KR101248047B1 - 신규한 중합체 - Google Patents
신규한 중합체 Download PDFInfo
- Publication number
- KR101248047B1 KR101248047B1 KR1020077023560A KR20077023560A KR101248047B1 KR 101248047 B1 KR101248047 B1 KR 101248047B1 KR 1020077023560 A KR1020077023560 A KR 1020077023560A KR 20077023560 A KR20077023560 A KR 20077023560A KR 101248047 B1 KR101248047 B1 KR 101248047B1
- Authority
- KR
- South Korea
- Prior art keywords
- substituted
- alkyl
- blocked
- aryl
- alkoxy
- 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.)
- Expired - Lifetime
Links
- 0 CC1C*(C)CC1 Chemical compound CC1C*(C)CC1 0.000 description 13
- PODXMJZWPPXECD-UHFFFAOYSA-N Brc(cc1)cc2c1c(ccc(Br)c1)c1c1c2nccn1 Chemical compound Brc(cc1)cc2c1c(ccc(Br)c1)c1c1c2nccn1 PODXMJZWPPXECD-UHFFFAOYSA-N 0.000 description 2
- LTZIIBSPYWTOQV-UHFFFAOYSA-N O=C(c(cc(cc1)Br)c1-c(c1c2)ccc2Br)C1=O Chemical compound O=C(c(cc(cc1)Br)c1-c(c1c2)ccc2Br)C1=O LTZIIBSPYWTOQV-UHFFFAOYSA-N 0.000 description 2
- NFZZRSGDSSYQRS-UHFFFAOYSA-N Oc1ccccc1-c1nc2c(cc(cc3)Br)c3c(ccc(Br)c3)c3c2[nH]1 Chemical compound Oc1ccccc1-c1nc2c(cc(cc3)Br)c3c(ccc(Br)c3)c3c2[nH]1 NFZZRSGDSSYQRS-UHFFFAOYSA-N 0.000 description 2
- MRPVFQPWNIBJAN-UHFFFAOYSA-N Bc1ccc(BOC(C)(C)C(C)O)cc1 Chemical compound Bc1ccc(BOC(C)(C)C(C)O)cc1 MRPVFQPWNIBJAN-UHFFFAOYSA-N 0.000 description 1
- XVVIVIJVMGCRIH-UHFFFAOYSA-N Brc(cc1)cc(c2nc(cccc3)c3nc2c2c3)c1c2ccc3Br Chemical compound Brc(cc1)cc(c2nc(cccc3)c3nc2c2c3)c1c2ccc3Br XVVIVIJVMGCRIH-UHFFFAOYSA-N 0.000 description 1
- JURXKRWETZZBHA-UHFFFAOYSA-N Brc(cc12)ccc1[nH]cc2-c1nc(c2cc(I)ccc2c(c2c3)ccc3I)c2[nH]1 Chemical compound Brc(cc12)ccc1[nH]cc2-c1nc(c2cc(I)ccc2c(c2c3)ccc3I)c2[nH]1 JURXKRWETZZBHA-UHFFFAOYSA-N 0.000 description 1
- UOJCDDLTVQJPGH-UHFFFAOYSA-N CC1(C)OB(c2ccc(B3OC(C)(C)C(C)(C)O3)cc2)OC1(C)C Chemical compound CC1(C)OB(c2ccc(B3OC(C)(C)C(C)(C)O3)cc2)OC1(C)C UOJCDDLTVQJPGH-UHFFFAOYSA-N 0.000 description 1
- CIUNGMVMJOCXFR-UHFFFAOYSA-N CC1(C=CC(O)=C2c3nc4c(cc(cc5)Br)c5c(ccc(Br)c5)c5c4[nH]3)C2=CC=CC1 Chemical compound CC1(C=CC(O)=C2c3nc4c(cc(cc5)Br)c5c(ccc(Br)c5)c5c4[nH]3)C2=CC=CC1 CIUNGMVMJOCXFR-UHFFFAOYSA-N 0.000 description 1
- FOBBTAHQXDNISH-UHFFFAOYSA-N CCCCC(CC)COc1cc(OCC(CC)CCCC)c(C=O)cc1 Chemical compound CCCCC(CC)COc1cc(OCC(CC)CCCC)c(C=O)cc1 FOBBTAHQXDNISH-UHFFFAOYSA-N 0.000 description 1
- JRTGAUPRINXUCF-UHFFFAOYSA-N CCCCC(CC)COc1ccc(-c2nc3c(cc(cc4)Br)c4c(ccc(Br)c4)c4c3[n]2-c2ccccc2)c(OCC(CC)CCCC)c1 Chemical compound CCCCC(CC)COc1ccc(-c2nc3c(cc(cc4)Br)c4c(ccc(Br)c4)c4c3[n]2-c2ccccc2)c(OCC(CC)CCCC)c1 JRTGAUPRINXUCF-UHFFFAOYSA-N 0.000 description 1
