KR101333697B1 - 벤즈이미다졸계 화합물 및 이를 포함하는 유기 광전 소자 - Google Patents
벤즈이미다졸계 화합물 및 이를 포함하는 유기 광전 소자 Download PDFInfo
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- KR101333697B1 KR101333697B1 KR1020090097762A KR20090097762A KR101333697B1 KR 101333697 B1 KR101333697 B1 KR 101333697B1 KR 1020090097762 A KR1020090097762 A KR 1020090097762A KR 20090097762 A KR20090097762 A KR 20090097762A KR 101333697 B1 KR101333697 B1 KR 101333697B1
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- PZOHSYHZZKQIKK-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(ccc(-c2cc(-c3cc(-[n]4c5ccccc5c5c4cccc5)cc(-c4nc5ccccc5[n]4-c4ccccc4)c3)ncn2)c2)c2c2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c(ccc(-c2cc(-c3cc(-[n]4c5ccccc5c5c4cccc5)cc(-c4nc5ccccc5[n]4-c4ccccc4)c3)ncn2)c2)c2c2c1cccc2 PZOHSYHZZKQIKK-UHFFFAOYSA-N 0.000 description 2
- CMWPRUBXUWQOLX-UHFFFAOYSA-N Brc1cc(-c2nc3ccccc3[n]2-c2ccccc2)cc(-c2cc(-[n]3c4ccccc4c4c3cccc4)cc(-[n]3c(cccc4)c4c4c3cccc4)c2)c1 Chemical compound Brc1cc(-c2nc3ccccc3[n]2-c2ccccc2)cc(-c2cc(-[n]3c4ccccc4c4c3cccc4)cc(-[n]3c(cccc4)c4c4c3cccc4)c2)c1 CMWPRUBXUWQOLX-UHFFFAOYSA-N 0.000 description 1
- IRRVEZBIHFSSFN-UHFFFAOYSA-N Brc1cc(Br)cc(-c2nc3ccccc3[n]2-c2ccccc2)c1 Chemical compound Brc1cc(Br)cc(-c2nc3ccccc3[n]2-c2ccccc2)c1 IRRVEZBIHFSSFN-UHFFFAOYSA-N 0.000 description 1
- KTBSDLMOXIFZBC-UHFFFAOYSA-N CC(C)(C)c(cc1)cc(c2cc(C(C)(C)C)ccc22)c1[n]2-c(cc1)ccc1-c1cc(-c(cc2)ccc2-[n]2c(ccc(C(C)(C)C)c3)c3c3cc(C(C)(C)C)ccc23)cc(-c2nc(cccc3)c3[n]2-c2ccccc2)c1 Chemical compound CC(C)(C)c(cc1)cc(c2cc(C(C)(C)C)ccc22)c1[n]2-c(cc1)ccc1-c1cc(-c(cc2)ccc2-[n]2c(ccc(C(C)(C)C)c3)c3c3cc(C(C)(C)C)ccc23)cc(-c2nc(cccc3)c3[n]2-c2ccccc2)c1 KTBSDLMOXIFZBC-UHFFFAOYSA-N 0.000 description 1
- GOGJGJYLRAUVOC-UHFFFAOYSA-N CC(C)Cc1ccc(c(cccc2)c2[n]2-c3cc(-c4nc5ccccc5[n]4-c4ccccc4)cc(-c4cccc(-c(cc5)ccc5-[n]5c6ccccc6c6c5cccc6)n4)c3)c2c1 Chemical compound CC(C)Cc1ccc(c(cccc2)c2[n]2-c3cc(-c4nc5ccccc5[n]4-c4ccccc4)cc(-c4cccc(-c(cc5)ccc5-[n]5c6ccccc6c6c5cccc6)n4)c3)c2c1 GOGJGJYLRAUVOC-UHFFFAOYSA-N 0.000 description 1
- LEHMGSJPWSSGBO-UHFFFAOYSA-N CC(C)Cc1ccc(c(cccc2)c2[n]2-c3cc(-c4nc5ccccc5[n]4-c4ccccc4)cc(-c4cccc(-c5cccc(-[n]6c(cccc7)c7c7c6cccc7)c5)n4)c3)c2c1 Chemical compound CC(C)Cc1ccc(c(cccc2)c2[n]2-c3cc(-c4nc5ccccc5[n]4-c4ccccc4)cc(-c4cccc(-c5cccc(-[n]6c(cccc7)c7c7c6cccc7)c5)n4)c3)c2c1 LEHMGSJPWSSGBO-UHFFFAOYSA-N 0.000 description 1
- ADMPYRNBAYKWOL-UHFFFAOYSA-N CC1(C)OB(c2cc(-[n]3c(cccc4)c4c4c3cccc4)cc(-[n]3c(cccc4)c4c4c3cccc4)c2)OC1(C)C Chemical compound CC1(C)OB(c2cc(-[n]3c(cccc4)c4c4c3cccc4)cc(-[n]3c(cccc4)c4c4c3cccc4)c2)OC1(C)C ADMPYRNBAYKWOL-UHFFFAOYSA-N 0.000 description 1
