JP2011514885A5 - - Google Patents
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- JP2011514885A5 JP2011514885A5 JP2010546263A JP2010546263A JP2011514885A5 JP 2011514885 A5 JP2011514885 A5 JP 2011514885A5 JP 2010546263 A JP2010546263 A JP 2010546263A JP 2010546263 A JP2010546263 A JP 2010546263A JP 2011514885 A5 JP2011514885 A5 JP 2011514885A5
- Authority
- JP
- Japan
- Prior art keywords
- substituted
- aromatic
- organic
- groups
- 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.)
- Granted
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- 125000003118 aryl group Chemical group 0.000 claims description 25
- 150000001875 compounds Chemical class 0.000 claims description 15
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- -1 9-phenanthrenyl Chemical group 0.000 claims description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 125000002950 monocyclic group Chemical group 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 101100118680 Caenorhabditis elegans sec-61.G gene Proteins 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 2
- 125000004437 phosphorous atom Chemical group 0.000 claims description 2
- 229910052698 phosphorus Inorganic materials 0.000 claims description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims 5
- DXBHBZVCASKNBY-UHFFFAOYSA-N 1,2-Benz(a)anthracene Chemical compound C1=CC=C2C3=CC4=CC=CC=C4C=C3C=CC2=C1 DXBHBZVCASKNBY-UHFFFAOYSA-N 0.000 claims 4
- YNPNZTXNASCQKK-UHFFFAOYSA-N phenanthrene Chemical compound C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims 3
- 239000010410 layer Substances 0.000 claims 3
- 239000000463 material Substances 0.000 claims 3
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims 2
- UJOBWOGCFQCDNV-UHFFFAOYSA-N 9H-carbazole Chemical compound C1=CC=C2C3=CC=CC=C3NC2=C1 UJOBWOGCFQCDNV-UHFFFAOYSA-N 0.000 claims 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- XBDYBAVJXHJMNQ-UHFFFAOYSA-N Tetrahydroanthracene Natural products C1=CC=C2C=C(CCCC3)C3=CC2=C1 XBDYBAVJXHJMNQ-UHFFFAOYSA-N 0.000 claims 2
- ZADPBFCGQRWHPN-UHFFFAOYSA-N boronic acid Chemical compound OBO ZADPBFCGQRWHPN-UHFFFAOYSA-N 0.000 claims 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- WDECIBYCCFPHNR-UHFFFAOYSA-N chrysene Chemical compound C1=CC=CC2=CC=C3C4=CC=CC=C4C=CC3=C21 WDECIBYCCFPHNR-UHFFFAOYSA-N 0.000 claims 2
- 239000002019 doping agent Substances 0.000 claims 2
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 claims 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 claims 2
- IFLREYGFSNHWGE-UHFFFAOYSA-N tetracene Chemical compound C1=CC=CC2=CC3=CC4=CC=CC=C4C=C3C=C21 IFLREYGFSNHWGE-UHFFFAOYSA-N 0.000 claims 2
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 2
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical compound [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims 2
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims 1
- VNDFYDZORAPFSA-UHFFFAOYSA-N 2-(2-phenylethenoxy)ethenylbenzene Chemical compound C=1C=CC=CC=1C=COC=CC1=CC=CC=C1 VNDFYDZORAPFSA-UHFFFAOYSA-N 0.000 claims 1
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims 1
- UWRZIZXBOLBCON-UHFFFAOYSA-N 2-phenylethenamine Chemical compound NC=CC1=CC=CC=C1 UWRZIZXBOLBCON-UHFFFAOYSA-N 0.000 claims 1
- SKKKJNPBIGQNEJ-UHFFFAOYSA-N 9h-fluorene-1,9-diamine Chemical compound C1=CC(N)=C2C(N)C3=CC=CC=C3C2=C1 SKKKJNPBIGQNEJ-UHFFFAOYSA-N 0.000 claims 1
