JPS61152689A - フタロシアニン化合物 - Google Patents
フタロシアニン化合物Info
- Publication number
- JPS61152689A JPS61152689A JP27949784A JP27949784A JPS61152689A JP S61152689 A JPS61152689 A JP S61152689A JP 27949784 A JP27949784 A JP 27949784A JP 27949784 A JP27949784 A JP 27949784A JP S61152689 A JPS61152689 A JP S61152689A
- Authority
- JP
- Japan
- Prior art keywords
- formula
- group
- compound
- product
- infrared
- 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.)
- Granted
Links
- 125000005843 halogen group Chemical group 0.000 claims abstract description 9
- 239000002184 metal Substances 0.000 claims abstract description 7
- 229910052751 metal Inorganic materials 0.000 claims abstract description 7
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 5
- 125000003118 aryl group Chemical group 0.000 claims abstract description 4
- -1 phthalocyanine compound Chemical class 0.000 claims description 9
- 125000004429 atom Chemical group 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 12
- 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 abstract description 9
- 150000001875 compounds Chemical class 0.000 abstract description 8
- 239000000463 material Substances 0.000 abstract description 5
- 238000006243 chemical reaction Methods 0.000 abstract description 3
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 abstract description 2
- 230000002745 absorbent Effects 0.000 abstract description 2
- 239000002250 absorbent Substances 0.000 abstract description 2
- 230000003287 optical effect Effects 0.000 abstract description 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- PSCMQHVBLHHWTO-UHFFFAOYSA-K indium(iii) chloride Chemical compound Cl[In](Cl)Cl PSCMQHVBLHHWTO-UHFFFAOYSA-K 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
- 238000000921 elemental analysis Methods 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000010521 absorption reaction Methods 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 4
- 239000006096 absorbing agent Substances 0.000 description 3
- JWAZRIHNYRIHIV-UHFFFAOYSA-N 2-naphthol Chemical compound C1=CC=CC2=CC(O)=CC=C21 JWAZRIHNYRIHIV-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 239000012043 crude product Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 239000010409 thin film Substances 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 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- 240000007124 Brassica oleracea Species 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical group ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- 229940126214 compound 3 Drugs 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 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 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000010408 film Substances 0.000 description 1
- 125000002425 furfuryl group Chemical group C(C1=CC=CO1)* 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 108091008695 photoreceptors Proteins 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 230000002747 voluntary effect Effects 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Landscapes
- Photoreceptors In Electrophotography (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27949784A JPS61152689A (ja) | 1984-12-26 | 1984-12-26 | フタロシアニン化合物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP27949784A JPS61152689A (ja) | 1984-12-26 | 1984-12-26 | フタロシアニン化合物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61152689A true JPS61152689A (ja) | 1986-07-11 |
| JPH0251558B2 JPH0251558B2 (enrdf_load_stackoverflow) | 1990-11-07 |
Family
ID=17611869
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP27949784A Granted JPS61152689A (ja) | 1984-12-26 | 1984-12-26 | フタロシアニン化合物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61152689A (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6445474A (en) * | 1987-04-06 | 1989-02-17 | Nippon Catalytic Chem Ind | Novel fluorine-containing phthalocyanine compound and production thereof |
| JPH02502099A (ja) * | 1987-02-13 | 1990-07-12 | イギリス国 | 置換フタロシアニン |
| JPH0635214A (ja) * | 1992-05-29 | 1994-02-10 | Xerox Corp | オクタ−置換フタロシアニンを含有する赤外光導電体 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60199890A (ja) * | 1984-02-17 | 1985-10-09 | チバ‐ガイギ アクチエンゲゼルシヤフト | 水溶性フタロシアニン化合物および光活性化剤としてのその用途 |
-
1984
- 1984-12-26 JP JP27949784A patent/JPS61152689A/ja active Granted
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60199890A (ja) * | 1984-02-17 | 1985-10-09 | チバ‐ガイギ アクチエンゲゼルシヤフト | 水溶性フタロシアニン化合物および光活性化剤としてのその用途 |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02502099A (ja) * | 1987-02-13 | 1990-07-12 | イギリス国 | 置換フタロシアニン |
| JPH07316449A (ja) * | 1987-02-13 | 1995-12-05 | Uk Government | フタロシアニン誘導体を含む近赤外吸収体又は光学的記録媒体 |
| US5506708A (en) * | 1987-02-13 | 1996-04-09 | The Secretary Of State For Defence In Her Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland | Substituted phthalocyanines |
| US5618929A (en) * | 1987-02-13 | 1997-04-08 | The Secretary Of State For Defence In Her Brittanic Majesty's Government Of The United Kingdom Of Great Britain And Northern Ireland | Substituted phthalocyanines |
| JPS6445474A (en) * | 1987-04-06 | 1989-02-17 | Nippon Catalytic Chem Ind | Novel fluorine-containing phthalocyanine compound and production thereof |
| JPH0635214A (ja) * | 1992-05-29 | 1994-02-10 | Xerox Corp | オクタ−置換フタロシアニンを含有する赤外光導電体 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0251558B2 (enrdf_load_stackoverflow) | 1990-11-07 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS5869870A (ja) | ピリミジン誘導体およびそれを有効成分とする高脂血症治療剤 | |
| JP3860616B2 (ja) | フタロシアニン化合物 | |
| JPH01228960A (ja) | スクアリリウムの化合物 | |
| JP2011162445A (ja) | アゾ−ホウ素錯体化合物およびその製造方法 | |
| JPS60142944A (ja) | スクアライン化合物の製造方法 | |
| JPS61152689A (ja) | フタロシアニン化合物 | |
| JPS61152685A (ja) | フタロシアニン化合物 | |
| JPS61152769A (ja) | フタロシアニン化合物 | |
| JPS60184083A (ja) | フタロシアニン化合物 | |
| WO2018216679A1 (ja) | テトラフェニルポルフィリン誘導体 | |
| JPH075551B2 (ja) | スクアリリウム化合物 | |
| JPS62111984A (ja) | アルキルシアノフタロシアニン化合物 | |
| JPS61218551A (ja) | スクアリリウム化合物 | |
| Williams et al. | Pyrido [2, 3‐H]‐2, 6‐naphthyridines. I. Synthesis and thermal reactions of the 2, 2′ bisacylazide of 3, 3′ bipyridine | |
| JPH06172361A (ja) | フタロシアニン化合物 | |
| JPH04360150A (ja) | ゲルマニウムフタロシアニン系光電変換剤 | |
| JP2976058B2 (ja) | オクタキス（ジアルコキシフェニル）フタロシアニン系化合物およびその遷移金属錯体 | |
| JPH0435515B2 (enrdf_load_stackoverflow) | ||
| JP3039182B2 (ja) | オリゴチオフェン誘導体およびその製造方法 | |
| JPS63159386A (ja) | テトラナフトポルフイラジン誘導体 | |
| JPH03220392A (ja) | 結晶変換によるチタニルフタロシアニンの製造方法 | |
| SU1154281A1 (ru) | 10-Алкилхиндолины в качестве промежуточных продуктов дл получени сенсибилизаторов электрофотографических слоев на основе поли- @ -эпоксипропилкарбазола и способ их получени | |
| JPH02283769A (ja) | 新規フタロシアニン化合物およびその製造方法 | |
| KR101201669B1 (ko) | 고용해도 및 고내구성을 가진 근적외선의 흡수 화합물 및 그것을 포함하는 근적외선 흡수 소재 | |
| Yao et al. | Efficient synthesis of a multifunctional dye conjugate for photorefractive applications |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |