JPH0378871B2 - - Google Patents
Info
- Publication number
- JPH0378871B2 JPH0378871B2 JP3999784A JP3999784A JPH0378871B2 JP H0378871 B2 JPH0378871 B2 JP H0378871B2 JP 3999784 A JP3999784 A JP 3999784A JP 3999784 A JP3999784 A JP 3999784A JP H0378871 B2 JPH0378871 B2 JP H0378871B2
- Authority
- JP
- Japan
- Prior art keywords
- phthalocyanine
- group
- formula
- vinyl
- usually
- 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.)
- Expired
Links
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical group 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 claims description 17
- -1 phthalocyanine compound Chemical class 0.000 claims description 8
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- 239000002244 precipitate Substances 0.000 description 5
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 5
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000010894 electron beam technology Methods 0.000 description 3
- 238000000921 elemental analysis Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 238000000862 absorption spectrum Methods 0.000 description 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910052759 nickel Inorganic materials 0.000 description 2
- 239000003208 petroleum Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- 238000005979 thermal decomposition reaction Methods 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical group OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 description 1
- VHSHLMUCYSAUQU-UHFFFAOYSA-N 2-hydroxypropyl methacrylate Chemical group CC(O)COC(=O)C(C)=C VHSHLMUCYSAUQU-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- 229920002433 Vinyl chloride-vinyl acetate copolymer Polymers 0.000 description 1
- 125000003647 acryloyl group Chemical group O=C([*])C([H])=C([H])[H] 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002265 electronic spectrum Methods 0.000 description 1
- 239000003822 epoxy resin Substances 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 239000012761 high-performance material Substances 0.000 description 1
- 238000002329 infrared spectrum Methods 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 238000001308 synthesis method Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Landscapes
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3999784A JPS60184083A (ja) | 1984-03-02 | 1984-03-02 | フタロシアニン化合物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3999784A JPS60184083A (ja) | 1984-03-02 | 1984-03-02 | フタロシアニン化合物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS60184083A JPS60184083A (ja) | 1985-09-19 |
| JPH0378871B2 true JPH0378871B2 (enrdf_load_stackoverflow) | 1991-12-17 |
Family
ID=12568566
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3999784A Granted JPS60184083A (ja) | 1984-03-02 | 1984-03-02 | フタロシアニン化合物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS60184083A (enrdf_load_stackoverflow) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6358439A (ja) * | 1986-08-29 | 1988-03-14 | Hiroyoshi Shirai | レジスト |
| US5516900A (en) * | 1993-09-14 | 1996-05-14 | Hirofusa Shirai | Phthalocyanine compounds containing either a polymerizable vinyl group, a nitro group, or an amino group |
| JPH07118273A (ja) * | 1993-10-22 | 1995-05-09 | Hiroyoshi Shirai | ナフタロシアニン系化合物および製造方法、ならびにナフタロシアニン系重合体および製造方法 |
| JP4576989B2 (ja) * | 2004-11-19 | 2010-11-10 | セイコーエプソン株式会社 | 着色剤およびそれを用いたインクジェット記録用インク組成物 |
| JP5836326B2 (ja) * | 2012-07-30 | 2015-12-24 | 富士フイルム株式会社 | 着色硬化性組成物およびカラーフィルタ |
-
1984
- 1984-03-02 JP JP3999784A patent/JPS60184083A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS60184083A (ja) | 1985-09-19 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP3860616B2 (ja) | フタロシアニン化合物 | |
| JPH0378871B2 (enrdf_load_stackoverflow) | ||
| US5087390A (en) | Tetraazaporphyrin dye mixtures | |
| EP0284369B1 (en) | 5- or 6-alkoxycarbonyl-2,3-dicyanonaphthalenes and process for production thereof | |
| JPH0643428B2 (ja) | フタロシアニン化合物の製造方法 | |
| JPH0635461B2 (ja) | フタロシアニン化合物 | |
| JPH01146845A (ja) | 新規なスクアリリウム化合物及びその製造方法 | |
| JPS61223056A (ja) | 新規なフタロシアニン誘導体及びその製造方法 | |
| JPH0653744B2 (ja) | アルキルシアノフタロシアニン化合物 | |
| JP6726521B2 (ja) | 光学活性基を有する置換ポリアセチレン及びその製造方法 | |
| JP2634430B2 (ja) | はしご状ポリシラン類及びその製造方法 | |
| JPS63312364A (ja) | フタロシアニン化合物 | |
| JPS61287964A (ja) | ｔ−ブチル置換フタロシアニン類及びその中間体の製造方法 | |
| JPS6094981A (ja) | 金属フタロシアニンジカルボン酸およびそのアルキルエステル | |
| JP2513487B2 (ja) | 新規なフタロシアニン化合物 | |
| JPS63313760A (ja) | 含フッ素アルコキシフタロニトリル | |
| JPH01230674A (ja) | スクアリリウム色素の製造方法 | |
| JP3863195B2 (ja) | フタロシアニン化合物 | |
| Wang et al. | Synthesis and photoconductivity study of VKCuPc monomer and its homopolymer | |
| JPS61152689A (ja) | フタロシアニン化合物 | |
| JPH07248570A (ja) | フォトクロミック光記録材料 | |
| JP2941342B2 (ja) | ベンゾトリアゾール系化合物 | |
| JP2504801B2 (ja) | ビチエニリデンビスベンゾキノン類、およびその製造法 | |
| JPS6259285A (ja) | フタロシアニン化合物 | |
| Ohsugi et al. | Polydiacethylenes with directly bound aromatic substituents for the enlarged third-order nonlinearity |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |