CN102341403B - 选自咔唑类、二苯并呋喃类、二苯并噻吩类和二苯并磷杂环戊二烯类的甲硅烷基和杂原子取代的化合物及其在有机电子器件中的应用 - Google Patents
选自咔唑类、二苯并呋喃类、二苯并噻吩类和二苯并磷杂环戊二烯类的甲硅烷基和杂原子取代的化合物及其在有机电子器件中的应用 Download PDFInfo
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- CN102341403B CN102341403B CN200980157855.2A CN200980157855A CN102341403B CN 102341403 B CN102341403 B CN 102341403B CN 200980157855 A CN200980157855 A CN 200980157855A CN 102341403 B CN102341403 B CN 102341403B
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- 0 CC(*C(O1)=O)C1=O Chemical compound CC(*C(O1)=O)C1=O 0.000 description 2
- FQYDUYPJRKRGJW-UHFFFAOYSA-N Brc(cc1c2c3)ccc1[o]c2ccc3[Si+](c1ccccc1)(c1ccccc1)c1ccccc1 Chemical compound Brc(cc1c2c3)ccc1[o]c2ccc3[Si+](c1ccccc1)(c1ccccc1)c1ccccc1 FQYDUYPJRKRGJW-UHFFFAOYSA-N 0.000 description 1
- KWKATQSNYWPMFJ-UHFFFAOYSA-N CC(C)(C)c(cc1)cc(c2c3ccc(C(C)(C)C)c2)c1[n]3-c(cc1c2c3)ccc1[o]c2ccc3[Si+](c1ccccc1)(c1ccccc1)c1ccccc1 Chemical compound CC(C)(C)c(cc1)cc(c2c3ccc(C(C)(C)C)c2)c1[n]3-c(cc1c2c3)ccc1[o]c2ccc3[Si+](c1ccccc1)(c1ccccc1)c1ccccc1 KWKATQSNYWPMFJ-UHFFFAOYSA-N 0.000 description 1
- UGDCGAHHWKEECA-UHFFFAOYSA-N CP(c1ccccc1)(c(cc1c2c3ccc([Si](c4ccccc4)(c4ccccc4)c4ccccc4)c2)ccc1[n]3-c1ccccc1)=O Chemical compound CP(c1ccccc1)(c(cc1c2c3ccc([Si](c4ccccc4)(c4ccccc4)c4ccccc4)c2)ccc1[n]3-c1ccccc1)=O UGDCGAHHWKEECA-UHFFFAOYSA-N 0.000 description 1
- VFHLTQSBQVCHPP-UHFFFAOYSA-N C[Si+](C)(c(cc1c2c3ccc(Br)c2)ccc1[n]3-c1ccccc1)c(cc1c2cc(Br)ccc22)ccc1[n]2-c1ccccc1 Chemical compound C[Si+](C)(c(cc1c2c3ccc(Br)c2)ccc1[n]3-c1ccccc1)c(cc1c2cc(Br)ccc22)ccc1[n]2-c1ccccc1 VFHLTQSBQVCHPP-UHFFFAOYSA-N 0.000 description 1
- SGBYSWUTSIVPBA-UHFFFAOYSA-N Cc(cc1c2c3)ccc1[o]c2ccc3-[n]1c(cccc2)c2c2c1cccc2 Chemical compound Cc(cc1c2c3)ccc1[o]c2ccc3-[n]1c(cccc2)c2c2c1cccc2 SGBYSWUTSIVPBA-UHFFFAOYSA-N 0.000 description 1
- FXUUZUCJAHGWSV-UHFFFAOYSA-N O=P(c1ccccc1)(c1ccccc1)c(cc1c2c3ccc([Si](c4ccccc4)(c4ccccc4)c4ccccc4)c2)ccc1[n]3-c1ccccc1 Chemical compound O=P(c1ccccc1)(c1ccccc1)c(cc1c2c3ccc([Si](c4ccccc4)(c4ccccc4)c4ccccc4)c2)ccc1[n]3-c1ccccc1 FXUUZUCJAHGWSV-UHFFFAOYSA-N 0.000 description 1
- DZUNWQZGHLUANP-UHFFFAOYSA-N c(cc1)ccc1[Si+](c1ccccc1)(c1ccccc1)c(cc1)cc2c1[o]c(c([Si+](c1ccccc1)(c1ccccc1)c1ccccc1)c1)c2cc1-[n]1c2ccccc2c2c1cccc2 Chemical compound c(cc1)ccc1[Si+](c1ccccc1)(c1ccccc1)c(cc1)cc2c1[o]c(c([Si+](c1ccccc1)(c1ccccc1)c1ccccc1)c1)c2cc1-[n]1c2ccccc2c2c1cccc2 DZUNWQZGHLUANP-UHFFFAOYSA-N 0.000 description 1
- UQCRAJQMGCHUPL-UHFFFAOYSA-N c1ccc(C2(c3ccccc3)c3ccccc3N(c(cc3c4c5)ccc3[o]c4ccc5[Si+](c3ccccc3)(c3ccccc3)c3ccccc3)c3c2cccc3)cc1 Chemical compound c1ccc(C2(c3ccccc3)c3ccccc3N(c(cc3c4c5)ccc3[o]c4ccc5[Si+](c3ccccc3)(c3ccccc3)c3ccccc3)c3c2cccc3)cc1 UQCRAJQMGCHUPL-UHFFFAOYSA-N 0.000 description 1
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having one nitrogen atom as the only ring hetero atom
- C07F9/572—Five-membered rings
- C07F9/5728—Five-membered rings condensed with carbocyclic rings or carbocyclic ring systems
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- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
- C07F7/0814—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring is substituted at a C ring atom by Si
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- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/65515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a five-membered ring
- C07F9/65517—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a five-membered ring condensed with carbocyclic rings or carbocyclic ring systems
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6553—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms
- C07F9/655345—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms the sulfur atom being part of a five-membered ring
- C07F9/655354—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having sulfur atoms, with or without selenium or tellurium atoms, as the only ring hetero atoms the sulfur atom being part of a five-membered ring condensed with carbocyclic rings or carbocyclic ring systems
