Patent Grant
11196005
The invention relates to a blend containing an electron acceptor and an electron donor, the acceptor being an n-type semiconductor which is a small molecule that does not contain a fullerene moiety, the electron donor being a p-type semiconductor which is a conjugated copolymer comprising donor and acceptor units in random sequence, to a formulation containing such a blend, to the use of the blend in organic electronic (OE) devices, especially organic photovoltaic (OPV) devices, perovskite-based solar cell (PSC) devices, organic photodetectors (OPD) and organic light emitting diodes (OLED), and to OE, OPV, PSC, OPD and OLED devices comprising the blend.
In recent years, there has been development of organic semiconducting (OSC) materials in order to produce more versatile, lower cost electronic devices. Such materials find application in a wide range of devices or apparatus, including organic field effect transistors (OFETs), organic light emitting diodes (OLEDs), perovskite-based solar cell (PSC) devices, organic photodetectors (OPDs), organic photovoltaic (OPV) cells, sensors, memory elements and logic circuits to name just a few. The organic semiconducting materials are typically present in the electronic device in the form of a thin layer, for example of between 50 and 300 nm thickness.
One particular area of importance is organic photovoltaics (OPV). Conjugated polymers have found use in OPVs as they allow devices to be manufactured by solution-processing techniques such as spin casting, dip coating or ink jet printing. Solution processing can be carried out cheaper and on a larger scale compared to the evaporative techniques used to make inorganic thin film devices. Currently, polymer based photovoltaic devices are achieving efficiencies above 10%.
Organic photodetectors (OPDs) are a further particular area of importance, for which conjugated light-absorbing polymers offer the hope of allowing efficient devices to be produced by solution-processing technologies, such as spin casting, dip coating or ink jet printing, to name a few only.
The photosensitive layer in an OPV or OPD device is usually composed of at least two materials, a p-type semiconductor, which is typically a conjugated polymer, an oligomer or a defined molecular unit, and an n-type semiconductor, which is typically a fullerene or substituted fullerene, graphene, a metal oxide, or quantum dots.
However, the OSC materials disclosed in prior art for use in OE devices have several drawbacks. They are often difficult to synthesize or purify (fullerenes), and/or do not absorb light strongly in the near IR (infra-red) spectrum >700 nm. In addition, other OSC materials do not often form a favourable morphology and/or donor phase miscibility for use in organic photovoltaics or organic photodetectors.
Therefore there is still a need for OSC materials for use in OE devices like OPVs and OPDs, which have advantageous properties, in particular good processibility, high solubility in organic solvents, good structural organization and film-forming properties. In addition, the OSC materials should be easy to synthesize, especially by methods suitable for mass production. For use in OPV and OPD devices, the OSC materials should especially have a low bandgap, which enables improved light harvesting by the photoactive layer and can lead to higher cell efficiencies, high stability and long lifetime.
It was an aim of the present invention to provide new OSC compounds, especially n-type OSCs, which can overcome the drawbacks of the OSCs from prior art, and which provide one or more of the above-mentioned advantageous properties, especially easy synthesis by methods suitable for mass production, good processibility, high stability, long lifetime in OE devices, good solubility in organic solvents, high charge carrier mobility, and a low bandgap. Another aim of the invention was to extend the pool of OSC materials and n-type OSCs available to the expert. Other aims of the present invention are immediately evident to the expert from the following detailed description.
The inventors of the present invention have found that one or more of the above aims can be achieved by providing a blend as disclosed and claimed hereinafter, which contains as electron acceptor an n-type OSC small molecule that is not a fullerene, and as electron donor a p-type conjugated OSC copolymer that comprises donor and acceptor units in random sequence. The random copolymer can be prepared by the use of two or more, preferably three or more, distinct monomers, wherein the repeat units formed from the monomers are dispersed in random or statistical sequence along the polymer chain.
It has been found that such a blend can advantageously be used in the photoactive layer of an optoelectronic device, like for example an OPV or OPD, where it leads to improved properties.
In prior art OPV devices are known, using in the photoactive layer, a blend of an n-type or acceptor material that is a non-fullerene compound, and a p-type or donor that is a conjugated copolymer being prepared from two monomers and having in the polymer chain an alternating (-ABABAB-) sequence of repeating units A and B formed from these monomers, like for example in Adv. Sci., 2015, 2, 1500096; Energy Environ. Sci., 2015, 8, 610; Nature Communications DOI: 10.1038/ncomms11585; Adv. Mater. 2015, 27, 7299; J. Am. Chem. Soc. 2016, 138(13), 4657; Macromolecules, 2016, 49(8), 2993; J. Am. Chem. Soc. 2016, 138(9), 2973.
However, a blend as disclosed and claimed hereinafter, where the n-type OSC is a non-fullerene and the p-type OSC is a random polymer, for use in the photoactive layer of an optoelectronic device has hitherto not been disclosed in prior art.
The invention relates to a blend containing an n-type organic semiconducting (OSC) compound which does not contain a fullerene moiety, and further containing a p-type OSC compound which is a conjugated copolymer comprising donor and acceptor units that are distributed in random sequence along the polymer backbone.
The invention further relates to a blend as described above and below, further comprising one or more compounds having one or more of a semiconducting, hole or electron transport, hole or electron blocking, insulating, binding, electrically conducting, photoconducting, photoactive or light emitting property.
The invention further relates to a blend as described above and below, further comprising a binder, preferably an electrically inert binder, very preferably an electrically inert polymeric binder.
The invention further relates to a blend as described above and below, further comprising one or more n-type semiconductors, preferably selected from conjugated polymers, small molecules and fullerenes or fullerene derivatives.
The invention further relates to a bulk heterojunction (BHJ) formed from a blend as described above and below.
The invention further relates to the use of a blend as described above and below as semiconducting, charge transporting, electrically conducting, photoconducting, photoactive or light emitting material.
The invention further relates to the use of a blend as described above and below in an electronic or optoelectronic device, or in the component of an optoelectronic device, or in an assembly comprising an electronic or optoelectronic device.
The invention further relates to a semiconducting, charge transporting, electrically conducting, photoconducting, photoactive or light emitting material, comprising a blend as described above and below.
The invention further relates to an electronic or optoelectronic device, or a component thereof, or an assembly comprising it, which comprises a blend as described above and below.
The invention further relates to an electronic or optoelectronic device, or a component thereof, or an assembly comprising it, which comprises a semiconducting, charge transporting, electrically conducting, photoconducting or light emitting material as described above and below.
The invention further relates to a formulation comprising a blend as described above and below, and further comprising one or more solvents, preferably selected from organic solvents.
The invention further relates to the use of a formulation as described above and below for the preparation of an electronic or optoelectronic device or a component thereof.
The invention further relates to an electronic or optoelectronic device or a component thereof, which is obtained through the use of a formulation as described above and below.
The electronic or optoelectronic device includes, without limitation, organic field effect transistors (OFET), organic thin film transistors (OTFT), organic light emitting diodes (OLED), organic light emitting transistors (OLET), organic light emitting electrochemical cell (OLEC), organic photovoltaic devices (OPV), organic photodetectors (OPD), organic solar cells, dye-sensitized solar cells (DSSC), organic photoelectrochemical cells (OPEC), perovskite-based solar cell (PSC) devices, laser diodes, Schottky diodes, photoconductors, photodetectors and thermoelectric devices.
Preferred devices are OFETs, OTFTs, OPVs, PSCs, OPDs and OLEDs, in particular OPDs and BHJ OPVs or inverted BHJ OPVs.
The component of the electronic or optoelectronic device includes, without limitation, charge injection layers, charge transport layers, interlayers, planarising layers, antistatic films, polymer electrolyte membranes (PEM), conducting substrates and conducting patterns.
The assembly comprising an electronic or optoelectronic device includes, without limitation, integrated circuits (IC), radio frequency identification (RFID) tags, security markings, security devices, flat panel displays, backlights of flat panel displays, electrophotographic devices, electrophotographic recording devices, organic memory devices, sensor devices, biosensors and biochips.
In addition the blend as described above and below can be used as electrode materials in batteries, or in components or devices for detecting and discriminating DNA sequences.
As used herein, the term “polymer” will be understood to mean a molecule of high relative molecular mass, the structure of which essentially comprises multiple repetitions of units derived, actually or conceptually, from molecules of low relative molecular mass (Pure Appl. Chem., 1996, 68, 2291). The term “oligomer” will be understood to mean a molecule of intermediate relative molecular mass, the structure of which essentially comprises a small plurality of units derived, actually or conceptually, from molecules of lower relative molecular mass (Pure Appl. Chem., 1996, 68, 2291). In a preferred meaning as used herein present invention a polymer will be understood to mean a compound having >1, i.e. at least 2 repeat units, preferably ≥5, very preferably ≥10, repeat units, and an oligomer will be understood to mean a compound with >1 and <10, preferably <5, repeat units.
Further, as used herein, the term “polymer” will be understood to mean a molecule that encompasses a backbone (also referred to as “main chain”) of one or more distinct types of repeat units (the smallest constitutional unit of the molecule) and is inclusive of the commonly known terms “oligomer”, “copolymer”, “homopolymer”, “random polymer” and the like. Further, it will be understood that the term polymer is inclusive of, in addition to the polymer itself, residues from initiators, catalysts and other elements attendant to the synthesis of such a polymer, where such residues are understood as not being covalently incorporated thereto.
Further, such residues and other elements, while normally removed during post polymerization purification processes, are typically mixed or co-mingled with the polymer such that they generally remain with the polymer when it is transferred between vessels or between solvents or dispersion media.
As used herein, in a formula showing a polymer or a repeat unit, an asterisk (*) will be understood to mean a chemical linkage to an adjacent unit or to a terminal group in the polymer backbone. In a ring, like for example a benzene or thiophene ring, an asterisk (*) will be understood to mean a C atom that is fused to an adjacent ring.
As used herein, the terms “repeat unit”, “repeating unit” and “monomeric unit” are used interchangeably and will be understood to mean the constitutional repeating unit (CRU), which is the smallest constitutional unit the repetition of which constitutes a regular macromolecule, a regular oligomer molecule, a regular block or a regular chain (Pure Appl. Chem., 1996, 68, 2291). As further used herein, the term “unit” will be understood to mean a structural unit which can be a repeating unit on its own, or can together with other units form a constitutional repeating unit.
As used herein, the expression “copolymer formed from donor and acceptor that are distributed in random sequence along the polymer backbone”, hereinafter also abbreviated as “random copolymer” or “statistical copolymer” will be understood to mean a copolymer comprising two or more repeat units, herein a donor and an acceptor unit, which are chemically distinct, i.e. which are not isomers of each other, and which are distributed in irregular sequence, i.e. random sequence or statistical sequence or statistical block sequence, along the polymer backbone.
The random copolymers according to the present invention do also include copolymers formed by repeat units which contain more than one subunit, for example diads, triads, tetrads or pentads, wherein at least one of these subunits is selected from donor and acceptor units, and wherein at least one repeat unit contains a donor unit and at least one repeat unit contains an acceptor unit.
Such a random copolymer can for example be prepared by the use of two, three or more distinct monomers as exemplarily shown in the polymerisation reaction schemes R1-R4 below. Therein, A, B and C represent structural units, wherein for example one of A and B is a donor unit and the other is an acceptor unit, and C is for example a spacer unit, and X1 and X2 represent reactive groups of the monomers. The reactive groups X1,2 are selected such that X1 can only react with X2 but not with another group X1, and X2 can only react with X1 but not with another group X2. The polymer backbones shown on the right side as reaction product are only exemplarily chosen to illustrate a random sequence, other random sequences are also possible.
X1-A-X1+X1—B—X1+X2—C—X2→-AC-BC-AC-AC-BC—BC-AC-BC—BC—BC—BC— Scheme R1
In Scheme R1, due to the choice of reactive groups X1 and X2, the units A, B and C form diads “AC” and “BC” which are distributed in random sequence. The polymer backbone formed by the reaction as illustrated in scheme R1 is represented by the following formula
*-[(AC)x—(BC)y]n—*
wherein x is the molar ratio of diads AC, y is the molar ratio of diads BC, and n is the total number of diads AC and BC.
X1-A-X2+X1—B—X2+X1—C—X2→-A-B—B—C-A-A-C—B—B—C—C—B-A-A-B—C— Scheme R2
In Scheme R2 the units A, B and C are distributed in random sequence. The polymer backbone formed by the reaction as illustrated in scheme R2 is represented by the following formula
*-[(A)x-(B)y—(C)z]n—*
wherein x is the molar ratio of units A, y is the molar ratio of units B, z is the molar ratio of units B, and n is the total number of units A, B and C.
X1-A-X2+X1—B—X2→—B-A-A-A-B—B-A-B—B—B-A-A-B-A- Scheme R3
In Scheme R3 the units A and B are distributed in random sequence. The polymer backbone formed by the reaction as illustrated in scheme R3 is represented by the following formula
*-[(A)x-(B)y]n—*
wherein x is the molar ratio of units A, y is the molar ratio of units B, and n is the total number of units A and B.
X1-A1-X1+X1-A1-X1+X2-D-X2→-DA1-DA1-DA2-DA1-DA2-DA2-DA1-DA2- Scheme R4
In Scheme R4 A1 and A2 represent different acceptor units and D represents a donor unit. Due to the choice of reactive groups X1 and X2, the units A1, A2 and D form diads “DA1” and “DA2” which are distributed in random sequence. The polymer backbone formed by the reaction as illustrated in scheme R1 is represented by the following formula
*-[(DA1)x-(DA2)y]n-*
wherein x is the molar ratio of diads DA1, y is the molar ratio of diads DA2, and n is the total number of diads DA1 and DA2.
X1-D1-X1+X1-D1-X1+X2-A-X2→-AD1-AD1-AD2-AD1-AD2-AD2-AD1-AD2- Scheme R5
In Scheme R4 D1 and D2 represent different donor units and A represents a donor unit. Due to the choice of reactive groups X1 and X2, the units D1, D2 and A form diads “AD1” and “AD2” which are distributed in random sequence. The polymer backbone formed by the reaction as illustrated in scheme R1 is represented by the following formula
*-[(AD1)x-(AD2)y]n-*
wherein x is the molar ratio of diads AD1, y is the molar ratio of diads AD2, and n is the total number of diads AD1 and AD2.
X1-D-A1-D-C—X1+X2-A2-C—X2→-D-A1-D-C-A2-C-D-A1-D-C-D-A1-D-C— Scheme R6
In Scheme R4 A1 and A2 represent different acceptor units, D represents a donor unit and C represents a spacer unit. The units D, and A1 and C are combined in a first monomer (a tetrad), and the units A2 and C are combined in a second monomer (a diad). Due to the choice of reactive groups X1 and X2, the units form diads “D-A1-D-C” and “A2-C” which are distributed in random sequence. The polymer backbone formed by the reaction as illustrated in scheme R1 is represented by the following formula
*-[(D-A1-D-C)x-(A2-C)y]n—*
wherein x is the molar ratio of tetrads D-A1-D-C, y is the molar ratio of diads A2-C, and n is the total number of tetrads D-A1-D-C and diads A1-C.
As used herein, the term “alternating copolymer” will be understood to mean a polymer which is not a random or statistical copolymer, and wherein two or repeat units which are chemcially distinct, are arranged in alternating sequence along the polymer backbone.
An alternating copolymer can for example be prepared by the use of two, three or more distinct monomers as exemplarily shown in the polymerisation reaction schemes A1 and A2 below, wherein A, B, C, X1 and X2 have the meanings given above. The polymer backbones shown on the right side as reaction product are only exemplarily chosen to illustrate an alternating sequence, longer or shorter sequences are also possible.
X1-A-X1+X2—B—X2→-A-B-A-B-A-B-A-B— Scheme A1
In Scheme A1 the units A and B are arranged in alternating sequence. The polymer backbone formed by the reaction as illustrated in scheme A1 is represented by the following formula
*-[A-B]n—*
wherein n is the total number of units A and B.
X1-A-B—C—X2→-A-B—C-A-B—C-A-B—C-A-B—C— Scheme A2
In Scheme A2 the units A, B and C are arranged in alternating sequence. The polymer backbone formed by the reaction as illustrated in scheme A2 is represented by the following formula
*-[A-B—C]n—*
wherein n is the total number of units A, B and C in the polymer backbone.
From scheme A it can be seen that an alternating copolymer formed from three or more different structural units A, B and C typically requires the use of more complex monomers where two or more of these structural units are combined.
As used herein, the expressions “copolymer formed from donor and acceptor that are distributed in random sequence along the polymer backbone”, “random copolymer” and “statistical copolymer” are understood not to include copolymers which are alternating but non-regioregular, for example wherein donor units and/or acceptor units that are chemically identical but of asymmetric nature are arranged along the polymer backbone in alternating but non-regioregular manner, like for example the following polymers wherein n, x and y are as defined in formula Pi below.
As used herein, a “terminal group” will be understood to mean a group that terminates a polymer backbone. The expression “in terminal position in the backbone” will be understood to mean a divalent unit or repeat unit that is linked at one side to such a terminal group and at the other side to another repeat unit. Such terminal groups include endcap groups, or reactive groups that are attached to a monomer forming the polymer backbone which did not participate in the polymerisation reaction, like for example a group having the meaning of R22 or R23 as defined below.
As used herein, the term “endcap group” will be understood to mean a group that is attached to, or replacing, a terminal group of the polymer backbone. The endcap group can be introduced into the polymer by an endcapping process. Endcapping can be carried out for example by reacting the terminal groups of the polymer backbone with a monofunctional compound (“endcapper”) like for example an alkyl- or arylhalide, an alkyl- or arylstannane or an alkyl- or arylboronate. The endcapper can be added for example after the polymerisation reaction. Alternatively the endcapper can be added in situ to the reaction mixture before or during the polymerisation reaction. In situ addition of an endcapper can also be used to terminate the polymerisation reaction and thus control the molecular weight of the forming polymer. Typical endcap groups are for example H, phenyl and lower alkyl.
As used herein, the term “small molecule” will be understood to mean a monomeric compound which typically does not contain a reactive group by which it can be reacted to form a polymer, and which is designated to be used in monomeric form. In contrast thereto, the term “monomer” unless stated otherwise will be understood to mean a monomeric compound that carries one or more reactive functional groups by which it can be reacted to form a polymer.
As used herein, the terms “donor” or “donating”, unless stated otherwise, will be understood to mean an electron donor, and will be understood to mean a chemical entity that donates electrons to another compound or another group of atoms of a compound. See also International Union of Pure and Applied Chemistry, Compendium of Chemical Technology, Gold Book, Version 2.3.2, 19. Aug. 2012, pages 477 and 480.
As used herein, the terms “acceptor” or “accepting” will be understood to mean an electron acceptor. The terms “electron acceptor”, “electron accepting” and “electron withdrawing” will be used interchangeably and will be understood to mean a chemical entity that accepts electrons transferred to it from another compound or another group of atoms of a compound. See also International Union of Pure and Applied Chemistry, Compendium of Chemical Technology, Gold Book, Version 2.3.2, 19. Aug. 2012, pages 477 and 480.
As used herein, the term “n-type” or “n-type semiconductor” will be understood to mean an extrinsic semiconductor in which the conduction electron density is in excess of the mobile hole density, and the term “p-type” or “p-type semiconductor” will be understood to mean an extrinsic semiconductor in which mobile hole density is in excess of the conduction electron density (see also, J. Thewlis, Concise Dictionary of Physics, Pergamon Press, Oxford, 1973).
As used herein, the term “leaving group” will be understood to mean an atom or group (which may be charged or uncharged) that becomes detached from an atom in what is considered to be the residual or main part of the molecule taking part in a specified reaction (see also Pure Appl. Chem., 1994, 66, 1134).
As used herein, the term “conjugated” will be understood to mean a compound (for example a polymer) that contains mainly C atoms with sp2-hybridisation (or optionally also sp-hybridisation), and wherein these C atoms may also be replaced by hetero atoms. In the simplest case this is for example a compound with alternating C—C single and double (or triple) bonds, but is also inclusive of compounds with aromatic units like for example 1,4-phenylene. The term “mainly” in this connection will be understood to mean that a compound with naturally (spontaneously) occurring defects, or with defects included by design, which may lead to interruption of the conjugation, is still regarded as a conjugated compound.
As used herein, unless stated otherwise the molecular weight is given as the number average molecular weight Mn or weight average molecular weight MW, which is determined by gel permeation chromatography (GPC) against polystyrene standards in eluent solvents such as tetrahydrofuran, trichloromethane (TCM, chloroform), chlorobenzene or 1,2,4-trichloro-benzene. Unless stated otherwise, chlorobenzene is used as solvent. The degree of polymerization, also referred to as total number of repeat units, n, will be understood to mean the number average degree of polymerization given as n=Mn/MU, wherein Mn is the number average molecular weight and MU is the molecular weight of the single repeat unit, see J. M. G. Cowie, Polymers: Chemistry & Physics of Modern Materials, Blackie, Glasgow, 1991.
As used herein, the term “carbyl group” will be understood to mean any monovalent or multivalent organic moiety which comprises at least one carbon atom either without any non-carbon atoms (like for example —C≡C—), or optionally combined with at least one non-carbon atom such as B, N, O, S, P, Si, Se, As, Te or Ge (for example carbonyl etc.).
As used herein, the term “hydrocarbyl group” will be understood to mean a carbyl group that does additionally contain one or more H atoms and optionally contains one or more hetero atoms like for example B, N, O, S, P, Si, Se, As, Te or Ge.
As used herein, the term “hetero atom” will be understood to mean an atom in an organic compound that is not a H- or C-atom, and preferably will be understood to mean B, N, O, S, P, Si, Se, Sn, As, Te or Ge.
A carbyl or hydrocarbyl group comprising a chain of 3 or more C atoms may be straight-chain, branched and/or cyclic, and may include spiro-connected and/or fused rings.
Preferred carbyl and hydrocarbyl groups include alkyl, alkoxy, thioalkyl, alkylcarbonyl, alkoxycarbonyl, alkylcarbonyloxy and alkoxycarbonyloxy, each of which is optionally substituted and has 1 to 40, preferably 1 to 25, very preferably 1 to 18 C atoms, furthermore optionally substituted aryl or aryloxy having 6 to 40, preferably 6 to 25 C atoms, furthermore alkylaryloxy, arylcarbonyl, aryloxycarbonyl, arylcarbonyloxy and aryloxycarbonyloxy, each of which is optionally substituted and has 6 to 40, preferably 7 to 40 C atoms, wherein all these groups do optionally contain one or more hetero atoms, preferably selected from B, N, O, S, P, Si, Se, As, Te and Ge.
Further preferred carbyl and hydrocarbyl group include for example: a C1-C40 alkyl group, a C1-C40 fluoroalkyl group, a C1-C40 alkoxy or oxaalkyl group, a C2-C40 alkenyl group, a C2-C40 alkynyl group, a C3-C40 allyl group, a C4-C40 alkyldienyl group, a C4-C40 polyenyl group, a C2-C40 ketone group, a C2-C40 ester group, a C6-C18 aryl group, a C6-C40 alkylaryl group, a C6-C40 arylalkyl group, a C4-C40 cycloalkyl group, a C4-C40 cycloalkenyl group, and the like. Preferred among the foregoing groups are a C1-C20 alkyl group, a C1-C20 fluoroalkyl group, a C2-C20 alkenyl group, a C2-C20 alkynyl group, a C3-C20 allyl group, a C4-C20 alkyldienyl group, a C2-C20 ketone group, a C2-C20 ester group, a C6-C12 aryl group, and a C4-C20 polyenyl group, respectively.
Also included are combinations of groups having carbon atoms and groups having hetero atoms, like e.g. an alkynyl group, preferably ethynyl, that is substituted with a silyl group, preferably a trialkylsilyl group.
The carbyl or hydrocarbyl group may be an acyclic group or a cyclic group. Where the carbyl or hydrocarbyl group is an acyclic group, it may be straight-chain or branched. Where the carbyl or hydrocarbyl group is a cyclic group, it may be a non-aromatic carbocyclic or heterocyclic group, or an aryl or heteroaryl group.
A non-aromatic carbocyclic group as referred to above and below is saturated or unsaturated and preferably has 4 to 30 ring C atoms. A non-aromatic heterocyclic group as referred to above and below preferably has 4 to 30 ring C atoms, wherein one or more of the C ring atoms are optionally replaced by a hetero atom, preferably selected from N, O, P, S, Si and Se, or by a —S(O)— or —S(O)2— group. The non-aromatic carbo- and heterocyclic groups are mono- or polycyclic, may also contain fused rings, preferably contain 1, 2, 3 or 4 fused or unfused rings, and are optionally substituted with one or more groups L, wherein
L is selected from F, Cl, —CN, —NC, —NCO, —NCS, —OCN, —SCN, —R0, —OR0, —SR0, —C(═O)X0, —C(═O)R0, —C(═O)—OR0, —O—C(═O)—R0, —NH2, —NHR0, —NR0R00, —C(═O)NHR0, —C(═O)NR0R00, —SO3R0, —SO2R0, —OH, —NO2, —CF3, —SF5, or optionally substituted silyl, or carbyl or hydrocarbyl with 1 to 30, preferably 1 to 20 C atoms that is optionally substituted and optionally comprises one or more hetero atoms, wherein X0 is halogen, preferably F or Cl, and R0, R00 denote H or straight-chain or branched alkyl with 1 to 20, preferably 1 to 12 C atoms that is optionally fluorinated.
Preferably L is selected from F, —CN, R0, —OR0, —SR0, —C(═O)—R0, —C(═O)—OR0, —O—C(═O)—R0, —O—C(═O)—OR0, —C(═O)—NHR0 and —C(═O)—NR0R00.
Further preferably L is selected from F or alkyl, alkoxy, oxaalkyl, thioalkyl, fluoroalkyl, fluoroalkoxy, alkylcarbonyl, alkoxycarbonyl, with 1 to 12 C atoms, or alkenyl or alkynyl with 2 to 12 C atoms.
Preferred non-aromatic carbocyclic or heterocyclic groups are tetrahydrofuran, indane, pyran, pyrrolidine, piperidine, cyclopentane, cyclohexane, cycloheptane, cyclopentanone, cyclohexanone, dihydro-furan-2-one, tetrahydro-pyran-2-one and oxepan-2-one.
An aryl group as referred to above and below preferably has 4 to 30 ring C atoms, is mono- or polycyclic and may also contain fused rings, preferably contains 1, 2, 3 or 4 fused or unfused rings, and is optionally substituted with one or more groups L as defined above.
A heteroaryl group as referred to above and below preferably has 4 to 30 ring C atoms, wherein one or more of the C ring atoms are replaced by a hetero atom, preferably selected from N, O, S, Si and Se, is mono- or polycyclic and may also contain fused rings, preferably contains 1, 2, 3 or 4 fused or unfused rings, and is optionally substituted with one or more groups L as defined above.
An arylalkyl or heteroarylalkyl group as referred to above and below preferably denotes —(CH2)a-aryl or —(CH2)a-heteroaryl, wherein a is an integer from 1 to 6, preferably 1, and “aryl” and “heteroaryl” have the meanings given above and below. A preferred arylalkyl group is benzyl which is optionally substituted by L.
As used herein, “arylene” will be understood to mean a divalent aryl group, and “heteroarylene” will be understood to mean a divalent heteroaryl group, including all preferred meanings of aryl and heteroaryl as given above and below.
Preferred aryl and heteroaryl groups are phenyl in which, in addition, one or more CH groups may be replaced by N, naphthalene, thiophene, selenophene, thienothiophene, dithienothiophene, fluorene and oxazole, all of which can be unsubstituted, mono- or polysubstituted with L as defined above. Very preferred aryl and heteroaryl groups are selected from pyrrole, preferably N-pyrrole, furan, pyridine, preferably 2- or 3-pyridine, pyrimidine, pyridazine, pyrazine, triazole, tetrazole, pyrazole, imidazole, isothiazole, thiazole, thiadiazole, isoxazole, oxazole, oxadiazole, thiophene, preferably 2-thiophene, selenophene, preferably 2-selenophene, 2,5-dithiophene-2′,5′-diyl, thieno[3,2-b]thiophene, thieno[2,3-b]thiophene, furo[3,2-b]furan, furo[2,3-b]furan, seleno[3,2-b]selenophene, seleno[2,3-b]selenophene, thieno[3,2-b]selenophene, thieno[3,2-b]furan, indole, isoindole, benzo[b]furan, benzo[b]thiophene, benzo[1,2-b;4,5-b′]dithiophene, benzo[2,1-b;3,4-b′]dithiophene, quinole, 2-methylquinole, isoquinole, quinoxaline, quinazoline, benzotriazole, benzimidazole, benzothiazole, benzisothiazole, benzisoxazole, benzoxadiazole, benzoxazole, benzothiadiazole, 4H-cyclopenta[2,1-b;3,4-b′]dithiophene, 7H-3,4-dithia-7-sila-cyclopenta[a]pentalene, all of which can be unsubstituted, mono- or polysubstituted with L as defined above. Further examples of aryl and heteroaryl groups are those selected from the groups shown hereinafter.
An alkyl group or an alkoxy group, i.e., where the terminal CH2 group is replaced by —O—, can be straight-chain or branched. Particularly preferred straight chains have 2, 3, 4, 5, 6, 7, 8, 12 or 16 carbon atoms and accordingly denote preferably ethyl, propyl, butyl, pentyl, hexyl, heptyl, octyl, dodecyl or hexadecyl, ethoxy, propoxy, butoxy, pentoxy, hexoxy, heptoxy, octoxy, dodecoxy or hexadecoxy, furthermore methyl, nonyl, decyl, undecyl, tridecyl, tetradecyl, pentadecyl, nonoxy, decoxy, undecoxy, tridecoxy or tetradecoxy, for example.
An alkenyl group, i.e., wherein one or more CH2 groups are replaced by —CH═CH— can be straight-chain or branched. It is preferably straight-chain, has 2 to 10 C atoms and accordingly is preferably vinyl, prop-1-, or prop-2-enyl, but-1-, 2- or but-3-enyl, pent-1-, 2-, 3- or pent-4-enyl, hex-1-, 2-, 3-, 4- or hex-5-enyl, hept-1-, 2-, 3-, 4-, 5- or hept-6-enyl, oct-1-, 2-, 3-, 4-, 5-, 6- or oct-7-enyl, non-1-, 2-, 3-, 4-, 5-, 6-, 7- or non-8-enyl, dec-1-, 2-, 3-, 4-, 5-, 6-, 7-, 8- or dec-9-enyl.
Especially preferred alkenyl groups are C2-C7-1E-alkenyl, C4-C7-3E-alkenyl, C5-C7-4-alkenyl, C6-C7-5-alkenyl and C7-6-alkenyl, in particular C2-C7-1E-alkenyl, C4-C7-3E-alkenyl and C5-C7-4-alkenyl. Examples for particularly preferred alkenyl groups are vinyl, 1E-propenyl, 1E-butenyl, 1E-pentenyl, 1E-hexenyl, 1E-heptenyl, 3-butenyl, 3E-pentenyl, 3E-hexenyl, 3E-heptenyl, 4-pentenyl, 4Z-hexenyl, 4E-hexenyl, 4Z-heptenyl, 5-hexenyl, 6-heptenyl and the like. Groups having up to 5 C atoms are generally preferred.
An oxaalkyl group, i.e., where one CH2 group is replaced by —O—, can be straight-chain. Particularly preferred straight-chains are 2-oxapropyl (=methoxymethyl), 2-(=ethoxymethyl) or 3-oxabutyl (=2-methoxyethyl), 2-, 3-, or 4-oxapentyl, 2-, 3-, 4-, or 5-oxahexyl, 2-, 3-, 4-, 5-, or 6-oxaheptyl, 2-, 3-, 4-, 5-, 6- or 7-oxaoctyl, 2-, 3-, 4-, 5-, 6-, 7- or 8-oxanonyl or 2-, 3-, 4-, 5-6-,7-, 8- or 9-oxadecyl, for example.
In an alkyl group wherein one CH2 group is replaced by —O— and one CH2 group is replaced by —C(O)—, these radicals are preferably neighboured. Accordingly these radicals together form a carbonyloxy group —C(O)—O— or an oxycarbonyl group —O—C(O)—. Preferably this group is straight-chain and has 2 to 6 C atoms. It is accordingly preferably acetyloxy, propionyloxy, butyryloxy, pentanoyloxy, hexanoyloxy, acetyloxymethyl, propionyloxymethyl, butyryloxymethyl, pentanoyloxymethyl, 2-acetyloxyethyl, 2-propionyloxyethyl, 2-butyryloxyethyl, 3-acetyloxypropyl, 3-propionyloxypropyl, 4-acetyloxybutyl, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, butoxycarbonyl, pentoxycarbonyl, methoxycarbonylmethyl, ethoxycarbonylmethyl, propoxycarbonylmethyl, butoxycarbonylmethyl, 2-(methoxycarbonyl)ethyl, 2-(ethoxycarbonyl)ethyl, 2-(propoxycarbonyl)ethyl, 3-(methoxycarbonyl)propyl, 3-(ethoxycarbonyl)propyl, 4-(methoxycarbonyl)-butyl.
An alkyl group wherein two or more CH2 groups are replaced by —O— and/or —C(O)O— can be straight-chain or branched. It is preferably straight-chain and has 3 to 12 C atoms. Accordingly, it is preferably bis-carboxy-methyl, 2,2-bis-carboxy-ethyl, 3,3-bis-carboxy-propyl, 4,4-bis-carboxy-butyl, 5,5-bis-carboxy-pentyl, 6,6-bis-carboxy-hexyl, 7,7-bis-carboxy-heptyl, 8,8-bis-carboxy-octyl, 9,9-bis-carboxy-nonyl, 10,10-bis-carboxy-decyl, bis-(methoxycarbonyl)-methyl, 2,2-bis-(methoxycarbonyl)-ethyl, 3,3-bis-(methoxycarbonyl)-propyl, 4,4-bis-(methoxycarbonyl)-butyl, 5,5-bis-(methoxycarbonyl)-pentyl, 6,6-bis-(methoxycarbonyl)-hexyl, 7,7-bis-(methoxycarbonyl)-heptyl, 8,8-bis-(methoxycarbonyl)-octyl, bis-(ethoxycarbonyl)-methyl, 2,2-bis-(ethoxycarbonyl)-ethyl, 3,3-bis-(ethoxycarbonyl)-propyl, 4,4-bis-(ethoxycarbonyl)-butyl, 5,5-bis-(ethoxycarbonyl)-hexyl.
A thioalkyl group, i.e., where one CH2 group is replaced by —S—, is preferably straight-chain thiomethyl (—SCH3), 1-thioethyl (—SCH2CH3), 1-thiopropyl (=—SCH2CH2CH3), 1-(thiobutyl), 1-(thiopentyl), 1-(thiohexyl), 1-(thioheptyl), 1-(thiooctyl), 1-(thiononyl), 1-(thiodecyl), 1-(thioundecyl) or 1-(thiododecyl), wherein preferably the CH2 group adjacent to the sp2 hybridised vinyl carbon atom is replaced.
A fluoroalkyl group can either be perfluoroalkyl CiF2i+1, wherein i is an integer from 1 to 15, in particular CF3, C2F5, C3F7, C4F9, C5F11, C6F13, C7F15 or CO8F17, very preferably C6F13, or partially fluorinated alkyl, preferably with 1 to 15 C atoms, in particular 1,1-difluoroalkyl, all of the aforementioned being straight-chain or branched.
Preferably “fluoroalkyl” means a partially fluorinated (i.e. not perfluorinated) alkyl group.
Alkyl, alkoxy, alkenyl, oxaalkyl, thioalkyl, carbonyl and carbonyloxy groups can be achiral or chiral groups. Particularly preferred chiral groups are 2-butyl (=1-methylpropyl), 2-methylbutyl, 2-methylpentyl, 3-methylpentyl, 2-ethylhexyl, 2-butyloctyl, 2-hexyldecyl, 2-octyldodecyl, 3,7-dimethyloctyl, 3,7,11-trimethyldodecyl, 2-propylpentyl, in particular 2-methylbutyl, 2-methylbutoxy, 2-methylpentoxy, 3-methyl-pentoxy, 2-ethyl-hexoxy, 2-butyloctoxyo, 2-hexyldecoxy, 2-octyldodecoxy, 3,7-dimethyloctoxy, 3,7,11-trimethyldodecoxy, 1-methylhexoxy, 2-octyloxy, 2-oxa-3-methylbutyl, 3-oxa-4-methyl-pentyl, 4-methylhexyl, 2-hexyl, 2-octyl, 2-nonyl, 2-decyl, 2-dodecyl, 6-methoxy-octoxy, 6-methyloctoxy, 6-methyloctanoyloxy, 5-methylheptyloxy-carbonyl, 2-methylbutyryloxy, 3-methylvaleroyloxy, 4-methylhexanoyloxy, 2-chloro-propionyloxy, 2-chloro-3-methylbutyryloxy, 2-chloro-4-methyl-valeryl-oxy, 2-chloro-3-methylvaleryloxy, 2-methyl-3-oxapentyl, 2-methyl-3-oxa-hexyl, 1-methoxypropyl-2-oxy, 1-ethoxypropyl-2-oxy, 1-propoxypropyl-2-oxy, 1-butoxypropyl-2-oxy, 2-fluorooctyloxy, 2-fluorodecyloxy, 1,1,1-trifluoro-2-octyloxy, 1,1,1-trifluoro-2-octyl, 2-fluoromethyloctyloxy for example. Very preferred are 2-methylbutyl, 2-ethylhexyl, 2-butyloctyl, 2-hexyldecyl, 2-octyldodecyl, 3,7-dimethyloctyl, 3,7,11-trimethyldodecyl, 2-hexyl, 2-octyl, 2-octyloxy, 1,1,1-trifluoro-2-hexyl, 1,1,1-trifluoro-2-octyl and 1,1,1-trifluoro-2-octyloxy.
Preferred achiral branched groups are isopropyl, isobutyl (=methylpropyl), isopentyl (=3-methylbutyl), tert. butyl, isopropoxy, 2-methyl-propoxy, 3-methylbutoxy and 3,7-dimethyloctyl.
In a preferred embodiment, the substituents on an aryl or heteroaryl ring are independently of each other selected from primary, secondary or tertiary alkyl, alkoxy, oxaalkyl, thioalkyl, alkylcarbonyl or alkoxycarbonyl with 1 to 30 C atoms, wherein one or more H atoms are optionally replaced by F, or aryl, aryloxy, heteroaryl or heteroaryloxy that is optionally alkylated, alkoxylated, alkylthiolated or esterified and has 4 to 30 ring atoms. Further preferred substituents are selected from the group consisting of the following formulae
wherein RSub1-3 denotes L as defined above and below and where at least one group RSub1-3 is alkyl, alkoxy, oxaalkyl, thioalkyl, alkylcarbonyl or alkoxycarbonyl with 1 to 24 C atoms, preferably 1 to 20 C atoms, that is optionally fluorinated, and wherein the dashed line denotes the link to the ring to which these groups are attached. Very preferred among these substituents are those wherein all RSub1-3 subgroups are identical.
As used herein, if an aryl(oxy) or heteroaryl(oxy) group is “alkylated or alkoxylated”, this means that it is substituted with one or more alkyl or alkoxy groups having from 1 to 24 C-atoms and being straight-chain or branched and wherein one or more H atoms are optionally substituted by an F atom.
Above and below, Y1 and Y2 are independently of each other H, F, Cl or CN.
