CN1304486C - 酞菁化合物,制备该酞菁化合物的方法以及含有该酞菁化合物的光记录介质 - Google Patents
酞菁化合物,制备该酞菁化合物的方法以及含有该酞菁化合物的光记录介质 Download PDFInfo
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- CN1304486C CN1304486C CNB038038838A CN03803883A CN1304486C CN 1304486 C CN1304486 C CN 1304486C CN B038038838 A CNB038038838 A CN B038038838A CN 03803883 A CN03803883 A CN 03803883A CN 1304486 C CN1304486 C CN 1304486C
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- sulfenyl
- phenoxy group
- amino
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- thiophenyl
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- -1 Phthalocyanine compound Chemical class 0.000 title claims abstract description 335
- 230000003287 optical effect Effects 0.000 title claims abstract description 47
- 238000000034 method Methods 0.000 title claims description 30
- 150000001875 compounds Chemical class 0.000 claims abstract description 83
- 239000000203 mixture Substances 0.000 claims abstract description 72
- 229910052751 metal Inorganic materials 0.000 claims abstract description 39
- 239000002184 metal Substances 0.000 claims abstract description 39
- 125000004429 atom Chemical group 0.000 claims abstract description 24
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 24
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 15
- 125000004414 alkyl thio group Chemical group 0.000 claims abstract description 14
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract description 12
- 125000005843 halogen group Chemical group 0.000 claims abstract description 10
- 150000002736 metal compounds Chemical group 0.000 claims abstract description 10
- 125000002813 thiocarbonyl group Chemical group *C(*)=S 0.000 claims abstract description 10
- 125000005110 aryl thio group Chemical group 0.000 claims abstract description 9
- 125000004104 aryloxy group Chemical group 0.000 claims abstract description 9
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 28
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 28
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 21
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 claims description 20
- 150000001721 carbon Chemical group 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 16
- YVNRUPSDZZZUQJ-UHFFFAOYSA-N [O].NC1=CC=CC=C1 Chemical compound [O].NC1=CC=CC=C1 YVNRUPSDZZZUQJ-UHFFFAOYSA-N 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 12
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- 125000003118 aryl group Chemical group 0.000 claims description 10
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 230000002140 halogenating effect Effects 0.000 claims description 8
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 7
- BFSVOASYOCHEOV-UHFFFAOYSA-N 2-diethylaminoethanol Chemical group CCN(CC)CCO BFSVOASYOCHEOV-UHFFFAOYSA-N 0.000 claims description 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 4
- 125000001544 thienyl group Chemical group 0.000 claims description 4
- UGRMITBWUVWUEB-UHFFFAOYSA-N 1-$l^{1}-oxidanyl-3-methylbenzene Chemical group CC1=CC=CC([O])=C1 UGRMITBWUVWUEB-UHFFFAOYSA-N 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 28
- 125000001424 substituent group Chemical group 0.000 abstract description 3
- 150000003457 sulfones Chemical group 0.000 abstract description 2
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- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 1
