KR19990087956A - 나프탈렌유도체및이를함유하는액정조성물 - Google Patents
나프탈렌유도체및이를함유하는액정조성물 Download PDFInfo
- Publication number
- KR19990087956A KR19990087956A KR1019990014400A KR19990014400A KR19990087956A KR 19990087956 A KR19990087956 A KR 19990087956A KR 1019990014400 A KR1019990014400 A KR 1019990014400A KR 19990014400 A KR19990014400 A KR 19990014400A KR 19990087956 A KR19990087956 A KR 19990087956A
- Authority
- KR
- South Korea
- Prior art keywords
- fluoro
- naphthalene
- phenyl
- group
- difluoro
- Prior art date
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- 239000004973 liquid crystal related substance Substances 0.000 title claims abstract description 119
- 239000000203 mixture Substances 0.000 title claims abstract description 78
- 150000002790 naphthalenes Chemical class 0.000 title claims abstract description 16
- 150000001875 compounds Chemical class 0.000 claims abstract description 218
- -1 Fluorine-substituted-2-phenylnaphthalene Chemical class 0.000 claims abstract description 135
- 239000011159 matrix material Substances 0.000 claims abstract description 26
- 125000001153 fluoro group Chemical group F* 0.000 claims description 95
- 229910052731 fluorine Inorganic materials 0.000 claims description 64
- 125000004432 carbon atom Chemical group C* 0.000 claims description 49
- 125000000217 alkyl group Chemical group 0.000 claims description 47
- 125000003545 alkoxy group Chemical group 0.000 claims description 41
- 125000003342 alkenyl group Chemical group 0.000 claims description 30
- 229910052801 chlorine Inorganic materials 0.000 claims description 26
- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 claims description 24
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 23
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 23
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 22
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 22
- 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 15
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 11
- 239000000126 substance Substances 0.000 claims description 10
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 9
- 101150065749 Churc1 gene Proteins 0.000 claims description 9
- 102100038239 Protein Churchill Human genes 0.000 claims description 9
- 125000005449 2-fluoro-1,4-phenylene group Chemical group [H]C1=C([*:2])C([H])=C(F)C([*:1])=C1[H] 0.000 claims description 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 7
- 229910052740 iodine Inorganic materials 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- 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 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 4
- XLJMAIOERFSOGZ-UHFFFAOYSA-M cyanate group Chemical group [O-]C#N XLJMAIOERFSOGZ-UHFFFAOYSA-M 0.000 claims description 4
- 238000006467 substitution reaction Methods 0.000 claims description 4
- 125000005653 3,5-difluoro-1,4-phenylene group Chemical group [H]C1=C(F)C([*:2])=C(F)C([H])=C1[*:1] 0.000 claims description 3
- 125000002252 acyl group Chemical group 0.000 claims description 3
- 125000004423 acyloxy group Chemical group 0.000 claims description 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 3
- 229940106189 ceramide Drugs 0.000 claims description 3
