JP2017513042A5 - - Google Patents
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- JP2017513042A5 JP2017513042A5 JP2016553373A JP2016553373A JP2017513042A5 JP 2017513042 A5 JP2017513042 A5 JP 2017513042A5 JP 2016553373 A JP2016553373 A JP 2016553373A JP 2016553373 A JP2016553373 A JP 2016553373A JP 2017513042 A5 JP2017513042 A5 JP 2017513042A5
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- 150000001875 compounds Chemical class 0.000 claims description 23
- 229910052731 fluorine Inorganic materials 0.000 claims description 17
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 15
- 239000011737 fluorine Substances 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 10
- ZYGHJZDHTFUPRJ-UHFFFAOYSA-N coumarin Chemical compound C1=CC=C2OC(=O)C=CC2=C1 ZYGHJZDHTFUPRJ-UHFFFAOYSA-N 0.000 claims description 9
- 125000000524 functional group Chemical group 0.000 claims description 9
- 125000001153 fluoro group Chemical group F* 0.000 claims description 8
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 7
- 229910052794 bromium Inorganic materials 0.000 claims description 7
- 229910052801 chlorine Inorganic materials 0.000 claims description 7
- 239000000460 chlorine Substances 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 239000004642 Polyimide Substances 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- -1 glycol ethers Chemical class 0.000 claims description 6
- 229920005575 poly(amic acid) Polymers 0.000 claims description 6
- 229920001721 polyimide Polymers 0.000 claims description 6
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims description 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 150000001408 amides Chemical class 0.000 claims description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 5
- 235000001671 coumarin Nutrition 0.000 claims description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 5
- 125000004185 ester group Chemical group 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- 235000021286 stilbenes Nutrition 0.000 claims description 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- DQFBYFPFKXHELB-UHFFFAOYSA-N Chalcone Natural products C=1C=CC=CC=1C(=O)C=CC1=CC=CC=C1 DQFBYFPFKXHELB-UHFFFAOYSA-N 0.000 claims description 4
- PJANXHGTPQOBST-VAWYXSNFSA-N Stilbene Natural products C=1C=CC=CC=1/C=C/C1=CC=CC=C1 PJANXHGTPQOBST-VAWYXSNFSA-N 0.000 claims description 4
- 235000005513 chalcones Nutrition 0.000 claims description 4
- 229930016911 cinnamic acid Natural products 0.000 claims description 4
- 235000013985 cinnamic acid Nutrition 0.000 claims description 4
- 229960000956 coumarin Drugs 0.000 claims description 4
- 150000003949 imides Chemical class 0.000 claims description 4
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 claims description 4
- PJANXHGTPQOBST-UHFFFAOYSA-N stilbene Chemical compound C=1C=CC=CC=1C=CC1=CC=CC=C1 PJANXHGTPQOBST-UHFFFAOYSA-N 0.000 claims description 4
- 150000007970 thio esters Chemical group 0.000 claims description 4
