JP2010525111A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2010525111A5 JP2010525111A5 JP2010504151A JP2010504151A JP2010525111A5 JP 2010525111 A5 JP2010525111 A5 JP 2010525111A5 JP 2010504151 A JP2010504151 A JP 2010504151A JP 2010504151 A JP2010504151 A JP 2010504151A JP 2010525111 A5 JP2010525111 A5 JP 2010525111A5
- Authority
- JP
- Japan
- Prior art keywords
- composition
- formula
- derived
- phosphorescent organometallic
- phosphorescent
- 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.)
- Pending
Links
- 239000000203 mixture Substances 0.000 claims 16
- 150000002902 organometallic compounds Chemical class 0.000 claims 7
- 229920000642 polymer Polymers 0.000 claims 5
- VQGHOUODWALEFC-UHFFFAOYSA-N 2-phenylpyridine Chemical compound C1=CC=CC=C1C1=CC=CC=N1 VQGHOUODWALEFC-UHFFFAOYSA-N 0.000 claims 4
- -1 acrylic ester Chemical class 0.000 claims 4
- 150000001875 compounds Chemical class 0.000 claims 4
- 239000000178 monomer Substances 0.000 claims 4
- NRSBAUDUBWMTGL-UHFFFAOYSA-N 2-(1-benzothiophen-2-yl)pyridine Chemical compound S1C2=CC=CC=C2C=C1C1=CC=CC=N1 NRSBAUDUBWMTGL-UHFFFAOYSA-N 0.000 claims 2
- QLPKTAFPRRIFQX-UHFFFAOYSA-N 2-thiophen-2-ylpyridine Chemical compound C1=CSC(C=2N=CC=CC=2)=C1 QLPKTAFPRRIFQX-UHFFFAOYSA-N 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 229910052733 gallium Inorganic materials 0.000 claims 2
- JVZRCNQLWOELDU-UHFFFAOYSA-N gamma-Phenylpyridine Natural products C1=CC=CC=C1C1=CC=NC=C1 JVZRCNQLWOELDU-UHFFFAOYSA-N 0.000 claims 2
- 239000003446 ligand Substances 0.000 claims 2
- SIOXPEMLGUPBBT-UHFFFAOYSA-M picolinate Chemical compound [O-]C(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-M 0.000 claims 2
- SMQUZDBALVYZAC-UHFFFAOYSA-N salicylaldehyde Chemical compound OC1=CC=CC=C1C=O SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 claims 2
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 claims 1
- POILWHVDKZOXJZ-ARJAWSKDSA-M (z)-4-oxopent-2-en-2-olate Chemical compound C\C([O-])=C\C(C)=O POILWHVDKZOXJZ-ARJAWSKDSA-M 0.000 claims 1
- LPCWDYWZIWDTCV-UHFFFAOYSA-N 1-phenylisoquinoline Chemical compound C1=CC=CC=C1C1=NC=CC2=CC=CC=C12 LPCWDYWZIWDTCV-UHFFFAOYSA-N 0.000 claims 1
- SSABEFIRGJISFH-UHFFFAOYSA-N 2-(2,4-difluorophenyl)pyridine Chemical compound FC1=CC(F)=CC=C1C1=CC=CC=N1 SSABEFIRGJISFH-UHFFFAOYSA-N 0.000 claims 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- KAJMDIRNTNSOLE-UHFFFAOYSA-N 2-naphthalen-1-yl-1,3-benzoxazole Chemical compound C1=CC=C2C(C=3OC4=CC=CC=C4N=3)=CC=CC2=C1 KAJMDIRNTNSOLE-UHFFFAOYSA-N 0.000 claims 1
- XBHOUXSGHYZCNH-UHFFFAOYSA-N 2-phenyl-1,3-benzothiazole Chemical compound C1=CC=CC=C1C1=NC2=CC=CC=C2S1 XBHOUXSGHYZCNH-UHFFFAOYSA-N 0.000 claims 1
- FIISKTXZUZBTRC-UHFFFAOYSA-N 2-phenyl-1,3-benzoxazole Chemical compound C1=CC=CC=C1C1=NC2=CC=CC=C2O1 FIISKTXZUZBTRC-UHFFFAOYSA-N 0.000 claims 1
- KLLLJCACIRKBDT-UHFFFAOYSA-N 2-phenyl-1H-indole Chemical compound N1C2=CC=CC=C2C=C1C1=CC=CC=C1 KLLLJCACIRKBDT-UHFFFAOYSA-N 0.000 claims 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims 1