As used herein, —CO—, —C(═O)— and —C(O)— will be understood to mean a carbonyl group, i.e. a group having the structure
As used herein, C═CR1R2 etc. will be understood to mean a group having the structure
Unless stated otherwise “optionally substituted” without mentioning the substitutent means optionally substituted by L.
As used herein, “halogen” includes F, Cl, Br or I, preferably F, Cl or Br. A halogen atom that represents a substituent on a ring or chain is preferably F or Cl, very preferably F. A halogen atom that represents a reactive group in a monomer is preferably Cl, Br or I, very preferably Br or I.
Above and below, “mirror image” means a moiety that is obtainable from another moiety by flipping it vertically or horizontally across an external symmetry plane or a symmetry plane extending through the moiety. For example the moiety
also includes the mirror images
The blend as described above and below shows the following advantageous properties:
In the blend as described above and below, preferably the n-type OSC compound is not a polymer.
Preferably the n-type OSC compound is a monomeric or oligomeric compound, very preferably a small molecule, which does not contain a fullerene moiety.
Preferably the n-type OSC compound which does not contain a fullerene moiety contains a polycyclic electron donating core and attached thereto one or two terminal electron withdrawing groups, and is preferably selected of formula N below
wherein w is 0 or 1.
More preferably the n-type OSC compound is selected of formula NI
wherein the individual radicals, independently of each other and on each occurrence identically or differently, have the following meanings
wherein a group
is not adjacent to another group
Preferred compounds of formula NI are those wherein i is 1, 2 or 3, very preferably 1.
Further preferred compounds of formula NI are those wherein i is 0, preferably selected of formula I
wherein the individual radicals, independently of each other and on each occurrence identically or differently, have the meanings given in formula NI.
The invention further relates to novel compounds of formula I and its subformulae, novel synthesis methods for preparing them, and novel intermediates used therein.
In a preferred embodiment the compound of formula NI or I contains at least one group Ar1 that denotes
In another preferred embodiment the compound of formula NI or I contains at least one group Ar1 that denotes
In another preferred embodiment the compound of formula NI or I contains at least one group Ar1 that denotes
In another preferred embodiment the compound of formula NI or I contains at least one group Ar1 that denotes
and at least one group Ar1 that denotes
In another preferred embodiment the compound of formula NI or I contains at least one group Ar1 that denotes
at least one group Ar1 that denotes
and at least one group Ar1 that denotes
Preferred compounds of formula NI and I are selected of subformula IA
wherein RT1, RT1, Ar2, Ar3, Ar4, Ar5, a and b have the meanings given in formula NI,
Ar1A, Ar1B and Ar1C have, independently of each other, and on each occurrence identically or differently, one of the meanings given for Ar1 in formula NI,
m1 is 0 or an integer from 1 to 10,
a2 and a3 are each 0, 1, 2 or 3, and
m1+a2+a3≤10.
Preferred compounds of formula IA are those wherein a2 is 1 or 2 and/or a3 is 1 or 2.
Further preferred compounds of formula IA are those wherein
is selected from the following formulae
wherein W1, V1 and R5 to R7, independently of each other and on each occurrence identically or differently, have the meanings given above,
W2 and W3 have independently of each other one of the meanings given for W1 in formula NI,
Further preferred compounds of formula IA are those wherein
is selected from the following formulae
wherein W1-3, V1,2 and R5 to R7, independently of each other and on each occurrence identically or differently, have the meanings given above.
Very preferred compounds of formula IA are those wherein
is selected from the following formulae
wherein R3 and R5 to R7, independently of each other and on each occurrence identically or differently, have the meanings given above.
Further very preferred compounds of formula IA are those wherein
is selected from the following formulae
wherein R3 and R5 to R7, independently of each other and on each occurrence identically or differently, have the meanings given above.
Preferred groups Ar1, Ar1A, Ar1B and Ar1C in formula NI, I and IA are selected from the following formulae
wherein R1-3, R5-7 and Z1 are as defined above and below, R4 has one of the meanings given for R3, and Z2 has one of the meanings given for Z1.
Preferred groups Ar2 in formula NI, I and IA are selected from the following formulae
Preferred groups Ar3 in formula NI, I and IA are selected from the following formulae
wherein R1-7 are as defined above and below.
In the compounds of formula NI, I and IA Ar4 and Ar5 are preferably arylene or heteroarylene as defined above.
In another preferred embodiment the compounds of formula NI, I and IA have an asymmetric polycyclic core formed by the groups Ar1-3, or by the groups Ar1A-1C and Ar2-3, respectively.
Preferred compounds of this embodiment are compounds of formula IA wherein
are different from each other and are not a mirror image of each other.
Further preferred compounds of this embodiment are compounds of formula NI, I or IA wherein [Ar1]m or [Ar1A]m1 respectively form an asymmetric group, i.e. a group that has no intrinsic mirror plane.
Further preferred are compounds of formula NI, I and IA that contain at least one group Ar1A, Ar1B or Ar1C that denotes
wherein one or both of R5 and R6 denote an electron withdrawing group Z1 or Z2.
Preferred compounds of formula NI, I and IA are selected from the following subformulae
wherein the individual radicals, independently of each other and on each occurrence identically or differently, have the following meanings
Preferred groups Ar11-3 in formula I1 are selected from the following formulae and their mirror images:
wherein the individual radicals, independently of each other and on each occurrence identically or differently, have the following meanings
Very preferred groups Ar11-13 in formula I1 are selected from the following formulae and their mirror images:
wherein U1 and R5-10 have the meanings given above and below.
In the compounds of formula I2 Ar21 is preferably selected from the group consisting of benzene, naphthalene, anthracene, phenanthrene and pyrene, all of which are substituted by one or more identical or different groups R21.
R21 is preferably selected from H or straight-chain, branched or cyclic alkyl with 1 to 30, preferably 1 to 20, C atoms, in which one or more CH2 groups are optionally replaced by —O—, —S—, —NR0—, —SiR0R00—, —CR0═CR00— or —C≡C— in such a manner that O and/or S atoms are not linked directly to one another, wherein R0 and R00 have the meanings given in formula I2.
R21 is very preferably selected from H, straight-chain or branched alkyl with 1 to 30, preferably 1 to 20, C atoms, in which one or more CH2 groups are optionally replaced by —O—, —CR0═CR00— or —C≡C— in such a manner that O atoms are not linked directly to one another.
Preferred groups Ar21 in formula I2 are selected from the following formulae and their mirror images:
wherein the individual radicals, independently of each other and on each occurrence identically or differently, have the following meanings
Preferred groups Ar22 in formula I2 are selected from the following formulae and their mirror images:
wherein W1,2 and R57 are as defined above.
Preferred groups Ar26 in formula I2 are selected from the following formulae and their mirror images:
wherein W1, W2, R5, R6 and R7 have the meanings given above.
Preferred groups Ar23 in formula I2 are selected from the following formulae and their mirror images:
wherein W1, W2, R5-8 have the meanings given above and R9 has one of the meanings given for R5-8.
Very preferred groups Ar21 in formula I2 are selected from the following formulae and their mirror images:
wherein R21-26 have the meanings given above.
Very preferably Ar21 in formula I2 denotes
wherein R21 and R22 have the meanings given above.
Very preferred groups Ar22 in formula I2 are selected from the following formulae and their mirror images:
wherein R5-7 have the meanings given above.
Very preferred groups Ar26 in formula I2 are selected from the following formulae and their mirror images:
wherein R5-7 have the meanings given above and below.
Very preferred groups Ar23 in formula I2 are selected from the following formulae and their mirror images:
wherein R5-9 have the meanings given above.
Preferred compounds of formula I3 are those wherein W1 and W2 denote S or Se, very preferably S.
Further preferred compounds of formula I3 are those wherein W1 and W2 have the same meaning, and preferably both denote S or Se, very preferably S.
Further preferred compounds of formula I3 are those wherein W1 and W2 have different meaning, and preferably one denotes S and the other Se. Preferred groups Ar32-33 in formula I3 are selected from the following formulae and their mirror images:
wherein W1,2, V1, R5-7 are as defined above.
Very preferred groups Ar32 and Ar33 in formula I3 are selected from the following formulae and their mirror images:
wherein R5-9 have the meanings given above and below.
In the compounds of formula I4 Ar41 is preferably selected from the group consisting of benzene, naphthalene, anthracene, phenanthrene and pyrene, all of which are unsubstituted or substituted by one or more identical or different groups L.
In the compounds of formula I4 Ar6 and Ar7, if present, are preferably selected from the following formulae and their mirror images
wherein W2 and W3 have independently of each other one of the meanings of W1 in formula I, and preferably denote S, and R5-7 are as defined below.
In the compounds of formula I4 preferred groups Ar41-43 are selected from the following formulae and their mirror images:
wherein W1,2 and R5-10 are as defined above, and W3 has one of the meanings given for W1.
Very preferred groups Ar41-43 in formula I4 are selected from the following formulae and their mirror images:
wherein R5-10 have the meanings given above and below.
In the compounds of formula I5 Ar51 is preferably selected from the group consisting of benzene, naphthalene, anthracene, phenanthrene and pyrene, all of which are substituted by at least one, preferably at least two, groups Z1, and are optionally further substituted by one or more identical or different groups L or R1.
Preferred groups Ar51 in formula I5 are selected from the following formulae and their mirror images:
wherein the individual radicals, independently of each other and on each occurrence identically or differently, have the following meanings
More preferred groups Ar51 are selected from the following formula:
wherein Z1 and Z2 are, independently of each other and on each occurrence identically or differently, an electron withdrawing group.
Very preferred groups Ar51 are selected from the following formula:
wherein Z1 and Z2 are independently of each other, and on each occurrence identically or differently, an electron withdrawing group.
Preferred groups Ar52 and Ar53 in formula I5 are selected from the following formulae and their mirror images:
wherein W1,2, V1, R5-7 are as defined above.
Very preferred groups Ar52 and Ar53 in formula I5 are selected from the following formulae and their mirror images:
wherein R5-7 have the meanings given above and below.
In the compounds of formula NI, I, IA and I1-I5 and their subformulae Ar4, Ar5, Ar54 and Ar55 are preferably arylene or heteroarylene as defined above.
Preferred groups Ar4, Ar5, Ar54 and Ar55 in formula NI, I, IA and I1-I5 and their subformulae are selected from the following formulae and their mirror images:
wherein W1,2, V1,2 and R5 to R8, independently of each other and on each occurrence identically or differently, have the meanings given above, and
Very preferred groups Ar4, Ar5, Ar54 and Ar55 in formula NI, I, IA and I1-I5 and their subformulae are selected from the following formulae and their mirror images.
wherein X1, X2, X3 and X4 have one of the meanings given for R1 above and below, and preferably denote alkyl, alkoxy, carbonyl, carbonyloxy, CN, H, F or Cl.
Preferred formulae AR1, AR2, AR5, AR6, AR7, AR8, AR9, AR10 and AR11 are those containing at least one, preferably one, two or four substituents X1-4 selected from F and Cl, very preferably F.
Very preferred compounds of formula NI, I, IA and I1-I5 are selected from the following subformulae
wherein R1, R2, R3, R4, RT1, RT2, Ar4, Ar5, Z1, Z2, a and b have the meanings given above.
In the compounds of formula NI, I, IA and I1-I5 and their subformulae, the electron withdrawing groups Z1 and Z2 are preferably selected from the group consisting of F, Cl, Br, —NO2, —CN, —CF3, —CF2—R*, —SO2—R*, —SO3—R*, —C(═O)—H, —C(═O)—R*, —C(═S)—R*, —C(═O)—CF2—R*, —C(═O)—OR*, —C(═S)—OR*, —O—C(═O)—R*, —O—C(═S)—R*, —C(═O)—SR*, —S—C(═O)—R*, —C(═O)NR*R**, —NR*—C(═O)—R*, —CH═CH(CN), —CH═C(CN)2, —C(CN)═C(CN)2, —CH═C(CN)(Ra), CH═C(CN)—C(═O)—OR*, —CH═C(CO—OR*)2, —CH═C(CO—NR*R**)2, wherein
Ra is aryl or heteroaryl, each having from 4 to 30 ring atoms, optionally containing fused rings and being unsubstituted or substituted with one or more groups L as defined above, or Ra has one of the meanings of L,
R* and R** independently of each other denote alkyl with 1 to 20 C atoms which is straight-chain, branched or cyclic, and is unsubstituted, or substituted with one or more F or Cl atoms or CN groups, or perfluorinated, and in which one or more C atoms are optionally replaced by —O—, —S—, —C(═O)—, —C(═S)—, —SiR0R00—, —NR0R00—, —CHR0═CR00— or —C≡C— such that O- and/or S-atoms are not directly linked to each other, or R* and R** have one of the meanings given for Ra, and R0 and R00 are as defined above.
Preferably Z1 and Z2 denote F, Cl, Br, NO2, CN or CF3, very preferably F, Cl or CN, most preferably F.
In the compounds of formula NI, I, IA and I1-I5 and their subformulae, the groups RT1 and RT2 are preferably selected from H, F, Cl, Br, —NO2, —ON, —CF3, R*, —CF2—R*, —O—R*, —S—R*, —SO2—R*, —SO3—R*, —C(═O)—H, —C(═O)—R*, —C(═S)—R*, —C(═O)—CF2—R*, —C(═O)—OR*, —C(═S)—OR*, —O—C(═O)—R*, —O—C(═S)—R*, —C(═O)—SR*, —S—C(═O)—R*, —C(═O)NR*R**, —NR*—C(═O)—R*, —NHR*, —NR*R**, —CR*═CR*R**, —C≡C—R*, —C≡C—SiR*R**R***, —SiR*R**R***, —CH═CH(CN), —CH═C(CN)2, —C(CN)═C(CN)2, —CH═C(CN)(Ra), CH═C(CN)—C(═O)—OR*, —CH═C(CO—OR*)2, —CH═C(CO—NR*R**)2, and the group consisting of the following formulae
wherein the individual radicals, independently of each other and on each occurrence identically or differently, have the following meanings
Preferred compounds of formula NI, I, IA and I1-I5 and their subformulae are those wherein both of RT1 and RT2 denote an electron withdrawing group.
Preferred electron withdrawing groups RT1 and RT2 are selected from —CN, —C(═O)—OR*, —C(═S)—OR*, —CH═CH(CN), —CH═C(CN)2, —C(CN)═C(CN)2, —CH═C(CN)(Ra), CH═C(CN)—C(═O)—OR*, —CH═C(CO—OR*)2, and formulae T1-T54.
Very preferred groups RT1 and RT2 are selected from the following formulae
wherein L, L′, Ra r and s have the meanings given above and below. Preferably in these formulae L′ is H. Further preferably in these formulae r is 0.
The above formulae T1-T54 are meant to also include their respective E- or Z-stereoisomer with respect to the C═C bond in ca-position to the adjacent group Ar4 or Ar5, thus for example the group
may also denote
In the compounds of formula NI, I and its subformulae preferably R1-4 are different from H.
In a preferred embodiment of the present invention, R1-4 in formula NI, I and its subformulae are selected from F, Cl or straight-chain or branched alkyl, alkoxy, sulfanylalkyl, sulfonylalkyl, alkylcarbonyl, alkoxycarbonyl and alkylcarbonyloxy, each having 1 to 20 C atoms and being unsubstituted or substituted by one or more F atoms.
In another preferred embodiment of the present invention, R1-4 in formula NI, I and its subformulae are selected from mono- or polycyclic aryl or heteroaryl, each of which is optionally substituted with one or more groups L as defined in formula NI and I and has 4 to 30 ring atoms, and wherein two or more rings may be fused to each other or connected with each other by a covalent bond.
In a preferred embodiment of the present invention, R5-10 in formula NI, I and its subformulae are H.
In another preferred embodiment of the present invention, at least one of R5-10 in formula NI, I and its subformulae is different from H.
In a preferred embodiment of the present invention, R5-10 in formula NI, I and its subformulae, when being different from H, are selected from F, Cl or straight-chain or branched alkyl, alkoxy, sulfanylalkyl, sulfonylalkyl, alkylcarbonyl, alkoxycarbonyl and alkylcarbonyloxy, each having 1 to 20 C atoms and being unsubstituted or substituted by one or more F atoms.
In another preferred embodiment of the present invention, R5-10 in formula NI, I and its subformulae, when being different from H, are selected from aryl or heteroaryl, each of which is optionally substituted with one or more groups RS as defined in formula NI, I and has 4 to 30 ring atoms.
Preferred aryl and heteroaryl groups R1-10 are selected from the following formulae
wherein R11-17, independently of each other, and on each occurrence identically or differently, denote H or have one of the meanings of L or R1 as given above and below.
Very preferred aryl and heteroaryl groups R1-10 are selected from the following formulae
wherein R11-15 are as defined above. Most preferably R1-R10 are selected from formulae SUB7-SUB14 as defined above.
In another preferred embodiment one or more of R1-10 in the compounds of formula NI, I and its subformulae denote a straight-chain, branched or cyclic alkyl group with 1 to 50, preferably 2 to 50, very preferably 2 to 30, more preferably 2 to 24, most preferably 2 to 16 C atoms, in which one or more CH2 or CH3 groups are replaced by a cationic or anionic group.
The cationic group is preferably selected from the group consisting of phosphonium, sulfonium, ammonium, uronium, thiouronium, guanidinium or heterocyclic cations such as imidazolium, pyridinium, pyrrolidinium, triazolium, morpholinium or piperidinium cation.
Preferred cationic groups are selected from the group consisting of tetraalkylammonium, tetraalkylphosphonium, N-alkylpyridinium, N,N-dialkylpyrrolidinium, 1,3-dialkylimidazolium, wherein “alkyl” preferably denotes a straight-chain or branched alkyl group with 1 to 12 C atoms and very preferably is selected from formulae SUB1-6.
Further preferred cationic groups are selected from the group consisting of the following formulae
wherein R1′, R2′, R3′ and R4′ denote, independently of each other, H, a straight-chain or branched alkyl group with 1 to 12 C atoms or non-aromatic carbo- or heterocyclic group or an aryl or heteroaryl group, each of the aforementioned groups having 3 to 20, preferably 5 to 15, ring atoms, being mono- or polycyclic, and optionally being substituted by one or more identical or different substituents L as defined above, or denote a link to the respective group R1-10.
In the above cationic groups of the above-mentioned formulae any one of the groups R1′, R2′, R3′ and R4′ (if they replace a CH3 group) can denote a link to the respective group R1-10, or two neighbored groups R1′, R2′, R3′ or R4′ (if they replace a CH2 group) can denote a link to the respective group R1-10.
The anionic group is preferably selected from the group consisting of borate, imide, phosphate, sulfonate, sulfate, succinate, naphthenate or carboxylate, very preferably from phosphate, sulfonate or carboxylate.
In a preferred embodiment of the present invention the groups RT1 and RT2 in formula NI, I and its subformulae are selected from alkyl with 1 to 16 C atoms which is straight-chain, branched or cyclic, and is unsubstituted, substituted with one or more F or Cl atoms or CN groups, or perfluorinated, and in which one or more C atoms are optionally replaced by —O—, —S—, —C(O)—, —C(S)—, —SiR0R00—, —NR0R00—, —CHR0═CR00— or —C≡C-such that O- and/or S-atoms are not directly linked to each other.
Further preferred compounds of formula NI, I and its subformulae are selected from the following preferred embodiments or any combination thereof:
In another preferred embodiment of the present invention the n-type OSC compound which does not contain a fullerene moiety is a naphthalene or perylene derivative.
Preferred naphthalene or perylene derivatives for use as n-type OSC compounds are described for example in Adv. Sci. 2016, 3, 1600117, Adv. Mater. 2016, 28, 8546-8551, J. Am. Chem. Soc., 2016, 138, 7248-7251 and J. Mater. Chem. A, 2016, 4, 17604.
Preferred n-type OSC compounds of this preferred embodiment are selected from the following formulae
wherein the individual radicals, independently of each other and on each occurrence identically or differently, have the following meanings
In another preferred embodiment of the present invention the blend contains two or more n-type OSC compounds.
Preferred blends of this preferred embodiment contain two or more n-type OSC compounds which do not contain a fullerene moiety.
Very preferred blends of this preferred embodiment contain two or more n-type OSC compounds, at least one of which is a compound of formula NI, I, IA, I1-I5 or their subformulae.
Further very preferred blends of this preferred embodiment contain two or more n-type OSC compounds, at least one of which is a compound of formula NI, I, IA, I1-I5 or their subformulae, and at least one other of which is a naphthalene or perylene derivative as described above and below.
In another preferred embodiment of the present invention the blend contains two or more n-type OSC compounds, at least one of which does not contain a fullerene moiety, and is very preferably selected of formula NI, I, IA, I1-I5 or their subformulae, and at least one other of which is a fullerene or substituted fullerene.
The substituted fullerene is for example an indene-C60-fullerene bisadduct like ICBA, or a (6,6)-phenyl-butyric acid methyl ester derivatized methano C60 fullerene, also known as “PCBM-C60” or “C60PCBM”, as disclosed for example in G. Yu, J. Gao, J. C. Hummelen, F. Wudl, A. J. Heeger, Science 1995, Vol. 270, p. 1789 ff and having the structure shown below, or structural analogous compounds with e.g. a C61 fullerene group, a C70 fullerene group, or a C71 fullerene group, or an organic polymer (see for example Coakley, K. M. and McGehee, M. D. Chem. Mater. 2004, 16, 4533).
Preferably the polymer according to the present invention is blended with an n-type semiconductor such as a fullerene or substituted fullerene of formula Full-I to form the active layer in an OPV or OPD device wherein,
In the formula Full-I and its subformulae, k preferably denotes 1, 2, 3 or, 4, very preferably 1 or 2.
The fullerene Cn in formula Full-I and its subformulae may be composed of any number n of carbon atoms Preferably, in the compounds of formula XII and its subformulae the number of carbon atoms n of which the fullerene Cn is composed is 60, 70, 76, 78, 82, 84, 90, 94 or 96, very preferably 60 or 70.
The fullerene Cn in formula Full-I and its subformulae is preferably selected from carbon based fullerenes, endohedral fullerenes, or mixtures thereof, very preferably from carbon based fullerenes.
Suitable and preferred carbon based fullerenes include, without limitation, (C60-1h)[5,6]fullerene, (C70-D5h)[5,6]fullerene, (C76-D2*)[5,6]fullerene, (C84-D2*)[5,6]fullerene, (C84-D2d)[5,6]fullerene, or a mixture of two or more of the aforementioned carbon based fullerenes.
The endohedral fullerenes are preferably metallofullerenes. Suitable and preferred metallofullerenes include, without limitation, La@C60, La@C82, Y@C82, Sc3N@C80, Y3N@C80, Sc3C2@C80 or a mixture of two or more of the aforementioned metallofullerenes.
Preferably the fullerene Cn is substituted at a [6,6] and/or [5,6] bond, preferably substituted on at least one [6,6] bond.
Primary and secondary adduct, named “Adduct” in formula Full-I and its subformulae, is preferably selected from the following formulae
wherein
Preferred compounds of formula Full-I are selected from the following subformulae:
wherein
RS1, RS2, RS3, RS4 RS5 and RS6 independently of each other, and on each occurrence identically or differently, denote H or have one of the meanings of RS as defined above and below.
Most preferably the substituted fullerene is PCBM-C60, PCBM-C70, bis-PCBM-C60, bis-PCBM-C70, ICMA-c60 (1′,4′-dihydro-naphtho[2′,3′:1,2][5,6]fullerene-C60), ICBA, oQDM-C60 (1′,4′-dihydro-naphtho[2′,3′:1,9][5,6]fullerene-C60-lh), or bis-oQDM-C60.
In another preferred embodiment of the present invention, the blend further comprises one or more n-type OSC compounds selected from conjugated OSC polymers in addition or alternatively to the small molecules. Preferred OSC polymers are described, for example, in Acc. Chem. Res., 2016, 49 (11), pp 2424-2434 and WO2013142841 A1.
Preferred n-type conjugated OSC polymers for use in this preferred embodiment comprise one or more units derived from perylene or naphthalene are poly[[N,N′-bis(2-octyldodecyl)naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,5′-(2,2′-bithiophene)], poly[[N,N′-bis(2-hexyldecyl)naphthalene-1,4,5,8-bis(dicarboximide)-2,6-diyl]-alt-5,5′-thiophene].
In the blend as described above and below, the p-type OSC compound is a conjugated copolymer comprising donor and acceptor units that are distributed in random sequence along the polymer chain.
Preferably the donor and acceptor units are selected from arylene or heteroarylene that has from 5 to 20 ring atoms, is mono- or polycyclic, optionally contains fused rings, are is unsubstituted or substituted by one or more identical or different groups L as defined above.
Further preferably the conjugated copolymer additionally comprises one or more spacer units, which are selected from arylene or heteroarylene that has from 5 to 20 ring atoms, is mono- or polycyclic, optionally contains fused rings, is unsubstituted or substituted by one or more identical or different groups L as defined above, and wherein these spacer units are located between the donor and acceptor units such that a donor unit and an acceptor unit are not directly connected to each other.
In a preferred embodiment the conjugated p-type OSC polymer comprises one or more donor units selected from formula DA and DB
wherein
In another preferred embodiment the conjugated p-type OSC polymer comprises one or more acceptor units of formula AA
wherein X13 and X14 independently of each other denote CR11 or N and R11 has the meanings given in formula DA.
Preferred acceptor units of formula AA are selected from the following subformulae
wherein R denotes alkyl with 1 to 20 C atoms, preferably selected from formulae SUB1-6.
In another preferred embodiment the conjugated p-type OSC polymer comprises one or more spacer units of formula Sp1 and/or Sp6
wherein R11 and R12 have the meanings given in formula DA.
Preferably the conjugated p-type OSC polymer consists of donor units selected from formulae DA and DB, acceptor units selected from formula AA and its subformulae AA1-AA7, and one or more spacer units of formula Sp1-Sp6.
In another preferred embodiment the p-type OSC conjugated polymer comprises, very preferably consists of, one or more units selected from the following formulae
-(D-Sp)- U1
-(A-Sp)- U2
-(D-A)- U3
-(D)- U4
-(A)- U5
-(D-A-D-Sp)- U6
-(D-Sp-A-Sp)- U7
-(Sp-A-Sp)- U8
-(Sp-D-Sp)- U9
wherein D denotes, on each occurrence identically or differently, a donor unit, A denotes, on each occurrence identically or differently, an acceptor unit and Sp denotes, on each occurrence identically or differently, a spacer unit, all of which are selected from arylene or heteroarylene that has from 5 to 20 ring atoms, is mono- or polycyclic, optionally contains fused rings, are is unsubstituted or substituted by one or more identical or different groups L as defined above, and wherein the polymer contains at least one unit selected from formulae U1-U9 containing a unit D and at least one unit selected from formulae U1-U9 containing a unit A.
Preferably in formulae U1-U9 D is selected of formula DA or DB, A is selected of formula AA or AA1-AA6, and Sp is selected of formula Sp1.
Very preferred are conjugated polymers selected from the following formulae
-[(D-Sp)x-(A-Sp)y]n- Pi
-[(D-A)x-(Sp-A)y]n- Pii
-[(D-A1)x-(D-A2)y]n- Piii
-[(D1-A)x-(D2-A)y]n- Piv
-[(D)x-(Sp-A-Sp)y]n- Pv
-[(D-Sp1)x-(Sp1-A-Sp2)y]n- Pvi
-[(D-Sp-A1-Sp)x-(A2-Sp)y]n- Pvi
-[(D-Sp-A1-Sp)x-(D-A2)y]n- Pvii
-[(D-A1-D-Sp)x-(A2-Sp)y]n- Pviii
-[(D-Sp-A1-Sp)x-(D-Sp-A2-Sp)y]n- Pix
-[(D-A1)x-(Sp-A1)y-(D-Sp1-A2-Sp1)z-(Sp2-A2-Sp)xx]n- Px
-[(D1-A1)x-(D2-A1)y-(D1-A2)z-(D2-A2)xx]n- Pxi
wherein A, D and Sp are as defined in formula U1-U9, A1 and A2 are different acceptor units having one of the meanings of A, D1 and D2 are different donor units having one of the meanings of D, Sp1 and Sp2 are different spacer units having one of the meanings of Sp, x, y, z and xx denote the molar fraction of the respective unit and are each, independently of one another >0 and <1, with x+y+z+xx=1, and n is an integer >1.
In the polymers of formula Pi-Pxi and their subformulae, x, y, z and xx are preferably from 0.1 to 0.9, very preferably from 0.25 to 0.75, most preferably from 0.4 to 0.6.
Preferably in the conjugated polymers of formulae Pi-Pxi the donor units D, D1 and D2 are selected from formulae DA or DB.
Further preferably in the conjugated polymers of formulae Pi-Pxi the acceptor units A, A1 and A2 are selected from formula AA or AA1-AA7.
Further preferably in the conjugated p-type OSC polymer, including but not limited to the polymers of formulae Pi-Pxi, the donor units or units D, D1 and d2 are selected from the following formulae
wherein R11, R12, R13, R14, R15, R16, R17 and R18 independently of each other denote H or have one of the meanings of L or R1 as defined above and below.
Preferably the conjugated p-type OSC polymer contains one or more donor units selected from the group consisting of the formulae D1, D7, D10, D11, D19, D22, D29, D30, D35, D36, D37, D44, D55, D84, D87, D88, D89, D93, D106, D111, D119, D140, D141, D146 and D150.
Further preferably in the conjugated p-type OSC polymer, including but not limited to the polymers of formulae Pi-Pxi, the acceptor units or units A, A1 and A2 are selected from the following formulae
wherein R11, R12, R13, R14, R15 and R16 independently of each other denote H or have one of the meanings of L or R1 as defined above and below.
Preferably the conjugated p-type OSC polymer contains one or more acceptor units selected from the group consisting of the formulae A1, A5, A7, A15, A16, A20, A74, A88, A92, A94, A98, A99, A103 and A104.
Further preferably in the conjugated p-type OSC polymer, including but not limited to the polymers of formulae Pi-Pxi, the spacer units or units Sp, Sp1 and Sp2 are selected from the following formulae
wherein R11, R12, R13, R14 independently of each other denote H or have one of the meanings of L or R1 as defined above.
In the formulae Sp1 to Sp17 preferably R11 and R12 are H. In formula Sp18 preferably R11-14 are H or F.
Preferably the conjugated p-type OSC polymer contains one or more spacer units selected from the group consisting of formulae Sp1, Sp6, Sp11 and Sp14.
Preferably the conjugated p-type OSC polymer contains, preferably consists of
In another preferred embodiment the conjugated p-type OSC polymer comprises, preferably consists of
one or more, preferably one, two, three or four, distinct repeating units D, and
one or more, preferably one, two or three, distinct repeating units A.
Preferably the conjugated p-type OSC polymer according to this preferred embodiment contains from one to six, very preferably one, two, three or four distinct units D and from one to six, very preferably one, two, three or four distinct units A, wherein d1, d2, d3, d4, d5 and d6 denote the molar ratio of each distinct unit D, and a1, a2, a3, a4, a5 and a6 denote the molar ratio of each distinct unit A, and
each of d1, d2, d3, d4, d5 and d6 is from 0 to 0.6, and d1+d2+d3+d4+d5+d6 is from 0.2 to 0.8, preferably from 0.3 to 0.7, and
each of a1, a2, a3, a4, a5 and a6 is from 0 to 0.6, and a1+a2+a3+a4+a5+d6 is from 0.2 to 0.8, preferably from 0.3 to 0.7, and
d1+d2+d3+d4+d5+d6+a1+a2+a3+a4+a5+a6 is from 0.8 to 1, preferably 1.
Preferably the conjugated p-type OSC polymer according to this preferred embodiment contains, preferably consists of
In the above conjugated polymers, like those of formula Pi and Pii, the total number of repeating units n is preferably from 2 to 10,000. The total number of repeating units n is preferably ≥5, very preferably ≥10, most preferably ≥50, and preferably ≤500, very preferably ≤1,000, most preferably ≤2,000, including any combination of the aforementioned lower and upper limits of n.
Very preferred conjugated polymers comprise one or more of the following subformulae as one or more repeating unit
wherein R11-20 independently of each other, and on each occurrence identically or differently denote H or have one of the meanings of L or R as defined above, x, y, z, xx, yy, zz, xy and xz are each, independently of one another >0 and <1, with x+y+z+xx+yy+zz+xy+xz=1, n is an integer >1, and X1, X2, X3 and X4 denote H, F or Cl, and in formula P5 and P7 at least one of R13 and R14 is different from at least one of R15 and R16.
In the formulae P1-P49 preferably one or more of X1, X2, X3 and X4 denote F, very preferably all of X1, X2, X3 and X4 denote F or X1 and X2 denote H and X3 and X4 denote F.
In the formulae P1-P39 and P49, preferably R11 and R12, when being different from H, are independently of each other, and on each occurrence identically or differently selected from the following groups:
Further preferably R11 and R12, when being different from H, denote F or formulae SUB1-6 with 2 to 30, preferably 2 to 20, C atoms that is optionally fluorinated.
In the formulae P1-P39 and P49, preferably R15 and R16 are H, and R13 and R14 are different from H.
In the formulae P1-P39 and P49, preferably R13, R14, R15 and R16, when being different from H, are independently of each other, and on each occurrence identically or differently selected from the following groups:
Further preferably R13, R14, R15 and R16, when being different from H, independently of each other, and on each occurrence identically or differently denote a structure of formulae SUB1-6 with 2 to 30, preferably 2 to 20, C atoms that is optionally fluorinated.
In the formulae P1-P49, preferably R17, R18, R19 and R20 when being different from H, independently of each other, and on each occurrence identically or differently are selected from the following groups:
In the formulae P40-P48, preferably R11, R12, R13 and R14, are independently of each other, and on each occurrence identically or differently selected from the following groups:
Further preferably R11, R12, R13 and R14 independently of each other, and on each occurrence identically or differently denote a structure of formulae SUB1-6 with 2 to 30, preferably 2 to 20, C atoms that is optionally fluorinated.
Further preferred are conjugated p-type OSC polymers of formula PT
R31-chain-R32 PT
wherein “chain” denotes a polymer chain selected of formula Pi-Pix or P1-P49, and R31 and R32 have independently of each other one of the meanings of R11 as defined above, or denote, independently of each other, H, F, Br, Cl, I, —CH2Cl, —CHO, —CR′═CR″2, —SiR′R″R′″, —SiR′X′X″, —SiR′R″X′, —SnR′R″R′″, —BR′R″, —B(OR′)(OR″), —B(OH)2, —O—SO2—R′, —C≡CH, —C≡C—SiR′3, —ZnX′ or an endcap group, X′ and X″ denote halogen, R′, R″ and R′″ have independently of each other one of the meanings of R0 given in formula 1, and preferably denote alkyl with 1 to 12 C atoms, and two of R′, R″ and R′″ may also form a cyclosilyl, cyclostannyl, cycloborane or cycloboronate group with 2 to 20 C atoms together with the respective hetero atom to which they are attached.
Preferred endcap groups R31 and R32 are H, C1-20 alkyl, or optionally substituted C6-12 aryl or C2-10 heteroaryl, very preferably H, phenyl or thiophene.
In another preferred embodiment of the present invention, the blend in addition to the p-type OSC conjugated random polymer, further comprises one or more p-type OSC compounds selected from small molecules.
The compounds and conjugated polymers of the present invention can be synthesized according to or in analogy to methods that are known to the skilled person and are described in the literature. Other methods of preparation can be taken from the examples.
For example, the compounds of the present invention can be suitably prepared by aryl-aryl coupling reactions, such as Yamamoto coupling, Suzuki coupling, Stille coupling, Sonogashira coupling, Heck coupling or Buchwald coupling. The educts can be prepared according to methods which are known to the person skilled in the art.
Preferred aryl-aryl coupling methods used in the synthesis methods as described above and below are Yamamoto coupling, Kumada coupling, Negishi coupling, Suzuki coupling, Stille coupling, Sonogashira coupling, Heck coupling, C—H activation coupling, Ullmann coupling or Buchwald coupling. Especially preferred are Suzuki coupling, Negishi coupling, Stille coupling and Yamamoto coupling. Suzuki coupling is described for example in WO 00/53656 A1. Negishi coupling is described for example in J. Chem. Soc., Chem. Commun., 1977, 683-684. Yamamoto coupling is described in for example in T. Yamamoto et al., Prog. Polym. Sci., 1993, 17, 1153-1205, or WO 2004/022626 A1. Stille coupling is described for example in Z. Bao et al., J. Am. Chem. Soc., 1995, 117, 12426-12435 and C—H activation is described for example in M. Leclerc et al, Angew. Chem. Int. Ed., 2012, 51, 2068-2071. For example, when using Yamamoto coupling, educts having two reactive halide groups are preferably used.
When using Suzuki coupling, educts having two reactive boronic acid or boronic acid ester groups or two reactive halide groups are preferably used. When using Stille coupling, edcuts having two reactive stannane groups or two reactive halide groups are preferably used. When using Negishi coupling, educts having two reactive organozinc groups or two reactive halide groups are preferably used.
Preferred catalysts, especially for Suzuki, Negishi or Stille coupling, are selected from Pd(0) complexes or Pd(II) salts. Preferred Pd(0) complexes are those bearing at least one phosphine ligand such as Pd(Ph3P)4. Another preferred phosphine ligand is tris(ortho-tolyl)phosphine, i.e. Pd(o-Tol3P)4. Preferred Pd(II) salts include palladium acetate, i.e. Pd(OAc)2. Alternatively the Pd(0) complex can be prepared by mixing a Pd(0) dibenzylideneacetone complex, for example tris(dibenzyl-ideneacetone)dipalladium(0), bis(dibenzylideneacetone)palladium(0), or Pd(II) salts e.g. palladium acetate, with a phosphine ligand, for example triphenylphosphine, tris(ortho-tolyl)phosphine or tri(tert-butyl)phosphine. Suzuki coupling is performed in the presence of a base, for example sodium carbonate, potassium carbonate, cesium carbonate, lithium hydroxide, potassium phosphate or an organic base such as tetraethylammonium carbonate or tetraethylammonium hydroxide. Yamamoto coupling employs a Ni(0) complex, for example bis(1,5-cyclooctadienyl) nickel(0).
As alternatives to halogens as described above, leaving groups of formula —O—SO2Z0 can be used wherein Z0 is an alkyl or aryl group, preferably C1-10 alkyl or C6-12 aryl. Particular examples of such leaving groups are tosylate, mesylate and triflate.
Especially suitable and preferred synthesis methods of the n-type OSC compounds of formula NI, I, IA, I1-I5 and their subformulae are illustrated in the synthesis schemes shown hereinafter.
Novel methods of preparing compounds of formula NI, I, IA, I1-I5 and their subformulae as described above and below are another aspect of the invention.
The blend according to the present invention may also comprise one or more additional monomeric or polymeric compounds having charge-transport, semiconducting, electrically conducting, photoconducting and/or light emitting semiconducting properties, or for example having hole blocking or electron blocking properties for use as interlayers or charge blocking layers in PSCs or OLEDs.
Thus, another aspect of the invention relates to a blend as described above and below having one or more of a charge-transport, semiconducting, electrically conducting, photoconducting, hole blocking and electron blocking property.
The blend according to the present invention can be prepared from the single compounds and/or polymers by conventional methods that are described in prior art and known to the skilled person. Typically the compounds and/or polymers are mixed with each other or dissolved in suitable solvents and the solutions combined.
Another aspect of the invention relates to a formulation comprising a blend as described above and below and one or more organic solvents.
