Patent Application
20230123170
The present invention relates to specific compounds, a material for an organic electroluminescence device comprising said specific compound, an organic electroluminescence device comprising said specific compound, an electronic equipment comprising said organic electroluminescence device and the use of said compounds in an organic electroluminescence device.
When a voltage is applied to an organic electroluminescence device (hereinafter may be referred to as an organic EL device), holes are injected to an emitting layer from an anode and electrons are injected to an emitting layer from a cathode. In the emitting layer, injected holes and electrons are re-combined and excitons are formed.
An organic EL device comprises an emitting layer between the anode and the cathode. Further, there may be a case where it has a stacked layer structure comprising an organic layer such as a hole-injecting layer, a hole-transporting layer, an electron-blocking layer, an electron-injecting layer, an electron-transporting layer, a hole-blocking layer etc.
EP 2 752 902 A1 relates to an organic electroluminescence device including: an anode; an emitting layer; an electron transporting zone; and a cathode in this sequence, in which the electron transporting zone comprises an aromatic heterocyclic derivative represented by formula (1)
wherein
(HAr)a-L1- (2),
and
Specifically mentioned compounds are:
In the examples in EP 2 752 902 A1, the compounds of formula (1) are employed in the (hole-)blocking layer.
WO 2017/016630 A1 relates to fluorene derivatives that are connected in one or more of the 1-, 1′-, 4-, or 4′-positions in any combination to a carbon atom of a diaryl substituted triazinyl or pyrimidinyl derivative. The compounds are suitable for use in electronic devices, in particular organic electroluminescent devices, comprising these compounds. In some embodiments, the compounds are used as matrix materials for phosphorescent or fluorescent emitters as well as a hole-blocking or an electron-transporting layer.
Specifically mentioned compounds are:
KR10-2018-0063710 A relates to an organic light-emitting compound represented by the following formula (I). The organic light-emitting compound is adopted as an electron-transporting material of an electron-transporting layer in an organic light-emitting device.
wherein
A specifically mentioned compound is:
KR10-2018-0063709 A relates to an organic light-emitting compound represented by the chemical formula (I). The compound is used as an electron-transporting material in an electron-transporting layer in organic light-emitting devices.
wherein
EP 2 752 902 A1
WO 2017/016630 A1
KR10-2018-0063710 A
KR10-2018-0063709 A
The specific structure and substitution pattern of polycyclic compounds have a significant impact on the performance of the polycyclic compounds in organic electronic devices.
The specific structure and substitution pattern of polycyclic compounds have a significant impact on the performance of the polycyclic compounds in organic electronic devices. Therefore, notwithstanding the developments described above, there remains a need for organic electroluminescence devices comprising new materials, especially charge-transporting materials, e.g. electron-transporting materials, charge-blocking materials, e.g. hole-blocking materials and/or dopant materials, to provide improved performance of electroluminescence devices.
Accordingly, it is an object of the present invention, with respect to the aforementioned related art, to provide further materials suitable for use in organic electroluminescence devices and further applications in organic electronics. More particularly, it should be possible to provide charge-transporting materials, e.g. electron-transporting materials, and/or charge-blocking materials, e.g. hole-blocking materials, and/or dopant materials for use in organic electroluminescence devices. The materials should be suitable especially for organic electroluminescence devices which comprise at least one emitter, which is a phosphorescence emitter and/or a fluorescence emitter.
Furthermore, the materials should be suitable for providing organic electroluminescence devices which ensure good performance of the organic electroluminescence devices, especially a high current efficiency (EQE) and/or a long lifetime and/or a low driving voltage.
Said object is solved by a polycyclic compound represented by formula (I):
wherein
R1 and R1′ each independently represents a C1 to C6 alkyl group;
R2 represents a substituted or unsubstituted C6 to C24 aryl group, a substituted or unsubstituted heteroaryl group having 3 to 9 carbon atoms or CN;
L represents a substituted or unsubstituted C6 to C40 arylene group;
m is 0, 1, 2, 3, 4 or 5;
n is 1, 2 or 3.
The specific polycyclic compounds of the present invention according to formula (I) may be used as a material, especially host, charge-transporting or charge-blocking material, that is highly suitable in organic electroluminescence devices. Moreover, thermally stable compounds are provided, especially resulting in organic electroluminescence devices having a high current efficiency (EQE) and/or a long lifetime and/or a low driving voltage.
The compounds of the present invention may also be used in further organic electronic devices than organic electroluminescence devices such as electrophotographic photoreceptors, photoelectric converters, organic solar cells (organic photovoltaics), switching elements, such as organic transistors, for example, organic FETs and organic TFTs, organic light emitting field effect transistors (OLEFETs), image sensors and dye lasers.
Accordingly, a further subject of the present invention is directed to an organic electronic device, comprising a compound according to the present invention. The organic electronic device is preferably an organic electroluminescence device (EL device). The term organic EL device (organic electroluminescence device) is used interchangeably with the term organic light-emitting diode (OLED) in the present application.
The compounds of formula (I) can in principal be used in any layer of an EL device, but are preferably used as charge-transporting, especially electron-transporting, charge-blocking, especially hole-blocking, material. Particularly, the compounds of formula (I) are used as electron-transporting material and/or hole-blocking material for phosphorescence or fluorescence emitters.
Hence, a further subject of the present invention is directed to a material for an organic electroluminescence device comprising at least one compound of formula (I) according to the present invention.
A further subject of the present invention is directed to an organic electroluminescence device which comprises an organic thin film layer between a cathode and an anode, wherein the organic thin film layer comprises one or more layers and comprises a light emitting layer, and at least one layer of the organic thin film layer comprises at least one compound of formula (I) according to the present invention.
A further subject of the present invention is directed to an electronic equipment comprising the organic electroluminescence device according the present invention.
A further subject of the present invention is directed to the use of a compound of formula (I) according to the present invention in an organic electroluminescence device. In said embodiment the compound of formula (I) is preferably used in an electron-transporting zone of the organic electroluminescence device. In the meaning of the present invention, the electron-transporting zone includes at least an electron-transporting layer and preferably also an electron-injection layer and/or a hole-blocking layer.
A further subject of the present invention is directed to an emitting layer, comprising a compound of formula (I) according to the present invention.
A further subject of the present invention is directed to an electron-transporting layer comprising a compound of formula (I) according to the present invention. Preferably, the electron-transporting layer is provided between the cathode and the light emitting layer of an EL device such as an OLED.
A further subject of the present invention is directed to a hole-blocking layer comprising a compound of formula (I) according to the present invention. Preferably, the hole-blocking layer is provided between the electron-transporting layer and the light emitting layer of an EL device such as an OLED.
The compounds of the invention are suitable for providing organic electroluminescence devices which ensure good performance of the organic electroluminescence devices, especially a high external quantum efficiency (EQE), long lifetime and/or low driving voltage.
The terms heteroaryl group having 3 to 9 carbon atoms, a C6 to C24 aryl group, C6 to C40 arylene group, an alkyl group having 1 to 25 carbon atoms, preferably a C1 to C6 alkyl group, are known in the art and generally have the following meaning, if said groups are not further specified in specific embodiments mentioned below:
The C6 to C24 aryl group, preferably C6 to C18 aryl group, may be a non-condensed aryl group or a condensed aryl group. Specific examples thereof include phenyl group, naphthyl group, phenanthryl group, biphenyl group, terphenyl group, quaterphenyl group, fluoranthenyl group, triphenylenyl group, phenanthrenyl group, fluorenyl group, anthracenyl, chrysenyl, spirofluorenyl group, 9,9-diphenylfluorenyl group, 9,9′-spirobi[9H-fluorene]-2-yl group, 9,9-dimethylfluorenyl group, benzo[c]phenanthrenyl group, benzo[a]triphenylenyl group, naphtho[1,2-c]phenanthrenyl group, naphtho[1,2-a]triphenylenyl group, dibenzo[a,c]triphenylenyl group, benzo[a]fluoranthenyl group, benzo[j]fluoranthenyl group, benzo[k]fluoranthenyl group and benzo[b]fluoranthenyl group, with phenyl group, naphthyl group, biphenyl group, terphenyl group, phenanthryl group, triphenylenyl group, fluorenyl group, spirobifluorenyl group, and fluoranthenyl group being preferred, and phenyl group, 1-naphthyl group, 2-naphthyl group, biphenyl-2-yl group, biphenyl-3-yl group, biphenyl-4-yl group, phenanthrene-9-yl group, phenanthrene-3-yl group, phenanthrene-2-yl group, triphenylene-2-yl group, 9,9-dimethylfluorene-2-yl group, fluoranthene-3-yl group, fluoranthene-2-yl group, fluoranthene-8-yl group being more preferred, and phenyl group, 1-naphthyl group, 2-naphthyl group, biphenyl-2-yl group, biphenyl-3-yl group and biphenyl-4-yl group being most preferred.
The heteroaryl group having 3 to 9 carbon atoms, preferably having 5 to 9 carbon atoms, may be a non-condensed heteroaryl group or a condensed heteroaryl group. Specific examples thereof include the residues of pyrrole ring, isoindole ring, benzofuran ring, isobenzofuran ring, benzothiophene, isoquinoline ring, quinoxaline ring, quinazoline, pyridine ring, pyrazine ring, pyrimidine ring, pyridazine ring, indole ring, quinoline ring, furan ring, thiophene ring, benzoxazole ring, benzothiazole ring, benzimidazole ring, triazine ring, oxazole ring, thiazole ring and imidazole ring with the pyridine ring and quinoline ring being preferred.
Examples of the alkyl group having 1 to 25 carbon atoms, preferably 1 to 8 carbon atoms, are methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, n-hexyl group, n-heptyl group, n-octyl group, n-nonyl group, n-decyl group, n-undecyl group, n-dodecyl group, n-tridecyl group, n-tetradecyl group, n-pentadecyl group, n-hexadecyl group, n-heptadecyl group, n-octadecyl group, neopentyl group and 1-methylpentyl group.
Further preferred are alkyl groups having 1 to 6 carbon atoms. Examples of the alkyl group having 1 to 6 carbon atoms are methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group, t-butyl group, n-pentyl group, n-hexyl group, neopentyl group and 1-methylpentyl group, with methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, s-butyl group, isobutyl group and t-butyl group being preferred.
The C6 to C40 arylene group, preferably C6 to C18 arylene group, may be a non-condensed arylene group or a condensed arylene group. Specific examples thereof include phenylene group, naphthylene group, biphenylene group, terphenylene group, quaterphenylene group, fluoranthene-diyl group, triphenylene-diyl group, phenanthrene-diyl group, fluorene-diyl group, anthracene-diyl, chrysene-diyl, spirofluorene-diyl group, 9,9-diphenylfluorene-diyl group, 9,9′-spirobi[9H-fluorene]-2-diyl group, 9,9-dimethylfluorene-diyl group, benzo[c]phenanthrene-diyl group, benzo[a]triphenylene-diyl group, naphtho[1,2-c]phenanthrene-diyl group, naphtho[1,2-a]triphenylene-diyl group, dibenzo[a,c]triphenylene-diyl group, benzo[a]fluoranthene-diyl group, benzo[j]fluoranthene-diylgroup, benzo[k]fluoranthene-diyl group and benzo[b]fluoranthene-diyl group, with phenylene group, naphthylene group, biphenylene group, terphenylene group, phenanthrene-diyl group, triphenylene-diyl group, fluorene-diyl group, spirobifluorene-diyl group, and fluoranthene-diyl group being preferred, and phenylene group, biphenylene group, terphenylene group, triphenylene-diyl group, and naphthylene group being more preferred, and phenylene group, biphenylene group and naphthylene group being most preferred.
Examples of the optional substituent(s) indicated by “substituted or unsubstituted” and “may be substituted” referred to above or hereinafter include a halogen atom, a cyano group, an alkyl group having 1 to 25, preferably 1 to 8 carbon atoms, a cycloalkyl group having 3 to 18, preferably 3 to 12 ring carbon atoms, an alkoxy group having 1 to 25, preferably 1 to 8 carbon atoms, a haloalkyl group having 1 to 25, preferably 1 to 5 carbon atoms, a haloalkoxy group having 1 to 25, preferably 1 to 5 carbon atoms, an alkylamino group having 1 to 25 carbon atoms, preferably 1 to 5 carbon atoms, a carboxyalkyl group having 1 to 25 carbon atoms, preferably 1 to 5 carbon atoms, a carboxamidalkyl group having 1 to 25 carbon atoms, preferably 1 to 5 carbon atoms, a silyl group, a C6 to C24 aryl group, preferably a C6 to C18 aryl group , an aryloxy group having 6 to 24, preferably 6 to 18 ring carbon atoms, an aralkyl group having 7 to 24, preferably 7 to 20 carbon atoms, an alkylthio group having 1 to 25, preferably 1 to 5 carbon atoms, an arylthio group having 6 to 24, preferably 6 to 18 ring carbon atoms, an arylamino group having 6 to 30 carbon atoms, preferably 6 to 18 carbon atoms, a carboxyaryl group having 6 to 24 carbon atoms, preferably 6 to 18 carbon atoms, a carboxamidaryl group having 6 to 24 carbon atoms, preferably 6 to 18 carbon atoms, and an heterocyclic group having 3 to 30 ring atoms, preferably 5 to 18 ring atoms.
