JP6174749B2 - ホウ素−窒素ヘテロ環を含む配位子をもつ金属錯体 - Google Patents
ホウ素−窒素ヘテロ環を含む配位子をもつ金属錯体 Download PDFInfo
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- JP6174749B2 JP6174749B2 JP2016075089A JP2016075089A JP6174749B2 JP 6174749 B2 JP6174749 B2 JP 6174749B2 JP 2016075089 A JP2016075089 A JP 2016075089A JP 2016075089 A JP2016075089 A JP 2016075089A JP 6174749 B2 JP6174749 B2 JP 6174749B2
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- 239000003446 ligand Substances 0.000 title description 118
- 229910052751 metal Inorganic materials 0.000 title description 36
- 239000002184 metal Substances 0.000 title description 36
- 150000001875 compounds Chemical class 0.000 claims description 142
- 125000003118 aryl group Chemical group 0.000 claims description 28
- 125000001072 heteroaryl group Chemical group 0.000 claims description 18
- 239000010410 layer Substances 0.000 description 62
- 239000000463 material Substances 0.000 description 47
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 38
- 229910052757 nitrogen Inorganic materials 0.000 description 26
- 229910052739 hydrogen Inorganic materials 0.000 description 24
- 239000001257 hydrogen Substances 0.000 description 24
- 125000000217 alkyl group Chemical group 0.000 description 23
- VQGHOUODWALEFC-UHFFFAOYSA-N 2-phenylpyridine Chemical compound C1=CC=CC=C1C1=CC=CC=N1 VQGHOUODWALEFC-UHFFFAOYSA-N 0.000 description 22
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 21
- 239000000243 solution Substances 0.000 description 20
- 239000012044 organic layer Substances 0.000 description 19
- 125000001424 substituent group Chemical group 0.000 description 19
- 150000002431 hydrogen Chemical class 0.000 description 18
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 18
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 17
- -1 arylkyl Chemical group 0.000 description 17
- 229910052796 boron Inorganic materials 0.000 description 16
- 239000000203 mixture Substances 0.000 description 16
- 125000003342 alkenyl group Chemical group 0.000 description 15
- 125000000304 alkynyl group Chemical group 0.000 description 15
- 125000003545 alkoxy group Chemical group 0.000 description 14
- KCQLSIKUOYWBAO-UHFFFAOYSA-N azaborinine Chemical compound B1=NC=CC=C1 KCQLSIKUOYWBAO-UHFFFAOYSA-N 0.000 description 14
- 230000015572 biosynthetic process Effects 0.000 description 14
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 14
- 239000000047 product Substances 0.000 description 13
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 12
- 229910052799 carbon Inorganic materials 0.000 description 12