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 claims 1
- VJHVLELNDFVKMS-UHFFFAOYSA-N 3-methoxy-2-phenylpyridine Chemical compound COC1=CC=CN=C1C1=CC=CC=C1 VJHVLELNDFVKMS-UHFFFAOYSA-N 0.000 claims 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 1
- YFPJFKYCVYXDJK-UHFFFAOYSA-N Diphenylphosphine oxide Chemical compound C=1C=CC=CC=1[P+](=O)C1=CC=CC=C1 YFPJFKYCVYXDJK-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
- 229910052771 Terbium Inorganic materials 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 229910052782 aluminium Inorganic materials 0.000 claims 1
- 229910052787 antimony Inorganic materials 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 229910052793 cadmium Inorganic materials 0.000 claims 1
- 229910052804 chromium Inorganic materials 0.000 claims 1
- 229910052802 copper Inorganic materials 0.000 claims 1
- CHYUXCABJMXHJN-UHFFFAOYSA-N diphenyl(sulfanylidene)phosphanium Chemical compound C=1C=CC=CC=1[P+](=S)C1=CC=CC=C1 CHYUXCABJMXHJN-UHFFFAOYSA-N 0.000 claims 1
- 229910052732 germanium Inorganic materials 0.000 claims 1
- 229910052737 gold Inorganic materials 0.000 claims 1
- 125000001475 halogen functional group Chemical group 0.000 claims 1
- 229910052738 indium Inorganic materials 0.000 claims 1
- 238000002347 injection Methods 0.000 claims 1
- 239000007924 injection Substances 0.000 claims 1
- 229910052741 iridium Inorganic materials 0.000 claims 1
- 229910052742 iron Inorganic materials 0.000 claims 1
- 229910052745 lead Inorganic materials 0.000 claims 1
- 229910052748 manganese Inorganic materials 0.000 claims 1
- 229910052753 mercury Inorganic materials 0.000 claims 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims 1
- 229910052750 molybdenum Inorganic materials 0.000 claims 1
- 125000002950 monocyclic group Chemical group 0.000 claims 1
- 229910052759 nickel Inorganic materials 0.000 claims 1
- 229910052758 niobium Inorganic materials 0.000 claims 1
- 229910052762 osmium Inorganic materials 0.000 claims 1
- 229910052763 palladium Inorganic materials 0.000 claims 1
- 229910052697 platinum Inorganic materials 0.000 claims 1
- VIXWGKYSYIBATJ-UHFFFAOYSA-N pyrrol-2-one Chemical compound O=C1C=CC=N1 VIXWGKYSYIBATJ-UHFFFAOYSA-N 0.000 claims 1
- 229910052702 rhenium Inorganic materials 0.000 claims 1
- 229910052703 rhodium Inorganic materials 0.000 claims 1
- 229910052707 ruthenium Inorganic materials 0.000 claims 1
- 229910052706 scandium Inorganic materials 0.000 claims 1
- 229910052709 silver Inorganic materials 0.000 claims 1
- 125000005415 substituted alkoxy group Chemical group 0.000 claims 1
- 125000000547 substituted alkyl group Chemical group 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 229910052715 tantalum Inorganic materials 0.000 claims 1
- 229910052713 technetium Inorganic materials 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 229910052716 thallium Inorganic materials 0.000 claims 1
- 229910052718 tin Inorganic materials 0.000 claims 1
- 229910052719 titanium Inorganic materials 0.000 claims 1
