JPS63211291A - 液晶材料 - Google Patents
液晶材料Info
- Publication number
- JPS63211291A JPS63211291A JP62044446A JP4444687A JPS63211291A JP S63211291 A JPS63211291 A JP S63211291A JP 62044446 A JP62044446 A JP 62044446A JP 4444687 A JP4444687 A JP 4444687A JP S63211291 A JPS63211291 A JP S63211291A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- liquid crystal
- alkyl
- phase
- compound
- 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.)
- Granted
Links
- 239000000463 material Substances 0.000 title abstract description 5
- 239000004973 liquid crystal related substance Substances 0.000 title description 22
- 150000001875 compounds Chemical class 0.000 claims abstract description 29
- 239000004990 Smectic liquid crystal Substances 0.000 claims abstract description 16
- 239000000203 mixture Substances 0.000 claims abstract description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 9
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 5
- 239000000126 substance Substances 0.000 claims 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 abstract description 9
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Substances C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract description 9
- 238000010992 reflux Methods 0.000 abstract description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 6
- 125000000217 alkyl group Chemical group 0.000 abstract description 6
- 150000002148 esters Chemical class 0.000 abstract description 5
- 230000005621 ferroelectricity Effects 0.000 abstract description 4
- 239000002904 solvent Substances 0.000 abstract description 4
- YPFDHNVEDLHUCE-UHFFFAOYSA-N 1,3-propanediol Substances OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 abstract description 3
- 229920000166 polytrimethylene carbonate Polymers 0.000 abstract description 3
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 abstract description 2
- VADKRMSMGWJZCF-UHFFFAOYSA-N 2-bromophenol Chemical compound OC1=CC=CC=C1Br VADKRMSMGWJZCF-UHFFFAOYSA-N 0.000 abstract 1
- 101100400378 Mus musculus Marveld2 gene Proteins 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000012071 phase Substances 0.000 description 24
- 239000005262 ferroelectric liquid crystals (FLCs) Substances 0.000 description 7
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
- 230000004044 response Effects 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 230000007704 transition Effects 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- 239000004988 Nematic liquid crystal Substances 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- QPRQEDXDYOZYLA-UHFFFAOYSA-N 2-methylbutan-1-ol Chemical compound CCC(C)CO QPRQEDXDYOZYLA-UHFFFAOYSA-N 0.000 description 2
- IWTBVKIGCDZRPL-UHFFFAOYSA-N 3-methylpentanol Chemical compound CCC(C)CCO IWTBVKIGCDZRPL-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- -1 Lithium aluminum hydride Chemical compound 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 235000011089 carbon dioxide Nutrition 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000012280 lithium aluminium hydride Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 238000010898 silica gel chromatography Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- OXPDQFOKSZYEMJ-UHFFFAOYSA-N 2-phenylpyrimidine Chemical compound C1=CC=CC=C1C1=NC=CC=N1 OXPDQFOKSZYEMJ-UHFFFAOYSA-N 0.000 description 1
- YNPVNLWKVZZBTM-UHFFFAOYSA-N 4-methylhexan-1-ol Chemical compound CCC(C)CCCO YNPVNLWKVZZBTM-UHFFFAOYSA-N 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 240000001548 Camellia japonica Species 0.000 description 1
- 241001643623 Enteles Species 0.000 description 1
- 238000004566 IR spectroscopy Methods 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 125000001309 chloro group Chemical group Cl* 0.000 description 1
- 230000003098 cholesteric effect Effects 0.000 description 1
- 235000018597 common camellia Nutrition 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005401 electroluminescence Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000004043 responsiveness Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Liquid Crystal (AREA)
- Liquid Crystal Substances (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62044446A JPS63211291A (ja) | 1987-02-26 | 1987-02-26 | 液晶材料 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62044446A JPS63211291A (ja) | 1987-02-26 | 1987-02-26 | 液晶材料 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS63211291A true JPS63211291A (ja) | 1988-09-02 |
JPH0572911B2 JPH0572911B2 (en, 2012) | 1993-10-13 |
Family
ID=12691715
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62044446A Granted JPS63211291A (ja) | 1987-02-26 | 1987-02-26 | 液晶材料 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS63211291A (en, 2012) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5035340B2 (ja) * | 2008-04-22 | 2012-09-26 | ユニマテック株式会社 | 含フッ素ボロン酸エステル化合物およびその製造法 |
-
1987
- 1987-02-26 JP JP62044446A patent/JPS63211291A/ja active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5035340B2 (ja) * | 2008-04-22 | 2012-09-26 | ユニマテック株式会社 | 含フッ素ボロン酸エステル化合物およびその製造法 |
Also Published As
Publication number | Publication date |
---|---|
JPH0572911B2 (en, 2012) | 1993-10-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS63107961A (ja) | 2−(アルキルオキシカルボニルオキシフエニル)−5−アルキルピリジン及び組成物 | |
US4835274A (en) | Liquid crystal compound | |
JPS62111939A (ja) | 光学活性β−フルオロヒドリン化合物 | |
JPH0764829B2 (ja) | 液晶化合物 | |
JPS63211291A (ja) | 液晶材料 | |
US4826979A (en) | Liquid crystal compound | |
JPH0341473B2 (en, 2012) | ||
JPS63284147A (ja) | 液晶性物質,その製造法及びそれを含有する液晶組成物 | |
JPH0825946B2 (ja) | フツ素置換ビフエニル誘導体 | |
JPS61109792A (ja) | 2−(4′−置換フエニル)−5−アルキル−1,3,2−ジオキサボリナン化合物,その製造法及びそれを含有する液晶組成物 | |
JP4007462B2 (ja) | ピリジニウム型イオン性化合物誘導体、その製造方法及び液晶物質 | |
JPS6197293A (ja) | 2−(4′−置換フエニル)−5−(4″−置換フエニル)−1,3,2−ジオキサボリナン化合物,その製造法及びそれを含有する液晶組成物 | |
JPH01245089A (ja) | 液晶材料 | |
JPH0778064B2 (ja) | 液晶材料 | |
JPS63316787A (ja) | 液晶材料 | |
JPH024893A (ja) | 液晶材料 | |
JPS62181237A (ja) | 液晶化合物及び液晶組成物 | |
JPH03151349A (ja) | 強誘電性液晶化合物 | |
JPH0629222B2 (ja) | 新規化合物とその製造法および液晶組成物 | |
JPH0320241A (ja) | 光学活性化合物、その中間体、これらの製造方法、液晶組成物及び液晶表示素子 | |
JPH0267252A (ja) | 光学活性化合物 | |
JPH02134361A (ja) | アルキルチオ安息香酸誘導体 | |
JPH03112954A (ja) | 光学活性化合物、その中間体と製法、及び液晶材料 | |
JPH0262850A (ja) | 液晶性化合物及びそれを含有する液晶組成物 | |
JPS6341446A (ja) | 新規な液晶性化合物及び液晶組成物 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |