NO894477L - Superdreiet flytendekrystalltegn. - Google Patents
Superdreiet flytendekrystalltegn.Info
- Publication number
- NO894477L NO894477L NO89894477A NO894477A NO894477L NO 894477 L NO894477 L NO 894477L NO 89894477 A NO89894477 A NO 89894477A NO 894477 A NO894477 A NO 894477A NO 894477 L NO894477 L NO 894477L
- Authority
- NO
- Norway
- Prior art keywords
- trans
- liquid
- atoms
- phenylene
- crystal mixture
- Prior art date
Links
- 239000000203 mixture Substances 0.000 claims abstract description 86
- 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 70
- 239000004988 Nematic liquid crystal Substances 0.000 claims abstract description 15
- 150000001875 compounds Chemical class 0.000 claims description 57
- 125000004432 carbon atom Chemical group C* 0.000 claims description 35
- -1 1,4-disubstituted 2,3-difluorobenzene compound Chemical class 0.000 claims description 27
- 229910052731 fluorine Inorganic materials 0.000 claims description 20
- 125000000217 alkyl group Chemical group 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
- 125000005450 2,3-difluoro-1,4-phenylene group Chemical group [H]C1=C([*:2])C(F)=C(F)C([*:1])=C1[H] 0.000 claims description 8
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims description 7
- 239000002019 doping agent Substances 0.000 claims description 7
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 7
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 6
- 239000011737 fluorine Substances 0.000 claims description 6
- HSFWRNGVRCDJHI-UHFFFAOYSA-N Acetylene Chemical compound C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 4
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
- 101100400378 Mus musculus Marveld2 gene Proteins 0.000 claims 2
- 239000013078 crystal Substances 0.000 claims 2
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 claims 2
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Substances N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 54
- QCNUKEGGHOLBES-KYZUINATSA-N CCC[C@H]1CC[C@H](C(O)=O)CC1 Chemical compound CCC[C@H]1CC[C@H](C(O)=O)CC1 QCNUKEGGHOLBES-KYZUINATSA-N 0.000 description 20
- JXPGQFKJNKWDKP-KTSLABGISA-N C1C[C@@H](CCC)CC[C@@H]1[C@@H]1CC[C@@H](C(O)=O)CC1 Chemical compound C1C[C@@H](CCC)CC[C@@H]1[C@@H]1CC[C@@H](C(O)=O)CC1 JXPGQFKJNKWDKP-KTSLABGISA-N 0.000 description 19
- RVLAXPQGTRTHEV-XYPYZODXSA-N CCCCC[C@H]1CC[C@H](C(O)=O)CC1 Chemical compound CCCCC[C@H]1CC[C@H](C(O)=O)CC1 RVLAXPQGTRTHEV-XYPYZODXSA-N 0.000 description 15
- BALGERHMIXFENA-MGCOHNPYSA-N CCCC[C@H]1CC[C@H](C(O)=O)CC1 Chemical compound CCCC[C@H]1CC[C@H](C(O)=O)CC1 BALGERHMIXFENA-MGCOHNPYSA-N 0.000 description 15
- XIHWAWBICWAQHQ-UHFFFAOYSA-N 3-(cyclohexylamino)benzonitrile Chemical compound N#CC1=CC=CC(NC2CCCCC2)=C1 XIHWAWBICWAQHQ-UHFFFAOYSA-N 0.000 description 13
