JPS6033552A - カラ−画像形成方法 - Google Patents

カラ−画像形成方法

Info

Publication number: JPS6033552A
Authority: JP; Japan
Prior art keywords: group; coupler; color; page; acid
Prior art date: 1983-08-04
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

Application number

JP14280183A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0365529B2 (fr

Inventor

Toshio Kawagishi

俊雄川岸

Tadahisa Sato

忠久佐藤

Nobuo Koyakata

古舘　信生

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Fujifilm Holdings Corp

Original Assignee

Fuji Photo Film Co Ltd

Priority date (The priority date 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 date listed.)

1983-08-04

Filing date

1983-08-04

Publication date

1985-02-20

1983-08-04 Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd

1983-08-04 Priority to JP14280183A priority Critical patent/JPS6033552A/ja

1985-02-20 Publication of JPS6033552A publication Critical patent/JPS6033552A/ja

1991-10-14 Publication of JPH0365529B2 publication Critical patent/JPH0365529B2/ja

Status Granted legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims abstract description 61
229910052709 silver Inorganic materials 0.000 claims abstract description 27
239000004332 silver Substances 0.000 claims abstract description 27
239000003795 chemical substances by application Substances 0.000 claims abstract description 11
125000001424 substituent group Chemical group 0.000 claims abstract description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 15
150000001412 amines Chemical class 0.000 claims description 7
230000003647 oxidation Effects 0.000 claims description 3
238000007254 oxidation reaction Methods 0.000 claims description 3
-1 aromatic primary amine Chemical class 0.000 abstract description 103
230000015572 biosynthetic process Effects 0.000 abstract description 13
239000000463 material Substances 0.000 abstract description 13
238000005859 coupling reaction Methods 0.000 abstract description 12
238000010168 coupling process Methods 0.000 abstract description 7
230000008878 coupling Effects 0.000 abstract description 6
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 abstract description 4
KNPMOBYRBAKHIM-UHFFFAOYSA-N 3h-pyrazolo[5,1-e]tetrazole Chemical group N1N=NN2N=CC=C21 KNPMOBYRBAKHIM-UHFFFAOYSA-N 0.000 abstract 1
239000000975 dye Substances 0.000 description 34
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 24
239000000839 emulsion Substances 0.000 description 22
150000001875 compounds Chemical class 0.000 description 21
235000013339 cereals Nutrition 0.000 description 14
125000003118 aryl group Chemical group 0.000 description 13
239000010410 layer Substances 0.000 description 13
229920000642 polymer Polymers 0.000 description 13
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 13
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 12
238000003786 synthesis reaction Methods 0.000 description 12
108010010803 Gelatin Proteins 0.000 description 10
238000010521 absorption reaction Methods 0.000 description 10
239000002253 acid Substances 0.000 description 10
239000008273 gelatin Substances 0.000 description 10
229920000159 gelatin Polymers 0.000 description 10
235000019322 gelatine Nutrition 0.000 description 10
235000011852 gelatine desserts Nutrition 0.000 description 10
229910052757 nitrogen Inorganic materials 0.000 description 9
239000000243 solution Substances 0.000 description 9
238000011161 development Methods 0.000 description 8
125000000623 heterocyclic group Chemical group 0.000 description 8
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 8
150000003839 salts Chemical class 0.000 description 8
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 8
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 7
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 7
125000000217 alkyl group Chemical group 0.000 description 7
239000000084 colloidal system Substances 0.000 description 7
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 7
150000003536 tetrazoles Chemical class 0.000 description 7
WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
238000000862 absorption spectrum Methods 0.000 description 6
QTBSBXVTEAMEQO-UHFFFAOYSA-N acetic acid Substances CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
239000007864 aqueous solution Substances 0.000 description 6
230000000052 comparative effect Effects 0.000 description 6
239000000203 mixture Substances 0.000 description 6
125000004433 nitrogen atom Chemical group N* 0.000 description 6
239000003960 organic solvent Substances 0.000 description 6
239000000047 product Substances 0.000 description 6
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 5
210000000988 bone and bone Anatomy 0.000 description 5
238000002156 mixing Methods 0.000 description 5
239000000178 monomer Substances 0.000 description 5
125000004430 oxygen atom Chemical group O* 0.000 description 5
230000001235 sensitizing effect Effects 0.000 description 5
239000000126 substance Substances 0.000 description 5
125000003396 thiol group Chemical group [H]S* 0.000 description 5
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 4
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 4
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 4
125000003545 alkoxy group Chemical group 0.000 description 4
125000002947 alkylene group Chemical group 0.000 description 4
125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 4
238000009835 boiling Methods 0.000 description 4
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 4
229910052801 chlorine Inorganic materials 0.000 description 4
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical class OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 4
150000002148 esters Chemical class 0.000 description 4
150000004820 halides Chemical class 0.000 description 4
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 4
239000002245 particle Substances 0.000 description 4
125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 4
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 4
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
239000002904 solvent Substances 0.000 description 4
229920002554 vinyl polymer Polymers 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
125000004442 acylamino group Chemical group 0.000 description 3
125000004466 alkoxycarbonylamino group Chemical group 0.000 description 3
125000004414 alkyl thio group Chemical group 0.000 description 3
150000001408 amides Chemical class 0.000 description 3
125000005110 aryl thio group Chemical group 0.000 description 3
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
125000001309 chloro group Chemical group Cl* 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
239000013078 crystal Substances 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
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 3
229940079593 drug Drugs 0.000 description 3
