JP2013506984A5 - - Google Patents
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- JP2013506984A5 JP2013506984A5 JP2012531434A JP2012531434A JP2013506984A5 JP 2013506984 A5 JP2013506984 A5 JP 2013506984A5 JP 2012531434 A JP2012531434 A JP 2012531434A JP 2012531434 A JP2012531434 A JP 2012531434A JP 2013506984 A5 JP2013506984 A5 JP 2013506984A5
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- JP
- Japan
- Prior art keywords
- electronic device
- matrix material
- organic
- anion
- salt
- 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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- 150000001450 anions Chemical class 0.000 claims description 10
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 4
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 4
- 125000000129 anionic group Chemical group 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 150000002891 organic anions Chemical class 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 2
- 239000005977 Ethylene Substances 0.000 claims description 2
- HCAUQPZEWLULFJ-UHFFFAOYSA-N benzo[f]quinoline Chemical group C1=CC=C2C3=CC=CC=C3C=CC2=N1 HCAUQPZEWLULFJ-UHFFFAOYSA-N 0.000 claims description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N butadiene group Chemical group C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 125000001792 phenanthrenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C=CC12)* 0.000 claims description 2
- WGDRAVMHLDKGGA-UHFFFAOYSA-N prop-2-en-1-imine Chemical group [CH2]C=C[NH] WGDRAVMHLDKGGA-UHFFFAOYSA-N 0.000 claims description 2
- 125000006413 ring segment Chemical group 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 claims 13
- 150000003839 salts Chemical class 0.000 claims 10
- -1 phosphate anion Chemical class 0.000 claims 9
- 150000001768 cations Chemical class 0.000 claims 7
- 229910052751 metal Inorganic materials 0.000 claims 6
- 239000002184 metal Substances 0.000 claims 6
- 229910019142 PO4 Inorganic materials 0.000 claims 3
- 239000002019 doping agent Substances 0.000 claims 3
- 239000010452 phosphate Substances 0.000 claims 3
- 238000000034 method Methods 0.000 claims 2
- 150000003967 siloles Chemical class 0.000 claims 2
- 239000000758 substrate Substances 0.000 claims 2
- XNCMQRWVMWLODV-UHFFFAOYSA-N 1-phenylbenzimidazole Chemical compound C1=NC2=CC=CC=C2N1C1=CC=CC=C1 XNCMQRWVMWLODV-UHFFFAOYSA-N 0.000 claims 1
- STTGYIUESPWXOW-UHFFFAOYSA-N 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline Chemical compound C=12C=CC3=C(C=4C=CC=CC=4)C=C(C)N=C3C2=NC(C)=CC=1C1=CC=CC=C1 STTGYIUESPWXOW-UHFFFAOYSA-N 0.000 claims 1
- XESMNQMWRSEIET-UHFFFAOYSA-N 2,9-dinaphthalen-2-yl-4,7-diphenyl-1,10-phenanthroline Chemical compound C1=CC=CC=C1C1=CC(C=2C=C3C=CC=CC3=CC=2)=NC2=C1C=CC1=C(C=3C=CC=CC=3)C=C(C=3C=C4C=CC=CC4=CC=3)N=C21 XESMNQMWRSEIET-UHFFFAOYSA-N 0.000 claims 1
- CELPGKFEUDCZOU-UHFFFAOYSA-N 2-naphthalen-2-yl-4,7-diphenyl-1,10-phenanthroline Chemical compound C1=CC=CC=C1C1=CC=NC2=C1C=CC1=C(C=3C=CC=CC=3)C=C(C=3C=C4C=CC=CC4=CC=3)N=C21 CELPGKFEUDCZOU-UHFFFAOYSA-N 0.000 claims 1
- ZVFQEOPUXVPSLB-UHFFFAOYSA-N 3-(4-tert-butylphenyl)-4-phenyl-5-(4-phenylphenyl)-1,2,4-triazole Chemical compound C1=CC(C(C)(C)C)=CC=C1C(N1C=2C=CC=CC=2)=NN=C1C1=CC=C(C=2C=CC=CC=2)C=C1 ZVFQEOPUXVPSLB-UHFFFAOYSA-N 0.000 claims 1
- BSVILDUORGWESI-UHFFFAOYSA-N 3-methyl-2-(4-naphthalen-2-ylphenyl)imidazo[4,5-f][1,10]phenanthroline Chemical compound C1=CC=CC2=CC(C3=CC=C(C=C3)C=3N(C4=C(C5=CC=CN=C5C5=NC=CC=C54)N=3)C)=CC=C21 BSVILDUORGWESI-UHFFFAOYSA-N 0.000 claims 1
