JPH0651465A - カラー写真要素及び写真画像の形成方法 - Google Patents

カラー写真要素及び写真画像の形成方法

Info

Publication number: JPH0651465A
Authority: JP; Japan
Prior art keywords: photographic; group; coupler; couplers; substituted
Prior art date: 1992-06-24
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.): Pending

Application number

JP14903693A

Other languages

English (en)

Japanese (ja)

Inventor

William J Begley

ジェームズベグレイウィリアム

Hans Gway Ling

グウェイリングハンス

Drake M Michno

マシューミチノドレイク

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.)

Eastman Kodak Co

Original Assignee

Eastman Kodak Co

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.)

1992-06-24

Filing date

1993-06-21

Publication date

1994-02-25

1993-06-21 Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co

1994-02-25 Publication of JPH0651465A publication Critical patent/JPH0651465A/ja

Status Pending legal-status Critical Current

Links

230000015572 biosynthetic process Effects 0.000 title description 5
239000003112 inhibitor Substances 0.000 claims abstract description 134
238000011161 development Methods 0.000 claims abstract description 70
239000000839 emulsion Substances 0.000 claims abstract description 46
-1 silver halide Chemical class 0.000 claims abstract description 45
229910052709 silver Inorganic materials 0.000 claims abstract description 43
239000004332 silver Substances 0.000 claims abstract description 43
238000012545 processing Methods 0.000 claims abstract description 31
150000001875 compounds Chemical class 0.000 claims abstract description 25
238000006243 chemical reaction Methods 0.000 claims abstract description 19
238000000034 method Methods 0.000 claims description 10
239000000463 material Substances 0.000 abstract description 18
239000003795 chemical substances by application Substances 0.000 abstract description 13
230000000979 retarding effect Effects 0.000 abstract 1
125000000217 alkyl group Chemical group 0.000 description 87
125000003118 aryl group Chemical group 0.000 description 82
239000000126 substance Substances 0.000 description 75
229910052739 hydrogen Inorganic materials 0.000 description 66
239000001257 hydrogen Substances 0.000 description 66
150000002431 hydrogen Chemical class 0.000 description 64
125000004432 carbon atom Chemical group C* 0.000 description 54
239000010410 layer Substances 0.000 description 53
239000000975 dye Substances 0.000 description 48
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 47
230000002411 adverse Effects 0.000 description 35
230000003381 solubilizing effect Effects 0.000 description 27
239000000460 chlorine Substances 0.000 description 25
125000001424 substituent group Chemical group 0.000 description 17
229910052799 carbon Inorganic materials 0.000 description 14
150000001721 carbon Chemical group 0.000 description 13
230000000694 effects Effects 0.000 description 13
108010010803 Gelatin Proteins 0.000 description 12
229920000159 gelatin Polymers 0.000 description 12
239000008273 gelatin Substances 0.000 description 12
235000019322 gelatine Nutrition 0.000 description 12
235000011852 gelatine desserts Nutrition 0.000 description 12
125000000547 substituted alkyl group Chemical group 0.000 description 12
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 10
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 10
BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 9
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
239000011229 interlayer Substances 0.000 description 7
ZUNKMNLKJXRCDM-UHFFFAOYSA-N silver bromoiodide Chemical compound [Ag].IBr ZUNKMNLKJXRCDM-UHFFFAOYSA-N 0.000 description 7
239000007864 aqueous solution Substances 0.000 description 6
238000011160 research Methods 0.000 description 6
238000005859 coupling reaction Methods 0.000 description 5
JAAIPIWKKXCNOC-UHFFFAOYSA-N 1h-tetrazol-1-ium-5-thiolate Chemical compound SC1=NN=NN1 JAAIPIWKKXCNOC-UHFFFAOYSA-N 0.000 description 4
FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 4
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 4
239000012964 benzotriazole Substances 0.000 description 4
230000008878 coupling Effects 0.000 description 4
238000010168 coupling process Methods 0.000 description 4
239000000203 mixture Substances 0.000 description 4
KPCHOCIEAXFUHZ-UHFFFAOYSA-N oxadiazole-4-thiol Chemical compound SC1=CON=N1 KPCHOCIEAXFUHZ-UHFFFAOYSA-N 0.000 description 4
230000035945 sensitivity Effects 0.000 description 4
JJJPTTANZGDADF-UHFFFAOYSA-N thiadiazole-4-thiol Chemical compound SC1=CSN=N1 JJJPTTANZGDADF-UHFFFAOYSA-N 0.000 description 4
INVVMIXYILXINW-UHFFFAOYSA-N 5-methyl-1h-[1,2,4]triazolo[1,5-a]pyrimidin-7-one Chemical compound CC1=CC(=O)N2NC=NC2=N1 INVVMIXYILXINW-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
241001479434 Agfa Species 0.000 description 3
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
239000007844 bleaching agent Substances 0.000 description 3
238000003384 imaging method Methods 0.000 description 3
239000000123 paper Substances 0.000 description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical compound O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 3
238000006467 substitution reaction Methods 0.000 description 3
239000006096 absorbing agent Substances 0.000 description 2
229960001413 acetanilide Drugs 0.000 description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 2
239000003153 chemical reaction reagent Substances 0.000 description 2
230000002860 competitive effect Effects 0.000 description 2
238000009792 diffusion process Methods 0.000 description 2
238000003379 elimination reaction Methods 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical class 0.000 description 2
125000000623 heterocyclic group Chemical group 0.000 description 2
230000000873 masking effect Effects 0.000 description 2
238000012986 modification Methods 0.000 description 2
230000004048 modification Effects 0.000 description 2
238000005691 oxidative coupling reaction Methods 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
239000002243 precursor Substances 0.000 description 2
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
230000005855 radiation Effects 0.000 description 2
239000002516 radical scavenger Substances 0.000 description 2
229910052702 rhenium Inorganic materials 0.000 description 2
229910052703 rhodium Inorganic materials 0.000 description 2
238000007363 ring formation reaction Methods 0.000 description 2
229910052701 rubidium Inorganic materials 0.000 description 2
ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 2
239000000243 solution Substances 0.000 description 2
230000003595 spectral effect Effects 0.000 description 2
150000003457 sulfones Chemical class 0.000 description 2
GVEYRUKUJCHJSR-UHFFFAOYSA-N (4-azaniumyl-3-methylphenyl)-ethyl-(2-hydroxyethyl)azanium;sulfate Chemical compound OS(O)(=O)=O.OCCN(CC)C1=CC=C(N)C(C)=C1 GVEYRUKUJCHJSR-UHFFFAOYSA-N 0.000 description 1
125000001989 1,3-phenylene group Chemical group [H]C1=C([H])C([*:1])=C([H])C([*:2])=C1[H] 0.000 description 1
IJHIIHORMWQZRQ-UHFFFAOYSA-N 1-(ethenylsulfonylmethylsulfonyl)ethene Chemical compound C=CS(=O)(=O)CS(=O)(=O)C=C IJHIIHORMWQZRQ-UHFFFAOYSA-N 0.000 description 1
125000006219 1-ethylpentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 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
125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 1
RTLKJCSGNBYCKJ-UHFFFAOYSA-N 3-oxo-3-phenylpropanamide Chemical compound NC(=O)CC(=O)C1=CC=CC=C1 RTLKJCSGNBYCKJ-UHFFFAOYSA-N 0.000 description 1
CSQXGPMRNVVHDI-UHFFFAOYSA-N 4-dodecoxy-n-[3-[(4-dodecoxyphenyl)sulfonylamino]-4-hydroxyphenyl]benzenesulfonamide Chemical compound C1=CC(OCCCCCCCCCCCC)=CC=C1S(=O)(=O)NC1=CC=C(O)C(NS(=O)(=O)C=2C=CC(OCCCCCCCCCCCC)=CC=2)=C1 CSQXGPMRNVVHDI-UHFFFAOYSA-N 0.000 description 1
XTBFKMDOQMQYPP-UHFFFAOYSA-N 4-n,4-n-diethylbenzene-1,4-diamine;hydron;chloride Chemical compound Cl.CCN(CC)C1=CC=C(N)C=C1 XTBFKMDOQMQYPP-UHFFFAOYSA-N 0.000 description 1
KHBQMWCZKVMBLN-UHFFFAOYSA-N Benzenesulfonamide Chemical compound NS(=O)(=O)C1=CC=CC=C1 KHBQMWCZKVMBLN-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
229920002284 Cellulose triacetate Polymers 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
229940090898 Desensitizer Drugs 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
241000408495 Iton Species 0.000 description 1
239000000020 Nitrocellulose Substances 0.000 description 1
235000008585 Pinus thunbergii Nutrition 0.000 description 1
241000218686 Pinus thunbergii Species 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
239000004743 Polypropylene Substances 0.000 description 1
229910021607 Silver chloride Inorganic materials 0.000 description 1
NNLVGZFZQQXQNW-ADJNRHBOSA-N [(2r,3r,4s,5r,6s)-4,5-diacetyloxy-3-[(2s,3r,4s,5r,6r)-3,4,5-triacetyloxy-6-(acetyloxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6s)-4,5,6-triacetyloxy-2-(acetyloxymethyl)oxan-3-yl]oxyoxan-2-yl]methyl acetate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](OC(C)=O)[C@H]1OC(C)=O)O[C@H]1[C@@H]([C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O1)OC(C)=O)COC(=O)C)[C@@H]1[C@@H](COC(C)=O)O[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@H]1OC(C)=O NNLVGZFZQQXQNW-ADJNRHBOSA-N 0.000 description 1
FJWGYAHXMCUOOM-QHOUIDNNSA-N [(2s,3r,4s,5r,6r)-2-[(2r,3r,4s,5r,6s)-4,5-dinitrooxy-2-(nitrooxymethyl)-6-[(2r,3r,4s,5r,6s)-4,5,6-trinitrooxy-2-(nitrooxymethyl)oxan-3-yl]oxyoxan-3-yl]oxy-3,5-dinitrooxy-6-(nitrooxymethyl)oxan-4-yl] nitrate Chemical compound O([C@@H]1O[C@@H]([C@H]([C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O)O[C@H]1[C@@H]([C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@@H](CO[N+]([O-])=O)O1)O[N+]([O-])=O)CO[N+](=O)[O-])[C@@H]1[C@@H](CO[N+]([O-])=O)O[C@@H](O[N+]([O-])=O)[C@H](O[N+]([O-])=O)[C@H]1O[N+]([O-])=O FJWGYAHXMCUOOM-QHOUIDNNSA-N 0.000 description 1