- 125000000623 heterocyclic group Chemical group 0.000 description 12
- 125000002524 organometallic group Chemical group 0.000 description 12
- 150000003384 small molecules Chemical class 0.000 description 12
- 238000003786 synthesis reaction Methods 0.000 description 12
- 230000032258 transport Effects 0.000 description 12
- OBUDOIAYABJUHQ-UHFFFAOYSA-N 1,4-azaborinine Chemical compound B1=CC=NC=C1 OBUDOIAYABJUHQ-UHFFFAOYSA-N 0.000 description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 10
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 10
- 239000002019 doping agent Substances 0.000 description 10
- 229910052760 oxygen Inorganic materials 0.000 description 10
- 229910052717 sulfur Inorganic materials 0.000 description 10
- 230000000903 blocking effect Effects 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 8
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 8
- 150000004696 coordination complex Chemical class 0.000 description 8
- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 8
- IYYZUPMFVPLQIF-UHFFFAOYSA-N dibenzothiophene Chemical compound C1=CC=C2C3=CC=CC=C3SC2=C1 IYYZUPMFVPLQIF-UHFFFAOYSA-N 0.000 description 8
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 8
- 239000007924 injection Substances 0.000 description 8
- 238000002347 injection Methods 0.000 description 8
- 238000004768 lowest unoccupied molecular orbital Methods 0.000 description 8
- 125000004433 nitrogen atom Chemical group N* 0.000 description 8
- 239000000758 substrate Substances 0.000 description 8
- TZHYBRCGYCPGBQ-UHFFFAOYSA-N [B].[N] Chemical compound [B].[N] TZHYBRCGYCPGBQ-UHFFFAOYSA-N 0.000 description 7
- 230000021615 conjugation Effects 0.000 description 7
- JVZRCNQLWOELDU-UHFFFAOYSA-N gamma-Phenylpyridine Natural products C1=CC=CC=C1C1=CC=NC=C1 JVZRCNQLWOELDU-UHFFFAOYSA-N 0.000 description 7
- 238000004770 highest occupied molecular orbital Methods 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 239000011368 organic material Substances 0.000 description 7
- 239000011541 reaction mixture Substances 0.000 description 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000000151 deposition Methods 0.000 description 6
- 230000005525 hole transport Effects 0.000 description 6
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 6
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 description 5
- QBWKPGNFQQJGFY-QLFBSQMISA-N 3-[(1r)-1-[(2r,6s)-2,6-dimethylmorpholin-4-yl]ethyl]-n-[6-methyl-3-(1h-pyrazol-4-yl)imidazo[1,2-a]pyrazin-8-yl]-1,2-thiazol-5-amine Chemical compound N1([C@H](C)C2=NSC(NC=3C4=NC=C(N4C=C(C)N=3)C3=CNN=C3)=C2)C[C@H](C)O[C@H](C)C1 QBWKPGNFQQJGFY-QLFBSQMISA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 125000003710 aryl alkyl group Chemical group 0.000 description 5