- 125000005732 2,6-difluoro-1,4-phenylene group Chemical group [H]C1=C(F)C([*:1])=C(F)C([H])=C1[*:2] 0.000 claims description 2
- YDNKGFDKKRUKPY-JHOUSYSJSA-N C16 ceramide Natural products CCCCCCCCCCCCCCCC(=O)N[C@@H](CO)[C@H](O)C=CCCCCCCCCCCCCC YDNKGFDKKRUKPY-JHOUSYSJSA-N 0.000 claims description 2
- ZVEQCJWYRWKARO-UHFFFAOYSA-N ceramide Natural products CCCCCCCCCCCCCCC(O)C(=O)NC(CO)C(O)C=CCCC=C(C)CCCCCCCCC ZVEQCJWYRWKARO-UHFFFAOYSA-N 0.000 claims description 2
- 125000001549 ceramide group Chemical group 0.000 claims description 2
- VVGIYYKRAMHVLU-UHFFFAOYSA-N newbouldiamide Natural products CCCCCCCCCCCCCCCCCCCC(O)C(O)C(O)C(CO)NC(=O)CCCCCCCCCCCCCCCCC VVGIYYKRAMHVLU-UHFFFAOYSA-N 0.000 claims description 2
- 230000004044 response Effects 0.000 abstract description 34
- 239000007788 liquid Substances 0.000 abstract description 8
- 238000004519 manufacturing process Methods 0.000 abstract description 5
- 239000000463 material Substances 0.000 abstract description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 132
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 120
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 114
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 103
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 78
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 72
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 62
- 239000002904 solvent Substances 0.000 description 57
- 230000015572 biosynthetic process Effects 0.000 description 54
- 238000003786 synthesis reaction Methods 0.000 description 54
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 39
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 38
- 239000012044 organic layer Substances 0.000 description 37
- 239000013078 crystal Substances 0.000 description 36
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 36
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 36
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 34
- 239000000243 solution Substances 0.000 description 34
- 238000003756 stirring Methods 0.000 description 32
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 31
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 30
- 239000000376 reactant Substances 0.000 description 27
- 238000010898 silica gel chromatography Methods 0.000 description 27
- 239000012071 phase Substances 0.000 description 25
- 239000010410 layer Substances 0.000 description 24
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 22
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 21
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 20
- 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 20
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 19
- RAYZALBEMJMGEA-UHFFFAOYSA-N 1-cyclohexylnaphthalene Chemical compound C1CCCCC1C1=CC=CC2=CC=CC=C12 RAYZALBEMJMGEA-UHFFFAOYSA-N 0.000 description 18
- 238000001816 cooling Methods 0.000 description 18
- 238000010992 reflux Methods 0.000 description 15
- 238000000034 method Methods 0.000 description 14
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 14
- 238000002360 preparation method Methods 0.000 description 14
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical class [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 13
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 12
