JP2013528929A5 - - Google Patents
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- JP2013528929A5 JP2013528929A5 JP2013503205A JP2013503205A JP2013528929A5 JP 2013528929 A5 JP2013528929 A5 JP 2013528929A5 JP 2013503205 A JP2013503205 A JP 2013503205A JP 2013503205 A JP2013503205 A JP 2013503205A JP 2013528929 A5 JP2013528929 A5 JP 2013528929A5
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- JP
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- Prior art keywords
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- unsubstituted
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- atoms
- 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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- 125000001072 heteroaryl group Chemical group 0.000 claims description 16
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 125000004429 atom Chemical group 0.000 claims 34
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 claims 22
- -1 carbonylthio Chemical group 0.000 claims 18
- 229910003849 O-Si Inorganic materials 0.000 claims 16
- 229910003872 O—Si Inorganic materials 0.000 claims 16
- 229910052799 carbon Inorganic materials 0.000 claims 16
- 229910052760 oxygen Inorganic materials 0.000 claims 16
- 229920006395 saturated elastomer Polymers 0.000 claims 15
- 239000003446 ligand Substances 0.000 claims 14
- 125000006413 ring segment Chemical group 0.000 claims 14
- 229910052717 sulfur Inorganic materials 0.000 claims 13
- 125000000609 carbazolyl group Chemical class C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims 12
- 150000001721 carbon Chemical group 0.000 claims 12
- 125000005842 heteroatom Chemical group 0.000 claims 12
- 125000004432 carbon atom Chemical group C* 0.000 claims 11
- 229910000073 phosphorus hydride Inorganic materials 0.000 claims 11
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 11
- 125000001424 substituent group Chemical group 0.000 claims 11
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims 11
- 239000000463 material Substances 0.000 claims 10
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims 9
- 229910000086 alane Inorganic materials 0.000 claims 9
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical compound [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims 9
- 150000001408 amides Chemical class 0.000 claims 9
- UORVGPXVDQYIDP-BJUDXGSMSA-N borane Chemical group [10BH3] UORVGPXVDQYIDP-BJUDXGSMSA-N 0.000 claims 9
- BGECDVWSWDRFSP-UHFFFAOYSA-N borazine Chemical compound B1NBNBN1 BGECDVWSWDRFSP-UHFFFAOYSA-N 0.000 claims 9
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 9
- 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 claims 9
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 claims 9
- 229910000078 germane Inorganic materials 0.000 claims 9
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine group Chemical group NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 9
- 125000005597 hydrazone group Chemical group 0.000 claims 9
- 125000001841 imino group Chemical group [H]N=* 0.000 claims 9
- 125000000018 nitroso group Chemical group N(=O)* 0.000 claims 9
- 125000003544 oxime group Chemical group 0.000 claims 9