- DHDHJYNTEFLIHY-UHFFFAOYSA-N 4,7-diphenyl-1,10-phenanthroline Chemical compound C1=CC=CC=C1C1=CC=NC2=C1C=CC1=C(C=3C=CC=CC=3)C=CN=C21 DHDHJYNTEFLIHY-UHFFFAOYSA-N 0.000 claims 1
- AOQKGYRILLEVJV-UHFFFAOYSA-N 4-naphthalen-1-yl-3,5-diphenyl-1,2,4-triazole Chemical compound C1=CC=CC=C1C(N1C=2C3=CC=CC=C3C=CC=2)=NN=C1C1=CC=CC=C1 AOQKGYRILLEVJV-UHFFFAOYSA-N 0.000 claims 1
- RFVBBELSDAVRHM-UHFFFAOYSA-N 9,10-dinaphthalen-2-yl-2-phenylanthracene Chemical compound C1=CC=CC=C1C1=CC=C(C(C=2C=C3C=CC=CC3=CC=2)=C2C(C=CC=C2)=C2C=3C=C4C=CC=CC4=CC=3)C2=C1 RFVBBELSDAVRHM-UHFFFAOYSA-N 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 1
- 239000007983 Tris buffer Substances 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims 1
- XZCJVWCMJYNSQO-UHFFFAOYSA-N butyl pbd Chemical compound C1=CC(C(C)(C)C)=CC=C1C1=NN=C(C=2C=CC(=CC=2)C=2C=CC=CC=2)O1 XZCJVWCMJYNSQO-UHFFFAOYSA-N 0.000 claims 1
- 238000010549 co-Evaporation Methods 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 229910052744 lithium Inorganic materials 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- RFDGVZHLJCKEPT-UHFFFAOYSA-N tris(2,4,6-trimethyl-3-pyridin-3-ylphenyl)borane Chemical compound CC1=C(B(C=2C(=C(C=3C=NC=CC=3)C(C)=CC=2C)C)C=2C(=C(C=3C=NC=CC=3)C(C)=CC=2C)C)C(C)=CC(C)=C1C1=CC=CN=C1 RFDGVZHLJCKEPT-UHFFFAOYSA-N 0.000 claims 1
- 238000007740 vapor deposition Methods 0.000 claims 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 229910004283 SiO 4 Inorganic materials 0.000 description 1
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 1
- NKVMCSDLYHGDMD-UHFFFAOYSA-N methanetetracarboxylic acid Chemical compound OC(=O)C(C(O)=O)(C(O)=O)C(O)=O NKVMCSDLYHGDMD-UHFFFAOYSA-N 0.000 description 1
- RKGQUTNLMXNUME-UHFFFAOYSA-N methanetricarboxylic acid Chemical compound OC(=O)C(C(O)=O)C(O)=O RKGQUTNLMXNUME-UHFFFAOYSA-N 0.000 description 1
- MZYHMUONCNKCHE-UHFFFAOYSA-N naphthalene-1,2,3,4-tetracarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=C(C(O)=O)C(C(O)=O)=C21 MZYHMUONCNKCHE-UHFFFAOYSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102009047880A DE102009047880A1 (de) | 2009-09-30 | 2009-09-30 | Organische elektronische Vorrichtung und Verfahren zu dessen Herstellung |
| DE102009047880.9 | 2009-09-30 | ||
| PCT/EP2010/064592 WO2011039323A2 (de) | 2009-09-30 | 2010-09-30 | Organische elektronische vorrichtung und verfahren zu dessen herstellung |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2013506984A JP2013506984A (ja) | 2013-02-28 |
| JP2013506984A5 true JP2013506984A5 (enExample) | 2013-07-25 |
| JP5757951B2 JP5757951B2 (ja) | 2015-08-05 |
Family
ID=43085757
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012531434A Expired - Fee Related JP5757951B2 (ja) | 2009-09-30 | 2010-09-30 | 有機電子装置およびその製造方法 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9520570B2 (enExample) |
| EP (1) | EP2483945B1 (enExample) |
| JP (1) | JP5757951B2 (enExample) |
| KR (1) | KR101770437B1 (enExample) |
| CN (1) | CN102576823B (enExample) |
| DE (1) | DE102009047880A1 (enExample) |
| WO (1) | WO2011039323A2 (enExample) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5722238B2 (ja) | 2010-01-15 | 2015-05-20 | 出光興産株式会社 | 含窒素複素環誘導体及びそれを含んでなる有機エレクトロルミネッセンス素子 |
| DE102012211869A1 (de) | 2012-07-06 | 2014-01-09 | Osram Opto Semiconductors Gmbh | Organisches Licht emittierendes Bauelement |
| DE102012217574A1 (de) | 2012-09-27 | 2014-03-27 | Siemens Aktiengesellschaft | Phosphoroxo-Salze als n-Dotierstoffe für die organische Elektronik |
