JP2013539750A - 新規有機電界発光化合物およびこれを使用する有機電界発光素子 - Google Patents
新規有機電界発光化合物およびこれを使用する有機電界発光素子 Download PDFInfo
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- JP2013539750A JP2013539750A JP2013529060A JP2013529060A JP2013539750A JP 2013539750 A JP2013539750 A JP 2013539750A JP 2013529060 A JP2013529060 A JP 2013529060A JP 2013529060 A JP2013529060 A JP 2013529060A JP 2013539750 A JP2013539750 A JP 2013539750A
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- substituted
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- aryl
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- 0 C*CC=CC1*(C)C(CCC(C(C)*2)(*=C)N)[C@]2C(*)*1C Chemical compound C*CC=CC1*(C)C(CCC(C(C)*2)(*=C)N)[C@]2C(*)*1C 0.000 description 17
- SDNQERUOELVIOF-UHFFFAOYSA-N c(cc1)cc(c2c3)c1[nH]c2ccc3-c1cccc2c1[s]c1c2cccc1 Chemical compound c(cc1)cc(c2c3)c1[nH]c2ccc3-c1cccc2c1[s]c1c2cccc1 SDNQERUOELVIOF-UHFFFAOYSA-N 0.000 description 3
- QUQDGEOUBORSRB-UHFFFAOYSA-N c(cc1)cc2c1[o]c1c2cccc1-c(cc12)ccc1[nH]c1c2c(cccc2)c2cc1 Chemical compound c(cc1)cc2c1[o]c1c2cccc1-c(cc12)ccc1[nH]c1c2c(cccc2)c2cc1 QUQDGEOUBORSRB-UHFFFAOYSA-N 0.000 description 3
- TXLRAQXGAKHLAO-UHFFFAOYSA-N c(cc1)cc(c2c3)c1[nH]c2ccc3-c1cccc2c1[o]c1c2cccc1 Chemical compound c(cc1)cc(c2c3)c1[nH]c2ccc3-c1cccc2c1[o]c1c2cccc1 TXLRAQXGAKHLAO-UHFFFAOYSA-N 0.000 description 2
- BPHYUWGUPNUAKW-UHFFFAOYSA-N c(cc1)cc2c1[nH]nc2-c1c2[o]c(cccc3)c3c2ccc1 Chemical compound c(cc1)cc2c1[nH]nc2-c1c2[o]c(cccc3)c3c2ccc1 BPHYUWGUPNUAKW-UHFFFAOYSA-N 0.000 description 2
- PVCZRPLJMFEXGE-UHFFFAOYSA-N c(cc1)ccc1-[n](c(cc1)c2cc1-c(cc1)cc3c1[nH]c1c3cccc1)c1c2c(cccc2)c2cc1 Chemical compound c(cc1)ccc1-[n](c(cc1)c2cc1-c(cc1)cc3c1[nH]c1c3cccc1)c1c2c(cccc2)c2cc1 PVCZRPLJMFEXGE-UHFFFAOYSA-N 0.000 description 2
- HVNBXJBAUNUPCC-UHFFFAOYSA-N C(C1)C=C(c(cccc2)c2S2)C2=C1c1ccc2[nH]c(cccc3)c3c2c1 Chemical compound C(C1)C=C(c(cccc2)c2S2)C2=C1c1ccc2[nH]c(cccc3)c3c2c1 HVNBXJBAUNUPCC-UHFFFAOYSA-N 0.000 description 1
- PBESWPOMHWAVRO-UHFFFAOYSA-N C(C1C=C2)=CC=CC1c(c1c3ccc(-c4ccc5[nH]c(cccc6)c6c5c4)c1)c2[n]3-c1ccccc1 Chemical compound C(C1C=C2)=CC=CC1c(c1c3ccc(-c4ccc5[nH]c(cccc6)c6c5c4)c1)c2[n]3-c1ccccc1 PBESWPOMHWAVRO-UHFFFAOYSA-N 0.000 description 1
- LDLJCSDQETWSQO-GGCSAXROSA-N C([C@H](C=C1)c(cc2c3c4cccc3)ccc2[n]4-c(cc2)ccc2-c2nc(cccc3)c3c(-c(cc3)ccc3-c3cc4ccccc4cc3)n2)c(c2c3ccc4c2cccc4)c1[n]3-c1ccccc1 Chemical compound C([C@H](C=C1)c(cc2c3c4cccc3)ccc2[n]4-c(cc2)ccc2-c2nc(cccc3)c3c(-c(cc3)ccc3-c3cc4ccccc4cc3)n2)c(c2c3ccc4c2cccc4)c1[n]3-c1ccccc1 LDLJCSDQETWSQO-GGCSAXROSA-N 0.000 description 1
- IJHMCELYOWGCIF-CDXXIHCBSA-N C/C=C(\C=C/C#C)/c1n[nH]c2ccccc12 Chemical compound C/C=C(\C=C/C#C)/c1n[nH]c2ccccc12 IJHMCELYOWGCIF-CDXXIHCBSA-N 0.000 description 1
- SXBCONQKVGMTPU-XDOYNYLZSA-N C/N=C(/c(cc1)ccc1-c1ccccc1)\c(cccc1)c1N Chemical compound C/N=C(/c(cc1)ccc1-c1ccccc1)\c(cccc1)c1N SXBCONQKVGMTPU-XDOYNYLZSA-N 0.000 description 1
- XYTBISUZJJIJTP-FVDSYPCUSA-N C/N=C(/c1cc(-c2c3[o]c(cccc4)c4c3ccc2)ccc1)\c1ccccc1N Chemical compound C/N=C(/c1cc(-c2c3[o]c(cccc4)c4c3ccc2)ccc1)\c1ccccc1N XYTBISUZJJIJTP-FVDSYPCUSA-N 0.000 description 1
- KLNPGDOCAGHKPE-UHFFFAOYSA-N C1C=CC=CC1[n]1c2cc(-c3n[nH]c4c3cccc4)ccc2c2ccccc12 Chemical compound C1C=CC=CC1[n]1c2cc(-c3n[nH]c4c3cccc4)ccc2c2ccccc12 KLNPGDOCAGHKPE-UHFFFAOYSA-N 0.000 description 1
- PCJCYWZFDBHLGN-UHFFFAOYSA-N CC(C)(C)c1n[nH]c2ccccc12 Chemical compound CC(C)(C)c1n[nH]c2ccccc12 PCJCYWZFDBHLGN-UHFFFAOYSA-N 0.000 description 1
- VIVZXDQTJQMLAI-UHFFFAOYSA-N CC(C)(c1c2)C(C=CCC3)=C3c1ccc2-c1n[nH]c2ccccc12 Chemical compound CC(C)(c1c2)C(C=CCC3)=C3c1ccc2-c1n[nH]c2ccccc12 VIVZXDQTJQMLAI-UHFFFAOYSA-N 0.000 description 1
- FOFCLEWSMSEBHS-UHFFFAOYSA-N CC(C1c2c3ccc(-c4ccc5[nH]c(cccc6)c6c5c4)c2)(C=Cc2c1cccc2)N3c1ccccc1 Chemical compound CC(C1c2c3ccc(-c4ccc5[nH]c(cccc6)c6c5c4)c2)(C=Cc2c1cccc2)N3c1ccccc1 FOFCLEWSMSEBHS-UHFFFAOYSA-N 0.000 description 1
- PCMDBYLTUMFUSY-UHFFFAOYSA-N CC1(C)c(cc(cc2)-c(cc3)cc(c4c(cccc5)c5ccc44)c3[n]4-c3nc(cccc4)c4c(-c(cc4)ccc4-c4ccccc4)n3)c2-c2c1cccc2 Chemical compound CC1(C)c(cc(cc2)-c(cc3)cc(c4c(cccc5)c5ccc44)c3[n]4-c3nc(cccc4)c4c(-c(cc4)ccc4-c4ccccc4)n3)c2-c2c1cccc2 PCMDBYLTUMFUSY-UHFFFAOYSA-N 0.000 description 1
- JUWGTHMXSZIOPB-UHFFFAOYSA-N CC1(C)c2cc(-c3n[nH]c4c3cccc4)ccc2-c2ccccc12 Chemical compound CC1(C)c2cc(-c3n[nH]c4c3cccc4)ccc2-c2ccccc12 JUWGTHMXSZIOPB-UHFFFAOYSA-N 0.000 description 1
- ICFSJJIABGSHNB-UHFFFAOYSA-N Cc1cc(C)cc(-c2nc(-[n]3c4ccc(cccc5)c5c4c4cc(-c(cc5c6c7cccc6)ccc5[n]7C5=CC=CCC5)ccc34)nc3c2cccc3)c1 Chemical compound Cc1cc(C)cc(-c2nc(-[n]3c4ccc(cccc5)c5c4c4cc(-c(cc5c6c7cccc6)ccc5[n]7C5=CC=CCC5)ccc34)nc3c2cccc3)c1 ICFSJJIABGSHNB-UHFFFAOYSA-N 0.000 description 1
- PXWDUBIXHILMTR-UHFFFAOYSA-N c(cc1)cc2c1[nH]nc2-c(cc1)ccc1-c1cccc2c1[s]c1ccccc21 Chemical compound c(cc1)cc2c1[nH]nc2-c(cc1)ccc1-c1cccc2c1[s]c1ccccc21 PXWDUBIXHILMTR-UHFFFAOYSA-N 0.000 description 1
- JKMTWYWJKYCSIA-UHFFFAOYSA-N c(cc1)cc2c1[s]c1c2cccc1-c1ccc2[nH]c3ccc(cccc4)c4c3c2c1 Chemical compound c(cc1)cc2c1[s]c1c2cccc1-c1ccc2[nH]c3ccc(cccc4)c4c3c2c1 JKMTWYWJKYCSIA-UHFFFAOYSA-N 0.000 description 1
- AKQIDHGDRLXWRS-UHFFFAOYSA-N c(cc1)ccc1-[n](c(cc1)c2cc1-c(cc1c3c4cccc3)ccc1[n]4-c1nc3ccccc3c(-c3c4[s]c(cccc5)c5c4ccc3)n1)c1c2c(cccc2)c2cc1 Chemical compound c(cc1)ccc1-[n](c(cc1)c2cc1-c(cc1c3c4cccc3)ccc1[n]4-c1nc3ccccc3c(-c3c4[s]c(cccc5)c5c4ccc3)n1)c1c2c(cccc2)c2cc1 AKQIDHGDRLXWRS-UHFFFAOYSA-N 0.000 description 1