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- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- IWOKCMBOJXYDEE-UHFFFAOYSA-N sulfinylmethane Chemical group C=S=O IWOKCMBOJXYDEE-UHFFFAOYSA-N 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 57
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- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound 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 19
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- 238000000576 coating method Methods 0.000 description 8
- KTWOOEGAPBSYNW-UHFFFAOYSA-N ferrocene Chemical compound [Fe+2].C=1C=C[CH-]C=1.C=1C=C[CH-]C=1 KTWOOEGAPBSYNW-UHFFFAOYSA-N 0.000 description 8
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- 239000011248 coating agent Substances 0.000 description 6
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- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- 125000004646 sulfenyl group Chemical group S(*)* 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- 125000001246 bromo group Chemical group Br* 0.000 description 5
- 229910052731 fluorine Inorganic materials 0.000 description 5
- JIKUXBYRTXDNIY-UHFFFAOYSA-N n-methyl-n-phenylformamide Chemical compound O=CN(C)C1=CC=CC=C1 JIKUXBYRTXDNIY-UHFFFAOYSA-N 0.000 description 5
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- QEGNUYASOUJEHD-UHFFFAOYSA-N 1,1-dimethylcyclohexane Chemical compound CC1(C)CCCCC1 QEGNUYASOUJEHD-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 4
- 229910052740 iodine Inorganic materials 0.000 description 4
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 238000002310 reflectometry Methods 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- 229920000178 Acrylic resin Polymers 0.000 description 3
- 239000004925 Acrylic resin Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 3
- 230000031709 bromination Effects 0.000 description 3
- 238000005893 bromination reaction Methods 0.000 description 3
- 238000005229 chemical vapour deposition Methods 0.000 description 3
- 125000000058 cyclopentadienyl group Chemical group C1(=CC=CC1)* 0.000 description 3
- 229910010272 inorganic material Inorganic materials 0.000 description 3
- 239000011147 inorganic material Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- MCTALTNNXRUUBZ-UHFFFAOYSA-N molport-000-691-724 Chemical compound [Pd+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 MCTALTNNXRUUBZ-UHFFFAOYSA-N 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 125000001624 naphthyl group Chemical group 0.000 description 3
- 230000010355 oscillation Effects 0.000 description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Substances [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 3
- 238000000746 purification Methods 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 description 2
- HXVNBWAKAOHACI-UHFFFAOYSA-N 2,4-dimethyl-3-pentanone Chemical compound CC(C)C(=O)C(C)C HXVNBWAKAOHACI-UHFFFAOYSA-N 0.000 description 2
- SZNYYWIUQFZLLT-UHFFFAOYSA-N 2-methyl-1-(2-methylpropoxy)propane Chemical compound CC(C)COCC(C)C SZNYYWIUQFZLLT-UHFFFAOYSA-N 0.000 description 2
- BNDRWEVUODOUDW-UHFFFAOYSA-N 3-Hydroxy-3-methylbutan-2-one Chemical compound CC(=O)C(C)(C)O BNDRWEVUODOUDW-UHFFFAOYSA-N 0.000 description 2
- SYBYTAAJFKOIEJ-UHFFFAOYSA-N 3-Methylbutan-2-one Chemical compound CC(C)C(C)=O SYBYTAAJFKOIEJ-UHFFFAOYSA-N 0.000 description 2
- 241000931526 Acer campestre Species 0.000 description 2
- 229910017083 AlN Inorganic materials 0.000 description 2
