CH643291A5 - Composition a base de cristal liquide pour dispositif electro-optique. - Google Patents
Composition a base de cristal liquide pour dispositif electro-optique. Download PDFInfo
- Publication number
- CH643291A5 CH643291A5 CH223980A CH223980A CH643291A5 CH 643291 A5 CH643291 A5 CH 643291A5 CH 223980 A CH223980 A CH 223980A CH 223980 A CH223980 A CH 223980A CH 643291 A5 CH643291 A5 CH 643291A5
- Authority
- CH
- Switzerland
- Prior art keywords
- anthraquinone
- group
- composition according
- dye
- formula
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 29
- 239000004973 liquid crystal related substance Substances 0.000 title claims description 24
- 239000000975 dye Substances 0.000 claims description 17
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 239000001000 anthraquinone dye Substances 0.000 claims description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 125000003277 amino group Chemical group 0.000 claims description 6
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 150000004056 anthraquinones Chemical class 0.000 claims description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 230000003098 cholesteric effect Effects 0.000 claims description 3
- 239000004988 Nematic liquid crystal Substances 0.000 claims description 2
- 239000013543 active substance Substances 0.000 claims description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
- -1 anthraquinone compound Chemical class 0.000 claims description 2
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 2
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- YXPSFIWVUKQCQB-UHFFFAOYSA-N 2,3-diaminoanthracene-1,4-dione Chemical compound C1=CC=C2C=C(C(C(N)=C(N)C3=O)=O)C3=CC2=C1 YXPSFIWVUKQCQB-UHFFFAOYSA-N 0.000 claims 1
- MCCNAVROTKFXJW-UHFFFAOYSA-N NC1=C(C(C2=CC3=CC=CC(C3=CC2=C1)=O)=O)N Chemical compound NC1=C(C(C2=CC3=CC=CC(C3=CC2=C1)=O)=O)N MCCNAVROTKFXJW-UHFFFAOYSA-N 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 230000001939 inductive effect Effects 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 11
- 239000000243 solution Substances 0.000 description 10
- 150000002148 esters Chemical group 0.000 description 8
- 238000005259 measurement Methods 0.000 description 5
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
- 238000010521 absorption reaction Methods 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- 239000000600 sorbitol Substances 0.000 description 2
- SHFGENOBPXWUJF-UHFFFAOYSA-N 2-(2-phenylphenyl)benzonitrile Chemical group N#CC1=CC=CC=C1C1=CC=CC=C1C1=CC=CC=C1 SHFGENOBPXWUJF-UHFFFAOYSA-N 0.000 description 1
- WLPATYNQCGVFFH-UHFFFAOYSA-N 2-phenylbenzonitrile Chemical group N#CC1=CC=CC=C1C1=CC=CC=C1 WLPATYNQCGVFFH-UHFFFAOYSA-N 0.000 description 1
- RZVHIXYEVGDQDX-UHFFFAOYSA-N 9,10-anthraquinone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3C(=O)C2=C1 RZVHIXYEVGDQDX-UHFFFAOYSA-N 0.000 description 1
- 239000004642 Polyimide Substances 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- 239000002262 Schiff base Substances 0.000 description 1
- 150000004753 Schiff bases Chemical class 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000004737 colorimetric analysis Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical compound C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000007704 transition 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
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/16—Amino-anthraquinones
- C09B1/20—Preparation from starting materials already containing the anthracene nucleus
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
- C09B1/50—Amino-hydroxy-anthraquinones; Ethers and esters thereof
- C09B1/54—Amino-hydroxy-anthraquinones; Ethers and esters thereof etherified
-
- 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
- C09K19/52—Liquid crystal materials characterised by components which are not liquid crystals, e.g. additives with special physical aspect: solvents, solid particles
- C09K19/60—Pleochroic dyes
- C09K19/603—Anthroquinonic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Liquid Crystal (AREA)
- Liquid Crystal Substances (AREA)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH223980A CH643291A5 (fr) | 1980-03-21 | 1980-03-21 | Composition a base de cristal liquide pour dispositif electro-optique. |
FR8011748A FR2478664A1 (fr) | 1980-03-21 | 1980-05-21 | Composition a base de cristal liquide pour dispositif electro-optique |
GB8107303A GB2074182B (en) | 1980-03-21 | 1981-03-09 | Liquid crystal compositions containing pleochroic material for an electro-optical device |
