JPS5832858A - 液晶性化合物 - Google Patents

Info

Publication number

JPS5832858A

JPS5832858A JP13233881A JP13233881A JPS5832858A JP S5832858 A JPS5832858 A JP S5832858A JP 13233881 A JP13233881 A JP 13233881A JP 13233881 A JP13233881 A JP 13233881A JP S5832858 A JPS5832858 A JP S5832858A

Authority

JP

Japan

Prior art keywords

liquid crystal

compound

acid

crystal compound

dielectric anisotropy

Prior art date

1981-08-24

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

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• 239000004973 liquid crystal related substance Substances 0.000 title description 22
• 150000001875 compounds Chemical class 0.000 title description 15
• 125000004432 carbon atom Chemical group C* 0.000 claims description 2
• 125000000217 alkyl group Chemical group 0.000 claims 1
• 239000000203 mixture Substances 0.000 description 10
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
• 239000000463 material Substances 0.000 description 7
• LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 6
• FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 6
• 238000006243 chemical reaction Methods 0.000 description 5
• 239000013078 crystal Substances 0.000 description 5
• LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
• VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
• 239000002253 acid Substances 0.000 description 4
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
• OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
• KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
• 238000000862 absorption spectrum Methods 0.000 description 3
• 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
• 235000013399 edible fruits Nutrition 0.000 description 3
• NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
• 239000004988 Nematic liquid crystal Substances 0.000 description 2
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
• 239000003054 catalyst Substances 0.000 description 2
• 150000002148 esters Chemical class 0.000 description 2
• XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
• 239000011541 reaction mixture Substances 0.000 description 2
• 238000010992 reflux Methods 0.000 description 2
• 239000002904 solvent Substances 0.000 description 2
• 230000007704 transition Effects 0.000 description 2
• ZOSBAYFWABIRBV-UHFFFAOYSA-N 1-pentylcyclohexane-1-carboxylic acid Chemical compound CCCCCC1(C(O)=O)CCCCC1 ZOSBAYFWABIRBV-UHFFFAOYSA-N 0.000 description 1
• -1 3-(p-n-pentylbiphenylcarbonyloxy)-6-n-hexanoyloxyphthalonitrile Chemical compound 0.000 description 1
• YELAFYCYHWPDBI-UHFFFAOYSA-N 5-pentyl-2-phenylbenzoic acid Chemical compound C(CCCC)C=1C=C(C(=CC1)C1=CC=CC=C1)C(=O)O YELAFYCYHWPDBI-UHFFFAOYSA-N 0.000 description 1
• 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 1
• PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
• 238000009835 boiling Methods 0.000 description 1
• 239000003795 chemical substances by application Substances 0.000 description 1
• 238000001816 cooling Methods 0.000 description 1
• 210000002858 crystal cell Anatomy 0.000 description 1
• 125000004093 cyano group Chemical group *C#N 0.000 description 1
• 239000006185 dispersion Substances 0.000 description 1
• 238000001035 drying Methods 0.000 description 1
• 230000005684 electric field Effects 0.000 description 1
• 239000007788 liquid Substances 0.000 description 1
• 238000004519 manufacturing process Methods 0.000 description 1
• 239000011159 matrix material Substances 0.000 description 1
• XGISHOFUAFNYQF-UHFFFAOYSA-N pentanoyl chloride Chemical compound CCCCC(Cl)=O XGISHOFUAFNYQF-UHFFFAOYSA-N 0.000 description 1
• LUMVCLJFHCTMCV-UHFFFAOYSA-M potassium;hydroxide;hydrate Chemical compound O.[OH-].[K+] LUMVCLJFHCTMCV-UHFFFAOYSA-M 0.000 description 1
• 239000002244 precipitate Substances 0.000 description 1
• UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
• 150000003839 salts Chemical class 0.000 description 1
• 238000003756 stirring Methods 0.000 description 1
• 238000005406 washing Methods 0.000 description 1

Cited By (3)