KR102095001B1 - 신규한 헤테로 고리 화합물 및 이를 이용한 유기발광 소자 - Google Patents
신규한 헤테로 고리 화합물 및 이를 이용한 유기발광 소자 Download PDFInfo
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- KR102095001B1 KR102095001B1 KR1020160119374A KR20160119374A KR102095001B1 KR 102095001 B1 KR102095001 B1 KR 102095001B1 KR 1020160119374 A KR1020160119374 A KR 1020160119374A KR 20160119374 A KR20160119374 A KR 20160119374A KR 102095001 B1 KR102095001 B1 KR 102095001B1
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- PSQANSIANLLSPC-UHFFFAOYSA-N Brc(ccc1c2[o]c3ccccc13)c2Br Chemical compound Brc(ccc1c2[o]c3ccccc13)c2Br PSQANSIANLLSPC-UHFFFAOYSA-N 0.000 description 1
- DHGXKKVKMZRHIN-UHFFFAOYSA-N C(C(C=C1)c2cc(-c3ncccc3)nc(-c3ccccn3)c2)C=C1c1c(c2ccccc2[s]2)c2cc(-c(cc2)ccc2-c2cc(-c3ncccc3)nc(-c3ccccn3)c2)c1 Chemical compound C(C(C=C1)c2cc(-c3ncccc3)nc(-c3ccccn3)c2)C=C1c1c(c2ccccc2[s]2)c2cc(-c(cc2)ccc2-c2cc(-c3ncccc3)nc(-c3ccccn3)c2)c1 DHGXKKVKMZRHIN-UHFFFAOYSA-N 0.000 description 1
- OILFKPAESXOIIH-UHFFFAOYSA-N CC1(C)OB(c(cc2)ccc2-c2nc(-c3ccccc3)nc(-c3ccccc3)c2)OC1(C)C Chemical compound CC1(C)OB(c(cc2)ccc2-c2nc(-c3ccccc3)nc(-c3ccccc3)c2)OC1(C)C OILFKPAESXOIIH-UHFFFAOYSA-N 0.000 description 1
- 0 Cc(c(c(c1c2c(*)c3*)c3c(*)c3*)c3N(*)*)c(*)c1c(*)c(*)c2N(*)[Al] Chemical compound Cc(c(c(c1c2c(*)c3*)c3c(*)c3*)c3N(*)*)c(*)c1c(*)c(*)c2N(*)[Al] 0.000 description 1
- QHQYTGCMOZTXTP-UHFFFAOYSA-N N#Cc(cc1)ccc1-c(cc1)ccc1-c1ccc2[s]c3ccccc3c2c1-c(cc1)ccc1-c(cc1)ccc1C#N Chemical compound N#Cc(cc1)ccc1-c(cc1)ccc1-c1ccc2[s]c3ccccc3c2c1-c(cc1)ccc1-c(cc1)ccc1C#N QHQYTGCMOZTXTP-UHFFFAOYSA-N 0.000 description 1
- FILGICZHDOQIRB-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c(cc2)ccc2-c2ccc3[s]c4ccccc4c3c2-c(cc2)ccc2-c2nc(cccc3)c3[n]2-c2ccccc2)nc2ccccc12 Chemical compound c(cc1)ccc1-[n]1c(-c(cc2)ccc2-c2ccc3[s]c4ccccc4c3c2-c(cc2)ccc2-c2nc(cccc3)c3[n]2-c2ccccc2)nc2ccccc12 FILGICZHDOQIRB-UHFFFAOYSA-N 0.000 description 1
- IAJGLDHYLPFFCR-UHFFFAOYSA-N c(cc1)ccc1-c1cc(-c(cc2)ccc2-c(ccc2c3[o]c4ccccc24)c3-c(cc2)ccc2-c2nc(-c3ccccc3)nc(-c3ccccc3)c2)nc(-c2ccccc2)n1 Chemical compound c(cc1)ccc1-c1cc(-c(cc2)ccc2-c(ccc2c3[o]c4ccccc24)c3-c(cc2)ccc2-c2nc(-c3ccccc3)nc(-c3ccccc3)c2)nc(-c2ccccc2)n1 IAJGLDHYLPFFCR-UHFFFAOYSA-N 0.000 description 1
- LIXVQPIWPUIVQI-UHFFFAOYSA-N c(cc1)ccc1-c1cc(-c(cc2)ccc2-c2ccc3[s]c4ccccc4c3c2-c(cc2)ccc2-c2nc(-c3ccccc3)nc(-c3ccccc3)c2)nc(-c2ccccc2)n1 Chemical compound c(cc1)ccc1-c1cc(-c(cc2)ccc2-c2ccc3[s]c4ccccc4c3c2-c(cc2)ccc2-c2nc(-c3ccccc3)nc(-c3ccccc3)c2)nc(-c2ccccc2)n1 LIXVQPIWPUIVQI-UHFFFAOYSA-N 0.000 description 1
