Patent Application
20150349277
The present invention relates to metal complexes and to electronic devices, in particular organic electroluminescent devices, comprising these metal complexes.
The structure of organic electroluminescent devices (OLEDs) in which organic semiconductors are employed as functional materials is described, for example, in U.S. Pat. No. 4,539,507, U.S. Pat. No. 5,151,629, EP 0676461 and WO 98/27136. The emitting materials employed here are increasingly organometallic complexes which exhibit phosphorescence instead of fluorescence (M. A. Baldo et al., Appl. Phys. Left. 1999, 75, 4-6). For quantum-mechanical reasons, an up to four-fold increase in the energy and power efficiency is possible using organometallic compounds as phosphorescence emitters. In general, however, there is still a need for improvement in OLEDs which exhibit triplet emission, in particular with respect to efficiency, operating voltage and lifetime.
In accordance with the prior art, the triplet emitters employed in phosphorescent OLEDs are, in particular, iridium complexes, such as, for example, iridium complexes which contain imidazophenanthridine derivatives or diimidazoquinazoline derivatives as ligands (WO 2007/095118). WO 2011/044988 discloses iridium complexes in which the ligand contains at least one carbonyl group. In general, further improvements, in particular with respect to efficiency, operating voltage, lifetime and/or thermal stability of the luminescence, are desirable in phosphorescent emitters.
The object of the present invention is therefore the provision of novel metal complexes which are suitable as emitters for use in OLEDs and at the same time result in improved properties of the OLED, in particular with respect to efficiency, operating voltage and/or lifetime.
Surprisingly, it has been found that certain metal chelate complexes, described in greater detail below, which contain a condensed-on aliphatic five-membered ring in the ligand achieve this object and exhibit improved properties in organic electroluminescent devices. In particular, these metal complexes exhibit improved efficiency and lifetime compared with the analogous metal complexes which do not contain this condensed-on aliphatic five-membered ring. The present invention therefore relates to these metal complexes and to electronic devices, in particular organic electroluminescent devices, which comprise these complexes.
The invention thus relates to a compound of the formula (1),
[Ir(L)n(L′)m] formula (1)
where the compound of the general formula (1) contains a moiety Ir(L)n of the formula (2):
where the following applies to the symbols and indices used:
The indices n and m here are selected so that the coordination number at the iridium corresponds in total to 6. This is dependent, in particular, on how many ligands L are present and whether the ligands L′ are mono- or bidentate ligands.
In the following description, “adjacent groups Y” or “adjacent groups X” means that the groups Y or X respectively are bonded directly to one another in the structure.
Furthermore, “adjacent” in the definition of the radicals means that these radicals are bonded to the same C atom or to C atoms which are bonded directly to one another or, if they are not bonded to directly bonded C atoms, they are bonded in the next-possible position in which a substituent can be bonded. This is explained again with reference to a specific ligand in the following diagrammatic representation of adjacent radicals:
An aryl group in the sense of this invention contains 6 to 40 C atoms; a heteroaryl group in the sense of this invention contains 2 to 40 C atoms and at least one heteroatom, with the proviso that the sum of C atoms and heteroatoms is at least 5. The heteroatoms are preferably selected from N, O and/or S. An aryl group or heteroaryl group here is taken to mean either a simple aromatic ring, i.e. benzene, or a simple heteroaromatic ring, for example pyridine, pyrimidine, thiophene, etc., or a condensed aryl or heteroaryl group, for example naphthalene, anthracene, phenanthrene, quinoline, isoquinoline, etc.
An aromatic ring system in the sense of this invention contains 6 to 60 C atoms in the ring system. A heteroaromatic ring system in the sense of this invention contains 2 to 60 C atoms and at least one heteroatom in the ring system, with the proviso that the sum of C atoms and heteroatoms is at least 5. The heteroatoms are preferably selected from N, O and/or S. An aromatic or heteroaromatic ring system in the sense of this invention is intended to be taken to mean a system which does not necessarily contain only aryl or heteroaryl groups, but instead in which, in addition, a plurality of aryl or heteroaryl groups may be connected by a non-aromatic unit (preferably less than 10% of the atoms other than H), such as, for example, an sp3-hybridised C, N or O atom or a carbonyl group. Thus, for example, systems such as 9,9′-spirobifluorene, 9,9-diarylfluorene, triarylamine, diaryl ether, stilbene, etc., are also intended to be taken to be aromatic ring systems in the sense of this invention, as are systems in which two or more aryl groups are interrupted, for example, by a linear or cyclic alkylene group or by a silylene group.
A cyclic alkyl, alkoxy or thioalkoxy group in the sense of this invention is taken to mean a monocyclic, bicyclic or polycyclic group.
For the purposes of the present invention, a C1- to C40-alkyl group, in which, in addition, individual H atoms or CH2 groups may be substituted by the above-mentioned groups, is taken to mean, for example, the radicals methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, 2-methylbutyl, n-pentyl, s-pentyl, tert-pentyl, 2-pentyl, neopentyl, cyclopentyl, n-hexyl, s-hexyl, tert-hexyl, 2-hexyl, 3-hexyl, cyclohexyl, 2-methylpentyl, neohexyl, n-heptyl, 2-heptyl, 3-heptyl, 4-heptyl, cycloheptyl, 1-methylcyclohexyl, n-octyl, 2-ethylhexyl, cyclooctyl, 1-bicyclo[2.2.2]octyl, 2-bicyclo[2.2.2]octyl, 2-(2,6-dimethyl)octyl, 3-(3,7-dimethyl)octyl, trifluoromethyl, pentafluoroethyl or 2,2,2-trifluoroethyl. An alkenyl group is taken to mean, for example, ethenyl, propenyl, butenyl, pentenyl, cyclopentenyl, hexenyl, cyclohexenyl, heptenyl, cycloheptenyl, octenyl, cyclooctenyl or cyclooctadienyl. An alkynyl group is taken to mean, for example, ethynyl, propynyl, butynyl, pentynyl, hexynyl, heptynyl or octynyl. A C1- to C40-alkoxy group is taken to mean, for example, methoxy, trifluoromethoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, i-butoxy, s-butoxy, t-butoxy or 2-methylbutoxy.
An aromatic or heteroaromatic ring system having 5-60 aromatic ring atoms, which may also in each case be substituted by the above-mentioned radicals R and which may be linked to the aromatic or heteroaromatic ring system via any desired positions, is taken to mean, for example, groups derived from benzene, naphthalene, anthracene, benzanthracene, phenanthrene, benzophenanthrene, pyrene, chrysene, perylene, fluoranthene, benzofluoranthene, naphthacene, pentacene, benzopyrene, biphenyl, biphenylene, terphenyl, terphenylene, fluorene, spirobifluorene, dihydrophenanthrene, dihydropyrene, tetrahydropyrene, cis- or trans-indenofluorene, cis- or trans-monobenzoindenofluorene, cis- or trans-dibenzoindenofluorene, truxene, isotruxene, spirotruxene, spiroisotruxene, furan, benzofuran, isobenzofuran, dibenzofuran, thiophene, benzothiophene, isobenzothiophene, dibenzothiophene, pyrrole, indole, isoindole, carbazole, indolocarbazole, indenocarbazole, pyridine, quinoline, isoquinoline, acridine, phenanthridine, benzo-5,6-quinoline, benzo-6,7-quinoline, benzo-7,8-quinoline, phenothiazine, phenoxazine, pyrazole, indazole, imidazole, benzimidazole, naphthimidazole, phenanthrimidazole, pyridimidazole, pyrazinimidazole, quinoxalinimidazole, oxazole, benzoxazole, naphthoxazole, anthroxazole, phenanthroxazole, isoxazole, 1,2-thiazole, 1,3-thiazole, benzothiazole, pyridazine, benzopyridazine, pyrimidine, benzopyrimidine, quinoxaline, 1,5-diazaanthracene, 2,7-diazapyrene, 2,3-diazapyrene, 1,6-diazapyrene, 1,8-diazapyrene, 4,5-diazapyrene, 4,5,9,10-tetraazaperylene, pyrazine, phenazine, phenoxazine, phenothiazine, fluorubin, naphthyridine, azacarbazole, benzocarboline, phenanthroline, 1,2,3-triazole, 1,2,4-triazole, benzotriazole, 1,2,3-oxadiazole, 1,2,4-oxadiazole, 1,2,5-oxadiazole, 1,3,4-oxadiazole, 1,2,3-thiadiazole, 1,2,4-thiadiazole, 1,2,5-thiadiazole, 1,3,4-thiadiazole, 1,3,5-triazine, 1,2,4-triazine, 1,2,3-triazine, tetrazole, 1,2,4,5-tetrazine, 1,2,3,4-tetrazine, 1,2,3,5-tetrazine, purine, pteridine, indolizine and benzothiadiazole.
The complexes according to the invention can be facial or pseudofacial, or they can be meridional or pseudomeridional.
In a preferred embodiment, the index n=3, i.e. the metal complex is homoleptic, and the index m=0.
In a further preferred embodiment, the index n=2 and m=1, and the complex according to the invention contains two ligands L and one bidentate ligand L′. It is preferred here for the ligand L′ to be a ligand which is coordinated to the iridium via one carbon atom and one nitrogen atom, one carbon atom and one oxygen atom, two oxygen atoms, two nitrogen atoms or one oxygen atom and one nitrogen atom.
In a further preferred embodiment, the index n=1 and m=2, and the complex according to the invention contains one ligand L and two bidentate ligands L′. This is preferred, in particular, if the ligand L′ is an ortho-metallated ligand which is coordinated to the iridium via one carbon atom and one nitrogen atom or one carbon atom and one oxygen atom.
In a further preferred embodiment of the invention, the compounds according to the invention contain a maximum of one group of the formula (3). They are thus preferably compounds of the following formulae (11), (12), (13) or (14),
where Y stands on each occurrence, identically or differently, for CR or N, and the other symbols and indices have the meanings given above.
In a preferred embodiment of the invention, a total of 0, 1 or 2 of the symbols Y and, if present, X in the ligand L stand for N. Particularly preferably, a total of 0 or 1 of the symbols Y and, if present, X in the ligand L stand for N. Especially preferably, the symbols Y in the ring which is coordinated to the iridium via the carbon atom stand, identically or differently on each occurrence, for CR.
Preferred embodiments of the formula (11) are the structures of the following formulae (11-1) to (11-5), preferred embodiments of the formula (12) are the structures of the following formulae (12-1) to (12-8), preferred embodiments of the formula (13) are the structures of the following formulae (13-1) to (13-8), and preferred embodiments of the formula (14) are the structures of the following formulae (14-1) to (14-9),
where the symbols and indices used have the meanings given above.
In a preferred embodiment of the invention, the group Y which is present in the ortho-position to the coordination to the iridium stands for CR. This radical R which is bonded in the ortho-position to the coordination to the iridium is preferably selected from the group consisting of H, D, F and methyl. This applies, in particular, in the case of facial, homoleptic complexes, while in the case of meridional or heteroleptic complexes, other radicals R in this position may also be preferred.
In a further embodiment of the invention, it is preferred, if one of the atoms Y or, if present, X stands for N, for a group R which is not equal to hydrogen or deuterium to be bonded as substituent adjacent to this nitrogen atom.
This substituent R is preferably a group selected from CF3, OCF3, alkyl or alkoxy groups having 1 to 10 C atoms, in particular branched or cyclic alkyl or alkoxy groups having 3 to 10 C atoms, a dialkylamino group having 2 to 10 C atoms, aromatic or heteroaromatic ring systems or aralkyl or heteroaralkyl groups. These groups are bulky groups. Furthermore, this radical R can preferably also form a ring with an adjacent radical R. These are then preferably structures of the formulae (4) to (10), as are present in accordance with the invention in the compounds of the present invention.
If the radical R which is adjacent to a nitrogen atom stands for an alkyl group, this alkyl group then preferably has 3 to 10 C atoms. It is furthermore preferably a secondary or tertiary alkyl group in which the secondary or tertiary C atom is either bonded directly to the ligand or is bonded to the ligand via a CH2 group. This alkyl group is particularly preferably selected from the structures of the following formulae (R-1) to (R-33), where in each case the linking of these groups to the ligand is also drawn in:
where Lig denotes the linking of the alkyl group to the ligand.
If the radical R which is adjacent to a nitrogen atom stands for an alkoxy group, this alkoxy group then preferably has 3 to 10 C atoms. This alkoxy group is preferably selected from the structures of the following formulae (R-34) to (R-47), where in each case the linking of these groups to the ligand is also drawn in:
where Lig denotes the linking of the alkoxy group to the ligand.
If the radical R which is adjacent to a nitrogen atom stands for a dialkylamino group, each of these alkyl groups then preferably has 1 to 8 C atoms, particularly preferably 1 to 6 C atoms. Examples of suitable alkyl groups are methyl, ethyl or the structures shown above as groups (R−1) to (R-33). The dialkylamino group is particularly preferably selected from the structures of the following formulae (R-48) to (R-55), where in each case the linking of these groups to the ligand is also drawn in:
where Lig denotes the linking of the dialkylamino group to the ligand.