- DQFBYFPFKXHELB-VAWYXSNFSA-N trans-chalcone Chemical compound C=1C=CC=CC=1C(=O)\C=C\C1=CC=CC=C1 DQFBYFPFKXHELB-VAWYXSNFSA-N 0.000 claims description 4
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims description 3
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 3
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 claims description 3
- QZHPTGXQGDFGEN-UHFFFAOYSA-N chromene Chemical compound C1=CC=C2C=C[CH]OC2=C1 QZHPTGXQGDFGEN-UHFFFAOYSA-N 0.000 claims description 2
- OTAFHZMPRISVEM-UHFFFAOYSA-N chromone Chemical compound C1=CC=C2C(=O)C=COC2=C1 OTAFHZMPRISVEM-UHFFFAOYSA-N 0.000 claims description 2
- 239000000412 dendrimer Substances 0.000 claims description 2
- 229920000736 dendritic polymer Polymers 0.000 claims description 2
- 239000000178 monomer Substances 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 15
- 239000004973 liquid crystal related substance Substances 0.000 claims 15
- 239000000203 mixture Substances 0.000 claims 15
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 15
- 235000013824 polyphenols Nutrition 0.000 claims 15
- 150000004984 aromatic diamines Chemical class 0.000 claims 8
- 239000011247 coating layer Substances 0.000 claims 7
- 150000004985 diamines Chemical class 0.000 claims 7
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims 4
- 239000002904 solvent Substances 0.000 claims 4
- 150000001735 carboxylic acids Chemical class 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 230000003287 optical effect Effects 0.000 claims 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 2
- 230000000996 additive effect Effects 0.000 claims 2
- 150000004982 aromatic amines Chemical class 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 239000011877 solvent mixture Substances 0.000 claims 2
- 150000001241 acetals Chemical class 0.000 claims 1
- 150000001298 alcohols Chemical class 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 229920001400 block copolymer Polymers 0.000 claims 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims 1
- 239000011248 coating agent Substances 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 150000004775 coumarins Chemical class 0.000 claims 1
- 125000006159 dianhydride group Chemical group 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 1
- 150000002334 glycols Chemical class 0.000 claims 1
- 150000008282 halocarbons Chemical class 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- 230000001939 inductive effect Effects 0.000 claims 1
- 229910052740 iodine Inorganic materials 0.000 claims 1
- 230000001678 irradiating effect Effects 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 150000002596 lactones Chemical class 0.000 claims 1
- 239000010410 layer Substances 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- 150000002825 nitriles Chemical class 0.000 claims 1
- 239000003960 organic solvent 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
- 150000007660 quinolones Chemical class 0.000 claims 1
- 150000001629 stilbenes Chemical class 0.000 claims 1
- 239000000758 substrate Substances 0.000 claims 1
- 125000006158 tetracarboxylic acid group Chemical group 0.000 claims 1
