JPH0430987B2 - - Google Patents

Info

Publication number: JPH0430987B2
Authority: JP; Japan
Prior art keywords: formula; group; dye; atom; hydrogen atom
Prior art date: 1985-06-12
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

Application number

JP7845086A

Other languages

English (en)

Japanese (ja)

Other versions

JPS62275163A (ja

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.)

1985-06-12

Filing date

1986-04-04

Publication date

1992-05-25

1985-06-12 Priority claimed from JP60-502692A external-priority patent/JPWO1986002170A1/ja

1986-04-04 Application filed filed Critical

1987-11-30 Publication of JPS62275163A publication Critical patent/JPS62275163A/ja

1992-05-25 Publication of JPH0430987B2 publication Critical patent/JPH0430987B2/ja

Status Granted legal-status Critical Current

Links

229920005989 resin Polymers 0.000 claims description 23
239000011347 resin Substances 0.000 claims description 23
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 16
230000002209 hydrophobic effect Effects 0.000 claims description 14
125000000217 alkyl group Chemical group 0.000 claims description 13
239000001000 anthraquinone dye Substances 0.000 claims description 12
125000005843 halogen group Chemical group 0.000 claims description 10
125000004432 carbon atom Chemical group C* 0.000 claims description 9
125000003277 amino group Chemical group 0.000 claims description 8
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
125000003118 aryl group Chemical group 0.000 claims description 7
125000000753 cycloalkyl group Chemical group 0.000 claims description 6
125000004430 oxygen atom Chemical group O* 0.000 claims description 6
229910052717 sulfur Inorganic materials 0.000 claims description 6
125000004434 sulfur atom Chemical group 0.000 claims description 6
125000003545 alkoxy group Chemical group 0.000 claims description 3
125000001841 imino group Chemical group [H]N=* 0.000 claims description 3
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
239000000049 pigment Substances 0.000 claims description 3
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 1
150000004056 anthraquinones Chemical class 0.000 claims 1
239000000975 dye Substances 0.000 description 66
239000004973 liquid crystal related substance Substances 0.000 description 22
-1 polyethylene terephthalate Polymers 0.000 description 19
230000010287 polarization Effects 0.000 description 18
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 15
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
238000000034 method Methods 0.000 description 14
238000010521 absorption reaction Methods 0.000 description 13
229920000139 polyethylene terephthalate Polymers 0.000 description 13
239000005020 polyethylene terephthalate Substances 0.000 description 13
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 10
LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 10
238000010438 heat treatment Methods 0.000 description 8
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
239000000463 material Substances 0.000 description 6
239000003960 organic solvent Substances 0.000 description 6
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
239000003086 colorant Substances 0.000 description 5
150000001875 compounds Chemical class 0.000 description 5
238000004040 coloring Methods 0.000 description 4
ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 4
239000000835 fiber Substances 0.000 description 4
230000001681 protective effect Effects 0.000 description 4
238000002834 transmittance Methods 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
239000004305 biphenyl Substances 0.000 description 3
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 3
230000000052 comparative effect Effects 0.000 description 3
239000013078 crystal Substances 0.000 description 3
235000019441 ethanol Nutrition 0.000 description 3
238000002844 melting Methods 0.000 description 3
230000008018 melting Effects 0.000 description 3
239000000203 mixture Substances 0.000 description 3
239000008188 pellet Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
241000974482 Aricia saepiolus Species 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
239000004952 Polyamide Substances 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
239000004642 Polyimide Substances 0.000 description 2
235000010290 biphenyl Nutrition 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
238000001816 cooling Methods 0.000 description 2
238000001914 filtration Methods 0.000 description 2
239000011521 glass Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000002156 mixing Methods 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
229920002647 polyamide Polymers 0.000 description 2
229920000728 polyester Polymers 0.000 description 2
229920001225 polyester resin Polymers 0.000 description 2
239000004645 polyester resin Substances 0.000 description 2
229920000573 polyethylene Polymers 0.000 description 2
229920001721 polyimide Polymers 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
OCJBOOLMMGQPQU-UHFFFAOYSA-N 1,4-dichlorobenzene Chemical compound ClC1=CC=C(Cl)C=C1 OCJBOOLMMGQPQU-UHFFFAOYSA-N 0.000 description 1
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
GCPNYYXFDSGAPA-UHFFFAOYSA-N 4-amino-n-(4-butylphenyl)benzamide Chemical compound C1=CC(CCCC)=CC=C1NC(=O)C1=CC=C(N)C=C1 GCPNYYXFDSGAPA-UHFFFAOYSA-N 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
239000004988 Nematic liquid crystal Substances 0.000 description 1
229920002292 Nylon 6 Polymers 0.000 description 1
239000004695 Polyether sulfone Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
239000004793 Polystyrene Substances 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
239000004990 Smectic liquid crystal Substances 0.000 description 1
239000006096 absorbing agent Substances 0.000 description 1
239000000980 acid dye Substances 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000004183 alkoxy alkyl group Chemical group 0.000 description 1
150000008064 anhydrides Chemical class 0.000 description 1
239000001055 blue pigment Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
IGARGHRYKHJQSM-UHFFFAOYSA-N cyclohexylbenzene Chemical compound C1CCCCC1C1=CC=CC=C1 IGARGHRYKHJQSM-UHFFFAOYSA-N 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
229940117389 dichlorobenzene Drugs 0.000 description 1
239000000982 direct dye Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000005357 flat glass Substances 0.000 description 1
239000012530 fluid Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
230000009477 glass transition Effects 0.000 description 1
229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
239000005457 ice water Substances 0.000 description 1
AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
150000002497 iodine compounds Chemical class 0.000 description 1
238000004898 kneading Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229920000620 organic polymer Polymers 0.000 description 1
229920003207 poly(ethylene-2,6-naphthalate) Polymers 0.000 description 1
229920003217 poly(methylsilsesquioxane) Polymers 0.000 description 1
229920001707 polybutylene terephthalate Polymers 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920006393 polyether sulfone Polymers 0.000 description 1
239000011112 polyethylene naphthalate Substances 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
229920002223 polystyrene Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000004800 polyvinyl chloride Substances 0.000 description 1
229920000915 polyvinyl chloride Polymers 0.000 description 1
239000000047 product Substances 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
238000000746 purification Methods 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000009877 rendering Methods 0.000 description 1
239000011342 resin composition Substances 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
238000004544 sputter deposition Methods 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000000859 sublimation Methods 0.000 description 1
230000008022 sublimation Effects 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
239000006228 supernatant Substances 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
229920003002 synthetic resin Polymers 0.000 description 1
239000000057 synthetic resin Substances 0.000 description 1
238000007740 vapor deposition Methods 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1