If the radical R which is adjacent to a nitrogen atom stands for an aralkyl group, this aralkyl group is then preferably selected from the structures of the following formulae (R-56) to (R-69), where in each case the linking of these groups to the ligand is also drawn in:
where Lig denotes the linking of the aralkyl group to the ligand, and the phenyl groups may in each case be substituted by one or more radicals R1.
If the radical R which is adjacent to a nitrogen atom stands for an aromatic or heteroaromatic ring system, this aromatic or heteroaromatic ring system then preferably has 5 to 30 aromatic ring atoms, particularly preferably 5 to 24 aromatic ring atoms. This aromatic or heteroaromatic ring system furthermore preferably contains no aryl or heteroaryl groups in which more than two aromatic six-membered rings are condensed directly onto one another. The aromatic or heteroaromatic ring system particularly preferably contains no condensed aryl or heteroaryl groups at all, and it very particularly preferably contains only phenyl groups. The aromatic ring system here is preferably selected from the structures of the following formulae (R-70) to (R-88), where in each case the linking of these groups to the ligand is also drawn in:
where Lig denotes the linking of the aromatic ring system to the ligand, and the phenyl groups may in each case be substituted by one or more radicals R1.
Furthermore, the heteroaromatic ring system is preferably selected from the structures of the following formulae (R-89) to (R-119), where in each case the linking of these groups to the ligand is also drawn in:
where Lig denotes the linking of the heteroaromatic ring system to the ligand, and the aromatic and heteroaromatic groups may in each case be substituted by one or more radicals R1.
The characterising feature of the present invention is, as described above, that two adjacent groups Y and/or, if present, two adjacent groups X in the moiety of the formula (2) stand for CR, and the respective radicals R, together with the C atoms, form a ring of one of the formulae (4) to (10).
The groups of the formulae (4) to (10) may be present in any position of the moiety of the formula (2) in which two groups Y or, if present, two groups X are bonded directly to one another. Preferred positions in which a group of the formulae (4) to (10) is present are the moieties of the following formulae (11a) to (14e),
where the symbols and indices used have the meanings given above, and * in each case indicates the position at which the two adjacent groups Y or X stand for CR and the respective radicals R, together with the C atoms, form a ring of one of the formulae (4) to (10).
In the structures of the formulae (4) to (10) depicted above and the further embodiments of these structures mentioned as preferred, a double bond is formally shown between the two carbon atoms. This represents a simplification of the chemical structure if these two carbon atoms are bonded into an aromatic or heteroaromatic system and the bond between these two carbon atoms is thus formally between the bond order of a single bond and that of a double bond. The drawing-in of the formal double bond should thus not be interpreted as limiting for the structure, but instead it is apparent to the person skilled in the art that this is an aromatic bond.
It is essential in the groups of the formulae (4) to (10) that these do not contain any acidic benzylic protons. Benzylic protons are taken to mean protons which are bonded to a carbon atom which is bonded directly to the ligand. The absence of acidic benzylic protons is achieved in the formulae (4) to (6) through A1 and A3, if they stand for C(R3)2, being defined in such a way that R3 is not equal to hydrogen. The absence of acidic benzylic protons is achieved in formulae (7) to (10) through it being a bicyclic structure. Owing to the rigid spatial arrangement, R1, if it stands for H, is significantly less acidic than benzylic protons, since the corresponding anion of the bicyclic structure is not mesomerism-stabilised. Even if R1 in formulae (7) to (10) stands for H, this is therefore a non-acidic proton in the sense of the present application.
In a preferred embodiment of the structure of the formulae (4) to (10), a maximum of one of the groups A1, A2 and A3 stands for a heteroatom, in particular for O or NR3, and the other groups stand for C(R3)2 or C(R1)2, or A1 and A3 stand, identically or differently on each occurrence, for O or NR3 and A2 stands for C(R1)2. In a particularly preferred embodiment of the invention, A1 and A3 stand, identically or differently on each occurrence, for C(R3)2 and A2 stands for C(R1)2 and particularly preferably for C(R3)2 or CH2.
Preferred embodiments of the formula (4) are thus the structures of the formulae (4-A), (4-B), (4-C) and (4-D), and a particularly preferred embodiment of the formula (4-A) are the structures of the formulae (4-E) and (4-F),
where R1 and R3 have the meanings given above, and A1, A2 and A3 stand, identically or differently on each occurrence, for O or NR3.
Preferred embodiments of the formula (5) are the structures of the following formulae (5-A) to (5-F),
where R1 and R3 have the meanings given above, and A1, A2 and A3 stand, identically or differently on each occurrence, for O or NR3.
Preferred embodiments of the formula (6) are the structures of the following formulae (6-A) to (6-E),
where R1 and R3 have the meanings given above, and A1, A2 and A3 stand, identically or differently on each occurrence, for O or NR3.
In a preferred embodiment of the structure of the formula (7), the radicals R1 which are bonded to the bridgehead stand for H, D, F or CH3. A2 furthermore preferably stands for C(R1)2 or 0, and particularly preferably for C(R3)2. Preferred embodiments of the formula (7) are thus the structures of the formulae (7-A) and (7-B), and a particularly preferred embodiment of the formula (7-A) is a structure of the formula (7-C),
where the symbols used have the meanings given above.
In a preferred embodiment of the structure of the formulae (8), (9) and (10), the radicals R1 which are bonded to the bridgehead stand for H, D, F or CH3. A2 furthermore preferably stands for C(R1)2. Preferred embodiments of the formulae (8), (9) and (10) are thus the structures of the formulae (8-A), (9-A) and (10-A),
where the symbols used have the meanings given above.
The group G in the formulae (7), (7-A), (7-B), (7-C), (8), (8-A), (9), (9-A), (10) and (10-A) furthermore preferably stands for a 1,2-ethylene group, which may be substituted by one or more radicals R2, where R2 preferably stands, identically or differently on each occurrence, for H or an alkyl group having 1 to 4 C atoms, or an ortho-arylene group having 6 to 10 C atoms, which may be substituted by one or more radicals R2, but is preferably unsubstituted, in particular an ortho-phenylene group, which may be substituted by one or more radicals R2, but is preferably unsubstituted.
In a further preferred embodiment of the invention, R3 in the groups of the formulae (4) to (10) and in the preferred embodiments stands, identically or differently on each occurrence, for F, a straight-chain alkyl group having 1 to 10 C atoms or a branched or cyclic alkyl group having 3 to 20 C atoms, where in each case one or more non-adjacent CH2 groups may be replaced by R2C═CR2 and one or more H atoms may be replaced by D or F, or an aromatic or heteroaromatic ring system having 5 to 14 aromatic ring atoms, which may in each case be substituted by one or more radicals R2; two radicals R3 here which are bonded to the same carbon atom may form an aliphatic or aromatic ring system with one another and thus form a spiro system; furthermore, R3 may form an aliphatic ring system with an adjacent radical R or R1.
In a particularly preferred embodiment of the invention, R3 in the groups of the formulae (4) to (10) and in the preferred embodiments stands, identically or differently on each occurrence, for F, a straight-chain alkyl group having 1 to 3 C atoms, in particular methyl, or an aromatic or heteroaromatic ring system having 5 to 12 aromatic ring atoms, each of which may be substituted by one or more radicals R2, but is preferably unsubstituted; two radicals R3 here which are bonded to the same carbon atom may form an aliphatic or aromatic ring system with one another and thus form a spiro system; furthermore, R3 may form an aliphatic ring system with an adjacent radical R or R1.
Examples of particularly suitable groups of the formula (4) are the groups (4-1) to (4-69) shown below:
Examples of particularly suitable groups of the formula (5) are the groups (5-1) to (5-14) shown below:
Examples of particularly suitable groups of the formulae (6), (9) and (10) are the groups (6-1), (9-1) and (10-1) shown below:
Examples of particularly suitable groups of the formula (7) are the groups (7-1) to (7-22) shown below:
Examples of particularly suitable groups of the formula (8) are the groups (8-1) to (8-5) shown below:
In particular, the use of condensed-on bicyclic structures of this type may also result in chiral ligands L owing to the chirality of the structures. Both the use of enantiomerically pure ligands and also the use of the racemate may be suitable here. It may also be suitable, in particular, to use not only one enantiomer of a ligand in the metal complex according to the invention, but intentionally both enantiomers, so that, for example, a complex (+L)2(−L)M or a complex (+L)(−L)2M forms, where +L or −L in each case denotes the corresponding+ or − enantiomer of the ligand. This may have advantages with respect to the solubility of the corresponding complex compared with complexes which contain only +L or only −L as ligand.
If further or other radicals R are bonded in the moiety of the formula (2), these radicals R are preferably selected on each occurrence, identically or differently, from the group consisting of H, D, F, N(R1)2, CN, Si(R1)3, C(═O)R1, a straight-chain alkyl group having 1 to 10 C atoms or an alkenyl group having 2 to 10 C atoms or a branched or cyclic alkyl group having 3 to 10 C atoms, each of which may be substituted by one or more radicals R1, where one or more H atoms may be replaced by D or F, or an aromatic or heteroaromatic ring system having 5 to 24 aromatic ring atoms, which may in each case be substituted by one or more radicals R1; two adjacent radicals R or R with R1 here may also form a mono- or polycyclic, aliphatic or aromatic ring system with one another. These radicals R are particularly preferably selected on each occurrence, identically or differently, from the group consisting of H, D, F, a straight-chain alkyl group having 1 to 6 C atoms or a branched or cyclic alkyl group having 3 to 10 C atoms, where one or more H atoms may be replaced by F, or an aromatic or heteroaromatic ring system having 5 to 18 aromatic ring atoms, which may in each case be substituted by one or more radicals R1; two adjacent radicals R or R with R1 here may also form a mono- or polycyclic, aliphatic or aromatic ring system with one another. In the case of an aromatic or heteroaromatic ring system, it is preferred for this to have not more than two aromatic 6-membered rings condensed directly onto one another, in particular absolutely no aromatic 6-membered rings condensed directly onto one another.
Preferred ligands L′, as can occur in compounds of the formula (1), are described below. The ligands L′ are by definition mono- or bidentate ligands. The ligands L′ are preferably neutral, monoanionic, dianionic or trianionic ligands, particularly preferably neutral or monoanionic ligands. Preference is given to bidentate ligands L′.
Preferred neutral, monodentate ligands L′ are selected from carbon monoxide, nitrogen monoxide, alkyl cyanides, such as, for example, acetonitrile, aryl cyanides, such as, for example, benzonitrile, alkyl isocyanides, such as, for example, methyl isonitrile, aryl isocyanides, such as, for example, benzoisonitrile, amines, such as, for example, trimethylamine, triethylamine, morpholine, phosphines, in particular halophosphines, trialkylphosphines, triarylphosphines or alkylarylphosphines, such as, for example, trifluorophosphine, trimethylphosphine, tricyclohexylphosphine, tri-tert-butylphosphine, triphenylphosphine, tris(pentafluorophenyl)phosphine, phosphites, such as, for example, trimethyl phosphite, triethyl phosphite, arsines, such as, for example, trifluoroarsine, trimethylarsine, tricyclohexylarsine, tri-tert-butylarsine, triphenylarsine, tris(pentafluorophenyl)arsine, stibines, such as, for example, trifluorostibine, trimethylstibine, tricyclohexylstibine, tri-tert-butylstibine, triphenylstibine, tris(pentafluorophenyl)stibine, nitrogen-containing heterocycles, such as, for example, pyridine, pyridazine, pyrazine, pyrimidine, triazine, and carbenes, in particular Arduengo carbenes.
Preferred monoanionic, monodentate ligands L′ are selected from hydride, deuteride, the halides F−, Cl−, Br− and I−, alkylacetylides, such as, for example, methyl-C≡C−, tert-butyl-C≡C−, arylacetylides, such as, for example, phenyl-C≡C−, cyanide, cyanate, isocyanate, thiocyanate, isothiocyanate, aliphatic or aromatic alcoholates, such as, for example, methanolate, ethanolate, propanolate, isopropanolate, tert-butylate, phenolate, aliphatic or aromatic thioalcoholates, such as, for example, methanethiolate, ethanethiolate, propanethiolate, isopropanethiolate, tert-thiobutylate, thiophenolate, amides, such as, for example, dimethylamide, diethylamide, diisopropylamide, morpholide, carboxylates, such as, for example, acetate, trifluoroacetate, propionate, benzoate, aryl groups, such as, for example, phenyl, naphthyl, and anionic, nitrogen-containing heterocycles, such as pyrrolide, imidazolide, pyrazolide. The alkyl groups in these groups are preferably C1-C20-alkyl groups, particularly preferably C1-C10-alkyl groups, very particularly preferably C1-C4-alkyl groups. An aryl group is also taken to mean heteroaryl groups. These groups are as defined above.
Preferred di- or trianionic ligands are O2−, S2−, carbides, which result in coordination in the form R—C≡M, and nitrenes, which result in coordination in the form R—N=M, where R generally stands for a substituent, and N.
Preferred neutral or mono- or dianionic, bidentate or polydentate ligands L′ are selected from diamines, such as, for example, ethylenediamine, N,N,N′,N′-tetramethylethylenediamine, propylenediamine, N,N,N′,N′-tetra-methylpropylenediamine, cis- or trans-diaminocyclohexane, cis- or trans-N,N,N′,N′-tetramethyldiaminocyclohexane, imines, such as, for example, 2-[1-(phenylimino)ethyl]pyridine, 2-[1-(2-methylphenylimino)ethyl]pyridine, 2-[1-(2,6-diisopropylphenylimino)ethyl]pyridine, 2-[1-(methylimino)ethyl]-pyridine, 2-[1-(ethylimino)ethyl]pyridine, 2-[1-(isopropylimino)ethyl]pyridine, 2-[1-(tert-butylimino)ethyl]pyridine, diimines, such as, for example, 1,2-bis(methylimino)ethane, 1,2-bis(ethylimino)ethane, 1,2-bis(isopropylimino)ethane, 1,2-bis(tert-butylimino)ethane, 2,3-bis(methylimino)butane, 2,3-bis(ethylimino)butane, 2,3-bis(isopropylimino)butane, 2,3-bis(tert-butylimino)butane, 1,2-bis(phenylimino)ethane, 1,2-bis(2-methylphenylimino)ethane, 1,2-bis(2,6-diisopropylphenylimino)ethane, 1,2-bis(2,6-di-tert-butylphenyl-imino)ethane, 2,3-bis(phenylimino)butane, 2,3-bis(2-methylphenylimino)butane, 2,3-bis(2,6-diisopropylphenylimino)butane, 2,3-bis(2,6-di-tert-butylphenyl-imino)butane, heterocycles containing two nitrogen atoms, such as, for example, 2,2′-bipyridine, o-phenanthroline, diphosphines, such as, for example, bis(diphenylphosphino)methane, bis(diphenylphosphino)ethane, bis(diphenylphosphino)propane, bis(diphenylphosphino)butane, bis(dimethylphosphino)methane, bis(dimethylphosphino)ethane, bis(dimethylphosphino)propane, bis(diethylphosphino)methane, bis(diethylphosphino)ethane, bis(diethylphosphino)propane, bis(di-tert-butylphosphino)methane, bis(di-tert-butylphosphino)ethane, bis(tert-butylphosphino)propane, 1,3-diketonates derived from 1,3-diketones, such as, for example, acetylacetone, benzoylacetone, 1,5-diphenylacetylacetone, dibenzoylmethane, bis(1,1,1-trifluoroacetyl)methane, 2,2,6,6-tetramethyl-3,5-heptanedione, 3-ketonates derived from 3-ketoesters, such as, for example, acetyl acetate, carboxylates derived from aminocarboxylic acids, such as, for example, pyridine-2-carboxylic acid, quinoline-2-carboxylic acid, glycine, N,N-dimethylglycine, alanine, N,N-dimethylaminoalanine, salicyliminates derived from salicylimines, such as, for example, methylsalicylimine, ethylsalicylimine, phenylsalicylimine, dialcoholates derived from dialcohols, such as, for example, ethylene glycol, 1,3-propylene glycol, and dithiolates derived from dithiols, such as, for example, 1,2-ethylenedithiol, 1,3-propylenedithiol.
In a further preferred embodiment of the invention, the ligands L′ are bidentate monoanionic ligands L′ which, with the iridium, form a cyclometallated five- or six-membered ring with at least one iridium-carbon bond, in particular a cyclometallated five-membered ring. These are, in particular, ligands as are generally used in the area of phosphorescent metal complexes for organic electroluminescent devices, i.e. ligands of the type phenylpyridine, naphthylpyridine, phenylquinoline, phenylisoquinoline, etc., each of which may be substituted by one or more radicals R. A multiplicity of ligands of this type is known to the person skilled in the art in the area of phosphorescent electroluminescent devices, and he will be able, without inventive step, to select further ligands of this type as ligand L′ for compounds of the formula (1). The combination of two groups, as represented by the following formulae (15) to (42), where one group is bonded via a neutral atom and the other group is bonded via a negatively charged atom, is generally particularly suitable for this purpose. The neutral atom here is, in particular, a neutral nitrogen atom or a carbene carbon atom and the negatively charged atom is, in particular, a negatively charged carbon atom, a negatively charged nitrogen atom or a negatively charged oxygen atom. The ligand L′ can then be formed from the groups of the formulae (15) to (42) by these groups bonding to one another in each case at the position denoted by #. The position at which the groups coordinate to the metal is denoted by *. Furthermore, two adjacent radicals R which are each bonded to the two groups of the formulae (15) to (42) form an aliphatic or aromatic ring system with one another.
The symbols used here have the same meaning as described above, E stands for O, S or CR2, and preferably a maximum of two symbols X in each group stand for N, particularly preferably a maximum of one symbol X in each group stands for N. Very particularly preferably, all symbols X stand for CR.
In a very particularly preferred embodiment of the invention, the ligand L′ is a monoanionic bidentate ligand formed from two of the groups of the formulae (15) to (42), where one of these groups is coordinated to the iridium via a negatively charged carbon atom and the other of these groups is coordinated to the iridium via a neutral nitrogen atom.
It may likewise be preferred for two adjacent symbols X in these ligands to stand for a group of one of the above-mentioned formulae (4) to (10).
The further preferred radicals R in the structures shown above are defined like the radicals R of the ligand L.
The ligands L and L′ may also be chiral, depending on the structure. This is the case, in particular, if they contain a bicyclic group of the formulae (7) to (10) or if they contain substituents, for example alkyl, alkoxy, dialkylamino or aralkyl groups, which have one or more stereocentres. Since the basic structure of the complex may also be a chiral structure, the formation of diastereomers and a plurality of enantiomer pairs is possible. The complexes according to the invention then encompass both the mixtures of the various diastereomers or the corresponding racemates and also the individual isolated diastereomers or enantiomers.
The compounds according to the invention may also be rendered soluble by suitable substitution, for example by relatively long alkyl groups (about 4 to 20 C atoms), in particular branched alkyl groups, or optionally substituted aryl groups, for example xylyl, mesityl or branched terphenyl or quaterphenyl groups. Compounds of this type are then soluble in adequate concentration in common organic solvents at room temperature in order to enable the complexes to be processed from solution, for example by printing processes.
The preferred embodiments mentioned above can be combined with one another as desired. In a particularly preferred embodiment of the invention, the preferred embodiments mentioned above apply simultaneously.
The compounds can also be employed as chiral, enantiomerically pure complexes which are able to emit circular-polarised light. This may have advantages, since the polarising filter on the device can thus be omitted. In addition, complexes of this type are also suitable for use in security labels, since, besides the emission, they also have the polarisation of the light as an easily readable feature.
The present invention furthermore relates to oligomers, polymers and dendrimers containing at least one compound according to the invention, where the compound, instead of one or more radicals, has a bond to the oligomer, polymer or dendrimer.
The metal complexes according to the invention can in principle be prepared by various processes. However, the processes described below have proven particularly suitable.
The present invention therefore furthermore relates to a process for the preparation of the compounds of the formula (1) according to the invention by reaction of the corresponding free ligands with iridium alkoxides of the formula (43), with iridium ketoketonates of the formula (44), with iridium halides of the formula (45) or with dimeric iridium complexes of the formula (46) or (47),
where the symbols and indices L′, m, n and R1 have the meanings indicated above, and Hal=F, Cl, Br or I.
It is likewise possible to use iridium compounds which carry both alkoxide and/or halide and/or hydroxyl and also ketoketonate radicals. These compounds may also be charged. Corresponding iridium compounds which are particularly suitable as starting materials are disclosed in WO 2004/085449. [IrCl2(acac)2]−, for example Na[IrCl2(acac)2], is particularly suitable. Further particularly suitable iridium starting materials are iridium(III) tris(acetylacetonate) and iridium(III) tris(2,2,6,6-tetramethyl-3,5-heptane-dionate).
The synthesis can also be carried out by reaction of the ligands L with iridium complexes of the formula [Ir(L′)2(HOMe)2]A or [Ir(L′)2(NCMe)2]A or by reaction of the ligands L′ with iridium complexes of the formula [Ir(L)2(HOMe)2]A or [Ir(L)2(NCMe)2]A, where A in each case represents a non-coordinating anion, such as, for example, triflate, tetrafluoroborate, hexafluorophosphate, etc., in dipolar protic solvents, such as, for example, ethylene glycol, propylene glycol, glycerol, diethylene glycol, triethylene glycol, etc.
The synthesis of the complexes is preferably carried out as described in WO 2002/060910 and in WO 2004/085449. Heteroleptic complexes can also be synthesised, for example, in accordance with WO 05/042548. The synthesis here can also be activated, for example, thermally, photochemically and/or by microwave radiation. Furthermore, the synthesis can also be carried out in an autoclave at elevated pressure and/or elevated temperature.
The reactions can be carried out without addition of solvents or melting aids in a melt of the corresponding ligands to be o-metallated. Solvents or melting aids can be added if necessary. Suitable solvents are protic or aprotic solvents, such as aliphatic and/or aromatic alcohols (methanol, ethanol, isopropanol, t-butanol, etc.), oligo- and polyalcohols (ethylene glycol, 1,2-propanediol, glycerol, etc.), alcohol ethers (ethoxyethanol, diethylene glycol, triethylene glycol, polyethylene glycol, etc.), ethers (di- and triethylene glycol dimethyl ether, diphenyl ether, etc.), aromatic, heteroaromatic and/or aliphatic hydrocarbons (toluene, xylene, mesitylene, chlorobenzene, pyridine, lutidine, quinoline, isoquinoline, tridecane, hexadecane, etc.), amides (DMF, DMAC, etc.), lactams (NMP), sulfoxides (DMSO) or sulfones (dimethyl sulfone, sulfolane, etc.). Suitable melting aids are compounds which are in solid form at room temperature, but melt on warming of the reaction mixture and dissolve the reactants, so that a homogeneous melt forms. Biphenyl, m-terphenyl, triphenylene, 1,2-, 1,3-, 1,4-bisphenoxybenzene, triphenylphosphine oxide, 18-crown-6, phenol, 1-naphthol, hydroquinone, etc., are particularly suitable.
For the processing of the compounds according to the invention from the liquid phase, for example by spin coating or by printing processes, formulations of the compounds according to the invention are necessary. These formulations can be, for example, solutions, dispersions or emulsions. It may be preferred to use mixtures of two or more solvents for this purpose. Suitable and preferred solvents are, for example, toluene, anisole, o-, m- or p-xylene, methyl benzoate, mesitylene, tetralin, veratrol, THF, methyl-THF, THP, chlorobenzene, dioxane, phenoxytoluene, in particular 3-phenoxytoluene, (−)-fenchone, 1,2,3,5-tetramethylbenzene, 1,2,4,5-tetramethylbenzene, 1-methylnaphthalene, 2-methylbenzothiazole, 2-phenoxyethanol, 2-pyrrolidinone, 3-methylanisole, 4-methylanisole, 3,4-dimethylanisole, 3,5-dimethylanisole, acetophenone, α-terpineol, benzothiazole, butyl benzoate, cumene, cyclohexanol, cyclohexanone, cyclohexylbenzene, decalin, dodecylbenzene, ethyl benzoate, indane, methyl benzoate, NMP, p-cymene, phenetole, 1,4-diisopropylbenzene, dibenzyl ether, diethylene glycol butyl methyl ether, triethylene glycol butyl methyl ether, diethylene glycol dibutyl ether, triethylene glycol dimethyl ether, diethylene glycol monobutyl ether, tripropylene glycol dimethyl ether, tetraethylene glycol dimethyl ether, 2-isopropylnaphthalene, pentylbenzene, hexylbenzene, heptylbenzene, octylbenzene, 1,1-bis(3,4-dimethylphenyl)ethane or mixtures of these solvents.
The present invention therefore furthermore relates to a formulation comprising a compound according to the invention and at least one further compound. The further compound may be, for example, a solvent, in particular one of the above-mentioned solvents or a mixture of these solvents. However, the further compound may also be a further organic or inorganic compound which is likewise employed in the electronic device, for example a matrix material. This further compound may also be polymeric.
The complexes of the formula (1) described above or the preferred embodiments indicated above can be used as active component in an electronic device. The present invention therefore furthermore relates to the use of a compound of the formula (1) or according to one of the preferred embodiments in an electronic device. The compounds according to the invention can furthermore be employed for the generation of singlet oxygen, in photocatalysis or in oxygen sensors.
The present invention still furthermore relates to an electronic device comprising at least one compound of the formula (1) or according to one of the preferred embodiments.