- KGXCHACLIFYNOP-VOTSOKGWSA-N [(e)-2-phenylethenyl]phosphane Chemical compound P\C=C\C1=CC=CC=C1 KGXCHACLIFYNOP-VOTSOKGWSA-N 0.000 claims 1
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 claims 1
- 150000001454 anthracenes Chemical class 0.000 claims 1
- 150000004982 aromatic amines Chemical class 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 239000004305 biphenyl Substances 0.000 claims 1
- 230000000903 blocking effect Effects 0.000 claims 1
- 238000005401 electroluminescence Methods 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 230000005669 field effect Effects 0.000 claims 1
- GVEPBJHOBDJJJI-UHFFFAOYSA-N fluoranthrene Natural products C1=CC(C2=CC=CC=C22)=C3C2=CC=CC3=C1 GVEPBJHOBDJJJI-UHFFFAOYSA-N 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 150000002430 hydrocarbons Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000012044 organic layer Substances 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 108091008695 photoreceptors Proteins 0.000 claims 1
- 238000010791 quenching Methods 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- 239000010409 thin film Substances 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 125000005309 thioalkoxy group Chemical group 0.000 description 2
- 125000005577 anthracene group Chemical group 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 125000001792 phenanthrenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3C=CC12)* 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102008008953.2 | 2008-02-13 | ||
| DE102008008953.2A DE102008008953B4 (de) | 2008-02-13 | 2008-02-13 | Neue Materialien für organische Elektrolumineszenzvorrichtungen |
| PCT/EP2009/001028 WO2009100925A1 (de) | 2008-02-13 | 2009-02-13 | Neue materialien für organische elektrolumineszenzvorrichtungen |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011514885A JP2011514885A (ja) | 2011-05-12 |
| JP2011514885A5 true JP2011514885A5 (enExample) | 2014-10-16 |
| JP5638960B2 JP5638960B2 (ja) | 2014-12-10 |
Family
ID=40718755
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010546263A Active JP5638960B2 (ja) | 2008-02-13 | 2009-02-13 | 有機エレクトロルミネセントデバイスのための新規材料 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8993123B2 (enExample) |
| EP (1) | EP2240425A1 (enExample) |
| JP (1) | JP5638960B2 (enExample) |
| KR (1) | KR101573096B1 (enExample) |
| CN (1) | CN101939279B (enExample) |
| DE (1) | DE102008008953B4 (enExample) |
| TW (1) | TWI473778B (enExample) |
| WO (1) | WO2009100925A1 (enExample) |
Families Citing this family (79)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102010048608A1 (de) * | 2010-10-15 | 2012-04-19 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
| JP5653179B2 (ja) * | 2010-11-05 | 2015-01-14 | キヤノン株式会社 | フェナンスレン化合物及びこれを用いた有機発光素子 |
| KR101432600B1 (ko) * | 2010-12-31 | 2014-08-21 | 제일모직주식회사 | 유기광전소자용 화합물 및 이를 포함하는 유기광전소자 |
| KR101996648B1 (ko) * | 2011-04-15 | 2019-07-04 | 에스에프씨 주식회사 | 신규한 화합물 및 이를 포함하는 유기전계발광소자 |
| CN110003199B (zh) | 2012-09-12 | 2022-09-23 | 出光兴产株式会社 | 新型化合物、有机电致发光元件用材料、有机电致发光元件和电子设备 |
| KR101963104B1 (ko) | 2012-10-31 | 2019-03-28 | 메르크 파텐트 게엠베하 | 전자 디바이스 |
| JP6306033B2 (ja) | 2012-11-12 | 2018-04-04 | メルク パテント ゲーエムベーハー | 電子素子のための材料 |
| KR102013879B1 (ko) * | 2012-11-30 | 2019-08-29 | 엘지디스플레이 주식회사 | 유기발광장치 및 그 제조방법 |
| WO2014106523A1 (de) | 2013-01-03 | 2014-07-10 | Merck Patent Gmbh | Elektronische vorrichtung |
| EP2941469A2 (de) | 2013-01-03 | 2015-11-11 | Merck Patent GmbH | Materialien für elektronische vorrichtungen |