- 229940125846 compound 25 Drugs 0.000 description 5
- 125000004122 cyclic group Chemical group 0.000 description 5
- 239000000412 dendrimer Substances 0.000 description 5
- 229920000736 dendritic polymer Polymers 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 230000005693 optoelectronics Effects 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 5
- 238000006467 substitution reaction Methods 0.000 description 5
- HWIATMHDQVGMFQ-UHFFFAOYSA-N 1,3-azaborinine Chemical compound B1=CC=CN=C1 HWIATMHDQVGMFQ-UHFFFAOYSA-N 0.000 description 4
- FCEHBMOGCRZNNI-UHFFFAOYSA-N 1-benzothiophene Chemical compound C1=CC=C2SC=CC2=C1 FCEHBMOGCRZNNI-UHFFFAOYSA-N 0.000 description 4
- 125000001054 5 membered carbocyclic group Chemical group 0.000 description 4
- 125000004008 6 membered carbocyclic group Chemical group 0.000 description 4
- 0 CB1N([C@](*)C=CCC(*)(CCCCC)I)c2ccccc2N1* Chemical compound CB1N([C@](*)C=CCC(*)(CCCCC)I)c2ccccc2N1* 0.000 description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 4
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 description 4
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 4
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 4
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 4
- YTPLMLYBLZKORZ-UHFFFAOYSA-N Thiophene Chemical compound C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 4
- SLGBZMMZGDRARJ-UHFFFAOYSA-N Triphenylene Natural products C1=CC=C2C3=CC=CC=C3C3=CC=CC=C3C2=C1 SLGBZMMZGDRARJ-UHFFFAOYSA-N 0.000 description 4
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 4
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 4
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 4
- CUFNKYGDVFVPHO-UHFFFAOYSA-N azulene Chemical compound C1=CC=CC2=CC=CC2=C1 CUFNKYGDVFVPHO-UHFFFAOYSA-N 0.000 description 4
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 4
- 239000004305 biphenyl Substances 0.000 description 4
- 235000010290 biphenyl Nutrition 0.000 description 4
- WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical compound C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 description 4
- DHFABSXGNHDNCO-UHFFFAOYSA-N dibenzoselenophene Chemical compound C1=CC=C2C3=CC=CC=C3[se]C2=C1 DHFABSXGNHDNCO-UHFFFAOYSA-N 0.000 description 4
- 235000019439 ethyl acetate Nutrition 0.000 description 4
- 230000005281 excited state Effects 0.000 description 4
- 125000004404 heteroalkyl group Chemical group 0.000 description 4
- 229910052741 iridium Inorganic materials 0.000 description 4
