JP2008195841A5 - - Google Patents
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- JP2008195841A5 JP2008195841A5 JP2007033012A JP2007033012A JP2008195841A5 JP 2008195841 A5 JP2008195841 A5 JP 2008195841A5 JP 2007033012 A JP2007033012 A JP 2007033012A JP 2007033012 A JP2007033012 A JP 2007033012A JP 2008195841 A5 JP2008195841 A5 JP 2008195841A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- light emitting
- light
- emitting device
- aryl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000463 material Substances 0.000 claims description 19
- 125000003118 aryl group Chemical group 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 9
- 125000001072 heteroaryl group Chemical group 0.000 claims description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 125000000732 arylene group Chemical group 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000004414 alkyl thio group Chemical group 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- 125000005013 aryl ether group Chemical group 0.000 claims description 3
- 150000004832 aryl thioethers Chemical group 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 125000005549 heteroarylene group Chemical group 0.000 claims description 3
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- 125000001624 naphthyl group Chemical group 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 125000005561 phenanthryl group Chemical group 0.000 claims description 3
- 125000001725 pyrenyl group Chemical group 0.000 claims description 3
- 125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 claims description 3
- 125000001424 substituent group Chemical group 0.000 claims description 3
- 239000002019 doping agent Substances 0.000 claims description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims 1
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Natural products C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims 1
- -1 anthracene compound Chemical class 0.000 claims 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 239000001301 oxygen Substances 0.000 claims 1
- 229910052698 phosphorus Inorganic materials 0.000 claims 1
- 239000011574 phosphorus Substances 0.000 claims 1
- 239000010703 silicon Substances 0.000 claims 1
- 229910052710 silicon Inorganic materials 0.000 claims 1
- 239000000758 substrate Substances 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- CAYQIZIAYYNFCS-UHFFFAOYSA-N (4-chlorophenyl)boronic acid Chemical compound OB(O)C1=CC=C(Cl)C=C1 CAYQIZIAYYNFCS-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- LWIHDJKSTIGBAC-UHFFFAOYSA-K tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- SDEAGACSNFSZCU-UHFFFAOYSA-N (3-chlorophenyl)boronic acid Chemical compound OB(O)C1=CC=CC(Cl)=C1 SDEAGACSNFSZCU-UHFFFAOYSA-N 0.000 description 1
- OMNWKPZIFZJANV-UHFFFAOYSA-N 1-(4-chlorophenyl)-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1C1=CC=C(Cl)C=C1 OMNWKPZIFZJANV-UHFFFAOYSA-N 0.000 description 1
- ORPVVAKYSXQCJI-UHFFFAOYSA-N 1-bromo-2-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1Br ORPVVAKYSXQCJI-UHFFFAOYSA-N 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000011259 mixed solution Substances 0.000 description 1
- IBHBKWKFFTZAHE-UHFFFAOYSA-N n-[4-[4-(n-naphthalen-1-ylanilino)phenyl]phenyl]-n-phenylnaphthalen-1-amine Chemical group C1=CC=CC=C1N(C=1C2=CC=CC=C2C=CC=1)C1=CC=C(C=2C=CC(=CC=2)N(C=2C=CC=CC=2)C=2C3=CC=CC=C3C=CC=2)C=C1 IBHBKWKFFTZAHE-UHFFFAOYSA-N 0.000 description 1