239000003814 drug Substances 0.000 description 3
229910052736 halogen Inorganic materials 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
PTFYQSWHBLOXRZ-UHFFFAOYSA-N imidazo[4,5-e]indazole Chemical compound C1=CC2=NC=NC2=C2C=NN=C21 PTFYQSWHBLOXRZ-UHFFFAOYSA-N 0.000 description 3
125000005462 imide group Chemical group 0.000 description 3
239000003112 inhibitor Substances 0.000 description 3
229910052742 iron Inorganic materials 0.000 description 3
239000007788 liquid Substances 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
IPSIPYMEZZPCPY-UHFFFAOYSA-N new fuchsin Chemical compound [Cl-].C1=CC(=[NH2+])C(C)=CC1=C(C=1C=C(C)C(N)=CC=1)C1=CC=C(N)C(C)=C1 IPSIPYMEZZPCPY-UHFFFAOYSA-N 0.000 description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
238000012545 processing Methods 0.000 description 3
238000006722 reduction reaction Methods 0.000 description 3
235000010265 sodium sulphite Nutrition 0.000 description 3
239000003381 stabilizer Substances 0.000 description 3
229910052717 sulfur Inorganic materials 0.000 description 3
238000005406 washing Methods 0.000 description 3
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 2
SZTBMYHIYNGYIA-UHFFFAOYSA-N 2-chloroacrylic acid Chemical compound OC(=O)C(Cl)=C SZTBMYHIYNGYIA-UHFFFAOYSA-N 0.000 description 2
XLLIQLLCWZCATF-UHFFFAOYSA-N 2-methoxyethyl acetate Chemical compound COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 description 2
PCLIMKBDDGJMGD-UHFFFAOYSA-N N-bromosuccinimide Chemical compound BrN1C(=O)CCC1=O PCLIMKBDDGJMGD-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
229910021607 Silver chloride Inorganic materials 0.000 description 2
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 2
125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
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125000002252 acyl group Chemical group 0.000 description 2
125000004423 acyloxy group Chemical group 0.000 description 2
125000004453 alkoxycarbonyl group Chemical group 0.000 description 2
125000005162 aryl oxy carbonyl amino group Chemical group 0.000 description 2
QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 2
JEHKKBHWRAXMCH-UHFFFAOYSA-N benzenesulfinic acid Chemical compound O[S@@](=O)C1=CC=CC=C1 JEHKKBHWRAXMCH-UHFFFAOYSA-N 0.000 description 2
125000003354 benzotriazolyl group Chemical class N1N=NC2=C1C=CC=C2* 0.000 description 2
235000019445 benzyl alcohol Nutrition 0.000 description 2
238000004061 bleaching Methods 0.000 description 2
239000007844 bleaching agent Substances 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
239000001273 butane Substances 0.000 description 2
CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
238000004040 coloring Methods 0.000 description 2
229920001577 copolymer Polymers 0.000 description 2
125000004093 cyano group Chemical group *C#N 0.000 description 2
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
238000000921 elemental analysis Methods 0.000 description 2
239000003480 eluent Substances 0.000 description 2
FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 2
230000001747 exhibiting effect Effects 0.000 description 2
238000010528 free radical solution polymerization reaction Methods 0.000 description 2
125000005843 halogen group Chemical group 0.000 description 2
125000005842 heteroatom Chemical group 0.000 description 2
238000005984 hydrogenation reaction Methods 0.000 description 2
238000003384 imaging method Methods 0.000 description 2
159000000014 iron salts Chemical class 0.000 description 2
150000002576 ketones Chemical class 0.000 description 2
125000005647 linker group Chemical group 0.000 description 2
DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 2
UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 0.000 description 2
OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 2
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 2
YRVUCYWJQFRCOB-UHFFFAOYSA-N n-butylprop-2-enamide Chemical compound CCCCNC(=O)C=C YRVUCYWJQFRCOB-UHFFFAOYSA-N 0.000 description 2
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
150000002825 nitriles Chemical class 0.000 description 2
125000001820 oxy group Chemical group [*:1]O[*:2] 0.000 description 2
JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
238000006116 polymerization reaction Methods 0.000 description 2
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
239000000843 powder Substances 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical compound N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 2
238000010898 silica gel chromatography Methods 0.000 description 2
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 2
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 2
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 2
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 2
239000011734 sodium Substances 0.000 description 2
VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
230000003595 spectral effect Effects 0.000 description 2
238000003756 stirring Methods 0.000 description 2
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125000000565 sulfonamide group Chemical group 0.000 description 2
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239000011593 sulfur Substances 0.000 description 2
125000004434 sulfur atom Chemical group 0.000 description 2
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 2
238000001308 synthesis method Methods 0.000 description 2
125000004149 thio group Chemical group *S* 0.000 description 2
NWZSZGALRFJKBT-KNIFDHDWSA-N (2s)-2,6-diaminohexanoic acid;(2s)-2-hydroxybutanedioic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O.NCCCC[C@H](N)C(O)=O NWZSZGALRFJKBT-KNIFDHDWSA-N 0.000 description 1
BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical class C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
YHMYGUUIMTVXNW-UHFFFAOYSA-N 1,3-dihydrobenzimidazole-2-thione Chemical class C1=CC=C2NC(S)=NC2=C1 YHMYGUUIMTVXNW-UHFFFAOYSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
OZFIGURLAJSLIR-UHFFFAOYSA-N 1-ethenyl-2h-pyridine Chemical compound C=CN1CC=CC=C1 OZFIGURLAJSLIR-UHFFFAOYSA-N 0.000 description 1
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 1
ZFYKDNCOQBBOST-UHFFFAOYSA-N 1-phenylbut-3-en-1-one Chemical compound C=CCC(=O)C1=CC=CC=C1 ZFYKDNCOQBBOST-UHFFFAOYSA-N 0.000 description 1
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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
229940093915 gynecological organic acid Drugs 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
230000002140 halogenating effect Effects 0.000 description 1
150000002367 halogens Chemical group 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hcl hcl Chemical compound Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
CRPAPNNHNVVYKL-UHFFFAOYSA-N hexadecane-1-sulfonamide Chemical group CCCCCCCCCCCCCCCCS(N)(=O)=O CRPAPNNHNVVYKL-UHFFFAOYSA-N 0.000 description 1
GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 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
229920001519 homopolymer Polymers 0.000 description 1
IKDUDTNKRLTJSI-UHFFFAOYSA-N hydrazine monohydrate Substances O.NN IKDUDTNKRLTJSI-UHFFFAOYSA-N 0.000 description 1
150000002430 hydrocarbons Chemical group 0.000 description 1
125000001165 hydrophobic group Chemical group 0.000 description 1
AKCUHGBLDXXTOM-UHFFFAOYSA-N hydroxy-oxo-phenyl-sulfanylidene-$l^{6}-sulfane Chemical class SS(=O)(=O)C1=CC=CC=C1 AKCUHGBLDXXTOM-UHFFFAOYSA-N 0.000 description 1
NXPHCVPFHOVZBC-UHFFFAOYSA-N hydroxylamine;sulfuric acid Chemical compound ON.OS(O)(=O)=O NXPHCVPFHOVZBC-UHFFFAOYSA-N 0.000 description 1
150000002460 imidazoles Chemical class 0.000 description 1
125000002883 imidazolyl group Chemical group 0.000 description 1
RSAZYXZUJROYKR-UHFFFAOYSA-N indophenol Chemical compound C1=CC(O)=CC=C1N=C1C=CC(=O)C=C1 RSAZYXZUJROYKR-UHFFFAOYSA-N 0.000 description 1
239000003999 initiator Substances 0.000 description 1
229940079865 intestinal antiinfectives imidazole derivative Drugs 0.000 description 1
150000004694 iodide salts Chemical class 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000002563 ionic surfactant Substances 0.000 description 1
150000002503 iridium Chemical class 0.000 description 1
QRXWMOHMRWLFEY-UHFFFAOYSA-N isoniazide Chemical compound NNC(=O)C1=CC=NC=C1 QRXWMOHMRWLFEY-UHFFFAOYSA-N 0.000 description 1
239000004816 latex Substances 0.000 description 1
229920000126 latex Polymers 0.000 description 1
PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
239000011976 maleic acid Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
239000001630 malic acid Substances 0.000 description 1
235000011090 malic acid Nutrition 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical group CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 description 1
125000001434 methanylylidene group Chemical group [H]C#[*] 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
125000006626 methoxycarbonylamino group Chemical group 0.000 description 1
WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 1
238000005065 mining Methods 0.000 description 1
239000011259 mixed solution Substances 0.000 description 1
FGTVYMTUTYLLQR-UHFFFAOYSA-N n-ethyl-1-phenylmethanesulfonamide Chemical group CCNS(=O)(=O)CC1=CC=CC=C1 FGTVYMTUTYLLQR-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 1
150000002832 nitroso derivatives Chemical class 0.000 description 1
238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
SYQMMCZWJAEWEK-UHFFFAOYSA-N octadecane-1-sulfonamide Chemical group CCCCCCCCCCCCCCCCCCS(N)(=O)=O SYQMMCZWJAEWEK-UHFFFAOYSA-N 0.000 description 1
WTBAHSZERDXKKZ-UHFFFAOYSA-N octadecanoyl chloride Chemical compound CCCCCCCCCCCCCCCCCC(Cl)=O WTBAHSZERDXKKZ-UHFFFAOYSA-N 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
QWOKKHXWFDAJCZ-UHFFFAOYSA-N octane-1-sulfonamide Chemical group CCCCCCCCS(N)(=O)=O QWOKKHXWFDAJCZ-UHFFFAOYSA-N 0.000 description 1
VECVSKFWRQYTAL-UHFFFAOYSA-N octyl benzoate Chemical compound CCCCCCCCOC(=O)C1=CC=CC=C1 VECVSKFWRQYTAL-UHFFFAOYSA-N 0.000 description 1
ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
150000004965 peroxy acids Chemical class 0.000 description 1
150000004986 phenylenediamines Chemical class 0.000 description 1
125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000172 poly(styrenesulfonic acid) Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
229940005642 polystyrene sulfonic acid Drugs 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000003755 preservative agent Substances 0.000 description 1
230000002265 prevention Effects 0.000 description 1
150000003142 primary aromatic amines Chemical class 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
PNXMTCDJUBJHQJ-UHFFFAOYSA-N propyl prop-2-enoate Chemical compound CCCOC(=O)C=C PNXMTCDJUBJHQJ-UHFFFAOYSA-N 0.000 description 1
239000011241 protective layer Substances 0.000 description 1
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
NDGRWYRVNANFNB-UHFFFAOYSA-N pyrazolidin-3-one Chemical class O=C1CCNN1 NDGRWYRVNANFNB-UHFFFAOYSA-N 0.000 description 1
125000003226 pyrazolyl group Chemical group 0.000 description 1
HBCQSNAFLVXVAY-UHFFFAOYSA-N pyrimidine-2-thiol Chemical class SC1=NC=CC=N1 HBCQSNAFLVXVAY-UHFFFAOYSA-N 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
150000004053 quinones Chemical class 0.000 description 1
230000005855 radiation Effects 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
238000006479 redox reaction Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical group [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
230000005070 ripening Effects 0.000 description 1
239000012266 salt solution Substances 0.000 description 1
238000004062 sedimentation Methods 0.000 description 1
230000035945 sensitivity Effects 0.000 description 1
230000008313 sensitization Effects 0.000 description 1
229940045105 silver iodide Drugs 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000012279 sodium borohydride Substances 0.000 description 1
229910000033 sodium borohydride Inorganic materials 0.000 description 1
APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
239000004317 sodium nitrate Substances 0.000 description 1
235000010344 sodium nitrate Nutrition 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
125000004079 stearyl 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])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])[H] 0.000 description 1
239000010959 steel Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
125000005504 styryl group Chemical group 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
125000001174 sulfone group Chemical group 0.000 description 1
125000004354 sulfur functional group Chemical group 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
239000011975 tartaric acid Substances 0.000 description 1
235000002906 tartaric acid Nutrition 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
150000003475 thallium Chemical class 0.000 description 1
JJJPTTANZGDADF-UHFFFAOYSA-N thiadiazole-4-thiol Chemical class SC1=CSN=N1 JJJPTTANZGDADF-UHFFFAOYSA-N 0.000 description 1
150000003557 thiazoles Chemical class 0.000 description 1
125000001544 thienyl group Chemical group 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
125000005323 thioketone group Chemical group 0.000 description 1
150000004886 thiomorpholines Chemical class 0.000 description 1
ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
125000005147 toluenesulfonyl group Chemical group C=1(C(=CC=CC1)S(=O)(=O)*)C 0.000 description 1
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
125000002889 tridecyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
150000003639 trimesic acids Chemical class 0.000 description 1
239000006097 ultraviolet radiation absorber Substances 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
150000003673 urethanes Chemical class 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1

