JP2020509426A5 - - Google Patents
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- JP2020509426A5 JP2020509426A5 JP2019547621A JP2019547621A JP2020509426A5 JP 2020509426 A5 JP2020509426 A5 JP 2020509426A5 JP 2019547621 A JP2019547621 A JP 2019547621A JP 2019547621 A JP2019547621 A JP 2019547621A JP 2020509426 A5 JP2020509426 A5 JP 2020509426A5
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- JP
- Japan
- Prior art keywords
- group
- composition according
- formula
- photoalignment
- substituted
- 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.)
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- -1 phenylenediacryloyl group Chemical group 0.000 claims description 16
- 150000001875 compounds Chemical class 0.000 claims description 11
- 125000000623 heterocyclic group Chemical group 0.000 claims description 5
- 125000005647 linker group Chemical group 0.000 claims description 5
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 5
- NQRYJNQNLNOLGT-UHFFFAOYSA-N tetrahydropyridine hydrochloride Natural products C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
- 229920005575 poly(amic acid) Polymers 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 3
- 150000004985 diamines Chemical class 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims 16
- 239000000463 material Substances 0.000 claims 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Chemical class C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 3
- USLPZCOPYRKTGY-UHFFFAOYSA-N 2-(2-phenylethenyl)benzonitrile Chemical group N#CC1=CC=CC=C1C=CC1=CC=CC=C1 USLPZCOPYRKTGY-UHFFFAOYSA-N 0.000 claims 2
- KDCGOANMDULRCW-UHFFFAOYSA-N 7H-purine Chemical compound N1=CNC2=NC=NC2=C1 KDCGOANMDULRCW-UHFFFAOYSA-N 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
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 239000004642 Polyimide Substances 0.000 claims 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 claims 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 125000000751 azo group Chemical group [*]N=N[*] 0.000 claims 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims 2
- 125000000332 coumarinyl group Chemical group O1C(=O)C(=CC2=CC=CC=C12)* 0.000 claims 2
- 239000004973 liquid crystal related substance Substances 0.000 claims 2
- 229920001721 polyimide Polymers 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
- 150000003852 triazoles Chemical class 0.000 claims 2
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical class C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 claims 1
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical class C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 claims 1
- AVRPFRMDMNDIDH-UHFFFAOYSA-N 1h-quinazolin-2-one Chemical compound C1=CC=CC2=NC(O)=NC=C21 AVRPFRMDMNDIDH-UHFFFAOYSA-N 0.000 claims 1
- VHMICKWLTGFITH-UHFFFAOYSA-N 2H-isoindole Chemical compound C1=CC=CC2=CNC=C21 VHMICKWLTGFITH-UHFFFAOYSA-N 0.000 claims 1
- HOJKELKQMFMGOY-UHFFFAOYSA-N 3h-2,1,3-benzoxathiazole Chemical compound C1=CC=C2NOSC2=C1 HOJKELKQMFMGOY-UHFFFAOYSA-N 0.000 claims 1
- YCIPQJTZJGUXND-UHFFFAOYSA-N Aglaia odorata Alkaloid Natural products C1=CC(OC)=CC=C1C1(C(C=2C(=O)N3CCCC3=NC=22)C=3C=CC=CC=3)C2(O)C2=C(OC)C=C(OC)C=C2O1 YCIPQJTZJGUXND-UHFFFAOYSA-N 0.000 claims 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims 1
- ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical class C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 claims 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 1
- 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 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- QZHPTGXQGDFGEN-UHFFFAOYSA-N chromene Chemical group C1=CC=C2C=C[CH]OC2=C1 QZHPTGXQGDFGEN-UHFFFAOYSA-N 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 125000004427 diamine group Chemical group 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
- 229920001519 homopolymer Polymers 0.000 claims 1
- 125000004957 naphthylene group Chemical group 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 230000003287 optical effect Effects 0.000 claims 1
- 125000004430 oxygen atom Chemical group O* 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- CPNGPNLZQNNVQM-UHFFFAOYSA-N pteridine Chemical compound N1=CN=CC2=NC=CN=C21 CPNGPNLZQNNVQM-UHFFFAOYSA-N 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 150000003222 pyridines Chemical class 0.000 claims 1
- VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical compound OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 claims 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical group C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- 239000011877 solvent mixture Substances 0.000 claims 1
- 230000000087 stabilizing effect Effects 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 125000006158 tetracarboxylic acid group Chemical group 0.000 claims 1
- 125000005730 thiophenylene group Chemical group 0.000 claims 1
- 125000003944 tolyl group Chemical group 0.000 claims 1
- DQFBYFPFKXHELB-VAWYXSNFSA-N trans-chalcone Chemical group C=1C=CC=CC=1C(=O)\C=C\C1=CC=CC=C1 DQFBYFPFKXHELB-VAWYXSNFSA-N 0.000 claims 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical group [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 claims 1
- 239000008096 xylene Substances 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 description 17
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 101150096517 PAA2 gene Proteins 0.000 description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 4
- XAFOTXWPFVZQAZ-UHFFFAOYSA-N 2-(4-aminophenyl)-3h-benzimidazol-5-amine Chemical compound C1=CC(N)=CC=C1C1=NC2=CC=C(N)C=C2N1 XAFOTXWPFVZQAZ-UHFFFAOYSA-N 0.000 description 3
- JVSWJIKNEAIKJW-UHFFFAOYSA-N 2-Methylheptane Chemical group CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 3
- WPYMKLBDIGXBTP-UHFFFAOYSA-N Benzoic acid Natural products OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 description 2
- ZWZYQZVBPLYOFM-UHFFFAOYSA-N 2-(3,5-dinitrophenyl)-1h-benzimidazole Chemical compound [O-][N+](=O)C1=CC([N+](=O)[O-])=CC(C=2NC3=CC=CC=C3N=2)=C1 ZWZYQZVBPLYOFM-UHFFFAOYSA-N 0.000 description 2
- 239000005711 Benzoic acid Substances 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 235000010233 benzoic acid Nutrition 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000002837 carbocyclic group Chemical group 0.000 description 2
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 125000006678 phenoxycarbonyl group Chemical group 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- 238000005160 1H NMR spectroscopy Methods 0.000 description 1
- JHNLZOVBAQWGQU-UHFFFAOYSA-N 380814_sial Chemical compound CS(O)(=O)=O.O=P(=O)OP(=O)=O JHNLZOVBAQWGQU-UHFFFAOYSA-N 0.000 description 1
- HLBLWEWZXPIGSM-UHFFFAOYSA-N 4-Aminophenyl ether Chemical compound C1=CC(N)=CC=C1OC1=CC=C(N)C=C1 HLBLWEWZXPIGSM-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
- 101001126234 Homo sapiens Phospholipid phosphatase 3 Proteins 0.000 description 1
