JPS6160113B2 - - Google Patents
Info
- Publication number
- JPS6160113B2 JPS6160113B2 JP477178A JP477178A JPS6160113B2 JP S6160113 B2 JPS6160113 B2 JP S6160113B2 JP 477178 A JP477178 A JP 477178A JP 477178 A JP477178 A JP 477178A JP S6160113 B2 JPS6160113 B2 JP S6160113B2
- Authority
- JP
- Japan
- Prior art keywords
- formula
- electro
- liquid crystal
- numbers
- nematic
- 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
- 239000004973 liquid crystal related substance Substances 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 7
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000008018 melting Effects 0.000 description 5
- 238000002844 melting Methods 0.000 description 5
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000004817 gas chromatography Methods 0.000 description 4
- 238000005259 measurement Methods 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 239000004988 Nematic liquid crystal Substances 0.000 description 3
- 238000010521 absorption reaction Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- CEQFOVLGLXCDCX-WUKNDPDISA-N methyl red Chemical compound C1=CC(N(C)C)=CC=C1\N=N\C1=CC=CC=C1C(O)=O CEQFOVLGLXCDCX-WUKNDPDISA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 230000010287 polarization Effects 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 238000001429 visible spectrum Methods 0.000 description 2
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- -1 2-substituted hydroquinone Chemical class 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- 235000016588 Rosa centifolia Nutrition 0.000 description 1
- 244000052585 Rosa centifolia Species 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000000374 eutectic mixture Substances 0.000 description 1
- 230000005669 field effect Effects 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 210000004681 ovum Anatomy 0.000 description 1
- GJLNWLVPAHNBQN-UHFFFAOYSA-N phenyl 4-hydroxybenzoate Chemical compound C1=CC(O)=CC=C1C(=O)OC1=CC=CC=C1 GJLNWLVPAHNBQN-UHFFFAOYSA-N 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
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- 238000004611 spectroscopical analysis Methods 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
- C09K19/06—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
- C09K19/3066—Cyclohexane rings in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers
- C09K19/3068—Cyclohexane rings in which the rings are linked by a chain containing carbon and oxygen atoms, e.g. esters or ethers chain containing -COO- or -OCO- groups
Landscapes
- Chemical & Material Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Liquid Crystal Substances (AREA)
- Liquid Crystal (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DD19733177A DD138473A3 (de) | 1977-02-11 | 1977-02-11 | Kristallin-fluessige substanzen |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS53113284A JPS53113284A (en) | 1978-10-03 |
JPS6160113B2 true JPS6160113B2 (hu) | 1986-12-19 |
Family
ID=5507341
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP477178A Granted JPS53113284A (en) | 1977-02-11 | 1978-01-19 | Liquid crystal matter |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPS53113284A (hu) |
CH (1) | CH639064A5 (hu) |
DD (1) | DD138473A3 (hu) |
DE (1) | DE2752975C2 (hu) |
GB (1) | GB1596011A (hu) |
SU (1) | SU920062A1 (hu) |
Families Citing this family (23)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4113647A (en) * | 1976-08-13 | 1978-09-12 | The Secretary Of State For Defence In Her Britannic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland | Liquid crystalline materials |
