JPH0224297B2 - - Google Patents
Info
- Publication number
- JPH0224297B2 JPH0224297B2 JP14066683A JP14066683A JPH0224297B2 JP H0224297 B2 JPH0224297 B2 JP H0224297B2 JP 14066683 A JP14066683 A JP 14066683A JP 14066683 A JP14066683 A JP 14066683A JP H0224297 B2 JPH0224297 B2 JP H0224297B2
- Authority
- JP
- Japan
- Prior art keywords
- film
- methylene group
- color
- lower alkyl
- films
- 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.)
- Expired
Links
- 239000000463 material Substances 0.000 claims description 30
- 239000000203 mixture Substances 0.000 claims description 29
- 239000000178 monomer Substances 0.000 claims description 27
- 230000003287 optical effect Effects 0.000 claims description 27
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 24
- 125000002947 alkylene group Chemical group 0.000 claims description 23
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- 239000004973 liquid crystal related substance Substances 0.000 claims description 15
- 230000004044 response Effects 0.000 claims description 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 10
- 229920000642 polymer Polymers 0.000 claims description 10
- -1 alkylene ether Chemical compound 0.000 claims description 9
- 125000005587 carbonate group Chemical group 0.000 claims description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 7
- 230000003098 cholesteric effect Effects 0.000 description 17
- 150000001875 compounds Chemical class 0.000 description 15
- 239000004986 Cholesteric liquid crystals (ChLC) Substances 0.000 description 8
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 7
- 230000001747 exhibiting effect Effects 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 4
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical group C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 239000003431 cross linking reagent Substances 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- INQDDHNZXOAFFD-UHFFFAOYSA-N 2-[2-(2-prop-2-enoyloxyethoxy)ethoxy]ethyl prop-2-enoate Chemical compound C=CC(=O)OCCOCCOCCOC(=O)C=C INQDDHNZXOAFFD-UHFFFAOYSA-N 0.000 description 2
- KUDUQBURMYMBIJ-UHFFFAOYSA-N 2-prop-2-enoyloxyethyl prop-2-enoate Chemical compound C=CC(=O)OCCOC(=O)C=C KUDUQBURMYMBIJ-UHFFFAOYSA-N 0.000 description 2
- 239000004988 Nematic liquid crystal Substances 0.000 description 2
- 239000004990 Smectic liquid crystal Substances 0.000 description 2
- DAKWPKUUDNSNPN-UHFFFAOYSA-N Trimethylolpropane triacrylate Chemical compound C=CC(=O)OCC(CC)(COC(=O)C=C)COC(=O)C=C DAKWPKUUDNSNPN-UHFFFAOYSA-N 0.000 description 2
- 238000002835 absorbance Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 2
- 235000012000 cholesterol Nutrition 0.000 description 2
- 150000001841 cholesterols Chemical class 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 2
- 229910052753 mercury Inorganic materials 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M methacrylate group Chemical group C(C(=C)C)(=O)[O-] CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- 229920006254 polymer film Polymers 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- QYIXCDOBOSTCEI-QCYZZNICSA-N (5alpha)-cholestan-3beta-ol Chemical group C([C@@H]1CC2)[C@@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@H](C)CCCC(C)C)[C@@]2(C)CC1 QYIXCDOBOSTCEI-QCYZZNICSA-N 0.000 description 1