The heterocyclic group having 3 to 30 ring atoms, preferably 5 to 18 ring atoms, may be a non-condensed heterocyclic group or a condensed heterocyclic group. Preferably, the heterocyclic group having 5 to 18 ring atoms is a heteroaryl group having 5 to 18 ring atoms. Specific examples thereof include the residues of pyrrole ring, isoindole ring, benzofuran ring, isobenzofuran ring, benzothiophene, dibenzothiophene ring, isoquinoline ring, quinoxaline ring, quinazoline, phenanthridine ring, phenanthroline ring, pyridine ring, pyrazine ring, pyrimidine ring, pyridazine ring, indole ring, quinoline ring, acridine ring, carbazole ring, furan ring, thiophene ring, benzoxazole ring, benzothiazole ring, benzimidazole ring, dibenzofuran ring, triazine ring, oxazole ring, oxadiazole ring, thiazole ring, thiadiazole ring, triazole ring, and imidazole ring with the residues of dibenzofuran ring, carbazole ring, and dibenzothiophene ring being preferred, and the residues of dibenzofuran-1-yl group, dibenzofuran-3-yl group, dibenzofuran-2-yl group, dibenzofuran-4-yl group, 9-phenylcarbazole-3-yl group, 9-phenylcarbazole-2-yl group, 9-phenylcarbazole-4-yl group, dibenzothiophene-2-ylgroup, and dibenzothiophene-4-yl, dibenzothiophene-1-yl group, and dibenzothiophene-3-yl group being more preferred.
The alkyl group having 1 to 25, preferably 1 to 8 carbon atoms, and the C6 to C24 aryl group, preferably C6 to C18 aryl group, are defined above.
Examples of the alkenyl group having 2 to 25 carbon atoms include those disclosed as alkyl groups having 2 to 25 carbon atoms but comprising at least one double bond, preferably one, or where possible, two or three double bonds.
Examples of the alkynyl group having 2 to 25 carbon atoms include those disclosed as alkyl groups having 2 to 25 carbon atoms but comprising at least one triple bond, preferably one, or where possible, two or three triple bonds.
Examples of the cycloalkyl group having 3 to 18 ring carbon atoms, preferably 3 to 12 ring carbon atoms include cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cyclooctyl group, and adamantyl group, with tyclopentyl group, and cyclohexyl group being preferred. Preferred are cycloalkyl groups having 3 to 6 ring carbon atoms, i.e. a cyclopropyl group, a cyclobutyl group, a cyclopentyl group or a cyclohexyl group.
The silyl group is an alkyl and/or aryl substituted silyl group. Examples of alkyl and/or aryl substituted silyl groups include alkylsilyl groups having 1 to 10 carbon atoms, preferably 1 to 5 carbon atoms, including trimethylsilyl group, triethylsilyl group, tributylsilyl group, dimethylethylsilyl group, t-butyldimethylsilyl group, propyldimethylsilyl group, dimethylisopropylsilyl group, dimethylpropylsilyl group, dimethylbutylsilyl group, dimethyltertiarybutylsilyl group, diethylisopropylsilyl group, alkylarylsilyl groups having 6 to 30 carbon atoms, preferably 6 to 18 carbon atoms, in the aryl part and 1 to 10 carbon atoms, preferably 1 to 5 carbon atoms, in the alkyl part including phenyldimethylsilyl group, diphenylmethylsilyl group, diphenyltertiarybutylsilyl group, and arylsilyl groups having 6 to 30 carbon atoms, preferably 6 to 18 carbon atoms, including a triphenylsilyl group, with trimethylsilyl, triphenylsilyl, diphenyltertiarybutylsilyl group and t-butyldimethylsilyl group being preferred.
Examples of halogen atoms include fluorine, chlorine, bromine, and iodine, with fluorine being preferred.
Examples of a haloalkyl group having 1 to 25 carbon atoms include the alkyl groups mentioned above wherein the hydrogen atoms thereof are partly or entirely substituted by halogen, preferably fluorine, atoms.
Examples of a haloalkoxy group having 1 to 25 carbon atoms include the alkoxy groups mentioned above wherein the hydrogen atoms thereof are partly or entirely substituted by halogen, preferably fluorine, atoms.
Examples of an alkylamino group (alkyl substituted amino group), preferably an alkylamino group having 1 to 25 ring carbon atoms include those having an alkyl portion selected from the alkyl groups mentioned above.
Examples of an arylamino group (aryl substituted amino group), preferably an arylamino group having 6 to 24 ring carbon atoms include those having an aryl portion selected from the aromatic hydrocarbon groups mentioned above.
Examples of the optional aralkyl group having 6 to 30 ring carbon atoms include benzyl group, 2-phenylpropane-2-yl group, 1-phenylethyl group, 2-phenylethyl group, 1-phenylisopropyl group, 2-phenylisopropyl group, phenyl-t-butyl group, α-naphthylmethyl group, 1-α-naphthylethyl group, 2-α-naphthylethyl group, 1-α-naphthylisopropyl group, 2-α-naphthylisopropyl group, β-naphthylmethyl group, 1-β-naphthylethyl group, 2-β-naphthylethyl group, 1-β-naphthylisopropyl group, 2-β-naphthylisopropyl group, 1-pyrrolylmethyl group, 2-(1-pyrrolyl)ethyl group, p-methylbenzyl group, m-methylbenzyl group, o-methylbenzyl group, p-chlorobenzyl group, m-chlorobenzyl group, o-chlorobenzyl group, p-bromobenzyl group, m-bromobenzyl group, o-bromobenzyl group, p-iodobenzyl group, m-iodobenzyl group, o-iodobenzyl group, p-hydroxybenzyl group, m-hydroxybenzyl group, o-hydroxybenzyl group, p-aminobenzyl group, m-aminobenzyl group, o-aminobenzyl group, p-nitrobenzyl group, m-nitrobenzyl group, o-nitrobenzyl group, p-cyanobenzyl group, m-cyanobenzyl group, o-cyanobenzyl group, 1-hydroxy-2-phenylisopropyl group, and 1-chloro-2-phenylisopropyl group.
Examples of a carboxyalkyl group (alkyl substituted carboxyl group), preferably a carboxyalkyl group having 1 to 25 carbon atoms, preferably 1 to 5 carbon atoms, include those having an alkyl portion selected from the alkyl groups mentioned above.
Examples of a carboxyaryl group (aryl substituted carboxyl group), preferably a carboxyaryl group having 6 to 24 carbon atoms, preferably 6 to 18 carbon atoms, include those having an aryl portion selected from the aromatic hydrocarbon groups mentioned above.
Examples of a carboxamidalkyl group (alkyl substituted amide group), preferably a carboxamidalkyl group having 1 to 25 carbon atoms, preferably 1 to 5 carbon atoms include those having an alkyl portion selected from the alkyl groups mentioned above.
Examples of a carboxamidaryl group (aryl substituted amide group), preferably a carboxamidaryl group having 6 to 24 carbon atoms, preferably 6 to 18 carbon atoms, include those having an aryl portion selected from the aromatic hydrocarbon groups mentioned above.
The optional substituent is preferably a fluorine atom, a cyano group, an alkyl group having 1 to 25 carbon atoms, an aryl group having 6 to 24 ring carbon atoms, preferably 6 to 18 ring carbon atoms, and an heterocyclic group having 3 to 30 ring atoms, preferably 5 to 18 ring atoms; more preferably a cyano group, a phenyl group, a naphthyl group, a biphenyl group, a terphenyl group, a phenanthryl group, a triphenylenyl group, a fluorenyl group, a spirobifluorenyl group, a fluoranthenyl group, a residue based on a dibenzofuran ring, a residue based on a carbazole ring, and a residue based on a dibenzothiophene ring, a methyl group, an ethyl group, a n-propyl group, an isopropyl group, a n-butyl group, a s-butyl group, an isobutyl group, a t-butyl group, a cyclopentyl group, and a cyclohexyl group.
The optional substituent mentioned above may be further substituted by one or more of the optional substituents mentioned above.
The number of the optional substituents depends on the group which is substituted by said substituent(s). Preferred are 1, 2, 3 or 4 optional substituents, more preferred are 1, 2 or 3 optional substituents, most preferred are 1 or 2 optional substituents. In a further preferred embodiment, the groups mentioned above are unsubstituted.
The “carbon number of a to b” in the expression of “substituted or unsubstituted X group having a to b carbon atoms” is the carbon number of the unsubstituted X group and does not include the carbon atom(s) of an optional substituent.
The hydrogen atom referred to herein includes isotopes different from neutron numbers, i.e., light hydrogen (protium), heavy hydrogen (deuterium) and tritium.
The term “unsubstituted” referred to by “unsubstituted or substituted” means that a hydrogen atom is not substituted by one of the groups mentioned above.
In the compounds of formula (I), R1 and R1′ each independently represents a C1 to C6 alkyl group. Preferably, R1 and R1′ each independently represents a C1 to C4 alkyl group, preferably methyl, ethyl, n-propyl or n-butyl. More preferably, R1 and R1′ represent methyl.
R2 represents a substituted or unsubstituted C6 to C24 aryl group, a substituted or unsubstituted heteroaryl group having 3 to 9 carbon atoms or CN. Preferably, R2 represents a substituted or unsubstituted C6 to C24 aryl group or a substituted or unsubstituted N containing heteroaryl group having 3 to 9 carbon atoms. More preferably, R2 represents a substituted or unsubstituted C6 to C14 aryl group or a substituted or unsubstituted N containing heteroaryl group having 5 to 9 carbon atoms. Most preferably, R2 represents substituted or unsubstituted phenyl, substituted or unsubstituted biphenyl, substituted or unsubstituted naphthyl, substituted or unsubstituted phenanthrenyl, substituted or unsubstituted anthracenyl, substituted or unsubstituted triphenylenyl, substituted or unsubstituted fluoranthenyl, substituted or unsubstituted pyridyl, substituted or unsubstituted benzimidazolyl or substituted or unsubstituted quinolinyl, further most preferably substituted or unsubstituted phenyl, substituted or unsubstituted biphenyl, substituted or unsubstituted naphthyl or substituted or unsubstituted pyridyl or substituted or unsubstituted quinolinyl.
Examples for suitable groups R2 are:
wherein R represents a C1 to C6 alkyl group or a substituted or unsubstituted C6 to C18 aryl group, and the dotted lines are bonding sites.
m is 0, 1, 2, 3, 4 or 5, preferably 0, 1, 2 or 3, more preferably 0, 1 or 2, In the case that m is at least 2, the residues R2 are the same or different. In a preferred embodiment, the compound of formula (I) comprises 0, 1, 2 or 3, preferably 0, 1 or 2 residues R2 which are not hydrogen.
L represents a substituted or unsubstituted C6 to C40 arylene group. Preferably, L represents a substituted or unsubstituted C6 to C18 arylene group, more preferably, a substituted or unsubstituted phenylene, a substituted or unsubstituted biphenylene, a substituted or unsubstituted terphenylene, a substituted or unsubstituted triphenylene-diyl, or a substituted or unsubstituted naphthylene. Most preferably, L represents a substituted or unsubstituted phenylene, a substituted or unsubstituted biphenylene, or a substituted or unsubstituted naphthylene.
n is 1, 2 or 3. In the case that n is at least 2, the groups L are the same or different.
Preferred groups -(L)n- in the case that n is 1 are: a substituted or unsubstituted phenylene, a substituted or unsubstituted biphenylene, or a substituted or unsubstituted naphthylene, more preferably a substituted or unsubstituted phenylene, or a substituted or unsubstituted biphenylene.
Preferred groups -(L)n- in the case that n is 2 (-(L)2-) are:
wherein the dotted lines are bonding sites.
Preferred groups -(L)n- are:
wherein the dotted lines are bonding sites.
Preferred compounds of formula (I) are defined as follows:
wherein
Preferably, the compounds of formula (I) have a molecular weight of 500 to 1000 g/mol, preferably 550 to 885 g/mol.
The compounds of formula (I) are preferably represented by the compounds of formulae (Ia), (Ib), (Ic) and (Id):
wherein the residues, groups and indices R1, R1′, R2, L, m and n have been described above.