JPS5483694A (en) * | 1977-12-16 | 1979-07-03 | Hitachi Ltd | Nematic liquid crystal body for display device |
DE2800553A1 (de) * | 1978-01-07 | 1979-07-12 | Merck Patent Gmbh | Cyclohexanderivate |
JPS5941983B2 (ja) * | 1978-02-17 | 1984-10-11 | 大日本インキ化学工業株式会社 | トランス(エカトリアル↓−エカトリアル)1,4↓−ジ置換シクロヘキサン誘導体 |
FR2419966A1 (fr) * | 1978-03-17 | 1979-10-12 | Thomson Csf | Cristal liquide de type diester presentant une phase smectique, a basse frequence d'isotropie dielectrique, et dispositif de visualisation utilisant ce cristal |
US4293434A (en) * | 1978-08-08 | 1981-10-06 | VEB Werk fur Fernsehelektronik Berlin im VEB Kombinat Mikroelektronik | Liquid crystal compounds |
US4279770A (en) * | 1978-09-20 | 1981-07-21 | Chisso Corporation | Liquid crystal 2,3-dicyano-hydroquinone derivatives |
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 |
US4309304A (en) * | 1979-11-01 | 1982-01-05 | Exxon Research & Engineering Co. | Liquid crystal compositions for multiplexed displays |
US4328116A (en) * | 1979-11-01 | 1982-05-04 | Minnesota Mining And Manufacturing Company | Liquid crystal compositions for multiplexed displays |
US4290905A (en) * | 1979-12-26 | 1981-09-22 | Kabushiki Kaisha Suwa Seikosha | Ester compound |
JPS572385A (en) * | 1980-06-06 | 1982-01-07 | Hitachi Ltd | Liquid crystal composition |
CH647230A5 (en) * | 1981-06-18 | 1985-01-15 | Hoffmann La Roche | Phenyl esters, and the use thereof as components of liquid-crystalline mixtures |
DE3221577A1 (de) * | 1981-06-25 | 1983-06-16 | VEB Werk für Fernsehelektronik im VEB Kombinat Mikroelektronik, DDR 1160 Berlin | Nematische fluessige kristalle und verfahren zur herstellung |
DE3332692A1 (de) * | 1983-09-10 | 1985-03-28 | Merck Patent Gmbh, 6100 Darmstadt | Anisotrope verbindungen und fluessigkristallmischungen |
US5252252A (en) * | 1983-09-10 | 1993-10-12 | Merck Patent Gesellschaft Mit Beschraenkter Haftung | Anisotropic compounds and liquid crystal mixtures |
GB2182656B (en) * | 1984-11-14 | 1988-02-10 | Nii Prikladnych | Liquid-crystal 4-n-pentyl-phenyl ethers of 4'-(trans-4 -n-alkylcyclohex-2-enoyloxy)benzoin acids |
EP0247466B1 (de) * | 1986-05-22 | 1993-11-24 | F. Hoffmann-La Roche Ag | Flüssigkristalline Derivate von Phenylbenzoat |
US5082589A (en) * | 1986-05-22 | 1992-01-21 | Hoffmann-La Roche Inc. | Liquid crystalline esters |
US5648021A (en) * | 1994-01-17 | 1997-07-15 | Hoechst Aktiengesellschaft | Phenanthrene derivatives and their use in liquid-crystalline mixtures |
DE4423098A1 (de) | 1994-07-01 | 1996-01-04 | Hoechst Ag | Verwendung von Pyrimidingruppen enthaltenden konjugierten Verbindungen als Elektrolumineszenzmaterialien |
KR101677764B1 (ko) * | 2009-04-21 | 2016-11-18 | 스미또모 가가꾸 가부시끼가이샤 | 화합물 |
-
1977
- 1977-02-11 DD DD19733177A patent/DD138473A3/xx not_active IP Right Cessation
- 1977-11-28 DE DE19772752975 patent/DE2752975C2/de not_active Expired
-
1978
- 1978-01-01 CH CH1456177A patent/CH639064A5/de not_active IP Right Cessation
- 1978-01-05 GB GB35278A patent/GB1596011A/en not_active Expired
- 1978-01-19 JP JP477178A patent/JPS53113284A/ja active Granted
- 1978-01-23 SU SU787770079A patent/SU920062A1/ru active
Also Published As
Publication number | Publication date |
---|---|
SU920062A1 (ru) | 1982-04-15 |
DD138473A3 (de) | 1979-11-07 |
DE2752975C2 (de) | 1985-07-18 |
CH639064A5 (en) | 1983-10-31 |
DE2752975A1 (de) | 1978-08-17 |
GB1596011A (en) | 1981-08-19 |
JPS53113284A (en) | 1978-10-03 |
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