- AZUXKVXMJOIAOF-UHFFFAOYSA-N 1-(2-hydroxypropoxy)propan-2-ol Chemical compound CC(O)COCC(C)O AZUXKVXMJOIAOF-UHFFFAOYSA-N 0.000 description 1
- OGBWMWKMTUSNKE-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)hexyl 2-methylprop-2-enoate Chemical compound CCCCCC(OC(=O)C(C)=C)OC(=O)C(C)=C OGBWMWKMTUSNKE-UHFFFAOYSA-N 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N 1-butanol Substances CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 description 1
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
- MZJCWIPSNONIMO-UHFFFAOYSA-N 2-[4-(2-carboxy-5-hexoxyphenyl)-3-methylphenyl]-4-hexoxybenzoic acid Chemical compound CCCCCCOC1=CC=C(C(O)=O)C(C=2C=C(C)C(=CC=2)C=2C(=CC=C(OCCCCCC)C=2)C(O)=O)=C1 MZJCWIPSNONIMO-UHFFFAOYSA-N 0.000 description 1
- ZCDADJXRUCOCJE-UHFFFAOYSA-N 2-chlorothioxanthen-9-one Chemical compound C1=CC=C2C(=O)C3=CC(Cl)=CC=C3SC2=C1 ZCDADJXRUCOCJE-UHFFFAOYSA-N 0.000 description 1
- HTWRFCRQSLVESJ-UHFFFAOYSA-N 3-(2-methylprop-2-enoyloxy)propyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCOC(=O)C(C)=C HTWRFCRQSLVESJ-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- JHWGFJBTMHEZME-UHFFFAOYSA-N 4-prop-2-enoyloxybutyl prop-2-enoate Chemical compound C=CC(=O)OCCCCOC(=O)C=C JHWGFJBTMHEZME-UHFFFAOYSA-N 0.000 description 1
- FIHBHSQYSYVZQE-UHFFFAOYSA-N 6-prop-2-enoyloxyhexyl prop-2-enoate Chemical compound C=CC(=O)OCCCCCCOC(=O)C=C FIHBHSQYSYVZQE-UHFFFAOYSA-N 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 229940126062 Compound A Drugs 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 1
- XMPIMLRYNVGZIA-CCEZHUSRSA-N [10,13-dimethyl-17-(6-methylheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1h-cyclopenta[a]phenanthren-3-yl] [(e)-octadec-9-enyl] carbonate Chemical compound C12CCC3(C)C(C(C)CCCC(C)C)CCC3C2CC=C2C1(C)CCC(OC(=O)OCCCCCCCC/C=C/CCCCCCCC)C2 XMPIMLRYNVGZIA-CCEZHUSRSA-N 0.000 description 1
- 150000003926 acrylamides Chemical class 0.000 description 1
- QYIXCDOBOSTCEI-UHFFFAOYSA-N alpha-cholestanol Natural products C1CC2CC(O)CCC2(C)C2C1C1CCC(C(C)CCCC(C)C)C1(C)CC2 QYIXCDOBOSTCEI-UHFFFAOYSA-N 0.000 description 1
- 229920006125 amorphous polymer Polymers 0.000 description 1
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- MSODWKQDERPZOY-UHFFFAOYSA-N bis[2-(2-hydroxycyclohexyl)phenyl]methanone Chemical compound OC1CCCCC1C1=CC=CC=C1C(=O)C1=CC=CC=C1C1C(O)CCCC1 MSODWKQDERPZOY-UHFFFAOYSA-N 0.000 description 1
- 235000011089 carbon dioxide Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- UVZUFUGNHDDLRQ-LLHZKFLPSA-N cholesteryl benzoate Chemical compound O([C@@H]1CC2=CC[C@H]3[C@@H]4CC[C@@H]([C@]4(CC[C@@H]3[C@@]2(C)CC1)C)[C@H](C)CCCC(C)C)C(=O)C1=CC=CC=C1 UVZUFUGNHDDLRQ-LLHZKFLPSA-N 0.000 description 1
- 238000002983 circular dichroism Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000010528 free radical solution polymerization reaction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000009477 glass transition Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000003384 imaging method Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- YDZANNORUSYHFB-UHFFFAOYSA-N phenacyl benzoate Chemical compound C=1C=CC=CC=1C(=O)COC(=O)C1=CC=CC=C1 YDZANNORUSYHFB-UHFFFAOYSA-N 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
- 238000002834 transmittance Methods 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 238000001429 visible spectrum Methods 0.000 description 1
- 230000000007 visual effect Effects 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