- AUONHKJOIZSQGR-UHFFFAOYSA-N oxophosphane Chemical compound P=O AUONHKJOIZSQGR-UHFFFAOYSA-N 0.000 claims 9
- 125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 claims 9
- 125000002577 pseudohalo group Chemical group 0.000 claims 9
- KXCAEQNNTZANTK-UHFFFAOYSA-N stannane Chemical group [SnH4] KXCAEQNNTZANTK-UHFFFAOYSA-N 0.000 claims 9
- 229940124530 sulfonamide Drugs 0.000 claims 9
- 150000003456 sulfonamides Chemical class 0.000 claims 9
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 9
- 125000005555 sulfoximide group Chemical group 0.000 claims 9
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims 9
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 9
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 claims 8
- 229910052736 halogen Inorganic materials 0.000 claims 8
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical compound [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 claims 8
- 125000003860 C1-C20 alkoxy group Chemical group 0.000 claims 7
- 229910019142 PO4 Inorganic materials 0.000 claims 7
- 125000000217 alkyl group Chemical group 0.000 claims 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims 7
- 239000010452 phosphate Substances 0.000 claims 7
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims 7
- 150000003462 sulfoxides Chemical class 0.000 claims 7
- 150000002367 halogens Chemical class 0.000 claims 6
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 4
- 230000000903 blocking effect Effects 0.000 claims 4
- 239000004020 conductor Substances 0.000 claims 4
- 229910052732 germanium Inorganic materials 0.000 claims 4
- 229910052751 metal Inorganic materials 0.000 claims 4
- 239000002184 metal Substances 0.000 claims 4
- 229910052710 silicon Inorganic materials 0.000 claims 4
- 125000005843 halogen group Chemical group 0.000 claims 3
- 238000002347 injection Methods 0.000 claims 3
- 239000007924 injection Substances 0.000 claims 3
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 239000011159 matrix material Substances 0.000 claims 2
- 230000003647 oxidation Effects 0.000 claims 2
- 238000007254 oxidation reaction Methods 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 229910052747 lanthanoid Inorganic materials 0.000 claims 1
- 150000002602 lanthanoids Chemical class 0.000 claims 1
- 150000002739 metals Chemical class 0.000 claims 1
- 230000000737 periodic effect Effects 0.000 claims 1
- 150000001716 carbazoles Chemical class 0.000 description 3
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 1
- 125000001041 indolyl group Chemical group 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10159162.6 | 2010-04-06 | ||
| EP10159162 | 2010-04-06 | ||
| PCT/IB2011/051453 WO2011125020A1 (en) | 2010-04-06 | 2011-04-05 | Substituted carbazole derivatives and use thereof in organic electronics |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013528929A JP2013528929A (ja) | 2013-07-11 |
| JP2013528929A5 true JP2013528929A5 (enExample) | 2014-05-22 |
| JP5931051B2 JP5931051B2 (ja) | 2016-06-08 |
Family
ID=44762071
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013503205A Active JP5931051B2 (ja) | 2010-04-06 | 2011-04-05 | 置換カルバゾール誘導体および有機エレクトロニクスにおけるその使用 |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP2556075B1 (enExample) |