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- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 229910021617 Indium monochloride Inorganic materials 0.000 description 2
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- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 2
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- VTDVIWPHJXANHZ-UHFFFAOYSA-M chloro(cyclopenta-2,4-dien-1-ylidene)methanolate;cyclopenta-1,3-diene;iron(2+) Chemical compound [Fe+2].C=1C=C[CH-]C=1.[O-]C(Cl)=C1C=CC=C1 VTDVIWPHJXANHZ-UHFFFAOYSA-M 0.000 description 2
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
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- FLLHEJPVLSEJRX-UHFFFAOYSA-N C(CCC)OC(CCCCCC)(OCCCCCC)OCCCCC Chemical compound C(CCC)OC(CCCCCC)(OCCCCCC)OCCCCC FLLHEJPVLSEJRX-UHFFFAOYSA-N 0.000 description 1
- AELZBYQHJCEGBO-UHFFFAOYSA-N CC(C)(C)C[O] Chemical compound CC(C)(C)C[O] AELZBYQHJCEGBO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 241001269238 Data Species 0.000 description 1
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- 230000010748 Photoabsorption Effects 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 229910052581 Si3N4 Inorganic materials 0.000 description 1
- 229910003691 SiBr Inorganic materials 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 229910008449 SnF 2 Inorganic materials 0.000 description 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 1
- 241000270666 Testudines Species 0.000 description 1
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 1
- VVFMKHRTYGDEPI-UHFFFAOYSA-N [Ti]C1=CC=CC=C1 Chemical compound [Ti]C1=CC=CC=C1 VVFMKHRTYGDEPI-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 125000002252 acyl group Chemical group 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- XYOVOXDWRFGKEX-UHFFFAOYSA-N azepine Chemical compound N1C=CC=CC=C1 XYOVOXDWRFGKEX-UHFFFAOYSA-N 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- DMEGYFMYUHOHGS-UHFFFAOYSA-N cycloheptane Chemical compound C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 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
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical compound C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 description 1
- 239000004914 cyclooctane Substances 0.000 description 1
- DIOQZVSQGTUSAI-NJFSPNSNSA-N decane Chemical compound CCCCCCCCC[14CH3] DIOQZVSQGTUSAI-NJFSPNSNSA-N 0.000 description 1
- 230000006837 decompression Effects 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- 229940117389 dichlorobenzene Drugs 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- UHESRSKEBRADOO-UHFFFAOYSA-N ethyl carbamate;prop-2-enoic acid Chemical compound OC(=O)C=C.CCOC(N)=O UHESRSKEBRADOO-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 230000022244 formylation Effects 0.000 description 1
- 238000006170 formylation reaction Methods 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 230000003760 hair shine Effects 0.000 description 1
- 125000001188 haloalkyl group Chemical group 0.000 description 1
- 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 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910017053 inorganic salt Inorganic materials 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 238000007733 ion plating Methods 0.000 description 1
- 229950001891 iprotiazem Drugs 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 125000005647 linker group Chemical group 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- ORUIBWPALBXDOA-UHFFFAOYSA-L magnesium fluoride Chemical compound [F-].[F-].[Mg+2] ORUIBWPALBXDOA-UHFFFAOYSA-L 0.000 description 1