- 239000002253 acid Substances 0.000 description 12
- 239000011777 magnesium Substances 0.000 description 12
- 229910052749 magnesium Inorganic materials 0.000 description 12
- 230000000704 physical effect Effects 0.000 description 12
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 11
- 238000002844 melting Methods 0.000 description 11
- 230000008018 melting Effects 0.000 description 11
- NFHFRUOZVGFOOS-UHFFFAOYSA-N palladium;triphenylphosphane Chemical compound [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 11
- NQEDLIZOPMNZMC-UHFFFAOYSA-N 4-propylcyclohexan-1-one Chemical compound CCCC1CCC(=O)CC1 NQEDLIZOPMNZMC-UHFFFAOYSA-N 0.000 description 10
- 239000003054 catalyst Substances 0.000 description 10
- 230000014759 maintenance of location Effects 0.000 description 10
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 10
- ZMXIYERNXPIYFR-UHFFFAOYSA-N 1-ethylnaphthalene Chemical compound C1=CC=C2C(CC)=CC=CC2=C1 ZMXIYERNXPIYFR-UHFFFAOYSA-N 0.000 description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
- RJTJVVYSTUQWNI-UHFFFAOYSA-N beta-ethyl naphthalene Natural products C1=CC=CC2=CC(CC)=CC=C21 RJTJVVYSTUQWNI-UHFFFAOYSA-N 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 8
- JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 8
- 239000004988 Nematic liquid crystal Substances 0.000 description 8
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 8
- 239000002585 base Substances 0.000 description 8
- 230000008859 change Effects 0.000 description 8
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 8
- 239000012046 mixed solvent Substances 0.000 description 8
- 150000004780 naphthols Chemical class 0.000 description 8
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 8
- WJKHJLXJJJATHN-UHFFFAOYSA-N triflic anhydride Chemical compound FC(F)(F)S(=O)(=O)OS(=O)(=O)C(F)(F)F WJKHJLXJJJATHN-UHFFFAOYSA-N 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 239000012267 brine Substances 0.000 description 7
- 238000003682 fluorination reaction Methods 0.000 description 7
- 150000002500 ions Chemical class 0.000 description 7
- 125000001624 naphthyl group Chemical group 0.000 description 7
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- 125000003118 aryl group Chemical group 0.000 description 6
- 238000010531 catalytic reduction reaction Methods 0.000 description 6
- 230000007423 decrease Effects 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 6
- QCYXGORGJYUYMT-UHFFFAOYSA-N nickel;triphenylphosphane Chemical compound [Ni].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 QCYXGORGJYUYMT-UHFFFAOYSA-N 0.000 description 6
- XHXFXVLFKHQFAL-UHFFFAOYSA-N phosphoryl trichloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 6
- SXIOKIYOBPGMBF-WKILWMFISA-N C1C[C@@H](CCC)CC[C@@H]1C1=CC=C(C=C(OC)C=C2)C2=C1 Chemical compound C1C[C@@H](CCC)CC[C@@H]1C1=CC=C(C=C(OC)C=C2)C2=C1 SXIOKIYOBPGMBF-WKILWMFISA-N 0.000 description 5
- 239000012043 crude product Substances 0.000 description 5
- 238000000605 extraction Methods 0.000 description 5
- 229910052739 hydrogen Inorganic materials 0.000 description 5
- 239000001257 hydrogen Substances 0.000 description 5
- 125000002524 organometallic group Chemical group 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 5