- FMBXJPBLCDYPRA-UHFFFAOYSA-N Cc1cccc(C)c1-c1cc(-c2nc3ccccc3[n]2-c2ccccc2)cc(-c2cccc(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)n2)c1 Chemical compound Cc1cccc(C)c1-c1cc(-c2nc3ccccc3[n]2-c2ccccc2)cc(-c2cccc(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)n2)c1 FMBXJPBLCDYPRA-UHFFFAOYSA-N 0.000 description 1
- DDDIAJWRVJUNDF-UHFFFAOYSA-N Cc1cccc(C)c1-c1cc(-c2nc3ccccc3[n]2-c2ccccc2)cc(-c2cncc(-c(cc3)ccc3-[n]3c(cccc4)c4c4c3cccc4)c2)c1 Chemical compound Cc1cccc(C)c1-c1cc(-c2nc3ccccc3[n]2-c2ccccc2)cc(-c2cncc(-c(cc3)ccc3-[n]3c(cccc4)c4c4c3cccc4)c2)c1 DDDIAJWRVJUNDF-UHFFFAOYSA-N 0.000 description 1
- XYXQLFIENLDYBC-UHFFFAOYSA-N Cc1cccc(C)c1-c1cc(-c2nc3ccccc3[n]2-c2ccccc2)cc(-c2cncc(-c3cc(-[n]4c(cccc5)c5c5c4cccc5)ccc3)c2)c1 Chemical compound Cc1cccc(C)c1-c1cc(-c2nc3ccccc3[n]2-c2ccccc2)cc(-c2cncc(-c3cc(-[n]4c(cccc5)c5c5c4cccc5)ccc3)c2)c1 XYXQLFIENLDYBC-UHFFFAOYSA-N 0.000 description 1
- ZVLXIOWRYDGDLF-UHFFFAOYSA-N c(cc1)ccc1-[n](c(cccc1)c1c1c2)c1ccc2-c1cc(-c2nc3ccccc3[n]2-c2ccccc2)cc(-c2cccc(-c3cc(-[n]4c5ccccc5c5c4cccc5)cc(-[n]4c5ccccc5c5ccccc45)c3)n2)c1 Chemical compound c(cc1)ccc1-[n](c(cccc1)c1c1c2)c1ccc2-c1cc(-c2nc3ccccc3[n]2-c2ccccc2)cc(-c2cccc(-c3cc(-[n]4c5ccccc5c5c4cccc5)cc(-[n]4c5ccccc5c5ccccc45)c3)n2)c1 ZVLXIOWRYDGDLF-UHFFFAOYSA-N 0.000 description 1
- HFQSNJJYUNANKA-UHFFFAOYSA-N c(cc1)ccc1-[n](c(cccc1)c1c1c2)c1ccc2-c1cc(-c2nc3ccccc3[n]2-c2ccccc2)cc(-c2cncc(-c3cccc(-[n]4c(cccc5)c5c5c4cccc5)c3)c2)c1 Chemical compound c(cc1)ccc1-[n](c(cccc1)c1c1c2)c1ccc2-c1cc(-c2nc3ccccc3[n]2-c2ccccc2)cc(-c2cncc(-c3cccc(-[n]4c(cccc5)c5c5c4cccc5)c3)c2)c1 HFQSNJJYUNANKA-UHFFFAOYSA-N 0.000 description 1
- WNKQGGBHDWUUFL-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c2cc(-[n]3c(cccc4)c4c4c3cccc4)cc(-c3nc4ccccc4[n]3-c3ccccc3)c2)nc2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c(-c2cc(-[n]3c(cccc4)c4c4c3cccc4)cc(-c3nc4ccccc4[n]3-c3ccccc3)c2)nc2c1cccc2 WNKQGGBHDWUUFL-UHFFFAOYSA-N 0.000 description 1
- QVNUJKICUBUOAR-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c2cc(-[n]3c4ccccc4c4c3cccc4)cc(-c3cc(-[n]4c5ccccc5c5c4cccc5)cc(-[n]4c5ccccc5c5c4cccc5)c3)c2)nc2ccccc12 Chemical compound c(cc1)ccc1-[n]1c(-c2cc(-[n]3c4ccccc4c4c3cccc4)cc(-c3cc(-[n]4c5ccccc5c5c4cccc5)cc(-[n]4c5ccccc5c5c4cccc5)c3)c2)nc2ccccc12 QVNUJKICUBUOAR-UHFFFAOYSA-N 0.000 description 1
- WBBJIBQCPVUQEZ-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c2cc(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)cc(-c(cc3)ccc3-[n]3c4ccccc4c4ccccc34)c2)nc2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c(-c2cc(-c(cc3)ccc3-[n]3c4ccccc4c4c3cccc4)cc(-c(cc3)ccc3-[n]3c4ccccc4c4ccccc34)c2)nc2c1cccc2 WBBJIBQCPVUQEZ-UHFFFAOYSA-N 0.000 description 1
- KNVBNLMRLXHGBJ-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c2cc(-c3cc(-[n]4c(cccc5)c5c5c4cccc5)ccc3)cc(-c3cccc(-[n]4c(cccc5)c5c5c4cccc5)c3)c2)nc2ccccc12 Chemical compound c(cc1)ccc1-[n]1c(-c2cc(-c3cc(-[n]4c(cccc5)c5c5c4cccc5)ccc3)cc(-c3cccc(-[n]4c(cccc5)c5c5c4cccc5)c3)c2)nc2ccccc12 KNVBNLMRLXHGBJ-UHFFFAOYSA-N 0.000 description 1