An electronic device is taken to mean a device which comprises an anode, a cathode and at least one layer, where this layer comprises at least one organic or organometallic compound. The electronic device according to the invention thus comprises an anode, a cathode and at least one layer which comprises at least one compound of the formula (1) given above. Preferred electronic devices here are selected from the group consisting of organic electroluminescent devices (OLEDs, PLEDs), organic integrated circuits (O-ICs), organic field-effect transistors (O-FETs), organic thin-film transistors (O-TFTs), organic light-emitting transistors (O-LETs), organic solar cells (O-SCs), organic optical detectors, organic photoreceptors, organic field-quench devices (O-FQDs), light-emitting electrochemical cells (LECs) or organic laser diodes (O-lasers), comprising at least one compound of the formula (1) given above in at least one layer. Particular preference is given to organic electroluminescent devices. Active components are generally the organic or inorganic materials which have been introduced between the anode and cathode, for example charge-injection, charge-transport or charge-blocking materials, but in particular emission materials and matrix materials. The compounds according to the invention exhibit particularly good properties as emission material in organic electroluminescent devices. A preferred embodiment of the invention is therefore organic electroluminescent devices.
The organic electroluminescent device comprises a cathode, an anode and at least one emitting layer. Apart from these layers, it may also comprise further layers, for example in each case one or more hole-injection layers, hole-transport layers, hole-blocking layers, electron-transport layers, electron-injection layers, exciton-blocking layers, electron-blocking layers, charge-generation layers and/or organic or inorganic p/n junctions. Interlayers, which have, for example, an exciton-blocking function and/or control the charge balance in the electroluminescent device, may likewise be introduced between two emitting layers. However, it should be pointed out that each of these layers does not necessarily have to be present.
The organic electroluminescent device here may comprise one emitting layer or a plurality of emitting layers. If a plurality of emission layers are present, these preferably have in total a plurality of emission maxima between 380 nm and 750 nm, resulting overall in white emission, i.e. various emitting compounds which are able to fluoresce or phosphoresce are used in the emitting layers. A preferred embodiment is three-layer systems, where the three layers exhibit blue, green and orange or red emission (see, for example, WO 2005/011013), or systems which have more than three emitting layers. A further preferred embodiment is two-layer systems, where the two layers exhibit either blue and yellow or cyan and orange emission. Two-layer systems are of particular interest for lighting applications. Embodiments of this type with the compounds according to the invention are particularly suitable, since they frequently exhibit yellow or orange emission. The white-emitting electroluminescent devices can be employed for lighting applications or as backlight for displays or with colour filters as displays.
In a preferred embodiment of the invention, the organic electroluminescent device comprises the compound of the formula (1) or the preferred embodiments indicated above as emitting compound in one or more emitting layers.
If the compound of the formula (1) is employed as emitting compound in an emitting layer, it is preferably employed in combination with one or more matrix materials. The mixture comprising the compound of the formula (1) and the matrix material comprises between 1 and 99% by vol., preferably between 2 and 90% by vol., particularly preferably between 3 and 40% by vol., especially between 5 and 15% by vol., of the compound of the formula (1), based on the entire mixture comprising emitter and matrix material. Correspondingly, the mixture comprises between 99 and 1% by vol., preferably between 98 and 10% by vol., particularly preferably between 97 and 60% by vol., in particular between 95 and 85% by vol., of the matrix material or matrix materials, based on the entire mixture comprising emitter and matrix material.
The matrix material employed can in general be all materials which are known for this purpose in accordance with the prior art. The triplet level of the matrix material is preferably higher than the triplet level of the emitter.
Suitable matrix materials for the compounds according to the invention are ketones, phosphine oxides, sulfoxides and sulfones, for example in accordance with WO 2004/013080, WO 2004/093207, WO 2006/005627 or WO 2010/006680, triarylamines, carbazole derivatives, for example CBP (N,N-biscarbazolylbiphenyl), m-CBP or the carbazole derivatives disclosed in WO 2005/039246, US 2005/0069729, JP 2004/288381, EP 1205527, WO 2008/086851 or US 2009/0134784, indolocarbazole derivatives, for example in accordance with WO 2007/063754 or WO 2008/056746, indenocarbazole derivatives, for example in accordance with WO 2010/136109 or WO 2011/000455, azacarbazoles, for example in accordance with EP 1617710, EP 1617711, EP 1731584, JP 2005/347160, bipolar matrix materials, for example in accordance with WO 2007/137725, silanes, for example in accordance with WO 2005/111172, azaboroles or boronic esters, for example in accordance with WO 2006/117052, diazasilole derivatives, for example in accordance with WO 2010/054729, diazaphosphole derivatives, for example in accordance with WO 2010/054730, triazine derivatives, for example in accordance with WO 2010/015306, WO 2007/063754 or WO 2008/056746, zinc complexes, for example in accordance with EP 652273 or WO 2009/062578, beryllium complexes, dibenzofuran derivatives, for example in accordance with WO 2009/148015, or bridged carbazole derivatives, for example in accordance with US 2009/0136779, WO 2010/050778, WO 2011/042107 or WO 2011/088877.
It may also be preferred to employ a plurality of different matrix materials as a mixture. Suitable for this purpose are, in particular, mixtures of at least one electron-transporting matrix material and at least one hole-transporting matrix material or mixtures of at least two electron-transporting matrix materials or mixtures of at least one hole- or electron-transporting matrix material and at least one further material having a large band gap, which is thus substantially electrically inert and does not participate or does not participate to a significant extent in charge transport, as described, for example, in WO 2010/108579. A preferred combination is, for example, the use of an aromatic ketone or a triazine derivative with a triarylamine derivative or a carbazole derivative as mixed matrix for the metal complex according to the invention.
It is furthermore preferred to employ a mixture of two or more triplet emitters together with a matrix. The triplet emitter having the shorter-wave emission spectrum serves as co-matrix for the triplet-emitter having the longer-wave emission spectrum. Thus, for example, blue- or green-emitting triplet emitters can be employed as co-matrix for the complexes of the formula (1) according to the invention.
The cathode preferably comprises metals having a low work function, metal alloys or multilayered structures comprising various metals, such as, for example, alkaline-earth metals, alkali metals, main-group metals or lanthanoids (for example Ca, Ba, Mg, Al, In, Mg, Yb, Sm, etc.). Also suitable are alloys comprising an alkali metal or alkaline-earth metal and silver, for example an alloy comprising magnesium and silver. In the case of multilayered structures, further metals which have a relatively high work function, such as, for example, Ag, may also be used in addition to the said metals, in which case combinations of the metals, such as, for example, Ca/Ag or Ba/Ag, are generally used. It may also be preferred to introduce a thin interlayer of a material having a high dielectric constant between a metallic cathode and the organic semiconductor. Suitable for this purpose are, for example, alkali metal or alkaline-earth metal fluorides, but also the corresponding oxides or carbonates (for example LiF, Li2O, BaF2, MgO, NaF, CsF, Cs2CO3, etc.). The layer thickness of this layer is preferably between 0.5 and 5 nm.
The anode preferably comprises materials having a high work function. The anode preferably has a work function of greater than 4.5 eV vs. vacuum. Suitable for this purpose are on the one hand metals having a high redox potential, such as, for example, Ag, Pt or Au. On the other hand, metal/metal oxide electrodes (for example Al/Ni/NiOx, Al/PtOx) may also be preferred. For some applications, at least one of the electrodes must be transparent or partially transparent in order either to facilitate irradiation of the organic material (O-SCs) or the coupling-out of light (OLEDs/PLEDs, O-LASERs). A preferred structure uses a transparent anode. Preferred anode materials here are conductive mixed metal oxides. Particular preference is given to indium tin oxide (ITO) or indium zinc oxide (IZO). Preference is furthermore given to conductive, doped organic materials, in particular conductive doped polymers.
All materials as are used in accordance with the prior art for the layers can generally be used in the further layers, and the person skilled in the art will be able to combine each of these materials with the materials according to the invention in an electronic device without inventive step.
The device is correspondingly structured (depending on the application), provided with contacts and finally hermetically sealed, since the lifetime of such devices is drastically shortened in the presence of water and/or air.
Preference is furthermore given to an organic electroluminescent device, characterised in that one or more layers are coated by means of a sublimation process, in which the materials are vapour-deposited in vacuum sublimation units at an initial pressure of usually less than 10 mbar, preferably less than 10−6 mbar. It is also possible for the initial pressure to be even lower, for example less than 10−7 mbar.
Preference is likewise given to an organic electroluminescent device, characterised in that one or more layers are coated by means of the OVPD (organic vapour phase deposition) process or with the aid of carrier-gas sublimation, in which the materials are applied at a pressure of between 10−5 mbar and 1 bar. A special case of this process is the OVJP (organic vapour jet printing) process, in which the materials are applied directly through a nozzle and thus structured (for example M. S. Arnold et al., Appl. Phys. Lett. 2008, 92, 053301).
Preference is furthermore given to an organic electroluminescent device, characterised in that one or more layers are produced from solution, such as, for example, by spin coating, or by means of any desired printing process, such as, for example, screen printing, flexographic printing or offset printing, but particularly preferably LITI (light induced thermal imaging, thermal transfer printing) or ink-jet printing. Soluble compounds are necessary for this purpose, which are obtained, for example, through suitable substitution.
The organic electroluminescent device may also be produced as a hybrid system by applying one or more layers from solution and applying one or more other layers by vapour deposition. Thus, for example, it is possible to apply an emitting layer comprising a compound of the formula (1) and a matrix material from solution and to apply a hole-blocking layer and/or an electron-transport layer on top by vacuum vapour deposition.
These processes are generally known to the person skilled in the art and can be applied by him without problems to organic electroluminescent devices comprising compounds of the formula (1) or the preferred embodiments indicated above.
The electronic devices according to the invention, in particular organic electroluminescent devices, are distinguished by the following surprising advantages over the prior art:
These advantages mentioned above are not accompanied by an impairment of the other electronic properties.
The invention is explained in greater detail by the following examples, without wishing to restrict it thereby. The person skilled in the art will be able to use the descriptions to synthesise further compounds according to the invention without inventive step and use them in electronic devices and will thus be able to carry out the invention throughout the range disclosed.
The following syntheses are carried out, unless indicated otherwise, in dried solvents under a protective-gas atmosphere. The metal complexes are additionally handled with exclusion of light or under yellow light. The solvents and reagents can be purchased, for example, from Sigma-ALDRICH or ABCR. The respective numbers in square brackets or the numbers indicated for individual compounds relate to the CAS numbers of the compounds known from the literature.
A mixture of 18.0 g (100 mmol) of 5-chloro-2,6-naphthyridin-1-ylamine [1392428-85-1], 15.3 g (150 mmol) of isobutylboronic acid [84110-40-7], 46.1 g (200 mmol) of tripotassium phosphate monohydrate, 2.5 g (6 mmol) of S-Phos, 674 mg (3 mmol) of palladium(II)acetate, 100 g of glass beads (diameter 3 mm), 400 ml of toluene and 6 ml of water is heated under reflux for 24 h. After cooling, the reaction mixture is washed three times with 200 ml of water each time, once with 200 ml of saturated sodium chloride solution, dried over sodium sulfate, and the solvent is then removed in vacuo. Recrystallisation three times from cyclohexane. Yield 14.9 g (74 mmol), 74%. Purity about 98.0% according to 1H-NMR.
The following compounds can be prepared analogously.
701261-35-0
98-80-6
Procedure in accordance with J. Langer et al., Synthesis, 2006, 16, 2697. A mixture of 3.4 g (10 mmol) of [benzoato-κC2,κO1](2,2″-bipyridine-κN1,κN1′)nickel(II) [76262-92-5] and 2.3 g (10 mmol) of (1R,3S,4S)-3-bromo-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one [10293-06-8] in 150 ml of THF is stirred at 50° C. for 30 h until a green suspension has formed. The THF is removed in vacuo, the residue is stirred for 1 h with 200 ml of 2 N hydrochloric acid and then extracted five times with 100 ml of dichloromethane each time. The combined organic phases are washed by shaking five times with 200 ml of saturated sodium carbonate solution each time. The combined aqueous phases are acidified using conc. hydrochloric acid and then extracted five times with 100 ml of dichloromethane each time. After drying over magnesium sulfate, the combined organic phases are freed from solvent, 100 ml of acetic anhydride are added to the residue, and the mixture is heated under reflux for 2 h. After removal of the acetic anhydride in vacuo, the residue is recrystallised once from acetone/n-heptane. Yield 1.8 g (7.1 mmol), 71%. Purity about 98.0% according to 1H-NMR.
The following compounds can be prepared analogously.
(1S,3R,4S)- 64474-54-0
(1R,3R,4S)- 1073-25-2
A) A total of five portions of 32 mmol of dicyclohexylcarbodiimide each are added every 2 h to a vigorously stirred mixture of 100 mmol of 1-aminoisoquinoline, 120 mmol of the ketocarboxylic acid, 5 mmol of 4-dimethylaminopyridine and 300 ml of dichloromethane at room temperature, and the mixture is then stirred for a further 16 h. The precipitated dicyclohexylurea is filtered off, rinsed with a little dichloromethane, the reaction mixture is evaporated to about 100 ml and chromatographed on silica gel with dichloromethane, where firstly by-products are eluted and the product is then eluted by changing over to ethyl acetate. The crude product obtained in this way as an oil is reacted further in B).
Procedure analogous to J. Heterocycl. Chem., 2004, 41, 2, 187. A mixture of 100 mmol of the carboxamide from A), 10 g of polyphosphoric acid and 45 ml of phosphoryl chloride is stirred at 100° C. for 60 h in an autoclave. After cooling, the reaction mixture is added to 500 ml of ice-water (note: exothermic!), adjusted to pH 8 using 10% by weight NaOH and extracted five times with 100 ml of dichloromethane each time. The combined dichloromethane extracts are washed once with 100 ml of water and once with 100 ml of saturated sodium chloride solution and then dried over magnesium sulfate. After evaporation, the residue is chromatographed on silica gel or recrystallised. The products obtained in this way are freed from low-boiling components and non-volatile secondary components by heating in a high vacuum or by fractional bulb-tube distillation or sublimation.
50 ml (100 mmol) of a solution of lithium diisopropylamide (2.0 M in THF, ether, benzene) are added dropwise to a solution, cooled to −78° C., of 100 mmol of the carboxamide from A) in 500 ml of THF, and the mixture is stirred for 15 min. A solution of 100 mmol of 1,1,1-trifluoro-N-phenyl-N-[(trifluoromethyl)sulfonyl]methanesulfonamide [37595-74-7] in 100 ml of THF is then added dropwise, the mixture is allowed to warm to 0° C. over the course of 1 h, the reaction mixture is re-cooled to −78° C., and 50 ml (100 mmol) of a solution of lithium diisopropylamide (2.0 M in THF, ether, benzene) are added dropwise. After removal of the cooling bath and warming to room temperature, the mixture is stirred at room temperature for a further 16 h, then quenched by addition of 15 ml of methanol, the solvent is removed in vacuo, the residue is taken up in 300 ml of ethyl acetate, washed three times with 200 ml of water each time, once with 200 ml of saturated sodium chloride solution and dried over magnesium sulfate. After evaporation, the residue is chromatographed on silica gel. The products obtained in this way are freed from low-boiling components and non-volatile secondary components by heating in a high vacuum or by fractional bulb-tube distillation or sublimation.
A) Use of 14.4 g (100 mmol) of 1-aminoisoquinoline [1532-84-9], 25.5 g (130 mmol) of (1R,2S,4R)-4,7,7-trimethyl-3-oxobicyclo[2.2.1]heptane-2-carboxylic acid [18530-30-8], 611 mg (5 mmol) of 4-dimethylaminopyridine [1122-58-3], 33.0 g (160 mmol) of dicyclohexylcarbodiimide [538-75-0]. Chromatography on silica gel (dichloromethane/ethyl acetate 10:1, vv). Yield: 24.2 g (75 mmol), 75%. Purity about 95% according to 1H-NMR. Mixture of the endo/exo and enol form.
24.2 g (75 mmol) of the carboxamide from A), 7.6 g of polyphosphoric acid, 35.0 ml of phosphoryl chloride. Chromatography on silica gel (elution with ethyl acetate, then changeover to ethyl acetate/methanol 1:1, vv). Alternatively, recrystallisation from ethanol. Fractional sublimation (p about 10−5 mbar, T=210° C.). Yield: 15.5 g (51 mmol), 68%. Purity about 99.5% according to 1H-NMR.
The following compounds can be prepared analogously.
1532-84-9
(1S,2R,4S)- 18530-29-5
(1R,2S,4S)- 59161-64-7
(1R,2S,4R)- 63984-45-2
60585-42-4
59161-63-6
102593-64-6
prepared from [95760- 70-6] by hydrolysis using PLE*
prepared from [61363- 31-3] by hydrolysis using PLE*
1238291-27-4
(1R,2S,4R)- 18530-30-8
1238291-28-5
(1R,2S,4R)- 63984-45-2
855829-20-8
60585-42-4
60585-42-4
946147-28-0
102593-64-6
59161-63-6
55270-26-3
(1R,2S,4R)- 18530-30-8
42398-74-3
(1R,2S,4R)- 18530-30-8
58814-44-1
(1R,2S,4R)- 18530-30-8
69300-78-3
(1R,2S,4R)- 18530-30-8
87895-17-8
59161-63-6
42398-74-3
60585-42-4
58814-44-1
59161-63-6
1238291-27-4
60585-42-4
A) A total of five portions of 32 mmol of dicyclohexylcarbodiimide each are added every 2 h to a vigorously stirred mixture of 100 mmol of 1,6-naphthyridin-5-ylamine, 120 mmol of the ketocarboxylic acid, 5 mmol of 4-dimethylaminopyridine and 300 ml of dichloromethane at room temperature, and the mixture is then stirred for a further 16 h. The precipitated dicyclohexylurea is filtered off, rinsed with a little dichloromethane, the reaction mixture is evaporated to about 100 ml and chromatographed on silica gel with dichloromethane, where firstly by-products are eluted and the product is then eluted by changing over to ethyl acetate. The crude product obtained in this way as an oil is reacted further in B).
Procedure analogous to J. Heterocycl. Chem., 2004, 41, 2, 187.
A mixture of 100 mmol of the carboxamide from A), 10 g of polyphosphoric acid and 45 ml of phosphoryl chloride is stirred at 100° C. for 60 h in an autoclave. After cooling, the reaction mixture is added to 500 ml of ice-water (note: exothermic!), adjusted to pH 8 using 10% by weight NaOH and extracted five times with 100 ml of dichloromethane each time. The combined dichloromethane extracts are washed once with 100 ml of water and once with 100 ml of saturated sodium chloride solution and then dried over magnesium sulfate. After evaporation, the residue is chromatographed on silica gel. The products obtained in this way are freed from low-boiling components and non-volatile secondary components by heating in a high vacuum or by fractional bulb-tube distillation or sublimation.
50 ml (100 mmol) of a solution of lithium diisopropylamide (2.0 M in THF, ether, benzene) are added dropwise to a solution, cooled to −78° C., of 100 mmol of the carboxamide from A) in 500 ml of THF, and the mixture is stirred for 15 min. A solution of 100 mmol of 1,1,1-trifluoro-N-phenyl-N-[(trifluoromethyl)sulfonyl]methanesulfonamide [37595-74-7] in 100 ml of THF is then added dropwise, the mixture is allowed to warm to 0° C. over the course of 1 h, the reaction mixture is re-cooled to −78° C., and 50 ml (100 mmol) of a solution of lithium diisopropylamide (2.0 M in THF, ether, benzene) are added dropwise. After removal of the cooling bath and warming to room temperature, the mixture is stirred at room temperature for a further 16 h, then quenched by addition of 15 ml of methanol, the solvent is removed in vacuo, the residue is taken up in 300 ml of ethyl acetate, washed three times with 200 ml of water each time, once with 200 ml of saturated sodium chloride solution and dried over magnesium sulfate. After evaporation, the residue is chromatographed on silica gel. The products obtained in this way are freed from low-boiling components and non-volatile secondary components by heating in a high vacuum or by fractional bulb-tube distillation or sublimation.
A) Use of 20.1 g (100 mmol) of 2-tert-butyl-1,6-naphthyridin-5-ylamine [1352329-32-8], 25.5 g (130 mmol) of (1R,2S,4R)-4,7,7-trimethyl-3-oxobicyclo[2.2.1]heptane-2-carboxylic acid [18530-30-8], 611 mg (5 mmol) of 4-dimethylaminopyridine [1122-58-3], 33.0 g (160 mmol) of dicyclohexylcarbodiimide [538-75-0]. Chromatography on silica gel (dichloromethane/ethyl acetate 10:1, w). Yield: 29.6 g (78 mmol), 78%. Purity about 95% according to 1H-NMR. Mixture of the endo/exo and enol form.
B) 29.6 g (78 mmol) of the carboxamide from A), 7.8 g of polyphosphoric acid, 35.1 ml of phosphoryl chloride. Chromatography on silica gel (elution with ethyl acetate, then changeover to ethyl acetate/methanol 1:1, vv). Alternatively, recrystallisation from ethanol. Fractional sublimation (p about 10−5 mbar, T=210° C.). Yield: 16.3 g (45 mmol), 58%. Purity about 99.5% according to 1H-NMR.
The following compounds can be prepared analogously.
(1S,2R,4S)- 18530-29-5
(1R,2S,4S)- 59161-64-7
63984-45-2
60585-42-4
59161-63-6
102593-64-6
Prepared from 95760-70-6 by hydrolysis using PLE*
Prepared from 61363- 31-3 by hydrolysis using PLE*
1351516-72-7
60585-42-4
1352329-33-9
(1R,2S,4R)- 18530-30-8
100 ml of a solution of lithium diisopropylamide (2.0 M in THF, ether, benzene) are added dropwise to a solution, cooled to −78° C., of 100 mmol of the ketone, and the mixture is stirred for 15 min. A solution of 100 mmol of 2-fluoro-3-cyanopyridine in 100 ml of THF is then added dropwise. After removal of the cooling bath and warming to room temperature, the mixture is stirred at room temperature for a further 3 h. After the THF has been stripped off in vacuo, the residue is taken up in 200 ml of ethylene glycol, 110 mmol of the β-amino ester hydrochloride are added, and the mixture is heated at 180° C. on a water separator for 6 h. The mixture is subsequently allowed to cool to 60° C., stirred in air for a further 2 h, poured into 1000 ml of water, adjusted to pH 9 using ammonium hydroxide and extracted five times with 200 ml of dichloromethane each time. The combined organic phases are washed three times with 200 ml of water each time and once with 200 ml of saturated sodium chloride solution and dried over magnesium sulfate. After evaporation, the residue is chromatographed on silica gel. The products obtained in this way are freed from low-boiling components and non-volatile secondary components by heating in a high vacuum or by fractional bulb-tube distillation or sublimation.
Use of 12.2 g (100 mmol) of 2-fluoro-3-cyanopyridine [3939-13-7], 15.2 g (100 mmol) of (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-one, 15.4 g (110 mmol) of β-alanine methyl ester hydrochloride [3196-73-4]. Chromatography on silica gel (dichloromethane/methanol 6:1, vv). Fractional sublimation (p about 10−5 mbar, T=200° C.). Yield: 7.0 g (23 mmol), 23%. Purity about 99% according to 1H-NMR.
The following compounds can be prepared analogously.
(1S,4R)- 2630-41-3
58564-88-8
4694-11-5
15189-14-7
24669-65-5
A mixture of 10 mmol of the isochromen-1-one and 11 mmol of the β-aminopropanamide in 20 ml of NMP is heated at 150° C. on a water separator for 60 h. After removal of the solvent in vacuo, the residue is taken up in 10 g of polyphosphoric acid, the mixture is homogenised and then heated at 220° C. for 1 h in air with stirring. After cooling, the residue is dissolved in 200 ml of water, rendered alkaline using solid NaOH and extracted three times with 100 ml of dichloromethane each time. The combined organic phases are washed once with 200 ml of water and once with 100 ml of saturated sodium chloride solution and dried over magnesium sulfate. The residue obtained after removal of the solvent is chromatographed on silica gel with ethyl acetate/n-heptane (1:1, w). The products obtained in this way are freed from low-boiling components and non-volatile secondary components by heating in a high vacuum or by fractional bulb-tube distillation or sublimation.
Use of 2.5 g (10 mmol) of S4, 969 mg (11 mmol) of 3-aminopropanamide [4726-85-6]. Fractional sublimation (p about 10−5 mbar, T=200° C.). Yield: 1.6 g (5.3 mmol), 53%. Purity about 99.5% according to 1H-NMR.
The following compounds can be prepared analogously.
S5
S6
S7
S7
3440-38-8
S8
S9
S10
Preparation analogous to 2a), using 2,6-naphthyridin-1-ylamines instead of 1,6-naphthyridin-5-ylamines.
A) Use of 20.1 g (100 mmol) of 5-isobutyl-2,6-naphthyridin-1-ylamine S1, 25.5 g (130 mmol) of (1R,2S,4R)-4,7,7-trimethyl-3-oxobicyclo[2.2.1]-heptane-2-carboxylic acid [18530-30-8], 611 mg (5 mmol) of 4-dimethylaminopyridine, 33.0 g (160 mmol) of dicyclohexylcarbodiimide. Chromatography on silica gel (dichloromethane/ethyl acetate 10:1, vv). Yield: 30.4 g (80 mmol), 80%. Purity about 95% according to 1H-NMR. Mixture of the endo/exo and enol form.
B) Variant A:
30.4 g (80 mmol) of the carboxamide from A), 7.8 g of polyphosphoric acid, 35.1 ml of phosphoryl chloride. Chromatography on silica gel (elution with ethyl acetate, then changeover to ethyl acetate/methanol 1:1, vv). Fractional sublimation (p about 10−5 mbar, T=200° C.). Yield: 14.9 g (41 mmol), 51%. Purity about 99.5% according to 1H-NMR.