| JP (1) | JP5931051B2 (enExample) |
| KR (1) | KR102018920B1 (enExample) |
| CN (1) | CN102933582A (enExample) |
| WO (1) | WO2011125020A1 (enExample) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2707456B1 (en) | 2011-05-10 | 2018-09-26 | Basf Se | Novel color converters |
| US9406848B2 (en) | 2011-06-10 | 2016-08-02 | Basf Se | Color converter |
| US8652656B2 (en) * | 2011-11-14 | 2014-02-18 | Universal Display Corporation | Triphenylene silane hosts |
| CN103204846A (zh) * | 2012-01-12 | 2013-07-17 | 昱镭光电科技股份有限公司 | 咔唑衍生物及其有机电激发光装置及制造方法 |
| KR102054229B1 (ko) * | 2012-01-13 | 2019-12-11 | 덕산네오룩스 주식회사 | 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치 |
| WO2013179645A1 (ja) * | 2012-05-30 | 2013-12-05 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子用材料及びそれを用いた有機エレクトロルミネッセンス素子 |
| CN102827196B (zh) * | 2012-09-12 | 2015-06-03 | 山西大学 | 一种含硼吲哚[3,2-b]咔唑衍生物及其制备方法和应用 |
| TWI599570B (zh) * | 2012-09-28 | 2017-09-21 | 新日鐵住金化學股份有限公司 | Compounds for organic electroluminescent devices and organic electroluminescent devices |
| WO2014050588A1 (ja) * | 2012-09-28 | 2014-04-03 | 新日鉄住金化学株式会社 | 有機電界発光素子用材料及びこれを用いた有機電界発光素子 |
| KR101547623B1 (ko) * | 2012-10-24 | 2015-08-26 | 주식회사 두산 | 유기 전계 발광 소자 |
| KR101684979B1 (ko) * | 2012-12-31 | 2016-12-09 | 제일모직 주식회사 | 유기광전자소자 및 이를 포함하는 표시장치 |
| JP6389459B2 (ja) * | 2013-06-14 | 2018-09-12 | 保土谷化学工業株式会社 | ジカルバゾール誘導体及び有機エレクトロルミネッセンス素子 |
| KR101759238B1 (ko) | 2013-09-05 | 2017-07-18 | 제일모직 주식회사 | 유기 광전자 소자용 화합물, 이를 포함하는 유기 광전자 소자 및 상기 유기 광전자 소자를 포함하는 표시장치 |
| CN103601747B (zh) * | 2013-11-27 | 2015-09-30 | 山西大学 | 一种基于吲哚[3,2-b]咔唑的芳基硼化合物及其制备和应用 |
| CN104046351B (zh) * | 2014-04-29 | 2016-11-16 | 中山大学 | 具有余辉发光性能的有机发光材料及其合成方法和应用 |
| US10749118B2 (en) | 2014-06-26 | 2020-08-18 | Samsung Display Co., Ltd. | Heterocyclic compound and organic light-emitting device including the same |
| TWI666803B (zh) * | 2014-09-17 | 2019-07-21 | 日商日鐵化學材料股份有限公司 | 有機電場發光元件及其製造方法 |
| CN104610329B (zh) * | 2015-02-04 | 2016-11-23 | 中国科学院长春应用化学研究所 | 双硼氮桥联联吡啶及用其制备的有机/高分子材料 |
| US20180029983A1 (en) * | 2015-02-16 | 2018-02-01 | Idemitsu Kosan Co., Ltd. | Compound, organic electroluminescent element material, organic electroluminescent element, and electronic device |
| KR102626916B1 (ko) | 2015-09-09 | 2024-01-19 | 삼성전자주식회사 | 축합환 화합물 및 이를 포함한 유기 발광 소자 |
| CN105295010A (zh) * | 2015-10-15 | 2016-02-03 | 中国科学院长春应用化学研究所 | 基于双硼氮桥联联吡啶的共轭聚合物及其制备方法与应用 |
| CN105198889A (zh) * | 2015-10-23 | 2015-12-30 | 西安近代化学研究所 | 一种6-芳基取代的咪唑并[4,5-c]吲哚并[2,3-a]咔唑衍生物及其制备方法 |
| JP6834400B2 (ja) * | 2016-11-22 | 2021-02-24 | ソニー株式会社 | 撮像素子、積層型撮像素子、撮像装置及び電子装置 |
| CN107337680B (zh) * | 2017-07-17 | 2019-02-22 | 江苏三月光电科技有限公司 | 一种以芴为核心的有机化合物及其在oled器件上的应用 |
| CN110272427B (zh) * | 2018-03-14 | 2022-03-29 | 江苏三月科技股份有限公司 | 一种以芴为核心的化合物、其制备方法及其在有机电致发光器件上的应用 |
| CN110092789B (zh) * | 2019-06-12 | 2021-10-22 | 贵州省中国科学院天然产物化学重点实验室(贵州医科大学天然产物化学重点实验室) | 一种吲哚并[2,3-b]咔唑衍生物及其应用 |
| CN112250685B (zh) * | 2020-11-25 | 2022-04-19 | 中钢集团南京新材料研究院有限公司 | 一种吲哚并[2,3-a]咔唑的制备方法 |
| JP7264182B2 (ja) * | 2021-02-03 | 2023-04-25 | ソニーグループ株式会社 | 撮像素子、積層型撮像素子、撮像装置及び電子装置 |
| CN113957480B (zh) * | 2021-11-09 | 2022-11-22 | 深圳先进技术研究院 | 电化学催化二氧化碳还原储能用铜基催化剂、电极、其制备方法及应用 |
