JP4948022B2 - 光学フィルター - Google Patents

光学フィルター Download PDF

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Publication number: JP4948022B2
Authority: JP; Japan
Prior art keywords: optical filter; group; layer; compound; refractive index
Prior art date: 2006-04-13
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 - Fee Related

Application number

JP2006111184A

Other languages

English (en)

Japanese (ja)

Other versions

JP2007286189A (ja

Inventor

信秀冨永

敦郎冨田

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.)

Adeka Corp

Original Assignee

Adeka 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.)

2006-04-13

Filing date

2006-04-13

Publication date

2012-06-06

2006-04-13 Application filed by Adeka Corp filed Critical Adeka Corp

2006-04-13 Priority to JP2006111184A priority Critical patent/JP4948022B2/ja

2007-04-03 Priority to TW096111835A priority patent/TWI424202B/zh

2007-04-12 Priority to KR1020070035891A priority patent/KR20070101792A/ko

2007-04-13 Priority to CN2007100961066A priority patent/CN101055328B/zh

2007-11-01 Publication of JP2007286189A publication Critical patent/JP2007286189A/ja

2012-06-06 Application granted granted Critical

2012-06-06 Publication of JP4948022B2 publication Critical patent/JP4948022B2/ja

Status Expired - Fee Related legal-status Critical Current

2026-04-13 Anticipated expiration legal-status Critical

Links

230000003287 optical effect Effects 0.000 title claims description 72
150000001875 compounds Chemical class 0.000 claims description 70
125000004432 carbon atom Chemical group C* 0.000 claims description 16
125000000217 alkyl group Chemical group 0.000 claims description 9
125000003118 aryl group Chemical group 0.000 claims description 7
125000003710 aryl alkyl group Chemical group 0.000 claims description 5
125000004093 cyano group Chemical group *C#N 0.000 claims description 5
125000005843 halogen group Chemical group 0.000 claims description 5
125000003277 amino group Chemical group 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
229910052799 carbon Inorganic materials 0.000 claims description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims description 2
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims description 2
125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 claims description 2
239000002023 wood Substances 0.000 claims description 2
239000010410 layer Substances 0.000 description 98
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229910052731 fluorine Inorganic materials 0.000 description 5
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ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical class [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 5
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UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 3
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239000004793 Polystyrene Substances 0.000 description 3
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238000000862 absorption spectrum Methods 0.000 description 3
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238000004458 analytical method Methods 0.000 description 3
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229920002678 cellulose Polymers 0.000 description 3
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 3
OVTCUIZCVUGJHS-UHFFFAOYSA-N dipyrrin Chemical compound C=1C=CNC=1C=C1C=CC=N1 OVTCUIZCVUGJHS-UHFFFAOYSA-N 0.000 description 3
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 3
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239000007788 liquid Substances 0.000 description 3
230000007257 malfunction Effects 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical class N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 description 3
229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 3
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229920000728 polyester Polymers 0.000 description 3
239000002861 polymer material Substances 0.000 description 3
238000006116 polymerization reaction Methods 0.000 description 3
229920002223 polystyrene Polymers 0.000 description 3
150000004033 porphyrin derivatives Chemical class 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
239000000126 substance Substances 0.000 description 3
239000006097 ultraviolet radiation absorber Substances 0.000 description 3
125000003229 2-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 2
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
229920002284 Cellulose triacetate Polymers 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 2
239000004593 Epoxy Substances 0.000 description 2
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 2
108010010803 Gelatin Proteins 0.000 description 2
ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical class C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
239000004372 Polyvinyl alcohol Substances 0.000 description 2
229920002472 Starch Polymers 0.000 description 2
XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
239000000783 alginic acid Substances 0.000 description 2
235000010443 alginic acid Nutrition 0.000 description 2
229920000615 alginic acid Polymers 0.000 description 2
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150000004781 alginic acids Chemical class 0.000 description 2
125000002723 alicyclic group Chemical group 0.000 description 2
239000002216 antistatic agent Substances 0.000 description 2