- YAIXQZKNYMQUHW-UHFFFAOYSA-N c(cc1)ccc1-c(cc1)ccc1-c(cc1)ccc1-c1n[nH]c2ccccc12 Chemical compound c(cc1)ccc1-c(cc1)ccc1-c(cc1)ccc1-c1n[nH]c2ccccc12 YAIXQZKNYMQUHW-UHFFFAOYSA-N 0.000 description 1
- HWCOABRTFHFJPO-UHFFFAOYSA-N c(cc1)ccc1-c(cc1)ccc1-c1n[nH]c2ccccc12 Chemical compound c(cc1)ccc1-c(cc1)ccc1-c1n[nH]c2ccccc12 HWCOABRTFHFJPO-UHFFFAOYSA-N 0.000 description 1
- WOKLEXWSINFSPY-UHFFFAOYSA-N c(cc1)ccc1-c(cc1)ccc1-c1nc(-[n](c(cc2)c3cc2-c(cc2)cc4c2[o]c2ccccc42)c2c3c(cccc3)c3cc2)nc2c1cccc2 Chemical compound c(cc1)ccc1-c(cc1)ccc1-c1nc(-[n](c(cc2)c3cc2-c(cc2)cc4c2[o]c2ccccc42)c2c3c(cccc3)c3cc2)nc2c1cccc2 WOKLEXWSINFSPY-UHFFFAOYSA-N 0.000 description 1
- MNBSJSLKJVGGBL-UHFFFAOYSA-N c(cc1)ccc1-c(cccc1)c1-c(cc1)ccc1-c1n[nH]c2ccccc12 Chemical compound c(cc1)ccc1-c(cccc1)c1-c(cc1)ccc1-c1n[nH]c2ccccc12 MNBSJSLKJVGGBL-UHFFFAOYSA-N 0.000 description 1
- ZINDBEYFEJGNRZ-UHFFFAOYSA-N c(cc1)ccc1-c1cc(-c(cc2)ccc2-c2n[nH]c3c2cccc3)ccc1 Chemical compound c(cc1)ccc1-c1cc(-c(cc2)ccc2-c2n[nH]c3c2cccc3)ccc1 ZINDBEYFEJGNRZ-UHFFFAOYSA-N 0.000 description 1
- QRUXFVGFIGSGJU-UHFFFAOYSA-N c(cc1)ccc1-c1cc(-c2cc(-c3n[nH]c4ccccc34)ccc2)ccc1 Chemical compound c(cc1)ccc1-c1cc(-c2cc(-c3n[nH]c4ccccc34)ccc2)ccc1 QRUXFVGFIGSGJU-UHFFFAOYSA-N 0.000 description 1
- UHDVQAVHUQRAPG-UHFFFAOYSA-N c(cc1)ccc1-c1nc(-[n](c(cccc2)c2c2c3)c2ccc3-c2cccc3c2[s]c2c3cccc2)nc2ccccc12 Chemical compound c(cc1)ccc1-c1nc(-[n](c(cccc2)c2c2c3)c2ccc3-c2cccc3c2[s]c2c3cccc2)nc2ccccc12 UHDVQAVHUQRAPG-UHFFFAOYSA-N 0.000 description 1
- CGRXRKTUPUWMLW-UHFFFAOYSA-N c(cc1)ccc1-c1nc(-[n](c2ccccc2c2c3)c2ccc3-c2cccc3c2[o]c2ccccc32)nc2ccccc12 Chemical compound c(cc1)ccc1-c1nc(-[n](c2ccccc2c2c3)c2ccc3-c2cccc3c2[o]c2ccccc32)nc2ccccc12 CGRXRKTUPUWMLW-UHFFFAOYSA-N 0.000 description 1
- XPYFGPCDTKXYQQ-UHFFFAOYSA-N c(cc1)ccc1-c1nc(-[n]2c3ccc(cccc4)c4c3c3c2ccc(-c(cc2)cc4c2c(cccc2)c2[n]4-c2ccccc2)c3)nc2c1cccc2 Chemical compound c(cc1)ccc1-c1nc(-[n]2c3ccc(cccc4)c4c3c3c2ccc(-c(cc2)cc4c2c(cccc2)c2[n]4-c2ccccc2)c3)nc2c1cccc2 XPYFGPCDTKXYQQ-UHFFFAOYSA-N 0.000 description 1
- HFGZDOUBEINRJN-UHFFFAOYSA-N c(cc1-2)ccc1-c1ccc(-c(cc3)ccc3-c3nc(-c(cc4)ccc4-[n](c(cccc4)c4c4c5)c4ccc5-c(cc45)ccc4[s]c4c5c(cccc5)c5cc4)nc4c3cccc4)c3c1c-2ccc3 Chemical compound c(cc1-2)ccc1-c1ccc(-c(cc3)ccc3-c3nc(-c(cc4)ccc4-[n](c(cccc4)c4c4c5)c4ccc5-c(cc45)ccc4[s]c4c5c(cccc5)c5cc4)nc4c3cccc4)c3c1c-2ccc3 HFGZDOUBEINRJN-UHFFFAOYSA-N 0.000 description 1