| KR20150026114A (ko) | 2013-08-30 | 2015-03-11 | 삼성디스플레이 주식회사 | 인데노피리딘계 화합물 및 이를 포함한 유기 발광 소자 |
| EP3057947B1 (de) * | 2013-10-14 | 2018-10-17 | Merck Patent GmbH | Materialien für elektronische vorrichtungen |
| EP3114102B1 (de) * | 2014-03-07 | 2017-12-06 | Merck Patent GmbH | Materialien für elektronische vorrichtungen |
| JP6305798B2 (ja) * | 2014-03-17 | 2018-04-04 | 出光興産株式会社 | 有機エレクトロルミネッセンス素子および電子機器 |
| EP3241253A1 (en) | 2014-12-29 | 2017-11-08 | Dow Global Technologies LLC | Compositions with triarylamine derivatives and oled device containing the same |
| KR102626977B1 (ko) | 2015-01-30 | 2024-01-19 | 메르크 파텐트 게엠베하 | 전자 디바이스용 재료 |
| KR102424977B1 (ko) | 2015-04-14 | 2022-07-26 | 삼성디스플레이 주식회사 | 축합환 화합물 및 이를 포함한 유기 발광 소자 |
| KR102471110B1 (ko) | 2015-08-11 | 2022-11-28 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| WO2017036573A1 (en) * | 2015-08-28 | 2017-03-09 | Merck Patent Gmbh | Compounds for electronic devices |
| KR102606275B1 (ko) | 2015-10-27 | 2023-12-05 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| KR102630644B1 (ko) | 2015-12-17 | 2024-01-30 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| JP7051691B2 (ja) | 2016-02-05 | 2022-04-11 | メルク パテント ゲーエムベーハー | 電子素子のための材料 |
| KR102603865B1 (ko) | 2016-04-21 | 2023-11-21 | 삼성디스플레이 주식회사 | 유기 발광 소자 |
| TWI764942B (zh) | 2016-10-10 | 2022-05-21 | 德商麥克專利有限公司 | 電子裝置 |
| DE102017008794A1 (de) | 2016-10-17 | 2018-04-19 | Merck Patent Gmbh | Materialien zur Verwendung in elektronischen Vorrichtungen |
| WO2018083053A1 (de) | 2016-11-02 | 2018-05-11 | Merck Patent Gmbh | Materialien für elektronische vorrichtungen |
| US11440925B2 (en) | 2016-11-08 | 2022-09-13 | Merck Patent Gmbh | Compounds for electronic devices |
| TW201833118A (zh) | 2016-11-22 | 2018-09-16 | 德商麥克專利有限公司 | 用於電子裝置之材料 |
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| EP3577101B1 (de) | 2017-02-02 | 2021-03-03 | Merck Patent GmbH | Materialien für elektronische vorrichtungen |
| US20200055822A1 (en) | 2017-03-02 | 2020-02-20 | Merck Patent Gmbh | Materials for organic electronic devices |
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| KR102734776B1 (ko) | 2017-07-28 | 2024-11-27 | 메르크 파텐트 게엠베하 | 전자 디바이스에 사용하기 위한 스피로바이플루오렌 유도체 |
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| US11751415B2 (en) | 2018-02-02 | 2023-09-05 | Oti Lumionics Inc. | Materials for forming a nucleation-inhibiting coating and devices incorporating same |
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| EP3598515B1 (en) * | 2018-07-18 | 2024-09-04 | Novaled GmbH | Compound and organic semiconducting layer, organic electronic device, display device and lighting device comprising the same |
| CN111349055B (zh) * | 2018-12-24 | 2023-04-21 | 烟台显华光电材料研究院有限公司 | 一类用作电致发光材料的多环化合物及应用 |
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-
2008
- 2008-02-13 DE DE102008008953.2A patent/DE102008008953B4/de active Active
-
2009
- 2009-02-10 TW TW98104217A patent/TWI473778B/zh active
- 2009-02-13 JP JP2010546263A patent/JP5638960B2/ja active Active
- 2009-02-13 WO PCT/EP2009/001028 patent/WO2009100925A1/de not_active Ceased
- 2009-02-13 CN CN200980104579.3A patent/CN101939279B/zh active Active
- 2009-02-13 EP EP09709699A patent/EP2240425A1/de not_active Withdrawn
- 2009-02-13 US US12/867,648 patent/US8993123B2/en active Active
- 2009-02-13 KR KR1020107019981A patent/KR101573096B1/ko active Active
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