- XYKCCZSKCZRZST-BIAGXBKMSA-N C1C[C@@H](CCCC)CC[C@@H]1[C@@H]1CC[C@@H](C(O)=O)CC1 Chemical compound C1C[C@@H](CCCC)CC[C@@H]1[C@@H]1CC[C@@H](C(O)=O)CC1 XYKCCZSKCZRZST-BIAGXBKMSA-N 0.000 description 12
- 150000002148 esters Chemical class 0.000 description 10
- VRDNRAMDWPJGBD-MVBYDDMTSA-N C(CC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)CCC Chemical compound C(CC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)CCC VRDNRAMDWPJGBD-MVBYDDMTSA-N 0.000 description 9
- ZHDZFSWIWPZWCF-KDNFAQGPSA-N C(CC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)C#N Chemical compound C(CC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)C#N ZHDZFSWIWPZWCF-KDNFAQGPSA-N 0.000 description 7
- PZUUMRKZMNIXKL-CYWFSMGFSA-N C(CC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)CCCCC Chemical compound C(CC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)CCCCC PZUUMRKZMNIXKL-CYWFSMGFSA-N 0.000 description 7
- LHHCXPLNJQVGFH-KESTWPANSA-N C(CC)[C@@H]1CC[C@H](CC1)C1=CC=C(C=C1)C#CC1=C(C(=C(C=C1)OCC)F)F Chemical compound C(CC)[C@@H]1CC[C@H](CC1)C1=CC=C(C=C1)C#CC1=C(C(=C(C=C1)OCC)F)F LHHCXPLNJQVGFH-KESTWPANSA-N 0.000 description 5
- RZTKFRNATFGMIZ-MLRKGSHFSA-N C(CC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)C Chemical compound C(CC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)C RZTKFRNATFGMIZ-MLRKGSHFSA-N 0.000 description 5
- SYCNHFWYTQQMNG-UHFFFAOYSA-N 2-fluoro-4-(4-pentylcyclohexyl)-1-[4-(4-propylcyclohexyl)phenyl]benzene Chemical group C1CC(CCCCC)CCC1C1=CC=C(C=2C=CC(=CC=2)C2CCC(CCC)CC2)C(F)=C1 SYCNHFWYTQQMNG-UHFFFAOYSA-N 0.000 description 4
- SRJLZDPWUSOULH-UHFFFAOYSA-N 2-fluoro-4-(4-propylcyclohexyl)-1-[4-(4-propylcyclohexyl)phenyl]benzene Chemical group C1CC(CCC)CCC1C1=CC=C(C=2C(=CC(=CC=2)C2CCC(CCC)CC2)F)C=C1 SRJLZDPWUSOULH-UHFFFAOYSA-N 0.000 description 4
- FNIPGBFUEZMVHZ-JOLHVKOESA-N C(CC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)F Chemical compound C(CC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)F FNIPGBFUEZMVHZ-JOLHVKOESA-N 0.000 description 4
- VRPANQODGRNWRV-GARHLSDISA-N CCCCC[C@H]1CC[C@@H](CC1)[C@H]1CC[C@@H](CC1)C(O)=O Chemical compound CCCCC[C@H]1CC[C@@H](CC1)[C@H]1CC[C@@H](CC1)C(O)=O VRPANQODGRNWRV-GARHLSDISA-N 0.000 description 4
- JRXXLCKWQFKACW-UHFFFAOYSA-N biphenylacetylene Chemical class C1=CC=CC=C1C#CC1=CC=CC=C1 JRXXLCKWQFKACW-UHFFFAOYSA-N 0.000 description 4
- PIRBSQJCLKEHQD-UHFFFAOYSA-N 1-ethoxy-2,3-difluoro-4-[2-(4-pentylphenyl)ethynyl]benzene Chemical compound C1=CC(CCCCC)=CC=C1C#CC1=CC=C(OCC)C(F)=C1F PIRBSQJCLKEHQD-UHFFFAOYSA-N 0.000 description 3
- PJPLBHHDTUICNN-UHFFFAOYSA-N 4-(4-butylphenyl)benzonitrile Chemical group C1=CC(CCCC)=CC=C1C1=CC=C(C#N)C=C1 PJPLBHHDTUICNN-UHFFFAOYSA-N 0.000 description 3
- DLLIPJSMDJCZRF-UHFFFAOYSA-N 4-(4-ethylphenyl)benzonitrile Chemical group C1=CC(CC)=CC=C1C1=CC=C(C#N)C=C1 DLLIPJSMDJCZRF-UHFFFAOYSA-N 0.000 description 3
- XFMPTZWVMVMELB-UHFFFAOYSA-N 4-(4-propylphenyl)benzonitrile Chemical group C1=CC(CCC)=CC=C1C1=CC=C(C#N)C=C1 XFMPTZWVMVMELB-UHFFFAOYSA-N 0.000 description 3
- 239000005209 4-Butyl-4'-cyanobiphenyl Substances 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000005449 2-fluoro-1,4-phenylene group Chemical group [H]C1=C([*:2])C([H])=C(F)C([*:1])=C1[H] 0.000 description 2
- 125000005451 3-fluoro-1,4-phenylene group Chemical group [H]C1=C([*:1])C([H])=C(F)C([*:2])=C1[H] 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- ADQFOQFNQXFZLH-JKIUYZKVSA-N C(CC)[C@@H]1CC[C@H](CC1)C1=CC=C(C=C1)C#CC1=CC=C(C=C1)OCC Chemical compound C(CC)[C@@H]1CC[C@H](CC1)C1=CC=C(C=C1)C#CC1=CC=C(C=C1)OCC ADQFOQFNQXFZLH-JKIUYZKVSA-N 0.000 description 2
- KPRYWLQZHXTLHW-SAIGFBBZSA-N C(CC)[C@@H]1CC[C@H](CC1)C1=CC=C(C=C1)C#CC1=CC=C(C=C1)OCCC Chemical compound C(CC)[C@@H]1CC[C@H](CC1)C1=CC=C(C=C1)C#CC1=CC=C(C=C1)OCCC KPRYWLQZHXTLHW-SAIGFBBZSA-N 0.000 description 2
- QMSJHOQHIGUNCV-AQYVVDRMSA-N C(CCCC)[C@@H]1CC[C@H](CC1)C1=CC=C(C=C1)C#CC1=C(C(=C(C=C1)OCC)F)F Chemical compound C(CCCC)[C@@H]1CC[C@H](CC1)C1=CC=C(C=C1)C#CC1=C(C(=C(C=C1)OCC)F)F QMSJHOQHIGUNCV-AQYVVDRMSA-N 0.000 description 2
- DWDNWOSCKGVDJM-UBBSCCEASA-N CCCCC[C@H]1CC[C@@H](CC1)OC(=O)[C@H]1CC[C@H](CCC)CC1 Chemical compound CCCCC[C@H]1CC[C@@H](CC1)OC(=O)[C@H]1CC[C@H](CCC)CC1 DWDNWOSCKGVDJM-UBBSCCEASA-N 0.000 description 2
- TYXZVPMEKLRAGX-OEOGMAASSA-N CCCCC[C@H]1CC[C@@H](CC1)c1ccc(cc1)-c1ccc(cc1F)[C@H]1CC[C@H](CCCCC)CC1 Chemical group CCCCC[C@H]1CC[C@@H](CC1)c1ccc(cc1)-c1ccc(cc1F)[C@H]1CC[C@H](CCCCC)CC1 TYXZVPMEKLRAGX-OEOGMAASSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- HNNIDTTUHQGPSU-HDJSIYSDSA-N FC1=C(C#N)C=CC(=C1F)CC[C@@H]1CC[C@H](CC1)CCC Chemical compound FC1=C(C#N)C=CC(=C1F)CC[C@@H]1CC[C@H](CC1)CCC HNNIDTTUHQGPSU-HDJSIYSDSA-N 0.000 description 2
- OVKKOUZDOLSHLG-SHTZXODSSA-N FC1=C(C#N)C=CC(=C1F)CC[C@@H]1CC[C@H](CC1)CCCC Chemical compound FC1=C(C#N)C=CC(=C1F)CC[C@@H]1CC[C@H](CC1)CCCC OVKKOUZDOLSHLG-SHTZXODSSA-N 0.000 description 2
- RSDRSTGBQYLQQC-WKILWMFISA-N FC1=C(C#N)C=CC(=C1F)CC[C@@H]1CC[C@H](CC1)CCCCC Chemical compound FC1=C(C#N)C=CC(=C1F)CC[C@@H]1CC[C@H](CC1)CCCCC RSDRSTGBQYLQQC-WKILWMFISA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 238000005352 clarification Methods 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- VRWLWAWGMIDUBE-UHFFFAOYSA-N 1-[2-(4-ethoxy-4-pentylcyclohexa-1,5-dien-1-yl)ethynyl]-2,3-difluorobenzene Chemical compound C1=CC(CCCCC)(OCC)CC=C1C#CC1=CC=CC(F)=C1F VRWLWAWGMIDUBE-UHFFFAOYSA-N 0.000 description 1
- DFRQRMYHMWAEBZ-UHFFFAOYSA-N 1-ethoxy-2,3-difluoro-4-[2-(4-propylphenyl)ethynyl]benzene Chemical compound C1=CC(CCC)=CC=C1C#CC1=CC=C(OCC)C(F)=C1F DFRQRMYHMWAEBZ-UHFFFAOYSA-N 0.000 description 1
- QRMMWBMCJKXXKV-UHFFFAOYSA-N 1-ethoxy-4-[2-(4-pentylphenyl)ethynyl]benzene Chemical compound C1=CC(CCCCC)=CC=C1C#CC1=CC=C(OCC)C=C1 QRMMWBMCJKXXKV-UHFFFAOYSA-N 0.000 description 1
- CANQHIHYVQMRAZ-UHFFFAOYSA-N 2-(4-ethoxy-2,3-difluorophenyl)-5-heptylpyrimidine Chemical compound N1=CC(CCCCCCC)=CN=C1C1=CC=C(OCC)C(F)=C1F CANQHIHYVQMRAZ-UHFFFAOYSA-N 0.000 description 1
- MPAIWVOBMLSHQA-UHFFFAOYSA-N 3,6-dihydroxybenzene-1,2-dicarbonitrile Chemical class OC1=CC=C(O)C(C#N)=C1C#N MPAIWVOBMLSHQA-UHFFFAOYSA-N 0.000 description 1
- ZYZGBFKAISVDEZ-UHFFFAOYSA-N 4-(4-butylphenyl)-2,3-difluorobenzonitrile Chemical group C1=CC(CCCC)=CC=C1C1=CC=C(C#N)C(F)=C1F ZYZGBFKAISVDEZ-UHFFFAOYSA-N 0.000 description 1
- NUBWOJAPHNDFOU-UHFFFAOYSA-N 4-(4-ethylphenyl)-2,3-difluorobenzonitrile Chemical group C1=CC(CC)=CC=C1C1=CC=C(C#N)C(F)=C1F NUBWOJAPHNDFOU-UHFFFAOYSA-N 0.000 description 1
- RHMPLDJJXGPMEX-UHFFFAOYSA-N 4-fluorophenol Chemical compound OC1=CC=C(F)C=C1 RHMPLDJJXGPMEX-UHFFFAOYSA-N 0.000 description 1
- RVLAXPQGTRTHEV-UHFFFAOYSA-N 4-pentylcyclohexane-1-carboxylic acid Chemical compound CCCCCC1CCC(C(O)=O)CC1 RVLAXPQGTRTHEV-UHFFFAOYSA-N 0.000 description 1
- JQKHCVKNAJSAIX-XYWHTSSQSA-N C(CC)[C@@H]1CC[C@H](CC1)C1=CC=C(C=C1)C#CC1=CC=C(C=C1)OC Chemical compound C(CC)[C@@H]1CC[C@H](CC1)C1=CC=C(C=C1)C#CC1=CC=C(C=C1)OC JQKHCVKNAJSAIX-XYWHTSSQSA-N 0.000 description 1
- GDRRTVPYGZVUSZ-HZCBDIJESA-N C(CC)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)C#CC1=CC=C(C=C1)OC Chemical compound C(CC)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)C#CC1=CC=C(C=C1)OC GDRRTVPYGZVUSZ-HZCBDIJESA-N 0.000 description 1
- YZCCJRXJJVFAMB-QWZLJSJVSA-N C(CC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)CC Chemical compound C(CC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)CC YZCCJRXJJVFAMB-QWZLJSJVSA-N 0.000 description 1
- DEWAVJLSNXMVGF-FUMLSLJBSA-N C(CCCC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)CCC Chemical compound C(CCCC)[C@@H]1CC[C@H](CC1)[C@@H]1CC[C@H](CC1)CCC1=CC=C(C=C1)CCC DEWAVJLSNXMVGF-FUMLSLJBSA-N 0.000 description 1
- 101100379079 Emericella variicolor andA gene Proteins 0.000 description 1
- 239000004990 Smectic liquid crystal Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 150000001934 cyclohexanes Chemical class 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000001564 phenyl benzoates Chemical class 0.000 description 1
- 102220062248 rs568171603 Human genes 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 230000010415 tropism 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
- C09K19/42—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
- C09K19/46—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40 containing esters
-
- 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
- C09K19/02—Liquid crystal materials characterised by optical, electrical or physical properties of the components, in general
- C09K19/0208—Twisted Nematic (T.N.); Super Twisted Nematic (S.T.N.); Optical Mode Interference (O.M.I.)