Classifications

- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/32—Colour coupling substances
- G03C7/36—Couplers containing compounds with active methylene groups
- G03C7/38—Couplers containing compounds with active methylene groups in rings
- G03C7/381—Heterocyclic compounds
- G03C7/382—Heterocyclic compounds with two heterocyclic rings
- G03C7/3825—Heterocyclic compounds with two heterocyclic rings the nuclei containing only nitrogen as hetero atoms

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

JP14280183A 1983-08-04 1983-08-04 カラ−画像形成方法 Granted JPS6033552A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP14280183A JPS6033552A (ja)	1983-08-04	1983-08-04	カラ−画像形成方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP14280183A JPS6033552A (ja)	1983-08-04	1983-08-04	カラ−画像形成方法

Publications (2)

Publication Number	Publication Date
JPS6033552A true JPS6033552A (ja)	1985-02-20
JPH0365529B2 JPH0365529B2 (fr)	1991-10-14

Family

ID=15323945

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP14280183A Granted JPS6033552A (ja)	1983-08-04	1983-08-04	カラ−画像形成方法

Country Status (1)

Country	Link
JP (1)	JPS6033552A (fr)

Cited By (49)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS61156048A (ja) *	1984-12-27	1986-07-15	Konishiroku Photo Ind Co Ltd	ハロゲン化銀写真感光材料
JPS61249968A (ja) *	1985-04-29	1986-11-07	Konishiroku Photo Ind Co Ltd	５−ヒドラジノ−１ｈ−ピラゾ−ル系化合物
EP0201033A2 (fr)	1985-04-30	1986-11-12	Konica Corporation	Procédé de traitement de matériaux photographiques couleurs à l'halogénure d'argent
EP0202616A2 (fr)	1985-05-16	1986-11-26	Konica Corporation	Procédé pour le développement couleur d'un matériau photographique à l'halogénure d'argent sensible à la lumière
JPS6210069A (ja) *	1985-07-05	1987-01-19	Konishiroku Photo Ind Co Ltd	５―アミノ―１ｈ―ピラゾール系化合物を用いる写真用マゼンタカプラーの合成方法
JPS62153953A (ja) *	1985-12-27	1987-07-08	Fuji Photo Film Co Ltd	カラ−写真感光材料
JPS62163052A (ja) *	1986-01-11	1987-07-18	Konishiroku Photo Ind Co Ltd	ハロゲン化銀写真感光材料
JPS62195659A (ja) *	1986-02-24	1987-08-28	Konishiroku Photo Ind Co Ltd	５−アミノ−１ｈ−ピラゾ−ル系化合物
JPS62228066A (ja) *	1986-02-24	1987-10-06	Konika Corp	５−ヒドラジノ−１ｈ−ピラゾ−ル系化合物
EP0242013A2 (fr)	1986-01-20	1987-10-21	Konica Corporation	Matériau photographique couleur à l'halogénure d'argent sensible à la lumière
JPS62252773A (ja) *	1986-03-29	1987-11-04	アグフア−ゲヴエルト・アクチエンゲゼルシヤフト	４−ハロゲン−ピラゾロン−５のイミノ誘導体及びその製造法
JPS6324251A (ja) *	1986-07-17	1988-02-01	Fuji Photo Film Co Ltd	カラ−写真感光材料
JPS63145281A (ja) *	1986-12-09	1988-06-17	Fuji Photo Film Co Ltd	ピラゾロアゾールアゾメチンシアン染料
EP0317983A2 (fr)	1987-11-27	1989-05-31	Fuji Photo Film Co., Ltd.	Matériau photographique couleur à l'halogénure d'argent
EP0320939A2 (fr)	1987-12-15	1989-06-21	Fuji Photo Film Co., Ltd.	Matériau photographique couleur à l'halogénure d'argent
EP0435334A2 (fr)	1989-12-29	1991-07-03	Fuji Photo Film Co., Ltd.	Produit photographique couleur à l'halogénure d'argent contenant un coupleur cyan coloré en jaune
EP0440195A2 (fr)	1990-01-31	1991-08-07	Fuji Photo Film Co., Ltd.	Produit photographique couleur à l'halogénure d'argent
EP0452984A1 (fr)	1985-09-25	1991-10-23	Fuji Photo Film Co., Ltd.	Procédé de traitement d'un matériau photographique à l'halogénure d'argent pour un emploi photographique
EP0452886A2 (fr)	1990-04-17	1991-10-23	Fuji Photo Film Co., Ltd.	Méthode de traitement d'un produit photographique couleur à l'halogénure d'argent
US5155016A (en) *	1988-07-27	1992-10-13	Fuji Photo Film Co., Ltd.	Silver halide color photographic material containing novel pyrazoloazole coupler and method to produce color image
EP0562476A1 (fr)	1992-03-19	1993-09-29	Fuji Photo Film Co., Ltd.	Emulsion photographique à l'halogénure d'argent et matériau photographique sensible à la lumière
EP0563708A1 (fr)	1992-03-19	1993-10-06	Fuji Photo Film Co., Ltd.	Emulsion photographique à l'halogénure d'argent et metériau sensible à la lumière l'utilisant
