EP0435334B1 - Produit photographique couleur à l'halogénure d'argent contenant un coupleur cyan coloré en jaune - Google Patents

Produit photographique couleur à l'halogénure d'argent contenant un coupleur cyan coloré en jaune Download PDF

Info

Publication number
EP0435334B1
EP0435334B1 EP90125708A EP90125708A EP0435334B1 EP 0435334 B1 EP0435334 B1 EP 0435334B1 EP 90125708 A EP90125708 A EP 90125708A EP 90125708 A EP90125708 A EP 90125708A EP 0435334 B1 EP0435334 B1 EP 0435334B1
Authority
EP
European Patent Office
Prior art keywords
group
silver halide
photographic material
coupler
substituted
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP90125708A
Other languages
German (de)
English (en)
Other versions
EP0435334A3 (en
EP0435334A2 (fr
Inventor
Keiji C/O Fuji Photo Film Co. Ltd. Mihayashi
Takayoshi C/O Fuji Photo Film Co. Ltd. Kamio
Atsuhiro C/O Fuji Photo Film Co. Ltd. Ohkawa
Masuzi C/O Fuji Photo Film Co. Ltd. Motoki
Hidetoshi C/O Fuji Photo Film Co. Ltd. Kobayashi
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.)
Filing date
Publication date
Priority claimed from JP27202490A external-priority patent/JPH03223751A/ja
Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd
Publication of EP0435334A2 publication Critical patent/EP0435334A2/fr
Publication of EP0435334A3 publication Critical patent/EP0435334A3/en
Application granted granted Critical
Publication of EP0435334B1 publication Critical patent/EP0435334B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

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
    • G03C7/3225—Combination of couplers of different kinds, e.g. yellow and magenta couplers in a same layer or in different layers of the photographic material

Definitions

  • This invention relates to a silver halide color photographic material. More particularly, it relates to a silver halide color photographic material comprising a yellow colored cyan coupler and a development inhibitor-releasing compound which has excellent color reproducibility and sharpness over the whole exposure range and whose color reproducibility and sharpness are scarcely affected by changes in processing.
  • JP-A-60-185950 As means for improving color reproducibility and sharpness, the compounds of formula (I) according to the present invention have been proposed in JP-A-60-185950 (the term "JP-A” as used herein means an "unexamined published Japanese patent application"
  • JP-A-61-233741 corresponding to U.S. Patent 4,618,571
  • JP-A-62-151850 JP-A-63-163454 (corresponding to U.S. Patent 4,824,772) and JP-A-63-281160.
  • Interlaminar and edge effects are improved, and color reproducibility and sharpness are also improved to some degree by these compounds.
  • the red-sensitive layer and the blue-sensitive layer are far away from each other, so that there are problems in that a sufficient interlaminar effect between these layers cannot be obtained by use of these compounds and a lowering in the sensitivity of the green-sensitive layer is caused.
  • EP-A-0 423 727 is state of the art according to Art. 54(3) EPC and discloses a photographic material comprising yellow coloured cyan couplers.
  • a first object of the present invention is to provide a photographic material which has excellent color reproducibility, and particularly red color reproducibility, over the whole exposure range.
  • a second object of the present invention is to provide a photographic material having excellent sharpness.
  • a third object of the present invention is to provide a photographic material which is less processing-dependent.
  • a fourth object of the present invention is to provide a photographic material which is highly sensitive.
  • a silver halide color photographic material comprising a support having thereon at least one red-sensitive silver halide emulsion layer containing a cyan coupler, at least one green-sensitive silver halide emulsion layer containing a magenta coupler and at least one blue-sensitive silver halide emulsion layer containing a yellow coupler, wherein the photographic material contains at least one compound represented by the following general formula (I) in an amount of 1 x 10 -6 to 1 x 10 -3 mol/m 2 A-(L 1 ) v -B-(L 2 ) w -DI (I) wherein A represents a group which is cleaved from (L 1 ) v -B-(L 2 ) w -DI by a reaction of the compound of formula (I) with an oxidation product of a developing agent; L 1 represents a bonding group which is cleaved from B after the cleavage of the bond
  • aliphatic group means an aliphatic hydrocarbon group which may be a saturated or unsaturated hydrocarbon group or a straight-chain, branched or cyclic hydrocarbon group such as an alkyl group, a cycloalkyl group, an alkenyl group, a cycloalkenyl group, an alkynyl group.
  • aryl group means at least a substituted or unsubstituted phenyl and naphthyl groups.
  • An acyl moiety e.g. in acyl group, acylamino group
  • a sulfonyl moiety e.g.
  • sulfonyl group means an aliphatic and aromatic sulfonyl moieties.
  • a carbamoyl group, sulfamoyl group, amino group and ureido group include unsubstituted and substituted groups thereof.
  • a heterocyclic group is a 3- to 8-membered having at least one of N, O and S atoms as hetero atom.
  • the compounds represented by general formula (I) are cleaved through the following reaction route during development to release DI: wherein A, L 1 , v, B, L 2 , w and DI have the same meaning as in formula (I); and QDI represents an oxidation product of a developing agent.
  • a in formula (I) represents a coupler moiety for color development or a moiety which is cleaved during development, and which is able to reduce the oxidation product of a developing agent, which exists during development.
  • Coupler moiety represented by A can be used as the coupler moiety represented by A, including yellow coupler moieties (e.g., open chain ketomethylene couplers moieties), magenta coupler moieties (e.g., 5-pyrazolone, pyrazoloimidazole and pyrazolotriazole coupler moieties), cyan coupler moieties (e.g., phenol and naphthol coupler moieties) and non-color forming coupler moieties (e.g., indanone and acetophenone coupler moieties).
  • Heterocyclic coupler moieties described in U.S. Patent 4,315,070, 4,183,752, 3,961,959 or 4,171,223 can be used.
  • Preferred examples of A include coupler moieties represented by formulas (Cp-1), (Cp-2), (Cp-3), (Cp-4), (Cp-5), (Cp-6), (Cp-7), (Cp-8), (Cp-9), and (Cp-10).
  • coupler moieties are preferred, because they have a high coupling rate.
  • the free bonds at the coupling positions represent the bonding positions of the groups which are eliminated by coupling.
  • the total number of carbon atoms in the group is 8 to 40, preferably 10 to 30. In other cases, the total number of carbon atoms is preferably not more than 15.
  • the couplers are bis type, telomer type or polymer type, any one of the above substituent groups is a bivalent group bonded to a repeating unit. In this case, the total numbers of carbon atoms may be beyond the above range.
  • R 41 represents an aliphatic group, an aromatic group or a heterocyclic group
  • R 42 represents an aromatic group or a heterocyclic group
  • R 43 , R 44 , and R 45 which may be the same or different, each represents a hydrogen atom, an aliphatic group, an aromatic group or a heterocyclic group.
  • R 51 has the same meaning as R 41 ; b is 0 or 1; R 52 and R 53 each has the same meaning as R 42 ; R 54 represents R 41 , or an integer of from 1 to 3 and when d is 2 or 3, plural R 59 groups may be the same or different, or each R 59 is a divalent group and these divalent groups may be linked to form a ring structure.
  • Typical examples of the divalent groups which form a ring structure include the following groups. wherein f is O or an integer of 1 to 4 and g is 0, 1 or 2.
  • R 60 has the same meaning as R 41 ;
  • R 61 has the same meaning as R 41 ;
  • R 62 represents R 41 , R 41 OCONH-, R 41 CONH- a halogen atom, a nitro group, a cyano group or R 43 CO-; and
  • e is 0 or an integer of 1 to 4.
  • R 62 or R 63 groups may be the same or different.
  • the aliphatic group is a saturated or unsaturated linear or cyclic straight-chain or branched chain, substituted or unsubstituted aliphatic hydrocarbon group preferably having 1 to 32 carbon atoms, preferably 1 to 22 carbon atoms.
  • Typical examples thereof include a methyl group, ethyl group, propyl group, isopropyl group, butyl group, t-butyl group, i-butyl group, t-amyl group, hexyl group, cyclohexyl group, 2-ethylhexyl group, octyl group, 1,1,3,3-tetramethylbutyl group, decyl group, dodecyl group, hexadecyl group and octadecyl group.
  • the aromatic group is a substituted or unsubstituted phenyl or naphthyl group preferably having 6 to 20 carbon atoms.
  • the heterocyclic group is preferably a 3-membered to 8-membered a substituted or unsubstituted heterocyclic group having 1 to 20 carbon atoms, preferably 1 to 7 carbon atoms wherein the hetero-atom is selected from a nitrogen, oxygen and sulfur atom.
  • heterocyclic group examples include a 2-pyridyl group, 2-thienyl group, 2-furyl group, 1-imidazolyl group, 1-indolyl group, phthalimido group, 1,3,4-thiadiazole-2-yl group, 2-quinolyl group, 2,4-dioxo-1,3-imidazolidine-5-yl group, 2,4-dioxo-1,3-imidazolidine-3-yl group, succinimido group, 1,2,4-triazole-2-yl group and 1-pyrazolyl group.