- JXJKRJNRDUJBDC-UHFFFAOYSA-N c(cc1)ccc1-c1cc(-c2cccc(-c(ccc3c4c5ccccc5[s]3)c4-c3cc(-c4nc(-c5ccccc5)nc(-c5ccccc5)c4)ccc3)c2)nc(-c2ccccc2)n1 Chemical compound c(cc1)ccc1-c1cc(-c2cccc(-c(ccc3c4c5ccccc5[s]3)c4-c3cc(-c4nc(-c5ccccc5)nc(-c5ccccc5)c4)ccc3)c2)nc(-c2ccccc2)n1 JXJKRJNRDUJBDC-UHFFFAOYSA-N 0.000 description 1
- FVMZTYYJKZQSHR-UHFFFAOYSA-N c(cc1)ccc1-c1cc(-c2ccccc2)nc(-c2cc(-c(ccc3c4c5ccccc5[s]3)c4-c3cccc(-c4nc(-c5ccccc5)cc(-c5ccccc5)n4)c3)ccc2)n1 Chemical compound c(cc1)ccc1-c1cc(-c2ccccc2)nc(-c2cc(-c(ccc3c4c5ccccc5[s]3)c4-c3cccc(-c4nc(-c5ccccc5)cc(-c5ccccc5)n4)c3)ccc2)n1 FVMZTYYJKZQSHR-UHFFFAOYSA-N 0.000 description 1
- RZJLUTQPBDQDBE-UHFFFAOYSA-N c(cc1)ccc1-c1ccc(-c(cc2)ccc2-c2cc(-c(cc3)ccc3-c3ccc(-c4ccccc4)nn3)c(c3ccccc3[s]3)c3c2)nn1 Chemical compound c(cc1)ccc1-c1ccc(-c(cc2)ccc2-c2cc(-c(cc3)ccc3-c3ccc(-c4ccccc4)nn3)c(c3ccccc3[s]3)c3c2)nn1 RZJLUTQPBDQDBE-UHFFFAOYSA-N 0.000 description 1
- IVSBATOSCCYMKT-UHFFFAOYSA-N c(cc1)ccc1-c1nc(-c(cc2)ccc2-c2ccc3[s]c4ccccc4c3c2-c(cc2)ccc2-c2nc(-c3ccccc3)cc(-c3ccccc3)n2)nc(-c2ccccc2)c1 Chemical compound c(cc1)ccc1-c1nc(-c(cc2)ccc2-c2ccc3[s]c4ccccc4c3c2-c(cc2)ccc2-c2nc(-c3ccccc3)cc(-c3ccccc3)n2)nc(-c2ccccc2)c1 IVSBATOSCCYMKT-UHFFFAOYSA-N 0.000 description 1
- UGOVHINBHKLZSJ-UHFFFAOYSA-N c(cc1)ccc1-c1nc(-c(cc2)ccc2-c2ccc3[s]c4ccccc4c3c2-c(cc2)ccc2-c2nc(-c3ccccc3)nc(-c3ccccc3)n2)nc(-c2ccccc2)n1 Chemical compound c(cc1)ccc1-c1nc(-c(cc2)ccc2-c2ccc3[s]c4ccccc4c3c2-c(cc2)ccc2-c2nc(-c3ccccc3)nc(-c3ccccc3)n2)nc(-c2ccccc2)n1 UGOVHINBHKLZSJ-UHFFFAOYSA-N 0.000 description 1
- TWBDEBMCPLNGDL-UHFFFAOYSA-N c(cc1)ccc1-c1nc(-c2ccccc2)nc(-c2cc(-c(ccc3c4c5ccccc5[s]3)c4-c3cccc(-c4nc(-c5ccccc5)nc(-c5ccccc5)n4)c3)ccc2)n1 Chemical compound c(cc1)ccc1-c1nc(-c2ccccc2)nc(-c2cc(-c(ccc3c4c5ccccc5[s]3)c4-c3cccc(-c4nc(-c5ccccc5)nc(-c5ccccc5)n4)c3)ccc2)n1 TWBDEBMCPLNGDL-UHFFFAOYSA-N 0.000 description 1
- IBALUGPEGXFBQN-UHFFFAOYSA-N c(cc1)ccc1-c1nnc(-c(cc2)ccc2-c2ccc3[s]c4ccccc4c3c2-c(cc2)ccc2-c2nnc(-c3ccccc3)[o]2)[o]1 Chemical compound c(cc1)ccc1-c1nnc(-c(cc2)ccc2-c2ccc3[s]c4ccccc4c3c2-c(cc2)ccc2-c2nnc(-c3ccccc3)[o]2)[o]1 IBALUGPEGXFBQN-UHFFFAOYSA-N 0.000 description 1
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- 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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- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/91—Dibenzofurans; Hydrogenated dibenzofurans
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- C07D333/50—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
- C07D333/76—Dibenzothiophenes
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Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
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KR1020160119374A KR102095001B1 (ko) | 2016-09-19 | 2016-09-19 | 신규한 헤테로 고리 화합물 및 이를 이용한 유기발광 소자 |