- AWJUIBRHMBBTKR-UHFFFAOYSA-N isoquinoline Chemical compound C1=NC=CC2=CC=CC=C21 AWJUIBRHMBBTKR-UHFFFAOYSA-N 0.000 description 4
- 150000002894 organic compounds Chemical class 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 125000005580 triphenylene group Chemical group 0.000 description 4
- LYUPJHVGLFETDG-UHFFFAOYSA-N 1-phenylbutan-2-ol Chemical compound CCC(O)CC1=CC=CC=C1 LYUPJHVGLFETDG-UHFFFAOYSA-N 0.000 description 3
- GDUANFXPOZTYKS-UHFFFAOYSA-N 6-bromo-8-[(2,6-difluoro-4-methoxybenzoyl)amino]-4-oxochromene-2-carboxylic acid Chemical compound FC1=CC(OC)=CC(F)=C1C(=O)NC1=CC(Br)=CC2=C1OC(C(O)=O)=CC2=O GDUANFXPOZTYKS-UHFFFAOYSA-N 0.000 description 3
- XASOHFCUIQARJT-UHFFFAOYSA-N 8-methoxy-6-[7-(2-morpholin-4-ylethoxy)imidazo[1,2-a]pyridin-3-yl]-2-(2,2,2-trifluoroethyl)-3,4-dihydroisoquinolin-1-one Chemical compound C(N1C(=O)C2=C(OC)C=C(C=3N4C(=NC=3)C=C(C=C4)OCCN3CCOCC3)C=C2CC1)C(F)(F)F XASOHFCUIQARJT-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 239000012267 brine Substances 0.000 description 3
- 229940125904 compound 1 Drugs 0.000 description 3
- 238000010586 diagram Methods 0.000 description 3
- 238000010348 incorporation Methods 0.000 description 3
- VVVPGLRKXQSQSZ-UHFFFAOYSA-N indolo[3,2-c]carbazole Chemical class C1=CC=CC2=NC3=C4C5=CC=CC=C5N=C4C=CC3=C21 VVVPGLRKXQSQSZ-UHFFFAOYSA-N 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- ZBELDPMWYXDLNY-UHFFFAOYSA-N methyl 9-(4-bromo-2-fluoroanilino)-[1,3]thiazolo[5,4-f]quinazoline-2-carboximidate Chemical compound C12=C3SC(C(=N)OC)=NC3=CC=C2N=CN=C1NC1=CC=C(Br)C=C1F ZBELDPMWYXDLNY-UHFFFAOYSA-N 0.000 description 3
- QCIQNIHAVQGDCD-UHFFFAOYSA-N n-formyl-n-pyridin-2-ylformamide Chemical compound O=CN(C=O)C1=CC=CC=N1 QCIQNIHAVQGDCD-UHFFFAOYSA-N 0.000 description 3
- 125000004430 oxygen atom Chemical group O* 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 3
- UAOUIVVJBYDFKD-XKCDOFEDSA-N (1R,9R,10S,11R,12R,15S,18S,21R)-10,11,21-trihydroxy-8,8-dimethyl-14-methylidene-4-(prop-2-enylamino)-20-oxa-5-thia-3-azahexacyclo[9.7.2.112,15.01,9.02,6.012,18]henicosa-2(6),3-dien-13-one Chemical compound C([C@@H]1[C@@H](O)[C@@]23C(C1=C)=O)C[C@H]2[C@]12C(N=C(NCC=C)S4)=C4CC(C)(C)[C@H]1[C@H](O)[C@]3(O)OC2 UAOUIVVJBYDFKD-XKCDOFEDSA-N 0.000 description 2
- GHYOCDFICYLMRF-UTIIJYGPSA-N (2S,3R)-N-[(2S)-3-(cyclopenten-1-yl)-1-[(2R)-2-methyloxiran-2-yl]-1-oxopropan-2-yl]-3-hydroxy-3-(4-methoxyphenyl)-2-[[(2S)-2-[(2-morpholin-4-ylacetyl)amino]propanoyl]amino]propanamide Chemical compound C1(=CCCC1)C[C@@H](C(=O)[C@@]1(OC1)C)NC([C@H]([C@@H](C1=CC=C(C=C1)OC)O)NC([C@H](C)NC(CN1CCOCC1)=O)=O)=O GHYOCDFICYLMRF-UTIIJYGPSA-N 0.000 description 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 2
