JPS61215663A - ナフタロシアニン化合物 - Google Patents
ナフタロシアニン化合物Info
- Publication number
- JPS61215663A JPS61215663A JP60057260A JP5726085A JPS61215663A JP S61215663 A JPS61215663 A JP S61215663A JP 60057260 A JP60057260 A JP 60057260A JP 5726085 A JP5726085 A JP 5726085A JP S61215663 A JPS61215663 A JP S61215663A
- Authority
- JP
- Japan
- Prior art keywords
- group
- naphthalocyanine compound
- naphthalocyanine
- aralkyl
- dicyanonaphthalene
- 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
- -1 Naphthalocyanine compound Chemical class 0.000 title claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 7
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 6
- 239000000126 substance Substances 0.000 claims description 4
- 239000000975 dye Substances 0.000 abstract description 8
- 125000003545 alkoxy group Chemical group 0.000 abstract description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract description 4
- 239000004202 carbamide Substances 0.000 abstract description 4
- 238000004040 coloring Methods 0.000 abstract description 4
- 239000004973 liquid crystal related substance Substances 0.000 abstract description 4
- LKKPNUDVOYAOBB-UHFFFAOYSA-N naphthalocyanine Chemical compound N1C(N=C2C3=CC4=CC=CC=C4C=C3C(N=C3C4=CC5=CC=CC=C5C=C4C(=N4)N3)=N2)=C(C=C2C(C=CC=C2)=C2)C2=C1N=C1C2=CC3=CC=CC=C3C=C2C4=N1 LKKPNUDVOYAOBB-UHFFFAOYSA-N 0.000 abstract description 4
- 230000003287 optical effect Effects 0.000 abstract description 4
- 125000005287 vanadyl group Chemical group 0.000 abstract description 4
- KNBYJRSSFXTESR-UHFFFAOYSA-N naphthalene-2,3-dicarbonitrile Chemical compound C1=CC=C2C=C(C#N)C(C#N)=CC2=C1 KNBYJRSSFXTESR-UHFFFAOYSA-N 0.000 abstract description 3
- 239000011347 resin Substances 0.000 abstract description 3
- 229920005989 resin Polymers 0.000 abstract description 3
- 238000004043 dyeing Methods 0.000 abstract description 2
- 238000010438 heat treatment Methods 0.000 abstract description 2
- 239000003973 paint Substances 0.000 abstract description 2
- 239000000463 material Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 11
- 238000000921 elemental analysis Methods 0.000 description 8
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 238000000862 absorption spectrum Methods 0.000 description 5
- 125000001424 substituent group Chemical group 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 4
- 125000001624 naphthyl group Chemical group 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 238000003786 synthesis reaction Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- KYPOHTVBFVELTG-OWOJBTEDSA-N (e)-but-2-enedinitrile Chemical compound N#C\C=C\C#N KYPOHTVBFVELTG-OWOJBTEDSA-N 0.000 description 3
- ULLVZUWGOZCGEC-UHFFFAOYSA-N 6-butoxynaphthalene-2,3-dicarbonitrile Chemical compound C1=C(C#N)C(C#N)=CC2=CC(OCCCC)=CC=C21 ULLVZUWGOZCGEC-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-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
- 238000001816 cooling Methods 0.000 description 3
- 239000012043 crude product Substances 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- FVAUCKIRQBBSSJ-UHFFFAOYSA-M sodium iodide Chemical compound [Na+].[I-] FVAUCKIRQBBSSJ-UHFFFAOYSA-M 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000004440 column chromatography Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000012015 optical character recognition Methods 0.000 description 2
- 239000012264 purified product Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 2
- IVUBJNPDPBDVLT-UHFFFAOYSA-N 2,15,28,41,53,55-hexaza-54,56-diazanidatridecacyclo[40.10.1.13,14.116,27.129,40.04,13.06,11.017,26.019,24.030,39.032,37.043,52.045,50]hexapentaconta-1,3,5,7,9,11,13,15,17,19,21,23,25,27(55),28,30,32,34,36,38,40,42(53),43,45,47,49,51-heptacosaene oxovanadium(2+) Chemical compound [V+2]=O.[N-]1C(N=C2C3=CC4=CC=CC=C4C=C3C(N=C3C4=CC5=CC=CC=C5C=C4C(=N4)[N-]3)=N2)=C(C=C2C(C=CC=C2)=C2)C2=C1N=C1C2=CC3=CC=CC=C3C=C2C4=N1 IVUBJNPDPBDVLT-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- DWAQJAXMDSEUJJ-UHFFFAOYSA-M Sodium bisulfite Chemical compound [Na+].OS([O-])=O DWAQJAXMDSEUJJ-UHFFFAOYSA-M 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 239000011011 black crystal Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 239000013058 crude material Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 239000000976 ink Substances 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910001507 metal halide Inorganic materials 0.000 description 1
