JPS6043659A - カラ−画像形成方法 - Google Patents

カラ−画像形成方法

Info

Publication number: JPS6043659A
Authority: JP; Japan
Prior art keywords: group; coupler; acid; color; nucleus
Prior art date: 1983-08-19
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

JP15135483A

Other languages

English (en)

Japanese (ja)

Other versions

JPH0365530B2 (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.)

1983-08-19

Filing date

1983-08-19

Publication date

1985-03-08

1983-08-19 Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd

1983-08-19 Priority to JP15135483A priority Critical patent/JPS6043659A/ja

1985-03-08 Publication of JPS6043659A publication Critical patent/JPS6043659A/ja

1991-10-14 Publication of JPH0365530B2 publication Critical patent/JPH0365530B2/ja

Status Granted legal-status Critical Current

Links

230000015572 biosynthetic process Effects 0.000 title description 13
-1 aromatic primary amine Chemical class 0.000 claims abstract description 120
239000003795 chemical substances by application Substances 0.000 claims abstract description 12
238000000034 method Methods 0.000 claims description 58
229910052709 silver Inorganic materials 0.000 claims description 25
239000004332 silver Substances 0.000 claims description 25
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
230000003647 oxidation Effects 0.000 claims description 3
238000007254 oxidation reaction Methods 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
150000004982 aromatic amines Chemical class 0.000 claims description 2
229920000642 polymer Polymers 0.000 abstract description 20
125000000217 alkyl group Chemical group 0.000 abstract description 14
125000003118 aryl group Chemical group 0.000 abstract description 14
238000010521 absorption reaction Methods 0.000 abstract description 9
238000005859 coupling reaction Methods 0.000 abstract description 8
125000003545 alkoxy group Chemical group 0.000 abstract description 7
238000010168 coupling process Methods 0.000 abstract description 6
238000002156 mixing Methods 0.000 abstract description 6
230000008878 coupling Effects 0.000 abstract description 5
229910052736 halogen Inorganic materials 0.000 abstract description 4
150000002367 halogens Chemical class 0.000 abstract description 3
VQKUGKZVMQAPFM-UHFFFAOYSA-N 1h-pyrazolo[1,5-b]pyrazole Chemical compound C1=CNN2N=CC=C21 VQKUGKZVMQAPFM-UHFFFAOYSA-N 0.000 abstract 1
239000000539 dimer Substances 0.000 abstract 1
239000000975 dye Substances 0.000 description 47
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 40
239000000839 emulsion Substances 0.000 description 21
229910052757 nitrogen Inorganic materials 0.000 description 18
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 17
239000000243 solution Substances 0.000 description 17
150000001875 compounds Chemical class 0.000 description 16
125000000623 heterocyclic group Chemical group 0.000 description 15
239000002253 acid Substances 0.000 description 14
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 13
239000000203 mixture Substances 0.000 description 11
239000000543 intermediate Substances 0.000 description 10
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
238000003786 synthesis reaction Methods 0.000 description 10
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239000007864 aqueous solution Substances 0.000 description 7
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 7
239000003960 organic solvent Substances 0.000 description 7
150000003839 salts Chemical class 0.000 description 7
ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 7
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108010010803 Gelatin Proteins 0.000 description 6
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239000002202 Polyethylene glycol Substances 0.000 description 6
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
150000001412 amines Chemical class 0.000 description 6
238000006243 chemical reaction Methods 0.000 description 6
239000000084 colloidal system Substances 0.000 description 6
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235000019322 gelatine Nutrition 0.000 description 6
235000011852 gelatine desserts Nutrition 0.000 description 6
125000004433 nitrogen atom Chemical group N* 0.000 description 6
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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 4
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CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 4
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PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 4
HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 4
238000000862 absorption spectrum Methods 0.000 description 4
230000002378 acidificating effect Effects 0.000 description 4
125000004442 acylamino group Chemical group 0.000 description 4
125000002947 alkylene group Chemical group 0.000 description 4
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 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
238000004061 bleaching Methods 0.000 description 4
DNSISZSEWVHGLH-UHFFFAOYSA-N butanamide Chemical group CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 description 4
229910052799 carbon Inorganic materials 0.000 description 4
125000001309 chloro group Chemical group Cl* 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
UKVIEHSSVKSQBA-UHFFFAOYSA-N methane;palladium Chemical compound C.[Pd] UKVIEHSSVKSQBA-UHFFFAOYSA-N 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
235000021317 phosphate Nutrition 0.000 description 4
239000000047 product Substances 0.000 description 4
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
230000001235 sensitizing effect Effects 0.000 description 4