The following compounds can be prepared analogously.
S1
(1R,2S,4S)- 59161-64-7
S2
(1R,2S,4R)- 63984-45-2
S2
60585-42-4
S3
59161-63-6
C: Synthesis of the Metal Complexes
1) Homoleptic Tris-Facial Iridium Complexes
A mixture of 10 mmol of trisacetylacetonatoiridium(III) [15635-87-7], 40 mmol of the ligand L, optionally 1-10 g, typically 3 g, of an inert high-boiling additive as melting aid or solvent, for example hexadecane, m-terphenyl, triphenylene, bisphenyl ether, 3-phenoxytoluene, 1,2-, 1,3-, 1,4-bisphenoxybenzene, triphenylphosphine oxide, sulfolane, 18-crown-6, triethylene glycol, glycerol, polyethylene glycols, phenol, 1-naphthol, hydroquinone, etc., and a glass-clad magnetic stirrer bar are melted under vacuum (10−5 mbar) into a thick-walled 50 ml glass ampoule. The ampoule is heated at the temperature indicated for the time indicated, with the molten mixture being stirred with the aid of a magnetic stirrer. In order to prevent sublimation of the ligands at relatively cold points of the ampoule, the entire ampoule must have the temperature indicated. Alternatively, the synthesis can be carried out in a stirred autoclave with glass insert. After cooling (NOTE: the ampoules are usually under pressure!), the ampoule is opened, the sinter cake is stirred for 3 h with 100 g of glass beads (diameter 3 mm) in 100 ml of a suspension medium (the suspension medium is selected so that the ligand is readily soluble therein, but the metal complex has low solubility therein; typical suspension media are methanol, ethanol, dichloromethane, acetone, THF, ethyl acetate, toluene, etc.) and mechanically digested at the same time. The fine suspension is decanted off from the glass beads, the solid is filtered off with suction, rinsed with 50 ml of the suspension medium and dried in vacuo. The dry solid is placed on an aluminium oxide bed (aluminium oxide, basic, activity grade 1) with a depth of 3-5 cm in a continuous hot extractor and then extracted with an extractant (initially introduced amount about 500 ml, the extractant is selected so that the complex is readily soluble therein at elevated temperature and has low solubility therein at low temperature; particularly suitable extractants are hydrocarbons, such as toluene, xylenes, mesitylene, naphthalene, o-dichlorobenzene, halogenated aliphatic hydrocarbons, acetone, ethyl acetate, cyclohexane). When the extraction is complete, the extractant is evaporated to about 100 ml in vacuo. Metal complexes which have excessively good solubility in the extractant are brought to crystallisation by dropwise addition of 200 ml of methanol. The solid of the suspensions obtained in this way is filtered off with suction, washed once with about 50 ml of methanol and dried. After drying, the purity of the metal complex is determined by means of NMR and/or HPLC. If the purity is below 99.5%, the hot-extraction step is repeated, with the aluminium oxide bed being omitted from the 2nd extraction. When a purity of 99.5-99.9% or better has been achieved, the metal complex is heated or sublimed. The heating is carried out in a high vacuum (p about 10−6 mbar) in the temperature range from about 200-300° C. The sublimation is carried out in a high vacuum (p about 10−6 mbar) in the temperature range from about 300-430° C., where the sublimation is preferably carried out in the form of a fractional sublimation. If chiral ligands are employed, the derived fac-metal complexes are obtained as a diastereomer mixture. The enantiomers Λ,Δ of point group C3 generally have significantly lower solubility in the extractant than the enantiomers of point group Cl, which consequently become enriched in the mother liquor. Separation of the C3 diastereomers from the C1 diastereomers in this way is frequently possible. In addition, the diastereomers can also be separated chromatographically. If ligands of point group C1 are employed in enantiomerically pure form, a diastereomer pair Λ,Δ of point group C3 is formed. The diastereomers can be separated by crystallisation or chromatography and thus obtained as enantiomerically pure compounds.
Procedure analogous to variant A, using 10 mmol of tris(2,2,6,6-tetramethyl-3,5-heptanedionato)iridium [99581-86-9] instead of 10 mmol of trisacetylacetonatoiridium(III) [15635-87-7]. The use of this starting material is advantageous since the build-up of pressure in the ampoule is frequently not as pronounced.
Chromatography on silica gel with ethyl acetate:
Diastereomer 1: Rf about 0.5
Diastereomer 2: Rf about 0 After elution of diastereomer 1, changeover to DMF in order to elute diastereomer 2.
Chromatography on silica gel with ethyl acetate:
Diastereomer 1: Rf about 0.7
Diastereomer 2: Rf about 0.2
After elution of diastereomer 1, changeover to DMF in order to elute diastereomer 2.
A mixture of 10 mmol of sodium bisacetylacetonatodichloroiridate(III) [770720-50-8] and 22 mmol of the ligand L, optionally 1-10 g of an inert high-boiling additive as melting aid or solvent, as described under 1), and a glass-clad magnetic stirrer bar are melted under vacuum (10−5 mbar) into a thick-walled 50 ml glass ampoule. The ampoule is heated at the temperature indicated for the time indicated, with the molten mixture being stirred with the aid of a magnetic stirrer. After cooling—NOTE: the ampoules are usually under pressure!—the ampoule is opened, the sinter cake is stirred for 3 h with 100 g of glass beads (diameter 3 mm) in 100 ml of the suspension medium indicated (the suspension medium is selected so that the ligand is readily soluble therein, but the chloro dimer of the formula [Ir(L)2Cl]2 has low solubility therein; typical suspension media are MeOH, EtOH, DCM, acetone, ethyl acetate, toluene, etc.) and mechanically digested at the same time. The fine suspension is decanted off from the glass beads, the solid ([Ir(L)2Cl]2 which also contains about 2 eq. of NaCl, called the crude chloro dimer below) is filtered off with suction and dried in vacuo.
The crude chloro dimer of the formula [Ir(L)2Cl]2 obtained in this way is suspended in a mixture of 75 ml of 2-ethoxyethanol and 25 ml of water, 15 mmol of the co-ligand CL or the co-ligand compound CL and 15 mmol of sodium carbonate are added. After 20 h under reflux, a further 75 ml of water are added dropwise, the mixture is cooled, the solid is filtered off with suction, washed three times with 50 ml of water each time and three times with 50 ml of methanol each time and dried in vacuo. The dry solid is placed on an aluminium oxide bed (aluminium oxide, basic, activity grade 1) with a depth of 3-5 cm in a continuous hot extractor and then extracted with the extractant indicated (initially introduced amount about 500 ml, the extractant is selected so that the complex is readily soluble therein at elevated temperature and has low solubility therein at low temperature; particularly suitable extractants are hydrocarbons, such as toluene, xylenes, mesitylene, naphthalene, o-dichlorobenzene, acetone, ethyl acetate, cyclohexane). When the extraction is complete, the extractant is evaporated to about 100 ml in vacuo. Metal complexes which have excessively good solubility in the extractant are brought to crystallisation by dropwise addition of 200 ml of methanol. The solid of the suspensions obtained in this way is filtered off with suction, washed once with about 50 ml of methanol and dried. After drying, the purity of the metal complex is determined by means of NMR and/or HPLC. If the purity is below 99.5%, the hot-extraction step is repeated; when a purity of 99.5-99.9% or better has been achieved, the metal complex is heated or sublimed. Besides the hot-extraction method of purification, the purification can also be carried out by chromatography on silica gel or aluminium oxide. The heating is carried out in a high vacuum (p about 10−6 mbar) in the temperature range from about 200-300° C. The sublimation is carried out in a high vacuum (p about 10−6 mbar) in the temperature range from about 300-400° C., where the sublimation is preferably carried out in the form of a fractional sublimation.
123-54-6 CL1
270° C./20 h/EtOH Ethyl acetate
Hexadecane 280° C./20 h/EtOH Ethyl acetate
280° C./20 h/EtOH Ethyl acetate
260° C./26 h/EtOH Ethyl acetate
280° C./24 h/EtOH Ethyl acetate
1118-71-4 CL2
280° C./20 h/EtOH Cyclohexane
280° C./25 h/EtOH Cyclohexane
280° C./20 h/EtOH Cyclohexane
98-98-6 CL3
280° C./20 h/EtOH Cyclohexane
18653-75-3 CL4
270° C./20 h/EtOH Toluene
14782-58-2 CL5
Hexadecane 280° C./20 h/EtOH Ethyl acetate
219508-27-7 CL6
Hexadecane 280° C./20 h/EtOH Toluene
219508-27-7 CL6
280° C./20 h/EtOH Toluene
See variant A, step 1.
The crude chloro dimer of the formula [Ir(L)2Cl]2 is suspended in 200 ml of THF, 10 mmol of the co-ligand CL, 10 mmol of silver(I) trifluoroacetate and 20 mmol of potassium carbonate are added to the suspension, and the mixture is heated under reflux for 24 h. After cooling, the THF is removed in vacuo. The residue is taken up in 200 ml of a mixture of ethanol and concentrated ammonia solution (1:1, vv). The suspension is stirred at room temperature for 1 h, the solid is filtered off with suction, washed twice with 50 ml of a mixture of ethanol and conc. ammonia solution (1:1, vv) each time and twice with 50 ml of ethanol each time and then dried in vacuo. Hot extraction or chromatography and sublimation as in variant A.
391604-55-0 CL7
280° C./24 h/EtOH Toluene
4350-51-0 CL8
Hexadecane 280° C./24 h/EtOH Toluene
1093072-00- 4 CL9
Hexadecane 280° C./24 h/EtOH Cyclohexane
152536- 39-5 CL10
280° C./24 h/EtOH Toluene
See variant A, step 1.
The crude chloro dimer of the formula [Ir(L)2Cl]2 is suspended in 500 ml of dichloromethane and 100 ml of ethanol, 10 mmol of silver(I) trifluoromethanesulfonate are added to the suspension, and the mixture is stirred at room temperature for 24 h. The precipitated solid (AgCl) is filtered off with suction via a short Celite bed, and the filtrate is evaporated to dryness in vacuo. The solid obtained in this way is taken up in 100 ml of ethylene glycol, 10 mmol of the co-ligand CL and 10 mmol of 2,6-dimethylpyridine are added, and the mixture is then stirred at 130° C. for 30 h. After cooling, the solid is filtered off with suction, washed twice with 50 ml of ethanol each time and dried in vacuo. Hot extraction or chromatography and sublimation as in variant A.
914306- 48-2 CL11
280° C./24 h/EtOH Toluene Purification by chromatography on silica gel Eluent tol:EA 9:1, vv
270° C./24 h/EtOH Toluene
39696-58-7 CL12
Hexadecane 280° C./24 h/EtOH Toluene
26274-35-1 CL13
270° C./24 h/EtOH Toluene Purification by chromatography on silica gel Eluent DCM
3297-72-1 CL14
Hexadecane 280° C./24 h/EtOH Toluene
A mixture of 10 mmol of the Ir complex Ir(L)2(CL1 or CL2), 11 mmol of the ligand L′, optionally 1-10 g of an inert high-boiling additive as melting aid or solvent, as described under 1), and a glass-clad magnetic stirrer bar are melted under vacuum into a 50 ml glass ampoule (10−5 mbar). The ampoule is heated at the temperature indicated for the time indicated, with the molten mixture being stirred with the aid of a magnetic stirrer. Further work-up, purification and sublimation as described under 1) Homoleptic tris-facial iridium complexes.
Hexadecane 280° C./45 h/EtOH Toluene
as Ir(L1)2(L25)
as Ir(L1)2(L25)
Procedure analogous to A. Joshi-Pangu et al., J. Am. Chem. Soc., 2011, 133, 22, 8478. 100 ml of tert-butylmagnesium chloride, 2 M solution in THF, are added dropwise to a solution, cooled to −10° C., of 20.9 g (100 mmol) of 8-bromo-1,6-naphthyridine [17965-74-1], 1.5 g (10 mmol) of nickel(II) chloride×1.5 H2O and 3.2 g (10 mmol) of 1,3-dicyclohexyl-1H-imidazolium tetrafluoroborate [286014-37-7] in 300 ml of THF, and the mixture is then stirred for a further 8 h. After warming to 0° C., 20 ml of water are added dropwise, 300 ml of saturated ammonium chloride solution and 500 ml of ethyl acetate are then added. After vigorous shaking, the org. phase is separated off, washed once with 500 ml of water and once with 300 ml of saturated sodium chloride solution and then dried over magnesium sulfate. After removal of the solvent, the residue is chromatographed on silica gel with ethyl acetate:heptane:triethylamine (1:2:0.05). Yield: 3.4 g (18 mmol), 18%. Purity about 98% according to 1H-NMR.