EP0563985A1 (fr)	1992-04-03	1993-10-06	Fuji Photo Film Co., Ltd.	Matériau photographique couleur à l'halogénure d'argent
EP0570006A1 (fr)	1992-05-15	1993-11-18	Fuji Photo Film Co., Ltd.	Matériau photographique à l'halogénure d'argent sensible à la lumière
EP0607905A2 (fr)	1993-01-18	1994-07-27	Fuji Photo Film Co., Ltd.	Matériau photographique à l'halogénure d'argent
EP0654705A2 (fr)	1993-11-24	1995-05-24	Fuji Photo Film Co., Ltd.	Composition de traitement photographique et méthode de traitement photographique utilisant cette composition
JPH07267932A (ja) *	1994-11-07	1995-10-17	Konica Corp	５−アミノ−１ｈ−ピラゾール系化合物
WO1996013755A1 (fr)	1994-10-26	1996-05-09	Eastman Kodak Company	Emulsions photographiques a sensibilite renforcee
EP0711804A2 (fr)	1994-11-14	1996-05-15	Ciba-Geigy Ag	Stabilisateurs à la lumière latents
EP0720049A2 (fr)	1990-05-09	1996-07-03	Fuji Photo Film Co., Ltd.	Composition de traitement photographique et méthode de traitement l'utilisant
EP0800113A2 (fr)	1996-04-05	1997-10-08	Fuji Photo Film Co., Ltd.	Marériau photographique couleur à l'halogénure d'argent sensible à la lumière
US6165229A (en) *	1996-03-22	2000-12-26	L'oreal	Imidazoloazole-containing compositions for dyeing keratin fibers; their use in dyeing as couplers; dyeing process
US6179882B1 (en)	1996-03-22	2001-01-30	L'oreal	Keratin fibre dye composition containing pyrazolopyrimidinoxo compounds, use thereof as dye couplers, and dyeing methods
US6210447B1 (en)	1996-03-22	2001-04-03	L'oreal	Compositions containing pyrazolin-3,5-dione couplers for use in keratin fiber dyeing methods and kits
US6231623B1 (en)	1996-03-22	2001-05-15	L'oreal S.A.	Methods of dyeing keratin fibers with compositions containing pyrazolo-azole couplers
US6238440B1 (en)	1996-03-22	2001-05-29	L'oreal S.A.	Keratin fibre dye compositions containing pyrrolo-azole compounds, use thereof as couplers, and dyeing method
WO2001057034A1 (fr) *	2000-02-07	2001-08-09	Bristol-Myers Squibb Co.	Inhibiteurs 3-aminopyrazole des kinases dependantes des cyclines
WO2001068043A2 (fr)	2000-03-14	2001-09-20	L'oreal	Compositions pour la teinture des fibres keratiniques contenant des derives de paraphenylenediamine a groupement pyrrolidinyle
US6322775B1 (en)	1996-03-22	2001-11-27	L'oreal S.A.	Cosmetic compositions containing pyrazolin-4,5-diones, novel pyrazolin-4,5-diones, preparation methods therefor and uses thereof
US6379397B2 (en)	1997-12-16	2002-04-30	L'oreal S.A.	Compositions for dyeing keratinous fibers comprising pyrazoloazoles; their use in dyeing as oxidation base and dyeing process; and novel pyrazoloazoles
US6391063B1 (en)	1998-11-20	2002-05-21	L'oreal	Composition for the oxidation dyeing of keratin fibers and dyeing process using this composition
US6395042B1 (en)	1998-11-20	2002-05-28	L'oréal	Composition for the oxidation dyeing of keratin fibers and dyeing process using this composition
US6702863B1 (en)	1999-06-22	2004-03-09	Lion Corporation	Hairdye composition
US6890362B2 (en)	2000-03-06	2005-05-10	L'oreal, S.A.	Oxidation dyeing composition for keratinous fibers and dyeing method using same
EP1582919A1 (fr)	2004-03-23	2005-10-05	Fuji Photo Film Co. Ltd.	Matériau photosensible à l'halogénure d'argent et matériau photothermographique
EP1635216A1 (fr)	2004-09-14	2006-03-15	Fuji Photo Film Co., Ltd.	Matériau photothermographique
EP1754758A2 (fr)	2005-08-17	2007-02-21	Fuji Photo Film Co., Ltd.	Composition d'encre comprenant un sel d'onium et un composé polymérisable par voie cationique, procédé d'impression a jet d'encre, produit imprimé, procédé de fabrication d'une plaque d'impression lithographique, et plaque d'impression lithographique
EP2145931A1 (fr)	2008-07-16	2010-01-20	Fujifilm Corporation	Composition photo-durcissable, composition d'encre, et procédé d'enregistrement à jet d'encre utilisant la composition d'encre
EP2169021A1 (fr)	2008-09-25	2010-03-31	Fujifilm Corporation	Composition d'encre, procédé d'enregistrement à jet d'encre, et matériau imprimé