  • the above-described aliphatic hydrocarbon group, aromatic group and heterocyclic group may optionally have one or more substituent groups.
  • substituent groups include a halogen atom, R 47 O-, R 47 OSO 2 -, a cyano group and a nitro group, wherein R 46 represents an aliphatic group, an aromatic group or a heterocyclic group and R 47 , R 48 and R 49 each represents an aliphatic group, an aromatic group, a heterocyclic group or a hydrogen atom.
  • the aliphatic group, the aromatic group and the heterocyclic group have the same meanings as those described above.
  • R 51 to R 63 and d and e are as follows.
  • R 51 is an aliphatic group or an aromatic group.
  • R 52 , R 53 and R 55 are each an aromatic group.
  • R 54 is preferably R 41 CONH- or R 56 and R 57 are each preferably an aliphatic group, an aromatic group, R 41 O- or R 41 S-; and R 58 is preferably an aliphatic group or an aromatic group.
  • R 59 is preferably a chlorine atom, an aliphatic group or 41 CONH-; d is preferably 1 or 2; and R 60 is preferably an aromatic group.
  • R 59 is preferably R 41 CONH-; d is preferably 1; and R 61 is preferably an aliphatic group or an aromatic group.
  • e is preferably 0 or 1;
  • R 62 is preferably R 41 OCONH-, R 41 CONH- or R 41 SO 2 NH- and these groups are preferably attached to the 5-position of the naphthol ring.
  • R 63 is preferably R 41 CONH-, R 41 SO 2 NH-, a nitro group or a cyano group.
  • R 63 is preferably R 43 OCO- or a R 43 CO-.
  • formula (I) represents a moiety which can conduct reduction
  • the compounds of formula (I) can be represented by formula (II) according on Kendall-Pelz rule.
  • a 1 -P-(X Y) n -Q-A 2 (II)
  • P and Q represent independently an oxygen atom or a substituted or unsubstituted imino group; at least one of the n X groups and the n Y groups represents a methine group having a group of -(L 1 ) v -B(L 2 ) w -DI as a substituent group and the other X and Y groups represent independently a substituted or unsubstituted methine group or a nitrogen atom; n represents an integer of 1 to 3 (when n is 2 or greater, the n X groups or n Y groups may be the same or different groups); and A 1 and A 2 each represents a hydrogen atom or a group which can be eliminated by an alkali.
  • any two substituents of P, X, Y, Q, A 1 and A 2 may be bivalent groups and may be combined together to form a ring structure. All such ring structures are included within the scope of the present invention.
  • P and Q are each a substituted or unsubstituted imino group, a sulfonyl or acyl group-substituted imino group is preferred, and P and Q can be represented by the following formulas:
  • the group represented by G is preferably a straight-chain or branched, linear or cyclic, saturated or unsaturated, substituted or unsubstituted aliphatic hydrocarbon group having 1 to 32 carbon atoms (containing carbon atoms of substituent), preferably 1 to 22 carbon atoms (e.g., methyl, ethyl, benzyl, phenoxybutyl, isopropyl), a substituted or unsubstituted aromatic group having 6 to 10 carbon atoms (e.g., phenyl, 4-methylphenyl, 1-naphthyl, 4-dodecyloxyphenyl), a 4-membered to 7-membered substituted or unsubstituted heterocyclic group containing at least one of a nitrogen atom, a sulfur atom and an oxygen atom as hetero atom and the group may be condensed with a benzene ring (e.g., 1-phenyl
  • substituent for G or G' include a halogen atom, a hydroxy group, a carboxy group, a sulfo group, a phospono group, a phosphino group, a cyano group, an alkoxy group, an aryl group, an aryloxy group, an alkoxycarbonyl group, an amino group, an ammoniumyl group, an acyl group, a carbonamido group, a sulfonamido group, a carbamoyl group, a sulfamoyl group and a sulfonyl group.
  • P and Q are preferably independently an oxygen atom or a group represented by formula (N-1).
  • a 1 and A 2 are each a group which can be eliminated by an alkali (hereinafter referred to as a precursor group)
  • a hydrolyzable group such as an acyl, alkoxycarbonyl, aryloxycarbonyl, carbamoyl, imidoyl, oxazolyl and sulfonyl groups (which preferably have 1 to 6 carbon atoms and which may be substituted with a substituent such as those cited in the definition of G); a precursor group which utilizes reverse Michael reactions as described in U.S.
  • Patent 4,009,029 a precursor group which utilizes, as an intramolecular nucleophilic group, an anion formed after a ring cleavage reaction as described in U.S. Patent 4,310,612; a precursor group which causes a cleavage reaction by the electron transfer of an anion through a conjugated system as described in U.S. Patents 3,674,478, 3,932,480 and 3,993,681; a precursor group which causes a cleavage reaction by the electron transfer of an anion reacted after ring cleavage as described in U.S. Patent 4,335,200; and a precursor group which utilizes an imidomethyl group as described in U.S. Patents 4,363,865 and 4,410,618.
  • the X and Y groups which do not represent a methine group having a group of -(L 1 ) v -B-(L 2 ) w -DI as a substituent preferably represent substituted or unsubstituted methine groups.
  • the mark * represents a position at which a group of -(L 1 ) v -B-(L 2 ) w -DI is attached; P, Q, A 1 and A 2 have the same meaning as in formula (II); R 64 is a substituent group; and q is 0 or an integer of 1 to 3. When q is 2 or greater, the two or more R 64 groups may be the same or different groups. When two R 64 groups are substituent groups attached to adjoining carbon atoms, they each may be a bivalent group and may be combined together to form a ring structure. All such ring structures are included within the scope of the present invention.
  • benzene condensed rings which include such ring structures as naphthanenes, benzonorbornenes, chromans, benzothiophenes, benzofurans, 2,3-dihydrobenzofurans or indenes. These condensed rings may have one or more substituent groups.
  • Preferred examples of the substituent groups for these condensed rings when two R 64 groups form a condensed ring and preferred examples of R 64 when the R 64 groups do not form a condensed ring include an R 41 group, a halogen atom, R 43 O-, R 43 S-, R 43 (R 44 )NCO-, R 43 OOC-, R 43 SO 2 -, R 43 (R 44 )NSO 2 -, R 43 CON(R 43 )-, R 41 SO 2 (R 43 )-, R 43 CO-, R 41 COO-, R 41 SO-, a nitro group, R 43 (R 44 )NCON-(R 45 )-, a cyano group, R 41 OCON(R 43 )-, R 43 OSO 2 -, R 43 (R 44 )N-, R 43 (R 44 )NSO 2 N(R 45 )-, and wherein R 41 , R 43 , R 44 and R 45 are as defined above.
  • a 1 and A 2 are preferably hydrogen atom.
  • the groups represented by L 1 and L 2 in formula (I) may be used or may not be used according to purpose.
  • Examples of the groups represented by L 1 and L 2 when used include the following bonding groups. In the following formulas, either the mark * represents a position at which A is bonded and the mark ** represents a position at which B is bonded, or the mark * represents a position at which B is bonded and the mark ** represents a position at which DI is bonded.
  • R 10 is a group which can be substituted to a benzene ring (typical substituents thereof being those already described above in the definition of R 64 );
  • R 11 has the same meaning as R 41 ;
  • R 12 is a hydrogen atom or one of the groups already described above in the definition of R 64 ; and
  • t is an integer of 0 to 4.
  • the group represented by B in formula (I) is preferably a group which can be oxidized and is capable of reducing an oxidation product of a developing agent, or a group which forms a substantially colorless compound by a coupling reaction with an oxidation product of a developing agent.
  • a 2 ', P', Q' and n' have the same meaning as A 2 , P, Q and n in formula (II), respectively, with the proviso that at least one of the n' X' groups and the n' Y' groups is a methine group having an (L 2 ) w -DI group as a substituent group and the other X' and Y' groups are a substituted (examples of the substituent include the same group as those in the definition for R 64 and a hydroxy group) or unsubstituted methine group or a nitrogen atom.
  • a 2 ', P', Q', X' and Y' When any two of A 2 ', P', Q', X' and Y' are a bivalent group, they may be combined together to form a ring structure. All such ring structures are included within the scope of the present invention. Examples of the ring structures include a benzene ring, an imidazole ring and a pyridine ring.
  • P' is preferably an oxygen atom and Q' is preferably an oxygen atom or a group represented by any one of the following formulas.
  • G is as defined in formulas (N-1) and (N-2).
  • Q' is an oxygen atom or an group.
  • Typical examples of the group represented by B in formula (I) include the following groups wherein the mark * represents a position where each group is bonded to A-(L 1 ) n in formula (I) and the mark ** represents a position where each group is bonded to (L 2 ) w -DI in formula (I).
  • R 13 has the same meaning as R 64 , R 14 and R 15 each have the same meaning as R 41 , l is an integer of 0 to 2, m is an integer of 0 to 3, and a is an integer of 0 or 1.