Preferred solvents are aliphatic hydrocarbons, chlorinated hydrocarbons, aromatic hydrocarbons, ketones, ethers and mixtures thereof. Additional solvents which can be used include 1,2,4-trimethylbenzene, 1,2,3,4-tetra-methyl benzene, pentylbenzene, mesitylene, cumene, cymene, cyclohexylbenzene, diethylbenzene, tetralin, decalin, 2,6-lutidine, 2-fluoro-m-xylene, 3-fluoro-o-xylene, 2-chlorobenzotrifluoride, N,N-dimethylformamide, 2-chloro-6-fluorotoluene, 2-fluoroanisole, anisole, 2,3-dimethylpyrazine, 4-fluoroanisole, 3-fluoroanisole, 3-trifluoro-methylanisole, 2-methylanisole, phenetol, 4-methylanisole, 3-methylanisole, 4-fluoro-3-methylanisole, 2-fluorobenzonitrile, 4-fluoroveratrol, 2,6-dimethylanisole, 3-fluorobenzo-nitrile, 2,5-dimethylanisole, 2,4-dimethylanisole, benzonitrile, 3,5-dimethyl-anisole, N,N-dimethylaniline, ethyl benzoate, 1-fluoro-3,5-dimethoxy-benzene, 1-methylnaphthalene, N-methylpyrrolidinone, 3-fluorobenzo-trifluoride, benzotrifluoride, dioxane, trifluoromethoxy-benzene, 4-fluorobenzotrifluoride, 3-fluoropyridine, toluene, 2-fluoro-toluene, 2-fluorobenzotrifluoride, 3-fluorotoluene, 4-isopropylbiphenyl, phenyl ether, pyridine, 4-fluorotoluene, 2,5-difluorotoluene, 1-chloro-2,4-difluorobenzene, 2-fluoropyridine, 3-chlorofluoro-benzene, 1-chloro-2,5-difluorobenzene, 4-chlorofluorobenzene, chloro-benzene, o-dichlorobenzene, 2-chlorofluorobenzene, p-xylene, m-xylene, o-xylene or mixture of o-, m-, and p-isomers. Solvents with relatively low polarity are generally preferred. For inkjet printing solvents and solvent mixtures with high boiling temperatures are preferred. For spin coating alkylated benzenes like xylene and toluene are preferred.
Examples of especially preferred solvents include, without limitation, dichloromethane, trichloromethane, chlorobenzene, o-dichlorobenzene, tetrahydrofuran, anisole, 2,4-dimethylanisole, 1-methylnaphthalene, morpholine, toluene, o-xylene, m-xylene, p-xylene, 1,4-dioxane, acetone, methylethylketone, 1,2-dichloroethane, 1,1,1-trichloroethane, 1,1,2,2-tetrachloroethane, ethyl acetate, n-butyl acetate, N,N-dimethylformamide, dimethylacetamide, dimethylsulfoxide, 1,5-dimethyltetraline, propiophenone, acetophenone, tetraline, 2-methylthiophene, 3-methylthiophene, decaline, indane, methyl benzoate, ethyl benzoate, mesitylene and/or mixtures thereof.
The total concentration of the solid compounds and polymers in the solution is preferably 0.1 to 10% by weight, more preferably 0.5 to 5% by weight. Optionally, the solution also comprises one or more binders to adjust the rheological properties, as described for example in WO 2005/055248 A1.
After the appropriate mixing and ageing, solutions are evaluated as one of the following categories: complete solution, borderline solution or insoluble. The contour line is drawn to outline the solubility parameter-hydrogen bonding limits dividing solubility and insolubility. ‘Complete’ solvents falling within the solubility area can be chosen from literature values such as published in “Crowley, J. D., Teague, G. S. Jr and Lowe, J. W. Jr., Journal of Paint Technology, 1966, 38 (496), 296”. Solvent blends may also be used and can be identified as described in “Solvents, W. H. Ellis, Federation of Societies for Coatings Technology, p 9-10, 1986”. Such a procedure may lead to a blend of ‘non’ solvents that will dissolve both the polymers of the present invention, although it is desirable to have at least one true solvent in a blend.
The blend according to the present invention can also be used in patterned OSC layers in the devices as described above and below. For applications in modern microelectronics it is generally desirable to generate small structures or patterns to reduce cost (more devices/unit area), and power consumption. Patterning of thin layers comprising a compound according to the present invention can be carried out for example by photolithography, electron beam lithography or laser patterning.
For use as thin layers in electronic or electrooptical devices the compounds, blends or formulations of the present invention may be deposited by any suitable method. Liquid coating of devices is more desirable than vacuum deposition techniques. Solution deposition methods are especially preferred. The formulations of the present invention enable the use of a number of liquid coating techniques. Preferred deposition techniques include, without limitation, dip coating, spin coating, ink jet printing, nozzle printing, letter-press printing, screen printing, gravure printing, doctor blade coating, roller printing, reverse-roller printing, offset lithography printing, dry offset lithography printing, flexographic printing, web printing, spray coating, curtain coating, brush coating, slot dye coating or pad printing.
Ink jet printing is particularly preferred when high resolution layers and devices needs to be prepared. Selected formulations of the present invention may be applied to prefabricated device substrates by ink jet printing or microdispensing. Preferably industrial piezoelectric print heads such as but not limited to those supplied by Aprion, Hitachi-Koki, InkJet Technology, On Target Technology, Picojet, Spectra, Trident, Xaar may be used to apply the organic semiconductor layer to a substrate. Additionally semi-industrial heads such as those manufactured by Brother, Epson, Konica, Seiko Instruments Toshiba TEC or single nozzle microdispensers such as those produced by Microdrop and Microfab may be used.
In order to be applied by ink jet printing or microdispensing, the compounds or polymers should be first dissolved in a suitable solvent. Solvents must fulfil the requirements stated above and must not have any detrimental effect on the chosen print head. Additionally, solvents should have boiling points >100° C., preferably >140° C. and more preferably >150° C. in order to prevent operability problems caused by the solution drying out inside the print head. Apart from the solvents mentioned above, suitable solvents include substituted and non-substituted xylene derivatives, di-C1-2-alkyl formamide, substituted and non-substituted anisoles and other phenol-ether derivatives, substituted heterocycles such as substituted pyridines, pyrazines, pyrimidines, pyrrolidinones, substituted and non-substituted N,N-di-C1-2-alkylanilines and other fluorinated or chlorinated aromatics.
A preferred solvent for depositing a blend according to the present invention by ink jet printing comprises a benzene derivative which has a benzene ring substituted by one or more substituents wherein the total number of carbon atoms among the one or more substituents is at least three. For example, the benzene derivative may be substituted with a propyl group or three methyl groups, in either case there being at least three carbon atoms in total. Such a solvent enables an ink jet fluid to be formed comprising the solvent with the compound or polymer, which reduces or prevents clogging of the jets and separation of the components during spraying. The solvent(s) may include those selected from the following list of examples: dodecylbenzene, 1-methyl-4-tert-butylbenzene, terpineol, limonene, isodurene, terpinolene, cymene, diethylbenzene. The solvent may be a solvent mixture, that is a combination of two or more solvents, each solvent preferably having a boiling point >100° C., more preferably >140° C. Such solvent(s) also enhance film formation in the layer deposited and reduce defects in the layer.
The ink jet fluid (that is mixture of solvent, binder and semiconducting compound) preferably has a viscosity at 20° C. of 1-100 mPa·s, more preferably 1-50 mPa·s and most preferably 1-30 mPa·s.
The blends and formulations according to the present invention can additionally comprise one or more further components or additives selected for example from surface-active compounds, lubricating agents, wetting agents, dispersing agents, hydrophobing agents, adhesive agents, flow improvers, defoaming agents, deaerators, diluents which may be reactive or non-reactive, auxiliaries, colourants, dyes or pigments, sensitizers, stabilizers, nanoparticles or inhibitors.
The blends according to the present invention are useful as charge transport, semiconducting, electrically conducting, photoconducting or light emitting materials in optical, electrooptical, electronic, electroluminescent or photoluminescent components or devices. In these devices, the compounds of the present invention are typically applied as thin layers or films.
Thus, the present invention also provides the use of the semiconducting blend or layer in an electronic device. The blend may be used as a high mobility semiconducting material in various devices and apparatus. The blend may be used, for example, in the form of a semiconducting layer or film. Accordingly, in another aspect, the present invention provides a semiconducting layer for use in an electronic device, the layer comprising a blend according to the invention. The layer or film may be less than about 30 microns. For various electronic device applications, the thickness may be less than about 1 micron thick. The layer may be deposited, for example on a part of an electronic device, by any of the aforementioned solution coating or printing techniques.
The invention additionally provides an electronic device comprising a blend or organic semiconducting layer according to the present invention. Especially preferred devices are OFETs, TFTs, ICs, logic circuits, capacitors, RFID tags, OLEDs, OLETs, OPEDs, OPVs, PSCs, OPDs, solar cells, laser diodes, photoconductors, photodetectors, electrophotographic devices, electrophotographic recording devices, organic memory devices, sensor devices, charge injection layers, Schottky diodes, planarising layers, antistatic films, conducting substrates and conducting patterns.
Especially preferred electronic device are OFETs, OLEDs, OPV, PSC and OPD devices, in particular PSC, OPD and bulk heterojunction (BHJ) OPV devices. In an OFET, for example, the active semiconductor channel between the drain and source may comprise the compound or composition of the invention. As another example, in an OLED device, the charge (hole or electron) injection or transport layer may comprise the blend of the invention.
The OPV or OPD device preferably further comprises a first transparent or semi-transparent electrode on a transparent or semi-transparent substrate on one side of the photoactive layer, and a second metallic or semi-transparent electrode on the other side of the photoactive layer.
Further preferably the OPV or OPD device comprises, between the photoactive layer and the first or second electrode, one or more additional buffer layers acting as hole transporting layer and/or electron blocking layer, which comprise a material such as metal oxide, like for example, ZTO, MoOx, NiOx, a conjugated polymer electrolyte, like for example PEDOT:PSS, a conjugated polymer, like for example polytriarylamine (PTAA), an insulating polymer, like for example nafion, polyethyleneimine or polystyrenesulphonate, an organic compound, like for example N,N′-diphenyl-N,N′-bis(1-naphthyl)(1,1′-biphenyl)-4,4′diamine (NPB), N,N′-diphenyl-N,N′-(3-methylphenyl)-1,1′-biphenyl-4,4′-diamine (TPD), or alternatively as hole blocking layer and/or electron transporting layer, which comprise a material such as metal oxide, like for example, ZnOx, TiOx, a salt, like for example LiF, NaF, CsF, a conjugated polymer electrolyte, like for example poly[3-(6-trimethylammoniumhexyl)thiophene], poly(9,9-bis(2-ethylhexyl)-fluorene]-b-poly[3-(6-trimethylammoniumhexyl)thiophene], or poly [(9,9-bis(3′-(N,N-dimethylamino)propyl)-2,7-fluorene)-alt-2,7-(9,9-dioctylfluorene)] or an organic compound, like for example tris(8-quinolinolato)-aluminium(III) (Alq3), 4,7-diphenyl-1,10-phenanthroline.
In a blend according to the present invention comprising a n-type OSC compound and a conjugated p-type polymer, the ratio polymer:compound is preferably from 5:1 to 1:5 by weight, more preferably from 3:1 to 1:3 by weight, most preferably 2:1 to 1:2 by weight.
The blend or formulation according to the present invention may also comprise a polymeric binder, preferably from 0.001 to 95% by weight. Examples of binder include polystyrene (PS), polydimethylsilane (PDMS), polypropylene (PP) and polymethylmethacrylate (PMMA).
A binder to be used in the blend or formulation as described before, which is preferably a polymer, may comprise either an insulating binder or a semiconducting binder, or mixtures thereof, may be referred to herein as the organic binder, the polymeric binder or simply the binder.
Preferably, the polymeric binder comprises a weight average molecular weight in the range of 1000 to 5,000,000 g/mol, especially 1500 to 1,000,000 g/mol and more preferable 2000 to 500,000 g/mol. Surprising effects can be achieved with polymers having a weight average molecular weight of at least 10000 g/mol, more preferably at least 100000 g/mol.
In particular, the polymer can have a polydispersity index Mw/Mn in the range of 1.0 to 10.0, more preferably in the range of 1.1 to 5.0 and most preferably in the range of 1.2 to 3.
Preferably, the inert binder is a polymer having a glass transition temperature in the range of −70 to 160° C., preferably 0 to 150° C., more preferably 50 to 140° C. and most preferably 70 to 130° C. The glass transition temperature can be determined by measuring the DSC of the polymer (DIN EN ISO 11357, heating rate 10° C. per minute).
The weight ratio of the polymeric binder to the OSC compound, like that of formula I, is preferably in the range of 30:1 to 1:30, particularly in the range of 5:1 to 1:20 and more preferably in the range of 1:2 to 1:10.
According to a preferred embodiment the binder preferably comprises repeating units derived from styrene monomers and/or olefin monomers. Preferred polymeric binders can comprise at least 80%, preferably 90% and more preferably 99% by weight of repeating units derived from styrene monomers and/or olefins.
Styrene monomers are well known in the art. These monomers include styrene, substituted styrenes with an alkyl substituent in the side chain, such as α-methylstyrene and α-ethylstyrene, substituted styrenes with an alkyl substituent on the ring such as vinyltoluene and p-methylstyrene, halogenated styrenes such as monochlorostyrenes, dichlorostyrenes, tribromostyrenes and tetrabromostyrenes.
Olefin monomers consist of hydrogen and carbon atoms. These monomers include ethylene, propylene, butylenes, isoprene and 1,3-butadiene.
According to a preferred embodiment of the present invention, the polymeric binder is polystyrene having a weight average molecular weight in the range of 50,000 to 2,000,000 g/mol, preferably 100,000 to 750,000 g/mol, more preferably in the range of 150,000 to 600,000 g/mol and most preferably in the range of 200,000 to 500,000 g/mol.
Further examples of suitable binders are disclosed for example in US 2007/0102696 A1. Especially suitable and preferred binders are described in the following.
The binder should preferably be capable of forming a film, more preferably a flexible film.
Suitable polymers as binders include poly(1,3-butadiene), polyphenylene, polystyrene, poly(α-methylstyrene), poly(α-vinylnaphtalene), poly(vinyltoluene), polyethylene, cis-polybutadiene, polypropylene, polyisoprene, poly(4-methyl-1-pentene), poly (4-methylstyrene), poly(chorotrifluoroethylene), poly(2-methyl-1,3-butadiene), poly(p-xylylene), poly(α-α-α′-α′tetrafluoro-p-xylylene), poly[1,1-(2-methyl propane)bis(4-phenyl)carbonate], poly(cyclohexyl methacrylate), poly(chlorostyrene), poly(2,6-dimethyl-1,4-phenylene ether), polyisobutylene, poly(vinyl cyclohexane), poly(vinylcinnamate), poly(4-vinylbiphenyl), 1,4-polyisoprene, polynorbornene, poly(styrene-block-butadiene); 31% wt styrene, poly(styrene-block-butadiene-block-styrene); 30% wt styrene, poly(styrene-co-maleic anhydride) (and ethylene/butylene) 1-1.7% maleic anhydride, poly(styrene-block-ethylene/butylene-block-styrene) triblock polymer 13% styrene, poly(styrene-block-ethylene-propylene-block-styrene) triblock polymer 37% wt styrene, poly(styrene-block-ethylene/butylene-block-styrene) triblock polymer 29% wt styrene, poly(1-vinylnaphthalene), poly(1-vinylpyrrolidone-co-styrene) 64% styrene, poly(1-vinylpyrrolidone-co-vinyl acetate) 1.3:1, poly(2-chlorostyrene), poly(2-vinylnaphthalene), poly(2-vinylpyridine-co-styrene) 1:1, poly(4,5-Difluoro-2,2-bis(CF3)-1,3-dioxole-co-tetrafluoroethylene) Teflon, poly(4-chlorostyrene), poly(4-methyl-1-pentene), poly(4-methylstyrene), poly(4-vinylpyridine-co-styrene) 1:1, poly(alpha-methylstyrene), poly(butadiene-graft-poly(methyl acrylate-co-acrylonitrile)) 1:1:1, poly(butyl methacrylate-co-isobutyl methacrylate) 1:1, poly(butyl methacrylate-co-methyl methacrylate) 1:1, poly(cyclohexylmethacrylate), poly(ethylene-co-1-butene-co-1-hexene) 1:1:1, poly(ethylene-co-ethylacrylate-co-maleic anhydride); 2% anhydride, 32% ethyl acrylate, poly(ethylene-co-glycidyl methacrylate) 8% glycidyl methacrylate, poly(ethylene-co-methyl acrylate-co-glycidyl meth-acrylate) 8% glycidyl metha-crylate 25% methyl acrylate, poly(ethylene-co-octene) 1:1, poly(ethylene-co-propylene-co-5-methylene-2-norbornene) 50% ethylene, poly(ethylene-co-tetrafluoroethylene) 1:1, poly(isobutyl methacrylate), poly(isobutylene), poly(methyl methacrylate)-co-(fluorescein O-methacrylate) 80% methyl methacrylate, poly(methyl methacrylate-co-butyl methacrylate) 85% methyl methacrylate, poly(methyl methacrylate-co-ethyl acrylate) 5% ethyl acrylate, poly(propylene-co-butene) 12% 1-butene, poly(styrene-co-allyl alcohol) 40% allyl alcohol, poly(styrene-co-maleic anhydride) 7% maleic anhydride, poly(styrene-co-maleic anhydride) cumene terminated (1.3:1), poly(styrene-co-methyl methacrylate) 40% styrene, poly(vinyltoluene-co-alpha-methylstyrene) 1:1, poly-2-vinylpyridine, poly-4-vinylpyridine, poly-alpha-pinene, polymethylmethacrylate, polybenzylmethacrylate, polyethylmethacrylate, polyethylene, polyethylene terephthalate, polyethylene-co-ethylacrylate 18% ethyl acrylate, polyethylene-co-vinylacetate 12% vinyl acetate, polyethylene-graft-maleic anhydride 0.5% maleic anhydride, polypropylene, polypropylene-graft-maleic anhydride 8-10% maleic anhydride, polystyrene poly(styrene-block-ethylene/butylene-block-styrene) graft maleic anhydride 2% maleic anhydride 1:1:1 others, poly(styrene-block-butadiene) branched 1:1, poly(styrene-block-butadiene-block-styrene), 30% styrene, poly(styrene-block-isoprene) 10% wt styrene, poly(styrene-block-isoprene-block-styrene) 17% wt styrene, poly(styrene-co-4-chloromethylstyrene-co-4-methoxymethylstyrene 2:1:1, polystyrene-co-acrylonitrile 25% acrylonitrile, polystyrene-co-alpha-methylstyrene 1:1, polystyrene-co-butadiene 4% butadiene, polystyrene-co-butadiene 45% styrene, polystyrene-co-chloromethylstyrene 1:1, polyvinylchloride, polyvinylcinnamate, polyvinylcyclohexane, polyvinylidenefluoride, polyvinylidenefluoride-co-hexafluoropropylene assume 1:1, poly(styrene-block-ethylene/propylene-block-styrene) 30% styrene, poly(styrene-block-ethylene/propylene-block-styrene) 18% styrene, poly(styrene-block-ethylene/propylene-block-styrene) 13% styrene, poly(styrene-block ethylene block-ethylene/propylene-block styrene) 32% styrene, poly(styrene-block ethylene block-ethylene/propylene-block styrene) 30% styrene, poly(styrene-block-ethylene/butylene-block-styrene) 31% styrene, poly(styrene-block-ethylene/butylene-block-styrene) 34% styrene, poly(styrene-block-ethylene/butylene-block-styrene) 30% styrene, poly(styrene-block-ethylene/butylene-block-styrene) 60%, styrene, branched or non-branched polystyrene-block-polybutadiene, polystyrene-block(polyethylene-ran-butylene)-block-polystyrene, polystyrene-block-polybutadiene-block-polystyrene, polystyrene-(ethylene-propylene)-diblock-copolymers (e.g. KRATON®-G1701E, Shell), poly(propylene-co-ethylene) and poly(styrene-co-methylmethacrylate).
Preferred insulating binders to be used in the formulations as described before are polystryrene, poly(α-methylstyrene), polyvinylcinnamate, poly(4-vinylbiphenyl), poly(4-methylstyrene), and polymethyl methacrylate. Most preferred insulating binders are polystyrene and polymethyl methacrylate.
The binder can also be selected from crosslinkable binders, like e.g. acrylates, epoxies, vinylethers, thiolenes etc. The binder can also be mesogenic or liquid crystalline.
The organic binder may itself be a semiconductor, in which case it will be referred to herein as a semiconducting binder. The semiconducting binder is still preferably a binder of low permittivity as herein defined. Semiconducting binders for use in the present invention preferably have a number average molecular weight (Mn) of at least 1500-2000, more preferably at least 3000, even more preferably at least 4000 and most preferably at least 5000. The semiconducting binder preferably has a charge carrier mobility of at least 10−5 cm2V−1s−11, more preferably at least 10−4 cm2V−1 s−1.
A preferred semiconducting binder comprises a homo-polymer or copolymer (including block-copolymer) containing arylamine (preferably triarylamine).
To produce thin layers in BHJ OPV devices the blends and formulations of the present invention may be deposited by any suitable method. Liquid coating of devices is more desirable than vacuum deposition techniques. Solution deposition methods are especially preferred. The formulations of the present invention enable the use of a number of liquid coating techniques. Preferred deposition techniques include, without limitation, dip coating, spin coating, ink jet printing, nozzle printing, letter-press printing, screen printing, gravure printing, doctor blade coating, roller printing, reverse-roller printing, offset lithography printing, dry offset lithography printing, flexographic printing, web printing, spray coating, curtain coating, brush coating, slot dye coating or pad printing. For the fabrication of OPV devices and modules area printing method compatible with flexible substrates are preferred, for example slot dye coating, spray coating and the like.
Suitable solutions or formulations containing the blend of an n-type OSC compound and a conjugated p-type polymer must be prepared. In the preparation of formulations, suitable solvent must be selected to ensure full dissolution of both component, p-type and n-type and take into account the boundary conditions (for example rheological properties) introduced by the chosen printing method.
Organic solvents are generally used for this purpose. Typical solvents can be aromatic solvents, halogenated solvents or chlorinated solvents, including chlorinated aromatic solvents. Examples include, but are not limited to chlorobenzene, 1,2-dichlorobenzene, chloroform, 1,2-dichloroethane, dichloromethane, carbon tetrachloride, toluene, cyclohexanone, ethylacetate, tetrahydrofuran, anisole, 2,4-dimethylanisole, 1-methylnaphthalene, morpholine, toluene, o-xylene, m-xylene, p-xylene, 1,4-dioxane, acetone, methylethylketone, 1,2-dichloroethane, 1,1,1-trichloroethane, 1,1,2,2-tetrachloroethane, ethyl acetate, n-butyl acetate, N,N-dimethylformamide, dimethylacetamide, dimethylsulfoxide, 1,5-dimethyltetraline, propiophenone, acetophenone, tetraline, 2-methylthiophene, 3-methylthiophene, decaline, indane, methyl benzoate, ethyl benzoate, mesitylene and combinations thereof.
The OPV device can for example be of any type known from the literature (see e.g. Waldauf et al., Appl. Phys. Lett., 2006, 89, 233517).
A first preferred OPV device according to the invention comprises the following layers (in the sequence from bottom to top):
A second preferred OPV device according to the invention is an inverted OPV device and comprises the following layers (in the sequence from bottom to top):
In the OPV devices of the present invention the p-type and n-type semiconductor materials are preferably selected from the materials, like the compound/polymer/fullerene systems, as described above
When the photoactive layer is deposited on the substrate, it forms a BHJ that phase separates at nanoscale level. For discussion on nanoscale phase separation see Dennler et al, Proceedings of the IEEE, 2005, 93 (8), 1429 or Hoppe et al, Adv. Func. Mater, 2004, 14(10), 1005. An optional annealing step may be then necessary to optimize blend morpohology and consequently OPV device performance.
Another method to optimize device performance is to prepare formulations for the fabrication of OPV(BHJ) devices that may include high boiling point additives to promote phase separation in the right way. 1,8-Octanedithiol, 1,8-diiodooctane, nitrobenzene, chloronaphthalene, and other additives have been used to obtain high-efficiency solar cells. Examples are disclosed in J. Peet, et al, Nat. Mater., 2007, 6, 497 or Frechet et al. J. Am. Chem. Soc., 2010, 132, 7595-7597.
Another preferred embodiment of the present invention relates to the use of a blend according to the present invention as dye, hole transport layer, hole blocking layer, electron transport layer and/or electron blocking layer in a DSSC or a PSC, and to a DSSC or PSC comprising a blend according to the present invention.
DSSCs and PSCs can be manufactured as described in the literature, for example in Chem. Rev. 2010, 110, 6595-6663, Angew. Chem. Int. Ed. 2014, 53, 2-15 or in WO2013171520A1
A preferred OE device according to the invention is a solar cell, preferably a PSC, comprising the light absorber which is at least in part inorganic as described below.
In a solar cell comprising the light absorber according to the invention there are no restrictions per se with respect to the choice of the light absorber material which is at least in part inorganic.
The term “at least in part inorganic” means that the light absorber material may be selected from metalorganic complexes or materials which are substantially inorganic and possess preferably a crystalline structure where single positions in the crystalline structure may be allocated by organic ions.
Preferably, the light absorber comprised in the solar cell according to the invention has an optical band-gap ≤2.8 eV and ≥0.8 eV.
Very preferably, the light absorber in the solar cell according to the invention has an optical band-gap ≤2.2 eV and ≥1.0 eV.
The light absorber used in the solar cell according to the invention does preferably not contain a fullerene. The chemistry of fullerenes belongs to the field of organic chemistry. Therefore fullerenes do not fulfil the definition of being “at least in part inorganic” according to the invention.
Preferably, the light absorber which is at least in part inorganic is a material having perovskite structure or a material having 2D crystalline perovskite structure.
The term “perovskite” as used above and below denotes generally a material having a perovskite crystalline structure or a 2D crystalline perovskite structure.
The term perovskite solar cell (PSC) means a solar cell comprising a light absorber which is a material having perovskite structure or a material having 2D crystalline perovskite structure.
The light absorber which is at least in part inorganic is without limitation composed of a material having perovskite crystalline structure, a material having 2D crystalline perovskite structure (e.g. CrystEngComm, 2010, 12, 2646-2662), Sb2S3 (stibnite), Sb2(SxSe(x-1))3, PbSxSe(x-1), CdSxSe(x-1), ZnTe, CdTe, ZnSxSe(x-1), InP, FeS, FeS2, Fe2S3, Fe2SiS4, Fe2GeS4, Cu2S, CuInGa, CuIn(SexS(1-x))2, Cu3SbxBi(x-1), (SySe(y-1))3, Cu2SnS3, SnSxSe(x-1), Ag2S, AgBiS2, BiSI, BiSeI, Bi2(SxSe(x-1))3, BiS(1-x)SexI, WSe2, AlSb, metal halides (e.g. BiI3, Cs2SnI6), chalcopyrite (e.g. CuInxGa(1-x)(SySe(1-y))2), kesterite (e.g. Cu2ZnSnS4, Cu2ZnSn(SexS(1-x))4, Cu2Zn(Sn1-xGex)S4) and metal oxide (e.g. CuO, Cu2O) or a mixture thereof.
Preferably, the light absorber which is at least in part inorganic is a perovskite.
In the above definition for light absorber, x and y are each independently defined as follows: (0≤x≤1) and (0≤y≤1).
Very preferably, the light absorber is a special perovskite namely a metal halide perovskite as described in detail above and below. Most preferably, the light absorber is an organic-inorganic hybrid metal halide perovskite contained in the perovskite solar cell (PSC).
In one particularly preferred embodiment of the invention, the perovskite denotes a metal halide perovskite with the formula ABX3,
where
Preferably, the monovalent organic cation of the perovskite is selected from alkylammonium, wherein the alkyl group is straight chain or branched having 1 to 6 C atoms, formamidinium or guanidinium or wherein the metal cation is selected from K+, Cs+ or Rb+.
Suitable and preferred divalent cations B are Ge2+, Sn2+ or Pb2+.
Suitable and preferred perovskite materials are CsSnI3, CH3NH3Pb(I1-xClx)3, CH3NH3PbI3, CH3NH3Pb(I1-xBrx)3, CH3NH3Pb(I1-x(BF4)x)3, CH3NH3Sn(I1-xClx)3, CH3NH3SnI3 or CH3NH3Sn(I1-xBrx)3 wherein x is each independently defined as follows: (0≤x≤1).
Further suitable and preferred perovskites may comprise two halides corresponding to formula Xa(3-x)Xb(x), wherein Xa and Xb are each independently selected from Cl, Br, or I, and x is greater than 0 and less than 3.
Suitable and preferred perovskites are also disclosed in WO 2013/171517, claims 52 to 71 and claims 72 to 79, which is entirely incorporated herein by reference. The materials are defined as mixed-anion perovskites comprising two or more different anions selected from halide anions and chalcogenide anions. Preferred perovskites are disclosed on page 18, lines 5 to 17. As described, the perovskite is usually selected from CH3NH3PbBrI2, CH3NH3PbBrCl2, CH3NH3PbIBr2, CH3NH3PbICl2, CH3NH3SnF2Br, CH3NH3SnF2I and (H2N═CH—NH2)PbI3zBr3(1-z), wherein z is greater than 0 and less than 1.
The invention further relates to a solar cell comprising the light absorber, preferably a PSC, as described above and below, wherein the blend according to the present invention is employed as a layer between one electrode and the light absorber layer.
The invention further relates to a solar cell comprising the light absorber, preferably a PSC, as described above and below, wherein the blend according to the present invention is comprised in an electron-selective layer.
The electron selective layer is defined as a layer providing a high electron conductivity and a low hole conductivity favoring electron-charge transport.
The invention further relates to a solar cell comprising the light absorber, preferably a PSC, as described above and below, wherein the blend according to the present invention is employed as electron transport material (ETM) or as hole blocking material as part of the electron selective layer.
Preferably, the blend according to the present invention is employed as electron transport material (ETM).
In an alternative preferred embodiment, the blend according to the present invention is employed as hole blocking material.
The device architecture of a PSC device according to the invention can be of any type known from the literature.
A first preferred device architecture of a PSC device according to the invention comprises the following layers (in the sequence from bottom to top):
A second preferred device architecture of a PSC device according to the invention comprises the following layers (in the sequence from bottom to top):
To produce electron selective layers in PSC devices according to the invention, the compounds of formula I, optionally together with other compounds or additives in the form of blends or mixtures, may be deposited by any suitable method. Liquid coating of devices is more desirable than vacuum deposition techniques. Solution deposition methods are especially preferred. Formulations comprising the compounds of formula NI and I enable the use of a number of liquid coating techniques. Preferred deposition techniques include, without limitation, dip coating, spin coating, ink jet printing, nozzle printing, letter-press printing, screen printing, gravure printing, doctor blade coating, roller printing, reverse-roller printing, offset lithography printing, dry offset lithography printing, flexographic printing, web printing, spray coating, curtain coating, brush coating, slot die coating or pad printing. For the fabrication of PSC devices and modules, deposition techniques for large area coating are preferred, for example slot die coating or spray coating.
Formulations that can be used to produce electron selective layers in optoelectronic devices according to the invention, preferably in PSC devices comprise one or more compounds of formula NI or I or preferred embodiments as described above in the form of blends or mixtures optionally together with one or more further electron transport materials and/or hole blocking materials and/or binders and/or other additives as described above and below, and one or more solvents.
The formulation may include or comprise, essentially consist of or consist of the said necessary or optional constituents as described above or below. All compounds or components which can be used in the formulations are either known or commercially available, or can be synthesised by known processes.
The formulation as described before may be prepared by a process which comprises:
In step (i) the solvent may be a single solvent for the n-type and p-type compounds and the organic binder and/or further electron transport material may each be dissolved in a separate solvent followed by mixing the resultant solutions to mix the compounds.
Alternatively, the binder may be formed in situ by mixing or dissolving an n-type and p-type compound in a precursor of a binder, for example a liquid monomer, oligomer or crosslinkable polymer, optionally in the presence of a solvent, and depositing the mixture or solution, for example by dipping, spraying, painting or printing it, on a substrate to form a liquid layer and then curing the liquid monomer, oligomer or crosslinkable polymer, for example by exposure to radiation, heat or electron beams, to produce a solid layer. If a preformed binder is used it may be dissolved together with the compound formula NI or I in a suitable solvent as described before, and the solution deposited for example by dipping, spraying, painting or printing it on a substrate to form a liquid layer and then removing the solvent to leave a solid layer. It will be appreciated that solvents are chosen which are able to dissolve all ingredients of the formulation, and which upon evaporation from the solution blend give a coherent defect free layer.
Besides the said components, the formulation as described before may comprise further additives and processing assistants. These include, inter alia, surface-active substances (surfactants), lubricants and greases, additives which modify the viscosity, additives which increase the conductivity, dispersants, hydrophobicising agents, adhesion promoters, flow improvers, antifoams, deaerating agents, diluents, which may be reactive or unreactive, fillers, assistants, processing assistants, dyes, pigments, stabilisers, sensitisers, nanoparticles and inhibitors.
Additives can be used to enhance the properties of the electron selective layer and/or the properties of any of the neighbouring layers and/or the performance of the optoelectronic device according to the invention. Additives can also be used to facilitate the deposition, the processing or the formation of the electron selective layer and/or the deposition, the processing or the formation of any of the neighbouring layers. Preferably, one or more additives are used which enhance the electrical conductivity of the electron selective layer and/or passivate the surface of any of the neighbouring layers.
Suitable methods to incorporate one or more additives include, for example exposure to a vapor of the additive at atmospheric pressure or at reduced pressure, mixing a solution or solid containing one or more additives and a material or a formulation as described or preferably described before, bringing one or more additives into contact with a material or a formulation as described before, by thermal diffusion of one or more additives into a material or a formulation as described before, or by ion-implantantion of one or more additives into a material or a formulation as described before.
Additives used for this purpose can be organic, inorganic, metallic or hybrid materials. Additives can be molecular compounds, for example organic molecules, salts, ionic liquids, coordination complexes or organometallic compounds, polymers or mixtures thereof. Additives can also be particles, for example hybrid or inorganic particles, preferably nanoparticles, or carbon based materials such as fullerenes, carbon nanotubes or graphene flakes.
Examples for additives that can enhance the electrical conductivity are for example halogens (e.g. I2, Cl2, Br2, ICI, ICI3, IBr and IF), Lewis acids (e.g. PF5, AsF5, SbF5, BF3, BCl3, SbCl5, BBr3 and SO3), protonic acids, organic acids, or amino acids (e.g. HF, HCl, HNO3, H2SO4, HClO4, FSO3H and ClSO3H), transition metal compounds (e.g. FeCl3, FeOCl, Fe(ClO4)3, Fe(4-CH3C6H4SO3)3, TiCl4, ZrCl4, HfCl4, NbF5, NbCl5, TaCl5, MoF5, MoCl5, WF5, WCl6, UF6 and LnCl3 (wherein Ln is a lanthanoid)), anions (e.g. Cl−, Br−, I−, I3−, HSO4−, SO42−, NO3−, ClO4−, BF4−, PF6−, AsF6−, SbF6−, FeCl4−, Fe(CN)63−, and anions of various sulfonic acids, such as aryl-SO3−), cations (e.g. H+, Li+, Na+, K+, Rb+, Cs+, Co3+ and Fe3+), O2, redox active salts (e.g. XeOF4, (NO2+) (SbF6−), (NO2+) (SbCl6−), (NO2+) (BF4−), NOBF4, NOPF6, AgClO4, H2IrCl6 and La(NO3)3.6H2O), strongly electron-accepting organic molecules (e.g. 2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane (F4-TCNQ)), transition metal oxides (e.g. WO3, Re2O7 and MoO3), metal-organic complexes of cobalt, iron, bismuth and molybdenum, (p-BrC6H4)3NSbCl6, bismuth(III) tris(trifluoroacetate), FSO2OOSO2F, acetylcholine, R4N+, (R is an alkyl group), R4P+ (R is a straight-chain or branched alkyl group 1 to 20), R6As+ (R is an alkyl group), R3S+ (R is an alkyl group) and ionic liquids (e.g. 1-Ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide). Suitable cobalt complexes beside of tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)-cobalt(III) tris(bis(trifluoromethylsulfonyl)imide)) are cobalt complex salts as described in WO 2012/114315, WO 2012/114316, WO 2014/082706, WO 2014/082704, EP 2883881 or JP 2013-131477.
Suitable lithium salts are beside of lithium bis(trifluoromethylsulfonyl)imide, lithium tris(pentafluoroethyl)trifluorophosphate, lithium dicyanamide, lithium methylsulfate, lithium trifluormethanesulfonate, lithium tetracyanoborate, lithium dicyanamide, lithium tricyanomethide, lithium thiocyanate, lithium chloride, lithium bromide, lithium iodide, lithium hexafluoroposphate, lithium tetrafluoroborate, lithium perchlorate, lithium hexafluoroantimonate, lithium hexafluoroarsenate or a combination of two or more. A preferred lithium salt is lithium bis(trifluoromethylsulfonyl)imide.
Preferably, the formulation comprises from 0.1 mM to 50 mM, preferably from 5 to 20 mM of the lithium salt.
Suitable device structures for PSCs comprising a compound formula NI or I and a mixed halide perovskite are described in WO 2013/171517, claims 52 to 71 and claims 72 to 79, which is entirely incorporated herein by reference.
Suitable device structures for PSCs comprising a compound formula and a dielectric scaffold together with a perovskite are described in WO 2013/171518, claims 1 to 90 or WO 2013/171520, claims 1 to 94 which are entirely incorporated herein by reference.
Suitable device structures for PSCs comprising a blend according to the present invention, a semiconductor and a perovskite are described in WO 2014/020499, claims 1 and 3 to 14, which is entirely incorporated herein by reference The surface-increasing scaffold structure described therein comprises nanoparticles which are applied and/or fixed on a support layer, e.g. porous TiO2.
Suitable device structures for PSCs comprising a blend according to the present invention and comprising a planar heterojunction are described in WO 2014/045021, claims 1 to 39, which is entirely incorporated herein by reference. Such a device is characterized in having a thin film of a light-absorbing or light-emitting perovskite disposed between n-type (electron conducting) and p-type (hole-conducting) layers. Preferably, the thin film is a compact thin film.
The invention further relates to a method of preparing a PSC as described above or below, the method comprising the steps of:
The invention relates furthermore to a tandem device comprising at least one device according to the invention as described above and below. Preferably, the tandem device is a tandem solar cell.
The tandem device or tandem solar cell according to the invention may have two semi-cells wherein one of the semi cells comprises the compounds, oligomers or polymers in the active layer as described or preferably described above. There exists no restriction for the choice of the other type of semi cell which may be any other type of device or solar cell known in the art.
There are two different types of tandem solar cells known in the art. The so called 2-terminal or monolithic tandem solar cells have only two connections. The two subcells (or synonymously semi cells) are connected in series. Therefore, the current generated in both subcells is identical (current matching). The gain in power conversion efficiency is due to an increase in voltage as the voltages of the two subcells add up. The other type of tandem solar cells is the so called 4-terminal or stacked tandem solar cell. In this case, both subcells are operated independently. Therefore, both subcells can be operated at different voltages and can also generate different currents. The power conversion efficiency of the tandem solar cell is the sum of the power conversion efficiencies of the two subcells.