-
- 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
- C09K19/3001—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
- C09K19/42—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
-
- 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
- C09K19/42—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40
- C09K19/44—Mixtures of liquid crystal compounds covered by two or more of the preceding groups C09K19/06 - C09K19/40 containing compounds with benzene rings directly linked
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Liquid Crystal Substances (AREA)
- Liquid Crystal (AREA)
- Enzymes And Modification Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19883807805 DE3807805A1 (de) | 1988-03-10 | 1988-03-10 | Supertwist-fluessigkristallanzeigeelement |
| DE3835803A DE3835803A1 (de) | 1988-03-10 | 1988-10-20 | Supertwist-fluessigkristallanzeigeelement und fluessigkristallmischung |
| PCT/EP1989/000178 WO1989008691A1 (en) | 1988-03-10 | 1989-02-27 | Supertwist liquid crystal display |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO894477D0 NO894477D0 (no) | 1989-11-09 |
| NO894477L true NO894477L (no) | 1989-11-09 |
Family
ID=25865727
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO89894477A NO894477L (no) | 1988-03-10 | 1989-11-09 | Superdreiet flytendekrystalltegn. |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US5178790A (ja) |
| EP (2) | EP0360851A1 (ja) |
| JP (1) | JPH02503445A (ja) |
| KR (1) | KR900700574A (ja) |
| CN (1) | CN1036029A (ja) |
| AT (1) | ATE80409T1 (ja) |
| AU (1) | AU3188789A (ja) |
| BR (1) | BR8906383A (ja) |
| DE (2) | DE3835803A1 (ja) |
| FI (1) | FI895339A0 (ja) |
| NO (1) | NO894477L (ja) |
| WO (1) | WO1989008691A1 (ja) |
Families Citing this family (34)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5536442A (en) * | 1987-09-25 | 1996-07-16 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Fluorinated liquid crystal compounds and liquid crystal medium containing same |
| US6004479A (en) | 1988-07-13 | 1999-12-21 | Merck Kgaa | Matrix liquid crystal display |
| DE3835804B4 (de) | 1988-10-20 | 2006-12-28 | Merck Patent Gmbh | Nematische Flüssigkristallmischung |
| US5387369A (en) * | 1988-10-20 | 1995-02-07 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Supertwist liquid crystal display |
| EP0365962B1 (de) * | 1988-10-20 | 1994-09-21 | MERCK PATENT GmbH | Matrix-Flüssigkristallanzeige |
| EP0393442A3 (de) * | 1989-04-19 | 1991-08-14 | MERCK PATENT GmbH | Supertwist-Flüssigkristallanzeige |
| DE59010890D1 (de) * | 1989-04-19 | 2000-01-20 | Merck Patent Gmbh | Supertwist-Flüssigkristallanzeige |
| JPH0373922A (ja) * | 1989-05-17 | 1991-03-28 | Seiko Epson Corp | 液晶表示装置 |
| US5229031A (en) * | 1989-05-17 | 1993-07-20 | Seiko Epson Corporation | Liquid crystal display device |
| US5516454A (en) * | 1989-07-13 | 1996-05-14 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Supertwist liquid crystal display |