  • B which is released and forms a compound exhibiting a reducing action
  • B include the reducing agents described in U.S. Patents 4,741,994 and 4,477,560, JP-A-61-102646, JP-A-61-107245, JP-A-61-113060, JP-A-64-13547, JP-A-64-13548 and JP-A-64-73346.
  • the group represented by B in formula (I) is a group which forms a substantially colorless compound by a coupling reaction with an oxidation product of a developing agent
  • examples of the group include phenol and naphthol coupler moieties, pyrazolone coupler moieties and indanone coupler moieties. These moieties are bonded to A-(L 1 ) v through an oxygen atom. These coupler moieties become couplers after release from A-(L 1 ) v and are coupled with oxidation products of developing agents.
  • colored dyes are formed, but when diffusibility is properly increased without any nondiffusing group, the dyes are dissolved into processing solutions during development and hence the dyes are substantially not left behind in the photographic material.
  • the dyes formed are diffusing dyes, they react with alkaline ingredients (e.g., hydroxyl ion, sulfite ion) in developing solutions during development; the dyes are decomposed and are made colorless; and hence the dyes are substantially not left behind in the photographic material even when colored dyes are formed.
  • alkaline ingredients e.g., hydroxyl ion, sulfite ion
  • B include the following groups wherein the mark * represents a position where each group is bonded to A-(L 1 ) v and the mark ** represents a position where each group is bonded to (L 2 ) w -DI
  • R 13 , R 14 and m are as defined above and R 16 has the same meaning as R 43 .
  • the group represented by B in formula (I) is preferably a group which reduces an oxidation product of a developing agent after release from A-(L 1 ) v .
  • the compounds represented by formula (I) according to the present invention may be in the form of a polymer. All such polymers are included within the scope of the present invention. Namely, the polymers are derived from a monomer compound represented by the following general formula (P-1) and composed of a repeating unit represented by the following general formula (P-II), or copolymers of the monomer compound with at least one non-color forming monomer which has at least one ethylene group and is incapable of coupling with oxidation products of aromatic primary amine developing agents. Two or more members of the above monomer compounds may be polymerized simultaneously.
  • RR represents a hydrogen atom, a lower alkyl group having 1 to 4 carbon atoms or a chlorine atom;
  • a 11 represents -CONH-, -NHCONH-, -NHCOO-, -COO- -SO 2 -, -CO-, -NHCO-, -SO 2 NH-, -NHSO 2 -, -OCO-, -OCONH-, -NH- or -O-;
  • a 12 represents -CONH- or -COO-;
  • a 13 represents a substituted or unsubstituted alkylene or an aralkylene group preferably having 1 to 10 carbon atoms, or an unsubstituted or substituted arylene group.
  • the alkylene group or alkylene moiety in the aralkylene group may be straight-chain or branched.
  • QQ represents a moiety of a compound represented by formula (I) and may be bonded to any site of A, L 1 , B and L 2 .
  • i, j, and k each represents 0 or 1, but there is no case where i, j and k are 0 simultaneously.
  • substituent groups for the alkylene group, the aralkylene group or the arylene group represented by A 13 include aryl (e.g., phenyl, naphthyl), nitro, hydroxyl, cyano, sulfo, alkoxy (e.g., methoxy), aryloxy (e.g., phenoxy), acyloxy (e.g., acetoxy), acylamino (e.g., acetylamino), sulfonamido (e.g., methanesulfonamido), sulfamoyl (e.g., methylsulfamoyl), halogen (e.g., fluorine, chlorine, bromine), carboxy, carbamoyl (e.g., methylcarbamoyl), alkoxycarbonyl (e.g., methoxycarbonyl) and sulfonyl (e.g., methylsulf
  • These non-color forming ethylenic unsaturated monomers may be used either alone or as a mixture of two or more of them.
  • moieties of conventional development inhibitors can be used.
  • a heterocyclic mercapto group, a 1-indazolyl group and a triazolyl group can be preferably used. More specifically, examples thereof include a tetrazolylthio group, a thiadiazolylthio group, an oxadiazolylthio group, a triazolylthio group, a benzoxazolylthio group, a benzothiazolylthio group, a benzimidazolylthio group, a 1-(or 2-)benztriazolyl group, a 1,2,4-triazole-1-(or 4-)yl group and a 1-indazolyl group.
  • substituent groups include aliphatic groups, aromatic groups, heterocyclic groups and those groups already described above in the definition of the substituent groups for the aromatic group.
  • the compounds of formula (I) according to the present invention can be synthesized by the methods described in U.S. Patents 4,618,571 and 4,770,982, JP-A-63-284159, JP-A-60-203943 and JP-A-63-23152.
  • the compounds of formula (I) according to the present invention be added to sensitive silver halide emulsion layers or adjoining layers in the photographic materials. It is particularly preferred that the compounds be added to the red-sensitive silver halide emulsion layer.
  • the compounds are used in an amount of 1 ⁇ 10 -6 to 1 ⁇ 10 -3 mol/m 2 , preferably 3 ⁇ 10 -6 to 5 ⁇ 10 -4 mol/m 2 , more preferably 1 ⁇ 10 -5 to 2 ⁇ 10 -6 mol/m 2 .
  • the yellow colored cyan couplers in the photographic material of the present invention refer to cyan couplers which have an absorption maximum at 400 nm to 500 nm in the visible absorption region of the couplers and which form cyan dyes having an absorption maximum at 630 nm to 750 nm in the visible absorption region by the coupling thereof with the oxidation product of an aromatic primary amine developing agent.
  • the amount of the yellow colored cyan coupler in the silver halide color photographic material of the present invention is preferably from 0.05 to 0.30 g/m 2 .
  • cyan couplers which release a moiety of a water-soluble compound.
  • the moiety include a 6-hydroxy-2-pyridone-5-ylazo group, a pyrazolone-4-ylazo group, a 2-acylaminophenylazo group or a 2-sulfonamidophenylazo group, and a 5-aminopyrazol-4-ylazo group by a coupling reaction with the oxidation product of an aromatic primary amine developing agent.
  • the water soluble compound should be dissolved out from the photographic material during development processing.
  • the compound is preferably soluble in a developing solution of pH 9 to 12 in an amount of at least 1 g/l, more preferably at least 3 g/l at 25°C.
  • the colored cyan couplers in the photographic material of the present invention can be represented by the following general formulas (CI) to (CIV).
  • Cp represents a cyan coupler moiety (T is bonded to the coupling site thereof); T represents a timing group; k represents an integer of 0 or 1; X represents an N-, O- or S-containing bivalent group which is bonded to (T) k through the N, O or S atom and which also is bonded to Q; and Q represents an arylene group or a bivalent heterocyclic group (preferably containing 6 to 12 carbon atoms, e.g., phenylene, naphthylene).
  • R 1 and R 2 are independently a hydrogen atom, a carboxyl group, a sulfo group, a cyano group, an aliphatic hydrocarbon group, an alicyclic hydrocarbon group, an aryl group, a heterocyclic group, a carbamoyl group, a sulfamoyl group, a carbonamido group, a sulfonamido group or an alkylsulfonyl group;
  • R 3 is a hydrogen atom, an aliphatic hydrocarbon group, an alicyclic hydrocarbon group, an aryl group or a heterocyclic group; and at least one of T, X, Q, R 1 , R 2 and R 3 has a water-soluble group (e.g., hydroxyl, carboxyl, sulfo, amino, ammoniumyl, phosphono, phosphino, hydroxysulfonyloxy).
  • a water-soluble group e.g.,
  • R 4 is an acyl group or a sulfonyl group
  • R 5 is a group which can be attached to the benzene ring
  • j is an integer of 0 to 4; when j is 2 or greater, the two or more R 5 groups may be the same or different
  • at least one of T, X, Q, R 4 and R 5 has a water-soluble group (e.g., hydroxyl, carboxyl, sulfo, phosphono, phosphino, hydroxysulfonyloxy, amino, ammoniumyl).
  • R 9 is a hydrogen atom, a carboxyl group, a sulfo group, a cyano group, an aliphatic hydrocarbon group, an alicyclic hydrocarbon group, an aryl group, an alkoxy group, a cycloalkyloxy group, an aryloxy group, a heterocyclic group, a carbamoyl group, a sulfamoyl group, a carbonamido group, a sulfonamido group, an alkylsulfonyl group, an alkoxycarbonyl group, an aryloxycarbonyl group or a sulfonyl group; R 10 is a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group or a heterocyclic group; and at least one of T, X, Q, R 9 and R 10 has a water-soluble group (e.g., hydroxyl, carb
  • Examples of the coupler moiety represented by Cp include conventional cyan coupler moiety (e.g., phenol and naphthol couplers).
  • Cp coupler moiety represented by general formulas (Cp-6), (Cp-7) and (Cp-8) among those exemplified in the description of the compounds of formula (I).
  • the timing group represented by T in formulas (CI) to (CIV) is a group which is cleaved from X after the cleavage of the bond between Cp and T by the coupling reaction of the couplers with an oxidation product of an aromatic primary amine developing agent.
  • the timing group is used for various purposes, e.g., stabilizing the couplers, controlling the release timing of X, etc.
  • Examples of the timing group include conventional timing groups represented by formulas (T-1) to (T-7) exemplified in the description of the compounds of formula (I).
  • k may be an integer of 0 or 1, it is generally preferred the case where k is 0, that is, Cp is directly bonded to X.
  • X is a bivalent group which is bonded to (T) k through an N, O or S atom.
  • X is -O-, -S-, -OSO 2 -, -OSO 2 NH- or a bivalent group which is bonded to (T) k through N, such as a heterocyclic group (e.g., a group derived from pyrrolidine, piperidine, morpholine, piperazine, pyrrole, pyrazole, imidazole, 1,2,4-triazole, benztriazole, succinimide, phthalimide, oxazolidine-2,4-dione, imidazolidine-2,4-dione, 1,2,4-triazolidine-3,5-dione) or a composite group derived from these groups and an alkylene group (e.g., methylene, ethylene, propylene), a cycloalkylene group (e.g., 1,4-cyclohex
  • the mark * represents the position where the group is bonded to (T) k ; the mark ** represents the position where the group is bonded to Q;
  • X 1 represents -O- or -S-;
  • L represents an alkylene group;
  • X 2 represents a single bond, -O-, -S-, -CO-, -OSO 2 NH- or NHSO 2 O-; and
  • m represents an integer of 0 to 3.
  • the sum total of carbon atoms (hereinafter referred to as the carbon number) in X is preferably 0 to 12, more preferably 0 to 8. Most preferably, X is -OCH 2 CH 2 O-.
  • Q is an arylene group or a bivalent heterocyclic group.
  • the arylene group may be a condensed ring and may have one or more substituent groups (examples of the substituent groups include halogen atom, hydroxyl, carboxyl, sulfo, nitro, cyano, amino, ammonium, phosphono, phosphino, alkyl, cycloalkyl, aryl, carbonamido, sulfonamido, alkoxy, aryloxy, acyl, sulfonyl, carboxyl, carbamoyl and sulfamoyl).
  • the arylene group has preferably 6 to 15 carbon atoms, more preferably 6 to 10 carbon atoms.
  • the heterocyclic group is a 3-membered to 8-membered, preferably 5-membered to 7-membered, monocyclic or condensed ring heterocyclic group containing at least one hetero-atom selected from the group consisting of N, O, S, P, Se and Te as a member of the heterocyclic ring (e.g., a group derived from pyridine, thiophene, furan, pyrrole, pyrazole, imidazole, thiazole, oxazole, benzthiazole, benzoxazole, benzofuran, benzothiophene, 1,3,4-thiodiazole, indole, and quinoline) and may have one or more substituent groups (examples of the substituent groups being the same as those for the arylene group of Q).
  • the carbon number is preferably 2
  • the aliphatic hydrocarbon group represented by R 1 , R 2 or R 3 may be any of a straight-chain and branched (e.g., alkyl), and may contain unsaturated bonds and may have one or more substituent groups (examples of the substituent groups include halogen atom, hydroxyl, carboxyl, sulfo, phosphono, phosphino, cyano, alkoxy, aryl, alkoxycarbonyl, amino, ammoniumyl, acyl, carbonamido, sulfonamido, carbamoyl, sulfamoyl, and sulfonyl).
  • substituent groups include halogen atom, hydroxyl, carboxyl, sulfo, phosphono, phosphino, cyano, alkoxy, aryl, alkoxycarbonyl, amino, ammoniumyl, acyl, carbonamido, sulfonamido, carbamo
  • R 1 , R 2 or R 3 is an alicyclic hydrocarbon group
  • the group is a 3-membered to 8-membered group which may have crosslinking groups, unsaturated bonds or substituent groups (examples of the substituent groups being the same as those described above in the definition of the substituent groups for the aliphatic hydrocarbon group of R 1 , R 2 or R 3 ).
  • R 1 , R 2 or R 3 is an aryl group
  • the aryl group may be a condensed ring and may have one or more substituent groups (examples of the substituent groups being an alkyl group, a cycloalkyl group and those described above in the definition of the substituent groups for the aliphatic hydrocarbon group of R 1 , R 2 or R 3 ).
  • the heterocyclic group is a 3-membered to 8-membered, preferably 5-membered to 7-membered, monocyclic or condensed ring heterocyclic group containing at least one hetero-atom selected from the group consisting of N, S, O, P, Se and Te as a member of the heterocyclic ring (e.g., imidazolyl, thienyl, pyrazolyl, thiazolyl, pyridyl, quinolynyl) and may have one or more substituent groups (examples of the substituent groups being the same as those described above in the definition of the substituent groups for the aryl group of R 1 , R 2 or R 3 ).
  • carboxyl group may include carboxylato group
  • sulfo group may include sulfonato group
  • phosphino group may include phosphinato group
  • phosphono group may include phosphonato group.
  • Counter ions are, for example, Li + , Na + , K + , ammonium.
  • R 1 is a hydrogen atom, a carboxyl group, an alkyl group having 1 to 10 carbon atoms (e.g., methyl, t-butyl, sulfomethyl, 2-sulfomethyl, carboxymethyl, 2-carboxymethyl, 2-hydroxymethyl, benzyl, ethyl, isopropyl) or an aryl group having 6 to 12 carbon atoms (e.g., phenyl, 4-methoxyphenyl, 4-sulfophenyl) with a hydrogen atom, a methyl group or a carboxyl group being particularly preferred.
  • an alkyl group having 1 to 10 carbon atoms e.g., methyl, t-butyl, sulfomethyl, 2-sulfomethyl, carboxymethyl, 2-carboxymethyl, 2-hydroxymethyl, benzyl, ethyl, isopropyl
  • an aryl group having 6 to 12 carbon atoms e.g., pheny
  • R 2 is a cyano group, a carboxyl group, a carbamoyl group having 1 to 10 carbon atoms, a sulfamoyl group having 0 to 10 carbon atoms, a sulfo group, an alkyl group having 1 to 10 carbon atoms (e.g., methyl, sulfomethyl), a sulfonyl group having 1 to 10 carbon atoms (e.g., methylsulfonyl, phenylsulfonyl), a carbonamido group having 1 to 10 carbon atoms (e.g., acetamido, benzamido) or a sulfonamido group having 1 to 10 carbon atoms (e.g., methanesulfonamido, toluenesulfonamido) with a cyano group, a carbamoyl group or a carboxyl group being particularly preferred.
  • R 3 is a hydrogen atom, an alkyl group having 1 to 12 carbon atoms (e.g., methyl, sulfomethyl, carboxymethyl, ethyl, n-butyl, benzyl, 4-sulfobenzyl) or an aryl group having 6 to 15 carbon atoms (e.g., phenyl, 4-carboxyphenyl, 3-carboxyphenyl, 4-methoxyphenyl, 2,4-dicarboxyphenyl, 2-sulfophenyl, 3-sulfophenyl, 4-sulfophenyl, 2,4-disulfophenyl, 2,5-disulfophenyl) among which an alkyl group having 1 to 7 carbon atoms or an aryl group having 6 to 10 carbon atoms is more preferred.
  • an alkyl group having 1 to 12 carbon atoms e.g., methyl, sulfomethyl, carboxymethyl, ethyl,
  • R 4 preferably is an acyl group represented by the following general formula (III) or a sulfonyl group represented by the following general formula (IV): R 11 SO 2 - (IV)
  • R 11 is an aliphatic hydrocarbon group
  • the group includes both straight-chain and branched groups (preferably having 1 to 6 carbon atoms), and may contain unsaturated bonds and may have one or more substituent groups (examples of the substituent groups include halogen atom, hydroxyl, carboxyl, sulfo, phosphono, phosphino, cyano, alkoxy, aryl, alkoxycarbonyl, amino, ammoniumyl, acyl, carbonamido, sulfonamido, carbamoyl, sulfamoyl, and sulfonyl).
  • R 11 is an alicyclic hydrocarbon group
  • the group is a 3-membered to 8-membered group which may contain crosslinking groups and unsaturated bonds and may have one or more substituent groups (examples of the substituent groups being those described above in the definition of the substituent groups for the aliphatic hydrocarbon group of R 11 ).
  • R 11 is an aryl group
  • the aryl group may be a condensed ring and may have one or more substituent groups (examples of the substituent groups include an alkyl group, a cycloalkyl group and those described above in the definition of the substituent groups for the aliphatic hydrocarbon group of R 11 ).
  • the heterocyclic group is a 3-membered to 8-membered (preferably 5-membered to 7-membered) monocyclic or condensed ring heterocyclic group containing at least one hetero-atom selected from the group consisting of N, S, O, P, Se and Te as a member of the heterocyclic ring (e.g., imidazolyl, thienyl, pyrazolyl, thiazolyl, pyridyl, quinolyl) and may have one or more substituent groups (examples of the substituent groups being those described above in the definition of the substituent groups for the aryl group of R 11 ).