- KTZQTRPPVKQPFO-UHFFFAOYSA-N 1,2-benzoxazole Chemical compound C1=CC=C2C=NOC2=C1 KTZQTRPPVKQPFO-UHFFFAOYSA-N 0.000 description 2
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 2
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 2
- FLBAYUMRQUHISI-UHFFFAOYSA-N 1,8-naphthyridine Chemical compound N1=CC=CC2=CC=CN=C21 FLBAYUMRQUHISI-UHFFFAOYSA-N 0.000 description 2
- BNRDGHFESOHOBF-UHFFFAOYSA-N 1-benzoselenophene Chemical compound C1=CC=C2[se]C=CC2=C1 BNRDGHFESOHOBF-UHFFFAOYSA-N 0.000 description 2
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 2
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
- BAXOFTOLAUCFNW-UHFFFAOYSA-N 1H-indazole Chemical compound C1=CC=C2C=NNC2=C1 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 description 2
- VEPOHXYIFQMVHW-XOZOLZJESA-N 2,3-dihydroxybutanedioic acid (2S,3S)-3,4-dimethyl-2-phenylmorpholine Chemical compound OC(C(O)C(O)=O)C(O)=O.C[C@H]1[C@@H](OCCN1C)c1ccccc1 VEPOHXYIFQMVHW-XOZOLZJESA-N 0.000 description 2
- QEBYEVQKHRUYPE-UHFFFAOYSA-N 2-(2-chlorophenyl)-5-[(1-methylpyrazol-3-yl)methyl]-4-[[methyl(pyridin-3-ylmethyl)amino]methyl]-1h-pyrazolo[4,3-c]pyridine-3,6-dione Chemical compound C1=CN(C)N=C1CN1C(=O)C=C2NN(C=3C(=CC=CC=3)Cl)C(=O)C2=C1CN(C)CC1=CC=CN=C1 QEBYEVQKHRUYPE-UHFFFAOYSA-N 0.000 description 2
- OXABPHKDQGRFTG-UHFFFAOYSA-N 2-chloro-1h-1,2-benzazaborinine Chemical compound C1=CC=C2C=CB(Cl)NC2=C1 OXABPHKDQGRFTG-UHFFFAOYSA-N 0.000 description 2
- KURPPWHPIYBYBS-UHFFFAOYSA-N 2-ethenylaniline Chemical compound NC1=CC=CC=C1C=C KURPPWHPIYBYBS-UHFFFAOYSA-N 0.000 description 2
- FSEXLNMNADBYJU-UHFFFAOYSA-N 2-phenylquinoline Chemical compound C1=CC=CC=C1C1=CC=C(C=CC=C2)C2=N1 FSEXLNMNADBYJU-UHFFFAOYSA-N 0.000 description 2
- OLGGLCIDAMICTA-UHFFFAOYSA-N 2-pyridin-2-yl-1h-indole Chemical compound N1C2=CC=CC=C2C=C1C1=CC=CC=N1 OLGGLCIDAMICTA-UHFFFAOYSA-N 0.000 description 2
- QMEQBOSUJUOXMX-UHFFFAOYSA-N 2h-oxadiazine Chemical compound N1OC=CC=N1 QMEQBOSUJUOXMX-UHFFFAOYSA-N 0.000 description 2
- DFRAKBCRUYUFNT-UHFFFAOYSA-N 3,8-dicyclohexyl-2,4,7,9-tetrahydro-[1,3]oxazino[5,6-h][1,3]benzoxazine Chemical compound C1CCCCC1N1CC(C=CC2=C3OCN(C2)C2CCCCC2)=C3OC1 DFRAKBCRUYUFNT-UHFFFAOYSA-N 0.000 description 2
- BWCDLEQTELFBAW-UHFFFAOYSA-N 3h-dioxazole Chemical compound N1OOC=C1 BWCDLEQTELFBAW-UHFFFAOYSA-N 0.000 description 2
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 2
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 2
- FBVBNCGJVKIEHH-UHFFFAOYSA-N [1]benzofuro[3,2-b]pyridine Chemical compound C1=CN=C2C3=CC=CC=C3OC2=C1 FBVBNCGJVKIEHH-UHFFFAOYSA-N 0.000 description 2