The invention furthermore relates to a module comprising a device according to the invention as described before or preferably described before.
The compounds and blends of the present invention can also be used as dye or pigment in other applications, for example as an ink dye, laser dye, fluorescent marker, solvent dye, food dye, contrast dye or pigment in coloring paints, inks, plastics, fabrics, cosmetics, food and other materials.
The blends of the present invention are also suitable for use in the semiconducting channel of an OFET. Accordingly, the invention also provides an OFET comprising a gate electrode, an insulating (or gate insulator) layer, a source electrode, a drain electrode and an organic semiconducting channel connecting the source and drain electrodes, wherein the organic semiconducting channel comprises a blend according to the present invention. Other features of the OFET are well known to those skilled in the art.
OFETs where an OSC material is arranged as a thin film between a gate dielectric and a drain and a source electrode, are generally known, and are described for example in U.S. Pat. Nos. 5,892,244, 5,998,804, 6,723,394 and in the references cited in the background section. Due to the advantages, like low cost production using the solubility properties of the compounds according to the invention and thus the processibility of large surfaces, preferred applications of these OFETs are such as integrated circuitry, TFT displays and security applications.
The gate, source and drain electrodes and the insulating and semiconducting layer in the OFET device may be arranged in any sequence, provided that the source and drain electrode are separated from the gate electrode by the insulating layer, the gate electrode and the semiconductor layer both contact the insulating layer, and the source electrode and the drain electrode both contact the semiconducting layer.
An OFET device according to the present invention preferably comprises:
The OFET device can be a top gate device or a bottom gate device. Suitable structures and manufacturing methods of an OFET device are known to the skilled in the art and are described in the literature, for example in US 2007/0102696 A1.
The gate insulator layer preferably comprises a fluoropolymer, like e.g. the commercially available Cytop 809M® or Cytop 107M® (from Asahi Glass). Preferably the gate insulator layer is deposited, e.g. by spin-coating, doctor blading, wire bar coating, spray or dip coating or other known methods, from a formulation comprising an insulator material and one or more solvents with one or more fluoro atoms (fluorosolvents), preferably a perfluorosolvent. A suitable perfluorosolvent is e.g. FC75® (available from Acros, catalogue number 12380). Other suitable fluoropolymers and fluorosolvents are known in prior art, like for example the perfluoropolymers Teflon AF® 1600 or 2400 (from DuPont) or Fluoropel® (from Cytonix) or the perfluorosolvent FC 43® (Acros, No. 12377). Especially preferred are organic dielectric materials having a low permittivity (or dielectric contant) from 1.0 to 5.0, very preferably from 1.8 to 4.0 (“low k materials”), as disclosed for example in US 2007/0102696 A1 or U.S. Pat. No. 7,095,044.
In security applications, OFETs and other devices with semiconducting materials according to the present invention, like transistors or diodes, can be used for RFID tags or security markings to authenticate and prevent counterfeiting of documents of value like banknotes, credit cards or ID cards, national ID documents, licenses or any product with monetary value, like stamps, tickets, shares, cheques etc.
Alternatively, the compounds and blends (hereinafter referred to as “materials”) according to the present invention can be used in OLEDs, e.g. as the active display material in a flat panel display applications, or as backlight of a flat panel display like e.g. a liquid crystal display. Common OLEDs are realized using multilayer structures. An emission layer is generally sandwiched between one or more electron-transport and/or hole-transport layers. By applying an electric voltage electrons and holes as charge carriers move towards the emission layer where their recombination leads to the excitation and hence luminescence of the lumophor units contained in the emission layer. The materials according to the present invention may be employed in one or more of the charge transport layers and/or in the emission layer, corresponding to their electrical and/or optical properties. Furthermore their use within the emission layer is especially advantageous, if the materials according to the present invention show electroluminescent properties themselves or comprise electroluminescent groups or compounds. The selection, characterization as well as the processing of suitable monomeric, oligomeric and polymeric compounds or materials for the use in OLEDs is generally known by a person skilled in the art, see, e.g., Müller et al, Synth. Metals, 2000, 111-112, 31-34, Alcala, J. Appl. Phys., 2000, 88, 7124-7128 and the literature cited therein.
According to another use, the materials according to the present invention, especially those showing photoluminescent properties, may be employed as materials of light sources, e.g. in display devices, as described in EP 0 889 350 A1 or by C. Weder et al., Science, 1998, 279, 835-837.
A further aspect of the invention relates to both the oxidised and reduced form of the materials according to the present invention. Either loss or gain of electrons results in formation of a highly delocalised ionic form, which is of high conductivity. This can occur on exposure to common dopants. Suitable dopants and methods of doping are known to those skilled in the art, e.g. from EP 0 528 662, U.S. Pat. No. 5,198,153 or WO 96/21659.
The doping process typically implies treatment of the semiconductor material with an oxidating or reducing agent in a redox reaction to form delocalised ionic centres in the material, with the corresponding counterions derived from the applied dopants. Suitable doping methods comprise for example exposure to a doping vapor in the atmospheric pressure or at a reduced pressure, electrochemical doping in a solution containing a dopant, bringing a dopant into contact with the semiconductor material to be thermally diffused, and ion-implantantion of the dopant into the semiconductor material.
When electrons are used as carriers, suitable dopants are for example halogens (e.g., I2, Cl2, Br2, ICI, ICI3, IBr and IF), Lewis acids (e.g., PF5, AsF5, SbF5, BF3, BCl3, SbCl5, BBr3 and SO3), protonic acids, organic acids, or amino acids (e.g., HF, HCl, HNO3, H2SO4, HClO4, FSO3H and ClSO3H), transition metal compounds (e.g., FeCl3, FeOCl, Fe(ClO4)3, Fe(4-CH3C6H4SO3)3, TiCl4, ZrCl4, HfCl4, NbF5, NbCl5, TaCl5, MoF5, MoCl5, WF5, WCl6, UF6 and LnCl3 (wherein Ln is a lanthanoid), anions (e.g., Cl−, Br−, I−, I3−, HSO4−, SO42−, NO3−, ClO4−, BF4−, PF6−, AsF6−, SbF6−, FeCl4−, Fe(CN)63−, and anions of various sulfonic acids, such as aryl-SO3−). When holes are used as carriers, examples of dopants are cations (e.g., H+, Li+, Na+, K+, Rb+ and Cs+), alkali metals (e.g., Li, Na, K, Rb, and Cs), alkaline-earth metals (e.g., Ca, Sr, and Ba), O2, XeOF4, (NO2+) (SbF6−), (NO2+) (SbCl6−), (NO2+) (BF4−), AgClO4, H2IrCl6, La(NO3)3.6H2O, FSO2OOSO2F, Eu, acetylcholine, R4N+, (R is an alkyl group), R4P+ (R is an alkyl group), R6As+ (R is an alkyl group), and R3S+ (R is an alkyl group).
The conducting form of the materials according to the present invention can be used as an organic “metal” in applications including, but not limited to, charge injection layers and ITO planarising layers in OLED applications, films for flat panel displays and touch screens, antistatic films, printed conductive substrates, patterns or tracts in electronic applications such as printed circuit boards and condensers.
The materials according to the present invention may also be suitable for use in organic plasmon-emitting diodes (OPEDs), as described for example in Koller et al., Nat. Photonics, 2008, 2, 684.
According to another use, the materials according to the present invention can be used alone or together with other materials in or as alignment layers in LCD or OLED devices, as described for example in US 2003/0021913. The use of charge transport compounds according to the present invention can increase the electrical conductivity of the alignment layer. When used in an LCD, this increased electrical conductivity can reduce adverse residual dc effects in the switchable LCD cell and suppress image sticking or, for example in ferroelectric LCDs, reduce the residual charge produced by the switching of the spontaneous polarisation charge of the ferroelectric LCs. When used in an OLED device comprising a light emitting material provided onto the alignment layer, this increased electrical conductivity can enhance the electroluminescence of the light emitting material.
The materials according to the present invention having mesogenic or liquid crystalline properties can form oriented anisotropic films as described above, which are especially useful as alignment layers to induce or enhance alignment in a liquid crystal medium provided onto said anisotropic film.
According to another use, the materials according to the present invention are suitable for use in liquid crystal (LC) windows, also known as smart windows.
The materials according to the present invention may also be combined with photoisomerisable compounds and/or chromophores for use in or as photoalignment layers, as described in US 2003/0021913 A1.
According to another use, the materials according to the present invention, especially their water-soluble derivatives (for example with polar or ionic side groups) or ionically doped forms, can be employed as chemical sensors or materials for detecting and discriminating DNA sequences. Such uses are described for example in L. Chen, D. W. McBranch, H. Wang, R. Helgeson, F. Wudl and D. G. Whitten, Proc. Natl. Acad. Sci. U.S.A., 1999, 96, 12287; D. Wang, X. Gong, P. S. Heeger, F. Rininsland, G. C. Bazan and A. J. Heeger, Proc. Natl. Acad. Sci. U.S.A., 2002, 99, 49; N. DiCesare, M. R. Pinot, K. S. Schanze and J. R. Lakowicz, Langmuir, 2002, 18, 7785; D. T. McQuade, A. E. Pullen, T. M. Swager, Chem. Rev., 2000, 100, 2537.
Unless the context clearly indicates otherwise, as used herein plural forms of the terms herein are to be construed as including the singular form and vice versa.
Throughout the description and claims of this specification, the words “comprise” and “contain” and variations of the words, for example “comprising” and “comprises”, mean “including but not limited to”, and are not intended to (and do not) exclude other components.
It will be appreciated that variations to the foregoing embodiments of the invention can be made while still falling within the scope of the invention. Each feature disclosed in this specification, unless stated otherwise, may be replaced by alternative features serving the same, equivalent or similar purpose. Thus, unless stated otherwise, each feature disclosed is one example only of a generic series of equivalent or similar features.
All of the features disclosed in this specification may be combined in any combination, except combinations where at least some of such features and/or steps are mutually exclusive. In particular, the preferred features of the invention are applicable to all aspects of the invention and may be used in any combination. Likewise, features described in non-essential combinations may be used separately (not in combination).
Above and below, unless stated otherwise percentages are percent by weight and temperatures are given in degrees Celsius.
The invention will now be described in more detail by reference to the following examples, which are illustrative only and do not limit the scope of the invention.
A solution of 2,5-bis(tributylstannyl)thiophene (15 g, 22.7 mmol), methyl 5-bromo-2-iodobenzoate (17.8 g, 52.1 mmol) and anhydrous toluene (350 cm3) is degassed by bubbling through a stream of nitrogen for 30 minutes. Tri-o-tolyl phosphine (0.17 g, 0.57 mmol) and bis(triphenylphosphine)palladium (II) dichloride (0.21 g, 0.29 mmol) are added and the degassing continued for 10 minutes. The reaction is stirred at 80° C. under nitrogen for 20 hours. After cooling to 23° C., the reaction mixture is poured into distilled water (250 cm3) and the organic layer decanted, washed with brine (2×100 cm3), dried over magnesium sulphate and filtered. Removal of the solvent in vacuo followed by purification by silica gel chromatography (dichloromethane:heptanes; 7:3) gave intermediate 1 as a yellow solid (3.6 g, 31%). 1H NMR (CDCl3, 400 MHz) 7.89 (2H, d, J 2.3), 7.64 (2H, dd, J 2, 8.3), 7.40 (2H, d, J 8.3), 6.99 (2H, s), 3.80 (6H, s).
To a mixture of 1-bromo-4-hexadecylbenzene (13.4 g, 35.1 mmol) anhydrous tetrahydrofuran (170 cm3) at −65° C. is added dropwise n-butyllithium (15 cm3, 37.2 mmol, 2.5 M in hexanes) over 30 minutes. The resulting suspension is left to stir at −65° C. for 4 hours before intermediate 1 (3.60 g, 7 mmol) is added in one portion. The reaction mixture is left to stir and to warm up slowly over 17 hours to 23° C. Distilled water (100 cm3) and tert-butyl methyl ether (100 cm3) are added and the mixture stirred for 30 minutes. The organic layer is decanted and the aqueous layer extracted by tert-butyl methyl ether (3×50 cm3). All organics are combined, dried over sulphate magnesium, filtered and the solvent removed in vacuo. The solid is purified by silica gel chromatography (heptane:ethyl acetate; 95:5) to give intermediate 2 as a yellow oil which solidified slowly upon standing (7.0 g, 64%). 1H NMR (CDCl3, 400 MHz) 7.39 (2H, dd, J 1.8, 7.8), 7.11 (8H, d, J 8.3), 7.04 (10H, m), 6.94 (2H, d, J 2.3), 5.90 (2H, s), 3.25 (2H, s), 2.61 (8H, m), 1.60 (8H, m), 1.24-1.29 (104H, m), 0.89 (12H, t, J 6.6).
To a mixture of intermediate 2 (7.4 g, 4.5 mmol) and dichloromethane (230 cm3) is added p-toluene sulfonic acid (1.7 g, 9 mmol) and the reaction mixture heated at reflux for 6 hours. After cooling to 23° C., the suspension is filtered off. Purification by recrystallisation (2-butanone) gave intermediate 3 as a beige solid (3.6 g, 50%). 1H NMR (CDCl3, 400 MHz) 7.31 (2H, dd, J 1.5, 6.6), 7.24 (2H, d, J 8.1), 7.17 (2H, d, J 1.5), 6.72 (8H, d, J 8.1), 6.61 (8H, d, J 8.1), 2.39-2.45 (8H, m), 1.52 (8H, m), 1.23-1.38 (104H, m), 0.89 (12H, t, J 6.6).
A solution of intermediate 3 (1.0 g, 0.6 mmol), tributyl-(5-[1,3]dioxolan-2-yl-thiophen-2-yl)-stannane (1.1 g, 2.5 mmol), tri-o-tolyl-phosphane (56.4 mg, 0.2 mmol) and anhydrous toluene (50 cm3) is degassed with nitrogen for 30 minutes. Tris(dibenzylideneacetone)dipalladium(0) (42.4 mg, 0.05 mmol) is added and the degassing continued for 20 minutes. The reaction is stirred at 105° C. for 17 hours. The resulting reaction mixture is let cool to 25° C., removal of the solvent in vacuo followed by purification by silica gel chromatography (40-60 petrol:diethyl ether; 7:3) gave intermediate 4 as a yellow/green solid (1.0 g, 92%). 1H NMR (CD2Cl2, 400 MHz) 7.42-7.56 (4H, m), 7.31 (2H, s), 7.02-7.11 (4H, m) 6.83 (8H, d, J 8.1), 6.68 (8H, d, J 8.3), 6.03 (2H, s), 3.93-4.18 (8H, m), 2.46 (8H, q, J 7.3), 1.46-1.64 (8H, m), 1.21-1.43 (104H, m), 0.86-0.96 (12H, m).
A solution of intermediate 4 (1.0 g, 0.6 mmol) in tetrahydrofuran (5 cm3) at 20° C. is added dropwise concentrated hydrochloric acid (0.3 cm3). The reaction mixture is stirred at 20° C. for 2 hours. The reaction is quenched with ice water (50 cm3). The solution is extracted with diethyl ether (3×30 cm3). The organic layers combined, dried over anhydrous magnesium sulfate and the solvent removed in vacuo. The crude product is dissolved in hot 40-60 petrol (20 cm3) which is added dropwise into acetone (60 cm3) to form a clear solution. On standing over 30 minutes an orange crystalline solid is formed, filtered, washed with ethanol to give intermediate 5 as a light orange solid (850 mg, 90%). 1H NMR (CD2Cl2, 400 MHz) 9.78-9.88 (2H, s), 7.59-7.72 (4H, m), 7.53 (2H, d, J 8.1), 7.41 (2H, d, J 1.0), 7.31 (2H, d, J 4.2), 6.77-6.92 (8H, m), 6.61-6.75 (8H, m), 2.35-2.58 (8H, m), 1.45-1.64 (10H, m), 1.20-1.42 (104H, m), 0.91 (12H, t, J 6.7).
Compound 1
To a three-necked round-bottomed flask is added intermediate 5 (0.8 g, 0.5 mmol), 2-(3-oxo-indan-1-ylidene)-malononitrile (0.65 g, 3.3 mmol), chloroform (50 cm3) and pyridine (2.6 cm3, 33.3 mmol). The mixture is degassed with nitrogen for 30 minutes and then heated to reflux for 12 hours. The resulting reaction mixture is let cool to 25° C. and poured into methanol (300 cm3), stirred for 1 hour to form a fine suspension which is collected by filtration. The crude product is purified by column chromatography (dichloromethane) to give product 1 as a dark red solid (0.5 g, 52%). 1H NMR (CD2Cl2, 400 MHz) 8.68 (2H, s), 8.57 (2H, dd, J 6.6 1.2), 7.81 (2H, s), 7.63-7.73 (6H, m), 7.60 (2H, dd, J 8.1, 1.7), 7.35-7.42 (4H, m), 7.26 (2H, d, J 4.4), 6.77 (8H, d, J 8.3), 6.61 (8H, d, J 8.6), 2.36 (8H, m), 1.44 (8H, m), 1.09-1.31 (104H, m), 0.73-0.84 (12H, m).
To a mixture of 2,8-dibromo-6,6,12,12-tetraoctyl-6,12-dihydro-indeno[1,2-b]fluorene (1500 mg, 1.74 mmol), tributyl-(5-[1,3]dioxolan-2-yl-thiophen-2-yl)-stannane (3.10 g, 6.97 mmol) and tri-o-tolyl-phosphine (159 mg, 0.523 mmol) is added degassed anhydrous toluene (50 cm3). The resulting solution is degassed with nitrogen for further 30 minutes. Tris(dibenzylideneacetone)dipalladium(0) (120 mg, 0.131 mmol) is then added and the mixture degassed for a further 20 minutes. The reaction mixture is then placed in to a pre-heated block and heated at 105° C. for 17 hours. After cooling to 23° C., the solvent is removed in vacuo. The resulting residue is dissolved in tetrahydrofuran (50 cm3) and concentrated hydrochloric acid (5 cm3) added followed by stirring at 23° C. for 2 hours. The solvent is removed in vacuo and the residue triturated with ethanol. The solid collected by filtration and washed with methanol to give to intermediate 6 (1.55 g, 96%) as a yellow solid. 1H NMR (CDCl3, 400 MHz) 0.65-0.83 (20H, m), 1.03-1.24 (40H, m), 2.10-2.19 (8H, m), 7.56 (2H, d, J 3.9), 7.72-7.87 (10H, m), 9.94 (2H, s).
Compound 2
A degassed mixture of intermediate 6 (250 mg, 0.329 mmol), 2-(3-oxo-indan-1-ylidene)-malononitrile (442 mg, 2.27 mmol), chloroform (25 cm3) and pyridine (1.8 cm3) is heated at reflux for 12 hours. After cooling to 23° C., the solvent is removed in vacuo, the residue is stirred in ethanol (150 cm3) at 50° C. for 1 hour and the resulting suspension is filtered through a silica pad and washed well with ethanol followed by acetone. The solvent removed in vacuo and the solid triturated in ethanol. The solid collected by filtration to give compound 2 (356 mg, 86%) as a dark blue solid. 1H NMR (CD2Cl2, 400 MHz) 0.64-0.85 (20H, m), 1.05-1.22 (40H, m), 2.13-2.27 (8H, m), 7.69 (2H, d, J 3.9), 7.79-8.03 (16H, m), 8.74 (2H, d, J 7.3), 8.93 (2H, s).
To a mixture of 2,8-dibromo-6,6-bis-(4-tert-butyl-phenyl)-12,12-dioctyl-6,12-dihydro-indeno[1,2-b]fluorene (1500 mg, 1.67 mmol), tributyl-(5-[1,3]dioxolan-2-yl-thiophen-2-yl)-stannane (2.97 g, 6.67 mmol) and tri-o-tolyl-phosphine (152 mg, 0.499 mmol) is added degassed anhydrous toluene (50 cm3). The resulting solution is degassed with nitrogen for further 30 minutes. Tris(dibenzylideneacetone)dipalladium(0) (114 mg, 0.125 mmol) is then added and the mixture degassed for a further 20 minutes. The reaction mixture is then placed in to a pre-heated block and heated at 105° C. for 17 hours. After cooling to 23° C., the solvent is removed in vacuo. The resulting residue is dissolved in tetrahydrofuran (50 cm3) and concentrated hydrochloric acid (5 cm3) added followed by stirring at 23° C. for 2 hours. The solvent is removed in vacuo and the residue triturated with ethanol. The solid collected by filtration and washed with methanol to give to intermediate 7 (1.25 g, 78%) as a yellow solid. 1H NMR (CDCl3, 400 MHz) 0.60-1.35 (48H, m), 1.94-2.04 (4H, m), 7.09-7.22 (8H, m), 7.31-7.40 (2H, m), 7.54-7.82 (10H, m), 9.79 (2H, s), 9.82 (2H, s).
Compound 3
A degassed mixture intermediate 7 (300 mg, 0.311 mmol), 2-(3-oxo-indan-1-ylidene)-malononitrile (423 mg, 2.18 mmol), chloroform (25 cm3) and pyridine (1.7 cm3) is heated at reflux for 12 hours. After cooling to 23° C., the solvent is removed in vacuo, the residue is stirred in ethanol (150 cm3) at 50° C. for 1 hour and the resulting suspension is filtered through a silica pad and washed well with ethanol followed by acetone. The solvent removed in vacuo and the solid triturated in ethanol. The solid collected by filtration to give compound 3 (130 mg, 32%) as a dark purple solid. 1H NMR (CD2Cl2, 400 MHz) 0.62-0.71 (10H, m), 0.96-1.12 (20H, m), 1.17-1.24 (18H, m), 2.05-2.13 (4H, m), 7.13-7.28 (8H, m), 7.41-7.43 (1H, m), 7.52-7.54 (1H, m), 7.63-7.88 (16H, m), 8.56-8.62 (2H, m), 8.73-8.80 (2H, m).
To a solution of 2,7-dibromo-4,4,9,9-tetrakis(4-octylphenyl)-4,9-dihydro-thieno[3′,2′:4,5]cyclopenta[1,2-b]thieno[2″,3″:3′,4′]cyclopenta[1′,2′:4,5]thieno[2,3-d]thiophene (0.5 g, 0.40 mmol) in anhydrous tetrahydrofuran (20 cm3) at −78° C. is added dropwise n-butyllithium (0.50 cm3, 1.3 mmol, 2.5 M in hexane) over 15 minutes. After addition, the reaction mixture is stirred at −78° C. for 60 minutes before a solution of N,N-dimethylformamide (0.8 cm3, 10.4 mmol) in anhydrous diethyl ether (20 cm3) is added in one go. The mixture is then allowed to warm to 23° C. over 17 hours. Dichloromethane (60 cm3) and water (250 cm3) is added and the mixture stirred at 23° C. for 30 minutes. The product is extracted with dichloromethane (3×60 cm3). The combined organics are washed with brine (30 cm3) and dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo to obtain crude. The crude is purified by column chromatography (40-60 petrol:diethyl ether; 9.5:0.5) to give intermediate 8 (0.13 g, 27%) as an orange yellow crystalline solid. 1H NMR (400 MHz, CDCl3) 9.81 (2H, s), 7.69 (2H, s), 7.12 (16H, m), 2.52-2.61 (8H, m), 1.30 (48H, bs), 0.79-0.92 (12H, m).
Compound 4
To a degassed solution of intermediate 8 (0.13 g, 0.11 mmol) and 3-(dicyanomethylidene)indan-1-one (1.5 g, 0.77 mmol) in chloroform (12 cm3) is added Pyridine (0.6 cm3, 7.69 mmol). The mixture is then degassed with nitrogen for 30 min and then heated at 70° C. for 15 h. The reaction mixture allowed to cool to 23° C. and the solvent removed in vacuo. The crude is purified by column chromatography (40-60 petrol:chloroform; 1:1) to give desired compound 4 (1.1 g, 65%) as a dark blue crystalline solid. 1H NMR (400 MHz, CDCl3) 8.87 (2H, s), 8.69 (2H, J 7.58 Hz, d), 7.91 (2H, J 7.09 Hz, d), 7.68-7.79 (6H, m), 7.08-7.18 (16H, m), 2.60 (8H, J 7.70 Hz, t), 1.62 (8H, J 7.09 Hz, q), 1.21-1.39 (40H, m), 0.88 (12H, J 6.48 Hz, t).
To a solution of 2,7-dibromo-4,4,9,9-tetrakis(4-octylphenyl)-4,9-dihydro-thieno[3′,2′:4,5]cyclopenta[1,2-b]thieno[2″,3″:3′,4′]cyclopenta[1′,2′:4,5]thieno[2,3-d]thiophene (2.00 g, 1.61 mmol) in anhydrous tetrahydrofuran (100 cm3) at −78° C. is added n-butyllithium (2.6 cm3, 6.5 mmol, 2.5 M in hexanes) over 10 minutes. The mixture is stirred at −78° C. for 1 hour before tributyltin chloride (2.0 cm3, 7.4 mmol) is added and the mixture stirred to 23° C. overnight. Methanol (10 cm3) is added and the material concentrated in vacuo. The crude product is then taken up in pentane (20 cm3), anhydrous magnesium sulfate added, filtered and the solid washed with additional pentane (3×10 cm3). The filtrate is then concentrated in vacuo and the solid triturated with methanol (3×20 cm3) and the product collected by filtration to give intermediate 9 (2.57 g, 96%) as a yellow waxy solid. 1H NMR (400 MHz, CDCl3, 45° C.) 7.16 (8H, d, J 8.2), 7.06 (10H, d, J 7.8), 2.55 (8H, t, J 7.8), 1.53-1.67 (20H, m), 1.22-1.41 (56H, m), 1.07-1.14 (8H, m), 0.84-0.97 (30H, m).
To a degassed solution of intermediate 9 (500 mg, 0.30 mmol) and 7-bromo-benzo[1,2,5]thiadiazole-4-carbaldehyde (161 mg, 0.66 mmol) in anhydrous toluene (36 cm3), tris(dibenzylideneacetone)dipalladium(0) (22 mg, 0.02 mmol) and tris(o-tolyl)phosphine (28 mg, 0.09 mmol) is added. After degassing the reaction mixture for 30 minutes it is heated at 80° C. for 1.5 hours. After cooling to 23° C., the mixture is concentrated in vacuo. The crude is then triturated with methanol (3×25 cm3) and the solid filtered to obtain intermediate 10 (357 mg, 84%) as a blue crystalline solid. 1H NMR (400 MHz, CDCl3) 10.69 (2H, s), 8.33 (2H, s), 8.19 (2H, d, J 7.8), 7.95 (2H, d, J 7.6), 7.25 (8H, d, J 8.3), 7.14 (8H, d, J 8.3), 2.58 (8H, t, J 7.8), 1.58-1.64 (8H, m), 1.20-1.38 (40H, m), 0.86 (12H, t, J 6.8).
Compound 5
To a solution of intermediate 10 (357 mg, 0.25 mmol) in anhydrous chloroform (27 cm3) is added pyridine (1.4 cm3, 17 mmol). The mixture is degassed with nitrogen before 3-ethyl-2-thioxo-thiazolidin-4-one (286 mg, 1.77 mmol) is added. After further degassing, the reaction mixture is heated at reflux for 2 days. Additional degassed anhydrous chloroform (20 cm3) is added and the reaction heated at reflux for a further 24 hours. Additional 3-ethyl-2-thioxo-thiazolidin-4-one (286 mg, 1.77 mmol) is added and the reaction heated at reflux for 24 hours before the reaction is cooled to 23° C., concentrated in vacuo and triturated with methanol (4×20 cm3) followed by diethyl ether (3×20 cm3). The triturated material is then heated at 90° C. in 2-butanone/water (4:1) (70 cm3) for 30 minutes, cooled to 0° C. and the solid collected by filtration and washed with additional cold 2-butanone (4×10 cm3) to give Compound 5 (233 mg, 54%) as a green/black powder. 1H NMR (400 MHz, CDCl3) 8.50 (2H, s), 8.27 (2H, s), 7.89 (2H, d, J 7.8), 7.66 (2H, d, J 7.8), 7.24 (8H, d, J 8.1), 7.13 (8H, d, J 8.3), 4.25 (4H, q, J 6.9), 2.57 (8H, t, J 7.7), 1.58-1.63 (8H, m), 1.20-1.37 (46H, m), 0.86 (12H, t, J 6.7).
Compound 6
To a solution of intermediate 10 (170 mg, 0.12 mmol) in anhydrous chloroform (13 cm3) is added pyridine (0.7 cm3, 8.7 mmol). The mixture is then degassed with nitrogen before 3-(dicyanomethylidene)indan-1-one (164 mg, 0.84 mmol) is added. The solution is then degassed further before heating at reflux for 40 minutes. The reaction is then added to methanol (150 cm3) and the precipitated product collected by filtration and washed with methanol (5 cm3). The solid is then passed through a silica plug (dichloromethane) to give Compound 6 (36 mg, 17%) as a black solid. 1H NMR (400 MHz, CDCl3) 9.56 (2H, s), 9.26 (2H, d, J 8.1), 8.72 (2H, d, J 7.8), 8.36 (2H, s), 7.93 (4H, d, J 7.8), 7.73-7.84 (4H, m), 7.22-7.25 (8H, m), 7.14 (8H, d, J 8.1), 2.57 (8H, t, J 7.7), 1.57-1.64 (8H, m), 1.24 (40H, m), 0.85 (12H, t, J 6.5).
To a solution of 2,8-dibromo-6,12-dihydro-6,6,12,12-tetrakis(4-dodecylphenyl)indeno[1,2-b]indeno[2′,1′:4,5]thieno[2,3-d]thiophene (500 mg, 0.34 mmol) in anhydrous toluene (41 cm3) is added tributyl-(5-[1,3]dioxolan-2-yl-thiophen-2-yl)-stannane (0.4 cm3, 0.9 mmol) before the solution is degassed with nitrogen.
Tris(dibenzylideneacetone)dipalladium(0) (25 mg, 0.03 mmol) and tris(o-tolyl)phosphine (31 mg, 0.10 mmol) are then added and after additional degassing the reaction mixture is heated at 80° C. for 24 hours. The reaction mixture is then concentrated in vacuo and triturated with methanol (3×50 cm3). The solid is then eluted though a silica plug (40-60 petrol:dichloromethane; 4:1 to 0:1) and triturated with 2-propanol (100 cm3) at 80° C., which with cooling to 0° C. and collection by filtration gives intermediate 11 (454 mg, 82%) as a sticky yellow solid. 1H NMR (400 MHz, CHCl3) 7.61 (2H, s), 7.52 (2H, d, J 8.1), 7.35 (2H, d, J 8.1), 7.18 (8H, d, J 7.9), 7.14 (2H, d, J 3.7), 7.09 (10H, d, J 8.1), 6.09 (2H, s), 4.10-4.19 (4H, m), 4.00-4.09 (4H, m), 2.55 (8H, t, J 7.8), 1.57-1.63 (8H, m), 1.21-1.36 (72H, m), 0.87 (12H, t, J 6.7).
Concentrated hydrochloric acid (0.2 cm3, 1.8 mmol, 32%) is added dropwise to a solution of intermediate 11 (454 mg, 0.28 mmol) in tetrahydrofuran (20 cm3) at 23° C. and the reaction mixture stirred for 2 hours. Water (0.5 cm3) is then added and the reaction mixture stirred for a further hour. Additional water (50 cm3) is then added and the solution extracted with ethyl acetate (50 cm3 then 25 cm3). The combined organic extracts are then washed with water (50 cm3) and brine (50 cm3), extracting the aqueous layer each time with additional ethyl acetate (25 cm3). The combined organic extracts are then dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The crude product is then stirred in a mixture of 40-60 petrol (125 cm3) and acetone (10 cm3) at 70° C. The mixture is then cooled to 0° C., filtered and the solid washed with 40-60 petrol (3×10 cm3) to give intermediate 12 (191 mg, 45%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 9.86 (2H, s), 7.68-7.72 (4H, m), 7.63 (2H, d, J 8.1), 7.41 (2H, d, J 7.8), 7.36 (2H, d, J 3.9), 7.18 (8H, d, J 8.1), 7.11 (8H, d, J 8.1), 2.56 (8H, t, J 7.8), 1.58-1.64 (8H, m), 1.19-1.37 (72H, m), 0.87 (12H, t, J 6.6).
Compound 7
To a solution of intermediate 12 (191 mg, 0.13 mmol) in anhydrous chloroform (13 cm3) is added pyridine (0.7 cm3, 8.7 mmol). The mixture is then degassed with nitrogen before 3-(dicyanomethylidene)indan-1-one (172 mg, 0.89 mmol) is added. The solution is then further degassed and stirred at 23° C. for 200 minutes. The reaction mixture is then added to methanol (200 cm3), the resulting precipitate collected by filtration and washed with methanol (3×10 cm3). The solid is then triturated with diethyl ether (4×10 cm3) to obtain Compound 7 (158 mg, 67%) as a black solid. 1H NMR (400 MHz, CDCl3) 8.86 (2H, s), 8.67-8.72 (2H, m), 7.92-7.97 (2H, m), 7.83 (2H, d, J 4.4), 7.71-7.81 (8H, m), 7.42-7.47 (4H, m), 7.22 (8H, d, J 8.2), 7.13 (8H, d, J 8.3), 2.58 (8H, t, J 7.7), 1.59-1.65 (8H, m), 1.18-1.39 (72H, m), 0.87 (12H, t, J 6.9).
To a degassed mixture of 2-bromo-5-(5-trimethylsilanyl-thieno[3,2-b]thiophen-2-yl)-terephthalic acid diethyl ester (4.77 g, 9.3 mmol), tributyl-thiophen-2-yl-stannane (3.6 cm3, 11 mmol) and anhydrous N,N-dimethylformamide (50 cm3) is added bis(triphenylphosphine)palladium(II) dichloride (330 mg, 0.47 mmol) and the mixture further degassed for 5 minutes. The mixture is then heated at 100° C. for 17 hours. The mixture allowed to cool slightly and the solvent removed in vacuo. The residue is purified by column chromatography (gradient from 40-60 petrol to dichloromethane) to give intermediate 13 (1.89 g, 39%) as a yellow solid. 1H NMR (CDCl3, 400 MHz) 7.78 (1H, s), 7.75 (1H, s), 7.31-7.34 (1H, m), 7.28 (1H, s), 7.20 (1H, s), 7.00-7.04 (2H, m), 4.16 (4H, quin, J 7.2), 1.09 (3H, t, J 7.2), 1.08 (3H, t, J 7.2), 0.30 (9H, s).
To a solution of 1-bromo-4-hexyl-benzene (5.3 g, 22 mmol) in anhydrous tetrahydrofuran (36 cm3) at −78° C. is added n-butyllithium (8.8 cm3, 22 mmol, 2.5 M in hexanes) dropwise over 30 minutes. The reaction is then stirred for a further 30 minutes. Intermediate 13 (1.89 g, 3.67 mmol) is then added as a solid in one portion and the reaction mixture stirred and allowed to warm to 23° C. over 17 hours. Water (100 cm3) is added and the product extracted with ether (2×100 cm3). The combined organics washed with brine (100 cm3), dried over anhydrous magnesium sulfate and filtered. To the solution is added amberlyst 15 strong acid (25 g) and the mixture degassed by vacuum/nitrogen 3 times. The mixture is then heated at reflux for 3 hours. The mixture allowed to cool to 23° C., filtered, the solid washed with ether (50 cm3) and the solvent removed from the filtrate in vacuo. The crude is purified by column chromatography (gradient from 40-60 petrol to 40-60 petrol:dichloromethane 3:2) to give intermediate 14 (2.45 g, 64%) as an orange solid. 1H NMR (CD2Cl2, 400 MHz) 7.56 (1H, s), 7.51 (1H, s), 7.33-7.36 (2H, m), 7.10-7.22 (16H, m), 7.05 (1H, d, J 4.7), 2.55-2.64 (8H, m), 1.51-1.66 (8H, m), 1.26-1.42 (24H, m), 0.85-0.95 (12H, m).
To intermediate 14 (2.45 g, 0.38 mmol) in anhydrous tetrahydrofuran (50 cm3) at 23° C. is added N-bromosuccinimide (880 mg, 178 mmol). The reaction is then stirred at 23° C. for 3 hours. Water (50 cm3) is added and the product extracted with dichloromethane (2×100 cm3). The combined organics dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is purified by column chromatography (gradient from 40-60 petrol to 40-60 petrol:dichloromethane 7:3) to give intermediate 15 (2.30 g, 87%) as a yellow solid. 1H NMR (CD2Cl2, 400 MHz) 7.50 (2H, s), 7.36 (1H, s), 7.10-7.20 (16H, m), 7.07 (1H, s), 2.55-2.64 (8H, m), 1.54-1.66 (8H, m), 1.28-1.41 (24H, m), 0.86-0.95 (12H, m).
To a solution of intermediate 15 (1.00 g, 0.89 mmol) in anhydrous tetrahydrofuran (30 cm3) at −78° C. is added dropwise n-butyllithium (1.1 cm3, 2.7 mmol, 2.5 M in hexanes) over 20 minutes. The solution is then stirred at −78° C. for 1 hour before addition of anhydrous N,N-dimethylformamide (0.34 cm3, 4.6 mmol). The reaction mixture is stirred and allowed to warm to 23° C. over 17 hours. Water (100 cm3) is added and the product extracted with ether (3×50 cm3). The organic layers are combined, dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is purified by column chromatography (gradient from 40-60 petrol to dichloromethane) to give intermediate 16 (220 mg, 24%) as a yellow solid. 1H NMR (CD2Cl2, 400 MHz) 9.92 (1H, s), 9.86 (1H, s), 8.01 (1H, s), 7.75 (1H, s), 7.71 (1H, s), 7.64 (1H, s), 7.12-7.22 (16H, m), 2.55-2.64 (8H, m), 1.51-1.66 (8H, m), 1.25-1.42 (24H, m), 0.85-0.95 (12H, m).
Compound 8
A solution of intermediate 16 (220 mg, 0.22 mmol), 2-(3-oxo-indan-1-ylidene)-malononitrile (293 mg, 1.51 mmol), chloroform (17 cm3) and pyridine (1.2 g, 15 mmol) is degassed with nitrogen for 30 minutes and then heated at reflux for 3 hours. After cooling to 23° C., the mixture is poured into methanol (200 cm3) and the resulting suspension filtered. The solid is washed with methanol (100 cm3), ether (200 cm3) and extracted with dichloromethane (250 cm3). The solvent from the dichloromethane extract removed in vacuo and the residue purified by column chromatography (gradient from 40-60 petrol to 40-60 petrol:dichloromethane 3:7) to give compound 8 (243 mg, 82%) as a black solid. 1H NMR (CD2Cl2, 400 MHz) 8.88-8.93 (2H, m), 8.69-8.74 (2H, m), 8.26 (1H, s), 7.92-7.98 (2H, m), 7.90 (1H, s), 7.76-7.87 (5H, m), 7.69 (1H, s), 7.14-7.30 (16H, m), 2.57-2.66 (8H, m), 1.51-1.69 (8H, m), 1.25-1.42 (24H, m), 0.83-0.96 (12H, m).
To a 1.0 M solution (tetrahydrofuran 1:1 toluene) of 2,2,6,6-tetramethylpiperidinylmagnesium chloride lithium chloride complex (200 cm3, 200 mmol) at −30° C. under inert atmosphere is added dropwise a solution of 1,4-dibromo-2,5-difluoro-benzene (23.6 g, 86.8 mmol) in anhydrous tetrahydrofuran (150 cm3) over 30 minutes. After addition, the reaction mixture is stirred at −30° C. for 7 hours before ethyl chloroformate (22.6 g, 208 mmol) is added in one go. The mixture is then allowed to warm to 23° C. over 17 hours. Aqueous hydrochloric acid (1.0 M, 500 cm3) is added and the mixture stirred at 23° C. for 30 minutes. The product is extracted with diethyl ether (3×100 cm3). The combined organics are dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude product is triturated with n-pentane to form a suspension. The product is filtered and washed with cold acetone, collected and dried under vacuum to give intermediate 17 (12.0 g, 33%) as a white solid. 1H NMR (300 MHz, CDCl3) 1.42 (6H, m), 4.49 (4H, q); 19F-NMR 108.72 (2F, s).
A mixture of intermediate 17 (2.8 g, 6.7 mmol), tributyl-thiophen-2-yl-stannane (6.0 g, 16 mmol), tri-o-tolyl-phosphine (164 mg, 0.54 mmol) and anhydrous toluene (150 cm3) is degassed by nitrogen for 25 minutes. To the mixture is added tris(dibenzylideneacetone) dipalladium(0) (123 mg, 0.14 mmol) and the mixture further degassed for 15 minutes. The mixture is stirred at 100° C. for 17 hours and the solvent removed in vacuo. Dichloromethane (200 cm3) and water (200 cm3) is added and the mixture stirred at 23° C. for 30 minutes. The product is extracted with dichloromethane (3×100 cm3). The combined organics are dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude product is triturated with light petroleum ether to form a suspension. The product is filtered, collected and dried under vacuum to give intermediate 18 (2.45 g, 86%) as a pale yellow solid. 1H NMR (300 MHz, CDCl3) 1.16 (6H, t, J 7.16), 4.23 (4H, q), 7.12 (2H, dd, J 5.1, 3.7), 7.21 (2H, dd, J 3.5, 0.9), 7.50 (2H, dd, J 5.1, 1.2).
To a solution of 1-bromo-4-hexylbenzene (3.86 g, 16 mmol) in anhydrous tetrahydrofuran (156 cm3) at −78° C. is added dropwise tert-butyllithium (18.8 cm3, 32.0 mmol, 1.7 M in pentane) over 45 minutes. After addition, the reaction mixture is stirred at −78° C. for 20 minutes before it is warmed to −40° C. and stirred for 40 minutes. The mixture is cooled to −78° C. and intermediate 18 (1.4 g, 3.2 mmol) added in one go. The mixture is then allowed to warm to 23° C. over 17 hours. Diethyl ether (200 cm3) and water (200 cm3) is added and the mixture stirred at 23° C. for 30 minutes. The product is extracted with diethyl ether (3×100 cm3). The combined organics are dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo to obtain crude diol intermediate as a pale yellow oily residue. To a solution of crude diol in anhydrous diethyl ether (100 cm3) is added amberlyst 15 strong acid (25.0 g). The resulting solution is stirred at 40° C. for 2 hours. The reaction mixture is allowed to cool to 23° C. and the solvent removed in vacuo. The crude is purified using silica gel column chromatography (40-60 petroleum ether). Fractions containing pure product are combined and the solvent removed in vacuo to give intermediate 19 (445 mg, 15%) as a cream solid. 1H NMR (400 MHz, CD2Cl2) 0.79 (12H, m) 1.10-1.32 (24H, m) 1.49 (8H, m) 2.34-2.62 (8H, m) 6.89 (2H, d, J 5.1) 6.93-7.14 (16H, m) 7.31 (2H, d, J 4.9).
1-Bromo-pyrrolidine-2,5-dione (394 mg, 2.22 mmol) is added portion wise to a solution of intermediate 19 (510 mg, 0.54 mmol) in anhydrous tetrahydrofuran (50 cm3) under a nitrogen atmosphere with absence of light at 0° C. After addition, the reaction mixture is stirred at 23° C. for 17 hours and then the reaction mixture is concentrated in vacuo. The residue is dissolved in warm 40-60 petroleum ether (20 cm3 at 50° C.) and purified using silica gel column chromatography eluting with a mixture of 40-60 petroleum ether and diethyl ether (9:1). Fractions containing pure product are combined and the solvent removed in vacuo to give intermediate 20 (590 mg, 99%) as a pale yellow crystalline solid. 1H NMR (400 MHz, CDCl3) 0.74-0.87 (12H, m) 1.13-1.33 (24H, m) 1.44-1.60 (8H, m) 2.42-2.58 (8H, m) 6.89 (2H, s) 6.96-7.14 (16H, m).
To a solution of intermediate 20 (550 mg, 0.50 mmol) in anhydrous tetrahydrofuran (20 cm3) at −78° C. is added dropwise n-butyllithium (0.6 cm3, 1.5 mmol, 2.5 M in hexane) over 15 minutes. After addition, the reaction mixture is stirred at −78° C. for 60 minutes and N,N-dimethylformamide (0.19 cm3, 2.5 mmol) added in one go. The mixture is then allowed to warm to 23° C. over 17 hours. Dichloromethane (200 cm3) and water (200 cm3) is added and the mixture stirred at 23° C. for 30 minutes. The product is extracted with dichloromethane (3×100 cm3). The combined organics are dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo to obtain an oily residue. The crude is triturated with ethanol (40 cm3) to produce a heavy suspension. The solid collected by filtration and washed well with ethanol to give intermediate 21 (110 mg, 22%) as a grey solid. 1H NMR (400 MHz, CDCl3) 0.70-0.90 (12H, m) 1.08-1.21 (24H, m) 1.23-1.55 (8H, m) 2.38-2.62 (8H, m) 6.95-7.15 (16H, m) 7.55 (2H, s) 9.77 (2H, s).
Compound 9
To a solution of intermediate 21 (110 mg, 0.11 mmol) in anhydrous chloroform (13 cm3) is added pyridine (0.6 cm3, 8 mmol). The mixture is then degassed with nitrogen before 3-(dicyanomethylidene) indan-1-one (150 mg, 0.77 mmol) is added. The solution is then further degassed and stirred at 23° C. for 20 minutes. The mixture is stirred at 60° C. for 17 hours. The solvent is removed in vacuo abd the crude is triturated with ethanol (150 cm3) at 60° C. to produce a heavy suspension. The crude is purified using silica gel column chromatography (dichloromethane). Fractions containing pure product are combined and the solvent removed in vacuo to give Compound 9 (120 mg, 81%) as a dark blue solid. 1H NMR (400 MHz, CDCl3) 0.80 (12H, m) 1.10-1.35 (24H, m) 1.54 (8H, m) 2.52 (8H, m) 6.99-7.16 (16H, m) 7.55-7.73 (6H, m) 7.77-7.92 (2H, m) 8.61 (2H, d, J 7.3) 8.78 (2H, s).
5-Dibromo-3,6-difluoro-terephthalic acid diethyl ester (10.7 g, 25.7 mmol), tributyl-thieno[3,2-b]thiophen-2-yl-stannane (32.4 g; 64.2 mmol) and tri(o-tolyl)-phosphine (63 mg, 0.21 mmol) are dissolved in toluene (43 cm3) and degassed with nitrogen. Bis(dibenzylidene-acetone)palladium(0) (300 mg, 0.51 mmol) is added and the reaction heated to 130° C. externally for 5 hours. The reaction mixture is concentrated in vacuo, dissolved in hot dichloromethane (500 cm3) and filtered through a silica pad. The filtrate is concentrated, suspended in 40-60 petrol and filtered. The filter cake is washed with petrol (3×20 cm3). The resulting solid is recrystallized (chloroform/methanol) to give intermediate 22 (7.45 g, 54%) as a pale yellow solid. 1H NMR (400 MHz, CDCl3) 1.14 (6H, t), 4.27 (4H, q), 7.29 (2H, q), 7.40 (2H, d), 7.45 (2H, d).
1-Bromo-4-hexyl-benzene (11.3 g, 46.8 mmol) is dissolved in anhydrous tetrahydrofuran (200 cm3) and placed in a cooling bath at −78° C. T-butyllithium (55.0 cm3, 93.5 mmol) is added dropwise over 10 minutes and the solution stirred for 40 minutes. Warmed to between −45° C. and −50° C. for 30 minutes. 2,5-Difluoro-3,6-bis-thieno[3,2-b]thiophen-2-yl-terephthalic acid diethyl ester (5.00 g, 9.35 mmol) is added as a single portion, the resulting suspension maintained at −40° C. to −50° C. for 70 minutes before slowly warming to 23° C. stirring over 17 hours. The reaction is quenched with water (100 cm3), extracted with ether (2×200 cm3) and the combined extracts dried over magnesium sulphate, filtered and concentrated in vacuo. The oil is dissolved in toluene (100 cm3) and degassed with nitrogen for 15 minutes. P-toluenesulphonic acid (3 g) is added and the reaction heated to 80° C. for 6 hours. The reaction mixture is concentrated in vacuo, passed through a silica plug eluting with 40-60 petrol and then dichloromethane to give intermediate 23 as a yellow solid (250 mg, 2.5%). 1H NMR (400 MHz, CD2Cl2) 0.90 (12H, m), 1.33 (24H, m), 1.62 (8H, m), 2.61 (8H, m), 7.16 (8H, d), 7.25 (8H, d), 7.38 (4H, m). 19F NMR 126.4 (2F, s).
Intermediate 23 (350 mg, 0.33 mmol) is dissolved in tetrahydrofuran (50 cm3), cooled to 0° C. and 1-bromopyrrolidine-2,5-dione (130 mg, 0.73 mmol) added portionwise. The reaction is allowed to warm to 23° C. and stirred over 17 hours. The reaction is concentrated in vacuo to dryness and triturated in methanol (2×10 cm3), filtered and washed with methanol (2×5 cm3) to give intermediate 24 as a yellow solid (257 mg, 64%). 1H NMR (400 MHz, CDCl3) 0.87 (12H, t), 1.26-1.35 (24H, m), 1.56 (8H, m), 2.57 (8H, t), 7.10 (8H, d), 7.17 (8H, d), 7.29 (2H, s).
Intermediate 24 (120 mg, 0.10 mmol), tributyl-(5-[1,3]dioxolan-2-yl-thiophen-2-yl)-stannane (0.11 cm3, 0.23 mmol), tris(o-tolyl)phosphine (9 mg, 0.03 mmol) and toluene (18 cm3, 170 mmol) are combined and purged with nitrogen. Tris(dibenzylideneacetone) dipalladium(0) (7 mg, 0.01 mmol) is added, the reaction purged with nitrogen and heated to 140° C. externally over 17 hours. The reaction mixture is concentrated in vacuo, dissolved in 1:1 40-60 petrol:dichloromethane and passed through a silica plug. The resulting yellow solution is concentrated then dissolved in tetrahydrofuran (15 cm3), 2N hydrochloric acid (5 cm3) is added, and the biphasic solution stirred over 17 hours at 23° C. The organic phase is concentrated in vacuo and purified by column chromatography (gradient from 40-60 petrol to dichloromethane) to give intermediate 25 as an orange solid (99 mg, 79%). 1H NMR (400 MHz, CDCl3) 0.88 (12H, t), 1.28-1.39 (24H, m), 1.60 (8H, m), 2.60 (8H, t), 7.16 (8H, d), 7.24 (10H, m), 7.60 (2H, s) 7.67 (2H, d) 9.87 (2H, s). 19F-NMR 124.76 (2F, s).
Compound 10
Intermediate 25 (99 mg, 0.08 mmol) is dissolved in anhydrous trichloromethane (8.3 cm), pyridine (0.4 cm3, 5.4 mmol) is added and the solution purged with nitrogen. 2-(3-Oxo-indan-1-ylidene)-malononitrile (105 mg, 0.54 mmol) is then added. The reaction is purged with nitrogen and stirred at 23° C. for 2 hours, poured onto methanol (100 cm3) and filtered. The filter cake is washed with methanol affording Compound 10 as a blue/black solid (98 mg, 77%)1H NMR (400 MHz, CDCl3) 0.79 (12H, t), 1.19-1.26 (24H, m), 1.48-1.58 (8H, m), 2.52 (8H, t), 7.06 (8H, d), 7.17 (8H, m), 7.25 (2H, d) 7.68-7.70 (4H, m) 7.86 (2H, d) 8.62 (2H, d) 8.76 (2H, s). 19F-NMR 124.41 (2F, s).
To a solution of 1-bromo-4-hexyl-benzene (6.24 g, 25.9 mmol) in anhydrous tetrahydrofuran (69 cm3) at −78° C., n-butyllithium (10 cm3, 25 mmol, 2.5 M in hexane) is added dropwise over 10 minutes. The reaction is allowed to stir at −78° C. for 80 minutes, before intermediate 1 (1.65 g, 3.23 mmol) is added in one portion. The reaction mixture is stirred at 23° C. for 17 hours, quenched by the addition of water (100 cm3) and stirred for 72 hours. The reaction is then extracted with ethyl acetate (2×50 cm3) and the combined organic extracts washed with water (100 cm3), extracting the aqueous layer with additional ethyl acetate (25 cm3). The combined organic extracts are further washed with brine (100 cm3), again extracting the aqueous layer with additional ethyl acetate (50 cm3), before drying the combined organic extracts over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. Partial purification is by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 4:1 to 3:2) to give the intermediate which is taken up in dichloromethane (125 cm3) and the mixture degassed. Toluene-4-sulfonic acid monohydrate (955 mg, 5.02 mmol) is added and the reaction heated at reflux for 17 hours, before cooling to 23° C. diluting with water (100 cm3). The organics are extracted with dichloromethane (2×25 cm3) and the combined organic extracts washed with brine (100 cm3) and the residual aqueous layer extracted with dichloromethane (25 cm3). The combined organic extracts are then dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. Purification is by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:0 to 3:1) followed by a further second column chromatography (40-60 petrol) purification to give intermediate 26 (902 mg, 26%) as a white crystalline solid. 1H NMR (400 MHz, CDCl3) 7.31 (2H, dd, J 8.1, 1.4), 7.24 (2H, d, J 8.1), 7.17 (2H, d, J 1.2), 6.69-6.76 (8H, m), 6.57-6.63 (8H, m), 2.35-2.49 (8H, m), 1.47-1.55 (8H, m), 1.26-1.38 (24H, m), 0.86-0.94 (12H, m).
An oven dried nitrogen flushed flask is charged with intermediate 26 (902 mg, 0.85 mmol) and anhydrous toluene (150 cm3). Tributyl-(5-[1,3]dioxolan-2-yl-thiophen-2-yl)-stannane (0.93 cm3, 2.0 mmol) is added. The solution is degassed with nitrogen for 30 minutes before tris(dibenzylideneacetone)dipalladium (62 mg, 0.07 mmol) and tri(o-tolyl)phosphine (78 mg, 0.26 mmol) are added and the degassing continued for a further 30 minutes. The reaction mixture is heated at 80° C. for 17 hours before concentration in vacuo. The resulting solid is triturated with methanol (5×10 cm3) and collected by filtration to give the intermediate which is used without further purification. To a stirred solution of the intermediate in anhydrous tetrahydrofuran (81 cm3) at 23° C., concentrated hydrochloric acid (0.65 cm3, 5.7 mmol, 32%) is added dropwise. After 50 minutes, water (2.0 cm3) is added and the reaction mixture stirred for a further 1 hour. The reaction mixture is then diluted with water (125 cm3) and extracted with dichloromethane (4×25 cm3). The combined organic extracts are then washed with brine (100 cm3), additionally extracting the aqueous layer with dichloromethane (2×25 cm3). The combined organic extracts are dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. Purification by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 7:3 to 2:3) gives intermediate 27 (586 mg, 61%) as an orange solid. 1H NMR (400 MHz, CDCl3) 9.82 (2H, s), 7.64 (2H, d, J 3.9), 7.54 (2H, dd, J 8.0, 1.6), 7.44 (2H, d, J 8.3), 7.35 (2H, d, J 1.2), 7.24 (2H, d, J 3.9), 6.79 (8H, d, J 8.3), 6.63 (8H, d, J 8.3), 2.35-2.49 (8H, m), 1.47-1.56 (8H, m), 1.26-1.37 (24H, m), 0.85-0.92 (12H, m).
Compound 11
To a solution of intermediate 27 (535 mg, 0.48 mmol) in anhydrous chloroform (51 cm3) is added pyridine (2.7 cm3, 33 mmol). The mixture is degassed with nitrogen for 20 minutes before 3-(dicyanomethylidene)indan-1-one (648 mg, 3.34 mmol) is added. The resulting solution is degassed for a further 10 minutes before stirring for 3 hours. The reaction mixture is then added to stirred methanol (500 cm3), washing in with additional methanol (25 cm3) and dichloromethane (25 cm3). The precipitate is collected by filtration and washed with methanol (5×10 cm3), warm methanol (5×10 cm3), 40-60 petrol (3×10 cm3), diethyl ether (3×10 cm3), 80-100 petrol (3×10 cm3) and acetone (3×10 cm3) to give Compound 11 (645 mg, 92%) as a blue/black solid. 1H NMR (400 MHz, CDCl3) 8.77 (2H, s), 8.64-8.70 (2H, m), 7.89-7.94 (2H, m), 7.71-7.79 (6H, m), 7.61 (2H, dd, J 8.1, 1.7), 7.44 (2H, d, J 1.5), 7.38 (2H, d, J 8.1), 7.29 (2H, d, J 4.2), 6.85 (8H, d, J 8.3), 6.68 (8H, d, J 8.3), 2.38-2.52 (8H, m), 1.49-1.60 (8H, m), 1.24-1.40 (24H, m), 0.88 (12H, t, J 6.9).
To a solution of 2,7-dibromo-4,4,9,9-tetrakis(4-octylphenyl)-4,9-dihydro-thieno[3′,2′:4,5]cyclopenta[1,2-b]thieno[2″,3″:3′,4′]cyclopenta[1′,2′:4,5]thieno[2,3-d]thiophene (500 mg, 0.34 mmol) in anhydrous toluene (150 cm3) is added tributyl-(5-[1,3]dioxolan-2-yl-thiophen-2-yl)-stannane (0.88 cm3, 1.94 mmol) before the solution is degassed with nitrogen. Tris(dibenzylideneacetone)dipalladium (59 mg, 0.03 mmol) and tris(o-tolyl)phosphine (74 mg, 0.24 mmol) are then added and after additional degassing, the reaction mixture is heated at 80° C. for 17 hours. The reaction mixture is then concentrated in vacuo and triturated with methanol (5×20 cm3) collecting the solid by filtration to give intermediate 28 (1.1 g, 99%) as an orange solid. 1H NMR (400 MHz, CDCl3) 7.12-7.19 (10H, m), 7.09 (8H, d, J 7.8), 7.00-7.05 (4H, m), 6.08 (2H, s), 4.08-4.17 (4H, m), 3.99-4.08 (4H, m), 2.56 (8H, t, J 7.8), 1.52-1.63 (8H, m), 1.22-1.35 (40H, m), 0.87 (12H, t, J 6.5).
Concentrated hydrochloric acid (0.5 cm3, 4.07 mmol, 32%) is added dropwise to a solution of intermediate 28 (1.1 g, 0.81 mmol) in tetrahydrofuran (57 cm3) at 23° C. and the reaction mixture stirred for 1 hour. Water (0.5 cm3) is then added and the reaction mixture stirred for a further 17 hours. Additional water (100 cm3) is then added and the solution extracted with ethyl acetate (50 cm3 then 25 cm3). The combined organic extracts are then washed with water (50 cm3) and brine (50 cm3), extracting the aqueous layer each time with additional ethyl acetate (20 cm3). The combined organic extracts are then dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The crude product is then triturated with methanol (3×15 cm3) with collection by filtration and the solid washed with 40-60 petrol (3×15 cm3) to give intermediate 29 (291 mg, 28%) as an orange solid. 1H NMR (400 MHz, CDCl3) 9.83 (2H, s), 7.64 (2H, d, J 3.9), 7.32 (2H, s), 7.20 (2H, d, J 3.9), 7.16 (8H, d, J 8.1), 7.11 (8H, d, J 8.0), 2.57 (8H, t, J 7.6), 1.54-1.64 (8H, m), 1.20-1.38 (40H, m), 0.82-0.92 (12H, m).
Compound 12
To a solution of intermediate 29 (287 mg, 0.22 mmol) in anhydrous chloroform (23 cm3) is added pyridine (1.3 cm3, 16 mmol). The mixture is then degassed with nitrogen before 3-(dicyanomethylidene)indan-1-one (300 mg, 1.54 mmol) is added. The solution is then further degassed and stirred at 23° C. for 3.25 hours. The reaction mixture is then added to methanol (300 cm3), the mixture concentrated in vacuo and the resulting solid triturated with methanol (3×25 cm3) with collection by filtration. The filtered solid is then washed with diethyl ether (2×10 cm3) and acetone (3×10 cm3). The partially purified product is then subjected to column chromatography, eluting with a graded solvent system (40-60 petrol:dichloromethane; 9.5:0.5 to 2:3) to give Compound 12 (86 mg, 24%) as a green/black solid. 1H NMR (400 MHz, CDCl3) 8.83 (2H, s), 8.69 (2H, d, J 7.6), 7.92 (2H, d, J 6.6), 7.69-7.79 (6H, m), 7.54 (2H, s), 7.29 (2H, d, J 4.4), 7.11-7.20 (16H, m), 2.59 (8H, t, J 7.7), 1.58-1.64 (8H, m), 1.21-1.38 (40H, m), 0.87 (12H, t, J 6.5).
To a solution of 2,7-dibromo-4,4,9,9-tetrakis(3-octylphenyl)-4,9-dihydro-thieno[3′,2′:4,5]cyclopenta[1,2-b]thieno[2″,3″:3′,4′]cyclopenta[1′,2′:4,5]thieno[2,3-d]thiophene (1.00 g, 0.77 mmol) in tetrahydrofuran (25 cm3) cooled to −78° C. is added dropwise n-butyllithium (0.92 cm3, 2.30 mmol, 2.5 M in hexanes). The reaction is stirred for one hour and quenched with N,N-dimethylformamide (1.13 cm3, 23.0 mmol) in a single portion. The reaction is warmed to 23° C. and stirred for 18 hours. The mixture is quenched with water (50 cm3) and extracted with dichloromethane (3×30 cm3). The resulting combined organic phase is washed with water (2×20 cm3), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The crude is purified by flash chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 6:4 to 4:6) to give intermediate 30 (330 mg, 36%) as an orange oil. 1H NMR (400 MHz, CDCl3) 9.73 (2H, s), 7.62 (2H, s), 7.14 (4H, t, J 8.0), 6.65-6.77 (m, 12H), 3.80 (8H, t, J 6.6), 1.58-1.69 (8H, m), 1.27-1.38 (8H, m), 1.01-1.30 (32H, m), 0.71-0.87 (12H, m).
Compound 13
To a degassed solution of intermediate 30 (330 mg, 0.27 mmol) and 3-(dicyanomethylidene)indan-1-one (373 mg, 1.92 mmol) in chloroform (8.25 cm3) is added pyridine (0.55 cm3, 6.86 mmol) and the mixture stirred at 23° C. for 2 hours. Methanol (50 cm3) is added and the resulting suspension filtered and washed with methanol (3×20 cm3). The resulting solid is purified by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:1 to 3:7) to give compound 13 (321 mg, 75%) as a blue solid. 1H NMR (400 MHz, CDCl3) 8.79 (2H, s), 8.53-8.67 (2H, m), 7.83 (2H, m), 7.61-7.73 (6H, m), 7.18 (4H, m), 6.67-6.81 (12H, m), 3.83 (8H, t, J 6.7), 1.68 (8H, m), 1.33 (8H, m), 1.12-1.29 (32H, m), 0.78 (12H, t, J 6.7).
To a solution of 2,5-dichloro-thieno[3,2-b]thiophene (17.3 g, 82.7 mmol) in anhydrous tetrahydrofuran (173 cm3) at 5° C. is added ethyl chloroformate (23.7 cm3, 248 mmol). A solution of 2,2,6,6-tetramethylpiperidinylmagnesium chloride lithium chloride complex (207 cm3; 207 mmol, 1.0 M in tetrahydrofuran) is then added dropwise over 1 hour. The reaction is slowly warmed to 23° C. and stirred for 42 hours. Water (200 cm3) is added, the mixture stirred for 10 minutes and the solid collected by filtration and washed with water (2×100 cm3). The solid is triturated in acetone (200 cm3), the solid collected by filtration and washed with acetone (2×100 cm3) to give intermediate 31 (26.6 g, 91%) as a white solid. 1H NMR (400 MHz, CDCl3) 4.46 (4H, q, J 7.1), 1.47 (6H, t, J 7.1).
Trimethyl-(5-tributylstannanyl-thiophen-2-yl)-silane (30.5 g, 61.7 mmol), intermediate 31 (10.0 g, 28.3 mmol) and tetrakis(triphenylphosphine)palladium(0) (657 mg, 0.57 mmol) are suspended in anhydrous toluene (100 cm3) and heated at 100° C. for 18 hours. The reaction is cooled to 23° C. and methanol (250 cm3) added. The suspension is cooled in an ice-bath, the solid collected by filtration and washed with methanol (200 cm3). The crude is purified by silica pad (dichloromethane) followed by flash chromatography eluting with 40-60 petrol:dichloromethane; 60:40 to give intermediate 32 (7.68 g, 46%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 7.42 (2H, d, J 3.5), 7.02 (2H, d, J 3.5), 4.19 (4H, q, J 7.1), 1.19 (6H, t, J 7.1), 0.15 (18H, s).
To a solution of 1-bromo-4-octyloxy-benzene (14.1 g, 49.5 mmol) in anhydrous tetrahydro-furan (73 cm3) at −78° C. is added dropwise t-butyllithium (58.2 cm3, 99.0 mmol, 1.7 M in pentane) over 20 minutes. The reaction is warmed to between −28° C. and −35° C. for 30 minutes. A second portion of 1-bromo-4-octyloxy-benzene (3.0 g, 11 mmol) is added and the reaction mixture stirred for 30 minutes. The reaction is cooled to −78° C. and a solution of intermediate 32 (4.89 g, 8.25 mmol) in anhydrous tetrahydrofuran (30 cm3) is rapidly added. The reaction is warmed to 23° C. and stirred for 60 hours. Water (50 cm3) is added and the organics extracted with ether (300 cm3). The organic phase is washed with water (3×100 cm3), dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude purified by column chromatography using a gradient solvent system (40-60 petrol:dichloromethane; 9:1 to 8:2) to give intermediate 33 (3.17 g, 29%) as a pale brown solid. 1H NMR (400 MHz, CDCl3) 7.16-7.23 (8H, m), 6.88 (2H, d, J 3.4), 6.78-6.85 (8H, m), 6.51 (2H, d, J 3.4), 3.97 (8H, t, J 6.6), 3.37 (2H, s), 1.75-1.84 (8H, m), 1.27-1.52 (40H, m), 0.82-0.95 (12H, m), 0.25 (18H, s).
To a solution of 2,7-dibromo-4,4,9,9-tetrakis(4-(octyloxy)phenyl)-4,9-dihydro-thieno[3′,2′:4,5]cyclopenta[1,2-b]thieno[2″,3″:3′,4′]cyclopenta[1′, 2′:4,5]thieno[2,3-d]thiophene (1.00 g, 0.77 mmol) in tetrahydrofuran (25 cm3) cooled to −78° C. is added dropwise n-butyllithium (0.92 cm3, 2.30 mmol, 2.5 M in hexanes). The reaction is stirred for a further 1 hour and quenched with N,N-dimethylformamide (1.13 cm3, 23.0 mmol) as a single portion. The reaction is warmed to 23° C. and stirred for 18 hours. The reaction is quenched with water (50 cm3), extracted with dichloromethane (3×30 cm3). The resulting organic phase is washed with water (2×20 cm3), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The crude is purified by flash chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 6:4 to 4:6) to give intermediate 34 (330 mg, 36%) as an orange oil. 1H NMR (400 MHz, CDCl3) 9.72 (2H, s), 7.58 (2H, s), 7.00-7.08 (8H, m), 6.69-6.82 (8H, m), 3.83 (8H, t, J 6.5), 1.61-1.71 (8H, m), 1.34 (8H, m), 1.11-1.33 (32H, m), 0.72-0.90 (12H, m).
To a degassed solution of intermediate 33 (6.00 g, 4.52 mmol) in toluene (240 cm3) is added amberlyst 15 strong acid (24 g), the mixture further degassed.purged and then heated at 75° C. for 18 hours. The solution is cooled to about 50° C., filtered and the solid washed with toluene (200 cm3). The filtrate is concentrated and triturated with 80-100 petrol (3×30 cm3) with the solid collected by filtration. The solid is dissolved in chloroform (120 cm3), N,N-dimethylformamide (5.3 g, 72 mmol) added and the solution cooled to 0° C. Phosphorus(V) oxychloride (10.4 g, 67.9 mmol) is added over 10 minutes. The reaction mixture is then heated at 65° C. for 18 hours. Aqueous sodium acetate solution (150 cm3, 2 M) is added at 65° C. and the reaction mixture stirred for 1 hour. Saturated aqueous sodium acetate solution is added until the mixture is pH 6 and the reaction stirred for a further 30 minutes. The aqueous phase is extracted with chloroform (2×25 cm3) and the combined organic layers washed with water (50 cm3), dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The solid is triturated in 80-100 petrol and the solid collected by filtration to give intermediate 34 (3.06 g, 56%) as an orange oil. 1H NMR (400 MHz, CDCl3) 9.72 (2H, s), 7.58 (2H, s), 7.00-7.08 (8H, m), 6.69-6.82 (8H, m), 3.83 (8H, t, J 6.5), 1.61-1.71 (8H, m), 1.34 (8H, m), 1.11-1.33 (32H, m), 0.72-0.90 (12H, m).
Compound 14
To a degassed solution of intermediate 34 (330 mg, 0.27 mmol) and 3-(dicyanomethylidene)indan-1-one (373 mg, 1.92 mmol) in chloroform (8.25 cm3) is added pyridine (0.55 cm3, 6.86 mmol) and the mixture stirred at 23° C. for 4 hours. Methanol (50 cm3) is added and the resulting suspension is filtered and washed with methanol (3×20 cm3). The crude is purified by column chromatography (40-60 petrol:dichloromethane; 1:1) to give compound 14 (141 mg, 33%) as a blue solid. 1H NMR (400 MHz, CDCl3) 8.79 (2H, s), 8.60 (2H, m), 7.75-7.91 (2H, m), 7.67 (4H, m), 7.61 (s, 2H), 7.04-7.12 (8H, m), 6.74-6.81 (8H, m), 3.85 (8H, t, J 6.5), 1.68 (8H, m), 1.11-1.43 (40H, m), 0.72-0.84 (12H, m).
To a solution of 1-bromo-3,5-dihexyl-benzene (9.00 g, 27.7 mmol) in anhydrous tetrahydrofuran (135 cm3) cooled to −78° C. is added dropwise a solution of n-butyllithium (11.1 cm3, 27.7 mmol, 2.5 M in hexanes) over 10 minutes. The reaction is stirred for one hour and methyl 5-bromo-2-[5-(4-bromo-2-methoxycarbonyl-phenyl)thieno[3,2-b]thiophen-2-yl]benzoate (3.13 g, 5.53 mmol) is added as a single portion. The reaction is warmed to 23° C. and stirred for 18 hours. The reaction is partitioned between diethyl ether (50 cm3) and water (100 cm3). The organic phase is washed with water (30 cm3), brine (30 cm3), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The crude is triturated with 40-60 petrol, and the solid suspended in toluene (50 cm3). p-Toluene sulphonic acid (2.5 g) is added and the reaction mixture and stirred for 17 hours. The suspension is filtered, concentrated in vacuo and purified via flash chromatography eluting with a mixture of DCM petroleum ether 40:60. The resulting material is triturated in acetone and the solid collected to give intermediate 35 (2.71 g, 34%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 7.42 (2H, d, J 1.7), 7.32 (2H, dd, J 8.1, 1.8), 7.11 (2H, d, J 8.1), 6.80 (4H, t, J 1.5), 6.71 (8H, d, J 1.5), 2.40 (16H, t, J 7.7), 1.38-1.48 (16H, m), 1.11-1.24 (48H, m), 0.70-0.79 (24H, m).
To a degassed solution of intermediate 35 (250 mg, 0.17 mmol), tributyl-(5-[1,3]dioxolan-2-yl-thiophen-2-yl)-stannane (0.18 cm3, 0.40 mmol) and tris(o-tolyl)phosphine (16 mg, 0.05 mmol) in toluene (12.5 cm3) is added bis(dibenzylideneacetone)palladium(0) (16 mg, 0.02 mmol) and the mixture further degassed. The reaction is then heated to an external temperature of 140° C. for 6 hours. The reaction mixture is allowed to cool and concentrated in vacuo. The crude is purified by flash chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:9 to 3:10). The resulting oil is dissolved in chloroform (30 cm3) and stirred with 2.5 N hydrochloric acid solution (10 cm3) for 18 hours. The organic phase is concentrated in vacuo and the residue purified by flash chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:4 to 1:4). The resulting solid is triturated in acetone and the solid collected by filtration to give intermediate 36 (170 mg, 65%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 9.78 (2H, s), 7.59-7.65 (4H, m), 7.55 (2H, dd, J 8.0, 1.6), 7.31 (2H, d, J 8.0), 7.24 (2H, d, J 3.9), 6.82 (4H, s), 6.78 (8H, s), 2.41 (16H, t, J 7.6), 1.39-1.49 (16H, m), 1.17 (48H, m), 0.69-0.85 (24H, m).
Compound 15
To a degassed solution of intermediate 36 (170 mg, 0.11 mmol) and 3-(dicyanomethylidene)indan-1-one (153 mg, 0.79 mmol) in chloroform (4.25 cm3) is added pyridine (0.63 cm3, 7.86 mmol) and the mixture stirred at 23° C. for 18 hours. Methanol (75 cm3) is added and the resulting suspension filtered and washed with methanol (3×10 cm3). The resulting solid is purified by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:1 to 2:3) to give Compound 15 (32 mg, 15%) as a blue solid. 1H NMR (400 MHz, CD2Cl2) 8.75 (2H, s), 8.55-8.64 (2H, m), 7.82-7.87 (2H, m), 7.64-7.80 (10H, m), 7.25-7.49 (4H, m), 6.80-6.87 (12H, m), 2.42 (16H, t, J 7.6), 1.47 (16H, m), 1.11-1.23 (48H, m), 0.67-0.75 (m, 24H).
To a solution of 1-bromo-3-hexyl-benzene (6.39 g, 26.5 mmol) and anhydrous tetrahydrofuran (45 cm3) at −78° C. is added dropwise a solution of n-butyllithium (10.6 cm3, 26.5 mmol, 2.5 M in hexanes) over 10 minutes. The reaction mixture is stirred for 1 hour and methyl 5-bromo-2-[5-(4-bromo-2-methoxycarbonyl-phenyl)thieno[3,2-b]thiophen-2-yl]benzoate (3.00 g, 5.3 mmol) added as a single portion. The reaction is warmed to 23° C. and stirred for 17 hours. The reaction is partitioned between diethyl ether (100 cm3) and water (100 cm3). The organic phase is washed with water (2×50 cm3), brine (20 cm3), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The resulting oil is triturated with 40-60 petrol and the solid suspended in toluene (40 cm3). p-Toluene sulphonic acid (2.0 g) is added and the reaction mixture stirred for 17 hours. The suspension is filtered and concentrated in vacuo. The resulting material is triturated in acetone at 50° C. and then filtered at 0° C. to give intermediate 37 (1.28 g, 22%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 7.51 (2H, d, J 1.7), 7.41 (2H, dd, J 8.1, 1.8), 7.13-7.25 (6H, m), 7.04-7.12 (8H, m), 6.92-6.98 (4H, m), 2.50-2.59 (m, 8H), 1.54 (8H, m), 1.18-1.24 (m, 24H), 0.79-0.88 (m, 12H).
To a degassed solution of intermediate 37 (250 mg, 0.22 mmol), tributyl-(5-[1,3]dioxolan-2-yl-thiophen-2-yl)-stannane (277 mg, 0.52 mmol) and tris(o-tolyl)phosphine (21 mg, 0.07 mmol) in toluene (12.5 cm3) is added bis(dibenzylideneacetone)palladium(0) (21 mg, 0.02 mmol). The solution is further degassed and then heated to an external temperature of 140° C. for 6 hours. The reaction mixture is concentrated in vacuo and purified by flash chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:1 to 1:3). The resulting oil is dissolved in chloroform (10 cm3) and stirred with 2.5 N hydrochloric acid (10 cm3) for 18 hours. The organic phase is washed with water (10 cm3) and brine (20 cm3) before being concentrated in vacuo. The resulting solid is triturated in acetone to give intermediate 38 (75 mg, 28%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 9.86 (2H, s), 7.67-7.74 (4H, m), 7.63 (2H, m), 7.41 (2H, d, J 8.0), 7.34 (2H, d, J 3.9), 7.06-7.23 (12H, m), 6.98-7.06 (4H, m), 2.56 (8H, t, J 7.6), 1.55 (8H, m), 1.19-1.33 (m, 24H), 0.82 (12H, m).
Compound 16
To a degassed solution of intermediate 38 (75 mg, 0.06 mmol) and 3-(dicyanomethylidene)indan-1-one (87 mg, 0.45 mmol) in chloroform (1.9 cm3) is added pyridine (0.36 cm3, 4.46 mmol) and the reaction mixture stirred at 23° C. for 18 hours. Methanol (40 cm3) is added and the resulting suspension filtered and washed with methanol (3×10 cm3). The resulting solid is purified by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:1 to 2:3) to give Compound 16 (63 mg, 65%) as a blue solid. 1H NMR (400 MHz CD2Cl2) 8.75 (2H, s), 8.60 (2H, dd, J 7.1, 11.4), 7.84 (2H, dd, J 6.9, 1.8), 7.63-7.80 (8H, m), 7.44 (2H, d, J 8.4), 7.39 (2H, d, J 4.2), 7.08-7.15 (8H, m), 7.04 (4H, d, J 7.6), 6.96 (4H, m), 2.49 (8H, t, J 7.6), 1.49 (8H, t, J 4.2), 1.09-1.26 (24H, m), 0.68-0.76 (12H, m).
Compound 17
To a solution of intermediate 10 (450 mg, 0.32 mmol) in anhydrous chloroform (34 cm3) is added pyridine (1.8 cm3, 22 mmol). The mixture is then degassed with nitrogen before malononitrile (148 mg, 2.24 mmol) is added. The solution is then further degassed and stirred at 23° C. for 41 hours. The reaction mixture is then added to methanol (350 cm3), washing in with additional methanol (2×10 cm3) and dichloromethane (2×5 cm3). Additional methanol (35 cm3) is then added and the mixture stirred at 23° C. for 50 minutes before filtration, washing the solid with methanol (3×20 cm3), 40-60 petrol (3×20 cm3), 80-100 petrol (3×20 cm3), cyclohexane (3×20 cm3), diethyl ether (4×20 cm3) and acetone (4×20 cm3) to give Compound 17 (429 mg, 89%) as a black solid. 1H NMR (400 MHz, CDCl3) 8.75 (2H, s), 8.68 (2H, d, J 8.1), 8.29 (2H, s), 7.78 (2H, d, J 7.8), 7.24 (8H, d, J 8.4), 7.14 (8H, d, J 8.3), 2.58 (8H, t, J 7.7), 1.56-1.65 (8H, m), 1.20-1.37 (40H, m), 0.85 (12H, t, J 6.9).
Compound 18
To a degassed solution of intermediate 34 (200 mg, 0.17 mmol) and 2-(3-ethyl-4-oxo-thiazolidin-2-ylidene)-malononitrile (225 mg, 1.16 mmol) in chloroform (5 cm3) is added pyridine (0.94 cm3, 12 mmol) followed by piperidine (992 mg, 11.7 mmol). The reaction is stirred at 23° C. for 18 hours and then precipitated with methanol (50 cm3), filtered and purified by flash chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 3:2 to 2:3). The isolated material is then triturated in acetone (10 cm3) and the solid collected by filtration to give Compound 18 (48 mg, 19%) as a blue solid. 1H NMR (400 MHz, CDCl3) 7.97 (2H, s), 7.30 (2H, s), 7.01-7.08 (8H, m), 6.72-6.79 (8H, m), 4.24 (4H, q, J 7.1), 3.84 (8H, t, J 6.5), 1.67 (8H, q, J 6.8), 1.30-1.40 (14H, m), 1.11-1.28 (32H, m), 0.76-0.84 (12H, m).
To a solution of 3-methoxy-thiophene (25.0 g, 219 mmol) in anhydrous N,N-dimethylformamide (100 cm3) at 0° C. is added dropwise, over 20 minutes, a solution of 1-bromo-pyrrolidine-2,5-dione (39.0 g, 219 mmol) in anhydrous N,N-dimethylformamide (150 cm3) and the reaction stirred to 23° C. for 65 hours. The reaction mixture is then diluted with diethyl ether (100 cm3), washed with brine (250 cm3) diluted with water (250 cm3) and the organic layer separated. The aqueous layer is then extracted with diethyl ether (2×100 cm3 then 50 cm3) and the combined organic extracts washed with brine (3×100 cm3) extracting the aqueous layer each time with diethyl ether (50 cm3). The combined organic extracts are then dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The crude is purified by silica plug, eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:0-4:1). The fractions containing product are concentrated in vacuo at 23° C. and rapidly placed on an ice water bath. Anhydrous tetrahydrofuran (150 cm3) is then added and the flask placed under nitrogen atmosphere. At 0° C. with stirring, additional anhydrous tetrahydrofuran (150 cm3) is added before the solution is cooled to −78° C. and lithium diisopropylamide (120 cm3, 240 mmol, 2.0 M in tetrahydrofuran/heptane/ethylbenzene) is added dropwise over 40 minutes. The reaction mixture is stirred at −78° C. for 2 hours before the reaction is quenched by the dropwise addition of anhydrous N,N-dimethylformamide (202 cm3, 2630 mmol), maintaining the reaction temperature at −78° C. The reaction is then allowed to warm to 23° C. with stirring over 17 hours before addition to ice (600 cm3), followed by the addition of pentane (400 cm3) and stirring for 17 hours. The pentane layer is isolated and the aqueous layer extracted with pentane (2×100 cm3). The combined pentane extracts are then washed with 20 wt % citric acid solution (2×150 cm3), water (150 cm3) and brine (150 cm3), extracting the aqueous layer each time with pentane (50 cm3). The combined pentane extracts are then dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The crude is then purified by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:0-3:2) to give intermediate 39 (1.96 g, 4%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 9.84 (1H, s), 6.90 (1H, s), 3.96 (3H, s).
To a degassed solution of intermediate 9 (700 mg, 0.42 mmol) and 2-bromo-3-methoxythiophene-5-carboxaldehyde (205 mg, 0.93 mmol) in anhydrous toluene (45 cm3), tris(dibenzylideneacetone)dipalladium (31 mg, 0.03 mmol) and tris(o-tolyl)phosphine (39 mg, 0.13 mmol) are added. The reaction is then further degassed for 20 minutes before heating to 80° C. for 17 hours. The reaction mixture is then concentrated in vacuo, triturated with methanol (5×20 cm3) and the solid filtered. The crude product is then purified by silica plug eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:1-1:4 then dichloromethane:methanol; 1:0-9.5:0.5). Final purification is achieved by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 2:3-1:4 then dichloromethane:methanol; 1:0-9:1) to give intermediate 40 (134 mg, 23%) as a dark brown solid. 1H NMR (400 MHz, CDCl3) 9.92 (2H, s), 7.31 (2H, s), 7.12-7.17 (8H, m), 7.08-7.12 (8H, m), 6.84 (2H, s), 4.01 (6H, s), 2.53-2.60 (8H, m), 1.54-1.64 (8H, m), 1.20-1.37 (40H, m), 0.87 (12H, t, J 6.9).
Compound 19
To a solution of intermediate 40 (134 mg, 0.10 mmol) in anhydrous chloroform (10 cm3) is added pyridine (0.6 cm3, 6.9 mmol). The mixture is then degassed with nitrogen before 3-(dicyanomethylidene)indan-1-one (134 mg, 0.69 mmol) is added. The solution is then further degassed and stirred at 23° C. for 20 minutes before additional anhydrous degassed chloroform (5 cm3) is added and the reaction stirred for a further 3 hours 20 minutes. The reaction mixture is then added to methanol (250 cm3), washing in with methanol (2×10 cm3) and dichloromethane (2×5 cm3). Additional methanol (50 cm3) is then added before the solid is filtered and then washed with additional methanol (10×10 cm3). The crude product is then partially purified by column chromatography using a graded solvent system (chloroform then dichloromethane:methanol; 9.5:0.5) with final purification achieved by trituration with methanol (3×10 cm3) washing the filtered solid with 40-60 petrol (3×10 cm3), cyclohexane (3×10 cm3) and diethyl ether (3×10 cm3) to give Compound 19 (58 mg, 34%) as a black solid. 1H NMR (400 MHz, CDCl3) 9.16 (2H, s), 8.62-8.67 (2H, m), 7.82-7.87 (2H, m), 7.63-7.72 (4H, m), 7.58 (2H, s), 7.12-7.19 (16H, m), 6.89 (2H, s), 4.13 (6H, s), 2.59 (8H, t, J 7.7), 1.57-1.65 (8H, m), 1.22-1.36 (40H, m), 0.87 (12H, t, J 6.8).
To a solution of 1-bromo-4-hexyl-benzene (10.0 g, 41.5 mmol) in anhydrous tetrahydrofuran (70 cm3) at −78° C. is added n-butyllithium (16.6 cm3, 41.5 mmol, 2.5 M in hexane) portion-wise over 10 minutes. The reaction is stirred for one hour and methyl 5-bromo-2-[5-(4-bromo-2-methoxycarbonyl-phenyl)thieno[3,2-b]thiophen-2-yl]benzoate (4.70 g, 8.29 mmol) added in a single portion. The reaction is warmed to 23° C. and stirred for 17 hours. The reaction is partitioned between diethyl ether (100 cm3) and water (100 cm3). The organic phase is washed with water (2×50 cm3), brine (20 cm3), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The resulting oil is triturated with 40-60 petrol, and the solid suspended in toluene (40 cm3), p-toluene sulphonic acid (2.0 g) added and the reaction mixture stirred at 23° C. for 17 hours. The suspension is filtered and concentrated in vacuo. The resulting material is triturated in acetone at 50° C. then filtered at 0° C. to give intermediate 41 (3.4 g, 37%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 7.52 (2H, d, J 1.7), 7.40 (2H, dd, J 8.1, 1.8), 7.21 (2H, d, J 8.1), 7.06-7.15 (m, 16H), 2.52-2.61 (m, 8H), 1.58 (8H, m), 1.22-1.40 (24H, m), 0.83-0.92 (12H, m).
To a degassed solution of intermediate 41 (250 mg, 0.22 mmol), tributyl-(5-[1,3]dioxolan-2-yl-thiophen-2-yl)-stannane (273 mg, 0.51 mmol) and tris(o-tolyl)phosphine (2 mg, 0.01 mmol) in toluene (12.5 cm3) is added bis(dibenzylideneacetone)palladium(0) (20 mg, 0.02 mmol). The solution is further degassed and heated to an external temperature of 140° C. for 18 hours. Methanol (20 cm3) is added, the suspension is stirred for 30 minutes, filtered and the solid washed with methanol (20 cm3). The resulting solid is purified by flash chromatography eluting with 40:60 petrol followed by dichloromethane. The resulting solid is dissolved in chloroform (30 cm3) and stirred with hydrochloric acid (10 cm3, 3 N) for 4 hours. The organic phase is washed with water (10 cm3), dried over anhydrous magnesium sulfate, filtered before being concentrated in vacuo then triturated in acetone to give intermediate 42 (160 mg, 61%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 9.78 (2H, s), 7.59-7.66 (4H, m), 7.55 (2H, dd, J 8.0, 1.5), 7.33 (2H, d, J 7.9), 7.28 (2H, d, J 3.9), 7.11 (8H, d, J 8.0), 7.03 (8H, d, J 8.0), 2.49 (8H, t, J 7.9), 1.51 (8H, m), 1.23 (24H, m), 0.71-0.83 (12H, m).
Compound 20
To a degassed solution of intermediate 42 (170 mg, 0.14 mmol) and 3-(dicyanomethylidene)indan-1-one (196 mg, 01.01 mmol) in chloroform (12.3 cm3) is added pyridine (799 mg, 10 mmol) and stirred at 23° C. for 18 hours. Methanol (30 cm3) is added and the resulting suspension filtered and the solid washed with methanol (30 cm3). The solid is triturated in acetone (10 cm3), filtered and washed with acetone (30 cm3) to give Compound 20 (214 mg, 97%) as a blue solid. 1H NMR (400 MHz, CDCl3) 8.87 (2H, s), 8.69-8.74 (2H, m), 7.92-8.00 (2H, m), 7.85 (2H, d, J 4.3), 7.72-7.82 (8H, m), 7.41-7.50 (m, 4H), 7.22 (8H, d, J 8.2), 7.14 (8H, d, J 8.1), 2.58 (8H, t, J 7.9), 1.57 (8H, m), 1.24-1.40 (24H, m), 0.82-0.91 (12H, m).
Compound 21
To a solution of intermediate 8 (303 mg, 0.27 mmol) in anhydrous chloroform (28 cm3) is added piperidine (0.1 cm3, 1.0 mmol). The mixture is then degassed with nitrogen before 2-(3-ethyl-4-oxothiazolidin-2-ylidene)malononitrile (134 mg, 0.69 mmol) is added. The solution is then further degassed and stirred at 23° C. for 17 hours. The reaction mixture is then added to methanol (300 cm3) washing in with methanol (3×5 cm3) and dichloromethane (5 cm3), before filtering the precipitate, washing in with methanol (2×10 cm3). The filtered solid is washed with additional methanol (3×10 cm3) and the crude product purified by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:1-2:3). Final purification is achieved by trituration with methanol (3×10 cm3) washing the filtered solid with 40-60 petrol (3×10 cm3), diethyl ether (10 cm3) and acetone (10 cm3) to give Compound 21 (144 mg, 36%) as a dark blue/black solid. 1H NMR (400 MHz, CDCl3) 8.05 (2H, s), 7.41 (2H, s), 7.10-7.16 (16H, m), 4.32 (4H, q, J 7.1), 2.58 (8H, t, J 7.8), 1.56-1.64 (8H, m), 1.40 (6H, t, J 7.1), 1.22-1.36 (40H, m), 0.87 (12H, t, J 6.9).
To a solution of 1-bromo-3,5-dihexyl-benzene (14.5 g, 44.6 mmol) in anhydrous tetrahydrofuran (60 cm3) at −78° C. is added dropwise n-butyllithium (17.8 cm3, 44.6 mmol, 2.5 M in hexane) over 10 minutes. The reaction is stirred for 2 hours and ethyl 2-[5-(3-ethoxycarbonyl-2-thienyl)thieno[3,2-b]thiophen-2-yl]thiophene-3-carboxylate (4.00 g, 8.92 mmol) added. The reaction is warmed to 23° C. and stirred for 17 hours. Water (100 cm3) added and the product extracted with ether (100 cm3). The organic phase is washed with water (2×50 cm3), dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is purified by flash chromatography eluting with 40-60 petrol then dichloromethane. The solid is suspended in toluene (40 cm3), p-toluene sulphonic acid (2.0 g) added and the reaction mixture heated at 60° C. for 4 hours. The solid is collected by filtration, washed with toluene (50 cm3) and purified by flash chromatography using a graded solvent system (40-60 petrol:dichloromethane; 1:0 to 95:5) to give intermediate 43 (2.5 g, 21%) as a pale brown oil. 1H NMR (400 MHz, CDCl3) 7.07 (2H, d, J 4.9), 6.96 (2H, d, J 4.9), 6.78 (4H, d, J 1.6), 6.74 (8H, d, J 1.5), 2.40 (16H, t, J 8.0), 1.40-1.48 (16H, m), 1.10-1.26 (48H, m), 0.69-0.82 (24H, m).
To intermediate 21 (0.50 g, 0.38 mmol), anhydrous N,N-dimethylformamide (0.40 cm3, 5.2 mmol) chloroform (20 cm3) at 0° C. is added dropwise phosphorus oxychloride (0.47 cm3, 5.0 mmol). The reaction is heated at 70° C. for 18 hours before cooling to 60° C., saturated aqueous sodium acetate solution (7 cm3) is added and the mixture stirred for 1 hour. The organic phase is separated and washed with water (20 cm3) dried with anhydrous sodium sulphate, filtered and the solvent removed in vacuo. The solid is triturated in acetone (3×5 cm3) to give intermediate 43 (400 mg, 76%) as a bright orange solid. 1H NMR (400 MHz, CD2Cl2) 9.78 (2H, s), 7.64 (2H, s), 6.90 (4H, d, J 1.6), 6.78 (8H, d, J 1.6), 2.46 (16H, d, J 7.9), 1.42-1.51 (16H, m), 1.17-1.28 (48H, m), 0.76-0.85 (24H, m).
Compound 22
To a degassed mixture of 2-(3-oxo-indan-1-ylidene)-malononitrile (100 mg, 0.5 mmol), intermediate 44 (100 mg, 0.07 mmol) and chloroform (10 cm3) is added pyridine (0.41 cm3, 5.1 mmol) and the mixture further degassed. The reaction mixture is stirred for 4 hours, methanol (40 cm3) added and the suspension filtered. The solid is then washed with methanol (40 cm3) to give Compound 22 (101 mg, 84%) as a dark blue solid. 1H NMR (400 MHz, CDCl3) 8.87 (2H, s), 8.64-8.71 (2H, m), 7.84-7.96 (2H, m), 7.67-7.79 (6H, m), 6.93-6.98 (4H, m), 6.77-6.83 (8H, m), 2.52 (16H, t, J 7.8), 1.53 (16H, d, J 7.9), 1.21-1.35 (46H, m), 0.80-0.88 (24H, m).
To a solution of triisopropyl-thieno[3,2-b]thiophen-2-yl-silane (11.86 g, 40.0 mmol) in anhydrous tetrahydrofuran (100 cm3) at −78° C. is added drop-wise n-butyllithium (20.8 cm3, 52.0 mmol, 2.5 M in hexane) over 20 minutes. After addition, the reaction mixture is stirred at −78° C. for 120 minutes and then tributyltin chloride (15.8 cm3, 56.0 mmol) is added in one go. The mixture is then allowed to warm to 23° C. over 17 hours and the solvent removed in vacuo. The crude is diluted in 40-60 petrol (250 cm3) and filtered through a zeolite plug (50 g). The plug is washed with additional 40-60 petrol (250 cm3). The solvent is removed in vacuo to give intermediate 45 (23.1 g, 99%) as a clear oil. 1H-NMR (400 MHz, CD2Cl2) 7.27 (1H, d J 0.7), 7.1 (1H, s), 1.35-1.63 (9H, m), 1.17-1.34 (12H, m), 0.98-1.13 (18H, m), 0.65-0.91 (12H, m).
A mixture of intermediate 31 (7.5 g, 21 mmol), intermediate 45 (17.8 g, 30.4 mm) and anhydrous toluene (300 cm3) is degassed by nitrogen for 25 minutes. To the mixture is added tetrakis(triphenylphosphine)palladium(O) (500 mg, 0.43 mmol) and the mixture further degassed for 15 minutes. The mixture is stirred at 85° C. for 17 hours. The reaction mixture is filtered hot through a celite plug (50 g) and washed through with hot toluene (100 cm3). The solvent reduced in vacuo to 100 cm3 and cooled in an ice bath to form a suspension. The product is filtered, washed with water (100 cm3) and methanol (100 cm3), collected and dried under vacuum to give intermediate 46 (9.5 g, 71%) as a yellow crystalline solid. 1H-NMR (400 MHz, CDCl3) 7.75 (2H, d, J 0.7), 7.30 (2H, d, J 0.7), 4.36 (4H, q, J 7.2), 1.23-1.43 (12H, m), 1.07 (36H, d, J 7.3).
To a suspension of 1-bromo-4-dodecyloxy-benzene (10.6 g, 30.9 mmol) in anhydrous tetrahydrofuran (167 cm3) at −78° C. is added dropwise tert-butyllithium (36.4 cm3, 61.8 mmol, 1.7 M in pentane) over 60 minutes. After addition, the reaction mixture is stirred at −78° C. for 120 minutes. Intermediate 46 (6.0 g, 6.9 mmol) is added in one go. The mixture is then allowed to warm to 23° C. over 17 hours. Diethyl ether (200 cm3) and water (200 cm3) are added and the mixture stirred at 23° C. for 30 minutes. The product is extracted with diethyl ether (3×200 cm3). The combined organics is dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is purified using silica gel column chromatography (40-60 petrol:diethyl ether; 7:3). The solid triturated with methanol (200 cm3) and collected by filtration to give intermediate 47 (10.3 g, 82%) as a cream solid. 1H NMR (400 MHz, CDCl3) 7.15-7.23 (10H, m), 6.77-6.85 (8H, m), 6.65 (2H, d, J 0.7), 3.45 (2H, s), 3.95 (8H, s), 1.71-1.85 (8H, m), 1.20-1.52 (72H, m), 1.11 (36H, d, J 7.3), 0.82-0.95 (12H, m).
Nitrogen gas is bubbled through a solution of intermediate 47 in anhydrous toluene (250 cm3) at 0° C. for 60 minutes. Amberlyst 15 strong acid (50 g) is added and the mixture degassed for a further 30 minutes. The resulting suspension is stirred at 70° C. for 2 hours. The reaction mixture allowed to cool to 23° C., filtered and the solvent removed in vacuo. The crude is triturated with acetone (200 cm3). The solid is filtered to give intermediate 48 (4.2 g, 89%) as a dark orange solid. 1H NMR (400 MHz, CDCl3) 7.28 (4H, m), 7.16-7.24 (8H, m), 6.75-6.93 (8H, m), 3.91 (8H, t, J 6.5), 1.67-1.82 (8H, m), 1.37-1.48 (8H, m), 1.19-1.37 (64H, m), 0.80-1.00 (12H, m).
To a solution of intermediate 48 (0.6 g, 0.41 mmol) in anhydrous tetrahydrofuran (24 cm3) at −78° C. is added dropwise n-butyllithium (0.7 cm3, 1.6 mmol, 2.5 M in hexane) over 10 minutes. After addition, the reaction mixture is stirred at −78° C. for 60 minutes. N,N-dimethylformamide (0.16 cm3, 2.4 mmol) is added in one go and the mixture is allowed to warm to 23° C. over 2 hours. Diethyl ether (50 cm3) and water (50 cm3) are added and the mixture stirred at 23° C. for 30 minutes. The product is extracted with diethyl ether (3×100 cm3). The combined organics are dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is purified using silica gel column chromatography (40-60 petrol:dichloromethane; 8:2) to give intermediate 49 (380 mg, 61%) as a dark red oil. 1H NMR (400 MHz, CDCl3) 9.90 (2H, s), 7.94 (2H, s), 7.08-7.23 (8H, m), 6.78-6.93 (8H, m), 3.91 (8H, t, J 6.5), 1.65-1.85 (8H, m), 1.17-1.51 (72H, m), 0.82-0.96 (12H, m).
Compound 23
To a solution of intermediate 49 (370 mg, 0.24 mmol) in anhydrous chloroform (26 cm3) is added pyridine (1.4 cm3, 17 mmol). The mixture is then degassed with nitrogen before 3-(dicyanomethylidene) indan-1-one (280 mg, 1.4 mmol) is added. The solution is then further degassed and stirred at 23° C. for 20 minutes. The mixture is stirred at 40° C. for 2 hours and then the solvent is removed in vacuo. The crude is triturated with ethanol (200 cm3) to produce a heavy suspension which is collected by filtration and the solid washed with acetone (50 cm3). The crude is dissolved in dichloromethane (20 cm3) added precipitated into acetone (250 cm3) to form a suspension. The solid collected by filtration to give Compound 23 (437 mg, 96%) as a gray solid. 1H NMR (400 MHz, CDCl3) 8.87 (2H, s), 8.63-8.74 (2H, m), 8.13 (2H, s), 7.87-7.97 (2H, m), 7.68-7.82 (4H, m), 7.23 (8H, d, J 8.8), 6.90 (8H, d, J 9.0), 3.92 (8H, t, J 6.5), 1.69-1.84 (8H, m), 1.16-1.52 (72H, m), 0.80-0.97 (12H, m).
To a solution of intermediate 49 (1.6 g, 1.1 mmol) in anhydrous tetrahydrofuran (47 cm3) at −78° C. is added dropwise n-butyllithium (1.7 cm3, 4.3 mmol, 2.5 M in hexane) over 20 minutes. After addition, the reaction mixture is stirred at −78° C. for 60 minutes. Tributyltin chloride (1.3 cm3, 4.9 mmol) is added in one go and then the mixture is allowed to warm to 23° C. over 72 hours. The solvent removed in vacuo. The crude is purified by passing through a zeolite plug (40-60 petrol) followed by triturating in ethanol (2×100 cm3) to give intermediate 50 (2.0 g, 88%) as a dark red oil. 1H NMR (400 MHz, CDCl3) 7.28 (2H, s), 7.18-7.24 (8H, m), 6.79-6.87 (8H, m), 3.91 (8H, t, J 6.6), 1.51-1.83 (32H, m), 1.20-1.48 (114H, m), 1.07-1.18 (15H, m), 0.76-1.03 (69H, m).
Compound 24
A mixture of intermediate 50 (700 mg, 0.34 mmol), 2-(7-bromo-benzo[1,2,5]thiadiazol-4-ylmethylene)-malononitrile (218 mg, 0.75 mmol), tri-o-tolyl-phosphine (31 mg, 0.75 mmol) and anhydrous toluene (41 cm3) is degassed by nitrogen for 10 minutes. To the mixture is added tris(dibenzylideneacetone) dipalladium(0) (25 mg, 0.03 mmol) and the mixture further degassed for 15 minutes. The mixture is stirred at 80° C. for 17 hours and the solvent removed in vacuo. Dichloromethane (200 cm3) and water (200 cm3) are added and the mixture stirred at 23° C. for 30 minutes. The product is extracted with dichloromethane (3×100 cm3). The combined organics are dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is dissolved in dichloromethane and precipitated into acetone. The solid collected by filtration to give Compound 24 (451 mg, 70%) as a grey solid. 1H NMR (400 MHz, CD2Cl2) 8.55-8.74 (6H, m), 7.83 (2H, d, J 7.8), 7.14 (8H, d, J 8.8), 6.77 (8H, d, J 8.8), 3.82 (8H, t, J 6.6), 1.58-1.69 (8H, m), 1.07-1.40 (72H, m), 0.68-0.85 (12H, m).
To a solution of 7-bromo-benzo[1,2,5]thiadiazole-4-carbaldehyde (2.0 g, 8.2 mmol) in anhydrous chloroform (875 cm3) is added pyridine (46.5 cm3, 576 mmol). The mixture is then degassed with nitrogen before 3-(dicyanomethylidene) indan-1-one (4.0 g, 21 mmol) is added. The solution is then further degassed and stirred for 20 minutes. The mixture is stirred at 40° C. for 17 hours. The solid collected by filtration and washed with acetone (200 cm3), water (200 cm3), diethyl ether (200 cm3) and dichloromethane (200 cm3) to give intermediate 51 (3.0 g, 86%) as a pale yellow solid with very limited solubility.
Compounds 25 and 26
A mixture of intermediate 50 (700 mg, 0.34 mmol), intermediate 51 (356 mg, 0.85 mmol), tri-o-tolyl-phosphine (31 mg, 0.10 mmol) and anhydrous toluene (36 cm3) is degassed by nitrogen for 10 minutes. To the mixture is added tris(dibenzylideneacetone) dipalladium(0) (25 mg, 0.03 mmol) and the mixture further degassed for 15 minutes. The mixture is stirred at 80° C. for 17 hours and the solvent removed in vacuo. The crude is stirred in acetone (200 cm3) to form a suspension and the solid collected by filtration. The crude is purified using silica gel column chromatography eluting with 40-60 petrol:dichloromethane; 8:2 to give compound 25 (217 mg, 30%) and compound 26 (136 mg, 22%) as a dark grey solids. Compound 92: 1H NMR (400 MHz, CD2Cl2) 9.32-9.52 (2H, m), 9.15 (2H, d, J 8.1), 8.52-8.75 (4H, m), 7.61-7.98 (8H, m), 7.16 (8H, d, J 8.8), 6.79 (8H, d, J 8.8), 3.83 (8H, t, J 6.5), 1.56-1.73 (8H, m), 0.94-1.38 (72H, m), 0.77 (12H, t, J 6.6). Compound 93: 1H NMR (400 MHz, CD2Cl2) 9.41 (1H, s), 9.14 (1H, d, J 8.0), 8.56-8.71 (2H, m), 7.57-7.97 (4H, m), 7.02-7.30 (10H, m), 6.74 (8H, dd, J 9.0 18.1), 3.70-3.91 (8H, m), 1.54-1.72 (8H, m), 1.06-1.72 (72H, m), 0.70-0.84 (12H, m).
To a solution of 1-bromo-3,5-bis-hexyloxy-benzene (8.96 g, 25.1 mmol) in anhydrous tetrahydrofuran (50 cm3) at −78° C. is added dropwise n-butyllithium (10.0 cm3, 25.1 mmol). The mixture is stirred at −78° C. for 2 hours before methyl 5-bromo-2-[5-(4-bromo-2-methoxycarbonyl-phenyl)-3a,6a-dihydrothieno[3,2-b]thiophen-2-yl]benzoate (2.85 g, 5.0 mmol) is added in one portion. The mixture is allowed to warm to 23° C. and stirred for 17 hours. The reaction is carefully poured onto water (100 cm3) and the organics extracted with dichloromethane (2×100 cm3) is added. The combined organic layer is dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The residue is purified by column chromatography (40-60 petol:dichloromethane; 6:4). The intermediate diol (3.42 g, 3.65 mmol) is taken up in toluene (200 cm3) and p-toluenesulfonic acid monohydrate (1.39 g, 7.30 mmol) added. The mixture is stirred at 50° C. for 90 minutes and the mixture allowed to cool to 23° C. Water (100 cm3) is added and the organic layer washed with water (100 cm3) and brine (100 cm3). The organic layer is dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude product is triturated in ice-cooled acetone and the solid collected by filtration to give intermediate 52 (3.08 g, 87%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 7.54 (2H, d, J 1.8), 7.39 (2H, dd, J 8.1, 1.8), 7.17 (2H, d, J 8.1), 6.32 (12H, bs), 3.83 (16H, td, J 6.6, 1.6), 1.69 (16H, p, J 6.8), 1.37 (16H, tq, J 9.2, 4.9, 2.9), 1.29 (32H, dp, J 7.4, 4.6, 3.8), 0.80-0.91 (24H, m).
To a degassed solution of intermediate 52 (1.04 g, 0.66 mmol), 2-tributylstannanyl-thiazole (0.62 cm3, 1.97 mmol) in toluene (50 cm3) and N,N-dimethylformamide (10 cm3) is added (tetrakis(triphenylphosphine))palladium(0) (76.1 mg, 0.07 mmol) and the mixture stirred at 110° C. for 5 days. The mixture is allowed to cool to 23° C. and the solvents removed in vacuo. The crude product is purified by column chromatography using a graded solvent system (40-60 petrol:dichloromethane: 6.5:4.5 to 3:7) to give intermediate 53 (973 mg, 93%) as a yellow oil. 1H NMR (400 MHz, CDCl3) 8.07 (2H, d, J 1.5), 7.94 (2H, dd, J 8.0, 1.5), 7.82 (2H, d, J 3.3), 7.40 (2H, d, J 7.9), 7.27 (2H, d, J 3.2), 6.43 (8H, d, J 2.2), 6.34 (4H, t, J 2.2), 3.86 (16H, td, J 6.6, 1.8), 1.65-1.73 (16H, m), 1.25-1.42 (48H, m), 0.81-0.89 (24H, m).
To a stirred solution of intermediate 53 (973 mg, 0.61 mmol) in anhydrous tetrahydrofuran (100 cm3) at −78° C. is added dropwise n-butyllithium (0.98 cm3, 2.5 mmol, 2.5 M in hexane). The reaction mixture is stirred for 2 hours before anhydrous N,N-dimethylformamide (0.21 cm3, 2.8 mmol) is added. The mixture is allowed to warm to 23° C., stirred for 4 hours and methanol (3 cm3) added. The mixture is diluted with Et2O (100 cm3) and washed with water (2×100 cm3). The organic layer is dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is purified by column chromatography using a graded solvent system (40-60 petrol:dichloromethane: 4:6 to 1:9) to give intermediate 54 (680 mg, 67%) as a red oil. 1H NMR (400 MHz, CDCl3) 10.01 (2H, s), 8.37 (2H, s), 8.12 (2H, d, J 1.5), 7.99 (2H, dd, J 8.0, 1.6), 7.42 (2H, d, J 8.0), 6.40 (8H, d, J 2.2), 6.34 (4H, t, J 2.2), 3.85 (16H, td, J 6.6, 1.7), 1.64-1.73 (16H, m), 1.22-1.47 (48H, m), 0.80-0.89 (24H, m).
Compound 27
To a degassed solution of intermediate 54 (200 mg, 0.12 mmol), 3-ethyl-2-thioxo-thiazolidin-4-one (59 mg, 0.36 mmol) anhydrous N,N-dimethylformamide (10 cm3) is added potassium carbonate (50 mg, 0.36 mmol) and the mixture is stirred for 16 hours. Dichloromethane is added and the organic layer washed with water (2×100 cm3), brine (100 cm3), dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The residue is triturated in acetone and the solid collected by filtration to give Compound 27 (69 mg, 29%) as a shiny red solid. 1H NMR (400 MHz, CDCl3) 8.11 (2H, d, J 1.7), 8.05 (2H, s), 7.96 (2H, dd, J 8.0, 1.7), 7.89 (2H, s), 7.42 (2H, d, J 8.0), 6.41 (8H, d, J 2.2), 6.35 (4H, t, J 2.2), 4.19 (4H, q, J 7.1), 3.82-3.90 (16H, m), 1.33-1.42 (16H, m), 1.38 (16H, dq, J 14.2, 6.6), 1.20-1.32 (38H, m), 0.85 (24H, t, J 6.8).
Compound 28
A mixture of intermediate 50 (500 mg, 0.24 mmol), 5-[1-(7-bromo-benzo[1,2,5]thiadiazol-4-yl)-meth-(E)-ylidene]-3-ethyl-2-thioxo-thiazolidin-4-one (197 mg, 0.51 mmol), tri-o-tolyl-phosphine (22 mg, 0.07 mmol) and anhydrous toluene (26 cm3) is degassed by nitrogen for 10 minutes. To the mixture is added tris(dibenzylideneacetone) dipalladium(0) (18 mg, 0.02 mmol) and the mixture further degassed for 15 minutes. The mixture is stirred at 90° C. for 17 hours and the solvent removed in vacuo. The crude is stirred in acetone (200 cm3) to form a suspension and the solid collected by filtration. The crude is purified using silica gel column chromatography eluted with 40-60 petrol:dichloromethane; 1:1 to give Compound 28 (193 mg, 38%) as a dark green solid. 1H NMR (400 MHz, CD2Cl2) 8.57 (2H, s), 8.34 (2H, s), 7.79 (2H, d, J 7.8), 7.58 (2H, d, J 7.8), 7.15 (8H, d, J 8.8), 6.77 (8H, d, J 8.6), 4.13 (4H, q, J 7.3), 3.81 (8H, t, J 6.5), 1.63 (8H, quin, J 6.9), 0.96-1.38 (78H, m), 0.77 (12H, t, J 6.6).
Compound 29
To a degassed solution of intermediate 54 (192 mg, 0.12 mmol) in chloroform (19 cm3) and pyridine (1 cm3) is added 2-(3-oxo-indan-1-ylidene)-malononitrile (68 mg, 0.35 mmol) and the mixture stirred for 2 hours. Aqueous hydrochloric acid (10 cm3, 2 M) is added and the mixture diluted with dichloromethane (50 cm3). The organic layer is washed with water (50 cm3) and brine (50 cm3), dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The residue is triturated in acetone and the solid collected by filtration to give Compound 29 (182 mg, 78%) as a blue powder. 1H NMR (400 MHz, CDCl3) 8.90 (2H, s), 8.74 (2H, d, J 7.2), 8.41 (2H, s), 8.28 (2H, d, J 1.6), 8.14 (2H, dd, J 8.0, 1.6), 7.95 (2H, d, J 7.2), 7.76-7.86 (4H, m), 7.45 (2H, d, J 8.1), 6.43 (8H, d, J 2.2), 6.36 (4H, t, J 2.2), 3.88 (16H, td, J 6.6, 1.7), 1.67-1.74 (16H, m), 1.35-1.42 (16H, m), 1.23-1.31 (32H, m), 0.84 (24H, t, J 7.0).
A mixture of intermediate 50 (400 mg, 0.19 mmol), 2-bromo-thiazole-5-carbaldehyde (112 mg, 0.58 mmol), tri-o-tolyl-phosphine (18 mg, 0.06 mmol) and anhydrous toluene (40 cm3) is degassed by nitrogen for 10 minutes. To the mixture is added tris(dibenzylideneacetone) dipalladium(0) (14 mg, 0.02 mmol) and the mixture further degassed for 15 minutes. The mixture is stirred at 90° C. for 17 hours and the solvent removed in vacuo. The crude is stirred in acetone (200 cm3) and the solid collected by filtration to give intermediate 55 (158 mg, 48%) as a dark purple solid. 1H-NMR (400 MHz, CD2Cl2) 9.89 (2H, s), 8.21 (2H, s), 7.82 (2H, s), 7.08 (8H, d, J 8.6), 6.68-6.81 (8H, m), 3.81 (8H, t, J 6.4), 1.64 (8H, brs), 1.10-1.36 (72H, m), 0.78 (12H, t, J 6.5).
Compound 30
To a solution of intermediate 55 (150 mg, 0.09 mmol) in anhydrous chloroform (9 cm3) is added pyridine (0.5 cm3, 6.2 mmol). The mixture is then degassed with nitrogen before 3-(dicyanomethylidene) indan-1-one (120 mg, 0.62 mmol) is added. The solution is then further degassed and stirred at 23° C. for 20 minutes before the solvent is removed in vacuo. The crude is triturated with ethanol (200 cm3) and the solid collected by filtration. The crude is purified using silica gel column chromatography eluted with 40-60 petrol:dichloromethane; 6:4 to give Compound 30 (17 mg, 9%) as a green solid. 1H NMR (400 MHz, CD2Cl2) 8.75 (2H, s), 8.61 (2H, d, J 7.3), 8.25 (2H, s), 7.94 (2H, s), 7.85 (2H, d, J 7.3), 7.70 (4H, quin, J 7.5), 7.02-7.16 (8H, d, J 8.8), 6.77 (8H, d, J 9.0), 3.82 (8H, t, J 6.4), 1.58-1.66 (8H, m), 1.07-1.39 (72H, m), 0.70-0.84 (12H, m).
Compound 31
To a degassed solution of intermediate 55 (169 mg, 0.10 mmol), pyridine (2 cm3) and chloroform (10 cm3) is added 1-ethyl-4-methyl-2,6-dioxo-1,2,5,6-tetrahydro-pyridine-3-carbonitrile (55 mg, 0.31 mmol) and the mixture stirred for 20 hours. Aqueous hydrochloric acid (10 cm3, 2 M) is added and the mixture diluted with dichloromethane (50 cm3). The organic layer is washed with water (50 cm3) and brine (50 cm3), dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is purified by column chromatography using a graded solvent system (40-60 petrol:dichloromethane: 2:8 to 0:1) followed by recrystallization (ethanol/dichloromethane) to give Compound 31 (69 mg, 34%) as a shiny blue solid. 1H NMR (400 MHz, CDCl3) 8.39 (2H, s), 8.24 (2H, d, J 1.5), 8.14 (2H, dd, J 8.1, 1.5), 7.90 (2H, s), 7.43 (2H, d, J 8.0), 6.42 (8H, d, J 2.1), 6.35 (4H, t, J 2.1), 4.07 (4H, q, J 7.1), 3.87 (16H, t, J 6.8), 2.65 (6H, s), 1.66-1.73 (16H, m), 1.32-1.43 (16H, m), 1.23-1.30 (38H, m), 0.85 (24H, t, J 6.9).
To a solution of intermediate 43 (1.60 g, 1.2 mmol) in anhydrous tetrahydrofuran (47 cm3) at −78° C. is added dropwise n-butyllithium (1.96 cm3, 4.9 mmol, 2.5 M in hexane) over 20 minutes. After addition, the reaction mixture is stirred at −78° C. for 60 minutes and then tributyltin chloride (1.5 cm3, 5.5 mmol) is added in one go. The mixture is then allowed to warm to 23° C. over 72 hours and the solvent removed in vacuo. The crude is purified by passing through a zeolite plug (40-60 petrol) followed by trituration in ethanol (2×100 cm3) to give a mixture of intermediate 56 and tributyltin chloride (2.7 g) as a dark brown oil. 1H NMR (400 MHz, CD2Cl2) 6.99 (2H, s), 6.64-6.85 (12H, m), 2.38 (16H, t, J 7.7), 0.57-1.69 (98H, m).
A mixture of intermediate 56 (1.5 g, 0.48 mmol), 7-bromo-benzo[1,2,5]thiadiazole-4-carbaldehyde (232 mg, 0.96 mmol), tri-o-tolyl-phosphine (44 mg, 0.14 mmol) and anhydrous toluene (51 cm3) is degassed by nitrogen for 10 minutes. To the mixture is added tris(dibenzylideneacetone) dipalladium(0) (35 mg, 0.04 mmol) and the mixture further degassed for 15 minutes. The mixture is stirred at 100° C. for 17 hours and the solvent removed in vacuo. The crude is purified using silica gel column chromatography eluting with 40-60 petrol:dichloromethane; 7:3 to give intermediate 57 (650 mg, 84%) as a dark blue solid. 1H NMR (400 MHz, CDCl3) 10.67-10.73 (2H, m), 8.34 (2H, s), 8.20 (2H, d, J 7.6), 7.93 (2H, d, J 7.6), 6.94 (12H, s), 2.54 (16H, t, J 7.7), 1.51-1.64 (16H, m), 1.20-1.36 (48H, m), 0.77-0.88 (24H, m).