  • carboxyl group may include carboxylato group
  • sulfo group may include sulfonato group
  • phosphino group may include phosphinato group
  • phosphono group may include phosphonato group.
  • Counter ions are for example, Li + , Na + , K + , ammonium.
  • R 11 is an alkyl group having 1 to 10 carbon atoms (e.g., methyl, carboxymethyl, sulfoethyl, cyanoethyl), a cycloalkyl group having 5 to 8 carbon atoms (e.g., cyclohexyl, 2-carboxycyclohexyl) or an aryl group having 6 to 10 carbon atoms (e.g., phenyl, 1-naphthyl, 4-sulfophenyl) among which an alkyl group having 1 to 3 carbon atoms and an aryl group having 6 carbon atoms are particularly preferred.
  • a cycloalkyl group having 5 to 8 carbon atoms e.g., cyclohexyl, 2-carboxycyclohexyl
  • an aryl group having 6 to 10 carbon atoms e.g., phenyl, 1-naphthyl, 4-sulfophenyl
  • R 5 is a group which can be attached to the benzene ring and is preferably an electron donative group. Particularly preferably, R 5 is a group of -NR 12 R 13 or -OR 14 which is preferably attached to the 4-position of the ring.
  • R 12 , R 13 and R 14 are each a hydrogen atom, an alkyl group, a cycloalkyl group, an aryl group or a heterocyclic group and each has the same meaning as R 11 .
  • R 12 and R 13 may be combined together to form a ring.
  • a nitrogen-containing heterocyclic ring wherein atoms other than the nitrogen all are carbon atoms is preferred.
  • j is an integer of 0 to 4, preferably 1 to 2, particularly preferably 1.
  • R 9 or R 10 is an aliphatic hydrocarbon group
  • the group may be any of a straight chain group and a branched group, may contain unsaturated bonds and may have one or more substituent groups (e.g., halogen atom, hydroxyl, carboxyl, sulfo, phosphono, phosphino, cyano, alkoxy, aryl, alkoxycarbonyl, amino, ammonium, acyl, carbonamido, sulfonamido, carbamoyl, sulfamoyl, sulfonyl).
  • substituent groups e.g., halogen atom, hydroxyl, carboxyl, sulfo, phosphono, phosphino, cyano, alkoxy, aryl, alkoxycarbonyl, amino, ammonium, acyl, carbonamido, sulfonamido, carbamoyl, sulfamoyl,
  • R 9 or R 10 is an alicyclic hydrocarbon group
  • the group is a 3-membered to 8-membered group which may have crosslinking groups, unsaturated bonds or substituent groups (examples of the substituent groups being those described above in the definition of the substituent groups for the aliphatic hydrocarbon group of R 9 or R 10 ).
  • R 9 or R 10 is an aryl group
  • the aryl group may be a condensed ring and may have one or more substituent groups (examples of the substituent groups being an alkyl group, a cycloalkyl group and those described above in the definition of the substituent groups for the alipahtic hydrocarbon group of R 9 or R 10 ).
  • the heterocyclic group is a 3-membered to 8-membered (preferably 5-membered to 7-membered) monocyclic or condensed ring heterocyclic group containing at least one hetero-atom selected from the group consisting of N, S, O, P, Se and Te as a member of the heterocyclic ring (e.g., imidazolyl, thienyl, pyrazolyl, thiazolyl, pyridyl, quinolinyl) and may have one or more substituent groups (examples of the substituent groups being those described above in the definition of the substituent groups for the aryl group of R 9 or R 10 ).
  • carboxyl group may include carboxylato group
  • sulfo group may include sulfonato group
  • phosphino group may include phosphinato group
  • phosphono group may include phosphonato group.
  • Counter ions are for example Li + , Na + , K + , ammonium.
  • R 9 is a cyano group, a carboxyl group, a carbamoyl group having 1 to 10 carbon atoms, an alkoxycarbonyl group having 2 to 10 carbon atoms, an aryloxycarbonyl group having 7 to 11 carbon atoms, a sulfamoyl group having 0 to 10 carbon atoms, a sulfo group, an alkyl group having 1 to 10 carbon atoms (e.g., methyl, carboxymethyl, sulfomethyl), a sulfonyl group having 1 to 10 carbon atoms (e.g., methylsulfonyl, phenylsulfonyl), a carbonamido group having 1 to 10 carbon atoms (e.g., acetamido, benzamido), a sulfonamido group having 1 to 10 carbon atoms (e.g., methanesulfonamido, toluene
  • R 10 is a hydrogen atom, an alkyl group having 1 to 12 carbon atoms (e.g., methyl, sulfomethyl, carboxymethyl, ethyl, 2-sulfoethyl, 2-carboxyethyl, 3-sulfopropyl, 3-carboxypropyl, 5-sulfopentyl, 5-carboxypentyl, 4-sulfobenzyl) or an aryl group having 6 to 15 carbon atoms (e.g., phenyl, 4-carboxyphenyl, 3-carboxyphenyl, 2,4-dicarboxyphenyl, 4-sulfophenyl, 3-sulfophenyl, 2,5-disulfophenyl, 2,4-disulfophenyl) among which an alkyl group having 1 to 7 carbon atoms or an aryl group having 6 to 10 carbon atoms is more preferred.
  • an alkyl group having 1 to 12 carbon atoms
  • Cp, X, Q, in formulas (CI) to (CIV) include the following groups.
  • the compound represented by formula (I) and the yellow colored cyan coupler each are incorporated in at least one of said silver halide emulsion layers and a light-insensitive intermediate layer adjacent thereto.
  • the compound represented by formula (I) is incorporated in the layer having the same color sensitivity as that of the layer containing the yellow colored cyan coupler.
  • the compound represented by general formula (I) and the yellow colored cyan coupler are contained in the same red-sensitive silver halide emulsion layer.
  • the colored couplers represented by formula (CI) can be generally synthesized by the diazo coupling reaction of a 6-hydroxy-2-pyridone compound with an aromatic diazonium salt or heterocyclic diazonium salt having a coupler structure.
  • the former 6-hydroxy-2-pyridone compounds can be synthesized by methods described in Klinsberg, Heterocyclic Compound - Pyridine and Its Derivatives, Part 3 (Interscience 1962); J. Am. Chem. Soc., Vol. 65, page 449 (1943); J. Chem. Tech. Biotechnol., Vol. 36, page 410 (1986); Tetrahedron, Vol. 22, page 445 (1966); JP-B-61-52827 (the term "JP-B” as used herein means an "examined Japanese patent publication”); West German Patents 2,162,612, 2,349,709 and 2,902,486; and U.S. Patent 3,763,170.
  • the latter diazonium salts can be synthesized according to the methods described in U.S. Patents 4,004,929 and 4,138,258, JP-A-61-72244 and JP-A-61-273543.
  • the diazo coupling reaction of the 6-hydroxy-2-pyridone compounds with the diazonium salts can be carried out in a solvent such as methanol, ethanol, methyl cellosolve, acetic acid, N,N-dimethylformamide, N,N-dimethylacetamide, tetrahydrofuran, dioxane, water or a mixture thereof.
  • reaction temperature is generally from -78 to +60°C, preferably from -20 to +30°C.
  • the resulting crude crystal was purified from hot methanol in the same manner as in Synthesis Example 1 to give 14.8 g of the desired coupler (YC-3) with a melting point of 246 to 251°C (decomposition).
  • the structure of the compound was confirmed by 1 HNMR spectrum, mass spectrum and elemental analysis.
  • the compound exhibited a maximum absorption wavelength in methanol at 457.6 nm and had a molecular extinction coefficient of 42700.
  • the compound was found to have good spectral absorption characteristics as a yellow colored coupler.
  • the coupler (YC-30) had a melting point of 154-6°C. The structure thereof was confirmed by 1 HNMR spectrum, mass spectrum and elemental analysis. The compound exhibited a maximum absorption wavelength in methanol at 458.2 nm and had a molecular extinction coefficient of 42800. The compound was found to have good spectral absorption characteristics as a yellow colored coupler.
  • the yellow colored cyan couplers represented by formulas (CII) to (CIV) can be synthesized by methods described in JP-B-58-6939 (the term "JP-B” as used herein means an "examined published Japanese patent publication") and JP-A-1-197563.
  • the couplers represented by general formula (CI) can be synthesized by the methods described in patent specifications cited above.
  • the couplers represented by formulas (CI) and (CII) are more preferred, and the couplers of formula (CI) are particularly preferred.
  • the yellow colored cyan couplers of the present invention be added to sensitive silver halide emulsion layers or light-insensitive intermediate layers adjacent thereto in the photographic materials. It is particularly preferred that the yellow colored cyan couplers be added to the red-sensitive emulsion layer.
  • the total amount of the couplers to be added to the photographic material is preferably 0.005 to 0.30 g/m 2 , more preferably 0.02 to 0.20 g/m 2 , most preferably 0.03 to 0.15 g/m 2 .