- MPSMMJPLERAHAL-UHFFFAOYSA-N (4-propylphenoxy)boronic acid Chemical compound CCCC1=CC=C(OB(O)O)C=C1 MPSMMJPLERAHAL-UHFFFAOYSA-N 0.000 description 4
- CAJAZWLCCNCVEY-UHFFFAOYSA-N 2-bromo-6-fluoronaphthalene Chemical compound C1=C(Br)C=CC2=CC(F)=CC=C21 CAJAZWLCCNCVEY-UHFFFAOYSA-N 0.000 description 4
- QBSUCBZRMNPVLH-UHFFFAOYSA-N 2-methoxy-6-(4-propylcyclohexen-1-yl)naphthalene Chemical compound C1C(CCC)CCC(C=2C=C3C=CC(OC)=CC3=CC=2)=C1 QBSUCBZRMNPVLH-UHFFFAOYSA-N 0.000 description 4
- 125000004975 3-butenyl group Chemical group C(CC=C)* 0.000 description 4
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 4
- YMQPKONILWWJQG-UHFFFAOYSA-N 4-bromo-1,2-difluorobenzene Chemical compound FC1=CC=C(Br)C=C1F YMQPKONILWWJQG-UHFFFAOYSA-N 0.000 description 4
- IOIPFCQWKLBXEJ-UHFFFAOYSA-N 6-(4-propylcyclohexyl)naphthalen-2-ol Chemical compound C1CC(CCC)CCC1C1=CC=C(C=C(O)C=C2)C2=C1 IOIPFCQWKLBXEJ-UHFFFAOYSA-N 0.000 description 4
- XWDODHHQFCLSOA-UHFFFAOYSA-N 6-bromo-1,2-difluoronaphthalene Chemical compound C1=C(Br)C=CC2=C(F)C(F)=CC=C21 XWDODHHQFCLSOA-UHFFFAOYSA-N 0.000 description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 4
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 239000004305 biphenyl Substances 0.000 description 4
- 235000010290 biphenyl Nutrition 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 230000018044 dehydration Effects 0.000 description 4
- 238000006297 dehydration reaction Methods 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 235000019253 formic acid Nutrition 0.000 description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 4
- UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 230000009467 reduction Effects 0.000 description 4
- 238000006722 reduction reaction Methods 0.000 description 4
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 4
- 235000017557 sodium bicarbonate Nutrition 0.000 description 4
- XHFLOLLMZOTPSM-UHFFFAOYSA-M sodium;hydrogen carbonate;hydrate Chemical class [OH-].[Na+].OC(O)=O XHFLOLLMZOTPSM-UHFFFAOYSA-M 0.000 description 4
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 4
- 229910052723 transition metal Inorganic materials 0.000 description 4
- 150000003624 transition metals Chemical class 0.000 description 4
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- 150000005481 1,2-diphenylethanes Chemical class 0.000 description 3
- IYBROFSZTOTUKI-UHFFFAOYSA-N 1-fluoro-6-(4-propylphenyl)-2-(3,4,5-trifluorophenyl)naphthalene Chemical compound C1=CC(CCC)=CC=C1C1=CC=C(C(F)=C(C=C2)C=3C=C(F)C(F)=C(F)C=3)C2=C1 IYBROFSZTOTUKI-UHFFFAOYSA-N 0.000 description 3
- ODWMPTMWRTZGCF-UHFFFAOYSA-N 1-fluoro-6-propylnaphthalen-2-ol Chemical compound FC1=C(O)C=CC2=CC(CCC)=CC=C21 ODWMPTMWRTZGCF-UHFFFAOYSA-N 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 3
- DKWBHFPTCMHAEG-UHFFFAOYSA-N 2-(3,4-difluorophenyl)-1-fluoro-6-propylnaphthalene Chemical compound C1=CC2=CC(CCC)=CC=C2C(F)=C1C1=CC=C(F)C(F)=C1 DKWBHFPTCMHAEG-UHFFFAOYSA-N 0.000 description 3
- ZAQDVGLDRSNBEW-UHFFFAOYSA-N 2-(3,4-difluorophenyl)-6-prop-1-ynylnaphthalene Chemical compound C1=CC2=CC(C#CC)=CC=C2C=C1C1=CC=C(F)C(F)=C1 ZAQDVGLDRSNBEW-UHFFFAOYSA-N 0.000 description 3