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6568—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms
- C07F9/65683—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms the ring phosphorus atom being part of a phosphine
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- C09K11/00—Luminescent materials, e.g. electroluminescent or chemiluminescent
- C09K11/06—Luminescent materials, e.g. electroluminescent or chemiluminescent containing organic luminescent materials
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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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- 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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- H10K85/60—Organic compounds having low molecular weight
- 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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- H10K2101/00—Properties of the organic materials covered by group H10K85/00
- H10K2101/10—Triplet emission
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K50/00—Organic light-emitting devices
- H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
- H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
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- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
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- General Health & Medical Sciences (AREA)
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- Spectroscopy & Molecular Physics (AREA)
- Electroluminescent Light Sources (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09150181 | 2009-01-07 | ||
| EP09150176.7 | 2009-01-07 | ||
| EP09150176 | 2009-01-07 | ||
| EP09150181.7 | 2009-01-07 | ||
| PCT/EP2009/067120 WO2010079051A1 (de) | 2009-01-07 | 2009-12-14 | Silyl- und heteroatom-substituierte verbindungen ausgewählt aus carbazolen, dibenzofuranen, dibenzothiophenen und dibenzophospholen und ihre anwendung in der organischen elektronik |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102341403A CN102341403A (zh) | 2012-02-01 |
| CN102341403B true CN102341403B (zh) | 2014-12-03 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200980157855.2A Active CN102341403B (zh) | 2009-01-07 | 2009-12-14 | 选自咔唑类、二苯并呋喃类、二苯并噻吩类和二苯并磷杂环戊二烯类的甲硅烷基和杂原子取代的化合物及其在有机电子器件中的应用 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US9458182B2 (enExample) |
| EP (1) | EP2393819B9 (enExample) |
| JP (1) | JP5808252B2 (enExample) |
| KR (1) | KR101693903B1 (enExample) |
| CN (1) | CN102341403B (enExample) |
| WO (1) | WO2010079051A1 (enExample) |
Families Citing this family (114)
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| ATE553111T1 (de) | 2006-02-10 | 2012-04-15 | Universal Display Corp | Metallkomplexe aus imidazoä1,2-füphenanthridin- liganden und deren verwendung in oled vorrichtungen |
| KR101092170B1 (ko) * | 2009-05-27 | 2011-12-13 | 단국대학교 산학협력단 | 카바졸계 포스핀 옥사이드 화합물 및 이를 포함하는 유기 전계 발광 소자 |
| KR101837095B1 (ko) * | 2009-10-28 | 2018-03-09 | 바스프 에스이 | 이종 리간드 카르벤 착체 및 유기 전자장치에서의 이의 용도 |
| KR101951851B1 (ko) | 2009-12-14 | 2019-02-26 | 유디씨 아일랜드 리미티드 | 디아자벤즈이미다졸로카르벤 리간드를 포함하는 금속 착물 및 oled에서의 그의 용도 |
| US8288187B2 (en) | 2010-01-20 | 2012-10-16 | Universal Display Corporation | Electroluminescent devices for lighting applications |
| US8691401B2 (en) | 2010-04-16 | 2014-04-08 | Basf Se | Bridged benzimidazole-carbene complexes and use thereof in OLEDS |
| JP5990515B2 (ja) | 2010-06-18 | 2016-09-14 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | ジベンゾフラン化合物と8−ヒドロキシキノリノラトアルカリ土類金属錯体または8−ヒドロキシキノリノラトアルカリ金属錯体との層を含む、有機電子デバイス |
| US9142792B2 (en) | 2010-06-18 | 2015-09-22 | Basf Se | Organic electronic devices comprising a layer comprising at least one metal organic compound and at least one metal oxide |