- SBHHKGFHJWTZJN-UHFFFAOYSA-N 1,3-dimethylcyclobutane-1,2,3,4-tetracarboxylic acid Chemical compound OC(=O)C1(C)C(C(O)=O)C(C)(C(O)=O)C1C(O)=O SBHHKGFHJWTZJN-UHFFFAOYSA-N 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- RHRNYXVSZLSRRP-UHFFFAOYSA-N 3-(carboxymethyl)cyclopentane-1,2,4-tricarboxylic acid Chemical compound OC(=O)CC1C(C(O)=O)CC(C(O)=O)C1C(O)=O RHRNYXVSZLSRRP-UHFFFAOYSA-N 0.000 description 1
- YGYCECQIOXZODZ-UHFFFAOYSA-N 4415-87-6 Chemical compound O=C1OC(=O)C2C1C1C(=O)OC(=O)C12 YGYCECQIOXZODZ-UHFFFAOYSA-N 0.000 description 1
- JYCTWJFSRDBYJX-UHFFFAOYSA-N 5-(2,5-dioxooxolan-3-yl)-3a,4,5,9b-tetrahydrobenzo[e][2]benzofuran-1,3-dione Chemical compound O=C1OC(=O)CC1C1C2=CC=CC=C2C(C(=O)OC2=O)C2C1 JYCTWJFSRDBYJX-UHFFFAOYSA-N 0.000 description 1
- LSLUFHBPDRKXSF-UHFFFAOYSA-N 5-(2,5-dioxooxolan-3-yl)-5-ethyl-4,9b-dihydro-3ah-benzo[e][2]benzofuran-1,3-dione Chemical compound C1C(C(OC2=O)=O)C2C2=CC=CC=C2C1(CC)C1CC(=O)OC1=O LSLUFHBPDRKXSF-UHFFFAOYSA-N 0.000 description 1
- DZQLOPHNOBORQP-UHFFFAOYSA-N 5-(2,5-dioxooxolan-3-yl)-5-methyl-4,9b-dihydro-3ah-benzo[e][2]benzofuran-1,3-dione Chemical compound C1C(C(OC2=O)=O)C2C2=CC=CC=C2C1(C)C1CC(=O)OC1=O DZQLOPHNOBORQP-UHFFFAOYSA-N 0.000 description 1
- SFJDTBCBRPQWIP-UHFFFAOYSA-N 5-(2,5-dioxooxolan-3-yl)-7-ethyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound O=C1OC(CC1C1CC2C(C(OC2=O)=O)C(=C1)CC)=O SFJDTBCBRPQWIP-UHFFFAOYSA-N 0.000 description 1
- DGQOZCNCJKEVOA-UHFFFAOYSA-N 5-(2,5-dioxooxolan-3-yl)-7-methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C(C(OC2=O)=O)C2C(C)=CC1C1CC(=O)OC1=O DGQOZCNCJKEVOA-UHFFFAOYSA-N 0.000 description 1
- VWRKHZDUJPWJKV-UHFFFAOYSA-N 6-(carboxymethyl)bicyclo[2.2.1]heptane-2,3,5-tricarboxylic acid Chemical compound C1C2C(C(O)=O)C(CC(=O)O)C1C(C(O)=O)C2C(O)=O VWRKHZDUJPWJKV-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 229940114081 cinnamate Drugs 0.000 description 1
- WOSVXXBNNCUXMT-UHFFFAOYSA-N cyclopentane-1,2,3,4-tetracarboxylic acid Chemical compound OC(=O)C1CC(C(O)=O)C(C(O)=O)C1C(O)=O WOSVXXBNNCUXMT-UHFFFAOYSA-N 0.000 description 1
- UFOIOXZLTXNHQH-UHFFFAOYSA-N oxolane-2,3,4,5-tetracarboxylic acid Chemical compound OC(=O)C1OC(C(O)=O)C(C(O)=O)C1C(O)=O UFOIOXZLTXNHQH-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP14155690 | 2014-02-19 | ||
| EP14155690.2 | 2014-02-19 | ||
| PCT/EP2015/052913 WO2015124483A1 (en) | 2014-02-19 | 2015-02-12 | Liquid crystal alignment composition, liquid crystal alignment film and liquid crystal display element |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017513042A JP2017513042A (ja) | 2017-05-25 |
| JP2017513042A5 true JP2017513042A5 (enExample) | 2018-03-15 |
| JP6636441B2 JP6636441B2 (ja) | 2020-01-29 |
Family
ID=50114300
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016553373A Active JP6636441B2 (ja) | 2014-02-19 | 2015-02-12 | 液晶配向組成物、液晶配向膜、及び液晶ディスプレイ素子 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US10442994B2 (enExample) |
| EP (1) | EP3107978B1 (enExample) |
| JP (1) | JP6636441B2 (enExample) |