- OUPYBBPMTKBVAP-UHFFFAOYSA-N 2-(3,4-difluorophenyl)-6-propylnaphthalene Chemical compound C1=CC2=CC(CCC)=CC=C2C=C1C1=CC=C(F)C(F)=C1 OUPYBBPMTKBVAP-UHFFFAOYSA-N 0.000 description 3
- AYFJBMBVXWNYLT-UHFFFAOYSA-N 2-bromo-6-methoxynaphthalene Chemical compound C1=C(Br)C=CC2=CC(OC)=CC=C21 AYFJBMBVXWNYLT-UHFFFAOYSA-N 0.000 description 3
- DEMSTJLFNCGWTN-UHFFFAOYSA-N 2-methoxy-6-propylnaphthalene Chemical compound C1=C(OC)C=CC2=CC(CCC)=CC=C21 DEMSTJLFNCGWTN-UHFFFAOYSA-N 0.000 description 3
- ZKBUKVMUIPLGRY-UHFFFAOYSA-N 6-(3,4-difluorophenyl)naphthalen-2-ol Chemical compound C1=CC2=CC(O)=CC=C2C=C1C1=CC=C(F)C(F)=C1 ZKBUKVMUIPLGRY-UHFFFAOYSA-N 0.000 description 3
- KXGCDWYZOVRFSZ-UHFFFAOYSA-N 6-(4-propylphenyl)naphthalen-2-ol Chemical compound C1=CC(CCC)=CC=C1C1=CC=C(C=C(O)C=C2)C2=C1 KXGCDWYZOVRFSZ-UHFFFAOYSA-N 0.000 description 3
- AWQKULXTGASLSW-UHFFFAOYSA-N 6-propylnaphthalen-2-ol Chemical compound C1=C(O)C=CC2=CC(CCC)=CC=C21 AWQKULXTGASLSW-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- AYTQGJGHKDNXCN-WGSAOQKQSA-N C1C[C@@H](CCC)CC[C@@H]1C#CC1=CC=CC2=CC(C=3C=C(F)C(F)=C(F)C=3)=CC=C12 Chemical compound C1C[C@@H](CCC)CC[C@@H]1C#CC1=CC=CC2=CC(C=3C=C(F)C(F)=C(F)C=3)=CC=C12 AYTQGJGHKDNXCN-WGSAOQKQSA-N 0.000 description 3
- VSDDZYQYSVKFTE-KOMQPUFPSA-N C1C[C@@H](CCC)CC[C@@H]1C1=C(O)C=CC2=CC=CC=C12 Chemical compound C1C[C@@H](CCC)CC[C@@H]1C1=C(O)C=CC2=CC=CC=C12 VSDDZYQYSVKFTE-KOMQPUFPSA-N 0.000 description 3
- QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 3
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- 238000000862 absorption spectrum Methods 0.000 description 1
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- 229910000102 alkali metal hydride Inorganic materials 0.000 description 1
- 150000008046 alkali metal hydrides Chemical class 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
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- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 1
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- 150000005379 cyclohexanecarboxylic acid derivatives Chemical class 0.000 description 1
- 150000001935 cyclohexenes Chemical class 0.000 description 1
- IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical class C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 1
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- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
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- 239000012153 distilled water Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
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- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
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- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
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- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
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- 125000005647 linker group Chemical group 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- AFRJJFRNGGLMDW-UHFFFAOYSA-N lithium amide Chemical class [Li+].[NH2-] AFRJJFRNGGLMDW-UHFFFAOYSA-N 0.000 description 1
- 229940102396 methyl bromide Drugs 0.000 description 1
- QEKXARSPUFVXIX-UHFFFAOYSA-L nickel(2+);triphenylphosphane;dibromide Chemical compound [Ni+2].[Br-].[Br-].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 QEKXARSPUFVXIX-UHFFFAOYSA-L 0.000 description 1