| DE4025550B4 (de) * | 1989-08-16 | 2007-05-03 | Merck Patent Gmbh | Phenylcyclohexane und flüssigkristallines Medium |
| US5456860A (en) * | 1990-03-31 | 1995-10-10 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Matrix liquid-crystal display |
| EP0476104B1 (en) * | 1990-04-02 | 1995-07-26 | MERCK PATENT GmbH | Nematic liquid crystal mixtures and a matrix liquid crystal display |
| WO1991016401A1 (de) * | 1990-04-13 | 1991-10-31 | MERCK Patent Gesellschaft mit beschränkter Haftung | Flüssigkristallines medium |
| DE69120245T2 (de) * | 1990-10-02 | 1996-11-28 | Merck Patent Gmbh | Flüssigkristallmedium |
| DE4032579A1 (de) * | 1990-10-13 | 1992-04-16 | Merck Patent Gmbh | Supertwist-fluessigkristallanzeige |
| DE59109091D1 (de) * | 1990-12-07 | 1999-03-04 | Merck Patent Gmbh | Supertwist-Flüssigkristallanzeige |
| EP0500210A3 (en) * | 1991-01-19 | 1992-10-21 | Sanyo Chemical Industries, Ltd. | Liquid crystal compounds and compositions |
| WO1992014800A1 (en) * | 1991-02-20 | 1992-09-03 | MERCK Patent Gesellschaft mit beschränkter Haftung | Nematic liquid-crystal composition |
| DE4107167B4 (de) * | 1991-03-06 | 2008-05-08 | Merck Patent Gmbh | Flüssigkristallmischung |
| DE69228733T2 (de) * | 1991-07-04 | 1999-11-11 | Herbert Plach | Flüssigkristallines Medium |
| EP0589331B1 (de) * | 1992-09-25 | 1997-04-09 | MERCK PATENT GmbH | Acetylen Derivate und sie enthaltende flüssigkristalline Mischungen |
| DE4340271A1 (de) * | 1993-11-26 | 1995-06-01 | Nokia Deutschland Gmbh | Flüssigkristallanzeige |
| US5626792A (en) * | 1994-09-06 | 1997-05-06 | Displaytech, Inc. | High birefringence liquid crystal compounds |
| DE19736445B4 (de) * | 1996-08-22 | 2006-06-08 | Asmo Co., Ltd., Kosai-shi | Türgliedverriegelungs-/entriegelungsvorrichtung |
| DE19828149A1 (de) * | 1997-07-04 | 1999-01-07 | Merck Patent Gmbh | Supertwist-Flüssigkristallanzeige |
| US20060038929A1 (en) * | 2004-08-18 | 2006-02-23 | Chenhui Wang | Tunable spectral imaging filter configured for UV spectral ranges |
| JP5961933B2 (ja) * | 2011-06-24 | 2016-08-03 | Dic株式会社 | 誘電率異方性が負である液晶組成物、及び該液晶組成物を用いた液晶表示素子 |
| JP5845653B2 (ja) * | 2011-06-24 | 2016-01-20 | Dic株式会社 | 誘電率異方性が負である液晶組成物、及び該液晶組成物を用いた液晶表示素子 |
| JP5834535B2 (ja) * | 2011-06-24 | 2015-12-24 | Dic株式会社 | 誘電率異方性が負である液晶組成物、及び該液晶組成物を用いた液晶表示素子 |
| JP5845654B2 (ja) * | 2011-06-24 | 2016-01-20 | Dic株式会社 | 誘電率異方性が負である液晶組成物、及び該液晶組成物を用いた液晶表示素子 |
| US20150159087A1 (en) * | 2012-05-28 | 2015-06-11 | Dic Corporation | Liquid crystal composition having negative dielectric anisotropy, and liquid crystal display device using the liquid crystal composition |
| CN107880900B (zh) * | 2016-09-29 | 2021-01-15 | 石家庄诚志永华显示材料有限公司 | 含有2,3,4-三取代苯的液晶化合物及其组合物 |
| CN107057717A (zh) * | 2016-12-19 | 2017-08-18 | 西安近代化学研究所 | 一种含氟液晶化合物 |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2967129D1 (en) * | 1979-05-28 | 1984-08-30 | Merck Patent Gmbh | Liquid-crystal compositions |
