JPWO2016035667A1 - 液晶組成物及びそれを使用した液晶表示素子 - Google Patents
液晶組成物及びそれを使用した液晶表示素子 Download PDFInfo
- Publication number
- JPWO2016035667A1 JPWO2016035667A1 JP2016525111A JP2016525111A JPWO2016035667A1 JP WO2016035667 A1 JPWO2016035667 A1 JP WO2016035667A1 JP 2016525111 A JP2016525111 A JP 2016525111A JP 2016525111 A JP2016525111 A JP 2016525111A JP WO2016035667 A1 JPWO2016035667 A1 JP WO2016035667A1
- Authority
- JP
- Japan
- Prior art keywords
- liquid crystal
- general formula
- group
- formula
- crystal composition
- 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.)
- Pending
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- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract description 178
- 239000000203 mixture Substances 0.000 title claims abstract description 135
- 239000011159 matrix material Substances 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 158
- 125000004432 carbon atom Chemical group C* 0.000 claims description 71
- 125000000217 alkyl group Chemical group 0.000 claims description 39
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 35
- 229910052731 fluorine Inorganic materials 0.000 claims description 27
- 125000001153 fluoro group Chemical group F* 0.000 claims description 27
- 125000003342 alkenyl group Chemical group 0.000 claims description 15
- 125000003545 alkoxy group Chemical group 0.000 claims description 14
- 125000002947 alkylene group Chemical group 0.000 claims description 12
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 11
- 125000005407 trans-1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])[C@]([H])([*:2])C([H])([H])C([H])([H])[C@@]1([H])[*:1] 0.000 claims description 10
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims description 8
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 7
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 5
- 125000004429 atom Chemical group 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 239000008096 xylene Substances 0.000 claims 1
- 230000004044 response Effects 0.000 abstract description 8
- 230000007547 defect Effects 0.000 abstract description 3
- 238000000034 method Methods 0.000 description 27
- 230000008569 process Effects 0.000 description 19
- -1 1,4-dioxane-2,5-diyl group Chemical group 0.000 description 16
- 239000000758 substrate Substances 0.000 description 13
- 0 CC(C)(C1)N(C)C(C)(C)CC1OC(CC(C(CC(OC1CC(C)(C)N(*)C(C)(C)C1)=O)C(OC1CC(C)(C)N(*)C(C)(C)C1)=O)C(OC1CC(C)(C)N(*)C(C)(C)C1)=O)=O Chemical compound CC(C)(C1)N(C)C(C)(C)CC1OC(CC(C(CC(OC1CC(C)(C)N(*)C(C)(C)C1)=O)C(OC1CC(C)(C)N(*)C(C)(C)C1)=O)C(OC1CC(C)(C)N(*)C(C)(C)C1)=O)=O 0.000 description 10
- 230000000704 physical effect Effects 0.000 description 10
- 229910052799 carbon Inorganic materials 0.000 description 7
- 125000005843 halogen group Chemical group 0.000 description 7
- 230000007704 transition Effects 0.000 description 7
- 238000012360 testing method Methods 0.000 description 6
- 206010047571 Visual impairment Diseases 0.000 description 5
- 150000001721 carbon Chemical group 0.000 description 5
- 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 5
- 238000011156 evaluation Methods 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
- 239000010408 film Substances 0.000 description 4
- 239000007791 liquid phase Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 125000004955 1,4-cyclohexylene group Chemical group [H]C1([H])C([H])([H])C([H])([*:1])C([H])([H])C([H])([H])C1([H])[*:2] 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 235000006708 antioxidants Nutrition 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 229920000642 polymer Polymers 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- 125000004959 2,6-naphthylene group Chemical group [H]C1=C([H])C2=C([H])C([*:1])=C([H])C([H])=C2C([H])=C1[*:2] 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000004985 Discotic Liquid Crystal Substance Substances 0.000 description 2
- 101000946040 Homo sapiens Lysosomal-associated transmembrane protein 4B Proteins 0.000 description 2
- 102100034726 Lysosomal-associated transmembrane protein 4B Human genes 0.000 description 2
- 239000004988 Nematic liquid crystal Substances 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical group C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 125000004093 cyano group Chemical group *C#N 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical group CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 1
- 125000005714 2,5- (1,3-dioxanylene) group Chemical group [H]C1([H])OC([H])([*:1])OC([H])([H])C1([H])[*:2] 0.000 description 1