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- XZWYZXLIPXDOLR-UHFFFAOYSA-N metformin Chemical compound CN(C)C(=N)NC(N)=N XZWYZXLIPXDOLR-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- UNBDDZDKBWPHAX-UHFFFAOYSA-N n,n-di(propan-2-yl)formamide Chemical compound CC(C)N(C=O)C(C)C UNBDDZDKBWPHAX-UHFFFAOYSA-N 0.000 description 1
- DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012454 non-polar solvent Substances 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([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])[H] 0.000 description 1
- RNVCVTLRINQCPJ-UHFFFAOYSA-N o-toluidine Chemical compound CC1=CC=CC=C1N RNVCVTLRINQCPJ-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000005447 octyloxy 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])O* 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- 230000000176 photostabilization Effects 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920005672 polyolefin resin Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920005990 polystyrene resin Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- KCTAWXVAICEBSD-UHFFFAOYSA-N prop-2-enoyloxy prop-2-eneperoxoate Chemical compound C=CC(=O)OOOC(=O)C=C KCTAWXVAICEBSD-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 description 1
- 229910010271 silicon carbide Inorganic materials 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000011343 solid material Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 description 1
- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 125000003375 sulfoxide group Chemical group 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- CMJCEVKJYRZMIA-UHFFFAOYSA-M thallium(i) iodide Chemical compound [Tl]I CMJCEVKJYRZMIA-UHFFFAOYSA-M 0.000 description 1
- DZXKSFDSPBRJPS-UHFFFAOYSA-N tin(2+);sulfide Chemical compound [S-2].[Sn+2] DZXKSFDSPBRJPS-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- CMSYDJVRTHCWFP-UHFFFAOYSA-N triphenylphosphane;hydrobromide Chemical compound Br.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 CMSYDJVRTHCWFP-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
- C09B47/18—Obtaining compounds having oxygen atoms directly bound to the phthalocyanine skeleton
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B47/00—Porphines; Azaporphines
- C09B47/04—Phthalocyanines abbreviation: Pc
- C09B47/08—Preparation from other phthalocyanine compounds, e.g. cobaltphthalocyanineamine complex
- C09B47/12—Obtaining compounds having alkyl radicals, or alkyl radicals substituted by hetero atoms, bound to the phthalocyanine skeleton
- C09B47/16—Obtaining compounds having alkyl radicals, or alkyl radicals substituted by hetero atoms, bound to the phthalocyanine skeleton having alkyl radicals substituted by nitrogen atoms
-
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/242—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers
- G11B7/244—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only
- G11B7/246—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes
- G11B7/248—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of recording layers comprising organic materials only containing dyes porphines; azaporphines, e.g. phthalocyanines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Optical Record Carriers And Manufacture Thereof (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Abstract
Description
化合物 | M | X | A | Y | m | Z | n |