- C09K19/36—Steroidal liquid crystal compounds
-
- 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
- C09K2019/0444—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by a linking chain between rings or ring systems, a bridging chain between extensive mesogenic moieties or an end chain group
- C09K2019/0448—Liquid crystal materials characterised by the chemical structure of the liquid crystal components, e.g. by a specific unit characterized by a linking chain between rings or ring systems, a bridging chain between extensive mesogenic moieties or an end chain group the end chain group being a polymerizable end group, e.g. -Sp-P or acrylate
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Liquid Crystal Substances (AREA)
- Polymerisation Methods In General (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US45008982A | 1982-12-15 | 1982-12-15 | |
US450089 | 1982-12-15 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS59109505A JPS59109505A (ja) | 1984-06-25 |
JPH0224297B2 true JPH0224297B2 (fr) | 1990-05-29 |
Family
ID=23786723
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP14066683A Granted JPS59109505A (ja) | 1982-12-15 | 1983-08-02 | 高分子液晶フィルム |
Country Status (8)
Country | Link |
---|---|
JP (1) | JPS59109505A (fr) |
BE (1) | BE897871A (fr) |
CA (1) | CA1214592A (fr) |
DE (1) | DE3340954C2 (fr) |
FR (1) | FR2537989B1 (fr) |
GB (1) | GB2132623B (fr) |
LU (1) | LU85102A1 (fr) |
NL (1) | NL186584C (fr) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2572813A1 (fr) * | 1984-11-07 | 1986-05-09 | Armstrong World Ind Inc | Procede pour preparer des revetements liquides polymeres presentant des reponses optiques multiples et revetements ainsi obtenus |
US4780383A (en) * | 1985-02-27 | 1988-10-25 | Armstrong World Industries, Inc. | Optical storage system having expanded capacity |
GB2185487B (en) * | 1986-01-16 | 1990-06-06 | Gen Electric Plc | Electro-optical material |
JPH02167527A (ja) * | 1986-05-19 | 1990-06-27 | Seiko Epson Corp | 液晶装置 |
US5073294A (en) * | 1990-03-07 | 1991-12-17 | Hercules Incorporated | Process of preparing compositions having multiple oriented mesogens |
JP2630044B2 (ja) * | 1990-07-17 | 1997-07-16 | 凸版印刷株式会社 | 可逆性感熱記録媒体およびその製造方法 |
JP2630045B2 (ja) * | 1990-09-21 | 1997-07-16 | 凸版印刷株式会社 | 可逆性感熱記録媒体およびその製造方法 |
US5629055A (en) * | 1994-02-14 | 1997-05-13 | Pulp And Paper Research Institute Of Canada | Solidified liquid crystals of cellulose with optically variable properties |
DE4418075C2 (de) * | 1994-05-24 | 2000-06-29 | Daimler Chrysler Ag | Effektlack bzw. Effektlackierung, insbesondere für Fahrzeugkarosserien, unter Verwendung von flüssigkristallinen Interferenzpigmenten |
DE4441651A1 (de) * | 1994-11-23 | 1996-04-25 | Basf Ag | Verfahren zur oberflächlichen Beschichtung von Substraten |
DE19520704A1 (de) * | 1995-06-09 | 1996-12-12 | Basf Ag | Polymerisierbare chirale Verbindungen und deren Verwendung |
GB2321717A (en) | 1997-01-31 | 1998-08-05 | Sharp Kk | Cholesteric optical filters |
DE19745647A1 (de) * | 1997-10-15 | 1999-04-22 | Basf Ag | Wärmeisolationsbeschichtung |
US7879256B2 (en) * | 2006-03-31 | 2011-02-01 | E. I. Du Pont De Nemours And Company | Liquid crystal compositions, polymer networks derived therefrom and process for making the same |
JP5510483B2 (ja) * | 2006-06-29 | 2014-06-04 | Jnc株式会社 | 重合性液晶組成物およびその用途 |