Below, examples for compounds of formula (I) are given:
The compounds of formula (I) are for example prepared by the following process:
wherein
wherein
The residues, groups and indices R1, R1′, R2, L, m and n have been described above.
In the case that Z in the compound of formula (II) is —BQ2, the compounds of formula (II) are for example prepared from the corresponding halides in the presence of a borylation reagent:
Suitable borylation reagents are boronic acids or boronic esters, for example alkyl-, alkenyl-, alkynyl-, and aryl-boronic esters. Preferred borylation reagents have the general formula (RO)2BH or (RO)2B—B(OR)2. For example, Pinacolborane (Hbpin), Bis(pinacolato)diboron (B2Pin2), and bis(catecholato)diborane (B2Cat2). Further suitable borylation reagents are dioxaborolanes, for example 2-isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane.
The borylation can be carried out in the presence or in the absence of a catalyst.
In the case that the borylation is carried out in the absence of a catalyst, the halide is for example treated with an organolithium reagent followed by borylation with a borylation agent. Suitable borylation agents are mentioned above.
In the case that the borylation is carried out in the presence of a catalyst, preferred catalysts are Pd catalysts. Suitable Pd catalysts are for example Pd(0) complexes with bidentate ligands like dba (dibenzylideneacetone), or Pd(II) salts like PdCl2 or Pd(OAc)2 in combination with bidentate phosphine ligands such as dppf ((diphenylphosphino)ferrocene), dppp ((diphenylphosphino)propane), BINAP (2,2′-Bis(diphenylphosphino)-1,1′-binaphthyl), Xantphos (4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene), DPEphos (Bis[(2-diphenylphosphino)phenyl]ether) or Josiphos, or in combination with monodentate phosphine-ligands like tri-phenylphosphine, tri-ortho-tolyl phosphine, tri-tertbutylphosphine, tricyclohexylphosphine, 2-Di-cyclohexylphosphino-2′,6′-dimethoxybiphenyl (SPhos), 2-Dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (XPhos), or N-heterocyclic carbenes such as 1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidene (IPr), 1,3-Dimesitylimidazol-2-ylidene (Imes).
Hal and —BQ2 are as defined above.
Josiphos:
wherein R and R′ are generally substituted or unsubstituted phenyl.
The compounds of formula (III) are for example prepared by coupling a compound of formula (IV) with a compound of formula (V) in the presence of a strong base like n-BuLi:
Details of the reaction steps and process conditions are mentioned in the examples of the present application. The production method of the compounds of formula (I) according to the present invention is not particularly limited and it is produced according to known methods, for example, by a Suzuki coupling as described in Journal of American Chemistry Society, 1999, 121, 9550 to 9561 or Chemical Reviews, 1995, 95, 2457 to 2483 or Kumada coupling described in Org. Lett., 2010, 12, 2298-2301 or Angew. Chem., 2002, 114, 4218-4221.
It has been found that the compounds of formula (I) are particularly suitable for use in applications in which charge carrier conductivity is required, especially for use in organic electronics applications, for example selected from switching elements such as organic transistors, e.g. organic FETs and organic TFTs, organic solar cells and organic light-emitting diodes (OLEDs).
The term organic EL device (organic electroluminescence device) is used interchangeably with the term organic light-emitting diode (OLED) in the present application; i.e. both terms have the same meaning in the sense of the present application.
The present invention further relates to a material for an organic EL device comprising at least one compound of formula (I).
The organic transistor generally includes a semiconductor layer formed from an organic layer with charge transport capacity; a gate electrode formed from a conductive layer; and an insulating layer introduced between the semiconductor layer and the conductive layer. A source electrode and a drain electrode are mounted on this arrangement in order thus to produce the transistor element. In addition, further layers known to those skilled in the art may be present in the organic transistor. The layers with charge transport capacity may comprise the compound of formula (I).
The organic solar cell (photoelectric conversion element) generally comprises an organic layer present between two plate-type electrodes arranged in parallel. The organic layer may be configured on a comb-type electrode. There is no particular restriction regarding the site of the organic layer and there is no particular restriction regarding the material of the electrodes. When, however, plate-type electrodes arranged in parallel are used, at least one electrode is preferably formed from a transparent electrode, for example an ITO electrode or a fluorine-doped tin oxide electrode. The organic layer is formed from two sublayers, i.e. a layer with p-type semiconductor properties or hole transport capacity, and a layer formed with n-type semiconductor properties or charge transport capacity. In addition, it is possible for further layers known to those skilled in the art to be present in the organic solar cell. The layers with charge transport capacity may comprise the compound of formula (I).
The compounds of formula (I) being particularly suitable in OLEDs for use as charge and/or exciton-blocking material, i.e. as electron/exciton-blocking material or as hole/exciton-blocking material, and/or charge-transporting material, i.e. hole-transporting material or electron-transporting material, preferably as electron-transporting material and/or hole-blocking material.
In the case of use of the inventive compounds of formula (I) in OLEDs, OLEDs having good overall properties, preferably a long lifetime, high external quantum efficiencies (EQE) and/or a low driving voltage are obtained.
According to one aspect of the present invention, a material for an organic electroluminescence device, comprising at least one compound of formula (I) is provided.
According to another aspect of the invention, the following organic electroluminescence device is provided, comprising at least one compound of formula (I). The organic electroluminescence device generally comprises: a cathode, an anode, and one or more organic thin film layers comprising an emitting layer disposed between the cathode and the anode, wherein at least one layer of the organic thin film layers comprises at least one compound of formula (I).
In the present specification, regarding “one or more organic thin film layers disposed between the cathode and the anode”, if only one organic layer is present between the cathode and the anode, it means the layer, and if plural organic layers are present between the cathode and the anode, it means at least one layer thereof.
According to another aspect of the invention, the use of a compound of formula (I) according to the present invention in an organic electroluminescence device is provided.
In one embodiment, the organic EL device has a hole-transporting layer between the anode and the emitting layer.
In one embodiment, the organic EL device has an electron-transporting layer between the cathode and the emitting layer.
In one embodiment, the organic EL device has a hole-blocking layer between the electron-transporting layer and the emitting layer.
Layer(s) between the Emitting Layer and the Anode:
In the organic EL device according to the present invention, one or more organic thin film layers may be present between the emitting layer and the anode. If only one organic layer is present between the emitting layer and the anode, it means that layer, and if plural organic layers are present, it means at least one layer thereof. For example, if two or more organic layers are present between the emitting layer and the anode, an organic layer nearer to the emitting layer is called the “hole-transporting layer”, and an organic layer nearer to the anode is called the “hole-injecting layer”. Each of the “hole-transporting layer” and the “hole-injecting layer” may be a single layer or may be formed of two or more layers. One of these layers may be a single layer and the other may be formed of two or more layers.
Layer(s) between the Emitting Layer and the Cathode:
Similarly, one or more organic thin film layers may be present between the emitting layer and the cathode, in the organic EL device according to the present invention (electron-transporting zone, at least including an electron-transporting layer and preferably also an electron-injecting layer and/or a hole-blocking layer). If only one organic layer is present between the emitting layer and the cathode it means that layer, and if plural organic layers are present, it means at least one layer thereof. For example, if two or more organic layers are present between the emitting layer and the cathode, an organic layer nearest to the emitting layer is called the “hole-blocking layer”, an organic layer nearest to the “hole-blocking layer” is called the “electron-transporting layer”, and an organic layer nearer to the cathode is called the “electron-injecting layer”. Each of the “hole-blocking layer”, “electron-transporting layer” and the “electron-injecting layer” may be a single layer or may be formed of two or more layers. One of these layers may be a single layer and the other may be formed of two or more layers.
The one or more organic thin film layers between the emitting layer and the cathode, preferably the “electron-transporting zone”, preferably comprises a compound represented by formula (I).
Therefore, in a preferred embodiment, the organic thin film layers of the organic electroluminescence device comprise an electron-transporting zone provided between the emitting layer and the cathode, wherein the electron-transporting zone comprises at least one compound represented by formula (I). The compound represented by formula (I) preferably functions as “hole-blocking” material in the hole-blocking layer and/or “electron-transporting” material in the electron-transporting layer.
In an exemplary embodiment, the one or more organic thin film layers of the organic EL device of the present invention at least include the emitting layer and an electron-transporting zone. The electron-transporting zone is provided between the emitting layer and the cathode and at least includes an electron-transporting layer and preferably also an electron injecting layer and/or a hole-blocking layer. The electron-transporting zone may include the electron-injecting layer and an electron-transporting layer and may further include a hole-blocking layer and optionally a space layer. In addition to the above layers, the one or more organic thin film layers may be provided by layers applied in a known organic EL device such as a hole-injecting layer, a hole transporting layer and an electron-blocking layer. The one or more organic thin film layers may include an inorganic compound.
An explanation will be made on the layer configuration of the organic EL device according to one aspect of the invention.
An organic EL device according to one aspect of the invention comprises a cathode, an anode, and one or more organic thin film layers comprising an emitting layer disposed between the cathode and the anode. The organic layer comprises at least one layer composed of an organic compound. Alternatively, the organic layer is formed by laminating a plurality of layers composed of an organic compound. The organic layer may further comprise an inorganic compound in addition to the organic compound.
At least one of the organic layers is an emitting layer. The organic layer may be constituted, for example, as a single emitting layer, or may comprise other layers which can be adopted in the layer structure of the organic EL device. The layer that can be adopted in the layer structure of the organic EL device is not particularly limited, but examples thereof include a hole-transporting zone (a hole-transporting layer, a hole-injecting layer, an electron-blocking layer, an exciton-blocking layer, etc.), an emitting layer, a spacing layer, and an electron-transporting zone (electron-transporting layer, electron-injecting layer, hole-blocking layer, etc.) provided between the cathode and the emitting layer.
The organic EL device according to one aspect of the invention may be, for example, a fluorescent or phosphorescent monochromatic light emitting device or a fluorescent/phosphorescent hybrid white light emitting device.
Further, it may be a simple type device having a single emitting unit or a tandem type device having a plurality of emitting units.
The “emitting unit” in the specification is the smallest unit that comprises organic layers, in which at least one of the organic layers is an emitting layer and light is emitted by recombination of injected holes and electrons.
In addition, the emitting layer described in the present specification is an organic layer having an emitting function. The emitting layer is, for example, a phosphorescent emitting layer, a fluorescent emitting layer or the like, and may be a single layer or a stack of a plurality of layers.
The “emitting unit” may be a stacked type unit having a plurality of phosphorescent emitting layers and/or fluorescent emitting layers. In this case, for example, a spacing layer for preventing excitons generated in the phosphorescent emitting layer from diffusing into the fluorescent emitting layer may be provided between the respective light-emitting layers.
As the simple type organic EL device, a device configuration such as anode/emitting unit/cathode can be given.
Examples for representative layer structures of the emitting unit are shown below. The layers in parentheses are provided arbitrarily:
The layer structure of the organic EL device according to one aspect of the invention is not limited to the examples mentioned above.
For example, when the organic EL device has a hole-injecting layer and a hole-transporting layer, it is preferred that a hole-injecting layer be provided between the hole-transporting layer and the anode. Further, when the organic EL device has an electron-injecting layer and an electron-transporting layer, it is preferred that an electron-injecting layer be provided between the electron-transporting layer and the cathode. Further, each of the hole-injecting layer, the hole-transporting layer, the electron-transporting layer and the electron-injecting layer may be formed of a single layer or be formed of a plurality of layers.
The plurality of phosphorescent emitting layers and/or fluorescent emitting layers may be emitting layers that emit mutually different colors. For example, the emitting unit (f) may include a hole-transporting layer/first phosphorescent layer (red light emission)/second, phosphorescent emitting layer (green light emission)/spacing layer/fluorescent emitting layer (blue light emission)/electron-transporting layer.
An electron-blocking layer may be provided between each light emitting layer and the hole-transporting layer or the spacing layer. Further, a hole-blocking layer may be provided between each emitting layer and the electron-transporting layer. By providing the electron-blocking layer or the hole-blocking layer, it is possible to confine electrons or holes in the emitting layer, thereby to improve the recombination probability of carriers in the emitting layer, and to improve light emitting efficiency.
As a representative device configuration of a tandem type organic EL device, for example, a device configuration such as anode/first emitting unit/intermediate layer/second emitting unit/cathode can be given:
The first emitting unit and the second emitting unit are independently selected from the above-mentioned emitting units, for example.
The intermediate layer is also generally referred to as an intermediate electrode, an intermediate conductive layer, a charge generating layer, an electron withdrawing layer, a connecting layer, a connector layer, or an intermediate insulating layer. The intermediate layer is a layer that supplies electrons to the first emitting unit and holes to the second emitting unit, and can be formed from known materials.