(1) | Cu | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 1 | H | 3 |
(2) | Pd | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 1 | H | 3 |
(3) | VO | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 1 | H | 3 |
(4) | FeCl | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 1 | H | 3 |
(5) | Zn | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 1 | H | 3 |
(6) | AlCl | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 1 | H | 3 |
(7) | MnOH | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 1 | H | 3 |
(8) | Cu | OCH[CH(CH3)2]2 | C=S | Fe(Cp)2 | 1 | H | 3 |
(9) | VO | OCH[CH(CH3)2]2 | C=S | Fe(Cp)2 | 1 | H | 3 |
(10) | TiO | OCH[CH(CH3)2]2 | C=S | Fe(Cp)2 | 1 | H | 3 |
(11) | Ni | OCH[CH(CH3)2]2 | C=S | Fe(Cp)2 | 1 | H | 3 |
(12) | Co | OCH[CH(CH3)2]2 | C=S | Fe(Cp)2 | 1 | H | 3 |
(13) | Cu | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 1 | Br,H | 1,2 |
(14) | Zn | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 1 | Br,H | 1,2 |
(15) | Pd | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 1 | Br,H | 2,1 |
(16) | Cu | OCH[CH(CH3)2]2 | SO2 | Fe(Cp)2 | 1 | H | 3 |
(17) | VO | OCH2C(CH3)2 | SO2 | Fe(Cp)2 | 1 | H | 3 |
(18) | GaBr | OCH2C(CH3)2 | SO2 | Fe(Cp)2 | 1 | H | 3 |
(19) | Cu | OCH(CH3)CH2CH(CH3)2 | C=O | Fe(Cp)2 | 1 | H | 3 |
(20) | VO | OCH(CH3)CH2CH(CH3)2 | SO | Fe(Cp)2 | 1 | H | 3 |
(21) | Rh | OCH(CH3)CH2CH(CH3)2 | SO | Fe(Cp)2 | 1 | H | 3 |
(22) | MO | OCH2CH(C2H5)2(CH2)3CH3 | C=NH | Fe(Cp)2 | 1 | H | 3 |
(23) | Cu | OCH2CH(C2H5)2(CH2)3CH3 | C=NH | Fe(Cp)2 | 1 | H | 3 |
(24) | VO | OCH2CH(C2H5)2(CH2)3CH3 | C=NH | Fe(Cp)2 | 1 | H | 3 |
(25) | VO | OCH2CH2CH(CH3)2 | C=NCH3 | Fe(Cp)2 | 1 | H | 3 |
(26) | Cu | OCH2CH2CH(CH3)2 | C=NCH3 | Fe(Cp)2 | 1 | H | 3 |
(27) | Ni | OCH2CH2CH(CH3)2 | C=NCH3 | Fe(Cp)2 | 1 | H | 3 |
(28) | MnOH | OCH2CH2CH(CH3)2 | C=NPh | Fe(Cp)2 | 1 | H | 3 |
(29) | SiCl2 | OCH2CH2CH(CH3)2 | C=NPh | Fe(Cp)2 | 1 | H | 3 |
(30) | ZrCl2 | OCH2CH2CH(CH3)2 | C=NPh | Fe(Cp)2 | 1 | H | 3 |
(31) | AlCl | OCH2CH2CH(CH3)2 | C=NOCH3 | Fe(Cp)2 | 1 | H | 3 |
(32) | GaBr | OCH2CH2CH(CH3)2 | C=NOCH3 | Fe(Cp)2 | 1 | H | 3 |
(33) | Cu | O(CH2)2N(CH3)2 | C=NOCH3 | Fe(Cp)2 | 1 | H | 3 |
(34) | VO | O(CH2)2N(C2H5)2 | C=NOH | Fe(Cp)2 | 1 | H | 3 |
(35) | Co | O(CH2)2N(C2H5)2 | C=NOH | Fe(Cp)2 | 1 | H | 3 |
(36) | InCl | O(CH2)2N(C2H5)2 | C=NOH | Fe(Cp)2 | 1 | H | 3 |
(37) | Cu | C(CH3)3 | C=O | Fe(Cp)2 | 1 | H | 3 |
(38) | VO | C(CH3)3 | C=O | Fe(Cp)2 | 1 | H | 3 |
(39) | Ni | C(CH3)3 | C=O | Fe(Cp)2 | 1 | H | 3 |
化合物 | M | X | A | Y | m | Z | n |
(40) | FeCl | CH(CH3)C2H5 | C=S | Fe(Cp)2 | 1 | H | 3 |
(41) | Cu | CH(CH3)C2H5 | C=S | Fe(Cp)2 | 1 | H | 3 |
(42) | VO | CH(CH3)C2H5 | C=S | Fe(Cp)2 | 1 | H | 3 |
(43) | Co | C(CH3)2(CH2)4CH3 | C=S | Fe(Cp)2 | 1 | H | 3 |
(44) | Sn | C(CH3)2(CH2)4CH3 | C=S | Fe(Cp)2 | 1 | H | 3 |
(45) | Al-Ph | C(CH3)2(CH2)4CH3 | C=S | Fe(Cp)2 | 1 | H | 3 |
(46) | In-Ph | C(CH3)2(CH2)4CH3 | C=S | Fe(Cp)2 | 1 | H | 3 |
(47) | Cu | C(CH3)2(CH2)4CH3 | C=S | Fe(Cp)2 | 1 | H | 3 |
(48) | VO | SCH(C2H5)2 | SO2 | Fe(Cp)2 | 1 | H | 3 |
(49) | Pd | SCH(C2H5)2 | SO2 | Fe(Cp)2 | 1 | H | 3 |
(50) | Cu | SCH(C2H5)2 | SO2 | Fe(Cp)2 | 1 | H | 3 |
(51) | Sn | S(CH2)7CH3 | SO | Fe(Cp)2 | 1 | H | 3 |
(52) | VO | S(CH2)7CH3 | SO | Fe(Cp)2 | 1 | H | 3 |
(53) | FeCl | S(CH2)7CH3 | SO | Fe(Cp)2 | 1 | H | 3 |
(54) | Cu | S(CH2)2N(CH3)2 | C=NH | Fe(Cp)2 | 1 | H | 3 |
(55) | Ni | S(CH2)2N(CH3)2 | C=NH | Fe(Cp)2 | 1 | H | 3 |
(56) | Rh | S(CH2)2N(CH3)2 | C=NH | Fe(Cp)2 | 1 | H | 3 |