1983
- 1983-08-04 JP JP14280183A patent/JPS6033552A/ja active Granted

Cited By (54)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS61156048A (ja) *	1984-12-27	1986-07-15	Konishiroku Photo Ind Co Ltd	ハロゲン化銀写真感光材料
JPS61249968A (ja) *	1985-04-29	1986-11-07	Konishiroku Photo Ind Co Ltd	５−ヒドラジノ−１ｈ−ピラゾ−ル系化合物
EP0201033A2 (fr)	1985-04-30	1986-11-12	Konica Corporation	Procédé de traitement de matériaux photographiques couleurs à l'halogénure d'argent
EP0202616A2 (fr)	1985-05-16	1986-11-26	Konica Corporation	Procédé pour le développement couleur d'un matériau photographique à l'halogénure d'argent sensible à la lumière
JPS6210069A (ja) *	1985-07-05	1987-01-19	Konishiroku Photo Ind Co Ltd	５―アミノ―１ｈ―ピラゾール系化合物を用いる写真用マゼンタカプラーの合成方法
EP0452984A1 (fr)	1985-09-25	1991-10-23	Fuji Photo Film Co., Ltd.	Procédé de traitement d'un matériau photographique à l'halogénure d'argent pour un emploi photographique
JPS62153953A (ja) *	1985-12-27	1987-07-08	Fuji Photo Film Co Ltd	カラ−写真感光材料
JPS62163052A (ja) *	1986-01-11	1987-07-18	Konishiroku Photo Ind Co Ltd	ハロゲン化銀写真感光材料
EP0242013A2 (fr)	1986-01-20	1987-10-21	Konica Corporation	Matériau photographique couleur à l'halogénure d'argent sensible à la lumière
JPS62228066A (ja) *	1986-02-24	1987-10-06	Konika Corp	５−ヒドラジノ−１ｈ−ピラゾ−ル系化合物
JPS62195659A (ja) *	1986-02-24	1987-08-28	Konishiroku Photo Ind Co Ltd	５−アミノ−１ｈ−ピラゾ−ル系化合物
JPS62252773A (ja) *	1986-03-29	1987-11-04	アグフア−ゲヴエルト・アクチエンゲゼルシヤフト	４−ハロゲン−ピラゾロン−５のイミノ誘導体及びその製造法
JPS6324251A (ja) *	1986-07-17	1988-02-01	Fuji Photo Film Co Ltd	カラ−写真感光材料
JPS63145281A (ja) *	1986-12-09	1988-06-17	Fuji Photo Film Co Ltd	ピラゾロアゾールアゾメチンシアン染料
EP0317983A2 (fr)	1987-11-27	1989-05-31	Fuji Photo Film Co., Ltd.	Matériau photographique couleur à l'halogénure d'argent
EP0320939A2 (fr)	1987-12-15	1989-06-21	Fuji Photo Film Co., Ltd.	Matériau photographique couleur à l'halogénure d'argent
US5155016A (en) *	1988-07-27	1992-10-13	Fuji Photo Film Co., Ltd.	Silver halide color photographic material containing novel pyrazoloazole coupler and method to produce color image
EP0435334A2 (fr)	1989-12-29	1991-07-03	Fuji Photo Film Co., Ltd.	Produit photographique couleur à l'halogénure d'argent contenant un coupleur cyan coloré en jaune
EP0440195A2 (fr)	1990-01-31	1991-08-07	Fuji Photo Film Co., Ltd.	Produit photographique couleur à l'halogénure d'argent
EP0452886A2 (fr)	1990-04-17	1991-10-23	Fuji Photo Film Co., Ltd.	Méthode de traitement d'un produit photographique couleur à l'halogénure d'argent
EP0720049A2 (fr)	1990-05-09	1996-07-03	Fuji Photo Film Co., Ltd.	Composition de traitement photographique et méthode de traitement l'utilisant
EP0562476A1 (fr)	1992-03-19	1993-09-29	Fuji Photo Film Co., Ltd.	Emulsion photographique à l'halogénure d'argent et matériau photographique sensible à la lumière
EP0563708A1 (fr)	1992-03-19	1993-10-06	Fuji Photo Film Co., Ltd.	Emulsion photographique à l'halogénure d'argent et metériau sensible à la lumière l'utilisant
EP0563985A1 (fr)	1992-04-03	1993-10-06	Fuji Photo Film Co., Ltd.	Matériau photographique couleur à l'halogénure d'argent
EP0570006A1 (fr)	1992-05-15	1993-11-18	Fuji Photo Film Co., Ltd.	Matériau photographique à l'halogénure d'argent sensible à la lumière
EP0607905A2 (fr)	1993-01-18	1994-07-27	Fuji Photo Film Co., Ltd.	Matériau photographique à l'halogénure d'argent
EP0654705A2 (fr)	1993-11-24	1995-05-24	Fuji Photo Film Co., Ltd.	Composition de traitement photographique et méthode de traitement photographique utilisant cette composition
WO1996013755A1 (fr)	1994-10-26	1996-05-09	Eastman Kodak Company	Emulsions photographiques a sensibilite renforcee
JPH07267932A (ja) *	1994-11-07	1995-10-17	Konica Corp	５−アミノ−１ｈ−ピラゾール系化合物
EP0711804A2 (fr)	1994-11-14	1996-05-15	Ciba-Geigy Ag	Stabilisateurs à la lumière latents