- QZLAKPGRUFFNRD-UHFFFAOYSA-N [1]benzoselenolo[3,2-b]pyridine Chemical compound C1=CN=C2C3=CC=CC=C3[se]C2=C1 QZLAKPGRUFFNRD-UHFFFAOYSA-N 0.000 description 2
- WIUZHVZUGQDRHZ-UHFFFAOYSA-N [1]benzothiolo[3,2-b]pyridine Chemical compound C1=CN=C2C3=CC=CC=C3SC2=C1 WIUZHVZUGQDRHZ-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
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- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
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- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
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- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
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Description
本出願は、2009年5月20日に出願した米国仮出願No.61/179,933号に基づく優先権を主張し、その開示を、その全体を参照により本明細書に明示して援用する。
本発明は、有機発光デバイス(OLED)に有利に用いることができる新規な有機物質に関する。より詳細には、本発明は、ホウ素−窒素ヘテロ環を含む新規な化合物とそのような化合物を含むデバイスに関する。
新規な群の有機物質を提供する。この物質は、ホウ素−窒素ヘテロ環を含む配位子をもつ化合物である。この物質はOLEDに有利に用いることができる。特に、この物質はそのようなデバイスにおいて発光ドーパントとして用いることができる。
特に、R1は水素であってよい。
一般にOLEDは、アノードとカソードの間に配置され且つこれらと電気的に接続された少なくとも1つの有機層を含む。電流が流された場合、その有機層(単数又は複数)中にアノードは正孔を注入し、カソードは電子を注入する。注入された正孔と電子は、それぞれ反対に帯電した電極に向かって移動する。同じ分子上に電子と正孔が局在した場合、励起エネルギー状態を有する、局在化した電子-正孔対である「励起子」が形成される。この励起子が発光機構によって緩和する時に光が発せられる。ある場合には、励起子はエキシマー又はエキシプレックス上に局在することもできる。非放射機構、例えば熱緩和も起こることがあるが、通常は好ましくないと考えられている。
及び、Baldoら,“Very high-efficiency green organic light-emitting devices based on electrophosphorescence”, Appl. Phys. Lett., vol. 75, No. 3, 4-6 (1999)(“Baldo-II”)、これらを参照により全体を援用する。リン光は、米国特許第7,279, 704号明細書の第5〜6欄により詳細に記載されており、これを参照により援用する。
ある側面では、R1は水素であることが好ましい。X2及びX3は独立に、炭素、窒素、及びホウ素からなる群から選択される。Bは、ホウ素−窒素ヘテロ環である。一つの側面では、Aは以下のものからなる群から選択されうる。
フタロシアニン又はポルフィリン誘導体、芳香族アミン誘導体、インドロカルバゾール誘導体、フルオロ炭化水素を含むポリマー、導電性ドーパントを伴うポリマー、導電性ポリマー(例えば、PEDOT/PSS)、ホスホン酸及びシラン誘導体などの化合物から誘導される自己組織化モノマー、金属酸化物誘導体(例えば、MoOx)、p型半導体有機化合物(例えば、1,4,5,8,9,12-ヘキサアザトリフェニレンヘキサンカルボニトリル)、金属錯体、及び架橋性化合物。
500 mLのメタノール中のナトリウムメトキシド(176 mL、25質量%、0.81 mmol)の溶液に2-アミノピリジン(30.0 g, 0.32 mmol)を添加し、得られた溶液を40℃で30分間撹拌した。ギ酸エチル(220 mL, 2.76 mol)を次に滴下して添加し、反応混合物を夜通し40℃で撹拌した。室温に冷やした後、250mLのH2Oと250mLのCH2Cl2を添加し、濃HCl(〜40 mL)をpH約5になるまで滴下して添加した。メタノールのほとんどを蒸発させ、得られた混合物を3×150mLのCH2Cl2で抽出した。一緒にした有機部分を250mLのH2Oと150mLの食塩水で洗い、Na2SO4上で乾燥させた。溶媒の蒸発後、20.2gの粗製固体を得て、これを140℃のオーブン温度でクーゲルロールで蒸留し、生成物として18.98gの白色固体を得た。
氷/塩浴中で、50mLのエーテル中のギ酸ナトリウム(59 g, 0.86 mol)の混合物に、アセチルクロライド(41 mL, 0.577 mol)を滴下ロートから迅速に添加した。反応混合物を夜通し撹拌し、得られた酢酸ギ酸無水物のエーテル溶液をさらに精製することなく用いた。