- MQBWRHXKTHMIBL-UHFFFAOYSA-N CCCCC(CC)COc1cccc2c1nc(c1cc(Br)ccc1c(c1c3)ccc3Br)c1n2 Chemical compound CCCCC(CC)COc1cccc2c1nc(c1cc(Br)ccc1c(c1c3)ccc3Br)c1n2 MQBWRHXKTHMIBL-UHFFFAOYSA-N 0.000 description 1
- AETTUDKAQCIDIJ-UHFFFAOYSA-N CCCCCCCCC(CCCCCC)C[n]1c(-c2c(cccc3)c3ccc2OCC(CCCCCC)CCCCCCCC)nc2c(cc(cc3)-c4ccc(C(C)(C)C(C)(C)c5cc6c7ncc(-c8ccccc8OCCCCCCCC)nc7c(cc(cc7)-c8ccc(C(C)(C)c9ccccc9)cc8)c7c6cc5)cc4)c3c(ccc(C(C)(C)c3ccccc3)c3)c3c12 Chemical compound CCCCCCCCC(CCCCCC)C[n]1c(-c2c(cccc3)c3ccc2OCC(CCCCCC)CCCCCCCC)nc2c(cc(cc3)-c4ccc(C(C)(C)C(C)(C)c5cc6c7ncc(-c8ccccc8OCCCCCCCC)nc7c(cc(cc7)-c8ccc(C(C)(C)c9ccccc9)cc8)c7c6cc5)cc4)c3c(ccc(C(C)(C)c3ccccc3)c3)c3c12 AETTUDKAQCIDIJ-UHFFFAOYSA-N 0.000 description 1
- CWHMPRGKQREGQO-UHFFFAOYSA-N CCCCCCCCC1(CCCCCCCC)c2cc(-c3cc4c5nc(-c(cc6)ccc6OCCCCCCCC)[n](CCCCCCCC)c5c(cc(C(C)(C)c5ccccc5)cc5)c5c4cc3)ccc2-c2ccc(C(C)(C)c3ccccc3)cc12 Chemical compound CCCCCCCCC1(CCCCCCCC)c2cc(-c3cc4c5nc(-c(cc6)ccc6OCCCCCCCC)[n](CCCCCCCC)c5c(cc(C(C)(C)c5ccccc5)cc5)c5c4cc3)ccc2-c2ccc(C(C)(C)c3ccccc3)cc12 CWHMPRGKQREGQO-UHFFFAOYSA-N 0.000 description 1
- FAHIZHKRQQNPLC-UHFFFAOYSA-N CCCCCCCCC1(CCCCCCCC)c2cc(B3OC(C)(C)C(C)(C)O3)ccc2-c2ccc(B3OC(C)(C)C(C)(C)O3)cc12 Chemical compound CCCCCCCCC1(CCCCCCCC)c2cc(B3OC(C)(C)C(C)(C)O3)ccc2-c2ccc(B3OC(C)(C)C(C)(C)O3)cc12 FAHIZHKRQQNPLC-UHFFFAOYSA-N 0.000 description 1
- VEEDCTFRROGDIB-UHFFFAOYSA-N CCCCCCCCOc(cccc1)c1-c1cnc(c2cc(Br)ccc2c(cc2)c3cc2Br)c3n1 Chemical compound CCCCCCCCOc(cccc1)c1-c1cnc(c2cc(Br)ccc2c(cc2)c3cc2Br)c3n1 VEEDCTFRROGDIB-UHFFFAOYSA-N 0.000 description 1
- KAKYXZCLYKKDGI-UHFFFAOYSA-N CCCCCCCC[n]1c(-c(cc2)ccc2OCCCCCCCC)nc2c(cc(cc3)Br)c3c(ccc(Br)c3)c3c12 Chemical compound CCCCCCCC[n]1c(-c(cc2)ccc2OCCCCCCCC)nc2c(cc(cc3)Br)c3c(ccc(Br)c3)c3c12 KAKYXZCLYKKDGI-UHFFFAOYSA-N 0.000 description 1
- UJNXQWLHGDNDOA-UHFFFAOYSA-N CCCCCCCC[n]1c(-c(cccc2)c2OCCCCCCCC)nc2c(cc(cc3)Br)c3c(ccc(Br)c3)c3c12 Chemical compound CCCCCCCC[n]1c(-c(cccc2)c2OCCCCCCCC)nc2c(cc(cc3)Br)c3c(ccc(Br)c3)c3c12 UJNXQWLHGDNDOA-UHFFFAOYSA-N 0.000 description 1
- QQILWDKSDITBLZ-UHFFFAOYSA-N FC(F)(F)Sc1nc(c2cc(Cl)ccc2c(cc2)c3cc2Cl)c3[n]1C1OCCCC1 Chemical compound FC(F)(F)Sc1nc(c2cc(Cl)ccc2c(cc2)c3cc2Cl)c3[n]1C1OCCCC1 QQILWDKSDITBLZ-UHFFFAOYSA-N 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Nc1ccccc1 Chemical compound Nc1ccccc1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- SMQUZDBALVYZAC-UHFFFAOYSA-N Oc1c(C=O)cccc1 Chemical compound Oc1c(C=O)cccc1 SMQUZDBALVYZAC-UHFFFAOYSA-N 0.000 description 1