5.1 g (30 mmol) of m-chloroperbenzoic acid are added in portions to a solution of 3.4 g (18 mmol) of 8-tert-butyl-1,6-naphthyridine in 50 ml of chloroform, and the mixture is then stirred at room temperature for 4 days. After addition of 200 ml of chloroform, the reaction solution is washed three times with 100 ml of a 10% potassium carbonate solution each time and dried over magnesium sulfate. The solid obtained after removal of the solvent is reacted further without further purification. Yield: 3.6 g (18 mmol) quantitative, purity: 95% according to 1H-NMR.
A) A mixture of 100 mmol of 1-haloisoquinoline (halogen=chlorine, bromine, iodine), 120 mmol of the β-ketocarboxylic acid amide, 300 mol of a base (sodium carbonate, potassium carbonate, caesium carbonate, potassium phosphate, etc.), 5 mmol of a bidentate phosphine (BINAP, xantphos) or 10 mmol of a monodentate phosphine (S-Phos, X-Phos, BrettPhos), 5 mmol of palladium(II) acetate and 100 g of glass beads (diameter 6 mm) in 500 ml of a solvent (dioxane, DMF, DMAC, etc.) is stirred vigorously at 80-150° C. for 16 h. After cooling, the solvent is removed in vacuo, the residue is taken up in 1000 ml of ethyl acetate, washed three times with 300 ml of water each time, once with 300 ml of saturated sodium chloride solution and then dried over magnesium sulfate.
B) The residue obtained after removal of the solvent in vacuo is cyclised as described in 1a) step B) variant 1.
A+B) Use of 16.4 g (100 mmol) of 1-chloroisoquinoline [19493-44-8], 22.2 g (120 mmol) of 2,2,5,5-tetramethyl-4-oxotetrahydrofuran-3-carboxamide [99063-20-4], 41.5 g (300 mmol) of potassium carbonate, 2.9 g (5 mmol) of xantphos, 1.1 g (5 mmol) of palladium(II) acetate, 500 ml of dioxane, T=110° C. Purification by column chromatography (silica gel, DCM:EA 5:1, vv) and recrystallisation three times from ethyl acetate/n-heptane. Fractional sublimation (p about 10−5 mbar, T=190° C.). Yield 4.5 g (15 mmol), 15%. Purity about 99.5% according to 1H-NMR.
The following compounds can be prepared analogously.
1003195-34-3
24188-78-1
58421-80-0
53491-80-8
1086385-19-4
1339335-80-6
A) Procedure analogous to M. Couturier et al., Org. Lett. 2006, 9, 1929. 100 mmol of oxalyl chloride are added dropwise at room temperature to a suspension of 100 mmol of the amide in 100 ml of 1,2-dichloroethane, and the mixture is then stirred at 50° C. for 3 h. After cooling to room temperature, 50 mmol of the isoquinoline N-oxide dissolved in 100 ml of 1,2-dichloroethane are added, and the mixture is stirred at room temperature for a further 24 h.
B) The residue obtained after removal of the solvent in vacuo is cyclised as described in 1a) step B) variant 1.
A+B) Use of 18.5 g (100 mmol) of tetrahydro-2,2,5,5-tetramethyl-4-oxo-3-furancarboxamide [99063-20-4], 8.6 ml (100 mmol) of oxalyl chloride [79-37-8] and 11.1 g (50 mmol) of 4-phenylisoquinoline N-oxide [65811-00-9]. Purification by column chromatography (silica gel, DCM:EA 5:1, vv) and recrystallisation three times from ethyl acetate/n-heptane. Fractional sublimation (p about 10−5 mbar, T=190° C.). Yield: 3.8 g (10 mmol), 20%. Purity about 99.5% according to 1H-NMR.
The following compounds can be prepared analogously.
S11
69604-10-0
872823-41-1
A) A mixture of 100 mmol of 2-isoquinolin-1-yl-2,4,10a-triazaphenanthrene-1,3-dione (dimeric isocyanate, synthesis analogous to 4737-19-3 in accordance with K. J. Duffy et al., WO2007150011) and 500 mmol of the enamine is stirred at 160° C. on a water separator for 16 h. The temperature is then slowly increased to about 280° C. until the secondary amine formed and the excess enamine have distilled off. After cooling, the residue is chromatographed.
A) Use of 34.0 g (100 mmol) of 2-isoquinolin-1-yl-2,4,10a-triazaphenanthrene-1,3-dione, 105.7 g (500 mmol) of 4-(2,2,5,5-tetramethyl-2,5-dihydrofuran-3-yl)morpholine (preparation analogous to 78593-93-8 in accordance with R. Carlson et al., Acta Chem. Scand. B, 1984, B38, 1, 49). Purification by column chromatography (silica gel, DCM:EA 5:1, vv) and recrystallisation three times from ethyl acetate/n-heptane. Fractional sublimation (p about 10−5 mbar, T=190° C.). Yield 5.3 g (18 mmol), 18%. Purity about 99.5% according to 1H-NMR.
The following compounds can be prepared analogously.
78593-93-8
5024-92-0
racemate
41455-20-3
A) An intimate mixture of 120 mmol of the 2-halobenzoic acid amide and 100 mmol of the β-ketocarboxylic acid amide is melted on a water separator and then stirred at 240° C. until (about 2 h) water no longer separates off. After cooling, the melt cake is washed by stirring with 200 ml of hot methanol/water (1:1, vv). The solid obtained after filtration and drying is reacted further in B).
B) 6 mmol of triphenylphosphine, 3 mmol of palladium(II) acetate, 3 mmol of copper(I) iodide and 150 mmol of the alkyne are added consecutively to a solution of 100 mmol of the 2-phenyl-1H-pyrimidin-4-one from A) in 200 ml of DMF and 100 ml of triethylamine, and the mixture is stirred at 70° C. for 5 h. After cooling, the precipitated triethylammonium hydrochloride is filtered off with suction, rinsed with a little DMF, and the filtrate is freed from the volatile components in vacuo. The residue is dissolved in 200 ml of nitrobenzene, 10 ml of water are added, the mixture is slowly heated to 200° C. and then stirred at 200° C. on a water separator for 6 h. The nitrobenzene is then distilled off completely at 200° C. by application of a slight reduced pressure. After cooling, the glassy residue is taken up in 150 ml of hot methanol, during which the product begins to crystallise. After cooling, the solid is filtered off with suction, rinsed with a little methanol and recrystallised again.
A+B) Use of 24.0 g (120 mmol) of 2-bromobenzamide [4001-73-4], 18.5 g (100 mmol) of tetrahydro-2,2,5,5-tetramethyl-4-oxo-3-furancarboxamide [99063-20-4], 1.6 g (6 mmol) of triphenylphosphine, 673 mg (3 mmol) of palladium(II) acetate, 571 mg (3 mmol) of copper(I) iodide and 14.7 g (150 mmol) of trimethylsilylacetylene [1066-54-2]. Recrystallisation three times from methanol. Fractional sublimation (p about 10−5 mbar, T=190° C.). Yield: 8.5 g (29 mmol), 29%. Purity about 99.5% according to 1H-NMR.
Ir(L60)3
A×11 mmol of N-halosuccinimide (halogen: CI, Br, I) are added at 30° C. with exclusion of light and air to a solution or suspension of 10 mmol of a complex which carries A×C—H groups (where A=1, 2 or 3) in the para-position to the iridium in 1000 ml of dichloromethane, and the mixture is stirred for 20 h. Complexes which have low solubility in DCM can also be reacted in other solvents (TCE, THF, DMF, etc.) and at elevated temperature. The solvent is subsequently substantially removed in vacuo. The residue is washed by boiling with 100 ml of MeOH, the solid is filtered off with suction, washed three times with 50 ml of methanol and then dried in vacuo.
5.9 g (33 mmol) of N-bromosuccinimide are added in one portion to a suspension, stirred at 30° C., of 11.0 g (10 mmol) of Ir(L1)3 in 1000 ml of DCM, and the mixture is then stirred for a further 20 h. After removal of about 200 ml of the DCM in vacuo, 100 ml of methanol are added to the lemon-yellow suspension, the solid is filtered off with suction, washed three times with about 50 ml of methanol and then dried in vacuo. Yield: 12.7 g (9.5 mmol), 95%; purity: about 99.5% according to 1H-NMR.
The following compounds can be prepared analogously:
Ir(L5)3
Ir(L5-Br)3
Ir(L22)3
Ir(L22-Br)3
Ir(L24)3
Ir(L24-Br)3
Ir(L42)3
Ir(L42-Br)3
0.6 mmol of tri-o-tolylphosphine and then 0.1 mmol of palladium(II) acetate are added to a suspension of 10 mmol of a brominated complex, 40-80 mmol of the boronic acid or boronic acid ester and 80 mmol of tripotassium phosphate in a mixture of 300 ml of toluene, 100 ml of dioxane and 300 ml of water, and the mixture is heated under reflux for 16 h. After cooling, 500 ml of water and 200 ml of toluene are added, the aqueous phase is separated off, the organic phase is washed three times with 200 ml of water, once with 200 ml of saturated sodium chloride solution and dried over magnesium sulfate. The mixture is filtered through a Celite bed, the bed is rinsed with toluene, the toluene is removed virtually completely in vacuo, 300 ml of ethanol are added, the precipitated crude product is filtered off with suction, washed three times with 100 ml of EtOH each time and dried in vacuo. The crude product is passed through a silica-gel column twice with toluene. The metal complex is finally heated or sublimed. The heating is carried out in a high vacuum (p about 10−6 mbar) in the temperature range from about 200-300° C. The sublimation is carried out in a high vacuum (p about 10−6 mbar) in the temperature range from about 300-400° C., where the sublimation is preferably carried out in the form of a fractional sublimation.
0.6 mmol of tri-o-tolylphosphine and then 0.1 mmol of palladium(II) acetate are added to a suspension of 10 mmol of a brominated complex, 40-80 mmol of the boronic acid or boronic acid ester and 60-100 mmol of the base (potassium fluoride, tripotassium phosphate, tripotassium phosphate monohydrate, tripotassium phosphate trihydrate, potassium carbonate, caesium carbonate, etc.) and 100 g of glass beads (diameter 3 mm) in 100-500 ml of an aprotic solvent (THF, dioxane, xylene, mesitylene, dimethylacetamide, NMP, DMSO, etc.) and optionally 5-10 mmol of water, and the mixture is heated under reflux for 1-24 h. Alternatively, other phosphines, such as tri-tert-butylphosphine, di-tert-butylphosphine, S-Phos, xantphos, etc., can be employed, where, in the case of these phosphines, the preferred phosphine:palladium ratio is 2:1 to 1.2:1. The solvent is removed in vacuo, the product is taken up in a suitable solvent (toluene, dichloromethane, ethyl acetate, etc.) and purified as described under A.
Use of 14.3 g (10 mmol) of Ir(L1-Br)3 and 14.0 g (40 mmol) of quarter-phenylboronic acid [1233200-59-3]. Yield: 10.6 g (5.5 mmol), 55%; purity: about 99.9% according to HPLC.
The following compounds can be prepared analogously:
Ir(L1-Br)3 + [952583-08-3] > Ir(101)3 A, as Ir(L100)3
Ir(L5-Br)3 + [1251825-65-6] > Ir(102)3 A, as Ir(L100)3
Ir(L22-Br)3 + [1071924-15-6] > Ir(103)3 A, as Ir(L100)3
Ir(L42-Br)3 + [84110-40-7] > Ir(104)3 B, tripotassium phosphate, toluene, 5 mmol of water, S-Phos
0.4 mmol of tri-tert-butylphosphine and then 0.3 mmol of palladium(II) acetate are added to a mixture of 10 mmol of the brominated complex, 40 mmol of the diarylamine or carbazole, 45 mmol of sodium tert-butoxide in the case of amines or 80 mmol of anhydrous tripotassium phosphate in the case of carbazoles, 100 g of glass beads (diameter 3 mm) and 300-500 ml of o-xylene or mesitylene, and the mixture is heated under reflux for 16 h with vigorous stirring. After cooling, the aqueous phase is separated off, washed twice with 200 ml of water, once with 200 ml of saturated sodium chloride solution and dried over magnesium sulfate. The mixture is filtered through a Celite bed, the bed is rinsed with o-xylene or mesitylene, the solvent is removed virtually completely in vacuo, 300 ml of ethanol are added, the precipitated crude product is filtered off with suction, washed three times with 100 ml of EtOH each time and dried in vacuo. The crude product is passed through a silica-gel column twice with toluene. The metal complex is finally heated or sublimed. The heating is carried out in a high vacuum (p about 10−6 mbar) in the temperature range from about 200-300° C. The sublimation is carried out in a high vacuum (p about 10−6 mbar) in the temperature range from about 300-400° C., where the sublimation is preferably carried out in the form of a fractional sublimation.
Use of 14.3 g (10 mmol) of Ir(L1-Br)3 and 12.9 g (40 mmol) of p-biphenyl-o-biphenylamine [1372775-52-4], mesitylene. Yield: 11.9 g (6.0 mmol) 60%; purity: about 99.8% according to HPLC.
