JPH0461035B2 - - Google Patents

Info

Publication number: JPH0461035B2
Authority: JP; Japan
Prior art keywords: group; formula; hydrogen atom; atom; liquid crystal
Prior art date: 1982-06-30
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 - Lifetime

Application number

JP57111689A

Other languages

English (en)

Japanese (ja)

Other versions

JPS594674A (ja

Inventor

Masaharu Kaneko

Tomio Yoneyama

Junko Iwanami

Shuji Imazeki

Akio Kobi

Mikio Sato

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Hitachi Ltd

Mitsubishi Kasei Corp

Original Assignee

Hitachi Ltd

Mitsubishi Kasei Corp

Priority date (The priority date 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 date listed.)

1982-06-30

Filing date

1982-06-30

Publication date

1992-09-29

1982-06-30 Application filed by Hitachi Ltd, Mitsubishi Kasei Corp filed Critical Hitachi Ltd

1982-06-30 Priority to JP11168982A priority Critical patent/JPS594674A/ja

1983-06-29 Priority to US06/509,051 priority patent/US4588517A/en

1983-06-29 Priority to EP83106353A priority patent/EP0098522B1/fr

1983-06-29 Priority to DE8383106353T priority patent/DE3380031D1/de

1984-01-11 Publication of JPS594674A publication Critical patent/JPS594674A/ja

1992-09-29 Publication of JPH0461035B2 publication Critical patent/JPH0461035B2/ja

Status Granted legal-status Critical Current

Links

239000004973 liquid crystal related substance Substances 0.000 claims description 58
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 39
125000000217 alkyl group Chemical group 0.000 claims description 21
239000000203 mixture Substances 0.000 claims description 21
125000003545 alkoxy group Chemical group 0.000 claims description 14
125000005843 halogen group Chemical group 0.000 claims description 13
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 12
125000003277 amino group Chemical group 0.000 claims description 10
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 9
229910052801 chlorine Inorganic materials 0.000 claims description 8
125000001309 chloro group Chemical group Cl* 0.000 claims description 8
125000004093 cyano group Chemical group *C#N 0.000 claims description 5
239000000126 substance Substances 0.000 claims description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
125000004183 alkoxy alkyl group Chemical group 0.000 claims description 2
125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 2
239000011159 matrix material Substances 0.000 claims description 2
125000001624 naphthyl group Chemical group 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims description 2
125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 2
229910052717 sulfur Inorganic materials 0.000 claims description 2
125000004434 sulfur atom Chemical group 0.000 claims description 2
239000000975 dye Substances 0.000 description 67
238000010521 absorption reaction Methods 0.000 description 10
239000000758 substrate Substances 0.000 description 9
-1 propylcyclohexyl group Chemical group 0.000 description 8
238000000862 absorption spectrum Methods 0.000 description 7
125000004663 dialkyl amino group Chemical group 0.000 description 7
150000001875 compounds Chemical class 0.000 description 6
238000001228 spectrum Methods 0.000 description 5
239000004988 Nematic liquid crystal Substances 0.000 description 4
238000002835 absorbance Methods 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
239000011521 glass Substances 0.000 description 4
239000000463 material Substances 0.000 description 4
239000013543 active substance Substances 0.000 description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
239000002253 acid Substances 0.000 description 2
IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical compound C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 2
125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 description 2
125000006850 spacer group Chemical group 0.000 description 2
DTGKSKDOIYIVQL-NQMVMOMDSA-N (+)-Borneol Natural products C1C[C@]2(C)[C@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-NQMVMOMDSA-N 0.000 description 1
DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 1
NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 description 1
125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 1
125000001331 3-methylbutoxy group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])O* 0.000 description 1
125000005917 3-methylpentyl group Chemical group 0.000 description 1
NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001299 aldehydes Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
238000013459 approach Methods 0.000 description 1
NEHNMFOYXAPHSD-UHFFFAOYSA-N beta-citronellal Natural products O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
230000003098 cholesteric effect Effects 0.000 description 1
238000004040 coloring Methods 0.000 description 1
238000012937 correction Methods 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
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 1
230000007423 decrease Effects 0.000 description 1
238000010586 diagram Methods 0.000 description 1
125000004915 dibutylamino group Chemical group C(CCC)N(CCCC)* 0.000 description 1
125000001664 diethylamino group Chemical group [H]C([H])([H])C([H])([H])N(*)C([H])([H])C([H])([H])[H] 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
230000000694 effects Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000007788 liquid Substances 0.000 description 1
238000000034 method Methods 0.000 description 1
UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000004115 pentoxy group Chemical group [*]OC([H])([H])C([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
239000000049 pigment Substances 0.000 description 1
229920006122 polyamide resin Polymers 0.000 description 1
125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
208000011580 syndromic disease Diseases 0.000 description 1

Landscapes

Liquid Crystal (AREA)

JP11168982A 1982-06-30 1982-06-30 ゲスト―ホスト型液晶組成物 Granted JPS594674A (ja)

Priority Applications (4)