Compound 32
To a solution of intermediate 57 (500 mg, 0.31 mmol) in anhydrous chloroform (33 cm3) at −30° C. is added pyridine (1.7 cm3, 22 mmol). The mixture is then degassed with nitrogen before 3-(dicyanomethylidene) indan-1-one (417 mg, 2.15 mmol) is added. The solution is then further degassed and stirred at −30° C. for 30 minutes. The ice bath is removed, the reaction is allowed to warm to 20° C. over 60 minutes and the solvent removed in vacuo. The crude is triturated with ethanol and the solid collected by filtration. The crude is purified using silica gel column chromatography eluted with 40-60 petrol:dichloromethane; 1:1 to give Compound 32 (205 mg, 34%) as a green solid. 1H NMR (400 MHz, CDCl3) 9.61 (2H, s), 9.32 (2H, d, J 8.1), 8.75 (2H, d, J 7.8), 8.39 (2H, s), 7.94-8.03 (4H, m), 7.76-7.91 (4H, m), 6.95 (12H, s), 2.56 (16H, t, J 7.7), 1.48-1.68 (m, 16H), 1.20-1.40 (48H, m), 0.76-0.95 (24H, m).
To a degassed solution of intermediate 52 (350 mg, 0.22 mmol), tributyl-thiophen-2-yl-stannane (248 mg, 0.66 mmol) and anhydrous toluene (20 cm3) are added tris(dibenzylideneacetone)dipalladium(0) (10 mg, 0.01 mmol) and 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (42 mg, 0.09 mmol) and the mixture stirred at 80° C. for 17 hours. The mixture is allowed to cool to 23° C. and the solvent removed in vacuo. The crude is purified by column chromatography using a graded solvent system (40-60 petrol:dichloromethane: 9:1 to 1:1) followed by trituration in ice-cold acetone. The solid is collected by filtration to give intermediate 58 (216 mg, 61%) as a yellow powder. 1H NMR (400 MHz, CDCl3) 7.68 (2H, d, J 1.6), 7.53 (2H, dd, J 7.9, 1.6), 7.32 (2H, d, J 7.9), 7.20-7.26 (4H, m), 7.04 (2H, dd, J 5.1, 3.6), 6.41 (8H, d, J 2.2), 6.32 (4H, t, J 2.2), 3.84 (16H, td, J 6.6, 2.2), 1.62-1.73 (16H, m), 1.32-1.42 (16H, m), 1.27 (32H, dq, J 7.3, 3.7, 3.0), 0.82-0.88 (24H, m).
To a mixture of anhydrous N,N-dimethylformamide (1 cm3) and anhydrous chloroform (10 cm3) at 0° C. is added phosphoroxychloride (0.04 cm3, 0.41 mmol). The mixture is allowed to warm up at 23° C. and stirred for 1 hour before cooling to 0° C. where intermediate 58 (216 mg, 0.14 mmol) is added. The mixture is then stirred at 60° C. for 17 hours. The mixture is allowed to cool to 23° C. and poured on saturated aqueous sodium bicarbonate solution (50 cm3) and stirred at 23° C. for 30 minutes. The aqueous layer is extracted with dichloromethane (100 cm3). The organic layer is washed with brine (50 cm3), dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is purified by column chromatography using a graded solvent system (40-60 petrol:dichloromethane: 1:1 to 0:1) to give intermediate 59 (49 mg, 22%) as a red solid. 1H NMR (400 MHz, CDCl3) 9.86 (2H, s), 7.73 (2H, d, J 1.7), 7.70 (2H, d, J 4.0), 7.61 (2H, dd, J 8.0, 1.7), 7.37 (2H, d, J 8.0), 7.34 (2H, d, J 4.0), 6.39 (8H d, J 2.2), 6.34 (4H, t, J 2.2), 3.85 (16H, m), 1.69 (16H, p, J 6.8), 1.23-1.45 (48H, m), 0.76-0.92 (24H, m).
Compound 33
To a degassed solution of intermediate 59 (59 mg, 0.04 mmol), anhydrous chloroform (10 cm3) and anhydrous pyridine (2 cm3) at 0° C. is added 2-(3-oxo-indan-1-ylidene)-malononitrile (21 mg, 0.11 mmol) and the reaction mixture is stirred at 0° C. for 2 hours. The reaction is quenched by addition of aqueous hydrochloric acid (5 cm3, 2 M). Dichloromethane (50 cm3) is added and the organic layer is washed with water (2×50 cm3) and brine (50 cm3), dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The residue is triturated in acetone and the solid collected by filtration to give Compound 33 (18 mg, 25%) as a black powder. 1H NMR (400 MHz, CDCl3) 8.86 (2H, s), 8.69-8.73 (2H, m), 7.91-7.94 (2H, m), 7.88 (2H, d, J 1.6), 7.84 (2H, d, J 4.3), 7.73-7.81 (6H, m), 7.46 (2H, d, J 4.2), 7.40 (2H, d, J 8.0), 6.42 (8H, d, J 2.2), 6.36 (4H, t, J 2.2), 3.88 (16H, td, J 6.5, 1.8), 1.71 (16H, p, J 6.7), 1.31-1.47 (16H, m), 1.22-1.32 (32H, m), 0.79-0.88 (24H, m).
To a suspension of 1-bromo-4-dodecylbenzene (3.626 g, 11.15 mmol) in anhydrous tetrahydrofuran (48 cm3) at −78° C., tert-butyllithium (13 cm3, 22 mmol, 1.7 M in pentane) is added dropwise over 30 minutes. After 40 minutes the reaction is allowed to warm to −30° C. before the reaction mixture is then re-cooled to −78° C. Additional 1-bromo-4-dodecylbenzene (362 mg, 1.11 mmol) is added and after 15 minutes ethyl 2-[5-(3-ethoxycarbonyl-2-thienyl)thieno[3,2-b]thiophen-2-yl]thiophene-3-carboxylate (1.00 g, 2.23 mmol) is added in one portion to the reaction mixture. This mixture is then allowed to stir at −78° C. for 20 minutes before removing allowing the mixture to warm to 23° C. Water (100 cm3) is added and the mixture stirred for 5 minutes. Diethyl ether (50 cm3) is then added and the organic layer extracted. The organic extract is then washed with saturated ammonium chloride solution (100 cm3), water (100 cm3) and brine (100 cm3), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The crude is purified by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:0 to 3:2) with final purification achieved by trituration with methanol (3×10 cm3), washing the filtered solid with 40-60 petrol (2×10 cm3), diethyl ether (10 cm3) and acetone (10 cm3) to give intermediate 60 (2.09 g, 70%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 7.12-7.17 (10H, m), 7.07-7.12 (8H, m), 6.64 (2H, s), 6.45 (2H, d, J 5.2), 3.24 (2H, s), 2.60 (8H, t, J 7.7), 1.57-1.65 (8H, m), 1.25-1.35 (72H, m), 0.89 (12H, t, J 6.8).
A degassed solution of intermediate 60 (1.00 g, 0.75 mmol) in anhydrous toluene (17 cm3) is added to a degassed suspension of Amberlist 15 strong acid (4.00 g) in toluene (18 cm3) and the reaction stirred at 50° C. for 80 minutes. After cooling the mixture to 23° C., the solid is removed by filtration and washed with toluene (3×50 cm3) and diethyl ether (3×50 cm3) and the filtrate concentrated in vacuo. Purification is achieved by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:0 to 4:1) to give intermediate 61 (582 mg, 60%) as a brown oil. 1H NMR (400 MHz, CD2Cl2) 7.23 (2H, d, J 4.9), 7.11-7.16 (8H, m), 7.05-7.10 (10H, m), 2.54 (8H, t, J 7.8), 1.53-1.61 (8H, m), 1.22-1.33 (72H, m), 0.87 (12H, t, J 6.9).
To a solution of intermediate 61 (582 mg, 0.45 mmol) in anhydrous tetrahydrofuran (27 cm3) at −78° C. is added n-butyllithium (0.43 cm3, 1.1 mmol, 2.5 M in hexanes) over 5 minutes. The mixture is stirred at −78° C. for 45 minutes before additional n-butyllithium (0.10 cm3, 0.25 mmol) is added. The mixture is stirred for an additional 5 minutes before tributyltin chloride (0.42 cm3, 1.56 mmol) is added and the mixture stirred to 23° C. over 17 hours. Methanol (15 cm3) is added and the material concentrated in vacuo. The crude product is then taken up in pentane and the suspension filtered through celite washing though with additional pentane. The filtrate is then concentrated in vacuo, the solid triturated with methanol (3×10 cm3) and the product collected by filtration to give intermediate 62 (790 mg, 94%) as a brown sticky solid. 1H NMR (400 MHz, CDCl3) 7.13-7.18 (8H, m), 7.03-7.09 (10H, m), 2.54 (8H, t, J 7.8), 1.51-1.60 (20H, m), 1.21-1.38 (84H, m), 1.06-1.13 (12H, m), 0.85-0.91 (30H, m).
To a degassed solution of intermediate 62 (438 mg, 0.23 mmol) and 7-bromo-benzo[1,2,5]thiadiazole-4-carbaldehyde (124 mg, 0.51 mmol) in anhydrous toluene (28 cm3), tris(dibenzylideneacetone)dipalladium (17 mg, 0.02 mmol) and tris(o-tolyl)phosphine (21 mg, 0.07 mmol) are added. After degassing the reaction mixture for a further 20 minutes it is heated at 80° C. for 17 hours. After cooling to 23° C., the mixture is concentrated in vacuo. The crude is then triturated with methanol (3×10 cm3) and the solid filtered, washing with acetone (3×10 cm3) to give intermediate 63 (320 mg, 84%) as a blue/black solid. 1H NMR (400 MHz, CDCl3) 10.69 (2H, s), 8.33 (2H, s), 8.19 (2H, d, J 7.6), 7.94 (2H, d, J 7.8), 7.22-7.27 (8H, m), 7.11-7.17 (8H, m), 2.58 (8H, t, J 7.9), 1.51-1.65 (8H, m), 1.18-1.38 (72H, m), 0.86 (12H, t, J 6.9).
Compound 34
To a solution of intermediate 63 (319 mg, 0.20 mmol) in anhydrous chloroform (21 cm3) is added anhydrous pyridine (1.1 cm3, 14 mmol). The mixture is then degassed with nitrogen before 3-(dicyanomethylidene)indan-1-one (266 mg, 1.37 mmol) is added and the reaction cooled to −40° C. The solution is further degassed for 10 minutes and with stirring, is allowed to warm before being held at −15 to −20° C. After 5 hours the reaction mixture is then added to methanol (100 cm3) washing in with dichloromethane (10 cm3) and methanol (2×10 cm3). Additional methanol (50 cm3) is added before the suspension is filtered. The crude product is purified by column chromatography, eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:0 to 1:1) to give Compound 34 (24 mg, 6%) as a black solid. 1H NMR (400 MHz, CDCl3) 9.58 (2H, s), 9.28 (2H, d, J 8.1), 8.73 (2H, d, J 7.8), 8.37 (2H, s), 7.94 (4H, d, J 7.6), 7.74-7.85 (4H, m), 7.23-7.27 (8H, m), 7.15 (8H, d, J 8.3), 2.58 (8H, t, J 7.8), 1.53-1.65 (8H, m), 1.18-1.38 (72H, m), 0.83-0.90 (12H, m).
Compound 35
To a degassed mixture of intermediate 34 (100 mg, 0.08 mmol) and 2:3 regiomeric mix of 2-(5-methyl-3-oxo-indan-1-ylidene)-malononitrile and 2-(6-methyl-3-oxo-indan-1-ylidene)-malononitrile (121 mg, 0.58 mmol) and chloroform (2.5 cm3) is added pyridine (0.47 cm3, 5.8 mmol). The solution is bubbled with nitrogen for 10 minutes and then stirred for 3 hours at 23° C. Methanol (20 cm3) is added and the suspension filtered and washed with methanol (20 cm3). The resulting solid is stirred in methyl ethyl ketone (5 cm3) at 95° C. for 2 hours, cooled to 23° C. and the solid collected by filtration. The solid is washed with methyl ethyl ketone (5 cm3) to give Compound 35 (107 mg, 81%) as a dark blue solid. 1H NMR (400 MHz, CD2Cl2) 8.85 (2H, m), 8.40-8.66 (2H, m), 7.49-7.93 (6H, m), 7.20 (8H, d, J 8.6), 6.87 (8H, d, J 8.5), 3.95 (8H, t, J 6.5), 2.54-2.61 (6H, m), 1.73-1.82 (8H, m), 1.41-1.52 (8H, m), 1.24-1.40 (32H, m), 0.90 (12H, t, J 6.6).
To a suspension of 1-bromo-4-dodecyloxybenzene (7.25 g, 21.2 mmol) in anhydrous tetrahydrofuran (91 cm3) at −78° C., tert-butyllithium (25 cm3, 42 mmol, 1.7 M in pentane) is added dropwise over 30 minutes. After 2 hours the reaction mixture is allowed to warm to −30° C. before re-cooling to −78° C. Additional 1-bromo-4-dodecyloxybenzene (720 mg, 2.11 mmol) and after 10 minutes ethyl 2-[5-(3-ethoxycarbonyl-2-thienyl)thieno[3,2-b]thiophen-2-yl]thiophene-3-carboxylate (1.91 g, 4.25 mmol) is added in one portion to the reaction mixture. This mixture is then allowed to stir to 23° C. over 17 hours. Water (50 cm3) and diethyl ether (25 cm3) are then added and the organic layer extracted. The residual aqueous layer is then additionally extracted with diethyl ether (50 cm3) and the combined organic extracts washed with brine (75 cm3), dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The crude is purified by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:0 to 3:7) to give intermediate 64 (4.10 g, 69%) as a brown oil which solidifies on standing to a yellow/brown solid. 1H NMR (400 MHz, CDCl3) 7.09-7.17 (10H, m), 6.79-6.85 (8H, m), 6.76 (2H, s), 6.43 (2H, d, J 5.1), 3.95 (8H, t, J 6.6), 3.25 (2H, s), 1.73-1.83 (8H, m), 1.41-1.50 (8H, m), 1.24-1.39 (64H, m), 0.89 (12H, t, J 6.9).
To a degassed solution of intermediate 64 (1.20 g, 0.85 mmol) in anhydrous toluene (20 cm3) is added a degassed suspension of Amberlist 15 strong acid (5.00 g) in toluene (20 cm3) and the reaction mixture stirred at 100° C. for 3 hours. The solid is removed through filtration and washed with toluene (3×50 cm3) and diethyl ether (3×50 cm3) before the filtrate is concentrated in vacuo. Purification is achieved by column chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:0 to 3:7) to give intermediate 65 (221 mg, 19%) as a brown oil. 1H NMR (400 MHz, CDCl3) 7.12-7.19 (10H, m), 7.04 (2H, d, J 4.9), 6.75-6.82 (8H, m), 3.89 (8H, t, J 6.48), 1.74 (8H, quin, J 7.1), 1.37-1.46 (8H, m), 1.19-1.36 (64H, m), 0.88 (12H, t, J 6.9).
To a solution of intermediate 65 (493 mg, 0.36 mmol) in anhydrous tetrahydrofuran (22 cm3) at −78° C. is added n-butyllithium (0.43 cm3, 1.1 mmol, 2.5 M in hexanes) over 5 minutes. The mixture is stirred at −78° C. for 1 hour. Tributyltin chloride (0.34 cm3, 1.3 mmol) is added and the mixture stirred to 23° C. over 17 hours. Methanol (15 cm3) is added and the material concentrated in vacuo. The crude product is then taken up in pentane and the suspension filtered through celite washing through with additional pentane. The filtrate is then concentrated in vacuo, to give the crude product 2,7-bis(tributylstannyl)-4,4,9,9-tetrakis(4-dodecyloxyphenyl)-4,9-dihydro-thieno[3′,2′:4,5]cyclopenta[1,2-b]thieno[2″,3″:3′,4′]cyclopenta[1′,2′:4,5]thieno[2,3-d]thiophene (948 mg, 0.49 mmol) as a dark brown oil, used without further purification. To a degassed solution of 2,7-bis(tributylstannyl)-4,4,9,9-tetrakis(4-dodecyloxyphenyl)-4,9-dihydro-thieno[3′,2′:4,5]cyclopenta[1,2-b]thieno[2″,3″:3′,4′]cyclopenta[1′,2′:4,5]thieno[2,3-d]thiophene (701 mg, 0.36 mmol) and 7-bromo-benzo[1,2,5]thiadiazole-4-carbaldehyde (192 mg, 0.79 mmol) in anhydrous toluene (43 cm3), tris(dibenzylideneacetone)dipalladium (26 mg, 0.03 mmol) and tris(o-tolyl)phosphine (33 mg, 0.11 mmol) is added. After degassing the reaction mixture for a further 20 minutes it is heated at 80° C. for 17 hours. After cooling to 23° C., the mixture is concentrated in vacuo. The crude is triturated with methanol (4×10 cm3) and the solid filtered. The crude product is then twice partially purified by column chromatography, eluting with two graded solvent systems (40-60 petrol:dichloromethane; 1:0 to 1:4) (40-60 petrol:diethyl ether; 1:0 to 9:1) isolating partially pure fractions. Final purification is then achieved by trituration with warm acetone and warm diethyl ether to give intermediate 66 (255 mg, 42%) as a blue/black solid. 1H NMR (400 MHz, CDCl3) 10.69 (2H, s), 8.31 (2H, s), 8.19 (2H, d, J 7.8), 7.94 (2H, d, J 7.6), 7.22-7.27 (8H, m), 6.82-6.88 (8H, m), 3.91 (8H, t, J 6.5), 1.75 (8H, quin, J 7.2), 1.37-1.46 (8H, m), 1.20-1.35 (64H, m), 0.87 (12H, t, J 6.9).
Compound 36
To a solution of intermediate 66 (255 mg, 0.15 mmol) in anhydrous chloroform (16 cm3) is added pyridine (0.85 cm3, 11 mmol). The mixture is then degassed with nitrogen before cooling to −40° C. 3-(Dicyanomethylidene)indan-1-one (205 mg, 1.05 mmol) is added and the solution is further degassed for 10 minutes and with stirring, is allowed to warm before being held at −15 to −20° C. After 4 hours the reaction mixture is then added to methanol (100 cm3) washing in with methanol (2×10 cm3) and dichloromethane (10 cm3). Additional methanol (50 cm3) is added and the suspension stirred for 10 minutes before the solid is collected by vacuum filtration, washing the solid with additional methanol (3×10 cm3). The crude product is purified by silica plug (40-60 petrol:dichloromethane; 1:4), concentrating the product in vacuo. The solid is then triturated with methanol (3×10 cm3) and collected by filtration, before being additionally washed with cyclohexane (3×10 cm3), diethyl ether (3×10 cm3), acetone (3×10 cm3), methyl ethyl ketone (10 cm3) and ethyl acetate (3×10 cm3) to give Compound 36 (203 mg, 66%) as a partially pure black solid. 1H NMR (400 MHz, CDCl3) 9.58 (2H, s), 9.28 (2H, d, J 8.6), 8.74 (2H, d, J 7.8), 8.36 (2H, s), 7.93-8.00 (4H, m), 7.75-7.86 (4H, m), 7.23-7.27 (8H, m), 6.83-6.89 (8H, m), 3.92 (8H, t, J 6.5), 1.70-1.80 (8H, m), 1.38-1.46 (8H, m), 1.18-1.37 (64H, m), 0.87 (12H, t, J 6.9).
To a solution of 6-bromo-benzo[b]thiophene (9.09 g, 42.6 mmol) in anhydrous tetrahydrofuran (150 cm3) at −30° C. is added dropwise lithium diisopropylamide (23.5 cm3, 46.9 mmol, 2.0 M in tetrahydrofuran/heptane/ethylbenzene). The mixture is stirred at −30° C. for 1 hour before triisopropylsilyltrifluoromethanesulfonate (14.4 g, 46.9 mmol) is added in one portion. The mixture is allowed to warm to 23° C. and stirred for 15 hours. Water (150 cm3) is added and the mixture diluted with diethyl ether (100 cm3). The aqueous layer is extracted with diethyl ether (2×50 cm3). The combined organic layer is washed with brine (50 cm3), dried over anhydrous magnesium sulphate, filtered and the solvent removed in vacuo. The residue slowly crystallises which is triturated in ethanol (150 cm3) to give intermediate 67 (11.5 g, 72%) as an off-white solid. 1H NMR (400 MHz, CDCl3) 8.04 (1H, d, J 1.8), 7.69 (1H, d, J 8.5), 7.46 (1H, s), 7.46 (1H, dd, J 8.6, 1.9), 1.37-1.47 (3H, m), 1.16 (18H, d, J 7.5).
To a solution of intermediate 67 (5.00 g, 13.5 mmol) in anhydrous tetrahydrofuran (100 cm3) at −78° C. is added dropwise n-butyllithium (6.0 cm3, 14.9 mmol; 2.5 M in hexane). The mixture is stirred at −78° C. for 2 hours before tributyl(chloro)stannane (4.0 cm3, 15 mmol) is added. The mixture is stirred at −78° C. for 30 minutes before it is allowed to warm to 23° C. and stirred for 20 hours. Water (100 cm3) is added and the mixture diluted with diethyl ether (100 cm3). The aqueous layer is extracted with diethylether (2×50 cm3). The combined organic layer is washed with brine (50 cm3), dried over anhydrous magnesium sulphate, filtered and the solvent removed in vacuo to give 8.90 g of crude intermediate 68 as a yellow oil. The residue is used for the next step without any further purification. 1H NMR (400 MHz, CDCl3) 8.01 (1H, d, J 0.9), 7.82 (1H, dd, J 7.7, 0.7), 7.49 (1H, d, J 0.9), 7.43 (1H, dd, J 7.7, 0.7), 1.54-1.67 (9H, m), 1.33-1.44 (12H, m), 1.17 (18H, d, J 7.3), 0.92 (12H, t, J 7.3).
To a degassed solution of intermediate 68 (1.80 g, 5.10 mmol) and intermediate 46 (7.8 g, 12 mmol, 90% purity) in anhydrous toluene (60 cm3) and anhydrous N,N-dimethylformamide (10 cm3) is added 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (850 mg, 1.78 mmol) and tris(dibenzylideneacetone)dipalladium(0) (187 mg, 0.20 mmol) and the mixture stirred at 80° C. for 20 hours. The reaction mixture is allowed to cool to 23° C. and the solvents removed in vacuo. The residue is triturated in ice-cooled diethyl ether (50 cm3), filtered off and the solid washed with 40-60 petrol (2×20 cm3) to give intermediate 69 (3.01 g, 68%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 8.15 (2H, d, J 1.6), 7.90 (2H, d, J 8.2), 7.62 (2H, dd, J 8.2, 1.6), 7.57 (2H, s), 4.34 (4H, q, J 7.1), 1.40-1.49 (6H, m), 1.32 (6H, t, J 7.1), 1.19 (36H, d, J 7.5).
To a solution of 1-bromo-4-octyloxy-benzene (2.48 g, 8.71 mmol) in anhydrous tetrahydrofuran (60 cm3) at −78° C. is added dropwise n-butyllithium (3.48 cm3, 8.71 mmol, 2.5 M in hexanes). The mixture is stirred for 2 hours before intermediate 69 (1.50 g, 1.74 mmol) is added. The cooling bath is removed and the mixture is allowed to warm up at 23° C. over 17 hours. The reaction mixture is poured onto water (100 cm3) and diluted with dichloromethane (150 cm3). The aqueous layer is extracted twice with dichloromethane (2×50 cm3). The combined organic layer is washed with brine (50 cm3), dried over anhydrous magnesium sulphate, filtered and the solvent removed in vacuo. The residue is taken up in anhydrous toluene (300 cm3) and 4-methylbenzenesulfonic acid hydrate (662 mg, 3.48 mmol) is added. The mixture is stirred at 80° C. for 4 hours. After cooling to 23° C., the reaction is quenched by addition of saturated aqueous sodium hydrogenocarbonate solution (50 cm3), and diluted with water (50 cm3) and dichloromethane (150 cm3). The aqueous layer is extracted with dichloromethane (50 cm3). The combined organic layer is washed with brine (50 cm3), dried over anhydrous magnesium sulphate, filtered and the solvent removed in vacuo. The residue is taken up in anhydrous tetrahydrofuran (40 cm3) and tetrabutylammonium fluoride (2.73 g, 10.4 mmol) added. The mixture is stirred for 2 hours and then diluted with water (50 cm3) and dichloromethane (100 cm3). The aqueous layer is extracted with dichloromethane (50 cm3). The combined organic layer is washed with brine (50 cm3), dried over anhydrous magnesium sulphate, filtered and the solvent removed in vacuo. The residue is purified by column chromatography using a graded solvent system (40-60 petrol:dichloromethane; 19:1 to 7:3) to give intermediate 70 (990 mg, 45%) as a yellow gummy solid. 1H NMR (400 MHz, CDCl3) 7.80 (2H, d, J 8.1), 7.47 (2H, d, J 8.0), 7.36 (2H, d, J 5.5), 7.28 (2H, d, J 7.27), 7.16-7.23 (8H, m), 6.77-6.84 (8H, m), 3.90 (8H, t, J 6.5), 1.69-1.78 (8H, m), 1.37-1.46 (8H, m), 1.22-1.36 (32H, m), 0.88 (12H, t, J 7.0).
To a stirred solution of intermediate 70 (574 mg, 0.46 mmol) in anhydrous tetrahydrofuran (20 cm3) at −78° C. is added dropwise n-butyllithium (0.74 cm3, 1.8 mmol, 2.5 M in hexane). The mixture is stirred for 1 hour before anhydrous N,N-dimethylformamide (0.14 cm3, 1.8 mmol) is added. The mixture is allowed to warm up at 23° C. and is stirred for 3 hours. The reaction mixture is poured onto saturated aqueous ammonium chloride solution (20 cm3) and diluted with dichloromethane (100 cm3). The aqueous layer is extracted with dichloromethane (20 cm3). The combined organic layer is washed with brine (50 cm3), dried over anhydrous magnesium sulphate, filtered and the solvent removed in vacuo. The residue is purified by column chromatography using a graded solvent system (cyclohexane:dichloromethane; 3:7 to 2:3) to give intermediate 71 (280 mg; 46%) as an orange solid. 1H NMR (400 MHz, CDCl3) 10.02 (2H, s), 8.03 (2H, s), 7.94 (2H, d, J 8.2), 7.54 (2H, d, J 8.1), 7.14-7.24 (8H, m), 6.79-6.85 (8H, m), 3.90 (8H, t, J 6.5), 1.67-1.79 (8H, m), 1.39-1.44 (8H, m), 1.20-1.36 (32H, m), 0.88 (12H, t, J 7.1).
Compound 37
To a degassed solution of intermediate 71 (250 mg, 0.19 mmol) in a mixture of pyridine (2 cm3) and chloroform (18 cm3) at 0° C. is added 2-(3-oxo-indan-1-ylidene)-malononitrile (112 mg, 0.58 mmol) is added and the mixture stirred at 0° C. for 3 hours. The reaction is quenched by addition of aqueous hydrochloric acid solution (10 cm3, 2 M) and the aqueous layer extracted with dichloromethane (20 cm3). The combined organic layer is washed with brine (50 cm3), dried over anhydrous magnesium sulphate, filtered and the solvent removed in vacuo. This residue is purified by column chromatography using a graded solvent system (40-60 petrol:dichloromethane; 3:2 to 3:7). The solid is triturated in ice-cooled acetone (30 cm3) and with diethylether (20 cm3) to give Compound 37 (135 mg, 42%) as a blue solid. 1H NMR (400 MHz, CD2Cl2) 8.85 (2H, s), 8.67 (2H, d, J 7.5), 8.24 (2H, s), 7.95 (4H, t, J 9.2), 7.75-7.83 (4H, m), 7.59 (2H, d, J 8.3), 7.23 (8H, d, J 8.4), 6.83 (8H, d, J 8.4), 3.87 (8H, t, J 6.6), 1.63-1.74 (8H, m), 1.31-1.39 (8H, m), 1.18-1.31 (32H, m), 0.82 (12H, t, J 7.0).
To a degassed mixture of 7-bromo-benzo[1,2,5]thiadiazole-4-carbaldehyde (500 mg, 2.0 mmol) and 3-ethyl-2-thioxo-thiazolidin-4-one (2.32 g, 14.4 mmol) and chloroform (220 cm3) is added pyridine (5.8 cm3, 72 mmol) and the reaction mixture further degassed for a 30 minutes. The reaction is then heated at 60° C. for 7 hours. The reaction is cooled to 23° C., filtered and the solid washed with dichloromethane (100 cm3) to give intermediate 72 (534 mg, 67%) as a green/brown solid. 1H NMR (400 MHz, CDCl3) 8.44 (1H, s), 7.98 (1H, d, J 7.7), 7.55 (1H, d, J 7.7), 4.25 (2H, q, J 7.2), 1.33 (3H, t, J 7.1).
To a solution of intermediate 52 (3.09 g, 1.96 mmol) in anhydrous tetrahydrofuran (200 cm3) at −78° C. is added dropwise n-butyllithium (3.1 cm3, 7.8 mmol, 2.5 M in hexane) and the mixture stirred for 90 minutes. Tributyltin chloride (2.4 cm3, 8.8 mmol) is added and the reaction mixture is allowed to warm to 23° C. and stirred for 15 hours. Methanol (2 cm3) is added followed by water (50 cm3) and diethyl ether (100 cm3). The aqueous layer is extracted with diethyl ether (2×20 cm3) and the combined organic layer is dried over anhydrous magnesium sulphate, filtered and the solvent removed in vacuo. The solid is washed with 40-60 petrol (2×10 cm3) and taken up in dichloromethane. Evaporation of the solvents under vacuum gives a yellow oil that slowly crystallises at 23° C. Trituration in ice cooled acetone (20 cm3) gives intermediate 73 (2.95 g, 75%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 7.57 (s, 2H), 7.36 (2H, d, J 7.4), 7.32 (2H, d, J 7.4), 6.39 (8H, d, J 2.2), 6.32 (4H, d, J 2.2), 3.73-3.91 (16H, m), 1.60-1.74 (16H, m), 1.43-1.55 (12H, m), 1.34-1.42 (16H, m), 1.20-1.34 (44H, m), 0.92-1.12 (12H, m), 0.84-0.89 (30H, m).
Compound 38
To a degassed solution of intermediate 73 (300 mg, 0.15 mmol) and intermediate 50 (174 mg, 0.45 mmol) in a mixture of anhydrous toluene (18 cm3) and anhydrous N,N-dimethylformamide (2 cm3) is added 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (57 mg, 0.12 mmol) and tris(dibenzylideneacetone)dipalladium(0) (13 mg, 0.01 mmol) and the reaction mixture heated at 80° C. for 5 days. The reaction mixture cooled to 23° C. and the solvents removed in vacuo. The residue is purified by column chromatography using a graded solvent system (40-60 petrol:dichloromethane; 7:3 to 1:4). This solid is recrystallized (ethanol/dichloromethane) to give Compound 38 (20 mg, 6%) as a deep red solid. 1H NMR (400 MHz, CDCl3) 8.55 (2H, s), 8.20 (2H, d, J 1.6), 8.02 (2H, dd, J 8.0, 1.6), 7.83 (2H, d, J 7.6), 7.76 (2H, d, J 7.6), 7.54 (2H, d, J 7.9), 6.50 (8H, d, J 2.2), 6.37 (4H, t, J 2.2), 4.27 (4H, q, J 7.1), 3.78-3.97 (16H, m), 1.64-1.77 (16H, m), 1.33-1.43 (22H, m), 1.26-1.31 (32H, m), 0.83-0.89 (24H, m).
Compound 39
To a degassed mixture of intermediate 34 (100 mg, 0.08 mmol) and 2-(5,6-difluoro-3-oxo-indan-1-ylidene)-malononitrile (96 mg, 0.42 mmol) are dissolved in chloroform (2.5 cm3) is added pyridine (0.47 cm3, 5.8 mmol). The solution is stirred at 23° C. for 6 hours. Methanol (35 cm3) is added, the solid collected by filtration and washed with methanol (20 cm3). The solid is triturated in acetone (2 cm3), filtered and washed with acetone (2×1 cm3) to give Compound 39 (133 mg, 98%) as a dark blue solid. 1H NMR (400 MHz, CDCl3) 8.77 (2H, s), 8.46 (2H, dd, J 9.5, 6.5), 7.55-7.65 (4H, m), 7.02-7.11 (8H, m), 6.71-6.81 (8H, m), 3.85 (8H, t, J 6.5), 1.62-1.74 (8H, m), 1.35 (8H, p, J 7.3, 6.8), 1.13-1.31 (32H, m), 0.73-0.84 (12H, m).
Compound 40
To a degassed solution of intermediate 71 (215 mg; 0.17 mmol; 1.00 eq.) in a mixture of pyridine (1 cm3) and chloroform (10 cm3) is added an equimolar mixture of 2-(5-methyl-3-oxo-indan-1-ylidene)-malononitrile and 2-(6-methyl-3-oxo-indan-1-ylidene)-malononitrile (103 mg, 0.50 mmol) and the mixture stirred for 4 hours. The reaction is quenched by addition of aqueous hydrochloric acid solution (10 cm3, 2 M) and the aqueous layer extracted with dichloromethane (20 cm3). The combined organic layer is washed with brine (50 cm3), dried over anhydrous magnesium sulphate, filtered and the solvent removed in vacuo. The residue is purified column chromatography using a graded solvent system (cyclohexane:dichloromethane; 3:7 to 1:4). The solid is triturated in acetone (30 cm3) and filtered off to give Compound 40 (73 mg, 23%) as a blue powder. 1H NMR (400 MHz, CDCl3) 8.84 (2H, d, J 2.5), 8.59 (1H, d, J 8.1), 8.50 (1H, s), 8.29 (2H, s), 7.94 (2H, d, J 8.2), 7.86 (1H, d, J 7.8), 7.77 (1H, d, J 1.6), 7.55 (2H, d, J 8.2), 7.28 (8H, d, J 8.7), 6.87 (8H, d, J 8.7), 3.91 8H, (t, J 6.5), 1.67-1.80 (8H, m), 1.35-1.47 (8H, m), 1.18-1.35 (32H, m), 0.87 (12H, t, J 6.6).
A mixture of intermediate 31 (7.1 g, 20 mmol), trimethyl-(5-tributylstannanyl-thiophen-2-yl)-silane (10 g, 23 mmol) and anhydrous toluene (300 cm3) is degassed by nitrogen for 25 minutes. To the mixture is added tetrakis(triphenylphosphine)palladium(0) (0.5 g, 0.4 mmol) and the mixture further degassed for 15 minutes. The mixture is stirred at 85° C. for 17 hours. The reaction mixture is filtered hot through a celite plug and washed through with hot toluene. The crude product is purified using silica gel column chromatography (40-60 petrol:dichloromethane: 4:1) to give intermediate 74 (2.3 g, 21%) as a pale yellow solid. 1H-NMR (400 MHz, CDCl3) 7.40 (1H, d, J 3.7), 6.99-7.03 (1H, m), 4.13-4.29 (4H, m), 1.15-1.28 (6H, m), 0.10-0.37 (9H, s).
A mixture of intermediate 74 (2.2 g, 4.6 mmol), intermediate 23 (3.4 g, 5.8 mmol) and anhydrous toluene (300 cm3) is degassed by nitrogen for 25 minutes. To the mixture is added tetrakis(triphenylphosphine)palladium(0) (0.5 g, 0.4 mmol) and the mixture further degassed for 15 minutes. The mixture is stirred at 85° C. for 17 hours. The reaction mixture is filtered hot through a celite plug and washed through with hot toluene. The crude product is stirred in acetone (100 cm3) for 1 hour to form a heavy suspension. The solid is collected by filtration to give intermediate 75 (3.2 g, 75%) as a pale brown solid. 1H NMR (400 MHz, CDCl3) 7.80-7.86 (1H, s), 7.65 (1H, d, J 3.4), 7.38 (1H, s), 7.24 (1H, d, J 3.4), 4.43 (4H, m), 1.31-1.51 (10H, m), 1.15 (18H, d, J 7.3), 0.38 (9H, s).
To a solution of 1-bromo-3,5-dihexyl-benzene (4.9 g, 15 mmol) in anhydrous tetrahydrofuran (100 cm3) at −78° C. is added dropwise n-butyllithium (6.0 cm3, 15.0 mmol, 2.5 M in hexane) over 30 minutes. After addition, the reaction mixture is stirred at −78° C. for 120 minutes. Intermediate 75 (2.2 g, 3.0 mmol) is added and the mixture allowed to warm to 23° C. over 17 hours. Diethyl ether (100 cm3) and water (100 cm3) are added and the mixture stirred at 23° C. for 30 minutes. The product is extracted with diethyl ether (3×100 cm3). The organics are combined and dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo to give intermediate 76 (2.30 g, 47%) as a brown oil. 1H NMR (400 MHz, CD2Cl2) 7.21 (1H, s), 7.06 (1H, s), 6.80-7.03 (12H, m), 6.42-6.55 (2H, m), 3.36 (2H, d, J 4.4), 2.44-2.62 (16H, m), 1.48-1.65 (16H, m), 1.24-1.35 (49H, m), 1.11-1.17 (18H, m), 0.83-0.94 (24H, m), 0.26 (9H, s).
Nitrogen gas is bubbled through a suspension of amberlyst 15 strong acid (8.8 g) in anhydrous diethyl ether (100 cm3) at 0° C. for 60 minutes. Intermediate 76 (2.2 g, 1.4 mmol) is added whilst the mixture is degassed for a further 30 minutes. The resulting suspension is stirred at 23° C. for 2 hours. The reaction mixture is filtered and the solvent removed in vacuo. The crude is taken up in anhydrous tetrahydrofuran (50 cm3) and tetrabutylammonium fluoride (2.7 cm3, 2.7 mmol, 1 M in tetrahydrofuran) added. The mixture is stirred for 1 hour. Diethyl ether (100 cm3) and water (200 cm3) are added and the mixture stirred for 30 minutes. The product is extracted with diethyl ether (3×100 cm3). The organics are combined and dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is purified using silica gel column chromatography (40-60 petrol:dichloromethane; 9:1) to give intermediate 77 (1.0 g, 54%) as a dark orange solid. 1H NMR (400 MHz, CDCl3) 7.25-7.31 (1H, m), 7.21-7.25 (1H, m), 7.17 (1H, d, J 4.9), 7.05 (1H, d, J 4.9), 6.81-6.91 (12H, m), 2.40-2.57 (16H, m), 1.54 (16H, d, J 6.8), 1.25 (48H, d, J 7.3), 0.85 (24H, q, J 6.2).
To a solution of intermediate 77 (500 mg, 0.37 mmol) in anhydrous tetrahydrofuran (22 cm3) at −78° C. is added dropwise n-butyllithium (0.6 cm3, 1.5 mmol, 2.5 M in hexane) over 10 minutes. After addition, the reaction mixture is stirred at −78° C. for 60 minutes. N,N-Dimethylformamide (0.15 cm3, 2.2 mmol) is added and the mixture allowed to warm to 23° C. over 17 hours. Diethyl ether (50 cm3) and water (50 cm3) are added and the mixture stirred at 23° C. for 30 minutes. The product is extracted with diethyl ether (3×100 cm3). The combined organics are dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is purified using silica gel column chromatography (40-60 petrol:dichloromethane; 8:2) to give intermediate 78 (95 mg, 18%) as a dark red oil. 1H NMR (400 MHz, CDCl3) 9.70-9.85 (1H, s), 9.69-9.75 (1H, s), 7.83-7.87 (1H, s), 7.56 (1H, s), 6.83 (4H, s), 6.71 (8H, dd, J 12.8, 1.3), 2.29-2.53 (16H, m), 1.36-1.55 (16H, m), 1.05-1.27 (48H, m), 0.76 (24H, q, J 6.8).