US6379395B1 (en)	1996-03-22	2002-04-30	L'oreal S.A.	Pyrazolopyrimidinoxo-containing compositions for dyeing keratin fibres; their use in dyeing as couplers; dyeing processes
US6551360B2 (en)	1996-03-22	2003-04-22	Laurent Vidal	Pyrazoline-3,5-dione-containing compositions for dyeing keratin fibres; their use in dyeing as couplers; dyeing process
US6179882B1 (en)	1996-03-22	2001-01-30	L'oreal	Keratin fibre dye composition containing pyrazolopyrimidinoxo compounds, use thereof as dye couplers, and dyeing methods
US6210447B1 (en)	1996-03-22	2001-04-03	L'oreal	Compositions containing pyrazolin-3,5-dione couplers for use in keratin fiber dyeing methods and kits
US6231623B1 (en)	1996-03-22	2001-05-15	L'oreal S.A.	Methods of dyeing keratin fibers with compositions containing pyrazolo-azole couplers
US6238440B1 (en)	1996-03-22	2001-05-29	L'oreal S.A.	Keratin fibre dye compositions containing pyrrolo-azole compounds, use thereof as couplers, and dyeing method
US6322775B1 (en)	1996-03-22	2001-11-27	L'oreal S.A.	Cosmetic compositions containing pyrazolin-4,5-diones, novel pyrazolin-4,5-diones, preparation methods therefor and uses thereof
US6165229A (en) *	1996-03-22	2000-12-26	L'oreal	Imidazoloazole-containing compositions for dyeing keratin fibers; their use in dyeing as couplers; dyeing process
EP0800113A2 (fr)	1996-04-05	1997-10-08	Fuji Photo Film Co., Ltd.	Marériau photographique couleur à l'halogénure d'argent sensible à la lumière
US6855827B2 (en)	1997-12-16	2005-02-15	L'oréal	Compositions for dyeing keratinous fibers comprising pyrazoloazoles; their use in dyeing as oxidation base and dyeing process; and novel pyrazoloazoles
US6379397B2 (en)	1997-12-16	2002-04-30	L'oreal S.A.	Compositions for dyeing keratinous fibers comprising pyrazoloazoles; their use in dyeing as oxidation base and dyeing process; and novel pyrazoloazoles
US6395042B1 (en)	1998-11-20	2002-05-28	L'oréal	Composition for the oxidation dyeing of keratin fibers and dyeing process using this composition
US6391063B1 (en)	1998-11-20	2002-05-21	L'oreal	Composition for the oxidation dyeing of keratin fibers and dyeing process using this composition
US6702863B1 (en)	1999-06-22	2004-03-09	Lion Corporation	Hairdye composition
US6482842B2 (en)	2000-02-07	2002-11-19	Bristol-Myers Squibb Company	3-aminopyrazole inhibitors of cyclin dependent kinases
WO2001057034A1 (fr) *	2000-02-07	2001-08-09	Bristol-Myers Squibb Co.	Inhibiteurs 3-aminopyrazole des kinases dependantes des cyclines
US6610724B2 (en)	2000-02-07	2003-08-26	Bristol-Myers Squibb Company	3-Aminopyrazole inhibitors of cyclin dependent kinases
US6890362B2 (en)	2000-03-06	2005-05-10	L'oreal, S.A.	Oxidation dyeing composition for keratinous fibers and dyeing method using same
WO2001068043A2 (fr)	2000-03-14	2001-09-20	L'oreal	Compositions pour la teinture des fibres keratiniques contenant des derives de paraphenylenediamine a groupement pyrrolidinyle
EP1582919A1 (fr)	2004-03-23	2005-10-05	Fuji Photo Film Co. Ltd.	Matériau photosensible à l'halogénure d'argent et matériau photothermographique
EP1635216A1 (fr)	2004-09-14	2006-03-15	Fuji Photo Film Co., Ltd.	Matériau photothermographique
EP1754758A2 (fr)	2005-08-17	2007-02-21	Fuji Photo Film Co., Ltd.	Composition d'encre comprenant un sel d'onium et un composé polymérisable par voie cationique, procédé d'impression a jet d'encre, produit imprimé, procédé de fabrication d'une plaque d'impression lithographique, et plaque d'impression lithographique
EP2145931A1 (fr)	2008-07-16	2010-01-20	Fujifilm Corporation	Composition photo-durcissable, composition d'encre, et procédé d'enregistrement à jet d'encre utilisant la composition d'encre
EP2169021A1 (fr)	2008-09-25	2010-03-31	Fujifilm Corporation	Composition d'encre, procédé d'enregistrement à jet d'encre, et matériau imprimé