| WO2011157779A1 (en) | 2010-06-18 | 2011-12-22 | Basf Se | Organic electronic devices comprising a layer of a pyridine compound and a 8-hydroxyquinolinolato earth alkaline metal, or alkali metal complex |
| US9067919B2 (en) | 2010-07-08 | 2015-06-30 | Basf Se | Use of dibenzofurans and dibenzothiophenes substituted by nitrogen-bonded five-membered heterocyclic rings in organic electronics |
| CN107266398A (zh) * | 2010-10-07 | 2017-10-20 | Udc 爱尔兰有限责任公司 | 用于电子应用的菲并[9,10‑b]呋喃 |
| US9079872B2 (en) | 2010-10-07 | 2015-07-14 | Basf Se | Phenanthro[9, 10-B]furans for electronic applications |
| WO2012080052A1 (en) | 2010-12-13 | 2012-06-21 | Basf Se | Bispyrimidines for electronic applications |
| US8362246B2 (en) | 2010-12-13 | 2013-01-29 | Basf Se | Bispyrimidines for electronic applications |
| DE102010056519B4 (de) * | 2010-12-27 | 2024-11-28 | Heliatek Gmbh | Optoelektronisches Bauelement mit dotierten Schichten |
| JP5330429B2 (ja) * | 2011-03-08 | 2013-10-30 | 株式会社東芝 | 有機電界発光素子、表示装置および照明装置 |
| US9806270B2 (en) | 2011-03-25 | 2017-10-31 | Udc Ireland Limited | 4H-imidazo[1,2-a]imidazoles for electronic applications |
| EP3034508B1 (en) | 2011-03-25 | 2019-12-04 | UDC Ireland Limited | 4h-imidazo[1,2-a]imidazoles for electronic applications |
| JP5914462B2 (ja) * | 2011-04-05 | 2016-05-11 | 株式会社Adeka | 新規化合物及び光電変換素子 |
| CN103503187B (zh) * | 2011-05-05 | 2016-11-02 | 默克专利有限公司 | 用于电子器件的化合物 |
| US8748012B2 (en) * | 2011-05-25 | 2014-06-10 | Universal Display Corporation | Host materials for OLED |
| CN102214801B (zh) * | 2011-06-09 | 2013-05-08 | 河北工业大学 | 双p型掺杂层的有机发光二极管 |
| US9315724B2 (en) | 2011-06-14 | 2016-04-19 | Basf Se | Metal complexes comprising azabenzimidazole carbene ligands and the use thereof in OLEDs |
| WO2012172482A1 (en) * | 2011-06-14 | 2012-12-20 | Basf Se | Metal complexes comprising azabenzimidazole carbene ligands and the use thereof in oleds |
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| JP2013063963A (ja) * | 2011-08-31 | 2013-04-11 | Semiconductor Energy Lab Co Ltd | 複素環化合物、発光素子、発光装置、電子機器、及び照明装置 |
| KR101992874B1 (ko) * | 2011-09-12 | 2019-06-26 | 닛테츠 케미컬 앤드 머티리얼 가부시키가이샤 | 유기 전계 발광 소자 |
| JP6031302B2 (ja) * | 2011-09-14 | 2016-11-24 | 出光興産株式会社 | ヘテロ芳香族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 |
| JP5825043B2 (ja) * | 2011-10-26 | 2015-12-02 | コニカミノルタ株式会社 | 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、有機エレクトロルミネッセンス素子の製造方法、表示装置及び照明装置 |
| CN103917542B (zh) | 2011-11-10 | 2018-03-27 | Udc 爱尔兰有限责任公司 | 用于电子应用的4H‑咪唑并[1,2‑a]咪唑 |
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| CN102417518A (zh) * | 2011-12-31 | 2012-04-18 | 济南大学 | 一类用于发光材料的有机硅化合物及其制备方法 |
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| KR102012047B1 (ko) | 2012-01-06 | 2019-08-19 | 유니버셜 디스플레이 코포레이션 | 효율이 큰 인광 물질 |
| WO2013118507A1 (ja) * | 2012-02-10 | 2013-08-15 | 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 |
| KR102357439B1 (ko) * | 2012-02-14 | 2022-02-08 | 메르크 파텐트 게엠베하 | 유기 전계발광 소자용 스피로비플루오렌 화합물 |
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| US9184399B2 (en) * | 2012-05-04 | 2015-11-10 | Universal Display Corporation | Asymmetric hosts with triaryl silane side chains |
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- 2009-12-14 EP EP09795397.0A patent/EP2393819B9/de active Active
- 2009-12-14 KR KR1020117018426A patent/KR101693903B1/ko active Active
- 2009-12-14 US US13/143,651 patent/US9458182B2/en active Active
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Also Published As
| Publication number | Publication date |
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| JP2012514618A (ja) | 2012-06-28 |
| CN102341403A (zh) | 2012-02-01 |
| US9458182B2 (en) | 2016-10-04 |
| KR101693903B1 (ko) | 2017-01-06 |
| JP5808252B2 (ja) | 2015-11-10 |
| EP2393819B1 (de) | 2017-01-25 |
| EP2393819B9 (de) | 2017-12-27 |
| KR20120057556A (ko) | 2012-06-05 |
| US20120012821A1 (en) | 2012-01-19 |
| EP2393819A1 (de) | 2011-12-14 |
| WO2010079051A1 (de) | 2010-07-15 |
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