| DE2933563A1 (de) * | 1979-07-18 | 1981-02-05 | Bbc Brown Boveri & Cie | Anisotrope verbindungen mit negativer dk-anisotropie |
| DE3042391A1 (de) * | 1980-11-10 | 1982-06-16 | Merck Patent Gmbh, 6100 Darmstadt | Fluorhaltige cyclohexylbiphenylderivate, diese enthaltende dielektrika und elektrooptisches anzeigeelement |
| EP0085995B1 (de) * | 1982-02-04 | 1986-04-09 | MERCK PATENT GmbH | Anisotrope Verbindungen und Flüssigkristallmischungen |
| DE3209178A1 (de) * | 1982-03-13 | 1983-09-15 | Merck Patent Gmbh, 6100 Darmstadt | Polyhalogenaromaten |
| EP0098070B2 (en) * | 1982-06-29 | 2000-12-13 | The Secretary of State for Defence in Her Britannic Majesty's Government of the United Kingdom of Great Britain and | Liquid crystal devices |
| DE3317597A1 (de) * | 1983-05-14 | 1984-11-15 | Merck Patent Gmbh, 6100 Darmstadt | Bicyclohexylethane |
| GB8314077D0 (en) * | 1983-05-20 | 1983-06-29 | Secr Defence | Disubstituted ethanes |
| IN161652B (ja) * | 1983-07-12 | 1988-01-09 | Bbc Brown Boveri & Cie | |
| DE3468860D1 (en) * | 1983-08-04 | 1988-02-25 | Merck Patent Gmbh | Nematic compounds |
| DE3401320A1 (de) * | 1984-01-17 | 1985-07-25 | Merck Patent Gmbh, 6100 Darmstadt | Ethanderivate |
| US4652088A (en) * | 1984-02-01 | 1987-03-24 | Hitachi, Ltd. | Liquid crystal display device |
| CH660003A5 (de) * | 1984-04-16 | 1987-03-13 | Merck Patent Gmbh | Anisotrope verbindungen und fk-mischungen mit diesen. |
| DE3433248A1 (de) * | 1984-09-11 | 1986-03-20 | Merck Patent Gmbh, 6100 Darmstadt | Elektrooptisches anzeigeelement |
| DE3506446A1 (de) * | 1985-02-23 | 1986-08-28 | Merck Patent Gmbh, 6100 Darmstadt | Pyrimidinderivate |
| DE3515373A1 (de) * | 1985-04-27 | 1986-11-06 | Merck Patent Gmbh, 6100 Darmstadt | Stickstoffhaltige heterocyclen |
| DE3518734A1 (de) * | 1985-05-24 | 1986-11-27 | Merck Patent Gmbh, 6100 Darmstadt | Smektische fluessigkristalline phasen |
| JPS61282328A (ja) * | 1985-06-10 | 1986-12-12 | Chisso Corp | シクロヘキサン誘導体 |
| DE3609141A1 (de) * | 1986-03-19 | 1987-09-24 | Merck Patent Gmbh | Elektrooptisches anzeigeelement |
| DE3752339T2 (de) * | 1986-05-19 | 2002-05-08 | Seiko Epson Corp., Tokio/Tokyo | Flüssigkristallanzeigevorrichtung |
| EP0247466B1 (de) * | 1986-05-22 | 1993-11-24 | F. Hoffmann-La Roche Ag | Flüssigkristalline Derivate von Phenylbenzoat |
| EP0255700B1 (en) * | 1986-08-04 | 1991-10-02 | Chisso Corporation | A tolan derivative and a liquid crystal mixture containing the same |
| ATE70133T1 (de) * | 1986-09-12 | 1991-12-15 | Hoffmann La Roche | Fluessigkristallanzeige. |
| DE3788276D1 (de) * | 1986-09-16 | 1994-01-05 | Merck Patent Gmbh | Flüssigkristalline phasen für elektrooptische anzeigeelemente basierend auf dem ecb-effekt. |
| DE3884545D1 (de) * | 1987-04-03 | 1993-11-04 | Merck Patent Gmbh | Fluessigkristalline phase, tolane enthaltend. |
| US4925590A (en) * | 1988-03-10 | 1990-05-15 | Merck Patent Gesellschaft Mit Beschrankter Haftung | Derivatives of 4-cyano-2,3-difluorophenol |