Hereinbelow, an explanation will be made on function, materials, etc. of each layer constituting the organic EL device described in the present specification.
The substrate is used as a support of the organic EL device. The substrate preferably has a light transmittance of 50% or more in the visible light region with a wavelength of 400 to 700 nm, and a smooth substrate is preferable. Examples of the material of the substrate include soda-lime glass, aluminosilicate glass, quartz glass, plastic and the like. As a substrate, a flexible substrate can be used. The flexible substrate means a substrate that can be bent (flexible), and examples thereof include a plastic substrate and the like. Specific examples of the material for forming the plastic substrate include polycarbonate, polyallylate, polyether sulfone, polypropylene, polyester, polyvinyl fluoride, polyvinyl chloride, polyimide, polyethylene naphthalate and the like. Also, an inorganic vapor deposited film can be used.
As the anode, for example, it is preferable to use a metal, an alloy, a conductive compound, a mixture thereof or the like and having a high work function (specifically, 4.0 eV or more). Specific examples of the material of the anode include indium oxide-tin oxide (ITO: Indium Tin Oxide), indium oxide-tin oxide containing silicon or silicon oxide, indium oxide-zinc oxide, indium oxide containing tungsten oxide or zinc oxide, graphene and the like. In addition, it is also possible to use gold, silver, platinum, nickel, tungsten, chromium, molybdenum, iron, cobalt, copper, palladium, titanium, and nitrides of these metals (e.g. titanium oxide).
The anode is normally formed by depositing these materials on the substrate by a sputtering method. For example, indium oxide-zinc oxide can be formed by a sputtering method by using a target in which 1 to 10 mass % zinc oxide is added relative to indium oxide. Further, indium oxide containing tungsten oxide or zinc oxide can be formed by a sputtering method by using a target in which 0.5 to 5 mass % of tungsten oxide or 0.1 to 1 mass % of zinc oxide is added relative to indium oxide.
As other methods for forming the anode, a vacuum deposition method, a coating method, an inkjet method, a spin coating method or the like can be given. When silver paste or the like is used, it is possible to use a coating method, an inkjet method or the like.
The hole-injecting layer formed in contact with the anode is formed by using a material that allows easy hole injection regardless of the work function of the anode. For this reason, in the anode, it is possible to use a common electrode material, e.g. a metal, an alloy, a conductive compound and a mixture thereof. Specifically, a material having a small work function such as alkaline metals such as lithium and cesium; alkaline earth metals such as calcium and strontium; alloys containing these metals (for example, magnesium-silver and aluminum-lithium); rare earth metals such as europium and ytterbium; and an alloy containing rare earth metals.
The hole-transporting layer is an organic layer that is formed between the emitting layer and the anode, and has a function of transporting holes from the anode to the emitting layer. If the hole-transporting layer is composed of plural layers, an organic layer that is nearer to the anode may often be defined as the hole-injecting layer. The hole-injecting layer has a function of injecting holes efficiently to the organic layer unit from the anode. Said hole-injecting layer is generally used for stabilizing hole injection from anode to hole-transporting layer which is generally consist of organic materials. Organic material having good contact with anode or organic material with p-type doping is preferably used for the hole-injecting layer.
p-doping usually consists of one or more p-dopant materials and one or more matrix materials. Matrix materials preferably have shallower HOMO level and p-dopant preferably have deeper LUMO level to enhance the carrier density of the layer. Aryl or heteroaryl amine compounds are preferably used as the matrix materials. Specific examples for the matrix material are the same as that for hole-transporting layer which is explained at the later part. Specific examples for p-dopant are the below mentioned acceptor materials, preferably the quinone compounds with one or more electron withdrawing groups, such as F4TCNQ, 1,2,3-Tris[(cyano)(4-cyano-2,3,5,6-tetrafluorophenyl)methylene]cyclopropane.
Acceptor materials, or fused aromatic hydrocarbon materials or fused heterocycles which have high planarity, are preferably used as p-dopant materials for the hole-injecting layer. Specific examples for acceptor materials are, the quinone compounds with one or more electron withdrawing groups, such as F4TCNQ(2,3,5,6-tetrafluoro-7,7,8,8-tetracyanoquinodimethane), and 1,2,3-tris[(cyano)(4-cyano-2,3,5,6-tetrafluorophenyl)methylene]cyclopropane; hexa-azatriphenylene compounds with one or more electron withdrawing groups, such as hexa-azatri-phenylene-hexanitrile; aromatic hydrocarbon compounds with one or more electron withdrawing groups; and aryl boron compounds with one or more electron withdrawing groups.
The ratio of the p-type dopant is preferably less than 20% of molar ratio, more preferably less than 10%, such as 1%, 3%, or 5%, related to the matrix material.
The hole-transporting layer is generally used for injecting and transporting holes efficiently, and aromatic or heterocyclic amine compounds are preferably used. Specific examples for compounds for the hole-transporting layer are represented by the general formula (H),
wherein
Preferably, at least one of Ar1 to Ar3 have additional one aryl or heterocyclic amine substituent, more preferably Ar1 has an additional aryl amino substituent, at the case of that it is preferable that Ar1 represents substituted or unsubstituted biphenylene group, substituted or unsubstituted fluorenylene group.
A second hole-transporting layer is preferably inserted between the first hole-transporting layer and the emitting layer to enhance device performance by blocking excess electrons or excitons.
Specific examples for second hole-transporting layer are the same as for the first hole-transporting layer. It is preferred that second hole-transporting layer has higher triplet energy to block triplet excitons, especially for phosphorescent green device, such as bicarbazole compounds, biphenylamine compounds, triphenylenyl amine compounds, fluorenyl amine compounds, carbazole substituted arylamine compounds, dibenzofuran substituted arylamine compounds, and dibenzothiophene substituted arylamine compounds.
This second hole-transporting layer also called electron-blocking layer provided adjacent to the emitting layer has a function of preventing leakage of electrons from the emitting layer to the hole-transporting layer.
The emitting layer is a layer containing a substance having a high emitting property (emitter material or dopant material). As the dopant material, various materials can be used. For example, a fluorescent emitting compound (fluorescent dopant), a phosphorescent emitting compound (phosphorescent dopant) or the like can be used. A fluorescent emitting compound is a compound capable of emitting light from the singlet excited state, and an emitting layer containing a fluorescent emitting compound is called a fluorescent emitting layer. Further, a phosphorescent emitting compound is a compound capable of emitting light from the triplet excited state, and an emitting layer containing a phosphorescent emitting compound is called a phosphorescent emitting layer.
The emitting layer preferably comprises at least one dopant material and at least one host material that allows it to emit light efficiently. In some literatures, a dopant material is called a guest material, an emitter or an emitting material. In some literatures, a host material is called a matrix material.
A single emitting layer may comprise plural dopant materials and plural host materials. Further, plural emitting layers may be present.
In the present specification, a host material combined with the fluorescent dopant is referred to as a “fluorescent host” and a host material combined with the phosphorescent dopant is referred to as the “phosphorescent host”. Note that the fluorescent host and the phosphorescent host are not classified only by the molecular structure. The phosphorescent host is a material for forming a phosphorescent emitting layer containing a phosphorescent dopant, but does not mean that it cannot be used as a material for forming a fluorescent emitting layer. The same can be applied to the fluorescent host.
No specific restrictions are generally imposed on the content of the dopant material in a host in the emitting layer. A person skilled in the art generally knows the concentration of a phosphorescent dopant respectively a fluorescent dopant usually present in a suitable host. In respect of sufficient emission and concentration quenching, the content is preferably 0.5 to 70 mass %, more preferably 0.8 to 30 mass %, further preferably 1 to 30 mass %, still further preferably 1 to 20 mass. The remaining mass of the emitting layer is generally provided by one or more host materials.
Suitable fluorescent dopants are generally known by a person skilled in the art. As a fluorescent dopant a fused polycyclic aromatic compound, a styrylamine compound, a fused ring amine compound, a boron-containing compound, a pyrrole compound, an indole compound, a carbazole compound can be given, for example. Among these, a fused ring amine compound, a boron-containing compound, carbazole compound is preferable.
As the fused ring amine compound, a diaminopyrene compound, a diaminochrysene compound, a diaminoanthracene compound, a diaminofluorene compound, a diaminofluorene compound with which one or more benzofuro skeletons are fused, or the like can be given.
As the boron-containing compound, a pyrromethene compound, a triphenylborane compound or the like can be given.
Suitable phosphorescent dopants are generally known by a person skilled in the art. As a phosphorescent dopant, a phosphorescent emitting heavy metal complex and a phosphorescent emitting rare earth metal complex can be given, for example.
As the heavy metal complex, an iridium complex, an osmium complex, a platinum complex or the like can be given. The heavy metal complex is for example an ortho-metalated complex of a metal selected from iridium, osmium and platinum.
Examples of rare earth metal complexes include terbium complexes, europium complexes and the like. Specifically, tris(acetylacetonate)(monophenanthroline)terbium(III) (abbreviation: Tb(acac)3(Phen)), tris(1,3-diphenyl-1,3-propandionate)(monophenanthroline)europium(III) (abbreviation: Eu(DBM)3(Phen)), tris[1-(2-thenoyl)-3,3,3-trifluoroacetonate](monophenanthroline)europium(III) (abbreviation: Eu(TTA)3(Phen)) or the like can be given. These rare earth metal complexes are preferable as phosphorescent dopants since rare earth metal ions emit light due to electronic transition between different multiplicity.
As a blue phosphorescent dopant, an iridium complex, an osmium complex, a platinum complex, or the like can be given, for example. Specifically, bis[2-(4′,6′-difluorophenyl)pyridinate-N,C2′]iridium(III) tetrakis(1-pyrazolyl)borate (abbreviation: FIr6), bis[2-(4′,6′-difluorophenyl) pyridinato-N,C2′]iridium(III) picolinate (abbreviation: Ir(CF3ppy)2(pic)), bis[2-(4′,6′-difluorophenyl)pyridinato-N,C2′]iridium(III) acetylacetonate (abbreviation: Flracac) or the like can be given.
As a green phosphorescent dopant, an iridium complex or the like can be given, for example. Specifically, tris(2-phenylpyridinato-N,C2′) iridium(III) (abbreviation: Ir(ppy)3), bis(1,2-diphenyl-1H-benzimidazolato)iridium(III) acetylacetonate (abbreviation: Ir(pbi)2(acac)), bis(benzo[h]quinolinato)iridium(III) acetylacetonate (abbreviation: Ir(bzq)2(acac)) or the like can be given.
As a red phosphorescent dopant, an iridium complex, a platinum complex, a terbium complex, an europium complex or the like can be given. Specifically, bis[2-(2′-benzo[4,5-α]thienyl)pyridinato-N,C3′]iridium(III) acetylacetonate (abbreviation: Ir(btp)2(acac)), bis(1-phenylisoquinolinato-N,C2′)iridium(III) acetylacetonate (abbreviation: Ir(piq)2(acac)), (acetylacetonato)bis[2,3-bis(4-fluorophenyl)quinoxalinato]iridium(III) (abbreviation: Ir(Fdpq)2(acac)), 2,3,7,8,12,13,17,18-octaethyl-21H,23H-porphyrin platinum(II) (abbreviation PtOEP) or the like can be given.
As host material, metal complexes such as aluminum complexes, beryllium complexes and zinc complexes; heterocyclic compounds such as indole compounds, pyridine compounds, pyrimidine compounds, triazine compounds, quinoline compounds, isoquinoline compounds, quinazoline compounds, dibenzofuran compounds, dibenzothiophene compounds, oxadiazole compounds, benzimidazole compounds, phenanthroline compounds; fused polyaromatic hydrocarbon (PAH) compounds such as a naphthalene compound, a triphenylene compound, a carbazole compound, an anthracene compound, a phenanthrene compound, a pyrene compound, a chrysene compound, a naphthacene compound, a fluoranthene compound; and aromatic amine compound such as triarylamine compounds and fused polycyclic aromatic amine compounds can be given, for example. Plural types of host materials can be used in combination.
As a fluorescent host, a compound having a higher singlet energy level than a fluorescent dopant is preferable. For example, a heterocyclic compound, a fused aromatic compound or the like can be given. As a fused aromatic compound, an anthracene compound, a pyrene compound, a chrysene compound, a naphthacene compound or the like are preferable. An anthracene compound is preferentially used as blue fluorescent host.