CN201710623704.8A CN107840835B (zh) | 2016-09-19 | 2017-07-27 | 新的杂环化合物及利用它的有机发光元件 |
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KR1020160119374A KR102095001B1 (ko) | 2016-09-19 | 2016-09-19 | 신규한 헤테로 고리 화합물 및 이를 이용한 유기발광 소자 |
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KR20180031224A KR20180031224A (ko) | 2018-03-28 |
KR102095001B1 true KR102095001B1 (ko) | 2020-03-30 |
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KR1020160119374A KR102095001B1 (ko) | 2016-09-19 | 2016-09-19 | 신규한 헤테로 고리 화합물 및 이를 이용한 유기발광 소자 |
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CN (1) | CN107840835B (zh) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR102017790B1 (ko) * | 2017-04-13 | 2019-09-03 | 주식회사 엘지화학 | 신규한 헤테로 고리 화합물 및 이를 이용한 유기발광 소자 |
KR102322698B1 (ko) * | 2018-06-22 | 2021-11-09 | 엘티소재주식회사 | 헤테로고리 화합물, 이를 포함하는 유기 발광 소자, 유기 발광 소자의 유기물층용 조성물 및 유기 발광 소자의 제조 방법 |
KR102288756B1 (ko) * | 2018-07-25 | 2021-08-10 | 주식회사 엘지화학 | 신규한 화합물 및 이를 이용한 유기발광 소자 |
KR20200011873A (ko) * | 2018-07-25 | 2020-02-04 | 롬엔드하스전자재료코리아유한회사 | 유기 전계 발광 화합물 및 이를 포함하는 유기 전계 발광 소자 |
KR102303746B1 (ko) * | 2018-10-05 | 2021-09-17 | 주식회사 엘지화학 | 신규한 화합물 및 이를 포함하는 유기발광 소자 |
KR20200074805A (ko) * | 2018-12-17 | 2020-06-25 | 두산솔루스 주식회사 | 유기 발광 화합물 및 이를 이용한 유기 전계 발광 소자 |
CN110143952A (zh) * | 2019-06-17 | 2019-08-20 | 上海天马有机发光显示技术有限公司 | 一种化合物、显示面板及显示装置 |
CN111018847A (zh) * | 2019-10-31 | 2020-04-17 | 陕西莱特光电材料股份有限公司 | 含氮化合物、电子元件及电子装置 |
CN110964009B (zh) * | 2019-11-15 | 2021-08-17 | 北京绿人科技有限责任公司 | 一种含菲啰啉结构的化合物及其应用和一种有机电致发光器件 |
CN111303134A (zh) * | 2020-03-25 | 2020-06-19 | 烟台显华化工科技有限公司 | 一种有机发光材料及有机电致发光器件 |
CN111269219B (zh) * | 2020-03-25 | 2023-05-30 | 烟台显华化工科技有限公司 | 一种有机发光材料及有机电致发光器件 |
KR102536903B1 (ko) * | 2020-08-13 | 2023-05-26 | 엘티소재주식회사 | 헤테로고리 화합물, 이를 포함하는 유기 발광 소자 및 유기 발광 소자의 유기물층용 조성물 |
CN116283943B (zh) * | 2023-05-23 | 2023-08-04 | 苏州驳凡熹科技有限公司 | 一种有机化合物、电致发光材料及电致发光器件 |
CN116761450A (zh) * | 2023-08-18 | 2023-09-15 | 苏州驳凡熹科技有限公司 | 一种有机电致发光元件 |
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JP2015063518A (ja) | 2013-08-30 | 2015-04-09 | 株式会社半導体エネルギー研究所 | 有機化合物、発光素子、発光装置、電子機器、及び照明装置 |
JP5831654B1 (ja) | 2015-02-13 | 2015-12-09 | コニカミノルタ株式会社 | 芳香族複素環誘導体、それを用いた有機エレクトロルミネッセンス素子、照明装置及び表示装置 |
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KR100430549B1 (ko) | 1999-01-27 | 2004-05-10 | 주식회사 엘지화학 | 신규한 착물 및 그의 제조 방법과 이를 이용한 유기 발광 소자 및 그의 제조 방법 |
EP2354135B1 (en) * | 2009-12-23 | 2013-09-18 | Semiconductor Energy Laboratory Co., Ltd. | Benzimidazol-2-yl-phenyl compound, light-emitting element, light-emitting device, electronic device, and lighting device |
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