| CN113980026B (zh) * | 2021-11-25 | 2024-03-29 | 上海钥熠电子科技有限公司 | 咔唑衍生物类胺化合物和包含其的有机电致发光器件 |
| CN114539270B (zh) * | 2021-12-09 | 2024-03-29 | 上海钥熠电子科技有限公司 | 含有咔唑衍生物的化合物及其在有机电致发光器件中的应用 |
| CN114551725A (zh) * | 2022-02-14 | 2022-05-27 | 西安交通大学 | 界面掺杂双层平面异质结有机太阳能电池及其制备方法 |
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| DE3835842A1 (de) * | 1988-10-21 | 1990-04-26 | Goedecke Ag | Indolocarbazol-derivate, verfahren zu deren herstellung und deren verwendung als arzneimittel |
| US5952115A (en) * | 1997-10-02 | 1999-09-14 | Xerox Corporation | Electroluminescent devices |
| JPWO2005077956A1 (ja) * | 2004-02-16 | 2007-10-18 | イハラケミカル工業株式会社 | 置換Ｓｙｍ−トリインドール |
| EP1805280B1 (en) * | 2004-09-20 | 2011-02-09 | LG Chem, Ltd. | Carbazole derivative and organic light emitting device using same |
| US7173140B2 (en) * | 2004-12-14 | 2007-02-06 | Xerox Corporation | Process to form compound with indolocarbazole moieties |
| US8217181B2 (en) * | 2004-12-30 | 2012-07-10 | E. I. Du Pont De Nemours And Company | Dihalogen indolocarbazole monomers and poly (indolocarbazoles) |
| CN101321755B (zh) * | 2005-12-01 | 2012-04-18 | 新日铁化学株式会社 | 有机电致发光元件用化合物及有机电致发光元件 |
| US20070224446A1 (en) * | 2006-03-24 | 2007-09-27 | Idemitsu Kosan Co., Ltd. | Material for organic electroluminescence device and organic electroluminescence device using the same |
| KR20090016684A (ko) * | 2006-06-02 | 2009-02-17 | 이데미쓰 고산 가부시키가이샤 | 유기 전기발광 소자용 재료 및 그것을 이용한 유기 전기발광 소자 |
| KR100955993B1 (ko) * | 2006-11-09 | 2010-05-04 | 신닛테츠가가쿠 가부시키가이샤 | 유기 전계 발광 소자용 화합물 및 유기 전계 발광 소자 |
| EP3345983B1 (de) * | 2007-07-05 | 2020-08-26 | UDC Ireland Limited | Verbindungen enthaltend mindestens eine disilylverbindung ausgewählt aus disilylcarbazolen, disilyldibenzofuranen, disilyldibenzothiophenen, disilyldibenzophospholen, disilyldibenzothiophen-s-oxiden und disilyldibenzothiophen-s, s-dioxiden |
| KR101082144B1 (ko) * | 2008-05-08 | 2011-11-09 | 신닛테츠가가쿠 가부시키가이샤 | 유기 전계 발광 소자용 화합물 및 유기 전계 발광 소자 |
| WO2009148062A1 (ja) * | 2008-06-05 | 2009-12-10 | 出光興産株式会社 | 多環系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 |
| EP2145936A3 (en) * | 2008-07-14 | 2010-03-17 | Gracel Display Inc. | Fluorene and pyrene derivatives and organic electroluminescent device using the same |
| KR101511072B1 (ko) * | 2009-03-20 | 2015-04-10 | 롬엔드하스전자재료코리아유한회사 | 신규한 유기 발광 화합물 및 이를 포함하는 유기 전계 발광소자 |
| KR20100118700A (ko) * | 2009-04-29 | 2010-11-08 | 다우어드밴스드디스플레이머티리얼 유한회사 | 신규한 유기 발광 화합물 및 이를 채용하고 있는 유기 전계 발광 소자 |
| WO2010131930A2 (ko) * | 2009-05-15 | 2010-11-18 | 제일모직 주식회사 | 유기광전소자용 화합물 및 이를 포함하는 유기광전소자 |
| JP5457907B2 (ja) * | 2009-08-31 | 2014-04-02 | 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 |
| KR101324788B1 (ko) * | 2009-12-31 | 2013-10-31 | (주)씨에스엘쏠라 | 유기 광소자 및 이를 위한 유기 광합물 |
-
2011
- 2011-04-05 CN CN2011800170789A patent/CN102933582A/zh active Pending
- 2011-04-05 KR KR1020127029018A patent/KR102018920B1/ko active Active
- 2011-04-05 EP EP11765150.5A patent/EP2556075B1/en active Active
- 2011-04-05 JP JP2013503205A patent/JP5931051B2/ja active Active
- 2011-04-05 WO PCT/IB2011/051453 patent/WO2011125020A1/en not_active Ceased
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