As a phosphorescent host, a compound having a higher triplet energy level as compared with a phosphorescent dopant is preferable. For example, a metal complex, a heterocyclic compound, a fused aromatic compound or the like can be given. Among these, an indole compound, a carbazole compound, a pyridine compound, a pyrimidine compound, a triazine compound, a quinolone compound, an isoquinoline compound, a quinazoline compound, a dibenzofuran compound, a dibenzothiophene compound, a naphthalene compound, a triphenylene compound, a phenanthrene compound, a fluoranthene compound or the like can be given.
Preferred host materials are substituted or unsubstituted polyaromatic hydrocarbon (PAH) compounds, substituted or unsubstituted polyheteroaromatic compounds, substituted or unsubstituted anthracene compounds, or substituted or unsubstituted pyrene compounds, preferably substituted or unsubstituted anthracene compounds or substituted or unsubstituted pyrene compounds, more preferably substituted or unsubstituted anthracene compounds, most preferably anthracene compounds represented by formula (10) below.
In the formula (10), Ar31 and Ar32 each independently represent a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms or a heterocyclic group having 5 to 50 ring atoms.
R81 to R88 each independently represent a hydrogen atom, a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms, a substituted or unsubstituted heterocyclic group having 5 to 50 ring atoms, a substituted or unsubstituted alkyl group having 1 to 50 carbon atoms, a substituted or unsubstituted alkoxy group having 1 to 50 carbon atoms, a substituted or unsubstituted aralkyl group having 7 to 50 carbon atoms, a substituted or unsubstituted aryloxy group having 6 to 50 ring carbon atoms, a substituted or unsubstituted arylthio group having 6 to 50 ring carbon atoms, a substituted or unsubstituted alkoxycarbonyl group having 2 to 50 carbon atoms, a substituted or unsubstituted silyl group, a carboxyl group, a halogen atom, a cyano group, a nitro group or a hydroxyl group.
In formula (10):
The aryl group having 6 to 50 ring carbon atoms is preferably an aryl group having 6 to 40 ring carbon atoms, more preferably an aryl group having 6 to 30 ring carbon atoms.
The heterocyclic group having 5 to 50 ring atoms is preferably a heterocyclic group having 5 to 40 ring atoms, more preferably a heterocyclic group having 5 to 30 ring atoms. More preferably, the heterocyclic group is a substituted or unsubstituted heteroaryl group having 5 to 30 ring atoms. Suitable substituted or unsubstituted heteroaryl groups are mentioned above.
The alkyl group having 1 to 50 carbon atoms is preferably an alkyl group having 1 to 30 carbon atoms, more preferably an alkyl group having 1 to 10 carbon atoms, further preferably an alkyl group having 1 to 5 carbon atoms.
The alkoxy group having 1 to 50 carbon atoms is preferably an alkoxy group having 1 to 30 carbon atoms, more preferably an alkoxy group having 1 to 10 carbon atoms, further preferably an alkoxy group having 1 to 5 carbon atoms.
The aralkyl group having 7 to 50 carbon atoms is preferably an aralkyl group having 7 to 30 carbon atoms, more preferably an aralkyl group having 7 to 20 carbon atoms.
The aryloxy group having 6 to 50 ring carbon atoms is preferably an aryloxy group having 6 to 40 ring carbon atoms, more preferably an aryloxy group having 6 to 30 ring carbon atoms.
The arylthio group having 6 to 50 ring carbon atoms is preferably an arylthio group having 6 to 40 ring carbon atoms, more preferably an arylthio group having 6 to 30 ring carbon atoms.
The alkoxycarbonyl group having 2 to 50 carbon atoms is preferably an alkoxycarbonyl group having 2 to 30 carbon atoms, more preferably an alkoxycarbonyl group having 2 to 10 carbon atoms, further preferably an alkoxycarbonyl group having 2 to 5 carbon atoms.
Examples of the halogen atom are a fluorine atom, a chlorine atom and a bromine atom.
Ar31 and Ar32 are preferably a substituted or unsubstituted aryl group having 6 to 50 ring carbon atoms.
The electron-transporting zone is an organic layer or a plurality of organic layers that is formed between the emitting layer and the cathode and has a function of transporting electrons from the cathode to the emitting layer. The electron-transporting zone therefore comprises at least one electron-transporting layer comprising an electron-transporting material. When the electron-transporting zone is formed of plural layers, an organic layer or an inorganic layer that is nearer to the cathode is often defined as the electron-injecting layer (see for example
According to one embodiment, it is therefore preferred that the electron-transporting zone comprises in addition to the electron-transporting layer one or more layer(s) like an electron-injecting layer to enhance efficiency and lifetime of the device, a hole-blocking layer or an exciton/triplet-blocking layer (layer 7 in
In one preferred embodiment of the present invention, the compound of the formula (I) is present in the electron-transporting zone, as an electron-transporting material, an electron-injecting material, a hole-blocking material, an exciton-blocking material and/or a triplet-blocking material. More preferably, the compound of the formula (I) is present in the electron-transporting zone as an electron-transporting material and/or a hole-blocking material.
According to one embodiment, it is preferred that an electron-donating dopant be contained in the interfacial region between the cathode and the emitting unit. Due to such a configuration, the organic EL device can have an increased luminance or a long life. Here, the electron-donating dopant means one having a metal with a work function of 3.8 eV or less. As specific examples thereof, at least one selected from an alkali metal, an alkali metal complex, an alkali metal compound, an alkaline earth metal, an alkaline earth metal complex, an alkaline earth metal compound, a rare earth metal, a rare earth metal complex and a rare earth metal compound or the like can be mentioned.
As the alkali metal, Li (work function: 2.9 eV), Na (work function: 2.36 eV), K (work function: 2.28 eV), Rb (work function: 2.16 eV), Cs (work function: 1.95 eV) and the like can be given. One having a work function of 2.9 eV or less is particularly preferable. Among them, K, Rb and Cs are preferable. Rb or Cs is further preferable. Cs is most preferable. As the alkaline earth metal, Ca (work function: 2.9 eV), Sr (work function: 2.0 eV to 2.5 eV), Ba (work function: 2.52 eV), Mg (work function: 3.68 eV) and the like can be given. One having a work function of 2.9 eV or less is particularly preferable. As the rare-earth metal, Sc, Y, Ce, Tb, Yb and the like can be given. One having a work function of 2.9 eV or less is particularly preferable.
Examples of the alkali metal compound include an alkali chalcogenide such as Li2O, Na2O, Cs2O, K2O, Na2S or Na2Se, and an alkali halide such as LiF, NaF, CsF, KF, LiCl, KCl and NaCl. Among them, LiF, Li2O and NaF are preferable. Examples of the alkaline earth metal compound include BaO, SrO, CaO, BeO, BaS, CaSe and mixtures thereof such as BaxSr1−xO (0<x<1) and BaxCa1−xO (0<x<1). Alkaline earth metal halides are for example fluorides such as CaF2, BaF2, SrF2, MgF2 and BeF2. Among them, BaO, SrO and CaO are preferable. Examples of the rare earth metal compounds include one or more oxides, nitrides, oxidized nitrides or halides, especially fluorides, containing at least one element selected from Yb, Sc, Y, Ce, Gd, Tb and the like, for example YbF3, ScF3, ScO3, Y2O3, Ce2O3, GdF3 and TbF3. Among these, YbF3, ScF3 and TbF3 are preferable. Further suitable dopants are one or more oxides, nitrides and oxidized nitrides of Al, Ga, In, Cd, Si, Ta, Sb and Zn and nitrides and oxidized nitrides of Ba, Ca, Sr, Yb, Li, Na and Mg.
The alkali metal complexes, the alkaline earth metal complexes and the rare earth metal complexes are not particularly limited as long as they contain, as a metal ion, at least one of alkali metal ions, alkaline earth metal ions, and rare earth metal ions. Meanwhile, preferred examples of the ligand include, but are not limited to, quinolinol, benzoquinolinol, acridinol, phenanthridinol, hydroxyphenyloxazole, hydroxyphenylthiazole, hydroxydiaryloxadiazole, hydroxydiarylthiadiazole, hydroxyphenylpyridine, hydroxyphenylbenzimidazole, hydroxybenzotriazole, hydroxyfluborane, bipyridyl, phenanthroline, phthalocyanine, porphyrin, cyclopentadiene, β-diketones, and azomethines.
Regarding the addition form of the electron-donating dopant, it is preferred that the electron-donating dopant be formed in a shape of a layer or an island in the interfacial region. A preferred method for the formation is a method in which an organic compound (a light emitting material or an electron-injecting material) for forming the interfacial region is deposited simultaneously with deposition of the electron-donating dopant by a resistant heating deposition method, thereby dispersing the electron-donating dopant in the organic compound.
In a case where the electron-donating dopant is formed into the shape of a layer, the light-emitting material or electron-injecting material which serves as an organic layer in the interface is formed into the shape of a layer. After that, a reductive dopant is solely deposited by the resistant heating deposition method to form a layer preferably having a thickness of from 0.1 nm to 15 nm. In a case where the electron-donating dopant is formed into the shape of an island, the emitting material or the electron-injecting material which serves as an organic layer in the interface is formed into the shape of an island. After that, the electron-donating dopant is solely deposited by the resistant heating deposition method to form an island preferably having a thickness of from 0.05 nm to 1 nm.
As the electron-transporting material used in the electron-transporting layer other than a compound of the formula (I), an aromatic heterocyclic compound having one or more hetero atoms in the molecule may preferably be used. In particular, a nitrogen-containing heterocyclic compound is preferable.
According to one embodiment, it is preferable that the electron-transporting layer comprises a nitrogen-containing heterocyclic metal chelate.
According to another embodiment, it is preferable that the electron-transporting layer comprises a substituted or unsubstituted nitrogen containing heterocyclic compound. Specific examples of preferred heterocyclic compounds for the electron-transporting layer are, 6-membered azine compounds; such as pyridine compounds, pyrimidine compounds, triazine compounds, pyrazine compounds, preferably pyrimidine compounds or triazine compounds; 6-membered fused azine compounds, such as quinolone compounds, isoquinoline compounds, quinoxaline compounds, quinazoline compounds, phenanthroline compounds, benzoquinoline compounds, benzoisoquinoline compounds, dibenzoquinoxaline compounds, preferably quinolone compounds, isoquinoline compounds, phenanthroline compounds; 5-membered heterocyclic compounds, such as imidazole compounds, oxazole compounds, oxadiazole compounds, triazole compounds, thiazole compounds, thiadiazole compounds; fused imidazole compounds, such as benzimidazole compounds, imidazopyridine compounds, naphthoimidazole compounds, benzimidazophenanthridine compounds, benzimidzobenzimidazole compounds, preferably benzimidazole compounds, imidazopyridine compounds or benzimidazophenanthridine compounds.
According to another embodiment, it is preferable the electron-transporting layer comprises a phosphine oxide compound represented as Arp1Arp2ArP3P═O. Arp1 to Arp3 are the substituents of phosphor atom and each independently represent substituted or unsubstituted above mentioned aryl group or substituted or unsubstituted above mentioned heterocyclic group.
According to another embodiment, it is preferable that the electron-transporting layer comprises aromatic hydrocarbon compounds. Specific examples of preferred aromatic hydrocarbon compounds for the electron-transporting layer are, oligo-phenylene compounds, naphthalene compounds, fluorene compounds, fluoranthenyl group, anthracene compounds, phenanthrene compounds, pyrene compounds, triphenylene compounds, benzanthracene compounds, chrysene compounds, benzphenanthrene compounds, naphthacene compounds, and benzochrysene compounds, preferably anthracene compounds, pyrene compounds and fluoranthene compounds.
A hole-blocking layer may be provided adjacent to the emitting layer, and has a function of preventing leakage of holes from the emitting layer to the electron-transporting layer. In order to improve hole-blocking capability, a material having a deep HOMO level is preferably used.
In a preferred embodiment, the organic electroluminescence device according to the present invention, comprises an electron-transporting zone, wherein the electron-transporting zone further comprises at least one of an electron-donating dopant and preferably an organic metal complex. Suitable dopants are mentioned above.
More preferably, the at least one of an electron-donating dopant and an organic metal complex is at least one selected from the group consisting of an alkali metal, an alkali metal compound, an alkali metal complex, an alkaline earth metal, an alkaline earth metal compound, an alkaline earth metal complex, a rare earth metal, a rare earth metal compound, and a rare earth metal complex.
For the cathode, a metal, an alloy, an electrically conductive compound, and a mixture thereof, each having a small work function (specifically, a work function of 3.8 eV or less) are preferably used. Specific examples of a material for the cathode include an alkali metal such as lithium and cesium; an alkaline earth metal such as magnesium, calcium, and strontium; an alloy containing these metals (for example, magnesium-silver, aluminum-lithium); a rare earth metal such as europium and ytterbium; and an alloy containing a rare earth metal.
