DE602004001417T2 - Flüssigkristallfilm und damit versehene Flüssigkristallanzeigevorrichtung - Google Patents
Flüssigkristallfilm und damit versehene Flüssigkristallanzeigevorrichtung Download PDFInfo
- Publication number
- DE602004001417T2 DE602004001417T2 DE602004001417T DE602004001417T DE602004001417T2 DE 602004001417 T2 DE602004001417 T2 DE 602004001417T2 DE 602004001417 T DE602004001417 T DE 602004001417T DE 602004001417 T DE602004001417 T DE 602004001417T DE 602004001417 T2 DE602004001417 T2 DE 602004001417T2
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- Prior art keywords
- liquid crystal
- film
- group
- meth
- substance
- Prior art date
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- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract description 279
- 125000003566 oxetanyl group Chemical group 0.000 claims abstract description 68
- 239000000126 substance Substances 0.000 claims abstract description 63
- 239000000463 material Substances 0.000 claims abstract description 62
- -1 acrylic compound Chemical class 0.000 claims abstract description 55
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims abstract description 35
- 239000010408 film Substances 0.000 claims description 142
- 239000012788 optical film Substances 0.000 claims description 39
- 239000000758 substrate Substances 0.000 claims description 39
- 150000001768 cations Chemical class 0.000 claims description 31
- 230000003287 optical effect Effects 0.000 claims description 12
- 239000005264 High molar mass liquid crystal Substances 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 238000010792 warming Methods 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- 239000004990 Smectic liquid crystal Substances 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
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- 239000010410 layer Substances 0.000 description 55
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- 238000000034 method Methods 0.000 description 35
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 25
- 150000001875 compounds Chemical class 0.000 description 23
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- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 8
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- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 6
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- UNMJLQGKEDTEKJ-UHFFFAOYSA-N (3-ethyloxetan-3-yl)methanol Chemical compound CCC1(CO)COC1 UNMJLQGKEDTEKJ-UHFFFAOYSA-N 0.000 description 4
- JVVRCYWZTJLJSG-UHFFFAOYSA-N 4-dimethylaminophenol Chemical compound CN(C)C1=CC=C(O)C=C1 JVVRCYWZTJLJSG-UHFFFAOYSA-N 0.000 description 4
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- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 4
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- 229920000297 Rayon Polymers 0.000 description 4
- NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 4
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- ZDYVRSLAEXCVBX-UHFFFAOYSA-N pyridinium p-toluenesulfonate Chemical compound C1=CC=[NH+]C=C1.CC1=CC=C(S([O-])(=O)=O)C=C1 ZDYVRSLAEXCVBX-UHFFFAOYSA-N 0.000 description 4
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- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
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- 125000003118 aryl group Chemical group 0.000 description 3
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- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 3
- 239000002964 rayon Substances 0.000 description 3
- 239000005361 soda-lime glass Substances 0.000 description 3