- KFBKRCXOTTUAFS-UHFFFAOYSA-N nickel;triphenylphosphane Chemical compound [Ni].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 KFBKRCXOTTUAFS-UHFFFAOYSA-N 0.000 description 1
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- 125000001979 organolithium group Chemical group 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- FCJSHPDYVMKCHI-UHFFFAOYSA-N phenyl benzoate Chemical compound C=1C=CC=CC=1C(=O)OC1=CC=CC=C1 FCJSHPDYVMKCHI-UHFFFAOYSA-N 0.000 description 1
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- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 1
- 229910000343 potassium bisulfate Inorganic materials 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- DEDZSLCZHWTGOR-UHFFFAOYSA-N propylcyclohexane Chemical compound CCCC1CCCCC1 DEDZSLCZHWTGOR-UHFFFAOYSA-N 0.000 description 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical group CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
- 125000006239 protecting group Chemical group 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- WBHQBSYUUJJSRZ-UHFFFAOYSA-M sodium bisulfate Chemical compound [Na+].OS([O-])(=O)=O WBHQBSYUUJJSRZ-UHFFFAOYSA-M 0.000 description 1
- 229910000342 sodium bisulfate Inorganic materials 0.000 description 1
- 229940079827 sodium hydrogen sulfite Drugs 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 125000003003 spiro group Chemical group 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000010189 synthetic method Methods 0.000 description 1
- CMUTXJXHVDKYAN-UHFFFAOYSA-L tetrabutylazanium difluoride Chemical compound [F-].[F-].CCCC[N+](CCCC)(CCCC)CCCC.CCCC[N+](CCCC)(CCCC)CCCC CMUTXJXHVDKYAN-UHFFFAOYSA-L 0.000 description 1
- 125000005757 tetralin-2,6-ylene group Chemical group [H]C1=C([*:2])C([H])=C2C(=C1[H])C([H])([H])C([H])([*:1])C([H])([H])C2([H])[H] 0.000 description 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
- C07C17/2637—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions between a compound containing only oxygen and possibly halogen as hetero-atoms and a halogenated hydrocarbon
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C19/00—Acyclic saturated compounds containing halogen atoms
- C07C19/08—Acyclic saturated compounds containing halogen atoms containing fluorine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
- C07C17/2632—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions involving an organo-magnesium compound, e.g. Grignard synthesis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
- C07C17/2635—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions involving a phosphorus compound, e.g. Wittig synthesis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
- C07C17/269—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions of only halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/35—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction
- C07C17/354—Preparation of halogenated hydrocarbons by reactions not affecting the number of carbon or of halogen atoms in the reaction by hydrogenation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/18—Polycyclic aromatic halogenated hydrocarbons
-
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Abstract
Description