DE19813109088 DE3109088A1 (de) | 1980-03-21 | 1981-03-10 | Zusammensetzungen auf fluessigkristallbasis und ihre verwendung in elektrooptischen vorrichtungen |
JP3669781A JPS56145969A (en) | 1980-03-21 | 1981-03-16 | Liquid crystal base composition for electrooptic device |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH223980A CH643291A5 (fr) | 1980-03-21 | 1980-03-21 | Composition a base de cristal liquide pour dispositif electro-optique. |
Publications (1)
Publication Number | Publication Date |
---|---|
CH643291A5 true CH643291A5 (fr) | 1984-05-30 |
Family
ID=4229101
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH223980A CH643291A5 (fr) | 1980-03-21 | 1980-03-21 | Composition a base de cristal liquide pour dispositif electro-optique. |
Country Status (5)
Country | Link |
---|---|
JP (1) | JPS56145969A (enrdf_load_stackoverflow) |
CH (1) | CH643291A5 (enrdf_load_stackoverflow) |
DE (1) | DE3109088A1 (enrdf_load_stackoverflow) |
FR (1) | FR2478664A1 (enrdf_load_stackoverflow) |
GB (1) | GB2074182B (enrdf_load_stackoverflow) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4360447A (en) * | 1979-03-16 | 1982-11-23 | Mitsui Toatsu Chemicals, Inc. | Composition for liquid crystal color display elements |
JPS56167779A (en) * | 1980-05-28 | 1981-12-23 | Mitsubishi Chem Ind Ltd | Liquid crystal composition |
DE3007198A1 (de) * | 1980-02-26 | 1981-09-03 | Siemens AG, 1000 Berlin und 8000 München | Pleochroitischer anthrachinon-farbstoff, verfahren zu seiner herstellung und verwendung des farbstoffs |
CA1158078A (en) * | 1980-09-08 | 1983-12-06 | Kensuke Okuda | Artificial dental root |
JPS5763377A (en) * | 1980-10-03 | 1982-04-16 | Mitsui Toatsu Chem Inc | Liquid crystal composition for color display |
DE3040102A1 (de) * | 1980-10-24 | 1982-06-03 | Merck Patent Gmbh, 6100 Darmstadt | Dichroitische anthrachinonfarbstoffe, diese enthaltende fluessigkristalline dielektrika und elektrooptisches anzeigeelement |
DE3046904A1 (de) * | 1980-12-12 | 1982-07-15 | Bayer Ag, 5090 Leverkusen | Anthrachinonfarbstoffe, verfahren zu ihrer herstellung ihre verwendung sowie fluessigkristalline materialien enthaltend anthrachinonfarbstoffe |
GB2094825B (en) | 1981-01-17 | 1984-09-12 | Mitsubishi Chem Ind | Liquid crystal compositions containing pleochroic anthraquinone dyes |
JPS57155282A (en) * | 1981-03-20 | 1982-09-25 | Mitsubishi Chem Ind Ltd | Liquid crystal composition |
DE3137298A1 (de) * | 1981-09-18 | 1983-04-14 | Bayer Ag, 5090 Leverkusen | Anthrachinonfarbstoffe |
JPS5876482A (ja) * | 1981-10-30 | 1983-05-09 | Alps Electric Co Ltd | 液晶混合物 |
JPS594651A (ja) * | 1982-07-01 | 1984-01-11 | Hitachi Ltd | 液晶組成物 |
EP0098736B1 (en) * | 1982-07-01 | 1989-12-06 | Mitsubishi Kasei Corporation | Anthraquinone dyes and liquid crystal compositions containing the dyes |
DE3374875D1 (en) * | 1982-11-29 | 1988-01-21 | Hoffmann La Roche | Coloured liquid crystal mixtures containing phenyl ethanes |
EP0120463B1 (en) * | 1983-03-23 | 1991-11-06 | Hitachi, Ltd. | Anthraquinone dyes and liquid crystal compositions including the same |
JPS59182879A (ja) * | 1983-04-01 | 1984-10-17 | Hitachi Ltd | 液晶組成物 |
JPS59179561A (ja) * | 1983-03-29 | 1984-10-12 | Hitachi Ltd | アントラキノン系色素および該色素を含有する液晶組成物 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1480825A (enrdf_load_stackoverflow) * | 1965-05-24 | 1967-08-09 | ||
DE1644453A1 (de) * | 1966-08-19 | 1971-04-08 | Basf Ag | Verfahren zur Herstellung von blauen Anthrachinonfarbstoffen |
JPS54134452A (en) * | 1978-04-10 | 1979-10-18 | Hitachi Ltd | Quest-host type liquid crystal display device |
JPS54157786A (en) * | 1978-05-23 | 1979-12-12 | Minnesota Mining & Mfg | Multiicoloring dyestuff and photoelectric display device |
-
1980
- 1980-03-21 CH CH223980A patent/CH643291A5/fr not_active IP Right Cessation
- 1980-05-21 FR FR8011748A patent/FR2478664A1/fr active Granted
-
1981
- 1981-03-09 GB GB8107303A patent/GB2074182B/en not_active Expired
- 1981-03-10 DE DE19813109088 patent/DE3109088A1/de not_active Withdrawn
- 1981-03-16 JP JP3669781A patent/JPS56145969A/ja active Pending
Also Published As
Publication number | Publication date |
---|---|
FR2478664B1 (enrdf_load_stackoverflow) | 1982-03-05 |
FR2478664A1 (fr) | 1981-09-25 |
GB2074182A (en) | 1981-10-28 |
DE3109088A1 (de) | 1982-04-29 |
JPS56145969A (en) | 1981-11-13 |
GB2074182B (en) | 1984-10-17 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PL | Patent ceased | ||
PL | Patent ceased |