Application Number	Priority Date	Filing Date	Title
JP11168982A JPS594674A (ja)	1982-06-30	1982-06-30	ゲスト―ホスト型液晶組成物
US06/509,051 US4588517A (en)	1982-06-30	1983-06-29	Liquid crystal composition
EP83106353A EP0098522B1 (fr)	1982-06-30	1983-06-29	Composition à base de cristaux liquides
DE8383106353T DE3380031D1 (en)	1982-06-30	1983-06-29	Liquid crystal composition

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP11168982A JPS594674A (ja)	1982-06-30	1982-06-30	ゲスト―ホスト型液晶組成物

Publications (2)

Publication Number	Publication Date
JPS594674A JPS594674A (ja)	1984-01-11
JPH0461035B2 true JPH0461035B2 (fr)	1992-09-29

Family

ID=14567672

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP11168982A Granted JPS594674A (ja)	1982-06-30	1982-06-30	ゲスト―ホスト型液晶組成物

Country Status (1)

Country	Link
JP (1)	JPS594674A (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN103336325A (zh) *	2012-02-28	2013-10-02	住友化学株式会社	偏光膜、圆偏振板及它们的制造方法

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH0662868B2 (ja) *	1985-01-30	1994-08-17	三井東圧化学株式会社	液晶表示用二色性トリスアゾ色素
JPH0653854B2 (ja) *	1985-05-31	1994-07-20	三井東圧化学株式会社	液晶表示用ポリアゾ系二色性色素
JPH0635552B2 (ja) *	1985-06-11	1994-05-11	三井東圧化学株式会社	二色性ジスアゾ色素
JP2579796B2 (ja) *	1988-03-12	1997-02-12	ダイソー株式会社	チオインジコ誘導体
JPH086047B2 (ja) *	1994-03-07	1996-01-24	三井東圧化学株式会社	液晶表示用二色性トリスアゾ色素
US5805528A (en) *	1996-03-05	1998-09-08	Furuno Electric Co., Ltd.	Underwater detection system
JP5203030B2 (ja) *	2008-04-25	2013-06-05	京セラドキュメントソリューションズ株式会社	電子写真感光体
TWI561588B (en) *	2011-10-22	2016-12-11	Archroma Ip Gmbh	Trisazo acid dyes
JP2019214691A (ja) *	2018-06-14	2019-12-19	山本化成株式会社	二色性化合物、液晶組成物および液晶素子

Citations (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5738857A (en) *	1980-06-30	1982-03-03	Gen Electric	Trisazo dye for liquid crystal composition
JPS57212283A (en) *	1981-06-13	1982-12-27	Bayer Ag	Azo dye-free liquid crystal substance

1982
- 1982-06-30 JP JP11168982A patent/JPS594674A/ja active Granted

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS5738857A (en) *	1980-06-30	1982-03-03	Gen Electric	Trisazo dye for liquid crystal composition
JPS57212283A (en) *	1981-06-13	1982-12-27	Bayer Ag	Azo dye-free liquid crystal substance

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN103336325A (zh) *	2012-02-28	2013-10-02	住友化学株式会社	偏光膜、圆偏振板及它们的制造方法

Also Published As

Publication number	Publication date
JPS594674A (ja)	1984-01-11

Publication	Publication Date	Title
JPS6344797B2 (fr)	1988-09-06
EP0068427B1 (fr)	1985-09-18	Composition à base de cristal liquide
JPH0466913B2 (fr)	1992-10-26
GB2094825A (en)	1982-09-22	Liquid crystal compositions containing pleochroic anthraquinone dyes
JPH0461035B2 (fr)	1992-09-29
JPH0517274B2 (fr)	1993-03-08
JPS59182878A (ja)	1984-10-17	ゲスト―　ホスト型液晶組成物
EP0293942B1 (fr)	1993-04-07	Composition liquide cristalline contenant un composé du type pléochroique-azo
JPS64439B2 (fr)	1989-01-06
JP2638930B2 (ja)	1997-08-06	液晶組成物
GB2064572A (en)	1981-06-17	Liquid crystal composition
JPH0613703B2 (ja)	1994-02-23	ゲスト―ホスト型液晶組成物
JPS59182877A (ja)	1984-10-17	ゲスト−ホスト型液晶組成物
JPH0517275B2 (fr)	1993-03-08
JP2537328B2 (ja)	1996-09-25	ゲスト−ホスト型液晶組成物
JP2561710B2 (ja)	1996-12-11	液晶組成物
JPH0234988B2 (fr)	1990-08-07
JPH0472875B2 (fr)	1992-11-19
JPS6121508B2 (fr)	1986-05-27
JPH0454714B2 (fr)	1992-09-01
JPH0517276B2 (fr)	1993-03-08
JPS61155465A (ja)	1986-07-15	ベンゾ（チオ）キサンテン系化合物及び該化合物を含有する液晶組成物
JPH0223595B2 (fr)	1990-05-24
JPH0455236B2 (fr)	1992-09-02
JPH042626B2 (fr)	1992-01-20

JPH0461035B2 - - Google Patents

Info

Links

Landscapes

Priority Applications (4)

Applications Claiming Priority (1)

Publications (2)

Family

ID=14567672

Family Applications (1)

Country Status (1)

Cited By (1)

Families Citing this family (9)

Citations (2)

Patent Citations (2)

Cited By (1)

Also Published As

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