Claims (20)
- 화학식 1의 나프탈렌 유도체.화학식 1위의 화학식 1에서,Ra는 탄소원자수 1 내지 7의 알콕실기 또는 1 내지 7개의 불소원자에 의해 치환될 수 있는 탄소원자수 1 내지 20의 알킬기, 알콕실기, 알콕시알킬기, 알케닐기또는 알케닐옥시기를 나타내고,a 및 b는 0 또는 1이며 a≥ b를 만족시키고,환 A 및 환 B는 각각 독립적으로 트랜스-1,4-사이클로헥실렌기, 1개 이상의 불소원자에 의해 치환될 수 있는 1,4-페닐렌기, 피리딘-2,5-디일기, 피리미딘-2,5-디일기, 피라진-2,5-디일기, 피리다진-3,6-디일기, 트랜스-1,3-디옥산-2,5-디일기, 트랜스데카하이드로나프탈렌-2,6-디일기 또는 테트라하이드로나프탈렌-2,6-디일기를 나타내며,La및 Lb는 각각 독립적으로 -CH2CH₂-, -CH2CH2CH2CH2-, -CH=CH-, -CH=CHCH2CH2-, -CH2CH2CH=CH-, -CH(CH3)CH2-, -CH2CH(CH3)-, -CF=CF-, -CF20-, -0CF2-, -CO0-, -0CO-, -C≡C- 또는 단일 결합을 나타내고,X¹내지 X6은 각각 독립적으로 수소원자 또는 불소원자를 나타내며,Za는 불소원자, 염소원자, 트리플루오로메톡시기, 탄소원자수 1 내지 7의 알콕실기 또는 1 내지 7개의 불소원자에 의해 치환될 수 있는 탄소원자수 1 내지 20의 알킬기, 알콕실기, 알케닐기 또는 알케닐옥시기를 나타내거나, 화학식 2a 또는 화학식 2b의 기를 나타내며,단 1) Za가 화학식 2a를 나타내는 경우, b는 0이고, Za가 화학식 2b를 나타내는 경우, a는 0이며, Za가 불소원자, 염소원자, 트리플루오로메톡시기, 탄소원자수 1 내지 7의 알콕실기 또는 1 내지 7개의 불소원자에 의해 치환될 수 있는 탄소원자수 1 내지 20의 알킬기, 알콕실기, 알케닐기 또는 알케닐옥시기를 나타내는 경우, a는 1이고,2) Za가 화학식 2a를 나타내며, 환 C가 불소원자에 의해 치환될 수 있는 1,4-페닐렌기를 나타내며, Zb가 불소원자, 염소원자, 트리플루오로메톡시기 또는 불소원자에 의해 치환될 수 있는 알킬기 또는 알콕실기를 나타내는 경우, Lc는 -CH2CH2CH2CH2-, -CH=CH-, -CH=CHCH2CH2-, -CH2CH2CH=CH-, -CH(CH3)CH2-, -CH2CH(CH3)-, -CF=CF-, -CF20- 또는 -0CF2-를 나타내고/나타내거나, X1내지 X6중의 1개 이상은 불소원자를 나타내고,3) Za가 알킬기 또는 알콕실기를 나타내는 경우, X1내지 X6중의 1개 이상은 불소원자를 나타내고/나타내거나, Lc는 -CH2CH2CH2CH2-, -CF=CF-, -CF20- 또는 -OCF2-를 나타내며,4) Za가 불소원자 또는 염소원자를 나타내며, La가 단일 결합을 나타내고, 환 A가 불소원자에 의해 치환될 수 있는 1,4-페닐렌기를 나타내는 경우, b는 O 또는 1이고, Lb는 단일 결합을 나타내며,5) a와 b가 O이고 X1이 불소원자이며 X2내지 X6이 수소원자를 나타내며 Lc가 단일 결합을 나타내는 경우, Zb는 불소원자, 염소원자, 수소원자, 트리플루오로메톡시기, 알케닐기, 알케닐옥시기, 시아네이트기 또는 시아노기를 나타낸다.화학식 2a화학식 2b위의 화학식 2a 및 화학식 2b에서,Lc및 Ld는 각각 독립적으로 -CH2CH2-, -CH2CH2CH2CH2-, -CH=CH-, -CH=CHCH2CH2-, -CHCH2CH=CH-, -CH(CH3)CH2-, -CH2CH(CH3)-, -CF=CF-, -CF2O-, -0CF2-, -CO0-, -OCO-, -C≡C- 또는 단일 결합을 나타내고,환 C 및 환 D는 각각 독립적으로 트랜스-1,4-사이클로헥실렌기, 1개 이상의 불소원자에 의해 치환될 수 있는 1,4-페닐렌기, 피리딘-2,5-디일기, 피리미딘-2,5-디일기, 피라진-2,5-디일기, 피리다진-3,6-디일기, 트랜스-1,3-디옥산-2,5-디일기, 트랜스데카하이드로나프탈렌-2,6-디일기 또는 테트라하이드로나프탈렌-2,6-디일기를 나타내며,Zb및 Zc는 불소원자, 염소원자, 브롬 원자, 요오드 원자, 수소원자, 시아노기, -SCN, -OCN, -R', -OR', -OCOR' 또는 -COOR'를 나타내고, R'는 탄소원자수 1 내지 20의 알킬기 또는 알콕시기 또는 탄소원자수 2 내지 20의 알케닐기 또는 알케닐옥시기를 나타내며, 이들 기는 탄소원자수 1 내지 10의 알콕실기, 아실기, 아실옥시기 또는 알콕시카보닐기에 의해 치환될 수 있고 이들 기 중에 함유된 수소원자는 1개 이상의 불소원자에 의해 치환될 수 있으며 치환 또는 측쇄에 의해 부재탄소가 생기는 경우, 광학 활성이어도 세라미체일 수 있다.
- 제1항에 있어서, a와 b가 1인 화학식 1의 화합물.
- 제1항에 있어서, a가 1이고, b가 0이며, Za가 불소원자, 염소원자, 트리플루오로메톡시기, 탄소원자수 1 내지 7의 알콕실기 또는 1 내지 7개의 불소원자에 의해 치환될 수 있는 탄소원자수 1 내지 20의 알킬기, 알콕실기, 알케닐기 및 알케닐옥시기로부터 선택되는 화학식 1의 화합물.
- 제1항에 있어서, a가 1이고, b가 0이며, Za가 화학식 2a의 기인 화학식 1의화합물.
- 제1항에 있어서, a와 b가 0이고, Za가 화학식 2a의 기인 화학식 1의 화합물.
- 제1항에 있어서, a와 b가 0이고, Za가 화학식 2b의 기인 화학식 1의 화합물.
- 제1항 내지 제6항 중의 어느 한 항에 있어서, La, Lb, Lc및 Ld가 각각 독립적으로 -CH2CH2- 및 단일 결합으로부터 선택되는 화학식 1의 화합물.
- 제1항 내지 제4항 및 제7항 중의 어느 한 항에 있어서, 환 A가 트랜스-1,4-사이클로헥실렌기, 1,4-페닐렌기, 2-플루오로-1,4-페닐렌기, 2,6-디플루오로-1,4-페닐렌기 및 트랜스데카하이드로나프탈렌-2,6-디일기로부터 선택되는 화학식 1의 화합물.
- 제1항, 제2항, 제7항 또는 제8항에 있어서, 환 B가 트랜스-1,4-사이클로헥실렌기인 화학식 1의 화합물.
- 제1항 및 제4항 내지 제7항 중의 어느 한 항에 있어서, 환 C 및 환 D가 각각 독립적으로 1,4-페닐렌기, 2-플루오로-1,4-페닐렌기, 3-플루오로-1,4-페닐렌기, 2,3-디플루오로-1,4-페닐렌기 및 3,5-디플루오로-1,4-페닐렌기로부터 선택되는 화학식 1의 화합물.
- 제1항 내지 제3항 및 제7항 내지 제9항 중의 어느 한 항에 있어서, Za가 1 내지 3개의 불소원자에 의해 치환될 수 있는 탄소원자수 4 내지 12의 알케닐기 및 탄소원자수 3 내지 12의 알케닐옥시기로부터 선택되는 화학식 1의 화합물.