- IBGBGRVKPALMCQ-UHFFFAOYSA-N Oc1ccc(C=O)cc1O Chemical compound Oc1ccc(C=O)cc1O IBGBGRVKPALMCQ-UHFFFAOYSA-N 0.000 description 1
- ORHMBFDIIXUXDT-UHFFFAOYSA-N Oc1cccc2nc(c(cc(cc3)Br)c3c(cc3)c4cc3Br)c4nc12 Chemical compound Oc1cccc2nc(c(cc(cc3)Br)c3c(cc3)c4cc3Br)c4nc12 ORHMBFDIIXUXDT-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
- H10K85/10—Organic polymers or oligomers
- H10K85/111—Organic polymers or oligomers comprising aromatic, heteroaromatic, or aryl chains, e.g. polyaniline, polyphenylene or polyphenylene vinylene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
- C08G61/124—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one nitrogen atom in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
- C08G61/125—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one oxygen atom in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G61/00—Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
- C08G61/12—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule
- C08G61/122—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides
- C08G61/123—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds
- C08G61/126—Macromolecular compounds containing atoms other than carbon in the main chain of the macromolecule derived from five- or six-membered heterocyclic compounds, other than imides derived from five-membered heterocyclic compounds with a five-membered ring containing one sulfur atom in the ring
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Electroluminescent Light Sources (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
- Thin Film Transistor (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Polyesters Or Polycarbonates (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05101936.2 | 2005-03-14 | ||
| EP05101936 | 2005-03-14 | ||
| EP05103648.1 | 2005-05-02 | ||
| EP05103648 | 2005-05-02 | ||
| PCT/EP2006/060538 WO2006097419A1 (en) | 2005-03-14 | 2006-03-08 | Novel polymers |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR20070119693A KR20070119693A (ko) | 2007-12-20 |
| KR101248047B1 true KR101248047B1 (ko) | 2013-03-27 |
Family
ID=36441419
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020077023560A Expired - Lifetime KR101248047B1 (ko) | 2005-03-14 | 2006-03-08 | 신규한 중합체 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US8445630B2 (enExample) |
| EP (1) | EP1858976B1 (enExample) |
| JP (1) | JP5541859B2 (enExample) |
| KR (1) | KR101248047B1 (enExample) |
| CN (1) | CN101142275B (enExample) |
| AT (1) | ATE445672T1 (enExample) |
| DE (1) | DE602006009775D1 (enExample) |