JP5119736B2 (ja) | 2006-06-29 | 2013-01-16 | Jnc株式会社 | 重合性液晶組成物およびその用途 |
JP5262076B2 (ja) * | 2007-11-14 | 2013-08-14 | Jnc株式会社 | 重合性メントール誘導体 |
JP2011137850A (ja) * | 2009-12-25 | 2011-07-14 | Dainippon Printing Co Ltd | 赤外線反射部材 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3409404A (en) * | 1963-11-13 | 1968-11-05 | Westinghouse Electric Corp | Analytical methods and devices employing cholesteric liquid crystalline materials |
US3594126A (en) * | 1969-04-30 | 1971-07-20 | Westinghouse Electric Corp | Temperature-limit detection |
CA1255653A (fr) * | 1982-12-15 | 1989-06-13 | Paul J. Shannon | Materiaux cristallins liquides pouvant servir a la preparation de pellicules de polymere |
-
1983
- 1983-07-06 CA CA000431937A patent/CA1214592A/fr not_active Expired
- 1983-08-02 JP JP14066683A patent/JPS59109505A/ja active Granted
- 1983-09-29 BE BE0/211610A patent/BE897871A/fr not_active IP Right Cessation
- 1983-11-11 DE DE19833340954 patent/DE3340954C2/de not_active Expired
- 1983-11-25 LU LU85102A patent/LU85102A1/de unknown
- 1983-12-02 FR FR8319297A patent/FR2537989B1/fr not_active Expired
- 1983-12-13 NL NL8304277A patent/NL186584C/xx not_active IP Right Cessation
- 1983-12-14 GB GB8333324A patent/GB2132623B/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
NL186584B (nl) | 1991-01-02 |
FR2537989B1 (fr) | 1987-06-05 |
GB2132623A (en) | 1984-07-11 |
LU85102A1 (de) | 1984-04-02 |
DE3340954A1 (de) | 1984-07-19 |
BE897871A (fr) | 1984-01-16 |
FR2537989A1 (fr) | 1984-06-22 |
NL186584C (nl) | 1991-01-02 |
GB2132623B (en) | 1987-06-10 |
NL8304277A (nl) | 1984-07-02 |
GB8333324D0 (en) | 1984-01-18 |
CA1214592A (fr) | 1986-11-25 |
JPS59109505A (ja) | 1984-06-25 |
DE3340954C2 (de) | 1986-07-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4637896A (en) | Polymeric liquid crystals | |
JPH0224297B2 (fr) | ||
Martinez et al. | Reconfigurable and spatially programmable chameleon skin‐like material utilizing light responsive covalent adaptable cholesteric liquid crystal elastomers | |
US6057008A (en) | Process for broadening cholesteric reflection bands of photopolymerizable cholesteric liquid crystals, and optical elements produced by this process | |
DE69921824T2 (de) | Zusammensetzungen | |
KR101285496B1 (ko) | 중합성 액정 화합물, 중합성 액정 조성물, 액정 중합체 및 광학 이방체 | |
JP4402429B2 (ja) | 光学素子 | |
US6773766B2 (en) | Utilization of polymerizable liquid crystal substances for the production of optical components | |
JPH055338B2 (fr) | ||
KR100604730B1 (ko) | 광학 성분의 제조를 위한 중합성 액정 물질의 사용 | |
JPH06322040A (ja) | 側鎖基重合体から製造した平板材料 | |
JPH04220402A (ja) | 液晶ポリマーから成るフィルムまたはファイバーの製造方法 | |
CN101296995A (zh) | 高清晰度的胆甾型液晶薄膜 | |
JP7389147B2 (ja) | 新規な重合性液晶 | |
JP4317136B2 (ja) | 重合性混合物 | |
JP3163539B2 (ja) | 液晶性配向膜、液晶性配向膜の製造方法及びそれを用いた光学素子 | |
JP2010143989A (ja) | 相分離構造の形成方法及び薄膜の製造方法 | |
JP2004070264A (ja) | 正負混合型光学リタデーションフィルムの製造方法、正負混合型光学リタデーションフィルム及びそれを使用する液晶ディスプレイエレメント及び液晶ディスプレイ装置 | |
KR20210150498A (ko) | 액정 화합물 | |
Van Der Zande et al. | Synthesis, Properties, and Photopolymerization of Liquid‐Crystalline Oxetanes: Application in Transflective Liquid‐Crystal Displays | |
KR100309749B1 (ko) | 측쇄그룹중합체로부터제조된평면물질 | |
CN116535569A (zh) | 一种无侧基丙烯酸酯液晶化合物及其制备方法 | |
CN113534509A (zh) | 一种光反射涂层及其制备方法和光学器件 | |
Hoischen et al. | Optical storage effect due to photopolymerization of mesogenic twin molecules | |
JP2003207615A (ja) | カラーフィルタおよびその製造方法 |