KJCVRFUGPWSIIH-UHFFFAOYSA-N 1-naphthol Chemical compound C1=CC=C2C(O)=CC=CC2=C1 KJCVRFUGPWSIIH-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
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HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 3
150000001253 acrylic acids Chemical class 0.000 description 3
125000002252 acyl group Chemical group 0.000 description 3
150000001408 amides Chemical class 0.000 description 3
238000009835 boiling Methods 0.000 description 3
210000000988 bone and bone Anatomy 0.000 description 3
125000001951 carbamoylamino group Chemical group C(N)(=O)N* 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
229910052801 chlorine Inorganic materials 0.000 description 3
239000011248 coating agent Substances 0.000 description 3
238000000576 coating method Methods 0.000 description 3
229920001577 copolymer Polymers 0.000 description 3
NQGIJDNPUZEBRU-UHFFFAOYSA-N dodecanoyl chloride Chemical compound CCCCCCCCCCCC(Cl)=O NQGIJDNPUZEBRU-UHFFFAOYSA-N 0.000 description 3
238000001035 drying Methods 0.000 description 3
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
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238000000605 extraction Methods 0.000 description 3
238000010438 heat treatment Methods 0.000 description 3
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150000002576 ketones Chemical class 0.000 description 3
125000005647 linker group Chemical group 0.000 description 3
239000007788 liquid Substances 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-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
238000006116 polymerization reaction Methods 0.000 description 3
238000006722 reduction reaction Methods 0.000 description 3
238000010992 reflux Methods 0.000 description 3
125000000565 sulfonamide group Chemical group 0.000 description 3
125000004434 sulfur atom Chemical group 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
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MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-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
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class 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
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CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
OJGMBLNIHDZDGS-UHFFFAOYSA-N N-Ethylaniline Chemical compound CCNC1=CC=CC=C1 OJGMBLNIHDZDGS-UHFFFAOYSA-N 0.000 description 2
JRNVZBWKYDBUCA-UHFFFAOYSA-N N-chlorosuccinimide Chemical compound ClN1C(=O)CCC1=O JRNVZBWKYDBUCA-UHFFFAOYSA-N 0.000 description 2
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206010070834 Sensitisation Diseases 0.000 description 2
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
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CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
150000001661 cadmium Chemical class 0.000 description 2
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
229910017052 cobalt Inorganic materials 0.000 description 2
239000010941 cobalt Substances 0.000 description 2
GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 2
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239000010949 copper Substances 0.000 description 2
239000013078 crystal Substances 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
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238000007720 emulsion polymerization reaction Methods 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
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
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150000004820 halides Chemical class 0.000 description 2
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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 2
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230000002194 synthesizing effect Effects 0.000 description 2
150000003536 tetrazoles Chemical class 0.000 description 2
125000004149 thio group Chemical group *S* 0.000 description 2
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TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 1
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AIGNCQCMONAWOL-UHFFFAOYSA-N 1,3-benzoselenazole Chemical class C1=CC=C2[se]C=NC2=C1 AIGNCQCMONAWOL-UHFFFAOYSA-N 0.000 description 1
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ODIRBFFBCSTPTO-UHFFFAOYSA-N 1,3-selenazole Chemical class C1=C[se]C=N1 ODIRBFFBCSTPTO-UHFFFAOYSA-N 0.000 description 1
OGYGFUAIIOPWQD-UHFFFAOYSA-N 1,3-thiazolidine Chemical compound C1CSCN1 OGYGFUAIIOPWQD-UHFFFAOYSA-N 0.000 description 1
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150000002475 indoles Chemical class 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
229910052740 iodine Inorganic materials 0.000 description 1
150000002500 ions Chemical class 0.000 description 1
150000002503 iridium Chemical class 0.000 description 1
150000002505 iron Chemical class 0.000 description 1
KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 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
125000001288 lysyl group Chemical group 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
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 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
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
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
YRVUCYWJQFRCOB-UHFFFAOYSA-N n-butylprop-2-enamide Chemical compound CCCCNC(=O)C=C YRVUCYWJQFRCOB-UHFFFAOYSA-N 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
SQDFHQJTAWCFIB-UHFFFAOYSA-N n-methylidenehydroxylamine Chemical class ON=C SQDFHQJTAWCFIB-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