MPLZNPZPPXERDA-UHFFFAOYSA-N [4-(diethylamino)-2-methylphenyl]azanium;chloride Chemical compound [Cl-].CC[NH+](CC)C1=CC=C(N)C(C)=C1 MPLZNPZPPXERDA-UHFFFAOYSA-N 0.000 description 1
SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 description 1
HOLVRJRSWZOAJU-UHFFFAOYSA-N [Ag].ICl Chemical compound [Ag].ICl HOLVRJRSWZOAJU-UHFFFAOYSA-N 0.000 description 1
DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
150000001241 acetals Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
125000003545 alkoxy group Chemical group 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
125000004414 alkyl thio group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 1
229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 description 1
150000007860 aryl ester derivatives Chemical class 0.000 description 1
QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
229910001864 baryta Inorganic materials 0.000 description 1
239000002585 base Substances 0.000 description 1
238000004061 bleaching Methods 0.000 description 1
125000001246 bromo group Chemical group Br* 0.000 description 1
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
125000005521 carbonamide group Chemical group 0.000 description 1
125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 description 1
229920002301 cellulose acetate Polymers 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
239000003086 colorant Substances 0.000 description 1
238000004040 coloring Methods 0.000 description 1
239000008139 complexing agent Substances 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000012937 correction Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
230000003247 decreasing effect Effects 0.000 description 1
239000000539 dimer Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
239000003814 drug Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
125000006575 electron-withdrawing group Chemical group 0.000 description 1
230000002708 enhancing effect Effects 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
239000011521 glass Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
CBEQRNSPHCCXSH-UHFFFAOYSA-N iodine monobromide Chemical compound IBr CBEQRNSPHCCXSH-UHFFFAOYSA-N 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
238000005259 measurement 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
239000000178 monomer Substances 0.000 description 1
150000004780 naphthols Chemical class 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229920001220 nitrocellulos Polymers 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
239000002667 nucleating agent Substances 0.000 description 1
238000010534 nucleophilic substitution reaction Methods 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
125000000962 organic group Chemical group 0.000 description 1
150000004989 p-phenylenediamines Chemical class 0.000 description 1
JOXIMZWYDAKGHI-UHFFFAOYSA-N p-toluenesulfonic acid Substances CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000008363 phosphate buffer Substances 0.000 description 1
229920006289 polycarbonate film Polymers 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229920000139 polyethylene terephthalate Polymers 0.000 description 1
239000005020 polyethylene terephthalate Substances 0.000 description 1
239000004848 polyfunctional curative Substances 0.000 description 1
229920006254 polymer film Polymers 0.000 description 1
229920000098 polyolefin Polymers 0.000 description 1
229920001155 polypropylene Polymers 0.000 description 1
230000008569 process Effects 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
MCSKRVKAXABJLX-UHFFFAOYSA-N pyrazolo[3,4-d]triazole Chemical class N1=NN=C2N=NC=C21 MCSKRVKAXABJLX-UHFFFAOYSA-N 0.000 description 1
230000009467 reduction Effects 0.000 description 1
239000011347 resin Substances 0.000 description 1
229920005989 resin Polymers 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
241000894007 species Species 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000003381 stabilizer Substances 0.000 description 1
125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
229940124530 sulfonamide Drugs 0.000 description 1
150000003456 sulfonamides Chemical class 0.000 description 1
150000003462 sulfoxides Chemical class 0.000 description 1
230000002194 synthesizing effect Effects 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000001043 yellow dye Substances 0.000 description 1
239000004711 α-olefin 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
- G03C7/305—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers
- G03C7/30594—Combination of substances liberating photographically active agents
- 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
- G03C7/305—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers
- G03C7/30576—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers characterised by the linking group between the releasing and the released groups, e.g. time-groups