- 125000004665 trialkylsilyl group Chemical group 0.000 claims 1
- 125000005106 triarylsilyl group Chemical group 0.000 claims 1
- 229910052721 tungsten Inorganic materials 0.000 claims 1
- 229910052720 vanadium Inorganic materials 0.000 claims 1
- 229910052727 yttrium Inorganic materials 0.000 claims 1
- 229910052725 zinc Inorganic materials 0.000 claims 1
- 229910052726 zirconium Inorganic materials 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/736,023 US20080258111A1 (en) | 2007-04-17 | 2007-04-17 | Polycarbazolyl(meth)acrylate light emissive compositions |
| PCT/US2008/059106 WO2008130805A1 (en) | 2007-04-17 | 2008-04-02 | Polycarbazolyl(meth)acrylate light emissive compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2010525111A JP2010525111A (ja) | 2010-07-22 |
| JP2010525111A5 true JP2010525111A5 (enExample) | 2011-05-19 |
Family
ID=39467317
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010504151A Pending JP2010525111A (ja) | 2007-04-17 | 2008-04-02 | ポリカルバゾリル(メタ)アクリレート発光組成物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20080258111A1 (enExample) |
| EP (1) | EP2139929B1 (enExample) |
| JP (1) | JP2010525111A (enExample) |
| KR (1) | KR20100015590A (enExample) |
| CN (1) | CN101663337B (enExample) |
| WO (1) | WO2008130805A1 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080262184A1 (en) * | 2007-04-17 | 2008-10-23 | General Electric Company | Polycarbazolyl(meth)acrylate light emissive compositions |
| KR20120103571A (ko) * | 2009-10-05 | 2012-09-19 | 손 라이팅 리미티드 | 다층구조의 유기 장치 |
| GB2505834A (en) * | 2011-07-04 | 2014-03-12 | Cambridge Display Tech Ltd | Organic light emitting composition, device and method |
| WO2014065779A2 (en) * | 2012-10-22 | 2014-05-01 | Empire Technology Development Llc | Protection of light emitting devices |
| US8803187B2 (en) | 2012-10-22 | 2014-08-12 | Empire Technology Development Llc | Protection of light emitting devices |
| KR20160094430A (ko) * | 2013-12-06 | 2016-08-09 | 메르크 파텐트 게엠베하 | 아크릴산 및/또는 메타크릴산 에스테르 단위를 포함하는 폴리머 결합제를 함유하는 조성물 |
| CN105489763B (zh) * | 2015-11-26 | 2018-05-15 | 电子科技大学 | 一种基于铱类配合物磷光材料掺杂的有机紫外探测器件 |
| CN106366260B (zh) * | 2016-09-26 | 2018-07-17 | 福建师范大学 | 一种黄光共聚物杂化材料及其制备方法 |
| CN106432636B (zh) * | 2016-09-26 | 2018-07-17 | 福建师范大学 | 含poss纳米杂化聚合物磷光材料及其制备方法 |
| CN115746202B (zh) * | 2022-11-07 | 2023-10-13 | 滁州康华电子材料有限公司 | 一种水处理剂及其制备方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3906245A1 (de) * | 1989-02-28 | 1990-09-06 | Basf Ag | Seitenstaendige carbazolyl-gruppen enthaltende poly(meth)acrylate und elektrophotographische aufzeichnungselemente, enthaltend dieselben |
| ATE431970T1 (de) * | 2001-06-20 | 2009-06-15 | Showa Denko Kk | Licht emittierendes material und organische leuchtdiode |
| US7250226B2 (en) * | 2001-08-31 | 2007-07-31 | Nippon Hoso Kyokai | Phosphorescent compound, a phosphorescent composition and an organic light-emitting device |
| CN100335462C (zh) * | 2003-09-05 | 2007-09-05 | 清华大学 | 咔唑衍生物及其在电致发光器件中的应用 |
| US6885026B1 (en) * | 2004-01-30 | 2005-04-26 | Eastman Kodak Company | Organic element for electroluminescent devices |
| JP2005285381A (ja) * | 2004-03-26 | 2005-10-13 | Fuji Photo Film Co Ltd | 有機電界発光素子 |
| JP2007277467A (ja) * | 2006-04-10 | 2007-10-25 | Sony Chemical & Information Device Corp | 硬化性樹脂組成物 |
-
2007
- 2007-04-17 US US11/736,023 patent/US20080258111A1/en not_active Abandoned
-
2008
- 2008-04-02 KR KR1020097021501A patent/KR20100015590A/ko not_active Ceased
- 2008-04-02 JP JP2010504151A patent/JP2010525111A/ja active Pending
- 2008-04-02 CN CN200880012618.2A patent/CN101663337B/zh not_active Expired - Fee Related
- 2008-04-02 WO PCT/US2008/059106 patent/WO2008130805A1/en not_active Ceased
- 2008-04-02 EP EP08744916.1A patent/EP2139929B1/en not_active Not-in-force
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2010525111A5 (enExample) | ||
| TWI237524B (en) | Organometallic compound and organic electroluminescent device including the same | |
| KR100582797B1 (ko) | 금속 함유 덴드리머 | |
| Tung et al. | Highly efficient red phosphorescent osmium (II) complexes for OLED applications | |
| Kavitha et al. | In search of high‐performance platinum (II) phosphorescent materials for the fabrication of red electroluminescent devices | |
| JP2005344124A5 (enExample) | ||
| JP2010530466A5 (enExample) | ||
| Turner et al. | Cyclometalated platinum complexes with luminescent quantum yields approaching 100% | |
| Wu et al. | Synthesis and characterization of metal complexes possessing the 5-(2-pyridyl) pyrazolate ligands: The observation of remarkable osmium-induced blue phosphorescence in solution at room temperature | |
| Carlson et al. | Divalent osmium complexes: Synthesis, characterization, strong red phosphorescence, and electrophosphorescence | |
| KR101271826B1 (ko) | 금속 착물 | |
| Fuertes et al. | Heteroleptic cycloplatinated N-heterocyclic carbene complexes: a new approach to highly efficient blue-light emitters | |
| JP2003515897A5 (enExample) | ||
| Zheng et al. | Thermally induced defluorination during a mer to fac transformation of a blue-green phosphorescent cyclometalated iridium (III) complex | |
| AU2002215322A1 (en) | Polymers having attached luminescent metal complexes and devices made with such polymers | |
| JP2010523528A5 (enExample) | ||
| JPWO2006132173A1 (ja) | 有機金属錯体及びこれを用いた有機電界発光素子 | |
| JP2010525112A5 (enExample) | ||
| CN1671818A (zh) | 共价键合到共轭聚合物上的金属配合物和含有这种组合物的电子器件 | |
| JP2010517253A (ja) | ポリマー状アニオン/カチオン | |
| Jia et al. | Novel phosphorescent cyclometalated organotin (IV) and organolead (IV) complexes of 2, 6-Bis (2 ‘-indolyl) pyridine and 2, 6-Bis [2 ‘-(7-azaindolyl)] pyridine | |
| JP2010525111A (ja) | ポリカルバゾリル(メタ)アクリレート発光組成物 | |
| Yang et al. | Amidate iridium (III) bis (2-pyridyl) phenyl complexes: application examples of amidate ancillary ligands in iridium (III)-cyclometalated complexes | |
| Page et al. | Highly photoluminescent nonconjugated polymers for single-layer light emitting diodes | |
| Kang et al. | Novel blue phosphorescent group 15 compounds MR3 (M= P, Sb, Bi; R= p-(N-7-azaindolyl) phenyl) |