| TW (1) | TW200640985A (enExample) |
| WO (1) | WO2006097419A1 (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019212183A1 (ko) * | 2018-05-03 | 2019-11-07 | 주식회사 엘지화학 | 중합성 액정 화합물, 광학 소자용 액정 조성물, 중합체, 광학 이방체 및 디스플레이 장치용 광학 소자 |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5541859B2 (ja) | 2005-03-14 | 2014-07-09 | チバ ホールディング インコーポレーテッド | 新規ポリマー |
| ATE492581T1 (de) * | 2006-02-10 | 2011-01-15 | Basf Se | Neuartige polymere |
| TW200804452A (en) * | 2006-03-13 | 2008-01-16 | Sumitomo Chemical Co | Method for production of conjugated polymer |
| KR101430420B1 (ko) * | 2006-07-14 | 2014-08-14 | 시바 홀딩 인크 | 전자 적용을 위한 신규한 전계발광 중합체 |
| CN101495433B (zh) | 2006-07-28 | 2014-11-26 | 西巴控股有限公司 | 新颖聚合物 |
| CN102977032B (zh) | 2006-09-14 | 2017-01-11 | Udc 爱尔兰有限责任公司 | 杂环桥联联苯及其在场致发光装置中的应用 |
| JP4393527B2 (ja) * | 2007-03-08 | 2010-01-06 | パナソニック株式会社 | 電極活物質および蓄電デバイス |
| US8628862B2 (en) * | 2007-09-20 | 2014-01-14 | Basf Se | Electroluminescent device |
| GB0811930D0 (en) * | 2008-06-30 | 2008-07-30 | Imec Inter Uni Micro Electr | Polymerisable compounds for making opto-electronic devices |
| JP5600891B2 (ja) * | 2009-05-15 | 2014-10-08 | 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、表示装置および照明装置 |
| BRPI1011853A2 (pt) | 2009-05-27 | 2019-09-24 | Basf Se | polímero, material, camada ou componente semicondutores orgânicos, dispositivo semicondutor, processos para a preparação de um dispositivo semicondutor orgânico, e de um polímero, e, uso do polímero e/ou do material, camada ou componente semicondutores orgãnicos. |
| WO2010145991A1 (en) | 2009-06-18 | 2010-12-23 | Basf Se | Phenanthroazole compounds as hole transporting materials for electro luminescent devices |
| US9079872B2 (en) | 2010-10-07 | 2015-07-14 | Basf Se | Phenanthro[9, 10-B]furans for electronic applications |
| 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 |
| DE102010048608A1 (de) * | 2010-10-15 | 2012-04-19 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
| 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 |
| CN107814821B (zh) | 2012-01-12 | 2025-03-07 | Udc爱尔兰有限责任公司 | 具有二苯并[f,h]喹喔啉的金属配合物 |
| EP2834284B1 (en) | 2012-04-02 | 2017-05-10 | Basf Se | Phenanthro[9,10-b]furan polymers and small molecules for electronic applications |
| KR101532299B1 (ko) * | 2012-10-11 | 2015-06-30 | 주식회사 엠비케이 | 신규한 전자수송 화합물 및 이를 포함하는 유기전기발광소자 |
| JP6454226B2 (ja) * | 2015-06-08 | 2019-01-16 | 出光興産株式会社 | 化合物、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、及び電子機器 |
| KR102134266B1 (ko) * | 2017-11-08 | 2020-07-15 | 삼성에스디아이 주식회사 | 모노머, 중합체, 유기막 조성물 및 패턴 형성 방법 |
| CN112679732B (zh) * | 2020-12-28 | 2021-10-26 | 华南理工大学 | 一类发光聚合物及其无金属催化剂聚合方法与应用 |
| CN114409876B (zh) * | 2021-12-13 | 2023-11-07 | 武汉工程大学 | 一种对镉和锌双金属离子识别的聚合物及其制备方法、应用和分析方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003064373A1 (de) | 2002-01-28 | 2003-08-07 | Sensient Imaging Technologies Gmbh | Triarylamin-derivate und verwendung in organischen elektrolumineszenten und elektrofotografischen vorrichtungen |
| WO2004005288A2 (en) * | 2002-07-10 | 2004-01-15 | E.I. Du Pont De Nemours And Company | Charge transport compositions comprising fluorinated phenanthroline derivatives |
| WO2005014689A2 (de) * | 2003-08-12 | 2005-02-17 | Covion Organic Semiconductors Gmbh | Konjugierte polymere enthaltend dihydrophenanthren-einheiten und deren verwendung |
Family Cites Families (36)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4215135A (en) | 1979-06-08 | 1980-07-29 | E. I. Du Pont De Nemours And Company | Antiinflammatory 2-substituted-1H-phenanthro[9,10-d]imidazoles |
| SU1001855A3 (ru) | 1978-10-02 | 1983-02-28 | Е.И.Дюпон Де Немур Энд Компани (Фирма) | Способ получени 2-замещенных-1н-фенантро[9,10- @ ]имидазолов или их солей |
| JPH02134644A (ja) | 1988-11-15 | 1990-05-23 | Canon Inc | 電子写真感光体 |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2019212183A1 (ko) * | 2018-05-03 | 2019-11-07 | 주식회사 엘지화학 | 중합성 액정 화합물, 광학 소자용 액정 조성물, 중합체, 광학 이방체 및 디스플레이 장치용 광학 소자 |
| KR20190127062A (ko) * | 2018-05-03 | 2019-11-13 | 주식회사 엘지화학 | 중합성 액정 화합물, 광학 소자용 액정 조성물, 중합체, 광학 이방체 및 디스플레이 장치용 광학 소자 |
| KR102196632B1 (ko) | 2018-05-03 | 2020-12-30 | 주식회사 엘지화학 | 중합성 액정 화합물, 광학 소자용 액정 조성물, 중합체, 광학 이방체 및 디스플레이 장치용 광학 소자 |
| US11674082B2 (en) | 2018-05-03 | 2023-06-13 | Lg Chem, Ltd. | Polymerizable liquid crystal compound, liquid crystal composition for optical element, polymer, optically anisotropic body, and optical element for display device |
Also Published As
| Publication number | Publication date |
|---|---|
| DE602006009775D1 (de) | 2009-11-26 |
| EP1858976A1 (en) | 2007-11-28 |
| CN101142275B (zh) | 2012-07-11 |
| US20090105447A1 (en) | 2009-04-23 |
| ATE445672T1 (de) | 2009-10-15 |
| TW200640985A (en) | 2006-12-01 |
| KR20070119693A (ko) | 2007-12-20 |
| US8445630B2 (en) | 2013-05-21 |
| CN101142275A (zh) | 2008-03-12 |
| JP5541859B2 (ja) | 2014-07-09 |
| JP2008538221A (ja) | 2008-10-16 |
| EP1858976B1 (en) | 2009-10-14 |
| WO2006097419A1 (en) | 2006-09-21 |
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