The following compound can be prepared analogously:
Ir(L5-Br)3 + [1257220-47-5] > Ir(201)3
A mixture of 10 mmol of the brominated complex, 13 mmol of copper(I) cyanide per bromine function and 300 ml of NMP is stirred at 200° C. for 20 h. After cooling, the solvent is removed in vacuo, the residue is taken up in 500 ml of dichloromethane, the copper salts are filtered off via Celite, the dichloromethane is evaporated virtually to dryness in vacuo, 100 ml of ethanol are added, the precipitated solid is filtered off with suction, washed twice with 50 ml of ethanol each time and dried in vacuo. Hot extraction and sublimation as in 1) variant A. The crude product can alternatively be chromatographed on silica gel with dichloromethane, optionally with addition of ethyl acetate, and then sublimed.
Use of 14.3 g (10 mmol) of Ir(L1-Br)3 and 3.5 g (39 mmol) of copper(I) cyanide. Yield: 5.4 g (4.6 mmol), 46%; purity: about 99.8% according to HPLC.
A mixture of 10 mmol of the brominated complex, 12 mmol of bis(pinacolato)diborane [73183-34-3] per bromine function, 30 mmol of potassium acetate, anhydrous, per bromine function, 0.2 mmol of tricyclohexylphosphine and 0.1 mmol of palladium(II) acetate and 300 ml of solvent (dioxane, DMSO, NMP, etc.) is stirred at 80-160° C. for 4-16 h. After removal of the solvent in vacuo, the residue is taken up in 300 ml of dichloromethane, THF or ethyl acetate, filtered through a Celite bed, the filtrate is evaporated in vacuo until crystallisation commences, and finally about 100 ml of methanol are added dropwise in order to complete the crystallisation. The compounds can be recrystallised from dichloromethane, ethyl acetate or THF with addition of methanol or alternatively cyclohexane.
Use of 14.3 g (10 mmol) of Ir(L1-Br)3 and 9.1 g (36 mmol) of bis(pinacolato)diborane [73183-34-3], DMSO, 140° C., 6 h, THF, recrystallisation from THF:methanol. Yield: 9.5 g (6.5 mmol) 65%; purity: about 99.7% according to HPLC.
The monomers (bromides and boronic acids or boronic acid esters, purity according to HPLC>99.8%) in the composition indicated in the table are dissolved or suspended in a mixture of 2 parts by volume of toluene:6 parts by volume of dioxane:1 part by volume of water in a total concentration of about 100 mmol/1.2 mol equivalents of tripotassium phosphate per Br functionality employed are then added, the mixture is stirred for a further 5 min., 0.03-0.003 mol equivalent of tri-ortho-tolylphosphine and then 0.005-0.0005 mol equivalent of palladium(II) acetate (phosphine to Pd ratio preferably 6:1) per Br functionality employed are then added, and the mixture is then heated under reflux for 2-3 h with very vigorous stirring. If the viscosity of the mixture increases excessively, it can be diluted with a mixture of 2 parts by volume of toluene:3 parts by volume of dioxane. After a total reaction time of 4-6 h, 0.05 mol equivalent per boronic acid functionality employed of a monobromoaromatic compound and then, 30 min. later, 0.05 mol equivalent per Br functionality employed of a monoboronic acid or a monoboronic acid ester are added for end capping, and the mixture is boiled for a further 1 h. After cooling, the mixture is diluted with 300 ml of toluene, the aqueous phase is separated off, the organic phase is washed twice with 300 ml of water each time, dried over magnesium sulfate, filtered through a Celite bed in order to remove palladium and then evaporated to dryness. The crude polymer is dissolved in THF (concentration about 10-30 g/1), and the solution is allowed to run slowly, with very vigorous stirring, into twice the volume of methanol. The polymer is filtered off with suction and washed three times with methanol. The reprecipitation process is repeated three times, the polymer is then dried to constant weight at 30-50° C. in vacuo.
The monomers (bromides and boronic acids or boronic acid esters, purity according to HPLC>99.8%) in the composition indicated in the table are dissolved or suspended in a solvent (THF, dioxane, xylene, mesitylene, dimethylacetamide, NMP, DMSO, etc.) in a total concentration of about 100 mmol/l. 3 mol equivalents of base (potassium fluoride, tripotassium phosphate, potassium carbonate, caesium carbonate, etc., in each case anhydrous) per Br functionality are then added, and the weight equivalent of glass beads (diameter 3 mm) is added, the mixture is stirred for a further 5 min., 0.03-0.003 mol equivalent of tri-ortho-tolylphosphine and then 0.005-0.0005 mol equivalent of palladium(II) acetate (phosphine:Pd ratio preferably 6:1) per Br functionality are then added, and the mixture is then heated under reflux for 2-3 h with very vigorous stirring. Alternatively, other phosphines, such as tri-tert-butylphosphine, di-tert-butylphosphine, S-Phos, xantphos, etc., can be employed, where the preferred phosphine:palladium ratio in the case of these phosphines is 2:1 to 1.3:1. After a total reaction time of 4-12 h, 0.05 mol equivalent of a monobromoaromatic compound and then, 30 min. later, 0.05 mol equivalent of a monoboronic acid or a monoboronic acid ester are added for end capping, and the mixture is boiled for a further 1 h. The solvent is substantially removed in vacuo, the residue is taken up in toluene, and the polymer is purified as described under variant A.
Composition of the polymers, mol %:
Molecular weights and yield of the polymers according to the invention:
OLEDs according to the invention and OLEDs in accordance with the prior art are produced by a general process in accordance with WO 2004/058911, which is adapted to the circumstances described here (layer-thickness variation, materials used).
The results for various OLEDs are presented in the following examples. Glass plates with structured ITO (indium tin oxide) form the substrates to which the OLEDs are applied. The OLEDs have in principle the following layer structure: substrate/hole-transport layer 1 (HTL1) consisting of HTM doped with 3% of NDP-9 (commercially available from Novaled), 20 nm/hole-transport layer 2 (HTL2)/optional electron-blocking layer (EBL)/emission layer (EML)/optional hole-blocking layer (HBL)/electron-transport layer (ETL)/optional electron-injection layer (EIL) and finally a cathode. The cathode is formed by an aluminium layer with a thickness of 100 nm.
Firstly, vacuum-processed OLEDs are described. For this purpose, all materials are applied by thermal vapour deposition in a vacuum chamber. The emission layer here always consists of at least one matrix material (host material) and an emitting dopant (emitter), which is admixed with the matrix material or matrix materials in a certain proportion by volume by coevaporation. An expression such as M3:M2:Ir(L1)3 (55%:35%:10%) here means that material M3 is present in the layer in a proportion by volume of 55%, M2 is present in the layer in a proportion of 35% and Ir(L1)3 is present in the layer in a proportion of 10%. Analogously, the electron-transport layer may also consist of a mixture of two materials. The precise structure of the OLEDs is shown in Table 1. The materials used for the production of the OLEDs are shown in Table 6.
The OLEDs are characterised by standard methods. For this purpose, the electroluminescence spectra, the current efficiency (measured in cd/A) and the voltage (measured at 1000 cd/m2 in V) are determined from current/voltage/luminance characteristic lines (IUL characteristic lines). For selected experiments, the lifetime is determined. The lifetime is defined as the time after which the luminous density has dropped to a certain proportion from a certain initial luminous density. The expression LT50 means that the lifetime given is the time at which the luminous density has dropped to 50% of the initial luminous density, i.e. from, for example, 1000 cd/m2 to 500 cd/m2. Depending on the emission colour, different initial luminances were selected. The values for the lifetime can be converted to a figure for other initial luminous densities with the aid of conversion formulae known to the person skilled in the art. The lifetime for an initial luminous density of 1000 cd/m2 is a usual figure here.
The compounds according to the invention can be employed, inter alia, as phosphorescent emitter materials in the emission layer in OLEDs. Compound Ir(Ref1)3 is used as comparison in accordance with the prior art. The results for the OLEDs are summarised in Table 2.
The iridium complexes according to the invention can also be processed from solution, where they result in OLEDs which are significantly simpler as far as the process is concerned, compared with the vacuum-processed OLEDs, with nevertheless good properties. The production of components of this type is based on the production of polymeric light-emitting diodes (PLEDs), which has already been described many times in the literature (for example in WO 2004/037887). The structure is composed of substrate/ITO/PEDOT (80 nm)/interlayer (80 nm)/emission layer (80 nm)/cathode. To this end, use is made of substrates from Technoprint (soda-lime glass), to which the ITO structure (indium tin oxide, a transparent, conductive anode) is applied. The substrates are cleaned with DI water and a detergent (Deconex 15 PF) in a clean room and then activated by a UV/ozone plasma treatment. An 80 nm layer of PEDOT (PEDOT is a polythiophene derivative (Baytron P VAI 4083sp.) from H. C. Starck, Goslar, which is supplied as an aqueous dispersion) is then applied as buffer layer by spin coating, likewise in the clean room. The spin rate required depends on the degree of dilution and the specific spin coater geometry (typically for 80 nm: 4500 rpm). In order to remove residual water from the layer, the substrates are dried by heating on a hotplate at 180° C. for 10 minutes. The interlayer used serves for hole injection, in this case HIL-012 from Merck is used. The interlayer may alternatively also be replaced by one or more layers, which merely have to satisfy the condition of not being detached again by the subsequent processing step of EML deposition from solution. In order to produce the emission layer, the emitters according to the invention are dissolved in toluene together with the matrix materials. The typical solids content of such solutions is between 16 and 25 g/l if, as here, the typical layer thickness of 80 nm for a device is to be achieved by means of spin coating. The solution-processed devices comprise an emission layer comprising (polystyrene):M5:M6:Ir(L)3 (25%:25%:40%:10%). The emission layer is applied by spin coating in an inert-gas atmosphere, in the present case argon, and dried by heating at 130° C. for 30 min. Finally, a cathode is applied by vapour deposition of barium (5 nm) and then aluminium (100 nm) (high-purity metals from Aldrich, particularly barium 99.99% (Order No. 474711); vapour-deposition equipment from Lesker, inter alia, typical vapour-deposition pressure 5×10−6 mbar). Optionally, firstly a hole-blocking layer and then an electron-transport layer and only then the cathode (for example Al or LiF/Al) can be applied by vacuum vapour deposition. In order to protect the device against air and atmospheric moisture, the device is finally encapsulated and then characterised. The OLED examples given have not yet been optimised, Table 3 summarises the data obtained.
The production of a polymeric organic light-emitting diode (PLED) has already been described many times in the literature (for example WO 2004/037887). The substrates are prepared as described under A: From soluble functional materials, then, under an inert-gas atmosphere (nitrogen or argon), firstly 20 nm of an interlayer (typically a hole-dominated polymer, here HIL-012 from Merck) and then 65 nm of the polymer layers are applied from toluene solution (concentration of interlayer 5 g/l). The two layers are dried by heating at 160° C. for at least 10 minutes. The cathode is then applied by vapour deposition of barium (5 nm) and then aluminium (100 nm). In order to protect the device against air and atmospheric moisture, the device is finally encapsulated and then characterised. The OLED examples given have not yet been optimised, Table 3 summarises the data obtained.
A white-emitting OLED having the following layer structure is produced in accordance with the general process from 1):
HTM
EBM
M1
M2
M3
M4 = HBM
M5
M6
Ir-R
Ir-G
ETM1
ETM2
D-Ir(Ref1)3 (in accordance with WO 2011/044988)
Polystyrene films are produced alongside one another on a glass specimen slide by applying a drop of a dichloromethane solution of polystyrene and an emitter (solids content of polystyrene about 10% by weight, solids content of emitter about 0.1% by weight) and evaporation of the solvent. The specimen slide is illuminated from above in a darkened room with the light of a UV lamp (commercially available lamp for viewing TLCs, emission wavelength 366 nm), while the stream of hot air from an adjustable hair dryer is directed against it from below. The temperature is increased successively and the thermal luminescence quenching, i.e. the partial or complete quenching of the luminescence, as a function of the temperature is followed with the eye.
Film 1: Polystyrene film comprising reference emitter IrPPy, fac-tris(2-phenylpyridine)iridium[94928-86-6]
Film 2: Polystyrene film comprising emitter Ir(L1)3 according to the invention
From a hot-air temperature of about 150° C., slow extinction of the luminescence of film 1 is evident; the luminescence of film 2 appears unchanged. Above about 200° C., the luminescence of film 1 is substantially extinguished, that of film 2 appears virtually unchanged. Even above about 250° C., only weak extinction of the luminescence of film 2 is observed.
On cooling of the films, the luminescence of both films returns and appears as intense as at the beginning of the experiment. The experiment can be repeated many times, which shows that this is a reversible temperature-dependent extinction phenomenon and not an irreversible decomposition of the samples.
| Number | Date | Country | Kind |
|---|---|---|---|
| 12008582.4 | Dec 2012 | DE | national |
| 13003485.3 | Jul 2013 | DE | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2013/003580 | 11/27/2013 | WO | 00 |