- 150000005309 metal halides Chemical class 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 125000002560 nitrile group Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000003884 phenylalkyl group Chemical group 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000010267 sodium hydrogen sulphite Nutrition 0.000 description 1
- 235000009518 sodium iodide Nutrition 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 150000003613 toluenes Chemical class 0.000 description 1
Landscapes
- Thermal Transfer Or Thermal Recording In General (AREA)
- Liquid Crystal Substances (AREA)
- Coloring (AREA)
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
- Photoreceptors In Electrophotography (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60057260A JPS61215663A (ja) | 1985-03-20 | 1985-03-20 | ナフタロシアニン化合物 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP60057260A JPS61215663A (ja) | 1985-03-20 | 1985-03-20 | ナフタロシアニン化合物 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61215663A true JPS61215663A (ja) | 1986-09-25 |
JPH0377230B2 JPH0377230B2 (enrdf_load_stackoverflow) | 1991-12-09 |
Family
ID=13050555
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP60057260A Granted JPS61215663A (ja) | 1985-03-20 | 1985-03-20 | ナフタロシアニン化合物 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61215663A (enrdf_load_stackoverflow) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6239286A (ja) * | 1985-08-13 | 1987-02-20 | Mitsubishi Chem Ind Ltd | 光学記録体 |
JPS6411153A (en) * | 1987-07-03 | 1989-01-13 | Mitsui Toatsu Chemicals | Near infrared-absorbing polymer composition |
JPH01294791A (ja) * | 1988-05-20 | 1989-11-28 | Canon Inc | 情報記録媒体 |
JPH0379683A (ja) * | 1989-08-22 | 1991-04-04 | Toyo Ink Mfg Co Ltd | 感熱転写材および検出方法 |
EP0464959A2 (en) | 1987-03-23 | 1992-01-08 | Hitachi Chemical Co., Ltd. | Naphthalocyanine derivatives and production processes thereof, as well as optical information recording media using the derivatives and production processes thereof |
US6197851B1 (en) | 1996-08-30 | 2001-03-06 | Eastman Chemical Company | Polyester compositions containing near infrared absorbing materials to improve reheat |
JP2003508615A (ja) * | 1999-09-06 | 2003-03-04 | バイエル アクチェンゲゼルシャフト | 成形組成物 |
WO2022130925A1 (ja) | 2020-12-16 | 2022-06-23 | 山本化成株式会社 | 媒体 |
-
1985
- 1985-03-20 JP JP60057260A patent/JPS61215663A/ja active Granted
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6239286A (ja) * | 1985-08-13 | 1987-02-20 | Mitsubishi Chem Ind Ltd | 光学記録体 |
EP0464959A2 (en) | 1987-03-23 | 1992-01-08 | Hitachi Chemical Co., Ltd. | Naphthalocyanine derivatives and production processes thereof, as well as optical information recording media using the derivatives and production processes thereof |
JPS6411153A (en) * | 1987-07-03 | 1989-01-13 | Mitsui Toatsu Chemicals | Near infrared-absorbing polymer composition |
JPH01294791A (ja) * | 1988-05-20 | 1989-11-28 | Canon Inc | 情報記録媒体 |
JPH0379683A (ja) * | 1989-08-22 | 1991-04-04 | Toyo Ink Mfg Co Ltd | 感熱転写材および検出方法 |
US6197851B1 (en) | 1996-08-30 | 2001-03-06 | Eastman Chemical Company | Polyester compositions containing near infrared absorbing materials to improve reheat |
JP2003508615A (ja) * | 1999-09-06 | 2003-03-04 | バイエル アクチェンゲゼルシャフト | 成形組成物 |
WO2022130925A1 (ja) | 2020-12-16 | 2022-06-23 | 山本化成株式会社 | 媒体 |
Also Published As
Publication number | Publication date |
---|---|
JPH0377230B2 (enrdf_load_stackoverflow) | 1991-12-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0134518B1 (en) | Naphthalocyanine compounds | |
US2155054A (en) | Coloring matters | |
JPS61215663A (ja) | ナフタロシアニン化合物 | |
JPH07286107A (ja) | フタロシアニン化合物 | |
JPS63308073A (ja) | フタロシアニン化合物 | |
JPH04273879A (ja) | フタロシアニン化合物 | |
JPS6023451A (ja) | ナフタロシアニン化合物 | |
JPH0813930B2 (ja) | 近赤外線吸収フィルター用高純度アントラキノン系色素 | |
JPS61268761A (ja) | ナフトキノン系緑色色素及びその製造方法 | |
JPS61215662A (ja) | ナフタロシアニン化合物 | |
JP2854908B2 (ja) | イミド化合物の製造方法 | |
US2818410A (en) | Dyes of the quinophthalone series | |
USRE34480E (en) | Naphthalocyanine compounds | |
JPH02283769A (ja) | 新規フタロシアニン化合物およびその製造方法 | |
JPH01100171A (ja) | フタロシアニン化合物の製造方法 | |
JPS63112592A (ja) | 近赤外吸収2:1型ニツケル錯体色素 | |
JPH01157944A (ja) | メチン系化合物、その製法及びそれを用いてなる光情報記録媒体 | |
JP3267745B2 (ja) | 新規イソインドレニン化合物およびその製造方法 | |
JPH0421684A (ja) | アザアヌレン化合物の新規な合成方法 | |
JPH05179150A (ja) | レーザー光記録媒体用アントラキノン系長波長吸収色素 | |
SU443048A1 (ru) | Способ получени медных комплексов макрогетероциклических соединений | |
JPH04124188A (ja) | テトラピラジノポルフィラジン誘導体 | |
DE1951157A1 (de) | Verfahren zur Herstellung von Benzoxazo- und Benzthiazo-isochinolonen | |
JPH0350270A (ja) | オキシチタニウムフタロシアニンの製造方法 | |
JPH01287175A (ja) | ナフタロシアニン化合物 |