| KR (1) | KR102284231B1 (enExample) |
| CN (1) | CN106029836B (enExample) |
| TW (1) | TWI682968B (enExample) |
| WO (1) | WO2015124483A1 (enExample) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR101879834B1 (ko) * | 2015-11-11 | 2018-07-18 | 주식회사 엘지화학 | 액정 배향막의 제조 방법, 이를 이용한 액정 배향막 및 액정 표시소자 |
| KR101697336B1 (ko) * | 2016-03-03 | 2017-01-17 | 주식회사 엘지화학 | 액정 배향막의 제조방법 |
| KR102637054B1 (ko) | 2016-06-28 | 2024-02-15 | 삼성디스플레이 주식회사 | 광배향제 및 액정 표시 장치 |
| JP7039166B2 (ja) * | 2016-09-30 | 2022-03-22 | 東京応化工業株式会社 | 樹脂組成物、硬化物の製造方法、及び硬化物 |
| JP7319924B2 (ja) * | 2017-03-03 | 2023-08-02 | ロリク・テクノロジーズ・アーゲー | 液晶層におけるプレチルト角を安定化させるための新規光配向組成物 |
| TWI710601B (zh) * | 2017-04-10 | 2020-11-21 | 奇美實業股份有限公司 | 軟性基板用組成物以及軟性基板 |
| JP7093058B2 (ja) * | 2017-04-25 | 2022-06-29 | 日産化学株式会社 | 液晶配向剤、液晶配向膜、及び液晶表示素子 |
| KR102030079B1 (ko) * | 2017-06-30 | 2019-10-08 | 주식회사 엘지화학 | 액정 배향제 조성물, 이를 이용한 액정 배향막의 제조 방법, 및 이를 이용한 액정 배향막 |
| JP6904216B2 (ja) * | 2017-10-30 | 2021-07-14 | Jnc株式会社 | 液晶配向膜を形成するための液晶配向剤、液晶配向膜およびこれを用いた液晶表示素子 |
| CN111212878B (zh) * | 2017-12-14 | 2022-06-14 | Jsr株式会社 | 液晶取向剂、液晶取向膜及其制造方法、及液晶元件 |
| KR102202054B1 (ko) * | 2018-01-22 | 2021-01-11 | 주식회사 엘지화학 | 액정 배향제 조성물, 이를 이용한 액정 배향막의 제조 방법, 및 이를 이용한 액정 배향막 |
| KR102273687B1 (ko) | 2018-05-17 | 2021-07-05 | 주식회사 엘지화학 | 액정 배향제 조성물, 이를 이용한 액정 배향막의 제조 방법, 및 이를 이용한 액정 배향막 |
| JP7093150B2 (ja) * | 2018-12-06 | 2022-06-29 | 日本化薬株式会社 | 硬化性樹脂組成物及びその硬化物 |
| WO2020189924A1 (ko) * | 2019-03-18 | 2020-09-24 | 삼성디스플레이 주식회사 | 발광 소자 용매, 광 분해성 증점제, 발광 소자 잉크 및 표시 장치의 제조 방법 |
| CN111848954B (zh) * | 2019-04-25 | 2023-10-17 | 北京鼎材科技有限公司 | 一种改性聚酰亚胺前驱体树脂、光敏树脂组合物及其用途 |
| CN110734771B (zh) * | 2019-09-27 | 2022-12-20 | 江苏三月科技股份有限公司 | 液晶取向剂、液晶取向膜及液晶显示元件 |
| CN111592891B (zh) * | 2020-06-12 | 2022-03-01 | 江苏三月科技股份有限公司 | 一种液晶取向剂及其制备的液晶取向膜、液晶显示元件 |
| WO2024125945A1 (en) * | 2022-12-16 | 2024-06-20 | Rolic Technologies AG | Composition for forming a liquid crystal alignment film |
| CN118852619A (zh) * | 2024-06-14 | 2024-10-29 | 上海交通大学 | 光敏聚合物及其制备方法、用途、正性光刻胶 |
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| KR101333709B1 (ko) * | 2011-01-24 | 2013-11-27 | 제일모직주식회사 | 액정 배향제, 이를 이용하여 제조한 액정 배향막 및 상기 액정 배향막을 포함하는 액정표시소자 |
| KR101444190B1 (ko) * | 2011-12-19 | 2014-09-26 | 제일모직 주식회사 | 액정 배향제, 이를 이용한 액정 배향막 및 상기 액정 배향막을 포함하는 액정표시소자 |
| KR101387735B1 (ko) * | 2011-12-22 | 2014-04-25 | 제일모직주식회사 | 액정 광배향제, 이를 이용한 액정 광배향막 및 상기 액정 광배향막을 포함하는 액정표시소자 |
| TWI461463B (zh) * | 2012-08-15 | 2014-11-21 | Daxin Materials Corp | 液晶配向劑、液晶配向膜及其液晶顯示元件 |
-
2015
- 2015-02-12 WO PCT/EP2015/052913 patent/WO2015124483A1/en not_active Ceased
- 2015-02-12 KR KR1020167025498A patent/KR102284231B1/ko active Active
- 2015-02-12 CN CN201580009545.1A patent/CN106029836B/zh active Active
- 2015-02-12 EP EP15705006.3A patent/EP3107978B1/en active Active
- 2015-02-12 US US15/119,934 patent/US10442994B2/en not_active Expired - Fee Related
- 2015-02-12 JP JP2016553373A patent/JP6636441B2/ja active Active
- 2015-02-16 TW TW104105206A patent/TWI682968B/zh active
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