- XOGFDDZNWYTPRY-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c2cc(-c3cc(-c4cc(-[n]5c6ccccc6c6c5cccc6)ccc4)nc(-c4cccc(-[n]5c(cccc6)c6c6c5cccc6)c4)c3)ccc2)nc2ccccc12 Chemical compound c(cc1)ccc1-[n]1c(-c2cc(-c3cc(-c4cc(-[n]5c6ccccc6c6c5cccc6)ccc4)nc(-c4cccc(-[n]5c(cccc6)c6c6c5cccc6)c4)c3)ccc2)nc2ccccc12 XOGFDDZNWYTPRY-UHFFFAOYSA-N 0.000 description 1
- MLPLPWVIZZDBMG-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c2cc(-c3cccc(-c(cc4)ccc4-[n]4c5ccccc5c5ccccc45)n3)cc(-[n]3c4ccccc4c4c3cccc4)c2)nc2ccccc12 Chemical compound c(cc1)ccc1-[n]1c(-c2cc(-c3cccc(-c(cc4)ccc4-[n]4c5ccccc5c5ccccc45)n3)cc(-[n]3c4ccccc4c4c3cccc4)c2)nc2ccccc12 MLPLPWVIZZDBMG-UHFFFAOYSA-N 0.000 description 1
- HBAUEIORDOGZJX-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c2ccc(-c3cc(-[n]4c5ccccc5c5c4cccc5)ccc3)c(-c3nc(cccc4)c4[n]3-c3ccccc3)c2)nc2ccccc12 Chemical compound c(cc1)ccc1-[n]1c(-c2ccc(-c3cc(-[n]4c5ccccc5c5c4cccc5)ccc3)c(-c3nc(cccc4)c4[n]3-c3ccccc3)c2)nc2ccccc12 HBAUEIORDOGZJX-UHFFFAOYSA-N 0.000 description 1
- UNUGIWSPDJOULV-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(ccc(-c2cc(-c3nc4ccccc4[n]3-c3ccccc3)cc(-c3cccc(-c4cccc(-[n]5c(cccc6)c6c6c5cccc6)c4)n3)c2)c2)c2c2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c(ccc(-c2cc(-c3nc4ccccc4[n]3-c3ccccc3)cc(-c3cccc(-c4cccc(-[n]5c(cccc6)c6c6c5cccc6)c4)n3)c2)c2)c2c2c1cccc2 UNUGIWSPDJOULV-UHFFFAOYSA-N 0.000 description 1
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- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/06—Benzimidazoles; Hydrogenated benzimidazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
- C07D235/08—Radicals containing only hydrogen and carbon atoms
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- 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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- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
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- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
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- H10K85/10—Organic polymers or oligomers
- H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
- H10K85/113—Heteroaromatic compounds comprising sulfur or selene, e.g. polythiophene
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- H10K85/30—Coordination compounds
- H10K85/321—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3]
- H10K85/324—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3] comprising aluminium, e.g. Alq3
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- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/30—Coordination compounds