239000000987 azo dye Substances 0.000 description 2
TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
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125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
239000005018 casein Substances 0.000 description 2
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 2
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JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
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SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
238000005401 electroluminescence Methods 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
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229910010272 inorganic material Inorganic materials 0.000 description 2
239000011147 inorganic material Substances 0.000 description 2
239000011630 iodine Substances 0.000 description 2
229910052740 iodine Inorganic materials 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
239000012948 isocyanate Substances 0.000 description 2
150000002513 isocyanates Chemical class 0.000 description 2
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
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150000004706 metal oxides Chemical class 0.000 description 2
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125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
239000000178 monomer Substances 0.000 description 2
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229910052757 nitrogen Inorganic materials 0.000 description 2
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UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 description 2
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125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
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239000002491 polymer binding agent Substances 0.000 description 2
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KKEYFWRCBNTPAC-UHFFFAOYSA-L terephthalate(2-) Chemical compound [O-]C(=O)C1=CC=C(C([O-])=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-L 0.000 description 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
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OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
125000002221 trityl group Chemical group [H]C1=C([H])C([H])=C([H])C([H])=C1C([*])(C1=C(C(=C(C(=C1[H])[H])[H])[H])[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
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JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 1
125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
CZSRXHJVZUBEGW-UHFFFAOYSA-N 1,2-thiazolidine Chemical group C1CNSC1 CZSRXHJVZUBEGW-UHFFFAOYSA-N 0.000 description 1
VSIYJQNFMOOGCU-UHFFFAOYSA-N 1-(cyclohexen-1-yl)cyclohexene Chemical group C1CCCC(C=2CCCCC=2)=C1 VSIYJQNFMOOGCU-UHFFFAOYSA-N 0.000 description 1
125000006030 1-methyl-3-butenyl group Chemical group 0.000 description 1
125000006018 1-methyl-ethenyl group Chemical group 0.000 description 1
238000005160 1H NMR spectroscopy Methods 0.000 description 1
HIYWOHBEPVGIQN-UHFFFAOYSA-N 1h-benzo[g]indole Chemical class C1=CC=CC2=C(NC=C3)C3=CC=C21 HIYWOHBEPVGIQN-UHFFFAOYSA-N 0.000 description 1
NBUKAOOFKZFCGD-UHFFFAOYSA-N 2,2,3,3-tetrafluoropropan-1-ol Chemical compound OCC(F)(F)C(F)F NBUKAOOFKZFCGD-UHFFFAOYSA-N 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
- C08J5/18—Manufacture of films or sheets
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/01—Hydrocarbons
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/16—Nitrogen-containing compounds
- C08K5/315—Compounds containing carbon-to-nitrogen triple bonds
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B1/00—Optical elements characterised by the material of which they are made; Optical coatings for optical elements
- G02B1/04—Optical elements characterised by the material of which they are made; Optical coatings for optical elements made of organic materials, e.g. plastics
- G—PHYSICS
- G02—OPTICS
- G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
- G02B5/00—Optical elements other than lenses
- G02B5/20—Filters
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J11/00—Gas-filled discharge tubes with alternating current induction of the discharge, e.g. alternating current plasma display panels [AC-PDP]; Gas-filled discharge tubes without any main electrode inside the vessel; Gas-filled discharge tubes with at least one main electrode outside the vessel
- H01J11/10—AC-PDPs with at least one main electrode being out of contact with the plasma
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2203/00—Applications
- C08L2203/16—Applications used for films

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Chemical & Material Sciences (AREA)
Physics & Mathematics (AREA)
Medicinal Chemistry (AREA)
Health & Medical Sciences (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
General Physics & Mathematics (AREA)
Optics & Photonics (AREA)
Manufacturing & Machinery (AREA)
Plasma & Fusion (AREA)
Materials Engineering (AREA)
Optical Filters (AREA)

JP2006111184A 2006-04-13 2006-04-13 光学フィルター Expired - Fee Related JP4948022B2 (ja)

Priority Applications (4)

Application Number	Priority Date	Filing Date	Title
JP2006111184A JP4948022B2 (ja)	2006-04-13	2006-04-13	光学フィルター
TW096111835A TWI424202B (zh)	2006-04-13	2007-04-03	Optical filter
KR1020070035891A KR20070101792A (ko)	2006-04-13	2007-04-12	광학필터
CN2007100961066A CN101055328B (zh)	2006-04-13	2007-04-13	滤光器