- LSKHYUSNCXKGSW-UHFFFAOYSA-N N-(2-aminophenyl)-3,5-dinitrobenzamide Chemical compound NC1=C(C=CC=C1)NC(C1=CC(=CC(=C1)[N+](=O)[O-])[N+](=O)[O-])=O LSKHYUSNCXKGSW-UHFFFAOYSA-N 0.000 description 1
- 101150033824 PAA1 gene Proteins 0.000 description 1
- 102100030450 Phospholipid phosphatase 3 Human genes 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 description 1
- WVIIMZNLDWSIRH-UHFFFAOYSA-N cyclohexylcyclohexane Chemical group C1CCCCC1C1CCCCC1 WVIIMZNLDWSIRH-UHFFFAOYSA-N 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2023072543A JP2023106407A (ja) | 2017-03-03 | 2023-04-26 | 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 |
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP17159210.8 | 2017-03-03 | ||
| EP17159210 | 2017-03-03 | ||
| EP17165423.9 | 2017-04-07 | ||
| EP17165423 | 2017-04-07 | ||
| PCT/EP2018/054816 WO2018158254A2 (en) | 2017-03-03 | 2018-02-27 | New photoalignment composition for the stabilization of the pre-tilt angle in liquid crystal layers |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2023072543A Division JP2023106407A (ja) | 2017-03-03 | 2023-04-26 | 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 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2020509426A JP2020509426A (ja) | 2020-03-26 |
| JP2020509426A5 true JP2020509426A5 (enExample) | 2021-03-25 |
| JP7319924B2 JP7319924B2 (ja) | 2023-08-02 |
Family
ID=61256968
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2019547621A Active JP7319924B2 (ja) | 2017-03-03 | 2018-02-27 | 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 |
| JP2023072543A Pending JP2023106407A (ja) | 2017-03-03 | 2023-04-26 | 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 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2023072543A Pending JP2023106407A (ja) | 2017-03-03 | 2023-04-26 | 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 |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US11561440B2 (enExample) |
| EP (1) | EP3628054B1 (enExample) |
| JP (2) | JP7319924B2 (enExample) |
| KR (1) | KR102533309B1 (enExample) |
| CN (1) | CN110392725B (enExample) |
| TW (1) | TWI794213B (enExample) |
| WO (1) | WO2018158254A2 (enExample) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| JP7218101B2 (ja) * | 2018-06-01 | 2023-02-06 | 株式会社ジャパンディスプレイ | 光配向膜用ワニス及び液晶表示装置 |
| CN113711117B (zh) * | 2019-03-29 | 2025-02-21 | 日产化学株式会社 | 液晶取向剂、液晶取向膜、液晶显示元件以及二胺 |
| CN111116911B (zh) * | 2019-12-30 | 2020-12-29 | 中山大学 | 一种含苯并恶唑和咔唑结构的聚酰亚胺及其制备方法和应用 |
| JP7643453B2 (ja) * | 2020-03-30 | 2025-03-11 | 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 |
| CN111575023B (zh) * | 2020-06-12 | 2022-03-01 | 江苏三月科技股份有限公司 | 一种化合物添加剂及其制备的液晶取向剂、液晶取向膜 |
| EP4008759A1 (en) * | 2020-11-20 | 2022-06-08 | Merck Patent GmbH | Polymerisable liquid crystal material and polymerised liquid crystal film |
| TWI774321B (zh) * | 2021-04-15 | 2022-08-11 | 李長榮化學工業股份有限公司 | 聚醯胺酸、聚醯亞胺、以及含有所述聚醯胺酸及聚醯亞胺之元件及其形成方法 |
| TWI887993B (zh) * | 2024-02-01 | 2025-06-21 | 奇美實業股份有限公司 | 光配向法用液晶配向劑、液晶配向膜、以及液晶顯示元件 |
| CN120737322B (zh) * | 2025-09-02 | 2025-11-28 | 西北工业大学 | 一种基于手性主链的液晶聚合物及其制备方法和应用 |
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|---|---|---|---|---|
| DE59209499D1 (de) | 1991-07-26 | 1998-10-22 | Rolic Ag | Orientierte Photopolymere und Verfahren zu ihrer Herstellung |
| SG50586A1 (en) | 1991-07-26 | 2000-05-23 | Rolic Ag | Liquid crystal display cell |