(57) | VO | OPhC(CH3)3 | C=NCH3 | Fe(Cp)2 | 1 | H | 3 |
(58) | Cu | OPhC(CH3)3 | C=NCH3 | Fe(Cp)2 | 1 | H | 3 |
(59) | Zn | OPhC(CH3)3 | C=NCH3 | Fe(Cp)2 | 1 | H | 3 |
(60) | VO | SPhC(CH3)3 | C=NPh | Fe(Cp)2 | 1 | H | 3 |
(61) | Cu | SPhC(CH3)3 | C=NPh | Fe(Cp)2 | 1 | H | 3 |
(62) | Pd | SPhC(CH3)3 | C=NPh | Fe(Cp)2 | 1 | H | 3 |
(63) | VO | SPhN(CH3)2 | C=NOH | Fe(Cp)2 | 1 | H | 3 |
(64) | Cu | SPhN(CH3)2 | C=NOH | Fe(Cp)2 | 1 | H | 3 |
(65) | Ni | SPhN(CH3)2 | C=NOH | Fe(Cp)2 | 1 | H | 3 |
(66) | Cu | OCH[CH(CH3)2]2 | C=O | Ru(Cp)2 | 1 | H | 3 |
(67) | VO | OCH[CH(CH3)2]2 | C=O | Ni(Cp)2 | 1 | H | 3 |
(68) | FeCl | OCH[CH(CH3)2]2 | C=O | Co(Cp)2 | 1 | H | 3 |
(69) | Pd | OCH[CH(CH3)2]2 | C=O | W(Cp)2 | 1 | H | 3 |
(70) | Zn | OCH[CH(CH3)2]2 | C=O | Er(Cp)2 | 1 | H | 3 |
(71) | Sn | OCH[CH(CH3)2]2 | C=O | Cr(Cp)2 | 1 | H | 3 |
(72) | Ni | OCH[CH(CH3)2]2 | C=S | Ti(Cp)2(OPh)2 | 1 | H | 3 |
(73) | Cu | OCH[CH(CH3)2]2 | C=S | La(Cp)3 | 1 | H | 3 |
(74) | VO | OCH[CH(CH3)2]2 | C=S | Sc(Cp)3 | 1 | H | 3 |
(75) | Cu | OCH[CH(CH3)2]2 | SO2 | Sc(Cp)3 | 1 | H | 3 |
(76) | VO | OCH[CH(CH3)2]2 | SO2 | Er(Cp)2 | 1 | H | 3 |
(77) | FeCl | OCH[CH(CH3)2]2 | SO2 | W(Cp)2 | 1 | H | 3 |
(78) | Cu | OCH[CH(CH3)2]2 | C=O | Co(Cp)2 | 1 | Br,H | 1,2 |
(79) | VO | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 1 | Br,H | 1,2 |
(80) | Pd | OCH[CH(CH3)2]2 | C=O | Er(Cp)2 | 1 | Br,H | 1,2 |
(81) | Cu | OCH[CH(CH3)2]2 | C=S | Fe(Cp)2 | 1 | Br,H | 1,2 |
(82) | VO | OCH[CH(CH3)2]2 | C=S | W(Cp)2 | 1 | Br,H | 1,2 |
(83) | Ni | OCH[CH(CH3)2]2 | C=S | Sc(Cp)3 | 1 | Br,H | 1,2 |
(84) | Cu | OCH[CH(CH3)2]2 | SO2 | Fe(Cp)2 | 1 | Br,H | 1,2 |
(85) | VO | OCH[CH(CH3)2]2 | SO2 | Fe(Cp)2 | 1 | Br,H | 1,2 |
(86) | Pb | OCH[CH(CH3)2]2 | SO2 | Co(Cp)2 | 1 | Br,H | 1,2 |
(87) | Pd | OCH[CH(CH3)2]2 | C=NH | Fe(Cp)2 | 1 | Br,H | 1,2 |
(88) | Cu | OCH[CH(CH3)2]2 | C=NH | La(Cp)3 | 1 | Br,H | 1,2 |
(89) | Co | OCH[CH(CH3)2]2 | C=NH | Ti(Cp)2(OPh)2 | 1 | Br,H | 1,2 |
化合物 | M | X | A | Y | m | Z | n |
(90) | InCl | SPhC(CH3)3 | C=O | Fe(Cp)2 | 1 | Br,H | 1,2 |
(91) | VO | SPhC(CH3)3 | C=O | Fe(Cp)2 | 1 | Br,H | 1,2 |
(92) | Cu | SPhC(CH3)3 | C=O | Fe(Cp)2 | 1 | Br,H | 1,2 |
(93) | Ni | SPhC(CH3)3 | C=S | Co(Cp)2 | 1 | Br,H | 1,2 |
(94) | Pb | SPhC(CH3)3 | C=S | Sc(Cp)3 | 1 | Br,H | 1,2 |
(95) | FeCl | SPhC(CH3)3 | C=S | W(Cp)2 | 1 | Br,H | 1,2 |
(96) | VO | SPhC(CH3)3 | SO2 | Fe(Cp)2 | 1 | Br,H | 1,2 |
(97) | Cu | SPhC(CH3)3 | SO2 | La(Cp)3 | 1 | Br,H | 1,2 |
(98) | Co | SPhC(CH3)3 | SO2 | Er(Cp)2 | 1 | Br,H | 1,2 |
(99) | AlCl | SPhC(CH3)3 | SO2 | Ti(Cp)2(OPh)2 | 1 | Br,H | 1,2 |
(100) | TiO | SPhC(CH3)3 | SO2 | Ti(Cp)2(OPh)2 | 1 | Br,H | 1,2 |
(101) | Cu | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 2 | H | 2 |
(102) | VO | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | 2 | H | 2 |
(103) | Cu | OCH[CH(CH3)2]2 | C=S | Fe(Cp)2 | 2 | H | 2 |
(104) | VO | OCH[CH(CH3)2]2 | C=S | Fe(Cp)2 | 2 | H | 2 |
(105) | Cu | OCH[CH(CH3)2]2 | SO2 | Fe(Cp)2 | 2 | H | 2 |
化合物 | M | X | A | Y | R | I | Z | n |
(106) | Cu | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | CH3,Ph | 1 | H | 3 |
(107) | Cu | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | CH3,CH3 | 1 | H | 3 |
(108) | Cu | OCH[CH(CH3)2]2 | C=S | Fe(Cp)2 | CH3,Ph | 1 | H | 3 |
(109) | Cu | OCH[CH(CH3)2]2 | C=S | Fe(Cp)2 | CH3,CH3 | 1 | H | 3 |
(110) | Pd | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | CH3,Ph | 1 | H | 3 |