50mLのTHF中の水素化ナトリウム(10.8 g, 60質量%, 0.27 mol)の懸濁液に、250mLのTHF中のN-(ピリジン-2-イル)ホルムアミド(22.4 g, 0.18 mol)の溶液を滴下して添加した。添加が終了したら、反応物を室温で30分間撹拌し、次に氷/塩浴中で冷やした。先の工程からの酢酸ギ酸無水物のエーテル溶液を一度に添加した。得られた混合物を氷浴中で30分間、次に夜通し室温で撹拌した。この混合物を1Lの氷水中に注ぎ、3×250mLのCH2Cl2で抽出した。一緒にした有機抽出物を2×250mLのH2Oで洗い、乾燥させ、溶媒留去して33.2gの固体を得た。この粗生成物を100%のCH2Cl2、次に90:10のCH2Cl2:EtOAcで溶出させるカラムクロマトグラフィー(シリカゲル)によって精製して14.2gの生成物を白色固体として単離した。
磁気攪拌機、熱電対、冷却管、窒素導入口、及び滴下ロートを備えた2Lの三ツ口フラスコ中で、トリフェニルホスフィン(82.5 g, 0.31 mol)及びテトラブロモメタン(103.5 g, 0.31 mol)を750mLのCH2Cl2に溶かした。亜鉛(20.27 g, 0.31 mol)を添加し、オレンジ色の混合物になった。この反応混合物を氷浴中で約10℃に冷やし、10分間撹拌した。100mLのCH2Cl2中のN-ホルミル-N-(ピリジン-2-イル)ホルムアミド(5.9 g, 0.04 mol)の溶液を、滴下ロートからゆっくり流しながら添加した。ピリジン(32.7 mL, 0.41 mol)を次に滴下ロートから添加した。反応温度は10℃から24℃に上がり、濃茶色に変わった。この反応混合物を夜通し撹拌し、室温にゆっくり温め、セライトを通して濾過した。ろ液を2×250mLの水と250mLの食塩水で洗い、乾燥させ、溶媒を蒸発させたところ約200gの黒色のガム状固体が残った。この粗製物質を75:25のヘキサン:CH2Cl2、次に50:50のヘキサン:CH2Cl2、最後に25:75のヘキサン:CH2Cl2で溶離させるフラッシュシリカカラム上でクロマトグラフィーを行い、14.9gの生成物を得た。
磁気攪拌機、滴下ロート、熱電対、及び窒素導入口を備え、オーブンで乾燥させた500mLの三ツ口フラスコに、無水塩化亜鉛(15.0 g, 0.11 mol)を仕込み、氷/塩浴中で冷やした。100mLのTHFを次に滴下して添加した。温度が0℃より低く保たれるようにしてブチルリチウム(134 mL, ヘキサン中2.5 M, 0.34 mol)を次に滴下して添加し、乳白色溶液が得られ、これを0℃で30分間撹拌した。氷/塩浴をドライアイス/アセトン浴に置き換えて、反応物を−75℃に冷やした。50mLのTHF中のN,N-ビス(2,2-ジブロモビニル)ピリジン-2-アミン(0.5 g, 0.011 mol)を滴下して添加し、反応物を−75℃で20時間撹拌した。なお−75℃において、THF中10%酢酸100mLを滴下して添加し、その冷たい溶液を150mLの1N HClに注いだ。反応混合物を3×100mLのエーテルで抽出し、一緒にした有機物を2×100mLの飽和NaHCO3で洗い、乾燥させ、溶媒留去して、生成物として3.0gの無色液体が残った。
tBuLi(4.9 mL, ペンタン中1.7 M、8.3 mmol)を、50mLのEt2O中のN,N-ビス((Z)-2-ブロモビニル)ピリジン-2-アミン(500 mg, 1.650 mmol)の溶液に−70℃で滴下して添加した。沈殿物が形成され、溶液は淡い橙色の混合物へとわずかに濃くなった。反応混合物を3時間−70℃において撹拌し、その間の時間に沈殿物が溶けた。10mLのエーテル中のジメチル(2,6-ジメチルフェニル)ボロネート(322 mg, 2.14 mmol)をその反応溶液中に滴下して添加し、これを次に室温までゆっくり温まるままにしておいた。反応物を、セライト栓を通して濾過し、濃縮して200mgの固体を得た。GC/MSによって生成物の形成を確認した。
2-(2-アミノフェニル)エタノール(5 g, 36.4 mmol)とKOH(2.0 g, 36.4 mmol)との混合物を200℃に4時間加熱した。冷却後、この混合物を減圧下で蒸留し、2.1gの生成物を得た。
BCl3(67.8 mL, ヘキサン中1.0 M)を40mLの無水トルエン中の2-ビニルアニリン(5.3 g, 44.3 mmol)の溶液に0℃で添加した。この混合物を0℃で1時間撹拌し、次に2時間還流させた。混合物を次に乾燥するまで溶媒留去し、直ちに次のステップに用いた。
イソプロピルマグネシウムブロマイド(9.2 mL, THF中2.0 M, 18.4 mmol)を2-ブロモピリジン(2.9 g, 18.4 mmol)と室温で2時間反応させることによって2-ピリジルマグネシウムブロマイドを形成させた。この2-ピリジルマグネシウムブロマイド溶液をつぎに無水THF(30 mL)中の2-クロロ-1,2-ジヒドロベンゾ[e][1,2]アザボリン(1.0 g, 6.12 mmol)に−78℃で添加した。この混合物を−78℃で2時間撹拌し、室温まで温めた。この混合物を水に注ぎ、酢酸エチルで抽出した。橙色の抽出液を乾燥させ、濃縮した。残留物をカラムクロマトグラフィーにかけて(ヘキサン中30%のEtOAc)0.5gの生成物を得た。
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US12/781,493 US8586203B2 (en) | 2009-05-20 | 2010-05-17 | Metal complexes with boron-nitrogen heterocycle containing ligands |
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EP2448947B1 (en) | 2016-04-20 |
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US8586203B2 (en) | 2013-11-19 |
US9673406B2 (en) | 2017-06-06 |
US20100295032A1 (en) | 2010-11-25 |
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