JP6201325B2

JP6201325B2 - キノフタロン色素単量体、およびそれを用いた着色性ポリマー、およびそれを用いた着色感光性組成物、およびその用途

キノフタロン色素単量体、およびそれを用いた着色性ポリマー、およびそれを用いた着色感光性組成物、およびその用途 Download PDF

Info

Publication number: JP6201325B2
Authority: JP; Japan
Prior art keywords: substituted; unsubstituted; group; parts; pigment
Prior art date: 2012-02-29
Legal status : Expired - Fee Related

Application number

JP2013015509A

Other languages

English (en)

Japanese (ja)

Other versions

JP2013209614A (ja

JP2013209614A5 (pt-PT

Inventor

直樹江草

清水　宏明

宏明清水

英範皆嶋

Current Assignee

Artience Co Ltd

Original Assignee

Toyo Ink SC Holdings Co Ltd

Priority date

2012-02-29

Filing date

2013-01-30

Publication date

2017-09-27

2013-01-30 Application filed by Toyo Ink SC Holdings Co Ltd filed Critical Toyo Ink SC Holdings Co Ltd

2013-01-30 Priority to JP2013015509A priority Critical patent/JP6201325B2/ja

2013-10-10 Publication of JP2013209614A publication Critical patent/JP2013209614A/ja

2015-11-26 Publication of JP2013209614A5 publication Critical patent/JP2013209614A5/ja

2017-09-27 Application granted granted Critical

2017-09-27 Publication of JP6201325B2 publication Critical patent/JP6201325B2/ja

Status Expired - Fee Related legal-status Critical Current

2033-01-30 Anticipated expiration legal-status Critical

Links

239000000178 monomer Substances 0.000 title claims description 141
239000000203 mixture Substances 0.000 title claims description 135
229920000642 polymer Polymers 0.000 title claims description 114
IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 claims description 112
239000000049 pigment Substances 0.000 claims description 101
238000004040 coloring Methods 0.000 claims description 65
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125000003118 aryl group Chemical group 0.000 claims description 59
239000003086 colorant Substances 0.000 claims description 59
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125000004432 carbon atom Chemical group C* 0.000 claims description 37
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239000011230 binding agent Substances 0.000 claims description 10
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238000002834 transmittance Methods 0.000 description 11
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CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 8
229910017053 inorganic salt Inorganic materials 0.000 description 8
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WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 7
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150000003254 radicals Chemical class 0.000 description 7
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PYRKKGOKRMZEIT-UHFFFAOYSA-N 2-[6-(2-cyclopropylethoxy)-9-(2-hydroxy-2-methylpropyl)-1h-phenanthro[9,10-d]imidazol-2-yl]-5-fluorobenzene-1,3-dicarbonitrile Chemical compound C1=C2C3=CC(CC(C)(O)C)=CC=C3C=3NC(C=4C(=CC(F)=CC=4C#N)C#N)=NC=3C2=CC=C1OCCC1CC1 PYRKKGOKRMZEIT-UHFFFAOYSA-N 0.000 description 6
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RSUCJIJELNXPQI-UHFFFAOYSA-N [4-[[4-(2-methylprop-2-enoyloxy)phenyl]methyl]phenyl] 2-methylprop-2-enoate Chemical class C1=CC(OC(=O)C(=C)C)=CC=C1CC1=CC=C(OC(=O)C(C)=C)C=C1 RSUCJIJELNXPQI-UHFFFAOYSA-N 0.000 description 3
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UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical class OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 3
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