| US4897216A (en) * | 1988-03-10 | 1990-01-30 | Merck Patent Gesellschaft Mit Beschrankter Haftung | 2,3-difluorophenol derivatives |
| DE3807910A1 (de) * | 1988-03-10 | 1989-09-21 | Merck Patent Gmbh | Verfahren zur herstellung von 2,3-difluorbenzolen |
-
1988
- 1988-10-20 DE DE3835803A patent/DE3835803A1/de not_active Withdrawn
-
1989
- 1989-02-27 AT AT89103412T patent/ATE80409T1/de not_active IP Right Cessation
- 1989-02-27 DE DE8989103412T patent/DE58902221D1/de not_active Expired - Fee Related
- 1989-02-27 JP JP1502559A patent/JPH02503445A/ja active Pending
- 1989-02-27 AU AU31887/89A patent/AU3188789A/en not_active Abandoned
- 1989-02-27 WO PCT/EP1989/000178 patent/WO1989008691A1/de not_active Application Discontinuation
- 1989-02-27 EP EP89902769A patent/EP0360851A1/de active Pending
- 1989-02-27 EP EP89103412A patent/EP0332005B1/de not_active Expired - Lifetime
- 1989-02-27 BR BR898906383A patent/BR8906383A/pt unknown
- 1989-02-27 KR KR1019890702085A patent/KR900700574A/ko not_active Application Discontinuation
- 1989-02-27 US US07/359,666 patent/US5178790A/en not_active Expired - Fee Related
- 1989-03-09 CN CN89101254A patent/CN1036029A/zh active Pending
- 1989-11-09 NO NO89894477A patent/NO894477L/no unknown
- 1989-11-09 FI FI895339A patent/FI895339A0/fi not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE3835803A1 (de) | 1990-04-26 |
| NO894477D0 (no) | 1989-11-09 |
| DE58902221D1 (de) | 1992-10-15 |
| CN1036029A (zh) | 1989-10-04 |
| AU3188789A (en) | 1989-10-05 |
| FI895339A0 (fi) | 1989-11-09 |
| ATE80409T1 (de) | 1992-09-15 |
| US5178790A (en) | 1993-01-12 |
| BR8906383A (pt) | 1990-08-28 |
| EP0332005B1 (de) | 1992-09-09 |
| WO1989008691A1 (en) | 1989-09-21 |
| JPH02503445A (ja) | 1990-10-18 |
| KR900700574A (ko) | 1990-08-16 |
| EP0332005A1 (de) | 1989-09-13 |
| EP0360851A1 (de) | 1990-04-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO894477L (no) | Superdreiet flytendekrystalltegn. | |
| JP3439776B2 (ja) | スーパーツィスト液晶ディスプレー | |
| JP5350118B2 (ja) | 電気光学液晶ディスプレイ | |
| KR100855336B1 (ko) | 액정 매질 | |
| KR100553789B1 (ko) | 비틀림네마틱액정표시장치및초비틀림네마틱액정표시장치 | |
| KR100649845B1 (ko) | 에스티엔 액정 디스플레이 | |
| JP5100939B2 (ja) | 液晶混合物 | |
| KR0153124B1 (ko) | 초비틀림 액정 표시장치 | |
| US5055224A (en) | Liquid crystal phase | |
| JP5105669B2 (ja) | 液晶化合物、液晶媒体および液晶ディスプレイ | |
| JPH10140157A (ja) | Ｔｎおよびｓｔｎ液晶ディスプレイ | |
| JP4896285B2 (ja) | スーパーツィストネマティック液晶ディスプレイ | |
| JPH04283291A (ja) | スーパーツイスト液晶ディスプレー | |
| US5286410A (en) | Supertwist liquid-crystal display | |
| JPH11218730A (ja) | Ｓｔｎ液晶ディスプレイ | |
| JPH02503446A (ja) | スーパーツイスト液晶表示体 | |
| JPH10158651A (ja) | スーパーツイスト液晶ディスプレイ | |
| JPH11116959A (ja) | Ｓｔｎ液晶ディスプレイ | |
| JP2660702B2 (ja) | 液晶組成物 | |
| JP2001011449A (ja) | Ｓｔｎ液晶ディスプレイ | |
| JP3004398B2 (ja) | スーパーツイスト液晶ディスプレー | |
| US5702640A (en) | High-multiplexed supertwist liquid-crystal display | |
| JP4638119B2 (ja) | 液晶媒体 | |
| JPH05508240A (ja) | 超ねじれ液晶ディスプレイ | |
| JP4132146B2 (ja) | 液晶混合物 |