(111) | Pd | OCH[CH(CH3)2]2 | C=S | Fe(Cp)2 | CH3,Ph | 1 | H | 3 |
(112) | Pd | OCH[CH(CH3)2]2 | C=O | Fe(Cp)2 | CH3,Ph | 1 | H,Br | 2,1 |
化合物 | M | X | Z | n |
(113) | Cu | OCH[CH(CH3)2]2 | H | 4 |
(114) | Cu | OCH[CH(CH3)2]2 | H,Br | 3,1 |
(115) | Cu | OCH[CH(CH3)2]2 | H,Br | 2,2 |
(116) | Pd | OCH[CH(CH3)2]2 | H | 4 |
(117) | Pd | OCH[CH(CH3)2]2 | H,Br | 3,1 |
(118) | Pd | OCH[CH(CH3)2]2 | H,Br | 2,2 |
(119) | Cu | OCH[CH(CH3)2]2 | H,NO2 | 3,1 |
混合物 | 酞善化合物(A) | 酞菁化合物(B) | 酞菁化合物(C) | 混合比率(LC),(A)/(B)/(C) |
(120) | (1)&(101) | (106) | (113) | 62/11/24 |
(121) | (1)&(101) | (106) | (113) | 45/10/44 |
(122) | (2) | (110) | (116) | 80/8/11 |
(123) | (2) | (110) | (116) | 61/10/26 |
(124) | (15)* | (112)* | (118)* | 50/5/47* |
(125) | (8)&(103) | (108) | (113) | 68/14/15 |
BETA=0% | BETA=10% | ||||||
记录激光功率 | 抖动 | 记录激光功率 | 抖动 | 实施例号 | |||
灵敏度 | 3T刻痕 | 3T槽脊 | 灵敏度 | 3T刻痕 | 3T槽脊 | 化合物/混合物 | |
实施例9 | ○ | ○ | ○ | ○ | ○ | ○ | (120) |
实施例10 | ○ | ○ | ○ | ○ | ○ | ○ | (125) |
实施例11 | ○ | ○ | ○ | ○ | ○ | ○ | (124) |
实施例12 | ○ | ○ | ○ | ○ | ○ | ○ | (121) |
实施例13 | ○ | ○ | ○ | ○ | ○ | ○ | (1) |
实施例14 | ○ | ○ | ○ | ○ | ○ | ○ | (8) |
实施例15 | ○ | ○ | ○ | ○ | ○ | ○ | (106) |
实施例16 | ○ | ○ | ○ | ○ | ○ | ○ | (108) |
实施例17 | ○ | ○ | ○ | ○ | ○ | ○ | (50) |
实施例18 | ○ | ○ | ○ | ○ | ○ | ○ | (66) |
实施例19 | ○ | ○ | ○ | ○ | ○ | ○ | (87) |
实施例20 | ○ | ○ | ○ | ○ | ○ | ○ | (89) |
实施例21 | ○ | ○ | ○ | ○ | ○ | ○ | (103) |
对比例1 | × | × | × | × | × | × | |
对比例2 | × | ○ | ○ | × | × | × |
Claims (6)
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JP39143/2002 | 2002-02-15 | ||
JP2002039143 | 2002-02-15 | ||
JP253836/2002 | 2002-08-30 | ||
JP2002253836 | 2002-08-30 |
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CN1633475A CN1633475A (zh) | 2005-06-29 |
CN1304486C true CN1304486C (zh) | 2007-03-14 |
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US (1) | US7332261B2 (zh) |
EP (1) | EP1482013B1 (zh) |
JP (1) | JP4220904B2 (zh) |
KR (1) | KR100957474B1 (zh) |
CN (1) | CN1304486C (zh) |
AT (1) | ATE367421T1 (zh) |
AU (1) | AU2003211973A1 (zh) |
DE (1) | DE60314998T2 (zh) |
HK (1) | HK1071154A1 (zh) |
TW (1) | TW593562B (zh) |
WO (1) | WO2003068865A1 (zh) |
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GB0225471D0 (en) * | 2002-11-01 | 2002-12-11 | Ciba Sc Holding Ag | Solvent composition and use thereof |
GB2426760B (en) * | 2005-05-25 | 2007-12-19 | Yen Cheng Tsai | Ferrocenylphthalocyanines and their use in optical recording media |
DE102008036670B3 (de) * | 2008-08-06 | 2009-11-26 | Leonhard Kurz Stiftung & Co. Kg | Folie, Verfahren zu deren Herstellung, sowie Verwendung |
EP2154140A1 (en) * | 2008-08-14 | 2010-02-17 | Orgchem Technologies, Inc. | Metallocenyl phthalocyanine compounds and use thereof in optical recording media |
US8206502B2 (en) * | 2008-12-15 | 2012-06-26 | Eastman Kodak Company | Titanyl phthalocyanine with improved milling properties |
JP6406863B2 (ja) * | 2014-04-24 | 2018-10-17 | キヤノン株式会社 | 電子写真感光体、電子写真感光体の製造方法、プロセスカートリッジおよび電子写真装置、ならびに、フタロシアニン結晶、フタロシアニン結晶の製造方法 |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4529688A (en) * | 1983-10-13 | 1985-07-16 | Xerox Corporation | Infrared sensitive phthalocyanine compositions |
JPH05247363A (ja) * | 1991-06-21 | 1993-09-24 | Mitsui Toatsu Chem Inc | フタロシアニン化合物またはその混合物のアモルファス体、及びその製造方法 |
CN1169128A (zh) * | 1995-12-25 | 1997-12-31 | 东洋油墨制造株式会社 | 光记录材料和光记录介质 |
EP0896327A1 (en) * | 1997-07-31 | 1999-02-10 | Ricoh Company, Ltd. | Optical information recording medium and method of producing the same |