Also Published As

Publication number	Publication date
JPH0365529B2 (fr)	1991-10-14

Publication	Publication Date	Title
JPS6033552A (ja)	1985-02-20	カラ−画像形成方法
JPS6165245A (ja)	1986-04-03	ハロゲン化銀カラ−写真感光材料
JPS6043659A (ja)	1985-03-08	カラ−画像形成方法
JPH0244051B2 (fr)	1990-10-02
JPS6322571B2 (fr)	1988-05-12
JPH0316013B2 (fr)	1991-03-04
JPH037101B2 (fr)	1991-01-31
JPS6147957A (ja)	1986-03-08	ハロゲン化銀カラ−写真感光材料
JPS60140241A (ja)	1985-07-25	ハロゲン化銀感光材料
JPH0413699B2 (fr)	1992-03-10
JPS6153644A (ja)	1986-03-17	ハロゲン化銀カラ−写真感光材料
JPH051930B2 (fr)	1993-01-11
JPH034892B2 (fr)	1991-01-24
JPS6291947A (ja)	1987-04-27	ハロゲン化銀カラ−写真感光材料
JPH0365532B2 (fr)	1991-10-14
JPS6128947A (ja)	1986-02-08	ハロゲン化銀カラ−写真感光材料
JPH043860B2 (fr)	1992-01-24
US4594313A (en)	1986-06-10	Color image forming process comprising blocked magenta dye forming coupler
JPS6286363A (ja)	1987-04-20	ハロゲン化銀カラ−写真感光材料
JPH053575B2 (fr)	1993-01-18
JPS62209457A (ja)	1987-09-14	カラ−画像形成方法
JPH0311458B2 (fr)	1991-02-18
JPS6165247A (ja)	1986-04-03	ハロゲン化銀カラ−写真感光材料
JPH0417413B2 (fr)	1992-03-25
JPS6292945A (ja)	1987-04-28	ハロゲン化銀カラ−写真感光材料