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 |
|---|---|---|---|
| EP14155690.2 | 2014-02-19 | ||
| EP14155690 | 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 (https=) | 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 (https=) |
| EP (1) | EP3107978B1 (https=) |
| JP (1) | JP6636441B2 (https=) |
| KR (1) | KR102284231B1 (https=) |
| CN (1) | CN106029836B (https=) |
| TW (1) | TWI682968B (https=) |
| WO (1) | WO2015124483A1 (https=) |
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 |
| US11561440B2 (en) * | 2017-03-03 | 2023-01-24 | Rolic Technologies AG | Photoalignment composition for the stabilization of the pre-tilt angle in liquid crystal layers |
| 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 |
| WO2019116702A1 (ja) * | 2017-12-14 | 2019-06-20 | Jsr株式会社 | 液晶配向剤、液晶配向膜及び液晶素子 |
| 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 |
| EP4634327A1 (en) * | 2022-12-16 | 2025-10-22 | Rolic Technologies AG | Composition for forming a liquid crystal alignment film |
| CN118852619B (zh) * | 2024-06-14 | 2026-03-20 | 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 EP EP15705006.3A patent/EP3107978B1/en not_active Not-in-force
- 2015-02-12 KR KR1020167025498A patent/KR102284231B1/ko active Active
- 2015-02-12 US US15/119,934 patent/US10442994B2/en not_active Expired - Fee Related
- 2015-02-12 CN CN201580009545.1A patent/CN106029836B/zh active Active
- 2015-02-12 JP JP2016553373A patent/JP6636441B2/ja active Active
- 2015-02-12 WO PCT/EP2015/052913 patent/WO2015124483A1/en not_active Ceased
- 2015-02-16 TW TW104105206A patent/TWI682968B/zh active
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