- 125000005409 triarylsulfonium group Chemical group 0.000 description 3
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
- 238000005160 1H NMR spectroscopy Methods 0.000 description 2
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
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- 101100272976 Panax ginseng CYP716A53v2 gene Proteins 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
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- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- CZFNISFYDPIDNM-UHFFFAOYSA-N n,n-dimethylformamide;oxolane Chemical compound CN(C)C=O.C1CCOC1 CZFNISFYDPIDNM-UHFFFAOYSA-N 0.000 description 2
- 230000006855 networking Effects 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
- 239000003505 polymerization initiator Substances 0.000 description 2
- BBEAQIROQSPTKN-UHFFFAOYSA-N pyrene Chemical compound C1=CC=C2C=CC3=CC=CC4=CC=C1C2=C43 BBEAQIROQSPTKN-UHFFFAOYSA-N 0.000 description 2
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- OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
- NDZFNTHGIIQMQI-UHFFFAOYSA-N 1-benzylpyridin-1-ium Chemical class C=1C=CC=C[N+]=1CC1=CC=CC=C1 NDZFNTHGIIQMQI-UHFFFAOYSA-N 0.000 description 1
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
- WJFKNYWRSNBZNX-UHFFFAOYSA-N 10H-phenothiazine Chemical compound C1=CC=C2NC3=CC=CC=C3SC2=C1 WJFKNYWRSNBZNX-UHFFFAOYSA-N 0.000 description 1
- BTJPUDCSZVCXFQ-UHFFFAOYSA-N 2,4-diethylthioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(CC)=CC(CC)=C3SC2=C1 BTJPUDCSZVCXFQ-UHFFFAOYSA-N 0.000 description 1
- FEWSKCAVEJNPBX-UHFFFAOYSA-N 2-(2-hydroxy-2-phenylacetyl)benzenesulfonic acid Chemical compound C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1S(O)(=O)=O FEWSKCAVEJNPBX-UHFFFAOYSA-N 0.000 description 1
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- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
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- 229920000742 Cotton Polymers 0.000 description 1
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical class C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 description 1
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- WYCLKHIHQYPHIP-UHFFFAOYSA-I acetyl chloride;pentachloro-$l^{5}-stibane Chemical class CC(Cl)=O.Cl[Sb](Cl)(Cl)(Cl)Cl WYCLKHIHQYPHIP-UHFFFAOYSA-I 0.000 description 1
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- 238000004458 analytical method Methods 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
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- 238000002360 preparation method Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 238000001226 reprecipitation Methods 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 150000003388 sodium compounds Chemical class 0.000 description 1
- 238000004528 spin coating Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000007669 thermal treatment Methods 0.000 description 1
- WBYWAXJHAXSJNI-VOTSOKGWSA-M trans-cinnamate Chemical compound [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229910052724 xenon Inorganic materials 0.000 description 1
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/38—Polymers
- C09K19/3833—Polymers with mesogenic groups in the side chain
- C09K19/3842—Polyvinyl derivatives
- C09K19/3852—Poly(meth)acrylate derivatives
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/08—Non-steroidal liquid crystal compounds containing at least two non-condensed rings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K19/00—Liquid crystal materials
- C09K19/04—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit
- C09K19/06—Non-steroidal liquid crystal compounds
- C09K19/34—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring
- C09K19/3402—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having oxygen as hetero atom
- C09K2019/3416—Non-steroidal liquid crystal compounds containing at least one heterocyclic ring having oxygen as hetero atom the heterocyclic ring being a four-membered ring, e.g. oxetane
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K2323/00—Functional layers of liquid crystal optical display excluding electroactive liquid crystal layer characterised by chemical composition
- C09K2323/03—Viewing layer characterised by chemical composition
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2003114322 | 2003-04-18 | ||
| JP2003114322A JP4246536B2 (ja) | 2003-04-18 | 2003-04-18 | 液晶フィルムおよび当該フィルムを搭載した液晶表示素子 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE602004001417D1 DE602004001417D1 (de) | 2006-08-17 |
| DE602004001417T2 true DE602004001417T2 (de) | 2006-11-16 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE602004001417T Expired - Lifetime DE602004001417T2 (de) | 2003-04-18 | 2004-04-15 | Flüssigkristallfilm und damit versehene Flüssigkristallanzeigevorrichtung |
Country Status (8)
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4246536B2 (ja) | 2003-04-18 | 2009-04-02 | 新日本石油株式会社 | 液晶フィルムおよび当該フィルムを搭載した液晶表示素子 |
| US7070838B2 (en) * | 2003-06-23 | 2006-07-04 | Chisso Petrochemical Corporation | Liquid crystalline compound, liquid crystal composition and their polymers |
| US7101595B2 (en) * | 2003-07-30 | 2006-09-05 | Chisso Corporation | Photo-curable fluorene derivative and composition containing the same |
| EP1524309B1 (en) * | 2003-10-15 | 2006-06-07 | Nippon Oil Corporation | Polymerizable liquid crystalline composition and liquid crystal film produced from the same |
| JP2006104307A (ja) * | 2004-10-04 | 2006-04-20 | Nippon Oil Corp | 重合性液晶組成物およびこの組成物を用いた液晶フィルム |
| JP2006337575A (ja) * | 2005-05-31 | 2006-12-14 | Nippon Oil Corp | ホメオトロピック配向液晶フィルムおよびそれを用いた装置 |
| EP1850155B1 (en) * | 2005-02-08 | 2012-11-14 | Nippon Oil Corporation | Homeotropically oriented liquid-crystal film, optical film comprising the same, and image display |
| JP2006220770A (ja) * | 2005-02-08 | 2006-08-24 | Nippon Oil Corp | 液晶フィルムおよび液晶表示素子 |
| JP4648854B2 (ja) | 2006-02-28 | 2011-03-09 | Ｊｘ日鉱日石エネルギー株式会社 | ジオキセタン化合物、カチオン重合性組成物および光学フィルム並びに液晶表示装置 |
| JP2007256761A (ja) * | 2006-03-24 | 2007-10-04 | Nippon Oil Corp | 楕円偏光板、その製造方法およびそれを用いた液晶表示装置 |
| JP4925709B2 (ja) | 2006-04-10 | 2012-05-09 | Ｊｘ日鉱日石エネルギー株式会社 | 接着性を向上させた液晶性組成物、該組成物からなる液晶フィルム、および該フィルムを搭載した液晶表示素子 |
| JP2008083613A (ja) * | 2006-09-29 | 2008-04-10 | Sony Corp | 液晶表示素子および液晶表示装置 |
| CN101798370B (zh) * | 2010-03-09 | 2012-06-06 | 湘潭大学 | 一种反应性侧链型液晶共聚物 |
| WO2014073578A1 (ja) * | 2012-11-07 | 2014-05-15 | 旭硝子株式会社 | 光重合性液晶組成物、光学補償膜、光学補償積層膜、電極基板、液晶装置用基板および液晶装置 |
| WO2014084687A1 (ko) * | 2012-11-29 | 2014-06-05 | 주식회사 엘지화학 | 광학 필름 |
| CN104558389B (zh) * | 2014-12-23 | 2018-04-27 | 湘潭大学 | 一种具有自愈合能力的液晶共聚物材料及其制备方法 |
| CN108698966B (zh) * | 2016-03-01 | 2022-03-22 | 日本瑞翁株式会社 | 包含单醚化物的溶液组合物的制造方法、溶液组合物、及聚合性化合物的制造方法 |
| JP6388053B2 (ja) * | 2017-04-28 | 2018-09-12 | 大日本印刷株式会社 | 光学フィルム用転写体、光学フィルム、光学フィルム用転写体の製造方法、光学フィルムの製造方法 |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4564563A (en) | 1983-09-30 | 1986-01-14 | Electro Materials Corp. Of America | Solderable conductor |
| JP2662814B2 (ja) | 1989-06-06 | 1997-10-15 | 株式会社リコー | 液晶性高分子の配向方法 |
| JP2660601B2 (ja) | 1990-06-27 | 1997-10-08 | 日本石油株式会社 | 液晶表示素子用補償板の製造法 |