JPH1148612A (ja) * | 1997-08-01 | 1999-02-23 | Mitsui Chem Inc | 光記録媒体 |
WO2000009522A1 (en) * | 1998-08-11 | 2000-02-24 | Ciba Specialty Chemicals Holding Inc. | Metallocenyl-phthalocyanines |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3315498B2 (ja) | 1992-12-02 | 2002-08-19 | 三井化学株式会社 | 光情報記録媒体、光情報記録媒体の記録層用組成物及び光情報記録媒体の製造方法 |
JPH08118800A (ja) | 1994-10-19 | 1996-05-14 | Mitsui Toatsu Chem Inc | 光記録媒体 |
US5683855A (en) * | 1995-03-09 | 1997-11-04 | Tdk Corporation | Printable members |
JPH0958123A (ja) | 1995-08-22 | 1997-03-04 | Mitsubishi Chem Corp | 光記録媒体 |
JP3666152B2 (ja) | 1996-12-18 | 2005-06-29 | 三菱化学株式会社 | 光記録媒体 |
JP3573600B2 (ja) | 1997-07-07 | 2004-10-06 | 富士写真フイルム株式会社 | 光情報記録媒体 |
JPH1170732A (ja) | 1997-08-28 | 1999-03-16 | Mitsubishi Chem Corp | 光学記録媒体 |
JP2002188018A (ja) | 2000-12-20 | 2002-07-05 | Mitsui Chemicals Inc | フタロシアニン化合物及びそれを用いた光記録媒体 |
JP2003072238A (ja) | 2001-09-03 | 2003-03-12 | Mitsui Chemicals Inc | 光記録媒体 |
JP4259849B2 (ja) * | 2002-10-24 | 2009-04-30 | 三井化学株式会社 | イミノメチル置換フタロシアニン化合物、及びこれを用いるメタロセン置換フタロシアニン化合物の製造方法 |
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2003
- 2003-02-14 AT AT03705136T patent/ATE367421T1/de not_active IP Right Cessation
- 2003-02-14 AU AU2003211973A patent/AU2003211973A1/en not_active Abandoned
- 2003-02-14 KR KR1020047012552A patent/KR100957474B1/ko not_active IP Right Cessation
- 2003-02-14 CN CNB038038838A patent/CN1304486C/zh not_active Expired - Fee Related
- 2003-02-14 DE DE60314998T patent/DE60314998T2/de not_active Expired - Lifetime
- 2003-02-14 US US10/504,089 patent/US7332261B2/en not_active Expired - Fee Related
- 2003-02-14 WO PCT/JP2003/001517 patent/WO2003068865A1/ja active IP Right Grant
- 2003-02-14 JP JP2003567982A patent/JP4220904B2/ja not_active Expired - Fee Related
- 2003-02-14 EP EP03705136A patent/EP1482013B1/en not_active Expired - Lifetime
- 2003-02-17 TW TW092103204A patent/TW593562B/zh not_active IP Right Cessation
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Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4529688A (en) * | 1983-10-13 | 1985-07-16 | Xerox Corporation | Infrared sensitive phthalocyanine compositions |
JPH05247363A (ja) * | 1991-06-21 | 1993-09-24 | Mitsui Toatsu Chem Inc | フタロシアニン化合物またはその混合物のアモルファス体、及びその製造方法 |
CN1169128A (zh) * | 1995-12-25 | 1997-12-31 | 东洋油墨制造株式会社 | 光记录材料和光记录介质 |
EP0896327A1 (en) * | 1997-07-31 | 1999-02-10 | Ricoh Company, Ltd. | Optical information recording medium and method of producing the same |
JPH1148612A (ja) * | 1997-08-01 | 1999-02-23 | Mitsui Chem Inc | 光記録媒体 |
WO2000009522A1 (en) * | 1998-08-11 | 2000-02-24 | Ciba Specialty Chemicals Holding Inc. | Metallocenyl-phthalocyanines |
Also Published As
Publication number | Publication date |
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EP1482013B1 (en) | 2007-07-18 |
ATE367421T1 (de) | 2007-08-15 |
DE60314998T2 (de) | 2008-04-03 |
CN1633475A (zh) | 2005-06-29 |
EP1482013A1 (en) | 2004-12-01 |
US20050201265A1 (en) | 2005-09-15 |
AU2003211973A1 (en) | 2003-09-04 |
TW593562B (en) | 2004-06-21 |
JP4220904B2 (ja) | 2009-02-04 |
US7332261B2 (en) | 2008-02-19 |
KR20040091039A (ko) | 2004-10-27 |
DE60314998D1 (de) | 2007-08-30 |
JPWO2003068865A1 (ja) | 2005-06-02 |
KR100957474B1 (ko) | 2010-05-14 |
HK1071154A1 (en) | 2005-07-08 |
WO2003068865A1 (fr) | 2003-08-21 |
EP1482013A4 (en) | 2005-06-15 |
TW200302854A (en) | 2003-08-16 |
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