JP2015036796A5 - - Google Patents
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- Publication number
- JP2015036796A5 JP2015036796A5 JP2013168928A JP2013168928A JP2015036796A5 JP 2015036796 A5 JP2015036796 A5 JP 2015036796A5 JP 2013168928 A JP2013168928 A JP 2013168928A JP 2013168928 A JP2013168928 A JP 2013168928A JP 2015036796 A5 JP2015036796 A5 JP 2015036796A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- general formula
- optical
- independently
- atom
- Prior art date
- 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.)
- Abandoned
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- 230000003287 optical effect Effects 0.000 claims description 59
- 239000000758 substrate Substances 0.000 claims description 34
- 239000000463 material Substances 0.000 claims description 27
- 125000003118 aryl group Chemical group 0.000 claims description 20
- 125000000217 alkyl group Chemical group 0.000 claims description 19
- 125000001424 substituent group Chemical group 0.000 claims description 14
- -1 metal complex compound Chemical class 0.000 claims description 13
- 125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 125000003342 alkenyl group Chemical group 0.000 claims description 8
- 238000009792 diffusion process Methods 0.000 claims description 5
- 125000000623 heterocyclic group Chemical group 0.000 claims description 5
- 125000004429 atom Chemical group 0.000 claims description 4
- 239000003086 colorant Substances 0.000 claims description 4
- 150000002500 ions Chemical class 0.000 claims description 4
- 239000010410 layer Substances 0.000 claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 4
- 238000010521 absorption reaction Methods 0.000 claims description 3
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 239000012790 adhesive layer Substances 0.000 claims description 2
- 125000001931 aliphatic group Chemical group 0.000 claims description 2
- 150000001450 anions Chemical class 0.000 claims description 2
- 238000004040 coloring Methods 0.000 claims description 2
- 229920000642 polymer Polymers 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 4
- 125000001072 heteroaryl group Chemical group 0.000 claims 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 2
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000004434 sulfur atom Chemical group 0.000 claims 2
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000001769 aryl amino group Chemical group 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 150000002736 metal compounds Chemical class 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 description 22
- 238000002360 preparation method Methods 0.000 description 15
- 125000003710 aryl alkyl group Chemical group 0.000 description 8
- 239000006185 dispersion Substances 0.000 description 8
- 239000004973 liquid crystal related substance Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 239000000976 ink Substances 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- YKENVNAJIQUGKU-UHFFFAOYSA-N tetraazaporphin Chemical class C=1C(C=N2)=NC2=NC(NN2)=NC2=CC(C=C2)=NC2=CC2=NC=1C=C2 YKENVNAJIQUGKU-UHFFFAOYSA-N 0.000 description 4
- 125000005462 imide group Chemical group 0.000 description 3
- 239000002096 quantum dot Substances 0.000 description 3
- 230000003595 spectral effect Effects 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 2
- 150000007933 aliphatic carboxylic acids Chemical group 0.000 description 2
- 238000005401 electroluminescence Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 description 1
- 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 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 1
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 102100030343 Antigen peptide transporter 2 Human genes 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 101800000849 Tachykinin-associated peptide 2 Proteins 0.000 description 1