Landscapes

Physics & Mathematics (AREA)
General Physics & Mathematics (AREA)
Silver Salt Photography Or Processing Solution Therefor (AREA)

JP14903693A 1992-06-24 1993-06-21 カラー写真要素及び写真画像の形成方法 Pending JPH0651465A (ja)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US90379592A	1992-06-24	1992-06-24
US903795		1992-06-24

Publications (1)

Publication Number	Publication Date
JPH0651465A true JPH0651465A (ja)	1994-02-25

Family

ID=25418086

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP14903693A Pending JPH0651465A (ja)	1992-06-24	1993-06-21	カラー写真要素及び写真画像の形成方法

Country Status (2)

Country	Link
EP (1)	EP0577183A1 (fr)
JP (1)	JPH0651465A (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE10335728B3 (de) *	2003-08-05	2005-01-20	Agfa-Gevaert Ag	Farbfotografisches Silberhalogenidmaterial

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5006448A (en) *	1989-06-15	1991-04-09	Eastman Kodak Company	Photographic material and process
US5026628A (en) *	1990-02-22	1991-06-25	Eastman Kodak Company	Photographic material and process comprising a compound capable of forming a wash-out dye
US5272043A (en) *	1991-06-28	1993-12-21	Eastman Kodak Company	Photographic material and process comprising DIR coupler

1993
- 1993-06-21 EP EP93201785A patent/EP0577183A1/fr not_active Withdrawn
- 1993-06-21 JP JP14903693A patent/JPH0651465A/ja active Pending

Also Published As

Publication number	Publication date
EP0577183A1 (fr)	1994-01-05

Publication	Publication Date	Title
JPS60185950A (ja)	1985-09-21	ハロゲン化銀カラ−感光材料
JPS6224252A (ja)	1987-02-02	ハロゲン化銀カラ−写真感光材料
CA1248803A (fr)	1989-01-17	Materiaux photographiques polychromes, a l'halogenure d'argent, photosensibles
JP3283917B2 (ja)	2002-05-20	マゼンタカプラー、抑制剤放出カプラー及びカルボンアミド化合物を含有するカラー写真材料
US4187110A (en)	1980-02-05	Silver halide photographic light-sensitive material
JPH0247650A (ja)	1990-02-16	カラー写真感光材料
JPH08240892A (ja)	1996-09-17	酸化された現像主薬の掃去剤を含有する写真要素
JP3193519B2 (ja)	2001-07-30	ハロゲン化銀カラー写真材料
EP0657776B1 (fr)	1998-08-12	Matériau photographique couleur à l'halogénure d'argent sensible à la lumière
JPH0651465A (ja)	1994-02-25	カラー写真要素及び写真画像の形成方法
JPS6370853A (ja)	1988-03-31	脱銀性の改良されたハロゲン化銀カラ−写真感光材料
JPH0651464A (ja)	1994-02-25	カラー写真要素及び写真画像の形成方法
JP2927374B2 (ja)	1999-07-28	ハロゲン化銀カラー写真感光材料
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