XNGIFLGASWRNHJ-UHFFFAOYSA-N o-dicarboxybenzene Natural products OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
SYQMMCZWJAEWEK-UHFFFAOYSA-N octadecane-1-sulfonamide Chemical group CCCCCCCCCCCCCCCCCCS(N)(=O)=O SYQMMCZWJAEWEK-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
235000005985 organic acids Nutrition 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
150000002916 oxazoles Chemical class 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
JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
KHUXNRRPPZOJPT-UHFFFAOYSA-N phenoxy radical Chemical group O=C1C=C[CH]C=C1 KHUXNRRPPZOJPT-UHFFFAOYSA-N 0.000 description 1
WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 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
XYFCBTPGUUZFHI-UHFFFAOYSA-O phosphonium Chemical compound [PH4+] XYFCBTPGUUZFHI-UHFFFAOYSA-O 0.000 description 1
235000011007 phosphoric acid Nutrition 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
150000003016 phosphoric acids Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
230000000379 polymerizing effect Effects 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920001296 polysiloxane Polymers 0.000 description 1
229910052700 potassium Inorganic materials 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
230000002028 premature Effects 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
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
125000006239 protecting group Chemical group 0.000 description 1
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical compound N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 1
125000003226 pyrazolyl group Chemical group 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 description 1
150000003233 pyrroles Chemical class 0.000 description 1
150000003236 pyrrolines Chemical class 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
230000003014 reinforcing effect Effects 0.000 description 1
KIWUVOGUEXMXSV-UHFFFAOYSA-N rhodanine Chemical class O=C1CSC(=S)N1 KIWUVOGUEXMXSV-UHFFFAOYSA-N 0.000 description 1
150000003283 rhodium Chemical class 0.000 description 1
230000005070 ripening Effects 0.000 description 1
229930182490 saponin Natural products 0.000 description 1
235000017709 saponins Nutrition 0.000 description 1
150000007949 saponins Chemical class 0.000 description 1
125000004469 siloxy group Chemical group [SiH3]O* 0.000 description 1
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 1
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
229910001961 silver nitrate Inorganic materials 0.000 description 1
125000003808 silyl group Chemical group [H][Si]([H])([H])[*] 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
239000012279 sodium borohydride Substances 0.000 description 1
229910000033 sodium borohydride Inorganic materials 0.000 description 1
229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
239000012312 sodium hydride Substances 0.000 description 1
229910000104 sodium hydride Inorganic materials 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
VUVFZUKPBAGTCQ-UHFFFAOYSA-M sodium;2,3-di(butan-2-yl)naphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(C(C)CC)C(C(C)CC)=CC2=C1 VUVFZUKPBAGTCQ-UHFFFAOYSA-M 0.000 description 1
230000003595 spectral effect Effects 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
239000001119 stannous chloride Substances 0.000 description 1
235000011150 stannous chloride Nutrition 0.000 description 1
150000003431 steroids Chemical class 0.000 description 1
238000003756 stirring Methods 0.000 description 1
229960002317 succinimide Drugs 0.000 description 1
150000005846 sugar alcohols Polymers 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
125000004964 sulfoalkyl group Chemical group 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
238000001308 synthesis method Methods 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
ARZGWBJFLJBOTR-UHFFFAOYSA-N tetradecanamide Chemical group CCCCCCCCCCCCCC(N)=O.CCCCCCCCCCCCCC(N)=O ARZGWBJFLJBOTR-UHFFFAOYSA-N 0.000 description 1
150000003475 thallium Chemical class 0.000 description 1
150000003557 thiazoles Chemical class 0.000 description 1
150000003549 thiazolines Chemical class 0.000 description 1
125000001544 thienyl group Chemical group 0.000 description 1
150000003568 thioethers Chemical class 0.000 description 1
UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 1
125000005147 toluenesulfonyl group Chemical group C=1(C(=CC=CC1)S(=O)(=O)*)C 0.000 description 1
150000003852 triazoles Chemical class 0.000 description 1
NJPOTNJJCSJJPJ-UHFFFAOYSA-N tributyl benzene-1,3,5-tricarboxylate Chemical compound CCCCOC(=O)C1=CC(C(=O)OCCCC)=CC(C(=O)OCCCC)=C1 NJPOTNJJCSJJPJ-UHFFFAOYSA-N 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 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
XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
239000006097 ultraviolet radiation absorber Substances 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
238000005406 washing Methods 0.000 description 1
229920003169 water-soluble polymer Polymers 0.000 description 1
239000011701 zinc Substances 0.000 description 1
150000003751 zinc Chemical class 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
- G03C7/3003—Materials characterised by the use of combinations of photographic compounds known as such, or by a particular location in the photographic element
- G03C7/3005—Combinations of couplers and photographic additives
- G03C7/3008—Combinations of couplers having the coupling site in rings of cyclic compounds and photographic additives
- G03C7/301—Combinations of couplers having the coupling site in pyrazoloazole rings and photographic additives