The cathode is usually formed by a vacuum vapor deposition or a sputtering method. Further, in the case of using a silver paste or the like, a coating method, an inkjet method, or the like can be employed.
Moreover, when the electron-injecting layer is provided, various electrically conductive materials such as aluminum, silver, ITO, graphene, indium oxide-tin oxide containing silicon or silicon oxide, selected independently from the work function, can be used to form a cathode. These electrically conductive materials are made into films using a sputtering method, an inkjet method, a spin coating method, or the like.
In the organic EL device, pixel defects based on leakage or a short circuit are easily generated since an electric field is applied to a thin film. In order to prevent this, it is preferred to insert an insulating thin layer between a pair of electrodes. Examples of materials used in the insulating layer include aluminum oxide, lithium fluoride, lithium oxide, cesium fluoride, cesium oxide, magnesium oxide, magnesium fluoride, calcium oxide, calcium fluoride, aluminum nitride, titanium oxide, silicon oxide, germanium oxide, silicon nitride, boron nitride, molybdenum oxide, ruthenium oxide, and vanadium oxide. A mixture thereof may be used in the insulating layer, and a laminate of a plurality of layers that include these materials can be also used for the insulating layer.
A spacing layer is a layer for example provided between a fluorescent emitting layer and a phosphorescent emitting layer when a fluorescent emitting layer and a phosphorescent emitting layer are stacked in order to prevent diffusion of excitons generated in the phosphorescent emitting layer to the fluorescent emitting layer or in order to adjust the carrier balance. Further, the spacing layer can be provided between the plural phosphorescent emitting layers.
Since the spacing layer is foe example provided between the emitting layers, the material used for the spacing layer is preferably a material having both electron-transporting capability and hole-transporting capability. In order to prevent diffusion of the triplet energy in adjacent phosphorescent emitting layers, it is preferred that the spacing layer have a triplet energy of 2.6 eV or more. As the material used for the spacing layer, the same materials as those used in the above-mentioned hole-transporting layer can be given.
A triplet-blocking layer (exciton-blocking layer) may be provided adjacent to the emitting layer.
The triplet-blocking layer has a function of preventing triplet excitons generated in the emitting layer from diffusing into neighboring layers to trap the triplet excitons within the emitting layer, thereby suppressing energy deactivation of the triplet excitons on molecules other than the emitting dopant in the electron-transporting layer.
When the triplet-blocking layer is provided in a phosphorescent device, triplet energy of a phosphorescent dopant in the emitting layer is denoted as ET d and triplet energy of a compound used as the triplet-blocking layer is denoted as ET TB. In an energy relationship of ET d<ET TB, triplet excitons of the phosphorescent dopant are trapped (cannot be transferred to another molecule) to leave no alternative route for energy deactivation other than emission on the dopant, so that highly efficient emission can be expected. However, when an energy gap (ΔET=ET TB−ET d) is small even though the relationship of ET d<ET TB is satisfied, under actual environments for driving a device (i.e., at around the room temperature), it is considered that triplet excitons can be transferred to another molecule irrespective of the energy gap LET by absorbing heat energy around the device. Particularly, since the excitons of the phosphorescent device have longer lifetime than those of a fluorescent device, influence by heat absorption during transfer of the excitons is more likely to be given on the phosphorescent device relative to the fluorescent device. A larger energy gap ΔET relative to heat energy at the room temperature is preferable, more preferably 0.1 eV or more, further preferable at 0.2 eV or more. On the other hand, in the fluorescent device, the organic-EL-device material according to the exemplary embodiment is usable as the triplet-blocking layer in the TTF device structure described in International Publication WO2010/134350A1.
The method for forming each layer of the organic EL device of the invention is not particularly limited unless otherwise specified. A known film-forming method such as a dry film-forming method, a wet film-forming method or the like can be used. Specific examples of the dry film-forming method include a vacuum deposition method, a sputtering method, a plasma method, an ion plating method, and the like. Specific examples of the wet film-forming method include various coating methods such as a spin coating method, a dipping method, a flow coating method, an inkjet method, and the like.
The film thickness of each layer of the organic EL device of the invention is not particularly limited unless otherwise specified. If the film thickness is too small, defects such as pin-holes are likely to occur to make it difficult to obtain a sufficient luminance. If the film thickness is too large, a high driving voltage is required to be applied, leading to a lowering in efficiency. In this respect, the film thickness is preferably 5 nm to 10 μm, and more preferably 10 nm to 0.2 μm.
The present invention further relates to an electronic equipment (electronic apparatus) comprising the organic electroluminescence device according to the present application. Examples of the electronic apparatus include display parts such as an organic EL panel module; display devices of television sets, mobile phones, smart phones, and personal computer, and the like; and emitting devices of a lighting device and a vehicle lighting device.
It should be noted that the invention is not limited to the above exemplary embodiments but may include any modification and improvement as long as such modification and improvement are compatible with the invention.
The following examples are included for illustrative purposes only and do not limit the scope of the claims. Unless otherwise stated, all parts and percentages are by weight.
The following examples are included for illustrative purposes only and do not limit the scope of the claims. Unless otherwise stated, all parts and percentages are by weight.
Compounds used in organic EL devices of Inventive Application Examples 1 to 8
Compounds used in organic EL devices of Comparative Application Examples 1 to 13
Other compounds used in organic EL devices of Application Examples 1 to 8 and Comparative Application Examples 1 to 13
A glass substrate with 130 nm-thick indium-tin-oxide (ITO) transparent electrode (manufactured by Geomatec Co., Ltd.) used as an anode was first treated with N2 plasma for 100 sec. This treatment also improved the hole-injection properties of the ITO. The cleaned substrate was mounted on a substrate holder and loaded into a vacuum chamber. Thereafter, the organic materials specified below were applied by vapor deposition to the ITO substrate at a rate of approx. 0.2-1 Å/sec at about 10−6-10−8 mbar. As a hole-injection layer, 10 nm-thick mixture of Compound HT and 3% by weight of Compound HI were applied. Then 80 nm-thick of Compound HT and 5 nm of Compound EB were applied as hole-transporting layer 1 and electron-blocking layer, respectively. Subsequently, a mixture of 4% by weight of an emitter Compound BD-1 and 96% by weight of host Compound BH-1 were applied to form a 25 nm-thick fluorescent-emitting layer. On the emitting layer, 5 nm-thick Compound HB was applied as an hole-blocking layer and 20 nm of mixture of 50% by weight of Comparative Compound 1 and lithium quinolate (Liq) as electron transporting layer. Finally, 1 nm-thick Yb was deposited as an electroninjection layer and 80 nm-thick Al was then deposited as a cathode to complete the device. The device was sealed with a glass lid and a getter in an inert nitrogen atmosphere with less than 1 ppm of water and oxygen. To characterize the OLED, electroluminescence spectra were recorded at various currents and voltages. In addition, the current-voltage characteristic was measured in combination with the luminance to determine luminous efficiency and external quantum efficiency (EQE). Lifetime of OLED device was measured as a decay of the luminance at constant current density of 50 mA/cm2 to 95% of its initial value. The device results are shown in Table 1.
The layer structure of the device was:
Comparative Application Example 1 was repeated except for using either the Compound 1, the Compound 2, the Compound 4, or the Compound 5 instead of the Comparative Compound 1 in the electron-transporting layer. The device results are shown in Table 1.
Comparative Application Example 1 was repeated except for using either the Comparative Compound 2 or the Comparative Compound 3 or the Comparative Compound 4 or the Comparative Compound 5 instead of the Comparative Compound 1 in the electron-transporting layer. The device results are shown in Table 1.
These results demonstrate that the efficiency is improved while the lifetime is retained in the case that the Inventive Compounds 1, 2, 4 and 5 are used instead of the Comparative Compounds 1, 2, 3, 4 and 5 as the electron transporting material in an OLED device.
Comparative Application Example 1 was repeated except for using: the Compound BH-2 instead of the Compoound BH-1 as a host in fluorescent-emitting layer; either the Comparative Compound 1 or the Comparative Compound 2 or the Comparative Compound 4 or the Comparative Compound 5 instead of the Compound HB in the hole-blocking layer; and mixture of 50% by weight of Compound ET-1 and lithium quinolate (Liq) instead of the mixture of 50% by weight of Comparative Compound 1 and lithium quinolate (Liq) in the electron-transporting layer. The device results are shown in Table 2.
Comparative Application Example 6 was repeated except for using the Compound 1 instead of the Comparative Compound 1 in the hole-blocking layer. The device results are shown in Table 2.
These results demonstrate that the efficiency and lifetime are improved in the case that the Compound 1 is used instead of the Comparative Compound 1 or the Comparative Compound 2 or the Comparative Compound 4 or the Comparative Compound 5 as hole-blocking material in an OLED device.
Comparative Application Example 6 was repeated except for using: Compound HB-2 instead of Comparative Compound 1 in the hole-blocking layer; and mixture of 50% by weight of either the Comparative Compound 1 or the Comparative Compound 2 or the Comparative Compound 3 or the Comparative Compound 5 and 50% by weight of lithium quinolate (Liq) instead of mixture of 50% by weight of Compound ET-1 and 50% by weight of lithium quinolate (Liq) in the electron-transporting layer. The device results are shown in Table 3.
Comparative Application Example 10 was repeated except for using either the Compound 3, the Compound 4 or the Compound 5 respectively instead of the Comparative Compound 1 in the electron-transporting layer. The device results are shown in Table 3.
These results demonstrate that the efficiency and lifetime of OLED are improved in the case that the Inventive Compounds 3, 4 and 5 are used instead of either the Comparative Compound 1 or the Comparative Compound 2 or the Comparative Compound 3 or the Comparative Compound 5 as the electron-transporting material in an OLED device.
Compounds synthesized in Comparative Preparation Examples 1 to 4
Step 1
In a 1 l three necked round-bottomed flask with magnetic stirrer, thermometer, reflux condenser were placed 4-bromo-9,9-dimethyl-9H-fluorene (10 g, 36.6 mmol), Bis(pinacolato)diboron (18.59 g, 73.2 mmol), Potassium acetate (10.78 g, 110 mmol) and Dioxane (400 ml). The white suspension was evacuated and backfilled with argon 5 times. Then Argon was bubbled through the suspension for 30 min. PdCl2(dppf) (0.897 g, 1.098 mmol) was added and the orange suspension was evacuated and backfilled with argon 5 times and then heated to reflux. After 6 hours the dark suspension was filtered hot through Hyflo, and washed 3× with Dioxane (100 ml each). The filtrate was concentrated to yield 30.1 g of a brown, viscous oil.
200 ml MeOH were added and put shortly into an ultasonic bath. The resulting suspension was cooled to 0° C. for 30 min with stirring, filtered and washed 3× with ice cold MeOH (25 ml each). The solid was dried in the hood over night to yield 9.28 g (79.2% of theory) of Intermediate 1 as a brown solid.
1H NMR (400 MHz, Tetrachloroethane-d2): δ 8.66-8.44 (m, 1H), 7.75 (dd, J=7.3, 1.4 Hz, 1H), 7.54 (dd, J=7.5, 1.3 Hz, 1H), 7.50-7.42 (m, 1H), 7.42-7.28 (m, 3H), 1.47 (d, J=2.5 Hz, 18H).
Step 2
A 1 l three necked round-bottomed flask with magnetic stirrer, thermometer was charged with 4-(4-bromophenyl)dibenzo[b,d]thiophene (20 g, 59.0 mmol), followed by THF (500 ml). The colorless, clear solution was cooled with an Aceton/dry ice-bath to −74° C. under Argon, before 2.5M n-BuLi (25.9 ml, 64.8 mmol) was added slowly within 15 min keeping the internal temperature between −76 and −73° C. The reaction mixture (green solution) was stirred at −74° C. for 1 hour.
A second 1 l three necked round-bottomed flask with magnetic stirrer, thermometer was charged with 2-([1,1′-biphenyl]-4-yl)-4,6-dichloro-1,3,5-triazine (35.6 g, 118 mmol) suspended in THF (250 ml). The mixture was cooled with an Aceton/dry ice-bath to −76° C., before the green solution from step 1 was added slowly with a canula over a period of 2.5 hours (internal temperature −76° C. to −73° C. during addition). The reaction mixture was stirred at −75° C. for 3 hours, then 500 ml MeOH were added to form a yellow precipitate that was filtered off, washed with MeOH and dried at 60° C./125 mbar overnight. The crude product was recrystallized from Chlorobenzene and then from Dichlorobenzene to yield 13 g (41.9% of theory) of Intermediate 2 as a yellow solid.