  • the yellow colored couplers in the photographic material of the present invention can be added in the same manner as in the addition of conventional couplers described hereinafter.
  • a polymer coupler obtained from at least one monomer represented by the following general formula (P) be used in the green-sensitive layer of the silver halide color photographic material (especially, the order of layers from the support is red-, green- and blue-sensitive layers, and the yellow colored coupler and the compound represented by formula (I) are incorporated to the red-sensitive layer) of the present invention:
  • R 121 represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms or a chlorine atom; -D- represents -COO-, -CONR 122 - or a substituted or unsubstituted phenylene group; -E- represents a substituted or unsubstituted alkylene, phenylene or aralkylene group; -F- represents -CONR 122 -, -NR 122 CONR 122 -, -NR 122 COO-, -NR 122 CO-, -OCONR 122 -, -NR 122 -, -COO-, -OCO-, -CO-, -O-, -S-, -SO 2 -, -NR 122 SO 2 -, or -SO 2 NR 122 -; R 122 represents a hydrogen atom or a substituted or unsubstituted, saturated or unsaturated aliphatic group or
  • substituents for groups represented by D, E, R 122 include a halogen atom, a hydroxy group, a carboxy group, a sulfo group, a phospono group, a phosphino group, a cyano group, an alkoxy group, an aryl group, an aryloxy group, an alkoxycarbonyl group, an amino group, an ammoniumyl group, an acyl group, a carbonamido group, a sulfonamido group, a carbamoyl group, a sulfamoyl group and a sulfonyl group.
  • T in formula (P) represents a magenta coupler moiety (which is bonded to ( ⁇ F) ⁇ r - at any one site of Ar, Z and R 133 ) represented by the following general formula (Q)
  • Ar represents known substituent groups at the 1-position of 2-pyrazoline-5-one couplers, such as an alkyl group, a substituted alkyl group (e.g., haloalkyl such as fluoroalkyl, cyanoalkyl, benzylalkyl), a substituted or unsubstituted heterocyclic group (e.g., 4-pyridyl group, 2-thiazolyl group), a substituted or unsubstituted aryl group (an example of a substituent group for the heterocyclic group and the aryl group includes an alkyl group, e.g., methyl and ethyl), an alkoxy group (e.g., methoxy, ethoxy), an aryloxy group (e.g., phenyloxy), an alkoxycarbonyl group (e.g., methoxycarbonyl), an acylamino group (e.g., acetylamino), a
  • substituent groups are a halogen atom, an alkyl group, an alkoxy group, an alkoxycarbonyl group and a cyano group.
  • R 133 represents a substituted or unsubstituted anilino group, an acylamino group (e.g., alkylcarbonamido, phenylcarbonamido, alkoxycarbonamido, phenyloxycarbonamido), a ureido group (e.g., alkylureido, phenylureido) or a sulfonamido group. These groups may be substituted.
  • an acylamino group e.g., alkylcarbonamido, phenylcarbonamido, alkoxycarbonamido, phenyloxycarbonamido
  • a ureido group e.g., alkylureido, phenylureido
  • sulfonamido group e.g., sulfonamido group.
  • substituent groups include a halogen atom (e.g., fluorine, chlorine, bromine), a straight-chain or branched alkyl group (e.g., methyl, t-butyl, octyl, tetradecyl), an alkoxy group (e.g., methoxy, ethoxy, 2-ethylhexyloxy, tetradecyloxy), an acylamino group (e.g., acetamido, benzamido, butane-amido, octaneamido, tetradecaneamido, ⁇ -(2,4-di-tert-amylphenoxy)acetamido, ⁇ -(2,4-di-tert-amylphenoxy)butylamido, ⁇ -(3-pentadecylphenoxy)hexaneamido, ⁇ -(4-hydroxy-3-tert-butyl
  • the alkyl group and alkyl moiety preferably has 1 to 36 carbon atoms and the aryl group preferably has 6 to 38 carbon atoms.
  • Z represents a halogen atom (e.g., chlorine atom, bromine atom), a group which is bonded through an oxygen atom and eliminated by a coupling reaction (e.g., acetoxy, propanoyloxy, benzoyloxy, ethoxyoxaloyloxy, pyruvvinyloxy, cinnamoyloxy, phenoxy, 4-cyanophenoxy, 4-titanium sulfonamidophenoxy, ⁇ -naphthoxy, 4-cyanoxy, 4-methanesulfonamidophenoxy, ⁇ -naphthoxy, 3-pentadecylphenoxy, benzyloxycarbonyloxy, ethoxy, 2-cyanoethoxy, benzyloxy, 2-phenethyloxy, 2-phenoxyethoxy, 5-phenyltetrazolyloxy, and 2-benzothiazolyloxy), a coupling eliminating group which is bonded through a nitrogen atom
  • Preferred coupling eliminating groups are those which are bonded through a nitrogen atom, and an especially preferred coupling eliminating group is a pyrazolyl gorup.
  • E represents a substituted or unsubstituted alkylene, aralkylene, or phenylene group preferably having 1 to 10 carbon atoms.
  • the alkylene group may be a straight-chain or branched-chain.
  • Examples of the alkylene group include a methylene group, a methylmethylene group, a dimethylmethylene group, a dimethylene group, a trimethylene group, a tetramethylene group, a pentamethylene group, a hexamethylene group, and a decylmethylene group.
  • An example of the aralkylene group include a benzylidene group.
  • An example of the phenylene group include a p-phenylene group, a m-phenylene group and a methylphenylene group.
  • substituents for the alkylene group, the aralkylene group or the phenylene group represented by E include an aryl group (e.g., phenyl), a nitro group, a hydroxyl group, a cyano group, a sulfo group, an alkoxy group (e.g., methoxy), an aryloxy group (e.g., phenoxy), an acyloxy gorup (e.g., acetoxy), an acylamino group (e.g., acetylamino), a sulfonamido group (e.g., methanesulfonamido), a sulfamoyl group (e.g., methylsulfamoyl), a halogen atom (e.g., fluorine, chlorine, and bromine), a carboxy group, a carbamoyl group (e.g., methylcarbamoyl), an alk
  • non-color forming ethylene monomers which are capable of copolymerizing with a coupler monomer represented by formula (P) and are incapable of coupling with an oxidized product of an aromatic primary amine developing agent include an acrylic acid ester, a methacrylic acid ester, a crotonic acid ester, a vinyl ester, a maleic acid diester, a fumaric acid diester, an itaconic acid diester, an acrylamide, a methacrylamide, a vinyl ether and a styrene.
  • acrylic acid ester examples include methylacrylate, ethylacrylate, n-propylacrylate, isopropylacrylate, n-butylacrylate, isobutylacrylate, terbutylacrylate, hexylacrylate, 2-ethylhexyl acrylate, acetoxyethyl acrylate, phenyl acrylate, 2-methoxy acrylate, 2-ethoxy acrylate and 2-(2-methoxyethoxy)ethyl acrylate.
  • methacrylic esters examples include methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, n-butyl methacrylate, tert-butyl methacrylate, cyclohexyl methacrylate, 2-hydroxyethyl methacrylate and 2-ethoxyethyl methacrylate.
  • crotonic esters examples include butyl crotonate and hexyl crotonate.
  • vinyl esters examples include vinyl acetate, vinyl propionate, vinyl butyrate, vinylmethoxy acetate and vinyl benzoate.
  • maleic diesters examples include diethyl maleate, dimethyl maleate and dibutyl maleate.
  • Examples of fumaric diesters include diethyl fumarate, dimethyl fumarate and dibutyl fumarate.
  • Examples of itaconic diesters include diethyl itaconate, dimethyl itaconate and dibutyl itaconate.
  • Examples of acrylamides include acrylamide, methyl acrylamide, ethyl acrylamide, propyl acrylamide, n-butyl acrylamide, tert-butyl acrylamide, cyclohexyl acrylamide, 2-methoxyethyl acrylamide, dimethyl acrylamide, diethyl acrylamide and phenyl acrylamide.
  • methacrylamides include methyl methacrylamide, ethyl methacrylamide, n-butyl methacrylamide, tert-butyl methacrylamide, 2-methoxy methacrylamide, dimethyl methacrylamide and diethyl methacrylamide.
  • vinyl ethers include methyl vinyl ether, butyl vinyl ether, hexyl vinyl ether, methoxyethyl vinyl ether and dimethylaminoethyl vinyl ether.
  • styrenes examples include styrene, methylstyrene, dimethylstyrene, trimethylstyrene, ethylstyrene, isopropylstyrene, butylstyrene, chloromethylstyrene, methoxystyrene, butoxystyrene, acetoxystyrene, chlorostyrene, dichlorostyrene, bromostyrene, methyl vinylbenzoate and 2-methylstyrene.