Compound 41
To a solution of intermediate 78 (100 mg, 0.07 mmol) in anhydrous chloroform (40 cm3) at 0° C. is added pyridine (0.4 cm3, 4.5 mmol). The mixture is then degassed with nitrogen before 2-(5,6-difluoro-3-oxo-indan-1-ylidene)-malononitrile (65 mg, 0.28 mmol) is added. The solution is further degassed and then stirred at 0° C. for 30 minutes. The ice bath is removed and the reaction is allowed to warm to 40° C. over 120 minutes. The mixture is diluted with 2-propanol (300 cm3) to form a suspension and the solid collected by filtration. The crude is dissolved in dichloromethane (100 cm3) then diluted with ethanol (300 cm3) to produce a heavy suspension which is collected by filtration to give Compound 41 (82 mg, 63%) as a blue/green solid. 1H NMR (400 MHz, CD2Cl2) 8.77 (2H, s), 8.42 (2H, dt, J 9.8, 6.1), 8.06 (1H, s), 7.67 (1H, s), 7.56 (2H, dt, J 11.4, 7.6), 6.66-6.96 (12H, m), 2.32-2.56 (16H, m), 1.35-1.57 (16H, m), 1.05-1.26 (48H, m), 0.63-0.80 (24H, m).
To a solution of intermediate 77 (500 mg, 0.37 mmol) in anhydrous tetrahydrofuran (22 cm3) at −78° C. is added dropwise n-butyllithium (0.6 cm3, 1.5 mmol, 2.5 M in hexane) over 10 minutes. After addition, the reaction mixture is stirred at −78° C. for 60 minutes before tributyltin chloride (0.4 cm3, 1.6 mmol) is added. The mixture is then allowed to warm to 23° C. over 72 hours. The solvent removed in vacuo, and the residue passed through a zeolite plug (40-60 petrol). The crude is suspended in ethanol (100 cm3) stirred for 30 minutes and the solvent decanted. This procedure is repeated twice to give partially purified intermediate 79 (860 mg) as a dark red oil. 1H NMR (400 MHz, CD2Cl2) 7.02-7.16 (1H, m), 6.82-6.93 (1H, m), 6.57-6.72 (12H, m), 2.20-2.32 (16H, m), 0.96-1.53 (48H, m), 0.54-0.78 (24H, m).
A mixture of intermediate 79 (712 mg, 0.37 mmol), 2-bromo-thiazole-5-carbaldehyde (178 mg, 0.73 mmol), tri-o-tolyl-phosphine (34 mg, 0.11 mmol) and anhydrous toluene (39 cm3) is degassed by nitrogen for 10 minutes. To the mixture is added tris(dibenzylideneacetone) dipalladium(0) (27 mg, 0.03 mmol) and the mixture further degassed for 15 minutes. The mixture is stirred at 80° C. for 17 hours and, after cooling to 23° C., the solvent removed in vacuo. The crude is stirred in 2-propanol (100 cm3) to form a suspension and the solid collected by filtration. The crude is purified using silica gel column chromatography (40-60 petrol:dichloromethane; 8:2) to give intermediate 80 (545 mg, 88%) as a dark blue solid. 1H NMR (400 MHz, CD2Cl2) 10.61 (2H, s), 8.67 (1H, s), 8.27 (1H, s), 8.10 (2H, d, J 7.6), 7.86 (2H, dd, J 11.9, 7.7), 6.84 (12H, d, J 12.0), 2.43 (16H, m), 1.43-1.57 (16H, m), 1.03-1.29 (48H, m), 0.63-0.80 (24H, m).
Compound 42
To a solution of intermediate 80 (120 mg, 0.07 mmol) in anhydrous chloroform (48 cm3) at 0° C. is added pyridine (0.2 cm3). The mixture is then degassed with nitrogen before 2-(5,6-difluoro-3-oxo-indan-1-ylidene)-malononitrile (66 mg, 0.29 mmol) is added. The solution is then further degassed and stirred at 0° C. for 20 minutes and at 23° C. for 3 hours. The mixture is diluted with ethanol (200 cm3) to produce a heavy suspension. The solid is collected by filtration and washed with methanol (50 cm3). The crude is suspended in a 1:1 mixture of acetone:diethyl ether (200 cm3) to form a suspension and stirred for 30 minutes. The solid is collected by filtration to give Compound 42 (110 mg, 73%) as a black solid. 1H NMR (400 MHz, CD2Cl2) 9.60 (2H, s), 9.31 (2H, t, J 8.4), 8.84 (1H, s), 8.57-8.65 (2H, m), 8.45 (1H, s), 8.04 (2H, dd, J 12.0, 8.1), 7.78 (2H, t, J 7.7), 6.93-7.03 (12H, m), 2.51-2.63 (16H, m), 1.57-1.66 (16H, m), 1.23-1.36 (48H, m), 0.79-0.90 (24H, m).
Compound 43
To a solution of intermediate 80 (150 mg, 0.09 mmol) in anhydrous chloroform (48 cm3) at 0° C. is added pyridine (0.3 cm3). The mixture is then degassed with nitrogen before a solution of 3-(dicyanomethylidene) indan-1-one (69 mg, 0.36 mmol) in chloroform (10 cm3) is added. The solution is then further degassed and stirred at 23° C. for 4 hours. The mixture is diluted with ethanol (500 cm3) to produce a heavy suspension. The solid is collected by filtration and washed with acetone (50 cm3) to give Compound 43 (98 mg, 54%) as a black solid. 1H NMR (400 MHz, CD2Cl2) 9.57 (2H, s), 9.33 (2H, t, J 7.9), 8.82 (1H, s), 8.76 (2H, d, J 7.3), 8.44 (1H, s), 8.01-8.07 (2H, m), 7.99 (2H, d, J 7.1), 7.78-7.90 (4H, m), 6.98 (12H, d, J 11.7), 2.48-2.62 (16H, m), 1.50-1.65 (24H, m), 1.20-1.41 (48H, m), 0.78-0.92 (24H, m).
3-Methoxy-thiophene (25.0 g, 219 mmol) and 2-ethyl-hexan-1-ol (51.4 cm3, 329 mmol) are dissolved in anhydrous toluene (500 cm3). With stirring 4-methylbenzenesulfonic acid hydrate (4.17 g, 21.9 mmol) is added and after 35 minutes at 23° C. the reaction is heated at reflux for 20 hours. The reaction is then cooled to 23° C. before additional toluene (50 cm3) is added. The solution is washed with water (2×250 cm3) and brine (250 cm3) before drying over magnesium sulfate, filtered and concented in vacuo. The crude product is purified by silica plug (40-60 petrol) followed by column chromatography (40-60 petrol), to give intermediate 81 (23.4 g, 50% yield) as a yellow tinged oil. 1H NMR (400 MHz, CDCl3) 7.18 (1H, dd, J 5.3, 3.1), 6.77 (1H, dd, J 5.3, 1.6), 6.24 (1H, dd, J 3.2, 1.5), 3.84 (2H, dd, J 5.8, 0.9), 1.72 (1H, spt, J 6.1), 1.26-1.56 (8H, m), 0.88-0.97 (6H, m).
To a solution of intermediate 81 (23.1 g, 109 mmol) in anhydrous N,N-dimethylformamide (330 cm3) at 0° C. is added a solution of 1-bromo-pyrrolidine-2,5-dione (19.4 g, 109 mmol) in anhydrous N,N-dimethylformamide (110 cm3). The reaction mixture is then stirred at 23° C. for 41 hours before adding to ice (2000 cm3) with stirring. Once melted, half of the aqueous suspension is extracted with 40-60 petrol (300 cm3). The aqueous layer is removed and the second half of the aqueous suspension extracted. The aqueous layers are additionally extracted in this manner with a second washing of 40-60 petrol (200 cm3). The organic extracts are then combined and washed with brine (2×200 cm3), dried over magnesium sulfate and filtered. Due to stability concerns, the bulk sample is not concentrated in vacuo and is allowed to remain in solution until immediately prior to use. 1H NMR of sample suggests quantitative yield of intermediate 82 as a yellow oil. 1H NMR (400 MHz, CDCl3) 7.19 (1H, d, J 5.9), 6.75 (1H, d, J 5.9), 3.93 (2H, d, J 5.9), 1.71 (1H, sept, J 6.1), 1.24-1.60 (8H, m), 0.88-0.98 (6H, m).
To a suspension of 1-bromo-4-hexylbenzene (10.3 g, 42.5 mmol) in anhydrous tetrahydrofuran (180 cm3) at −78° C. is added tert-butyllithium (50 cm3, 85 mmol, 1.7 M in pentane) over 30 minutes. The reaction is then allowed to warm to −30° C., before re-cooling to −78° C. Additional 1-bromo-4-hexylbenzene (1.00 g, 4.15 mmol) is then added to ensure consumption of any residual tert-butyllithium. Ethyl 2-[5-(3-ethoxycarbonyl-2-thienyl)thieno[3,2-b]thiophen-2-yl]thiophene-3-carboxylate (3.81 g, 8.50 mmol) is then added in one portion to the reaction mixture and the mixture allowed to stir at 23° C. for 17 hours. The reaction is diluted with diethyl ether (100 cm3) and washed with water (200 cm3). The organic layer is diluted with diethyl ether (100 cm3) then further washed with water (200 cm3) and brine (100 cm3). The organic layer is then dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The crude product is then purified by column chromatography using a graded solvent system (40-60 petrol:dichloromethane; 1:0 to 2:3) to give intermediate 83 (5.61 g, 66% yield) as a light yellow oil. 1H NMR (400 MHz, CDCl3) 7.07-7.18 (18H, m), 6.65 (2H, s), 6.45 (2H, d, J 5.4), 3.25 (2H, s), 2.60 (8H, t, J 7.7), 1.58-1.66 (8H, m), 1.24-1.39 (24H, m), 0.87-0.92 (12H, m).
To a degassed suspension of amberlyst 15 strong acid (10.8 g) in anhydrous toluene (65 cm3) is added a degassed solution of intermediate 83 (2.69 g, 2.68 mmol) in anhydrous toluene (64 cm3) and the reaction mixture stirred at 23° C. for 15 minutes. The reaction mixture is then heated at 40° C. for 70 minutes and at 50° C. for a further 45 minutes. The reaction is then filtered through a layered bed of celite:magnesium sulfate:celite washing with toluene (3×40 cm3) and diethyl ether (5×50 cm3). The mixture is then concentrated in vacuo and purified by column chromatography, eluting with a graded solvent system (40-60 petrol:dichloromethane; 1:0 to 1:9) to give intermediate 84 (540 mg, 21%) as a yellow solid. 1H NMR (400 MHz, CDCl3) 7.12-7.18 (10H, m), 7.05-7.10 (10H, m), 2.55 (8H, t, J 7.8), 1.51-1.63 (8H, m), 1.23-1.37 (24H, m), 0.84-0.90 (12H, m).
A solution of intermediate 84 (1.15 g, 1.19 mmol) in anhydrous tetrahydrofuran (70 cm3) is cooled to −78° C. before n-butyllithium (1.4 cm3, 3.6 mmol, 2.5 M in hexanes) is added via syringe. The mixture is then stirred at −78° C. for 1 hour before tributyltin chloride (1.1 cm3, 4.2 mmol) is added. The mixture is stirred at 23° C. for 17 hours, methanol (20 cm3) added and after stirring for 6 hours the reaction mixture is concentrated in vacuo. The crude is triturated with methanol (3×10 cm3) and then added to a solution of intermediate 61 (785 mg, 2.69 mmol) (freshly concentrated in vacuo) in anhydrous toluene (150 cm3). The solution is then degassed with nitrogen before tris(dibenzylideneacetone)dipalladium (90 mg, 0.10 mmol) and tris(o-tolyl)phosphine (112 mg, 0.368 mmol) are added. The reaction mixture is then further degassed before heating at 80° C. with continued degassing for 19 hours. The reaction is then stirred at 23° C. for 4 days after which it is concentrated in vacuo. The crude material is then partially purified by silica plug using a graded solvent system (petrol 40-60:dichloromethane; 1:0-2:3). The partially purified material is then triturated with methanol (6×10 cm3), taken up in anhydrous tetrahydrofuran (58 cm3) and cooled to −78° C. To this mixture is added dropwise n-butyllithium (1.4 cm3, 3.5 mmol, 2.5 M in hexanes) and the reaction mixture stirred for 1 hour. The reaction is then quenched by the addition of N,N-dimethylformamide (2.3 cm3, 30 mmol) and after 1 hour at −78° C. the reaction is allowed to stir at 23° C. for 15 hours. The reaction is diluted with diethyl ether (150 cm3) and washed with water (150 cm3) with added brine (20 cm3). The organic layer is then isolated and the aqueous layer additionally extracted with diethyl ether (50 cm3). The combined organic layers are then further washed with water (100 cm3) with added brine (20 cm3) and brine (100 cm3) before they are dried over magnesium sulfate, filtered and concentrated in vacuo. The crude product is purified by column chromatography using a graded solvent system (40-60 petrol:dichloromethane; 1:0 to 2:3) followed by further column chromatography using a graded solvent system (80-100 petrol:diethyl ether; 1:0 to 6:3) to give intermediate 85 (285 mg, 17% yield over 3 steps) as a black solid. 1H NMR (400 MHz, CDCl3) 9.73 (2H, s), 7.44 (2H, s), 7.41 (2H, s), 7.17 (8H, d, J 8.2), 7.11 (8H, d, J 8.2), 4.08 (4H, d, J 5.1), 2.57 (8H, t, J 7.8), 1.81 (2H, spt, J 6.0), 1.43-1.66 (16H, m), 1.22-1.40 (32H, m), 0.82-1.00 (24H, m).
Compound 44
To a solution of intermediate 85 (150 mg, 0.104 mmol) in anhydrous chloroform (11 cm3) is added pyridine (0.59 cm3) and the solution degassed for 25 minutes. The reaction mixture is then cooled to −20° C. and 2-(5,6-difluoro-3-oxo-indan-1-ylidene)-malononitrile (95 mg, 0.41 mmol) is added. The reaction mixture is then degassed for a further 15 minutes and allowed to warm to 23° C. over 3 hours. The cooling bath is then removed and the reaction stirred at 23° C. for a further 2 hours before the reaction is added to stirring methanol (200 cm3) washing in with dichloromethane (10 cm3). After 30 minutes the precipitate is collected by filtration, washed with methanol (3×10 cm3) to give Compound 44 (132 mg, 68% yield) as a black solid. 1H NMR (400 MHz, CDCl3) 8.67 (2H, s), 8.52 (2H, dd, J 10.2, 6.5), 7.67 (2H, s), 7.61-7.66 (2H, m), 7.51 (2H, s), 7.16-7.21 (8H, m), 7.11-7.16 (8H, m), 4.15 (4H, d, J 5.4), 2.60 (8H, t, J 7.7), 1.86 (2H, spt, J 6.1), 1.50-1.69 (16H, m), 1.25-1.43 (32H, m), 1.01 (6H, t, J 7.5), 0.92-0.97 (6H, m), 0.85-0.92 (12H, m).
To a solution of 1-bromo-4-hexyloxy-benzene (1.43 g, 5.57 mmol) in anhydrous tetrahydrofuran (20 cm3) at −78° C. is added tert-butyllithium (6.55 cm3, 11.1 mmol, 1.7 M in pentane) over 5 minutes. The reaction mixture is then stirred for 45 minutes. Intermediate 32 (550 mg, 0.93 mmol) is added as a single portion, the cooling removed and the reaction mixture stirred at 23° C. for 17 hours. Water (50 cm3) and diethyl ether (50 cm3) are added. The organic phase is washed with water (2×30 cm3), dried over magnesium sulphate, filtered and concentrated in vacuo. The resulting solid is slurried in 40-60 petrol (10 cm3), filtered and washed with 40-60 petrol (2×10 cm3) to give intermediate 86 (1.13 g, 76%) as a pale green solid. 1H NMR (400 MHz, CDCl3) 7.11-7.22 (8H, m), 6.85 (2H, d, J 3.4), 6.75-6.82 (7H, m), 6.49 (2H, d, J 3.4), 3.94 (8H, t, J 6.6), 3.34 (2H, s), 1.67-1.84 (8H, m), 1.39-1.52 (8H, m), 1.25-1.38 (16H, m), 0.86-0.95 (12H, m), 0.22 (s, 18H).
A solution of intermediate 86 (850 mg, 0.70 mmol) dissolved in toluene (34 cm3) at 75° C. is degassed with a flow of nitrogen for 20 minutes. Amberlyst 15 strong acid (4.0 g) is added and the reaction mixture degassed for a further 10 minutes and stirred for 17 hours. The reaction is allowed to cool to 23° C., filtered and the solid washed with toluene (50 cm3). The combined organic phases is concentrated in vacuo. The intermediate material is dissolved in chloroform (17 cm3), N,N-dimethylformamide (819 mg, 11.2 mmol) is added and the solution cooled to 0° C. Phosphoryl chloride (1.61 g, 10.5 mmol) is added over 10 minutes, the cooling removed and the reaction stirred at 65° C. for 17 hours. An aqueous solution of sodium acetate (100 cm3, 6 M) is added and the biphasic solution stirred at 65° C. for 2 hours. The mixture extracted with dichloromethane (15 cm3) and the combined organic phases washed with water (2×20 cm3), dried over anhydrous magnesium sulphate, filtered and concentrated in vacuo. The solid is triturated in 40-60 petrol (10 cm3) and collected by filtration to give intermediate 87 (763 mg, 63%) as an orange solid. 1H NMR (400 MHz, CD2Cl2) 9.80 (2H, s), 7.69 (2H, s), 7.00-7.28 (8H, m), 6.60-6.91 (8H, m), 3.91 (8H, t, J 6.6), 1.61-1.85 (8H, m), 1.38-1.51 (8H, m), 1.32 (16H, m), 0.82-0.98 (12H, m).
Compound 45
Intermediate 87 (200 mg, 0.18 mmol) and 2-(3-oxo-indan-1-ylidene)-malononitrile (250 mg, 1.28 mmol) are dissolved in chloroform (5 cm3) and nitrogen bubbled through the suspension for 20 minutes. Pyridine (30.6 cm3; 379 mmol) is added and nitrogen passed through the solution for a further 20 minutes. The solution is stirred for 17 hours. Methanol (35 cm3) is added and the solid collected by filtration and washed with methanol (3×10 cm3). The solid is triturated in acetone (5 cm3), filtered and washed with acetone (3×2 cm3). The material is purified on silica gel eluting with a graded solvent system (40-60 petrol:dichloromethane; 11:9 to 2:3) to give Compound 45 (66 mg, 25%) as a blue solid. 1H NMR (400 MHz, CDCl3) 8.86 (2H, s), 8.68 (2H, d, J 7.4), 7.86-7.95 (2H, m), 7.70-7.78 (4H, m), 7.68 (2H, s), 7.14 (8H, d, J 8.7), 6.84 (8H, d, J 8.5), 3.92 (8H, t, J 6.5), 1.75 (8H, m), 1.39-1.47 (8H, m), 1.27-1.35 (16H, m), 0.88 (12H, m).
Compound 46
Intermediate 87 (200 mg, 0.18 mmol) and 2-(5-methyl-3-oxo-indan-1-ylidene)-malononitrile (268 mg, 1.28 mmol) are dissolved in chloroform (5 cm3) and nitrogen bubbled through the suspension for 20 minutes. Pyridine (1.04 cm3, 12.9 mmol) is added and nitrogen passed through the solution for a further 20 minutes. The solution is stirred for 17 hours. Methanol (35 cm3) added and the solid collected by filtration and washed with methanol (3×10 cm3). The solid is triturated in acetone (5 cm3), filtered and washed with acetone (3×2 cm3). The material is purified on silica gel eluting with a graded solvent system (40-60 petrol:dichloromethane; 11:9 to 2:3) to give Compound 46 (69 mg, 26%) as a blue solid. 1H NMR (400 MHz, CD2Cl2) 8.82-8.88 (2H, m), 8.48-8.59 (2H, m), 7.55-7.86 (6H, m), 7.16-7.25 (8H, m), 6.82-6.91 (8H, m), 3.95 (8H, t, J 6.6), 2.55-2.59 (6H, m), 1.71-1.83 (8H, m), 1.42-1.52 (8H, m), 1.31-1.40 (16H, m), 0.88-0.95 (12H, m).
To a solution of 1-bromo-4-((S)-2-methyl-butoxy)-benzene (1.21 g, 4.98 mmol) in anhydrous tetrahydrofuran (20 cm3) at −78° C. is added tert-butyllithium (5.9 cm3, 10.0 mmol, 1.7 M in pentane) over 5 minutes and the reaction mixture stirred for 1 hour. Intermediate 32 (531 mg, 0.90 mmol) is added as a single portion, the cooling removed and the reaction mixture stirred for 65 hours. Water (25 cm3) is added, the mixture stirred for 20 minutes and extracted with ether (25 cm3). The organic portion is washed with water (2×15 cm3), dried over anhydrous magnesium sulphate, filtered, concentrated in vacuo and azeotroped with 40-60 petrol (10 cm3). The solid is collected by filtration and triturated in 40-60 petrol (10 cm3), filtered and washed with 40-60 petrol (2×10 cm3) to give intermediate 88 (785 mg, 68%) as a white solid. 1H NMR (400 MHz, CD2Cl2) 7.15-7.23 (m, 8H), 6.92 (4H, dd, J 3.4, 1.94), 6.83 (8H, dd, J 8.8, 2.1), 6.56 (2H, dd, J 3.5, 1.9), 3.70-3.91 (8H, m), 3.33 (2H, d, J 2.0), 1.82-1.95 (4H, m), 1.48-1.67 (4H, m), 1.22-1.38 (4H, m), 1.00-1.07 (12H, m), 0.87-1.00 (12H, m), 0.24-0.30 (18H, m).
To a degassed mixture of intermediate 88 (785 mg, 0.68 mmol) and toluene (31 cm3) at 75° C. is added Amberlyst 15 strong acid (3.20 g) and the mixture further degassed for 10 minutes. The reaction mixture is then stirred for 17 hours. The suspension is filtered, washed with toluene (50 cm3) and the solvent removed in vacuo. The solid is dissolved in chloroform (15.7 cm3) and N,N-dimethylformamide (793 mg, 10.9 mmol) added. The solution is cooled to 0° C. and phosphorus oxychloride (1.56 g, 10.2 mmol) added over 10 minutes. The cooling is removed and the reaction heated at 65° C. for 17 hours. An aqueous sodium acetate solution (50 cm3, 10 M) is added and the mixture stirred for 3 hours. The solution is extracted with chloroform (15 cm3). The combined organic phases are washed with water (2×20 cm3), dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is purified by flash chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 2:3 to 4:1) to give intermediate 89 (260 mg, 37%) as an orange solid. 1H NMR (400 MHz, CD2Cl2) 9.83 (2H, d, J 0.9), 7.72 (2H, s), 7.17 (8H, d, J 8.6), 6.85 (8H, d, J 8.7), 3.68-3.85 (8H), 1.79-1.91 (4H, m), 1.49-1.61 (4H, m), 1.21-1.34 (4H, m), 1.01 (12H, d, J 6.7), 0.95 (12H, t, J 7.5).
Compound 47
To a degassed mixture of intermediate 89 (108 mg, 0.10 mmol), 2-(5-methyl-3-oxo-indan-1-ylidene)-malononitrile (152 mg, 0.73 mmol) and chloroform (2.7 cm3) is added pyridine (0.59 cm3, 7.3 mmol) and the mixture degassed for a further 10 minutes. The reaction mixture stirred for 5 hours and methanol (30 cm3) added. The solid is collected by filtration and washed with methanol (2×10 cm3). The crude is purified by flash chromatography eluting with a graded solvent system (40-60 petrol:dichloromethane; 9:11 to 1:3) to give Compound 47 (75 mg, 51%) as a blue solid. 1H NMR (400 MHz, CDCl3) 8.75 (2H, s), 8.37-8.51 (2H, s), 7.41-7.75 (6H, s), 7.04-7.12 (8H, s), 6.74-6.82 (8H, m), 3.58-3.77 (8H, m), 2.44-2.50 (6H, m), 1.70-1.82 (4H, m), 1.39-1.55 (4H, m), 1.09-1.23 (4H, m), 0.92 (12H, d, J 6.7), 0.85 (12H, t, J 7.5).
Compound 48
A solution of intermediate 89 (135 mg, 0.130 mmol) in chloroform (10 cm3) and pyridine (0.75 cm3) is degassed for 10 minutes with nitrogen. 2-(3-Oxo-indan-1-ylidene)-malononitrile (180 mg, 0.91 mmol) is added in one portion and the reaction mixture is stirred at 23° C. for 150 minutes. Methanol (15 cm3) is added and the obtained precipitate is collected by filtration and washed with methanol (3×10 cm3). The solid is filtered through a pad of silica (40-60 petrol:dichloromethane; 2:3). Concentration in vacuo followed by trituration in refluxing acetone (20 cm3) and then in a 3:1 mixture of acetone:chloroform (40 cm3) gives Compound 48 (144 mg, 79%) as a dark blue powder. 1H NMR (400 MHz, CDCl3) 8.84 (2H, s), 8.61-8.67 (2H, m), 7.84-7.90 (2H, m), 7.63-7.72 (6H, m), 7.13-7.21 (8H, m), 6.83-6.90 (8H, m), 3.81 (4H, m), 3.72 (4H, m), 1.78-1.92 (4H, m, J 6.6), 1.56 (4H, m), 1.26 (4H, m), 1.00 (12H, d, J 6.7), 0.94 (12H, t, J 7.5).
Compound 49
To a degassed solution of intermediate 44 (200 mg, 0.147 mmol) and pyridine (0.83 cm3, 10 mmol) in anhydrous chloroform (40 cm3) at −10° C. is added a degassed solution of 2-(5,6-difluoro-3-oxo-indan-1-ylidene)-malononitrile (135 mg, 0.587 mmol) in anhydrous chloroform (8 cm3) over 10 minutes. The resulting solution is then degassed for a further 30 minutes, warmed to 23° C. and stirred for 4 hours. The reaction mixture is diluted with 2-propanol (300 cm3) and stirred for 1 hour. The resulting solid is collected by filtration and washed with 2-propanol (100 cm3) and ethanol (100 cm3). The solid is then suspended in dichloromethane (50 cm3) and then poured into methanol (500 cm3). The solid is collected by filtration and washed with methanol (100 cm3) and ice-cold acetone (100 cm3) to give Compound 49 (108 mg, 41%) as a dark blue solid. 1H NMR (400 MHz, CDCl3) 8.77 (2H, s), 8.45 (2H, dd, J 9.9, 6.5), 7.52-7.66 (4H, m), 6.88 (4H, s), 6.72 (8H, d, J 1.5), 2.34-2.52 (16H, m), 1.38-1.48 (16H, m), 1.19 (48H, d, J 2.0), 0.67-0.88 (24H, m).
To a solution of 1-bromo-3,5-dihexyl-benzene (5.21 g, 16.0 mmol) in anhydrous tetrahydrofuran (100 cm3) at −78° C. is added dropwise n-butyllithium (6.4 cm3, 16 mmol, 2.5 M in hexane) over 30 minutes. The reaction mixture is then stirred for 2 hours. Intermediate 46 (2.80 g, 3.21 mmol) is then added and the reaction mixture allowed to warm to 23° C. and stirred for 17 hours. Water (100 cm3) is added and the mixture stirred for a further 1 hour. Diethyl ether (100 cm3) is added and the organic layer washed with water (2×50 cm3), dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude is purified by column chromatography using a graded solvent system (40-60 petrol:dichloromethane; 19:1 to 1:4) to give intermediate 90 (3.54 g, 63%) as a pale yellow oil. 1H NMR (400 MHz, CD2Cl2) 7.23 (2H, s), 6.86-7.01 (12H, m), 6.51 (2H, s), 3.41 (2H, s), 2.42-2.61 (16H, m), 1.49-1.61 (16H, m), 1.22-1.45 (54H, m), 1.15 (36H, d, J 7.3), 0.78-0.95 (24H, m).
To a degassed suspension of amberlyst 15 strong acid (12 g) in anhydrous diethyl ether (100 cm3) at 0° C. is added intermediate 90 (2.95 g, 1.67 mmol) followed by degassing for a further 30 minutes. The resulting suspension is allowed to warm to 23° C. and stirred for 1 hour. The reaction mixture is filtered through a thin celite plug and washed well with diethyl ether (200 cm3). The crude is then purified by column chromatography (40-60 petrol) and then taken up in anhydrous tetrahydrofuran (50 cm3) and cooled to 0° C. To the mixture is added a solution of tetrabutylammonium fluoride (3.34 cm3, 3.34 mmol, 1 M in tetrahydrofuran) and the resulting mixture stirred for 30 minutes at 23° C. The solvent is then removed in vacuo and the residue suspended in methanol (200 cm3) and stirred for 30 minutes. The solid collected by filtration to give intermediate 91 (2.02 g, 85%) as a dark orange solid. 1H NMR (400 MHz, CDCl3) 7.13-7.21 (4H, m), 6.71-6.84 (12H, m), 2.33-2.49 (16H, m), 1.38-1.48 (16H, m), 1.08-1.22 (48H, m), 0.70-0.80 (24H, m).
To a solution of intermediate 91 (600 mg, 0.42 mmol) in anhydrous tetrahydrofuran (25 cm3) at −78° C. is added dropwise n-butyllithium (0.68 cm3, 1.7 mmol, 2.5 M in hexane) over 10 minutes. The mixture is then stirred at −78° C. for 1 hour before anhydrous N,N-dimethylformamide (0.17 cm3, 2.5 mmol) is added. The cooling is then removed and the reaction mixture stirred at 23° C. for 2 hours. Water (50 cm3) is added and the mixture stirred for 30 minutes. The organics are extracted with diethyl ether (3×50 cm3), combined, dried over anhydrous magnesium sulfate, filtered and the solvent removed in vacuo. The crude product is purified by column chromatography using a graded solvent system (40-60 petrol:dichloromethane; 1:0 to 4:1) to give intermediate 92 (450 mg, 72%) as a dark red sticky solid. 1H NMR (400 MHz, CDCl3) 9.79 (2H, s), 7.85 (2H, s), 6.83 (4H, s), 6.71 (8H, d, J 1.0), 2.41 (16H, t, J 7.6), 1.39-1.50 (16H, m), 1.15 (48H, br. s), 0.70-0.80 (24H, m).
Compound 50
To a degassed solution of intermediate 92 (300 mg, 0.20 mmol) and pyridine (1.15 cm3) in anhydrous chloroform (40 cm3) at −10° C. is added a degassed solution of 2-(5,6-difluoro-3-oxo-indan-1-ylidene)-malononitrile (187 mg, 0.814 mmol) in anhydrous chloroform (8 cm3) over 10 minutes. The reaction mixture is then degassed for a further 30 minutes, warmed to 23° C. and stirred for 5 hours. The reaction mixture is diluted with methanol (300 cm3) and stirred for 65 hours. The solid collected by filtration, washed with ethanol (100 cm3) and methanol (100 cm3) to give Compound 117 (62 mg, 16%) as a dark green solid. 1H NMR (400 MHz, CD2Cl2) 8.90 (2H, s), 8.55 (2H, dd, J 10.1, 6.5), 8.19 (2H, s), 7.67 (2H, t, J 7.5), 6.85-7.10 (12H, m), 2.56 (16H, t, J 7.6), 1.46-1.67 (16H, m), 1.13-1.45 (48H, m), 0.70-0.93 (24H, m).
Polymer 2
2,6-Bis-trimethylstannanyl-benzo[1,2-b;4,5-b′]dithiophene-4,8-dicarboxylic acid didodecyl ester (250.0 mg, 0.27 mmol), 4,7-bis-(5-bromo-thiophen-2-yl)-5,6-bis-octyloxy-benzo[1,2,5]thiadiazole (190.0 mg, 0.27 mmol), tri-o-tolyl-phosphine (6.5 mg, 21 μmol) and tris(dibenzylideneacetone)dipalladium (4.9 mg, 5.3 μmol) are weighed into a microwave vial and then the microwave vial sealed. Degassed chlorobenzene (2.7 cm3) is then added and the mixture further purged with nitrogen for 5 minutes. The reaction mixture is placed in a pre-heated oil bath at 140° C. and stirred for 30 minutes. The reaction mixture allowed to cool slightly and poured into methanol (200 cm3), the solid collected by filtration and washed with methanol (50 cm3). The solid subjected to sequential Soxhlet extraction, acetone, 40-60 petrol, cyclohexane, chloroform and chlorobenzene. The chlorobenzene fraction is precipitated into stirred methanol (200 cm3) and the solid collected by filtration to give polymer 2 (252 mg, 81%) as a black solid. GPC (1,2,4-trichlorobenzene, 140° C.) Mn=96,000 g/mol, Mw=300,000 g/mol.
Current-voltage characteristics are measured using a Keithley 2400 SMU while the solar cells are illuminated by a Newport Solar Simulator at 100 mW-cm−2 white light. The solar simulator is equipped with AM1.5G filters. The illumination intensity is calibrated using a Si photodiode. All the device preparation and characterization is done in a dry-nitrogen atmosphere.
Power conversion efficiency is calculated using the following expression
where FF is defined as
OPV device characteristics for a blend which contains either random polymer 1 or alternating polymer 2 as shown below and an acceptor compound of prior art or according to the invention, and is coated from an organic solution. Details of the solution composition are shown in Table 1.
Polymer 1 and its preparation are disclosed in WO 2011/131280 A1.
ITIC and its preparation are disclosed in CN105315298.
IDIC and its preparation are disclosed in JACS, 2016, 138, 2973.
ITIC-Th and its preparation are disclosed in JACS, 2016, 138, 4955.
IEIC and its preparation are disclosed in CN104557968.
FBR and IDTBR and their preparation are disclosed in Nature Materials DOI: 10.1038/NMAT 4797
Inverted Bulk Heterojunction Organic Photovoltaic Devices
Organic photovoltaic (OPV) devices are fabricated on pre-patterned ITO-glass substrates (13 Ω/sq.) purchased from LUMTEC Corporation. Substrates are cleaned using common solvents (acetone, iso-propanol, deionized-water) in an ultrasonic bath. A layer of commercially available aluminium zinc oxide (AlZnO, Nanograde) was applied as a uniform coating by doctor blade at 40° C. The AlZnO Films are then annealed at 100° C. for 10 minutes in air. Active material solutions (i.e. polymer+acceptor) are prepared to fully dissolve the solutes. Thin films are blade-coated in air atmosphere to achieve active layer thicknesses between 50 and 800 nm as measured using a profilometer. A short drying period follows to ensure removal of any residual solvent.
Typically, blade-coated films are dried at 70° C. for 2 minutes on a hotplate. Next the devices are transferred into an air atmosphere. On top of the active layer 0.1 mL of a conducting polymer poly(ethylene dioxythiophene) doped with poly(styrene sulfonic acid) [PEDOT:PSS Clevios HTL Solar SCA 434 (Heraeus)] was spread and uniformly coated by doctor blade at 70° C. Afterwards Ag (100 nm) cathodes are thermally evaporated through a shadow mask to define the cells.
Table 1 shows the formulation characteristics of the individual photoactive material solutions, comprising a polymer as electron donor component and a compound according to the invention as electron acceptor component.
Inverted Device Properties
Table 2 shows the device characteristics for the individual OPV devices comprising a photoactive layer with a BHJ formed from the active material (acceptor/polymer) solutions of Table 1.
From Table 2 it can be seen that the random polymer 1 shows improved performance over the comparative polymer 2 when combined with the non-fullerene acceptors from the present invention.
Devices are fabricated onto glass substrates with six pre-patterned ITO dots of 5 mm diameter to provide the bottom electrode. The ITO substrates are cleaned using a standard process of ultrasonication in Decon90 solution (30 minutes) followed by washing with de-ionized water (×3) and ultrasonication in de-ionized water (30 minutes). The ZnO ETL layer was deposited by blade coating or spin coating a ZnO nanoparticle dispersion onto the substrate and drying on a hotplate for 10 minutes at a temperature between 100 and 140° C. A formulation of random polymer 3 and compound as disclosed herein was prepared at a ratio of between 1:2 and 2:1 in o-dichlorobezene or o-xylene with 0-10% co-solvent at a concentration of between 18 and 40 mg/ml, and stirred for 17 hours at a temperature of between 23° C. and 60° C. The active layer was deposited using blade coating (K101 Control Coater System from RK). The stage temperature was set to 30° C. or 70° C., the blade gap set between 2-15 μm and the speed set between 2-8 m/min targeting a final dry film thickness of 500-1000 nm. Following coating the active layer was annealed at 100° C. for 10-15 minutes. The HTL layer was either MoO3 or WO3. Where the HTL was WO3 nanoparticles (WO3 NPs, Nanograde Ltd) it was coated by the blade coating technique, with a thickness of 50 nm. Where the HTL was MoO3, it was deposited by E-beam vacuum deposition from MoO3 pellets at a rate of 1 Å/s, targeting 15 nm thickness. Finally, the top silver electrode was deposited by thermal evaporation through a shadow mask, to achieve Ag thickness between 30-80 nm.
Random polymer 3 and its preparation are disclosed in WO 2011/131280 A1.
The J-V curves were measured using a Keithley 4200 system under light and dark conditions at a bias from +5 to −5 V. The light source was a 580 nm LED with power 0.5 mW/cm2.
The EQE, which is a key device parameter, of OPD devices were characterized between 400 and 1100 nm under −2V bias, using an External Quantum Efficiency (EQE) Measurement System from LOT-QuantumDesign Europe.
Table 3 shows the characteristics of the individual formulations. The polymer used is random polymer 3. The solvent is either o-dichlorobenzene (oDCB) or o-xylene with 0-10% co-solvent (oXyl).
Tables 4, 5 and 6 show the EQE values for the individual OPD devices comprising a photoactive layer with a BHJ formed from the photoactive acceptor/polymer formulations of Table 3.
From Tables 4, 5 and 6 it can be seen that OPD devices can be successfully prepared using a blend of random polymer 3 and small molecular acceptor, as disclosed herein, which is not a fullerene.
| Number | Date | Country | Kind |
|---|---|---|---|
| 16192351 | Oct 2016 | EP | regional |
| 16192352 | Oct 2016 | EP | regional |
| 16196564 | Oct 2016 | EP | regional |
| 16200289 | Nov 2016 | EP | regional |
| 16200807 | Nov 2016 | EP | regional |
| 16202329 | Dec 2016 | EP | regional |
| 17175533 | Jun 2017 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2017/074958 | 10/2/2017 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2018/065356 | 4/12/2018 | WO | A |
| Number | Name | Date | Kind |
|---|---|---|---|
| 10053542 | Mitchell et al. | Aug 2018 | B2 |
| 20110114184 | Brown | May 2011 | A1 |
| 20160141534 | Navarro et al. | May 2016 | A1 |
| 20160155946 | Blouin | Jun 2016 | A1 |
| Number | Date | Country |
|---|---|---|
| 14029453 | Feb 2014 | WO |
| 15004393 | Jan 2015 | WO |
| Entry |
|---|
| Chen et al. (Macromolecules 2011, 44, 8415-8424. |
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| Number | Date | Country | |
|---|---|---|---|
| 20190237672 A1 | Aug 2019 | US |