- H10K85/341—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H10K85/342—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising iridium
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- Electroluminescent Light Sources (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR20080100726 | 2008-10-14 | ||
| KR1020080100726 | 2008-10-14 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20100041690A KR20100041690A (ko) | 2010-04-22 |
| KR101333697B1 true KR101333697B1 (ko) | 2013-11-27 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020090097762A Active KR101333697B1 (ko) | 2008-10-14 | 2009-10-14 | 벤즈이미다졸계 화합물 및 이를 포함하는 유기 광전 소자 |
Country Status (7)
| Country | Link |
|---|---|
| US (2) | US20110272676A1 (https=) |
| EP (1) | EP2344611B1 (https=) |
| JP (1) | JP5694939B2 (https=) |
| KR (1) | KR101333697B1 (https=) |
| CN (1) | CN102159668A (https=) |
| TW (1) | TWI530493B (https=) |
| WO (1) | WO2010044607A1 (https=) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2020111601A1 (ko) * | 2018-11-27 | 2020-06-04 | 주식회사 엘지화학 | 신규한 화합물 및 이를 포함하는 유기발광 소자 |
Families Citing this family (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102272262B (zh) | 2008-12-30 | 2014-09-10 | 第一毛织株式会社 | 有机光电装置用新化合物和包括该化合物的有机光电装置 |
| CN102596939B (zh) * | 2009-09-16 | 2014-08-13 | 日东电工株式会社 | 用于有机发光二极管发射层的化合物 |
| JP5620125B2 (ja) * | 2010-01-28 | 2014-11-05 | ユー・ディー・シー アイルランド リミテッド | 有機電界発光素子 |
| WO2012012295A1 (en) * | 2010-07-19 | 2012-01-26 | Nitto Denko Corporation | Phototherapy devices and methods comprising substituted carbazole compounds |
| JP5872861B2 (ja) * | 2010-11-30 | 2016-03-01 | 株式会社半導体エネルギー研究所 | カルバゾール化合物 |
| US8426040B2 (en) * | 2010-12-22 | 2013-04-23 | Nitto Denko Corporation | Compounds for use in light-emitting devices |
| CN103459551B (zh) * | 2011-01-27 | 2016-06-15 | 日东电工株式会社 | 包含任意取代的三联苯和四联苯化合物的光疗装置和方法 |
| US8933243B2 (en) | 2011-06-22 | 2015-01-13 | Nitto Denko Corporation | Polyphenylene host compounds |
| KR101474797B1 (ko) | 2011-08-08 | 2014-12-19 | 제일모직 주식회사 | 유기광전자소자용 화합물 및 이를 포함하는 유기발광소자 |
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2011
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Also Published As
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|---|---|
| EP2344611B1 (en) | 2014-02-26 |
| US9530970B2 (en) | 2016-12-27 |
| EP2344611A1 (en) | 2011-07-20 |
| JP5694939B2 (ja) | 2015-04-01 |
| EP2344611A4 (en) | 2012-04-04 |
| CN102159668A (zh) | 2011-08-17 |
| WO2010044607A1 (en) | 2010-04-22 |
| US20130256641A1 (en) | 2013-10-03 |
| KR20100041690A (ko) | 2010-04-22 |
| JP2012505829A (ja) | 2012-03-08 |
| TWI530493B (zh) | 2016-04-21 |
| US20110272676A1 (en) | 2011-11-10 |
| TW201022232A (en) | 2010-06-16 |
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