1H NMR (300 MHz, Chloroform-d): δ 8.87-8.80 (m, 2H), 8.79-8.72 (m, 2H), 8.28-8.20 (m, 2H), 8.03-7.95 (m, 2H), 7.92-7.80 (m, 3H), 7.77-7.69 (m, 2H), 7.68-7.40 (m, 7H).
Step 3
A 250 ml three necked round-bottomed flask with magnetic stirrer, thermometer and reflux condenser was charged with Intermediate 2 (3.0 g, 5.70 mmol), Intermediate 1 (2.009 g, 6.27 mmol), tetrabutylammonium bromide (0.092 g, 0.285 mmol) and K2CO3 (2.364 g, 17.11 mmol), followed by Toluene (120 ml) and Water (30 ml). The reaction mixture was evacuated three times and flushed with nitrogen. Afterwards nitrogen was bubbled through the reaction mixture for 30 minutes, before Pd(PPh3)4 (0.330 g, 0.285 mmol) was added. The yellow suspension was stirred at reflux for 16 hours. The brown solution was filtered through a pad of silica and washed with Toluene. The Toluene phase was washed with water, dried over Mg2SO4 and concentrated to give 4.78 g of a brown oil.
The product was purified by chromatography using Heptane/Methylene Chloride=9:1 as eluent followed by crystallization from Cyclohexane to yield 2.37 g (57.7% of theory) of Compound 1 as a white solid.
1H NMR (300 MHz, Methylene Chloride-d2): δ 8.99-8.90 (m, 2H), 8.90-8.83 (m, 2H), 8.31-8.17 (m, 2H), 8.05-7.96 (m, 3H), 7.96-7.81 (m, 4H), 7.80-7.68 (m, 3H), 7.64 (dd, J=4.5, 0.8 Hz, 2H), 7.59-7.46 (m, 6H), 7.46-7.39 (m, 1H), 7.35 (td, J=7.5, 1.1 Hz, 1H), 7.16 (ddd, J=7.9, 7.3, 1.3 Hz, 1H), 1.59 (s, 6H).
Step 1
A 500 ml three necked round-bottomed flask with magnetic stirrer, thermometer was charged with 4-(3-bromophenyl)dibenzo[b,d]thiophene (20 g, 59.0 mmol), followed by THF (300 ml). The colorless, clear solution was cooled with an Aceton/dry ice-bath to −74° C. under Argon, before 2.5M n-BuLi (28.3 ml, 70.7 mmol) was added slowly within 30 min keeping the internal temperature below −73° C. The reaction mixture (green solution) was stirred at −74° C. for 1 hour. A second 2 l three necked round-bottomed flask with magnetic stirrer, thermometer was charged with 2,4-dichloro-6-phenyl-1,3,5-triazine (33.3 g, 147 mmol) dissolved in THF (600 ml). The solution was cooled with an Aceton/dry ice-bath to −76° C., before the green solution prepared above was added slowly with a canula over a period of 35 min (internal temperature kept below −73° C. during addition). The reaction mixture was stirred at −75° C. for 1 hour, then warmed to room temperature and stirred at that temperature for 1 hour. The reaction mixture was concentrated to 70 g solution, added to 1 l MeOH under vigorous stirring. The suspension formed was stirred for 5 min at room temperature, filtered and washed 3× with MeOH (100 ml each) and dried at ambient conditions over night to yield 13.02 g of a slightly greenish solid. The crude product was dissolved in 300 ml Toluene under reflux, 20 g silica were added and stirred for 5 min. The mixture was filtered hot through Hyflo, washed 3× with hot Toluene (100 ml each). The filtrate was concentrated to 115 g solution, then cooled to room temperature with stirring, then to 0° C. and stirred for 2 hours. The suspension formed was filtered, washed 2× with ice cold Toluene (10 ml each) and 4× with MeOH (50 ml each). The residue was dried at room temperature/125 mbar overnight to yield 10.96 g (41.3% of theory) of Intermediate 3 as a white solid
1H NMR (400 MHz, Tetrachloroethane-d2): δ 9.01 (t, J=1.8 Hz, 1H), 8.71 (dt, J=7.8, 1.4 Hz, 1H), 8.68-8.61 (m, 2H), 8.29-8.16 (m, 2H), 8.05 (dt, J=7.7, 1.4 Hz, 1H), 7.93-7.84 (m, 1H), 7.75 (t, J=7.8 Hz, 1H), 7.72-7.61 (m, 3H), 7.61-7.45 (m, 4H).
Step 2
The Step 3 of the synthesis of Compound 1 was repeated, but using Intermediate 3 (3.00 g, 6.67 mmol) instead of Intermediate 2 and Intermediate 1 (2.56 g, 8.00 mmol) to yield 2.5 g (61.7% of theory) of Compound 2 as a white solid.
1H NMR (400 MHz, Chloroform-d): δ 10.46 (t, J=1.7 Hz, 1H), 10.12 (dt, J=8.0, 1.4 Hz, 1H), 10.09-10.04 (m, 2H), 9.56-9.50 (m, 2H), 9.33 (dt, J=7.8, 1.4 Hz, 1H), 9.29-9.21 (m, 2H), 9.17-9.13 (m, 1H), 9.05 (t, J=7.8 Hz, 1H), 9.00-8.76 (m, 10H), 8.62 (td, J=7.4, 1.1 Hz, 1H), 8.48-8.42 (m, 1H), 1.87 (s, 6H).
Step 1
The Step 2 of the synthesis of Compound 1 was repeated, but using 4-(4-bromophenyl)dibenzo[b,d]-furan (10 g, 30.9 mmol) instead of 4-(4-bromophenyl)dibenzo[b,d]thiophene and 2-([1,1′-biphenyl]-4-yl)-4,6-dichloro-1,3,5-triazine (23.37 g, 77 mmol) to yield 4.75 g (30.1% of theory) of Intermediate 4 as a white solid.
1H NMR (400 MHz, Tetrachloroethane-d2): δ 8.86-8.79 (m, 1H), 8.79-8.70 (m, 1H), 8.21-8.15 (m, 1H), 8.13-7.97 (m, 4H), 7.95-7.89 (m, 2H), 7.87-7.81 (m, 1H), 7.78-7.65 (m, 4H), 7.59-7.38 (m, 6H).
Step 2
The Step 3 of the synthesis of Compound 1 was repeated, but using Intermediate 4 (4.26 g, 8.35 mmol) instead of Intermediate 2 and Intermediate 1 (3.21 g, 10.02 mmol) to yield 4.7 g (84% of theory) of Comparative Compound 1 as a white solid.
1H NMR (400 MHz, Tetrachloroethane-d2): δ 9.01-8.93 (m, 2H), 8.93-8.84 (m, 2H), 8.26-8.17 (m, 2H), 8.04 (dtd, J=7.8, 4.5, 1.4 Hz, 3H), 7.98 (d, J=7.8 Hz, 1H), 7.90-7.83 (m, 2H), 7.81-7.65 (m, 5H), 7.61-7.50 (m, 6H), 7.50-7.40 (m, 2H), 7.37 (td, J=7.4, 1.1 Hz, 1H), 7.19 (td, J=7.6, 1.2 Hz, 1H), 1.62 (s, 6H).
Step 1
In a dry 250 ml three necked round-bottomed flask with magnetic stirrer, thermometer were placed 4-bromo-9,9-dimethyl-9H-fluorene (9.56 g, 35 mmol) and 75 ml of THF abs under Ar. The clear, colorless solution was cooled to −78° C. with an acetone/CO2 bath. Within 15 minutes 2.5M BuLi in hexane (16.8 ml, 42 mmol) was added and then stirred at −78° C. for 40 minutes. In a separate dry 250 ml three necked round-bottomed flask with magnetic stirrer and thermometer was placed 2,4-dichloro-6-phenyl-1,3,5-triazine (11.06 g, 49 mmol) in 75 ml THF abs under Ar and cooled to −78° C. To this white suspension the solution prepared above was added with a canula within 20 minutes. The resulting brown solution was stirred at −78° C. for 30 minutes, then warmed to room temperature within 1 hour and stirred at room temperature for 2 hours. The solvent was evaporated to yield 16.9 g of crude product. This was purified by CombiFlash using Heptane/Toluene=1:1 as an eluent to yield 8.93 g (67% of theory) of Intermediate 5 as yellow resin.
1H NMR (300 MHz, Chloroform-d): δ 8.69-8.57 (m, 2H), 7.98-7.84 (m, 2H), 7.69-7.59 (m, 2H), 7.58-7.42 (m, 4H), 7.35 (td, J=7.4, 1.1 Hz, 1H), 7.22-7.14 (m, 1H), 1.56 (s, 6H).
Step 2
The Step 1 of the synthesis of Compound 1 was repeated except for using 4-(4-bromophenyl)-dibenzo[b,d]thiophene (23.75 g, 70 mmol) instead of 4-bromo-9,9-dimethyl-9H-fluorene to yield 21.56 g (80% of theory) of Intermediate 6 as a beige solid.
1H NMR (300 MHz, Chloroform-d): δ 8.23-8.13 (m, 2H), 8.04-7.95 (m, 2H), 7.89-7.81 (m, 1H), 7.81-7.74 (m, 2H), 7.57 (t, J=7.5 Hz, 1H), 7.53-7.42 (m, 3H), 1.40 (s, 12H).
Step 3
The Step 3 of the synthesis of Compound 1 was repeated except for using Intermediate 5 (3.84 g, 10 mmol) instead of Intermediate 2 and Intermediate 6 (4.25 g, 11 mmol) instead of Intermediate 1 to yield 4.92 g (81% of theory) of Compound 3 as a white solid.
1H NMR (300 MHz, Tetrachloroethane-d2): δ 9.00-8.92 (m, 2H), 8.88-8.79 (m, 2H), 8.31-8.18 (m, 2H), 8.09-7.95 (m, 4H), 7.91 (dt, J=6.6, 2.9 Hz, 1H), 7.77-7.47 (m, 10H), 7.38 (td, J=7.4, 1.1 Hz, 1H), 7.20 (td, J=7.6, 1.2 Hz, 1H), 1.63 (s, 6H).
Step 1
The Step 3 of the synthesis of Compound 1 was repeated except for using 1-bromobenzo[b,d]thiophene (13.16 g, 50 mmol) instead of Intermediate 2 and (4-chlorophenyl)boronic acid (9.38 g, 60 mmol) instead of Intermediate 1 to yield 14.14 g (96% of theory) of Intermediate 7 as a colorless resin.
1H NMR (300 MHz, Chloroform-d): δ 7.89 (dd, J=7.9, 1.1 Hz, 1H), 7.84 (dt, J=8.0, 1.0 Hz, 1H), 7.56-7.44 (m, 3H), 7.44-7.34 (m, 3H), 7.28-7.09 (m, 3H).
Step 2
In a 250 ml three necked round-bottomed flask with magnetic stirrer, thermometer and reflux condenser were placed Intermediate 7 (13.56 g, 46 mmol), Bis(pinacolato)diboron (14.02 g, 55.2 mmol), potassium acetate (11.29 g, 115 mmol) and Dioxane (125 ml). The suspension was evacuated and backfilled with Ar 6 times. Then Ar was bubbled through the suspension for 15 minutes. Pd2(dba)3 (0.84 g, 0.92 mmol) and S-Phos (0.76 g, 1.04 mmol) were added, the red suspension was evacuated and backfilled with Ar 5 times and then heated to reflux for 9 hours. To the beige suspension 250 ml of Toluene and 250 ml of Water were added and stirred to form a solution. The layers were separated and the aqueous layer extracted 1 time with 150 ml of Toluene. The combined organic layers were washed 1 time with 200 ml of Water and 1 time with 150 ml of brine, dried over Na2SO4, filtered and evaporated to yield 23.4 g of a brown resin. The crude product was purified by CombiFlash chromatography using a gradient of Heptane/Toluene=60%:40% to Toluene 100% to yield 12.85 g (72% of theory) of Intermediate 8 as a white foam.
1H NMR (300 MHz, Chloroform-d): δ 8.03-7.94 (m, 2H), 7.87 (dd, J=8.0, 1.1 Hz, 1H), 7.82 (dt, J=8.0, 1.0 Hz, 1H), 7.55-7.42 (m, 3H), 7.35 (ddd, J=8.1, 7.0, 1.3 Hz, 1H), 7.26-7.18 (m, 2H), 7.09 (ddd, J=8.3, 7.1, 1.2 Hz, 1H), 1.43 (s, 12H).
Step 3
The Step 3 of the synthesis of Compound 3 was repeated except for using Intermediate 8 (4.64 g, 12 mmol) instead of Intermediate 6 and Intermediate 5 (3.84 g, 10 mmol) to yield 4.64 g (76% of theory) of Compound 4 as a white foam.