- MPIAGWXWVAHQBB-UHFFFAOYSA-N [3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]-2-(prop-2-enoyloxymethyl)propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(COC(=O)C=C)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C MPIAGWXWVAHQBB-UHFFFAOYSA-N 0.000 description 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 1
- 125000004414 alkyl thio group Chemical group 0.000 description 1
- 125000005577 anthracene group Chemical group 0.000 description 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical group OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 125000004744 butyloxycarbonyl group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229940125904 compound 1 Drugs 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
- 238000005424 photoluminescence Methods 0.000 description 1
- 229920000139 polyethylene terephthalate Polymers 0.000 description 1
- 239000005020 polyethylene terephthalate Substances 0.000 description 1
- FBCQUCJYYPMKRO-UHFFFAOYSA-N prop-2-enyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC=C FBCQUCJYYPMKRO-UHFFFAOYSA-N 0.000 description 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
- 125000004742 propyloxycarbonyl group Chemical group 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 238000000411 transmission spectrum Methods 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2013168928A JP2015036796A (ja) | 2013-08-15 | 2013-08-15 | 光学基材、及び表示装置 |
| KR20140104466A KR20150020110A (ko) | 2013-08-15 | 2014-08-12 | 광학 기재 및 표시 장치 |
| TW103127698A TW201510099A (zh) | 2013-08-15 | 2014-08-13 | 光學基材及顯示裝置 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2013168928A JP2015036796A (ja) | 2013-08-15 | 2013-08-15 | 光学基材、及び表示装置 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2015036796A JP2015036796A (ja) | 2015-02-23 |
| JP2015036796A5 true JP2015036796A5 (ko) | 2015-04-02 |
Family
ID=52579025
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013168928A Abandoned JP2015036796A (ja) | 2013-08-15 | 2013-08-15 | 光学基材、及び表示装置 |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JP2015036796A (ko) |
| KR (1) | KR20150020110A (ko) |
| TW (1) | TW201510099A (ko) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6927285B2 (ja) | 2017-03-23 | 2021-08-25 | コニカミノルタ株式会社 | 光学フィルム、その製造方法、それを具備した偏光板及び表示装置 |
| US20200347289A1 (en) * | 2017-10-17 | 2020-11-05 | Ns Materials Inc. | Resin molded product, method for producing the same, and wavelength conversion member |
| JP7223966B2 (ja) * | 2018-06-28 | 2023-02-17 | パナソニックＩｐマネジメント株式会社 | 色覚補正フィルタ及び光学部品 |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02572A (ja) * | 1987-09-29 | 1990-01-05 | Fuji Photo Film Co Ltd | 光学的情報記録媒体 |
| JPH02251802A (ja) * | 1989-03-24 | 1990-10-09 | Fuji Photo Film Co Ltd | 光反射体 |
| JP2000193820A (ja) * | 1998-10-20 | 2000-07-14 | Fuji Photo Film Co Ltd | 光学フィルタ― |
| AU5248000A (en) * | 1999-06-17 | 2001-01-09 | Fuji Photo Film Co., Ltd. | Optical filter |
| JP2004107566A (ja) * | 2002-09-20 | 2004-04-08 | Tomoegawa Paper Co Ltd | ポリメチン系色素含有粘着剤及びそれを用いたプラズマディスプレイ用前面フィルタ |
| JP2006063195A (ja) * | 2004-08-27 | 2006-03-09 | Mitsui Chemicals Inc | 粘着シート |
| JP2006189751A (ja) * | 2004-12-10 | 2006-07-20 | Mitsubishi Chemicals Corp | ディスプレイ用光学フィルター |
| JP2008304677A (ja) * | 2007-06-07 | 2008-12-18 | Nitto Denko Corp | 色補正フィルター、画像表示装置および液晶表示装置 |
| JP2008304678A (ja) * | 2007-06-07 | 2008-12-18 | Nitto Denko Corp | 色補正フィルター、画像表示装置および液晶表示装置 |
| JP5840435B2 (ja) * | 2011-09-27 | 2016-01-06 | 富士フイルム株式会社 | 着色組成物、着色硬化膜、カラーフィルタ、カラーフィルタの製造方法、液晶表示装置、固体撮像素子、並びに、新規なジピロメテン金属錯体化合物又はその互変異性体 |
-
2013
- 2013-08-15 JP JP2013168928A patent/JP2015036796A/ja not_active Abandoned
-
2014
- 2014-08-12 KR KR20140104466A patent/KR20150020110A/ko not_active Application Discontinuation
- 2014-08-13 TW TW103127698A patent/TW201510099A/zh unknown
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