| DE102013106949A1 (de) * | 2013-07-02 | 2015-01-08 | Osram Opto Semiconductors Gmbh | Optoelektronisches Bauelement, organische funktionelle Schicht und Verfahren zur Herstellung eines optoelektronischen Bauelements |
| EP2960315A1 (de) | 2014-06-27 | 2015-12-30 | cynora GmbH | Organische Elektrolumineszenzvorrichtung |
| JP6954833B2 (ja) | 2014-09-17 | 2021-10-27 | サイノーラ・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | エミッタとして使用するための有機分子 |
| DE102015210388A1 (de) * | 2015-06-05 | 2016-12-08 | Siemens Aktiengesellschaft | Organische Heterozyklische Alkalimetallsalze als n-Dotierstoffe in der Organischen Elektronik |
| EP3312896B1 (en) * | 2016-10-24 | 2021-03-31 | Novaled GmbH | Organic electroluminescent device comprising a redox-doped electron transport layer and an auxiliary electron transport layer |
| JP2019026619A (ja) * | 2017-08-03 | 2019-02-21 | 国立大学法人山形大学 | ターピリジン誘導体、及びそれを用いた有機電子素子 |
| CN109994651B (zh) * | 2017-12-29 | 2020-12-25 | 昆山国显光电有限公司 | 一种有机电致发光器件及其制备方法 |
| KR102291411B1 (ko) * | 2019-12-09 | 2021-08-23 | 엘티소재주식회사 | 헤테로고리 화합물 및 이를 포함하는 유기 발광 소자 |
| US20210336151A1 (en) * | 2020-04-28 | 2021-10-28 | Semiconductor Energy Laboratory Co., Ltd. | Light-Emitting Device Material, Electron-Transport Layer Material, Organic Compound, Light-Emitting Device, Light-Emitting Apparatus, Electronic Device, and Lighting Device |
| CN112194614B (zh) * | 2020-10-14 | 2022-04-26 | 新乡医学院 | 一种特异性识别Fe3+的三联吡啶荧光探针及其合成方法和应用 |
| CN114695799A (zh) * | 2020-12-29 | 2022-07-01 | 常州强力昱镭光电材料有限公司 | 一种有机电致发光元件 |
| CN112903331B (zh) * | 2021-02-25 | 2022-07-29 | 北京空间飞行器总体设计部 | 一种水升华器供水压力地面等效模拟装置及方法 |
| KR20230162926A (ko) * | 2021-03-26 | 2023-11-29 | 도레이 카부시키가이샤 | 유기 el 표시 장치 및 그 제조 방법 |
| CN115207228B (zh) * | 2021-04-08 | 2025-06-03 | 常州强力电子新材料股份有限公司 | 有机电致发光元件 |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6064151A (en) * | 1997-12-08 | 2000-05-16 | Motorola, Inc. | Organic electroluminescent device with enhanced performance |
| JP2004193011A (ja) | 2002-12-12 | 2004-07-08 | Fuji Photo Film Co Ltd | 有機電界発光素子 |
| JP4366106B2 (ja) | 2003-04-30 | 2009-11-18 | キヤノン株式会社 | 発光素子 |
| US7608855B2 (en) | 2004-04-02 | 2009-10-27 | Spansion Llc | Polymer dielectrics for memory element array interconnect |
| US7622200B2 (en) | 2004-05-21 | 2009-11-24 | Semiconductor Energy Laboratory Co., Ltd. | Light emitting element |
| JP4988152B2 (ja) * | 2004-08-03 | 2012-08-01 | 株式会社Ａｄｅｋａ | 蛍光性陰イオンおよび蛍光性陽イオンからなる塩 |
| JP2007226043A (ja) | 2006-02-24 | 2007-09-06 | Mitsubishi Paper Mills Ltd | 酸化亜鉛膜の形成方法及び透明導電性基材 |
| DE102006053644A1 (de) | 2006-11-14 | 2008-06-12 | Siemens Ag | Neuartiges hochleitfähiges organisches Ladungsträgertransportmaterial |
| JP5656338B2 (ja) * | 2007-03-12 | 2015-01-21 | ケミプロ化成株式会社 | 新規な１，１０−フェナントロリン誘導体、電子輸送材料、電子注入材料およびそれを含有する有機電界発光素子 |
| JP5008584B2 (ja) * | 2008-02-15 | 2012-08-22 | 富士フイルム株式会社 | 有機電界発光素子及び表示装置 |
| JP5515234B2 (ja) | 2008-03-31 | 2014-06-11 | 住友化学株式会社 | 中間層形成塗布液、および有機エレクトロルミネッセンス素子の製造方法、並びに有機エレクトロルミネッセンス素子 |
-
2009
- 2009-09-30 DE DE102009047880A patent/DE102009047880A1/de not_active Withdrawn
-
2010
- 2010-09-30 JP JP2012531434A patent/JP5757951B2/ja not_active Expired - Fee Related
- 2010-09-30 KR KR1020127010788A patent/KR101770437B1/ko not_active Expired - Fee Related
- 2010-09-30 EP EP10759683.5A patent/EP2483945B1/de active Active
- 2010-09-30 US US13/499,542 patent/US9520570B2/en active Active
- 2010-09-30 WO PCT/EP2010/064592 patent/WO2011039323A2/de not_active Ceased
- 2010-09-30 CN CN201080044055.2A patent/CN102576823B/zh active Active
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