Landscapes

Optical Filters (AREA)

JP7845086A 1985-06-12 1986-04-04 アントラキノン系色素およびこれを用いた偏光フイルム Granted JPS62275163A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
JP60-502692A JPWO1986002170A1 (ja)		1985-06-12	偏光フィルム
WO85/00328		1985-06-12

Publications (2)

Publication Number	Publication Date
JPS62275163A JPS62275163A (ja)	1987-11-30
JPH0430987B2 true JPH0430987B2 (fr)	1992-05-25

Family

ID=18527196

Family Applications (3)

Application Number	Title	Priority Date	Filing Date
JP61078452A Expired - Lifetime JPH07104448B2 (ja)	1985-06-12	1986-04-04	ペリレン系色素を用いた偏光フイルム
JP7845186A Granted JPS62270664A (ja)	1985-06-12	1986-04-04	キノフタロン系色素およびこれを用いた偏光フイルム
JP7845086A Granted JPS62275163A (ja)	1985-06-12	1986-04-04	アントラキノン系色素およびこれを用いた偏光フイルム

Family Applications Before (2)

Application Number	Title	Priority Date	Filing Date
JP61078452A Expired - Lifetime JPH07104448B2 (ja)	1985-06-12	1986-04-04	ペリレン系色素を用いた偏光フイルム
JP7845186A Granted JPS62270664A (ja)	1985-06-12	1986-04-04	キノフタロン系色素およびこれを用いた偏光フイルム

Country Status (1)

Country	Link
JP (3)	JPH07104448B2 (fr)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH02167723A (ja) *	1988-12-22	1990-06-28	Chisso Corp	平面集光着色圧延シート又はフィルム及びその製造方法
US5659039A (en) *	1994-02-25	1997-08-19	Mitsui Toatsu Chemicals, Inc.	Quinophthalone compounds
WO1998037068A1 (fr) *	1997-02-21	1998-08-27	Bristol-Myers Squibb Company	Derives d'acide benzoïque et composes apparentes utilises comme agents antiarythmiques
US6432327B2 (en) *	1999-12-29	2002-08-13	Younger Mfg. Co.	Formed polyethylene terephthalate polarizing film for incorporation in optical-grade plastic parts
JP4525280B2 (ja) *	2004-09-30	2010-08-18	三菱化学株式会社	異方性色素膜用色素、異方性色素膜形成用組成物、異方性色素膜及び偏光素子
EP2051129B1 (fr)	2006-08-10	2018-04-04	Mitsui Chemicals, Inc.	Lentille polarisante en plastique et procede servant a produire celle-ci
EP2244111B1 (fr)	2008-02-07	2019-05-15	Mitsui Chemicals, Inc.	Lentille de polarisation en plastique et son procédé de fabrication
WO2012020570A1 (fr) *	2010-08-12	2012-02-16	三井化学株式会社	Lentille polarisante en matière plastique, son procédé de production et film polarisant
JP5937673B2 (ja)	2012-03-06	2016-06-22	三井化学株式会社	プラスチック偏光レンズ及びその製造方法
WO2016175585A1 (fr)	2015-04-29	2016-11-03	주식회사 트리아펙스	Film de polarisation, son procédé de fabrication et lentille de polarisation le comprenant
EP3858931A4 (fr)	2018-09-26	2022-06-15	Mitsui Chemicals, Inc.	Couche fonctionnelle comprenant une couche adhésive, stratifié et son utilisation
US12064908B2 (en)	2019-05-16	2024-08-20	Mitsui Chemicals, Inc.	Injection molding apparatus, injection molding method and production method of molded product using injection molding apparatus, and laminated lens
EP4318103A4 (fr)	2021-03-22	2025-03-26	Mitsui Chemicals, Inc.	Procédé de production de lentille photochromique et lentille photochromique