- IWNVVLAXMQFSLL-UHFFFAOYSA-N c(cc12)ccc1[nH]nc2-c(cc1)ccc1-c1c2[o]c(cccc3)c3c2ccc1 Chemical compound c(cc12)ccc1[nH]nc2-c(cc1)ccc1-c1c2[o]c(cccc3)c3c2ccc1 IWNVVLAXMQFSLL-UHFFFAOYSA-N 0.000 description 1
- BAXOFTOLAUCFNW-UHFFFAOYSA-N c1n[nH]c2ccccc12 Chemical compound c1n[nH]c2ccccc12 BAXOFTOLAUCFNW-UHFFFAOYSA-N 0.000 description 1
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- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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- H05B33/00—Electroluminescent light sources
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- H10K50/00—Organic light-emitting devices
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- H10K85/342—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising iridium
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- H10K85/60—Organic compounds having low molecular weight
- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6574—Polycyclic condensed heteroaromatic hydrocarbons comprising only oxygen in the heteroaromatic polycondensed ring system, e.g. cumarine dyes
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- H10K85/649—Aromatic compounds comprising a hetero atom
- H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
- H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
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- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
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- C09K2211/1044—Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1088—Heterocyclic compounds characterised by ligands containing oxygen as the only heteroatom
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1092—Heterocyclic compounds characterised by ligands containing sulfur as the only heteroatom
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
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- H10K2101/00—Properties of the organic materials covered by group H10K85/00
- H10K2101/10—Triplet emission
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
- Plural Heterocyclic Compounds (AREA)
- Laminated Bodies (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR20100091545 | 2010-09-17 | ||
| KR10-2010-0091545 | 2010-09-17 | ||
| KR10-2011-0092422 | 2011-09-14 | ||
| KR1020110092422A KR101477614B1 (ko) | 2010-09-17 | 2011-09-14 | 신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 전계 발광 소자 |
| PCT/KR2011/006810 WO2012036482A1 (en) | 2010-09-17 | 2011-09-16 | Novel organic electroluminescent compounds and organic electroluminescent device using the same |
Related Child Applications (1)
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10071993B2 (en) | 2010-09-21 | 2018-09-11 | Semiconductor Energy Laboratory Co., Ltd. | Carbazole derivative, light-emitting element material and organic semiconductor material |
| JP2015053488A (ja) * | 2010-09-21 | 2015-03-19 | 株式会社半導体エネルギー研究所 | 有機半導体素子 |
| US9450188B2 (en) | 2010-09-21 | 2016-09-20 | Semiconductor Energy Laboratory Co., Ltd. | Carbazole derivative, light-emitting element material and organic semiconductor material |
| JP2013546171A (ja) * | 2010-10-13 | 2013-12-26 | ローム・アンド・ハース・エレクトロニック・マテリアルズ・コリア・リミテッド | 有機電子材料のための新規化合物、およびこれを使用する有機電界発光素子 |
| JP2016145225A (ja) * | 2011-03-08 | 2016-08-12 | ローム・アンド・ハース・エレクトロニック・マテリアルズ・コリア・リミテッド | 新規な有機エレクトロルミネッセンス化合物およびそれを用いる有機エレクトロルミネッセンス素子 |
| JPWO2012128298A1 (ja) * | 2011-03-24 | 2014-07-24 | 出光興産株式会社 | ビスカルバゾール誘導体およびこれを用いた有機エレクトロルミネッセンス素子 |
| JP2014514344A (ja) * | 2011-05-03 | 2014-06-19 | ローム・アンド・ハース・エレクトロニック・マテリアルズ・コリア・リミテッド | 新規な有機電界発光化合物および同化合物を使用した有機電界発光素子 |
| JP2014522401A (ja) * | 2011-05-30 | 2014-09-04 | ローム・アンド・ハース・エレクトロニック・マテリアルズ・コリア・リミテッド | 有機エレクトロニクス材料用の新規化合物およびそれを使用した有機エレクトロルミネッセンス素子 |
| JP2017515809A (ja) * | 2014-05-02 | 2017-06-15 | ローム・アンド・ハース・エレクトロニック・マテリアルズ・コリア・リミテッド | 有機電界発光化合物及びそれを含む有機電界発光デバイス |
| JP2017523153A (ja) * | 2014-06-27 | 2017-08-17 | ヒソン・マテリアル・リミテッドHeesung Material Ltd. | 複素環化合物及びそれを用いた有機発光素子 |
| US10644244B2 (en) | 2014-06-27 | 2020-05-05 | Lt Materials Co., Ltd. | Heterocyclic compound and organic light emitting device using same |
| US10035765B2 (en) | 2014-10-14 | 2018-07-31 | Lg Chem, Ltd. | Nitrogen-containing polycyclic compound and organic light emitting device using same |
| JP2017533884A (ja) * | 2014-10-14 | 2017-11-16 | エルジー・ケム・リミテッド | 含窒素多環化合物及びこれを用いる有機発光素子 |
| JP2019501868A (ja) * | 2015-10-13 | 2019-01-24 | ローム・アンド・ハース・エレクトロニック・マテリアルズ・コリア・リミテッド | 有機電界発光化合物及びそれを含む有機電界発光デバイス |
| JP2022515619A (ja) * | 2018-12-27 | 2022-02-21 | エルティー・マテリアルズ・カンパニー・リミテッド | 多環化合物およびこれを含む有機発光素子 |
| JP7329266B2 (ja) | 2018-12-27 | 2023-08-18 | エルティー・マテリアルズ・カンパニー・リミテッド | 多環化合物およびこれを含む有機発光素子 |
| WO2025192265A1 (ja) * | 2024-03-13 | 2025-09-18 | キヤノン株式会社 | 有機化合物及び有機発光素子 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP6672416B2 (ja) | 2020-03-25 |
| JP2019050382A (ja) | 2019-03-28 |
| EP2616462A4 (en) | 2014-02-19 |
| CN103221406A (zh) | 2013-07-24 |
| CN109020960A (zh) | 2018-12-18 |
| CN109020960B (zh) | 2022-05-10 |
| KR101477614B1 (ko) | 2014-12-31 |
| WO2012036482A1 (en) | 2012-03-22 |
| TW201224110A (en) | 2012-06-16 |
| JP2017031167A (ja) | 2017-02-09 |
| KR20120030009A (ko) | 2012-03-27 |
| EP2616462A1 (en) | 2013-07-24 |
| TWI560258B (en) | 2016-12-01 |
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