- 제1항 내지 제3항 및 제7항 내지 제9항 중의 어느 한 항에 있어서, Za가 1 내지 7개의 불소원자에 의해 치환될 수 있는 탄소원자수 1 내지 12의 알킬기 및 알콕실기로부터 선택되는 화학식 1의 화합물.
- 제12항에 있어서, Za가 트리플루오로메톡시기인 화학식 1의 화합물.
- 제1항 내지 제13항 중의 어느 한 항에 있어서, X1이 불소원자인 화학식 1의 화합물.
- 제14항에 있어서, X2가 불소원자인 화학식 1의 화합물.
- 제2항 또는 제3항에 있어서, X1및 X2가 불소원자인 화학식 1의 화합물.
- 제1항에 따르는 화학식 1의 화합물을 함유하는 액정 조성물.
- 제17항에 있어서, 액티브 매트릭스 구동용으로 사용되는 액정 조성물.
- 제17항에 따르는 액정 조성물을 구성 요소로 하는 액정 소자.
- 제18항에 따르는 액정 조성물을 사용한 액티브 매트릭스 구동 액정 표시소자.
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JP11214798A JP4258033B2 (ja) | 1998-04-22 | 1998-04-22 | 6−フルオロナフタレン誘導体である新規液晶性化合物とそれを含有する液晶組成物 |
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JP98-191471 | 1998-07-07 | ||
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JP34842898A JP4487327B2 (ja) | 1998-12-08 | 1998-12-08 | 6−トリフルオロメトキシナフタレン誘導体である新規液晶性化合物とそれを含有する液晶組成物及びその製造方法 |
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1999
- 1999-04-21 CA CA002269561A patent/CA2269561C/en not_active Expired - Fee Related
- 1999-04-22 US US09/296,550 patent/US6468607B1/en not_active Expired - Lifetime
- 1999-04-22 EP EP02024918A patent/EP1452514B1/en not_active Expired - Lifetime
- 1999-04-22 EP EP02022912A patent/EP1273562B1/en not_active Expired - Lifetime
- 1999-04-22 KR KR1019990014400A patent/KR100611518B1/ko not_active IP Right Cessation
- 1999-04-22 SG SG9901903A patent/SG85639A1/en unknown
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- 1999-04-22 EP EP99107369A patent/EP0952135B1/en not_active Expired - Lifetime
- 1999-04-22 DE DE69923024T patent/DE69923024T2/de not_active Expired - Lifetime
- 1999-04-22 CN CNB991095235A patent/CN1291958C/zh not_active Expired - Lifetime
- 1999-04-22 DE DE69942212T patent/DE69942212D1/de not_active Expired - Lifetime
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- 2000-03-28 HK HK05100439.4A patent/HK1068328A1/xx not_active IP Right Cessation
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EP1273562B1 (en) | 2009-07-22 |
HK1050674A1 (en) | 2003-07-04 |
DE69923024D1 (de) | 2005-02-10 |
EP1273562A1 (en) | 2003-01-08 |
KR100611518B1 (ko) | 2006-08-11 |
EP0952135B1 (en) | 2005-01-05 |
US6468607B1 (en) | 2002-10-22 |
SG85639A1 (en) | 2002-01-15 |
CA2269561C (en) | 2007-06-05 |
CN1246469A (zh) | 2000-03-08 |
EP1452514B1 (en) | 2010-03-31 |
HK1068328A1 (en) | 2005-04-29 |
HK1030595A1 (en) | 2001-05-11 |
US7145047B2 (en) | 2006-12-05 |
DE69941162D1 (de) | 2009-09-03 |
CA2269561A1 (en) | 1999-10-22 |
EP0952135A1 (en) | 1999-10-27 |
US20030136944A1 (en) | 2003-07-24 |
CN1291958C (zh) | 2006-12-27 |
DE69923024T2 (de) | 2005-12-01 |
EP1452514A1 (en) | 2004-09-01 |
DE69942212D1 (de) | 2010-05-12 |
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