- UEHQKVMRKBARNQ-UHFFFAOYSA-N n-naphthalen-1-yl-n-phenyl-9h-carbazol-3-amine Chemical compound C1=CC=CC=C1N(C=1C2=CC=CC=C2C=CC=1)C1=CC=C(NC=2C3=CC=CC=2)C3=C1 UEHQKVMRKBARNQ-UHFFFAOYSA-N 0.000 description 1
- 230000010355 oscillation Effects 0.000 description 1
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- 229910000404 tripotassium phosphate Inorganic materials 0.000 description 1
- 235000019798 tripotassium phosphate Nutrition 0.000 description 1
- 229910021642 ultra pure water Inorganic materials 0.000 description 1
- 239000012498 ultrapure water Substances 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007033012A JP2008195841A (ja) | 2007-02-14 | 2007-02-14 | 発光素子材料および発光素子 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2007033012A JP2008195841A (ja) | 2007-02-14 | 2007-02-14 | 発光素子材料および発光素子 |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2008195841A JP2008195841A (ja) | 2008-08-28 |
JP2008195841A5 true JP2008195841A5 (enrdf_load_stackoverflow) | 2010-03-25 |
Family
ID=39755087
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2007033012A Pending JP2008195841A (ja) | 2007-02-14 | 2007-02-14 | 発光素子材料および発光素子 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2008195841A (enrdf_load_stackoverflow) |
Families Citing this family (37)
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US7723722B2 (en) | 2007-03-23 | 2010-05-25 | Semiconductor Energy Laboratory Co., Ltd. | Organic compound, anthracene derivative, and light-emitting element, light-emitting device, and electronic device using anthracene derivative |
KR101579918B1 (ko) * | 2007-04-25 | 2015-12-24 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 유기 화합물, 안트라센 유도체, 및 안트라센 유도체를 사용한 발광소자, 발광장치, 및 전자 기기 |
JP5501656B2 (ja) * | 2008-05-16 | 2014-05-28 | 株式会社半導体エネルギー研究所 | 組成物、薄膜の作製方法、及び発光素子の作製方法 |
JP5459903B2 (ja) * | 2008-09-02 | 2014-04-02 | 株式会社半導体エネルギー研究所 | アントラセン誘導体、発光素子、発光装置、電子機器、及び照明装置 |
CN102224150B (zh) * | 2008-11-25 | 2015-08-12 | 出光兴产株式会社 | 芳香族胺衍生物以及有机电致发光元件 |
JP5609256B2 (ja) * | 2009-05-20 | 2014-10-22 | 東ソー株式会社 | 2−アミノカルバゾール化合物及びその用途 |
JP5716270B2 (ja) * | 2009-10-20 | 2015-05-13 | 東ソー株式会社 | カルバゾール化合物およびその用途 |
KR101929151B1 (ko) * | 2009-10-20 | 2018-12-13 | 토소가부시키가이샤 | 카바졸 화합물 및 그 용도 |
JP5585044B2 (ja) * | 2009-10-20 | 2014-09-10 | 東ソー株式会社 | カルバゾール化合物及びその用途 |
JP5750821B2 (ja) * | 2009-11-09 | 2015-07-22 | 三菱化学株式会社 | 有機化合物、有機電界発光素子材料、有機電界発光素子用組成物、有機電界発光素子、有機el表示装置及び有機el照明 |
EP2518038A4 (en) * | 2009-12-21 | 2013-06-26 | Idemitsu Kosan Co | PYRENE DERIVATIVE AND ORGANIC ELECTROLUMINESCENT ELEMENT THEREWITH |
EP2521197B8 (en) * | 2009-12-28 | 2019-03-27 | NIPPON STEEL Chemical & Material Co., Ltd. | Organic electroluminescent element |
JP5623996B2 (ja) | 2010-09-21 | 2014-11-12 | 株式会社半導体エネルギー研究所 | カルバゾール誘導体 |
JP5856266B2 (ja) * | 2010-09-21 | 2016-02-09 | 株式会社半導体エネルギー研究所 | 有機半導体素子 |
US9337432B2 (en) * | 2010-12-09 | 2016-05-10 | Nippon Steel & Sumkin Chemical Co., Ltd. | Organic electroluminescent element |
TWI545175B (zh) * | 2010-12-17 | 2016-08-11 | 半導體能源研究所股份有限公司 | 有機化合物,發光元件,發光裝置,電子裝置,以及照明裝置 |
CN106187859A (zh) * | 2011-07-22 | 2016-12-07 | 株式会社半导体能源研究所 | 二苯并[c,g]咔唑化合物、发光元件、发光装置、显示装置、照明装置以及电子设备 |
EP2762478A1 (en) * | 2011-09-15 | 2014-08-06 | Idemitsu Kosan Co., Ltd | Aromatic amine derivative and organic electroluminescence element using same |