1H NMR (300 MHz, Chloroform-d): δ 9.00-8.90 (m, 2H), 8.89-8.77 (m, 2H), 8.04 (dd, J=7.7, 1.3 Hz, 1H), 8.00 (dt, J=7.9, 0.9 Hz, 1H), 7.92 (dd, J=7.9, 1.1 Hz, 1H), 7.85 (dt, J=8.1, 0.9 Hz, 1H), 7.75-7.45 (m, 9H), 7.42-7.28 (m, 4H), 7.21-7.02 (m, 2H), 1.60 (s, 6H).
Step 1
The Step 1 of the synthesis of Compound 3 was repeated except for using 2-([1,1′-biphenyl]-3-yl)-4,6-dichloro-1,3,5-triazine (6.35 g, 21 mmol) instead of 2,4-dichloro-6-phenyl-1,3,5-triazine and 4-bromo-9,9-dimethyl-9H-fluorene (9.56 g, 35 mmol) to yield 5.82 g (84% of theory) of Intermediate 9 as a white foam.
1H NMR (300 MHz, Chloroform-d): δ 8.87 (d, J=1.9 Hz, 1H), 8.60 (dt, J=7.8, 1.4 Hz, 1H), 7.99-7.90 (m, 2H), 7.87 (dt, J=7.8, 1.5 Hz, 1H), 7.66 (dt, J=7.8, 1.7 Hz, 3H), 7.61 (t, J=7.8 Hz, 1H), 7.54-7.31 (m, 6H), 7.25-7.13 (m, 1H), 1.56 (s, 6H).
Step 2
The Step 3 of the synthesis of Compound 3 was repeated except for using Intermediate 9 (4.14 g, 9.0 mmol) instead of Intermediate 5 and Intermediate 6 (3.82 g, 9.9 mmol) to yield 3.98 g (64% of theory) of Compound 5 as a white solid.
1H NMR (300 MHz, Chloroform-d): δ 9.07 (t, J=1.8 Hz, 1H), 9.00-8.89 (m, 2H), 8.80 (dt, J=7.8, 1.4 Hz, 1H), 8.27-8.15 (m, 2H), 8.09-8.00 (m, 2H), 8.00-7.94 (m, 2H), 7.91-7.82 (m, 2H), 7.79-7.71 (m, 2H), 7.71-7.62 (m, 2H), 7.62-7.57 (m, 2H), 7.57-7.45 (m, 6H), 7.45-7.40 (m, 1H), 7.36 (td, J=7.5, 1.2 Hz, 1H), 7.19 (td, J=7.6, 1.2 Hz, 1H), 1.61 (s, 6H).
Step 1
The Step 1 of the synthesis of Compound 1 was repeated, but using 2-bromo-9,9-dimethyl-9H-fluorene (10 g, 36.6 mmol) instead of 4-bromo-9,9-dimethyl-9H-fluorene to yield 10.86 g (93% of theory) of Intermediate 10 as a grey solid.
1H NMR (300 MHz, Tetrachloroethane-d2) δ 7.93 (s, 1H), 7.88-7.75 (m, 3H), 7.54-7.48 (m, 1H), 7.44-7.37 (m, 2H), 1.56 (s, 6H), 1.42 (s, 12H).
Step 2
The Step 2 of the synthesis of Compound 1 was repeated, but using 2-(4-bromophenyl) dibenzo[b,d]thiophene (12 g, 35.4 mmol) instead of 4-(4-bromophenyl) dibenzo[b,d]thiophene and 2,4-dichloro-6-phenyl-1,3,5-triazine (20 g, 88 mmol) instead of 2-([1,1′-biphenyl]-4-yl)-4,6-dichloro-1,3,5-triazine to yield 5.43 g (34% of theory) of Intermediate 11 as a white solid.
1H NMR (300 MHz, Tetrachloroethane-d2) δ 8.80-8.74 (m, 2H), 8.70-8.64 (m, 2H), 8.46 (d, J=1.7 Hz, 1 H), 8.33-8.26 (m, 1H), 8.02 (d, J=8.3 Hz, 1 H), 7.97-7.90 (m, 3H), 7.83 (dd, J=8.3, 1.8 Hz, 1H), 7.73-7.51 (m, 5H).
Step 3
The Step 3 of the synthesis of Compound 1 was repeated, but using Intermediate 11 (7.34 g, 16.31 mmol) instead of Intermediate 2 and Intermediate 10 (6.27 g, 19.58 mmol) instead of Intermediate 1 to yield 4.03 g (40.6% of theory) of Comparative Compound 2 as a white solid.
1H NMR (300 MHz, Tetrachloroethane-d2) δ 8.98-8.92 (m, 2H), 8.85 (td, J=4.8, 3.1 Hz, 4H), 8.50 (d, J=1.7 Hz, 1H), 8.35-8.27 (m, 1H), 8.07-7.83 (m, 7H), 7.74-7.62 (m, 3H), 7.59-7.52 (m, 3H), 7.44 (dd, J=5.6, 3.1 Hz, 2H), 1.67 (s, 6H).
Step 1
In a 100 ml three necked round bottomed flask were placed magnesium (0.474 g, 19.52 mmol) and THF abs. (20 ml) under Argon. In a separate 50 ml three necked round bottomed flask was placed 4-bromo-9,9-dimethyl-9H-fluorene (4.44 g, 16.27 mmol) and THF (20 ml) and then transferred to a dropping funnel using a canula. About 2 ml of this solution were added to the first vessel and the Grignard reaction was started by the addition of a small grain of iodine and heating to reflux with a heat gun. The rest of the solution with the starting material was then added drop by drop. The reaction mixture was heated to reflux for 3 hours and then cooled to room temperature.
In a 250 ml three necked round bottomed flask were placed 2,4,6-trichloro-1,3,5-triazine (3 g, 16.27 mmol) dissolved in THF (60 ml) and cooled to −15° C. with an ice/NaCl bath. The Grignard reagent was then added to this solution with a canula within 30 min. keeping the internal temperature below −10° C. The reaction mixture was warmed to room temperature and stirred overnight. The reaction mixture was cooled to 0° C. with an ice bath and slowly 50 ml HCl 2N were added. 250 ml of Ethyl acetate were added, the phases separated and the organic phase washed four times with water (150 ml each), dried with MgSO4, filtered and concentrated to yield 5.78 g of an orange solid.
The crude product was purified by CombiFlash using Heptane/CH2Cl2=80:20 to 60:40 as eluent to yield 2.8 g (50.3% of theory) of Intermediate 12 as white solid.
1H NMR (300 MHz, Tetrachloroethane-d2) δ 7.90 (td, J=8.0, 1.1 Hz, 2H), 7.70 (dd, J=7.5, 1.2 Hz, 1H), 7.54-7.37 (m, 3H), 7.30 (td, J=7.5, 1.3 Hz, 1H), 1.53 (s, 6H).
Step 2
The Step 3 of the synthesis of Compound 3 was repeated, but using Intermediate 12 (2.30 g, 6.72 mmol) instead of Intermediate 5 and Intermediate 6 (6.23 g, 16.13 mmol) to yield 2.0 g (37.7% of theory) of Comparative Compound 4 as a white solid.
1H NMR (300 MHz, Tetrachloroethane-d2) δ 9.01-8.93 (m, 4H), 8.29-8.21 (m, 4H), 8.08-7.98 (m, 6H), 7.94-7.87 (m, 2H), 7.76-7.51 (m, 11H), 7.38 (td, J=7.4, 1.1 Hz, 1H), 7.22 (ddd, J=8.1, 7.3, 1.2 Hz, 1H), 1.62 (s, 6H).
Step 1
The Step 1 of the synthesis of Compound 4 was repeated, but using 4-bromodibenzo-[b,d]thiophene (30 g, 114 mmol) instead of 1-bromodibenzo[b,d]thiophene and phenylboronic acid (15.29 g, 125 mmol) instead of (4-chlorophenyl)boronic acid to yield 26.46 g (89.3% of theory) of Intermediate 13 as a white solid.
1H NMR (300 MHz, Tetrachloroethane-d2) δ 8.25-8.16 (m, 2H), 7.89-7.84 (m, 1H), 7.79-7.75 (m, 2H), 7.63-7.44 (m, 7H).
Step 2
In a 100 ml three necked round bottomed flask were placed Intermediate 13 (26.46 g, 102 mmol) and 230 ml THF abs under Argon. The clear colourless solution was cooled to −78° C. with an acetone/dry ice bath. Butyllithium 2.5M in Hexane (44.7 ml, 112 mmol) was added drop by drop within 15 min. keeping the internal temperature below −70° C. The resulting orange solution was stirred for 10 min. at −78° C., then warmed up to 0° C. and stirred at that temperature for 3 hours.
The red solution was cooled to −78° C. and 1,2-dibromoethane (17.52 ml, 203 mmol) was added drop by drop within 15 min. keeping the internal temperature below −70° C. The yellow solution was stirred at room temperaure overnight. The reaction mixture was concentrated to yield 54.9 g of an orange viscous oil. 150 ml MeOH were added and the mixture put in an ultrasonic bath for 20 min. and then cooled to room temperature with stirring. The suspension was filtered, washed three times with MeOH (10 ml each) and dried at room temperature/125 mbar overnight to yield 24.43 g (70.6% of theory) of Intermediate 14 as white solid.
1H NMR (300 MHz, Tetrachloroethane-d2) δ 8.16 (td, J=7.9, 1.2 Hz, 2H), 7.79-7.75 (m, 2H), 7.67-7.54 (m, 5H), 7.52-7.48 (m, 1H), 7.41 (t, J=7.8 Hz, 1H).
Step 3
The Step 1 of the synthesis of Compound 4 was repeated, but using Intermediate 14 (19.7 g, 114 mmol) instead of 1-bromodibenzo[b,d]thiophene and (4-chlorophenyl)boronic acid (9.53g, 61.0 mol) to yield 13.0 g (60.3% of theory) of Intermediate 15 as a white solid.
1H NMR (300 MHz, Tetrachloroethane-d2) δ 8.22 (ddd, J=7.8, 3.0, 1.2 Hz, 2H), 7.77-7.71 (m, 2H), 7.70-7.58 (m, 4H), 7.57-7.44 (m, 7H).
Step 4
The Step 2 of the synthesis of Compound 4 was repeated, but using Intermediate 15 (8 g, 21.57 mmol) instead of Intermediate 7 to yield 9.59 g (96% of theory) of Intermediate 16 as a beige solid.
1H NMR (300 MHz, Tetrachloroethane-d2) δ 8.22 (ddd, J=7.8, 3.0, 1.2 Hz, 2H), 7.98-7.92 (m, 2H), 7.76-7.70 (m, 4H), 7.61 (td, J=7.6, 1.1 Hz, 2H), 7.56-7.49 (m, 4H), 7.47-7.41 (m, 1H), 1.37 (s, 12H).
Step 5
The Step 2 of the synthesis of Compound 1 was repeated, but using 4-bromo-9,9-dimethyl-9H-fluorene (8.0 g, 29.3 mmol) instead of 4-(4-bromophenyl)dibenzo[b,d]thiophene and 2-([1,1′-biphenyl]-4-yl)-4,6-dichloro-1,3,5-triazine (13.27 g, 43.9 mmol) to yield 5.13 g (38.5% of theory) of Intermediate 16 as a white solid.
1H NMR (300 MHz, Tetrachloroethane-d2) δ 8.77-8.72 (m, 2H), 7.99-7.89 (m, 2H), 7.88-7.82 (m, 2H), 7.80-7.72 (m, 3H), 7.61-7.39 (m, 6H), 7.26 (ddd, J=8.5, 7.3, 1.3 Hz, 1H), 1.61 (s, 6H).
Step 6
The Step 3 of the synthesis of Compound 3 was repeated, but using Intermediate 17 (5.18 g, 11.26 mmol) instead of Intermediate 5 and Intermediate 16 (5.73, 12.39 mmol) instead of Intermediate 6 to yield 3.2 g (37.4% of theory) of Comparative, Compound 5 as a white solid.
1H NMR (300 MHz, Tetrachloroethane-d2) δ 8.96-8.89 (m, 2H), 8.89-8.83 (m, 2H), 8.26 (ddd, J=10.2, 7.4, 1.7 Hz, 2H), 8.05-7.93 (m, 4H), 7.85 (d, J=8.3 Hz, 2H), 7.80-7.41 (m, 17H), 7.35 (t, J=7.4 Hz, 1H), 7.17 (t, J=7.6 Hz, 1H), 1.61 (s, 6H).
The compounds of the present invention can also be synthesized using the following intermediates.
| Number | Date | Country | Kind |
|---|---|---|---|
| 20157524.8 | Feb 2020 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2021/005389 | 2/5/2021 | WO |