- SBFXKDGHQRHHGO-UHFFFAOYSA-N CC(C)(C1NC1)C(CC1)CCC1N Chemical compound CC(C)(C1NC1)C(CC1)CCC1N SBFXKDGHQRHHGO-UHFFFAOYSA-N 0.000 description 1
- DQFBYFPFKXHELB-UHFFFAOYSA-N Chalcone Natural products C=1C=CC=CC=1C(=O)C=CC1=CC=CC=C1 DQFBYFPFKXHELB-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 206010027146 Melanoderma Diseases 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 125000004423 acyloxy group Chemical group 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000003302 alkenyloxy group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 125000001231 benzoyloxy group Chemical group C(C1=CC=CC=C1)(=O)O* 0.000 description 1
- 235000005513 chalcones Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 230000003098 cholesteric effect Effects 0.000 description 1
- 229940114081 cinnamate Drugs 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 150000001934 cyclohexanes Chemical class 0.000 description 1
- 238000007872 degassing Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000012769 display material Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000013213 extrapolation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical class N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 125000006850 spacer group Chemical group 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- DQFBYFPFKXHELB-VAWYXSNFSA-N trans-chalcone Chemical compound C=1C=CC=CC=1C(=O)\C=C\C1=CC=CC=C1 DQFBYFPFKXHELB-VAWYXSNFSA-N 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
- 125000005580 triphenylene group Chemical group 0.000 description 1
- YGPLLMPPZRUGTJ-UHFFFAOYSA-N truxene Chemical class C1C2=CC=CC=C2C(C2=C3C4=CC=CC=C4C2)=C1C1=C3CC2=CC=CC=C21 YGPLLMPPZRUGTJ-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
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K19/54—Additives having no specific mesophase characterised by their 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
- 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
- C09K19/10—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
- C09K19/12—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings at least two benzene rings directly linked, e.g. biphenyls
-
- 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
- C09K19/10—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings
- C09K19/20—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing at least two benzene rings linked by a chain containing carbon and oxygen atoms as chain links, e.g. esters or ethers
-
- 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
- C09K19/30—Non-steroidal liquid crystal compounds containing at least two non-condensed rings containing saturated or unsaturated non-aromatic rings, e.g. cyclohexane 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
- C09K19/32—Non-steroidal liquid crystal compounds containing condensed ring systems, i.e. fused, bridged or spiro ring systems
-
- 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
-
- G—PHYSICS
- G02—OPTICS
- G02F—OPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
- G02F1/00—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
- G02F1/01—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour
- G02F1/13—Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour based on liquid crystals, e.g. single liquid crystal display cells
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Nonlinear Science (AREA)
- General Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Liquid Crystal Substances (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2014181212 | 2014-09-05 | ||
| JP2014181212 | 2014-09-05 | ||
| PCT/JP2015/074199 WO2016035667A1 (fr) | 2014-09-05 | 2015-08-27 | Composition de cristaux liquides, et élément d'affichage à cristaux liquides mettant en œuvre celle-ci |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016214330A Division JP2017031428A (ja) | 2014-09-05 | 2016-11-01 | 液晶組成物及びそれを使用した液晶表示素子 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPWO2016035667A1 true JPWO2016035667A1 (ja) | 2017-04-27 |
Family
ID=55439732
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016525111A Pending JPWO2016035667A1 (ja) | 2014-09-05 | 2015-08-27 | 液晶組成物及びそれを使用した液晶表示素子 |
| JP2016214330A Pending JP2017031428A (ja) | 2014-09-05 | 2016-11-01 | 液晶組成物及びそれを使用した液晶表示素子 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016214330A Pending JP2017031428A (ja) | 2014-09-05 | 2016-11-01 | 液晶組成物及びそれを使用した液晶表示素子 |
Country Status (5)
| Country | Link |
|---|---|
| JP (2) | JPWO2016035667A1 (fr) |
| KR (1) | KR101955953B1 (fr) |
| CN (1) | CN106661455A (fr) |
| TW (1) | TWI697551B (fr) |