  • Examples of other monomers include allyl compounds (e.g., allyl acetate), vinyl ketones (e.g., methyl vinyl ketone), vinyl heterocyclic compounds (e.g., vinylpyridine), glycidyl esters (e.g., glycidyl acrylate), unsaturated nitriles (e.g., acrylonitrile), acrylic acid, methacrylic acid, itaconic acid, maleic acid, monoalkyl itaconates (e.g., monomethyl itaconate), monoalkyl maleates (e.g., monomethyl maleate), citraconic acid, vinylsulfonic acid, acryloyloxyalkylsulfonic acids (e.g., cryloyloxymethylsulfonic acid) and acrylamidoalkylsulfonic acids (e.g., 2-acrylamido-2-methylethanesulfonic acid).
  • These acids may be in the form of a salt such as an al
  • preferred comonomers are acrylic esters, methacrylic esters, styrenes, maleic esters, acrylamides and methacrylamides.
  • These monomers may be used either alone or in a combination of two or more of them.
  • a combination of n-butyl acrylate and styrene, a combination of n-butyl acrylate and butylstyrene and a combination of t-butyl methacrylamide and n-butyl acrylamide can be used.
  • the color forming moiety corresponding to formula (P) account for 5 to 80% by weight of the above magenta coupler.
  • the ratio of the color forming moiety in the coupler be 30 to 70% by weight.
  • the equimolecular weight grams of polymer containing one mol of monomer coupler is about 250 to 4,000, but is not limited thereto.
  • the above polymer couplers are preferably added to silver halide emulsion layers or adjoining light-insensitive layers thereto.
  • a magenta polymer coupler is preferably contained in the green-sensitive silver halide emulsion layer or in a light-insensitive layer adjacent thereto.
  • magenta polymer couplers when used in the green sensitive silver halide emulsion layers are used in an amount of 0.005 to 0.5 mol, preferably 0.03 to 0.25 mol (in terms of coupler monomer) per mol of silver used in the same layer.
  • the polymer couplers are used in the light-insensitive layers, the polymer couplers are used in a coating weight of 0.01 to 1.0 g/m 2 , preferably 0.1 to 0.5 g/m 2 .
  • the polymer couplers may be prepared by emulsifying and dispersing a solution of a lipophilic polymer coupler in the form of latex in an organic solvent in an aqueous gelatin solution, said polymer coupler being obtained by polymerizing a monomer coupler in the manner mentioned above.
  • the polymer coupler may be prepared directly by an emulsion polymerization method.
  • a method for emulsifying and dispersing the lipophilic polymer coupler in the form of a latex in an aqueous gelatin solution is described in U.S. Patent 3,451,820.
  • Emulsion polymerization can be carried out by using the methods described in U.S. Patents 4,080,211 and 3,370,952.
  • the syntheses of the above magenta polymer couplers are carried out by using the compounds described in JP-A-56-5543, JP-A-57-94752, JP-A-57-176038, JP-A-57-204038, JP-A-58-28745, JP-A-58-10738, JP-A-58-42044 and JP-A-58-145944 as polymerization initiators and solvents.
  • the polymerization temperature is set depending on the molecular weights of polymers to be synthesized, the types of initiators, etc.
  • the polymerization can be conducted at a temperature of from below 0°C to higher than 100°C, but polymerization is usually conducted at a temperature of 30 to 100°C.
  • magenta polymer couplers which can be used in the present invention include, but are not limited to, the following compounds (the suffix of parenthesis represents molar ratio).
  • the photographic material of the present invention has a support having thereon at least one blue-sensitive silver halide emulsion layer, green-sensitive silver halide emulsion layer and red-sensitive silver halide emulsion layer.
  • a support having thereon at least one blue-sensitive silver halide emulsion layer, green-sensitive silver halide emulsion layer and red-sensitive silver halide emulsion layer.
  • a typical example is a silver halide photographic material having at least one sensitive layer composed of a plurality of silver halide emulsion layers having substantially the same color sensitivity, but different light sensitivity, the sensitive layer being a unit sensitive layer having color sensitivity to any one of blue light, green light and red light.
  • the unit sensitive layers are generally arranged in the order of a red-sensitive layer, a green-sensitive layer and a blue-sensitive layer from the support.
  • the arrangement may be in the reverse order to that described above according to purpose. Further, the arrangement may be such that a different light-sensitive layer is inserted into the same color sensitive layers.
  • Non-sensitive layers such as various interlayers may be provided between silver halide sensitive layers, or on the uppermost layer or lowermost layer thereof.
  • the interlayers may contain couplers, or DIR compounds described in JP-A-61-43748, JP-A-59-113438, JP-A-59-113440, JP-A-61-20037 and JP-A-61-20038.
  • the inter layers may also contain color mixing inhibitors as used conventionally.
  • a plurality of silver halide emulsion layers which constitute each unit sensitive layer preferably include a two-layer structure consisting of a high-sensitivity emulsion layer and a low-sensitivity emulsion layer as described in West German Patent 1,121,470 and U.K. Patent 923,045. It is preferred that the layers are disposed such that light sensitivity is lower toward the support.
  • a non-sensitive layer may be provided between silver halide emulsion layers.
  • the low-sensitivity emulsion layer may be provided on the farther side from the support and the high-sensitivity emulsion layer may be provided on the side nearer to the support as described in JP-A-57-112751, JP-A-62-200350, JP-A-62-206541 and JP-A-62-206543.
  • the layer may be arranged in order of low-sensitivity blue-sensitive layer (BL)/high-sensitivity blue-sensitive layer (BH)/ high-sensitivity green-sensitive layer (GH)/low-sensitivity green-sensitive layer (GL)/high-sensitivity red-sensitive layer (RH)/low-sensitivity red-sensitive layer (RL) from the outermost layer, or in order of BH/BL/GL/GH/RH/RL, or in order of BH/BL/GH/GL/RL/RH.
  • BL low-sensitivity blue-sensitive layer
  • BH high-sensitivity blue-sensitive layer
  • GH high-sensitivity green-sensitive layer
  • GL low-sensitivity green-sensitive layer
  • RH high-sensitivity red-sensitive layer
  • RL low-sensitivity red-sensitive layer
  • the arrangement may be made in order of blue-sensitive layer/GH/RH/GL/RL from the outermost layer as described in JP-B-55-34932. Further, the arrangement may be made in order of blue-sensitive layer/GL/RL/GH/RH from the outermost layer as described in JP-A-56-25738 and JP-A-62-63936.
  • the layer structure contains three layers having different light sensitivity in such an arrangement that the upper layer is a silver halide emulsion layer having the highest light sensitivity, the medium layer is a silver halide emulsion layer having a light sensitivity lower than that of the upper layer and the lower layer is a silver halide emulsion layer having a light sensitivity lower than that of the medium layer so that light sensitivity becomes lower toward the support in order as described in JP-B-49-15495.
  • the arrangement may be made in order of medium-sensitive emulsion layer/high-sensitivity emulsion layer/low-sensitivity emulsion layer from the outermost layer as described in JP-A-59-202464.
  • the arrangement may be made in order of high-sensitivity emulsion layer/low sensitivity emulsion layer/medium-sensitivity emulsion layer or in order of low sensitivity emulsion layer/medium-sensitivity emulsion layer/high-sensitivity emulsion layer.
  • the layer structure is composed of four or more layers, the above-described various arrangements can be made.
  • a donor layer (CL) having a multilayer effect and different in spectral sensitivity distribution from the principal sensitive layers such as BL, GL and RL are provided adjacent to or near the principal sensitive layers to improve color reproducibility, said donor layer being described in U.S. Patents 4,663,271, 4,705,744 and 4,707,436, JP-A-62-160448 and JP-A-63-89850.
  • the preferred silver halide contained in the photographic emulsions of the photographic materials of the present invention is silver iodobromide, silver iodochloride or silver iodochlorobromide, each having a silver iodide content of not higher than about 30 mol%. Particularly preferred is silver iodobromide or silver iodochlorobromide, each having a silver iodide content of 2 mol% to 25 mol%.
  • Silver halide grains in the photographic emulsions may have a regular crystal form such as cube, octahedron or tetradecahedron, an irregular crystal form such as a sphere or tabular form, a crystal having a defect such as a twinning plane or a composite form thereof.
  • the size of silver halide grains may be in the range of from fine grains having a grain size of not larger than about 0.2 ⁇ m to large-size grains having a grain size of about 10 ⁇ m in terms of the diameter of projected area. Any of a polydisperse emulsion and monodisperse emulsion may be used.
  • the silver halide photographic emulsions of the present invention can be prepared according to the methods described in Research Disclosure (RD) No. 17643 (December 1978) pp 22-23 I. Emulsion Preparation and Types ; ibid. No. 18716 (November 1979), p. 648; ibid. No. 307105 (November 1989), pp 863-865; P. Glafkides, Chimie et Phisique Photographique (Paul Montel 1967), G.F. Duffin, Photographic Emulsion Chemistry (Focal Press 1966) and V.L. Zelikman et al, Making and Coating Photographic Emulsion (Focal Press 1964).
  • Tabular grains having an aspect ratio of not lower than about 5 can be used in the present invention.