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)

JP15135483A 1983-08-19 1983-08-19 カラ−画像形成方法 Granted JPS6043659A (ja)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP15135483A JPS6043659A (ja)	1983-08-19	1983-08-19	カラ−画像形成方法

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP15135483A JPS6043659A (ja)	1983-08-19	1983-08-19	カラ−画像形成方法

Publications (2)

Publication Number	Publication Date
JPS6043659A true JPS6043659A (ja)	1985-03-08
JPH0365530B2 JPH0365530B2 (fr)	1991-10-14

Family

ID=15516712

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP15135483A Granted JPS6043659A (ja)	1983-08-19	1983-08-19	カラ−画像形成方法

Country Status (1)

Country	Link
JP (1)	JPS6043659A (fr)

Cited By (37)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
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
EP0242013A2 (fr)	1986-01-20	1987-10-21	Konica Corporation	Matériau photographique couleur à l'halogénure d'argent sensible à la lumière
EP0253390A2 (fr)	1986-07-17	1988-01-20	Fuji Photo Film Co., Ltd.	Support photographique et matériau photosensible couleur
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
EP0313083A2 (fr)	1987-10-22	1989-04-26	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
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
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
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
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
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
- 1983-08-19 JP JP15135483A patent/JPS6043659A/ja active Granted

Cited By (40)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
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
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
EP0242013A2 (fr)	1986-01-20	1987-10-21	Konica Corporation	Matériau photographique couleur à l'halogénure d'argent sensible à la lumière
EP0253390A2 (fr)	1986-07-17	1988-01-20	Fuji Photo Film Co., Ltd.	Support photographique et matériau photosensible couleur
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
EP0313083A2 (fr)	1987-10-22	1989-04-26	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
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
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Also Published As

Publication number	Publication date
JPH0365530B2 (fr)	1991-10-14

Publication	Publication Date	Title
JPS6043659A (ja)	1985-03-08	カラ−画像形成方法
JPH0365529B2 (fr)	1991-10-14
JPH0244051B2 (fr)	1990-10-02
JPH037101B2 (fr)	1991-01-31
JPS6322571B2 (fr)	1988-05-12
JPH0260167B2 (fr)	1990-12-14
JPS6116063B2 (fr)	1986-04-28
JPS6116059B2 (fr)	1986-04-28
JPH0250457B2 (fr)	1990-11-02
JPS60262159A (ja)	1985-12-25	ハロゲン化銀カラ−写真感光材料
JPH0413699B2 (fr)	1992-03-10
JPH0365531B2 (fr)	1991-10-14
JPH0365532B2 (fr)	1991-10-14
GB2032638A (en)	1980-05-08	Silver photographic material containing yellow coupler
JPS6128947A (ja)	1986-02-08	ハロゲン化銀カラ−写真感光材料
JPH0562729B2 (fr)	1993-09-09
JPS62209457A (ja)	1987-09-14	カラ−画像形成方法
JPS6286363A (ja)	1987-04-20	ハロゲン化銀カラ−写真感光材料
JPS60262157A (ja)	1985-12-25	ハロゲン化銀カラ−写真感光材料
JPS6023855A (ja)	1985-02-06	カラ−写真感光材料
JPS63307453A (ja)	1988-12-15	マゼンタ色素形成カプラ−
JPS62257158A (ja)	1987-11-09	ハロゲン化銀カラ−写真感光材料
JPS5927895B2 (ja)	1984-07-09	黄色カプラ−
JPH0380296B2 (fr)	1991-12-24
EP0558146B1 (fr)	1995-04-05	Matériau photographique et procédé comprenant un coupleur pyrazolotriazole