| WO (1) | WO2016035667A1 (fr) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR102165665B1 (ko) * | 2016-12-27 | 2020-10-14 | 제이엔씨 주식회사 | 액정 조성물 및 액정 표시 소자 |
| JP7024254B2 (ja) * | 2017-08-24 | 2022-02-24 | Dic株式会社 | 液晶組成物及び液晶表示素子 |
| JP7151081B2 (ja) * | 2017-12-28 | 2022-10-12 | Dic株式会社 | 液晶表示素子 |
| CN109837097B (zh) * | 2019-03-29 | 2023-06-02 | 石家庄诚志永华显示材料有限公司 | 液晶组合物、液晶显示元件、液晶显示器 |
| CN109837098A (zh) * | 2019-03-29 | 2019-06-04 | 石家庄诚志永华显示材料有限公司 | 液晶组合物、液晶显示元件、液晶显示器 |
| JP2021092681A (ja) * | 2019-12-11 | 2021-06-17 | Dic株式会社 | 液晶表示素子および液晶表示装置 |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002256267A (ja) * | 2000-12-27 | 2002-09-11 | Dainippon Ink & Chem Inc | 抗酸化性液晶組成物 |
| JP2004507607A (ja) * | 2000-08-30 | 2004-03-11 | クラリアント インターナショナル リミテッド | 液晶混合物 |
| JP2006137856A (ja) * | 2004-11-12 | 2006-06-01 | Dainippon Ink & Chem Inc | 重合性液晶組成物及び当該組成物の硬化物 |
| JP2007137921A (ja) * | 2005-11-15 | 2007-06-07 | Chisso Corp | 液晶組成物および液晶表示素子 |
| JP2011519985A (ja) * | 2008-04-22 | 2011-07-14 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | 液晶媒体 |
| WO2013182271A1 (fr) * | 2012-06-05 | 2013-12-12 | Merck Patent Gmbh | Milieu cristal liquide et écran à cristaux liquides |
| JP2014084462A (ja) * | 2012-10-18 | 2014-05-12 | Merck Patent Gmbh | 液晶媒体、その安定化方法、および液晶ディスプレイ |
| JP5534381B1 (ja) * | 2012-08-22 | 2014-06-25 | Ｄｉｃ株式会社 | ネマチック液晶組成物 |
| JP5534115B1 (ja) * | 2012-10-17 | 2014-06-25 | Ｄｉｃ株式会社 | ネマチック液晶組成物 |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8909766D0 (en) | 1989-04-28 | 1989-06-14 | Merck Patent Gmbh | Mesogenic compounds with a trifluoroalkyl terminal group |
| DE4217248B4 (de) | 1991-06-05 | 2005-06-16 | Merck Patent Gmbh | Vinylverbindungen |
| DE4215277B4 (de) | 1992-05-09 | 2006-06-08 | Merck Patent Gmbh | Benzolderivate und ihre Verwendung für ein flüssigkristallines Medium |
| JPH06235925A (ja) | 1993-02-10 | 1994-08-23 | Matsushita Electric Ind Co Ltd | 液晶表示素子の製造方法 |
| DE4308028B4 (de) | 1993-03-13 | 2012-08-16 | Merck Patent Gmbh | 1,2,2,2-Tetrafluorethylether und flüssigkristallines Medium |
| DE4338164A1 (de) | 1993-11-09 | 1995-05-11 | Merck Patent Gmbh | Verfahren zur Herstellung von substituiertem 2,2-Difluorethoxybenzol |
| US5422035A (en) | 1993-05-10 | 1995-06-06 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Benzene derivatives, and liquid-crystalline medium |
| DE4414874A1 (de) | 1993-05-10 | 1994-11-17 | Merck Patent Gmbh | Benzolderivate und flüssigkristallines Medium |
| DE4416272C2 (de) | 1993-05-19 | 2003-09-11 | Merck Patent Gmbh | Partiell fluorierte Benzolderivate |
| DE4416256B4 (de) | 1993-05-19 | 2013-03-07 | Merck Patent Gmbh | Partiell fluorierte Benzolderivate und flüssigkristallines Medium |
| DE4428766B4 (de) | 1993-08-28 | 2013-11-28 | Merck Patent Gmbh | Benzolderivate und flüssigkristallines Medium |
| WO1996005159A1 (fr) | 1994-08-06 | 1996-02-22 | Merck Patent Gmbh | Derives benzeniques et milieu a cristaux liquides |
| TW371312B (en) | 1995-04-12 | 1999-10-01 | Chisso Corp | Fluorine-substituted liquid-crystal compound, liquid-crystal composition and liquid-crystal display device |
| JP3823354B2 (ja) | 1995-12-05 | 2006-09-20 | チッソ株式会社 | 酸素原子含有結合基を持つアルケニル化合物、液晶組成物および液晶表示素子 |
| JPH09291282A (ja) * | 1996-04-26 | 1997-11-11 | Sumitomo Chem Co Ltd | 安定化した液晶材料およびこれを用いた液晶素子 |
| DE69737690T2 (de) | 1996-11-28 | 2008-01-31 | Chisso Corp. | Fluorsubstituierte benzolderivate, flüssigkristallzubereitung und flüssigkristallanzeigeelement |
| DE10150198A1 (de) | 2001-10-12 | 2003-04-24 | Merck Patent Gmbh | Flüssigkristallines Medium |
| DE10340534B4 (de) | 2002-09-24 | 2015-06-25 | Merck Patent Gmbh | Flüssigkristallines Medium und seine Verwendung |
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| JP2007002083A (ja) * | 2005-06-23 | 2007-01-11 | Optrex Corp | 液晶光学素子 |
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2015
- 2015-08-27 WO PCT/JP2015/074199 patent/WO2016035667A1/fr active Application Filing
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- 2015-08-27 JP JP2016525111A patent/JPWO2016035667A1/ja active Pending
- 2015-08-27 CN CN201580044681.4A patent/CN106661455A/zh active Pending
- 2015-08-31 TW TW104128600A patent/TWI697551B/zh active
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2016
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Also Published As
| Publication number | Publication date |
|---|---|
| TWI697551B (zh) | 2020-07-01 |
| KR20170021843A (ko) | 2017-02-28 |
| WO2016035667A1 (fr) | 2016-03-10 |
| CN106661455A (zh) | 2017-05-10 |
| KR101955953B1 (ko) | 2019-03-08 |
| TW201623590A (zh) | 2016-07-01 |
| JP2017031428A (ja) | 2017-02-09 |
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