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS50105721A (fr) *	1974-01-29	1975-08-20
JPS51102036A (ja) *	1975-03-07	1976-09-09	Teijin Ltd	Kobunshizairyonochakushokuhoho
JPS58124621A (ja) *	1982-01-22	1983-07-25	Mitsui Toatsu Chem Inc	偏光フイルムの製造方法
JPS5936181A (ja) *	1982-08-25	1984-02-28	Mitsui Toatsu Chem Inc	カラ−液晶組成物
JPS59182877A (ja) *	1983-04-01	1984-10-17	Hitachi Ltd	ゲスト−ホスト型液晶組成物
JPS59182878A (ja) *	1983-04-01	1984-10-17	Hitachi Ltd	ゲスト―　ホスト型液晶組成物
JPS59223786A (ja) *	1983-06-03	1984-12-15	Alps Electric Co Ltd	カラ−液晶表示素子用二色性色素

1986
- 1986-04-04 JP JP61078452A patent/JPH07104448B2/ja not_active Expired - Lifetime
- 1986-04-04 JP JP7845186A patent/JPS62270664A/ja active Granted
- 1986-04-04 JP JP7845086A patent/JPS62275163A/ja active Granted

Also Published As

Publication number	Publication date
JPS62275163A (ja)	1987-11-30
JPS62270664A (ja)	1987-11-25
JPH07104448B2 (ja)	1995-11-13
JPS62269901A (ja)	1987-11-24
JPH0436189B2 (fr)	1992-06-15

Publication	Publication Date	Title
EP0198082B1 (fr)	1992-07-15	Film polarisant
EP0348964B1 (fr)	1995-05-10	Film polarisant
JPH0436189B2 (fr)	1992-06-15
US4128496A (en)	1978-12-05	Dichroic liquid crystal compositions
EP0275077B1 (fr)	1992-02-05	Compositions d'anthraquinone et film polarisant les contenant
JPH07207169A (ja)	1995-08-08	偏光フィルム用アゾ系色素及びこれを用いた偏光フィルム
JPS5884858A (ja)	1983-05-21	液晶組成物及び表示体
JPS61285259A (ja)	1986-12-16	二色性色素およびこれを用いた偏光フイルム
JPH01103667A (ja)	1989-04-20	アントラキノン系色素および該色素を用いた偏光フィルム
JP2954306B2 (ja)	1999-09-27	アントラキノン系偏光フィルム用色素及び該色素を用いた偏光フィルム
US5382465A (en)	1995-01-17	Anthraquinonic colorant and polarizing film containing the colorant
US4607097A (en)	1986-08-19	Dichromatic coloring matter for a colored liquid crystal display element
JPS62277471A (ja)	1987-12-02	アントラキノン化合物及びそれを含有する液晶組成物
US5659039A (en)	1997-08-19	Quinophthalone compounds
JP2966973B2 (ja)	1999-10-25	アントラキノン系色素及び該色素を用いた偏光フィルム
JP2955329B2 (ja)	1999-10-04	アントラキノン系黄色色素及び該色素を用いた偏光フィルム
JP3100461B2 (ja)	2000-10-16	二色性アゾ色素及びこれを用いた偏光フィルム
EP0300770A2 (fr)	1989-01-25	Film polarisant contenant des colorants anthraquinoniques
JPWO1986002170A1 (ja)	1986-07-03	偏光フィルム
GB2041962A (en)	1980-09-17	Guest-host liquid crystal composition
JPS62265356A (ja)	1987-11-18	二色性アゾ色素およびこれを用いた偏光フイルム
JPH042626B2 (fr)	1992-01-20
JPS58157883A (ja)	1983-09-20	液晶用二色性色素
JPS636056A (ja)	1988-01-12	アントラキノン染料およびこれを含む液晶組成物
HK1012021A (en)	1999-09-30	Quinophtalone compounds and polarizing films using same