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP2006111184A JP4948022B2 (ja)	2006-04-13	2006-04-13	光学フィルター

Publications (2)

Publication Number	Publication Date
JP2007286189A JP2007286189A (ja)	2007-11-01
JP4948022B2 true JP4948022B2 (ja)	2012-06-06

Family

ID=38758035

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP2006111184A Expired - Fee Related JP4948022B2 (ja)	2006-04-13	2006-04-13	光学フィルター

Country Status (4)

Country	Link
JP (1)	JP4948022B2 (zh)
KR (1)	KR20070101792A (zh)
CN (1)	CN101055328B (zh)
TW (1)	TWI424202B (zh)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP5459446B1 (ja) *	2013-04-30	2014-04-02	横浜ゴム株式会社	紫外線硬化型樹脂組成物及びこれを用いる積層体

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Publication number	Priority date	Publication date	Assignee	Title
JP5924698B2 (ja)	2010-05-04	2016-05-25	ユニバーサルシティスタジオズリミテッドライアビリティカンパニー	画像を変換する方法及び装置
CN102858884B (zh)	2010-09-22	2015-10-21	株式会社艾迪科	染料及着色感光性组合物
EP2669339B1 (en) *	2011-01-25	2017-01-18	Adeka Corporation	Novel compound, dye and colored photosensitive composition
EP2677364A4 (en)	2011-02-18	2015-05-13	Adeka Corp	LIGHT-SENSITIVE COLOR COMPOSITION
EP2700679A4 (en)	2011-04-20	2015-01-07	Adeka Corp	NEW COMPOUND WITH ALPHA -CYANOACRYLATE STRUCTURE, DYE, AND COLORING PHOTOSENSITIVE COMPOSITION
JP5916361B2 (ja) *	2011-12-01	2016-05-11	株式会社Adeka	染料及び着色感光性組成物
WO2013109972A2 (en)	2012-01-20	2013-07-25	Regents Of The University Of Minnesota	Therapeutic compounds
JP5955583B2 (ja) *	2012-02-24	2016-07-20	株式会社Adeka	新規化合物、染料及び着色感光性組成物
JP5961437B2 (ja) *	2012-04-25	2016-08-02	株式会社ニコン・エシロール	プラスチック眼鏡レンズ
JP6142398B2 (ja) *	2012-12-28	2017-06-07	山田化学工業株式会社	色補正フィルタ、照明装置及びディスプレイ装置
JP2014191190A (ja) *	2013-03-27	2014-10-06	Fujifilm Corp	赤外線吸収性組成物、赤外線カットフィルタ、カメラモジュール及びカメラモジュールの製造方法
CN105793362A (zh) *	2013-12-18	2016-07-20	横滨橡胶株式会社	紫外线固化型树脂组合物以及叠层体
JP5651797B1 (ja) *	2014-06-30	2015-01-14	尾池工業株式会社	ハードコート転写フィルムの製造方法及びハードコート転写フィルム並びにハードコート層を備えた高分子樹脂板又は高分子樹脂フィルム。
JP6851464B2 (ja) *	2017-03-31	2021-03-31	富士フイルム株式会社	樹脂成形体、及びブルーライトカット積層体
KR102777592B1 (ko) *	2018-04-19	2025-03-10	가부시키가이샤 아데카	화합물, 광 흡수제, 조성물 및 광학 필터
JP2021009244A (ja) *	2019-07-02	2021-01-28	株式会社トッパンＴｏｍｏｅｇａｗａオプティカルフィルム	表示装置
KR20240133419A (ko) *	2023-02-28	2024-09-04	동우 화인켐 주식회사	점착제 조성물, 이에 의해 구현된 점착시트 및 광학소자