| US6608661B1 (en) | 1992-07-08 | 2003-08-19 | Rolic Ag | Photo-oriented polymer network material having desired azimuthal orientation and tilt angle and method for its production |
| EP0611981B1 (de) | 1993-02-17 | 1997-06-11 | F. Hoffmann-La Roche Ag | Optisches Bauelement |
| US6160597A (en) | 1993-02-17 | 2000-12-12 | Rolic Ag | Optical component and method of manufacture |
| EP0756193B1 (de) | 1995-07-28 | 2016-02-17 | Rolic AG | Verfahren zur Erzeugung von Kippwinkeln in photoorientierten Polymernetzwerkschichten |
| EP1386910A1 (en) * | 2002-07-30 | 2004-02-04 | Rolic AG | Photoactive materials |
| JP4653421B2 (ja) * | 2004-06-08 | 2011-03-16 | 株式会社 日立ディスプレイズ | 液晶表示装置 |
| KR20080011118A (ko) * | 2006-07-28 | 2008-01-31 | 제이에스알 가부시끼가이샤 | 액정 배향제, 액정 배향막 및 액정 표시 소자 |
| KR101257929B1 (ko) * | 2006-09-20 | 2013-04-24 | 엘지디스플레이 주식회사 | 액정표시패널 및 그 제조방법 |
| CN101687763B (zh) | 2007-05-25 | 2014-02-19 | 罗利克有限公司 | 包含脂环基的光可交联材料 |
| KR100882586B1 (ko) * | 2007-10-10 | 2009-02-13 | 제일모직주식회사 | 액정 광배향제, 이를 포함하는 액정 광배향막, 및 이를포함하는 액정 표시 장치 |
| CN101903494B (zh) | 2007-12-21 | 2016-03-02 | 罗利克有限公司 | 光校准组合物 |
| US9499649B2 (en) * | 2007-12-21 | 2016-11-22 | Rolic Ag | Functionalized photoreactive compounds |
| JP5483005B2 (ja) * | 2009-03-31 | 2014-05-07 | Ｊｓｒ株式会社 | 液晶配向剤および液晶表示素子 |
| JP2010266477A (ja) * | 2009-05-12 | 2010-11-25 | Jsr Corp | 液晶配向剤および液晶表示素子 |
| TWI490316B (zh) | 2009-07-09 | 2015-07-01 | Rolic Ag | 用於光學或光電元件之含酯基液晶 |
| JP5428643B2 (ja) * | 2009-08-24 | 2014-02-26 | Ｊｎｃ株式会社 | 液晶配向剤、液晶配向膜および液晶表示素子 |
| JP5668907B2 (ja) * | 2009-12-25 | 2015-02-12 | Jsr株式会社 | 液晶配向剤、液晶配向膜および液晶表示素子 |
| JP5387428B2 (ja) * | 2010-01-26 | 2014-01-15 | Ｊｎｃ株式会社 | 液晶配向剤、液晶配向膜および液晶表示素子 |
| TWI448790B (zh) * | 2011-05-13 | 2014-08-11 | Chi Mei Corp | 液晶配向膜及液晶顯示元件 |
| CN103702970B (zh) | 2011-08-02 | 2018-10-19 | 罗利克有限公司 | 光配向材料 |
| JP6525590B2 (ja) | 2011-08-25 | 2019-06-05 | ロリク アーゲーＲｏｌｉｃ Ａｇ | 光反応性化合物 |
| TWI520985B (zh) * | 2012-07-18 | 2016-02-11 | 奇美實業股份有限公司 | 液晶配向劑、液晶配向膜及液晶顯示元件 |
| JP6213281B2 (ja) | 2013-03-19 | 2017-10-18 | Jnc株式会社 | 感光性ジアミン、液晶配向剤および液晶表示素子 |
| TWI513737B (zh) * | 2013-11-29 | 2015-12-21 | Daxin Materials Corp | 液晶配向劑、液晶配向膜和液晶顯示元件 |
| US10442994B2 (en) * | 2014-02-19 | 2019-10-15 | Rolic Ag | Liquid crystal alignment composition, liquid crystal alignment film and liquid crystal display element |
| JP6492688B2 (ja) * | 2014-04-23 | 2019-04-03 | Jsr株式会社 | 液晶配向剤、液晶配向膜及びその製造方法、並びに液晶表示素子 |
| WO2016052285A1 (ja) | 2014-09-30 | 2016-04-07 | シャープ株式会社 | 配向膜及び液晶表示装置 |
| TWI685525B (zh) | 2014-11-12 | 2020-02-21 | 日商日產化學工業股份有限公司 | 液晶配向劑、液晶配向膜及液晶顯示元件 |
| CN107438653B (zh) | 2015-03-31 | 2022-01-07 | 罗利克有限公司 | 光致配向组合物 |
| TW201704292A (zh) * | 2015-07-20 | 2017-02-01 | 奇美實業股份有限公司 | 液晶配向劑、液晶配向膜以及液晶顯示元件 |
| 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 |
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2018
- 2018-02-27 JP JP2019547621A patent/JP7319924B2/ja active Active
- 2018-02-27 US US16/490,179 patent/US11561440B2/en active Active
- 2018-02-27 WO PCT/EP2018/054816 patent/WO2018158254A2/en not_active Ceased
- 2018-02-27 KR KR1020197026889A patent/KR102533309B1/ko active Active
- 2018-02-27 EP EP18706530.5A patent/EP3628054B1/en active Active
- 2018-02-27 CN CN201880015522.5A patent/CN110392725B/zh active Active
- 2018-03-02 TW TW107107072A patent/TWI794213B/zh active
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2023
- 2023-04-26 JP JP2023072543A patent/JP2023106407A/ja active Pending
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