JP6115075B2 (ja) * | 2011-10-26 | 2017-04-19 | 東ソー株式会社 | 4−アミノカルバゾール化合物及びその用途 |
EP2772483B1 (en) * | 2011-10-26 | 2017-03-29 | Tosoh Corporation | 4-aminocarbazole compound and use of same |
WO2014088285A1 (ko) * | 2012-12-06 | 2014-06-12 | 덕산하이메탈(주) | 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 |
KR102098093B1 (ko) * | 2012-12-06 | 2020-04-08 | 덕산네오룩스 주식회사 | 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 |
JP6032107B2 (ja) * | 2013-04-16 | 2016-11-24 | 東ソー株式会社 | 2,5−ジアミノカルバゾール化合物及びその用途 |
KR101550429B1 (ko) * | 2013-04-30 | 2015-09-08 | (주)피엔에이치테크 | 새로운 유기전계발광소자용 화합물 및 그를 포함하는 유기전계발광소자 |
TW201542524A (zh) | 2013-09-09 | 2015-11-16 | Tosoh Corp | 2-胺基咔唑化合物及其用途 |
KR102106803B1 (ko) * | 2013-11-14 | 2020-05-06 | 덕산네오룩스 주식회사 | 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 |
US10418564B2 (en) | 2014-04-11 | 2019-09-17 | Merck Patent Gmbh | Materials for organic electroluminescent devices |
KR101512059B1 (ko) | 2014-10-06 | 2015-04-14 | 덕산네오룩스 주식회사 | 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 |
WO2017052138A2 (ko) * | 2015-09-25 | 2017-03-30 | 주식회사 엘지화학 | 아민계 화합물 및 이를 포함하는 유기 발광 소자 |
WO2017122669A1 (ja) * | 2016-01-15 | 2017-07-20 | 東ソー株式会社 | カルバゾール化合物及びその用途 |
JP6848424B2 (ja) * | 2016-01-15 | 2021-03-24 | 東ソー株式会社 | カルバゾール化合物及びその用途 |
KR102844041B1 (ko) * | 2016-02-26 | 2025-08-11 | 가부시키가이샤 한도오따이 에네루기 켄큐쇼 | 유기 화합물, 발광 소자, 발광 장치, 전자 기기, 및 조명 장치 |
JP2018123083A (ja) * | 2017-01-31 | 2018-08-09 | 出光興産株式会社 | 新規アントラセン誘導体、有機エレクトロルミネッセンス素子用材料、有機エレクトロルミネッセンス素子用材料溶液、有機エレクトロルミネッセンス素子及び電子機器 |
CN110590827B (zh) * | 2019-09-30 | 2023-02-03 | 武汉天马微电子有限公司 | 一种有机电致发光化合物及其应用 |
KR102680021B1 (ko) * | 2021-03-08 | 2024-06-28 | 주식회사 엘지화학 | 신규한 화합물 및 이를 포함한 유기 발광 소자 |
KR102654812B1 (ko) * | 2021-03-08 | 2024-04-03 | 주식회사 엘지화학 | 유기 발광 소자 |
CN114957094A (zh) * | 2022-06-09 | 2022-08-30 | 北京八亿时空液晶科技股份有限公司 | 一种多取代咔唑衍生物及其应用 |
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JP3649302B2 (ja) * | 1996-05-23 | 2005-05-18 | 出光興産株式会社 | 有機電界発光素子 |
JP3148176B2 (ja) * | 1998-04-15 | 2001-03-19 | 日本電気株式会社 | 有機エレクトロルミネッセンス素子 |
JP4429438B2 (ja) * | 1999-01-19 | 2010-03-10 | 出光興産株式会社 | アミノ化合物及びそれを用いた有機エレクトロルミネッセンス素子 |
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JP4220696B2 (ja) * | 2001-10-16 | 2009-02-04 | 三井化学株式会社 | 炭化水素化合物、有機電界発光素子用材料および有機電界発光素子 |
JP2004002351A (ja) * | 2002-03-27 | 2004-01-08 | Tdk Corp | 有機el素子 |
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US7541097B2 (en) * | 2003-02-19 | 2009-06-02 | Lg Display Co., Ltd. | Organic electroluminescent device and method for fabricating the same |
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TWI373506B (en) * | 2004-05-21 | 2012-10-01 | Toray Industries | Light-emitting element material and light-emitting material |
JP4906048B2 (ja) * | 2004-11-30 | 2012-03-28 | 株式会社半導体エネルギー研究所 | 発光素子、発光装置、及び電子機器 |
JP2007039431A (ja) * | 2005-03-28 | 2007-02-15 | Semiconductor Energy Lab Co Ltd | アントラセン誘導体、発光素子用材料、発光素子、発光装置及び電子機器 |
EP2479814B1 (en) * | 2005-03-28 | 2015-07-22 | Semiconductor Energy Laboratory Co, Ltd. | Light emitting device comprising a carbazole-anthracene derivative |
JP5041767B2 (ja) * | 2005-08-31 | 2012-10-03 | 株式会社半導体エネルギー研究所 | カルバゾール誘導体、発光素子用材料、発光素子、発光装置及び電子機器 |
-
2007
- 2007-02-14 JP JP2007033012A patent/JP2008195841A/ja active Pending
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