| DE4126422A1 (de) * | 1991-08-09 | 1993-02-11 | Bayer Ag | Vertraegliche polymermischungen mit thermoplastischen polycarbonaten |
| JP2952449B2 (ja) | 1992-06-03 | 1999-09-27 | 日石三菱株式会社 | 液晶表示素子用補償板の製造法 |
| DE69419120T2 (de) | 1993-12-24 | 1999-10-28 | Dainippon Ink & Chemicals | Polymerisierbare Flüssigkristallzusammensetzung und optisch anisotroper Film, der eine solche Zusammensetzung enthält |
| US5773178A (en) * | 1996-09-13 | 1998-06-30 | Japan Synthetic Rubber Co, Ltd. | Process for producing a patterned anisotropic polymeric film |
| JPH10120640A (ja) | 1996-10-21 | 1998-05-12 | Nitto Denko Corp | ビスアジド化合物、液晶ポリマー及び配向フィルム |
| FR2758557B1 (fr) * | 1997-01-21 | 1999-11-12 | Toagosei Co Ltd | Compose ayant un groupe oxetanyle, son procede de preparation et composition de durcissement |
| US6338808B1 (en) * | 1999-03-31 | 2002-01-15 | Fuji Photo Film Co., Ltd. | Liquid crystal composition comprising liquid crystal molecules and alignment promoter |
| JP2000319527A (ja) | 1999-05-10 | 2000-11-21 | Nitto Denko Corp | 不飽和脂環式化合物、添加系液晶ポリマー及び液晶ポリマー配向フィルムの製造方法 |
| DE60114518T2 (de) * | 2000-07-06 | 2006-08-10 | Fuji Photo Film Co. Ltd., Minamiashigara | Flüssigkristallzusammensetzung, die Flüssigkristallmoleküle und Ausrichtungsmittel enthält |
| DE60118776T2 (de) * | 2000-10-04 | 2007-06-06 | Koninklijke Philips Electronics N.V. | Polymerisierbare, flüssigkristalline dioxetane, deren herstellung und verwendung |
| JP2002294240A (ja) * | 2001-03-30 | 2002-10-09 | Fuji Photo Film Co Ltd | 棒状液晶性分子の配向方法および光学異方性素子 |
| JP4673502B2 (ja) * | 2001-06-07 | 2011-04-20 | Ｊｘ日鉱日石エネルギー株式会社 | 主鎖型液晶性ポリエステル、液晶性組成物、液晶フィルムの製造方法、光学フィルムおよび表示装置 |
| JP4911844B2 (ja) | 2001-09-20 | 2012-04-04 | Ｊｘ日鉱日石エネルギー株式会社 | 液晶フィルムの製造方法、光学フィルムおよび液晶表示装置 |
| US7244798B2 (en) * | 2002-10-01 | 2007-07-17 | Nippon Oil Corporation | (Meth) acrylic compound having an oxetanyl group and liquid crystal film produced by using same |
| JP4246536B2 (ja) * | 2003-04-18 | 2009-04-02 | 新日本石油株式会社 | 液晶フィルムおよび当該フィルムを搭載した液晶表示素子 |
| US6953862B2 (en) * | 2003-05-06 | 2005-10-11 | National Starch And Chemical Investment Holding Corporation | Oxetane compounds containing styrenic functionality |
| EP1524309B1 (en) * | 2003-10-15 | 2006-06-07 | Nippon Oil Corporation | Polymerizable liquid crystalline composition and liquid crystal film produced from the same |
| JP4586520B2 (ja) * | 2004-04-07 | 2010-11-24 | チッソ株式会社 | 光重合性オキセタン誘導体およびそれらを含む液晶組成物 |
-
2003
- 2003-04-18 JP JP2003114322A patent/JP4246536B2/ja not_active Expired - Lifetime
-
2004
- 2004-04-14 US US10/825,557 patent/US7125590B2/en active Active
- 2004-04-15 DE DE602004001417T patent/DE602004001417T2/de not_active Expired - Lifetime
- 2004-04-15 EP EP04009010A patent/EP1469058B1/en not_active Expired - Lifetime
- 2004-04-15 AT AT04009010T patent/ATE332347T1/de not_active IP Right Cessation
- 2004-04-16 KR KR1020040026311A patent/KR101059587B1/ko active IP Right Grant
- 2004-04-16 TW TW093110680A patent/TWI255293B/zh not_active IP Right Cessation
- 2004-04-16 CN CNB200410055254XA patent/CN100458519C/zh not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP4246536B2 (ja) | 2009-04-02 |
| TWI255293B (en) | 2006-05-21 |
| US20040209006A1 (en) | 2004-10-21 |
| CN1595250A (zh) | 2005-03-16 |
| EP1469058A1 (en) | 2004-10-20 |
| US7125590B2 (en) | 2006-10-24 |
| ATE332347T1 (de) | 2006-07-15 |
| EP1469058B1 (en) | 2006-07-05 |
| DE602004001417D1 (de) | 2006-08-17 |
| KR20040090917A (ko) | 2004-10-27 |
| TW200424292A (en) | 2004-11-16 |
| JP2004315736A (ja) | 2004-11-11 |
| CN100458519C (zh) | 2009-02-04 |
| KR101059587B1 (ko) | 2011-08-25 |
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