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4601532A (en) *	1983-05-09	1986-07-22	Minnesota Mining And Manufacturing Company	Narrow band light absorbing filter
US4791023A (en) *	1984-07-07	1988-12-13	Fuji Photo Film Co., Ltd.	Infrared absorbent and optical material using the same
EP0723167A3 (en) *	1995-01-17	1997-04-02	Mitsubishi Chem Corp	Light-curing composition for color filter
JP3873320B2 (ja) *	1995-08-07	2007-01-24	三菱化学株式会社	カラーフィルター用光重合性組成物
JP3750292B2 (ja) *	1997-06-27	2006-03-01	Ｊｓｒ株式会社	光選択吸収性樹脂成形品、その製造方法および光学フィルター
TWI225227B (en) *	2000-02-01	2004-12-11	Mitsui Chemicals Inc	A displaying filter, a display device and a manufacturing method thereof
WO2001057833A1 (fr) *	2000-02-01	2001-08-09	Mitsui Chemicals Inc.	Filtre pour affichage, afficheur et procede de production a cet effet
JP2002122731A (ja) *	2000-10-17	2002-04-26	Fuji Photo Film Co Ltd	光学フィルター
JP2003105206A (ja) *	2001-09-28	2003-04-09	Mitsui Chemicals Inc	光吸収剤およびその用途
JP2004102223A (ja) *	2002-07-15	2004-04-02	Fuji Photo Film Co Ltd	有機ｅｌディスプレイ素子用フィルター
JP2004258183A (ja) *	2003-02-25	2004-09-16	Toyo Ink Mfg Co Ltd	カラーフィルタおよびカラーフィルタ用着色組成物

2006
- 2006-04-13 JP JP2006111184A patent/JP4948022B2/ja not_active Expired - Fee Related
2007
- 2007-04-03 TW TW096111835A patent/TWI424202B/zh not_active IP Right Cessation
- 2007-04-12 KR KR1020070035891A patent/KR20070101792A/ko active Search and Examination
- 2007-04-13 CN CN2007100961066A patent/CN101055328B/zh not_active Expired - Fee Related

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP5459446B1 (ja) *	2013-04-30	2014-04-02	横浜ゴム株式会社	紫外線硬化型樹脂組成物及びこれを用いる積層体

Also Published As

Publication number	Publication date
TW200804873A (en)	2008-01-16
CN101055328A (zh)	2007-10-17
TWI424202B (zh)	2014-01-21
JP2007286189A (ja)	2007-11-01
KR20070101792A (ko)	2007-10-17
CN101055328B (zh)	2012-09-26

Publication	Publication Date	Title
JP4948022B2 (ja)	2012-06-06	光学フィルター
JP4785541B2 (ja)	2011-10-05	光学フィルター
JP5475244B2 (ja)	2014-04-16	シアニン化合物、該化合物を用いた光学フィルター及び光学記録材料
JP5535664B2 (ja)	2014-07-02	色調補正剤、スクアリリウム化合物及び光学フィルター
JP5431001B2 (ja)	2014-03-05	シアニン化合物及び該シアニン化合物を含有する光学フィルター
JP4781123B2 (ja)	2011-09-28	光学フィルター
JP6760926B2 (ja)	2020-09-23	メロシアニン化合物
JP5078386B2 (ja)	2012-11-21	新規化合物、該化合物を用いた光学フィルター及び光学記録材料
JP5159128B2 (ja)	2013-03-06	メロシアニン化合物、該化合物を用いた光学フィルター及び光学記録材料
JP2008250022A (ja)	2008-10-16	光学フィルター
JP4785588B2 (ja)	2011-10-05	光学フィルター
JP2011016879A (ja)	2011-01-27	蛍光消光材料、フィルム形成用組成物及び光学フィルター
JP2019082544A (ja)	2019-05-30	光学フィルタ
JP4901188B2 (ja)	2012-03-21	シアニン化合物及び該シアニン化合物を用いた光学フィルター
JP4912010B2 (ja)	2012-04-04	ジオキシノン構造を有する化合物並びに該化合物を用いた光学フィルター及び光学記録材料
JP4502791B2 (ja)	2010-07-14	光学フィルター
CN101519414B (zh)	2014-07-09	花青化合物以及使用该化合物的滤光器

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JP4948022B2 - 光学フィルター - Google Patents

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Priority Applications (4)

Applications Claiming Priority (1)

Publications (2)

Family

ID=38758035

Family Applications (1)

Country Status (4)

Cited By (1)

Families Citing this family (17)

Family Cites Families (11)

Cited By (1)

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