  • the tabular grains can be easily prepared by the methods described in Gutoff, Photographic Science and Engineering , Vol. 14, pp 248-257 (1970), U.S. Patents 4,434,226, 4,414,310, 4,433,048 and 4,439,520 and U.K. Patent 2,112,157.
  • Grains having a uniform crystal structure or a crystal structure different in halogen composition between the interior thereof and the surface thereof can be used.
  • Grains having a laminar crystal structure may be used.
  • Silver halide having a different composition may be joined to the grains by epitaxial growth.
  • a compound such as silver rhodanide or lead oxide other than silver halide may be joined to the grains.
  • a mixture of grains having various crystal forms may be used.
  • Silver halide emulsions are usually subjected to physical ripening, chemical ripening and spectral sensitization and then used. Additives used for these stages are described in Research Disclosure No. 17643, ibid. No. 18716 and ibid. No. 30716 and listed in a Table below.
  • non-light-sensitive finely divided silver halide grains are used in the present invention.
  • non-sensitive finely divided silver halide grains refers to finely divided silver halide grains which are not light-sensitive during imagewise exposure for obtaining a dye image and are substantially not developed in the processing stage. Grains which are previously not fogged are preferable.
  • Finely divided silver halide grains have a silver bromide content of 0 to 100 mol% and may optionally contain silver chloride and/or silver iodide. Grains containing 0.5 to 10 mol% of silver iodide are preferred.
  • Finely divided silver halide grains have a mean grain size (the mean value of diameters of the circles having areas corresponding to projected areas) of preferably 0.01 to 0.5 ⁇ m, more preferably 0.02 to 0.2 ⁇ m.
  • Finely divided silver halide grains can be prepared in the same manner as in the preparation of usual light-sensitive silver halides. In the preparation of finely divided silver halide grains, it is not necessary that the surfaces of silver halide grains be optically sensitized or spectrally-sensitized. However, it is preferred that a conventional stabilizer such as triazole, azaindene, benzthiazolium, a mercapto compound or a zinc compound be added before the finely divided silver halide grains are added to coating solutions. Colloidal silver is preferably incorporated in layers containing the finely divided silver halide grains.
  • color couplers can be used in the present invention. Examples thereof are described in patent specifications cited in the above-described Research Disclosure No. 17643, VII-C to G and ibid. No. 307105, VII-C to G.
  • yellow couplers include those described in U.S. Patents 3,933,501, 4,022,620, 4,326,024, 4,401,752 and 4,248,961, JP-B-58-10739, U.K. Patents 1,425,020 and 1,476,760, U.S. Patents 3,973,968, 4,314,023 and 4,511,649 and European Patent 249,473A.
  • magenta couplers are preferred as magenta couplers. Particularly preferred are magenta couplers described in U.S. Patents 4,310,619 and 4,351,897, European Patent 73,636, U.S. Patents 3,061,432 and 3,725,067, Research Disclosure No. 24220 (June 1984), JP-A-60-33552, Research Disclosure No. 24230 (June 1984), JP-A-60-43659, JP-A-61-72238, JP-A-60-35730, JP-A-55-118034, JP-A-60-185951, U.S. Patents 4,500,630, 4,540,654 and 4,556,630 and WO88/04795.
  • cyan couplers phenol coupelrs and naphthol couplers may be used.
  • Preferred cyan couplers include those described in U.S. Patents 4,052,212, 4,146,396, 4,228,233, 4,296,200, 2,369,929, 2,801,171, 2,772,162, 2,895,826, 3,772,002, 3,758,308, 4,334,011 and 4,327,173, West German Patent Application (Laid-Open) No. 3,329,729, European Patents 121,365A and 249,453A, U.S. Patents 3,446,622, 4,333,999, 4,775,616, 4,451,559, 4,427,767, 4,690,889, 4,254,212 and 4,296,199 and JP-A-61-42658.
  • couplers which release imagewise nucleating agents or development accelerators during development there are preferred those described in U.K. Patents 2,097,140 and 2,131,188, JP-A-59-157638 and JP-A-59-170840.
  • Couplers used in the present invention can be introduced into photographic materials by various known dispersion methods.
  • Examples of the high-boiling organic solvents which have a boiling point of not lower than 175°C at normal pressure used in the oil-in-water dispersion method include phthalic esters (e.g., dibutyl phthalate, dicyclohexyl phthalate, di-2-ethylhexyl phthalate, decyl phthalate, bis(2,4-di-t-amylphenyl) phthalate, bis(2,4-di-t-amylphenyl) isophthalate, bis(1,1-diethylpropyl) phthalate), phosphoric or phosphonic esters (e.g., triphenyl phosphate, tricresyl phosphate, 2-ethylhexyl diphenyl phosphate, tricyclohexyl phosphate, tri-2-ethylhexyl phosphate, tridodecyl phosphate, tributoxyethyl phosphate,
  • Organic solvents having a boiling point of not lower than about 30°C, preferably not lower than about 50°C, but not higher than about 160°C can be used as co-solvents.
  • the co-solvents include ethyl acetate, butyl acetate, ethyl propionate, methyl ethyl ketone, cyclohexanone, 2-ethoxyethyl acetate and dimethylformamide.
  • antiseptic and antifungal agents such as 1,2-benzoisothiazoline-3-one, n-butyl p-hydroxybenzoate, phenol, 4-chloro-3,5-dimethylphenol, 2-phenoxyethanol and 2-(4-thiazolyl)benzimidazole described in JP-A-63-257747, JP-A-62-272248 and JP-A-1-80941 and phenethyl alcohol are added to the color photographic materials of the present invention.
  • antiseptic and antifungal agents such as 1,2-benzoisothiazoline-3-one, n-butyl p-hydroxybenzoate, phenol, 4-chloro-3,5-dimethylphenol, 2-phenoxyethanol and 2-(4-thiazolyl)benzimidazole described in JP-A-63-257747, JP-A-62-272248 and JP-A-1-80941 and phenethyl alcohol are added to the color photographic materials of the present invention.
  • the present invention can be applied to various color photographic materials.
  • Typical examples of the color photographic materials according to the present invention include general-purpose and movie color negative films, reversal color films for slide or TV, color paper, color positive films and reversal color paper.
  • Examples of supports which can be used in the present invention include those described in the above-described RD No. 17643 (page 28), RD No. 18716 (right column of page 647 to left column of page 648) and RD No. 307105 (page 879).
  • the total of the layer thicknesses of the entire hydrophilic colloid layers on the emulsion layer side thereof is preferably not more than 28 ⁇ m, more preferably not more than 23 ⁇ m, still more preferably not more than 18 ⁇ m, particularly preferably not more than 16 ⁇ m.
  • the layer-swelling rate T 1/2 is preferably not longer than 30 seconds, more preferably not longer than 20 seconds.
  • the layer thickness refers to a layer thickness obtained by measuring the thickness of a layer at 25°C and 55% RH under air conditioning (2 days).
  • the layer-swelling rate T 1/2 can be measured by known method in the field of photography, for example, by using a swellometer described in A. Green et al., Photogr. Sci.
  • T 1/2 is defined as the time taken until layer thickness reaches 1/2 of saturated layer thickness when processing is conducted with a color developing solution at 30°C for 3 min 15 sec and 90% of the attainable maximum swollen layer thickness is referred to as saturated layer thickness.
  • the layer-swelling rate T 1/2 can be controlled by adding a hardening agent to gelatin as a binder or by changing conditions with time after coating.
  • a swelling ratio of 150 to 400% is preferred.
  • the swelling ratio can be calculated from the maximum swollen layer thickness under the above conditions by using the formula (maximum swollen layer thickness - layer thickness)/layer thickness.
  • the color photographic materials of the present invention can be developed according to conventional methods described in RD No. 17643 (pp 28-29), RD No. 18716 (left column to right column of page 651) and RD No. 307105 (pp 880-881).
  • Color developing solutions which can be used in the processing of the photographic materials of the present invention are preferably aqueous alkaline solutions mainly composed of aromatic primary amine color developing agents. Aminophenol compounds are useful as the color developing agents and p-phenylenediamine compounds are preferred as the color developing agents.
  • Typical examples thereof include 3-methyl-4-amino-N,N-diethylaniline, 3-methyl-4-amino-N-ethyl-N- ⁇ -hydroxyethylaniline, 3-methyl-4-amino-N-ethyl-N- ⁇ -methanesulfonamidoethylaniline, 3-methyl-4-amino-N-ethyl-N- ⁇ -methoxyethylaniline and salts thereof such as sulfate, hydrochloride and p-toluenesulfonate.
  • 3-methyl-4-amino-N-ethyl-N- ⁇ -hydroxyethylaniline sulfate is particularly preferred. These compounds may be used either alone or in combination of two or more of them according to purpose.
  • the color developing solutions contain pH buffering agents such as alkali metal carbonates, borates and phosphates, developed restrainers such as chlorides, bromides, iodides, benzimidazoles, benzothiazoles and mercapto compounds and anti-fogging agents.
  • pH buffering agents such as alkali metal carbonates, borates and phosphates
  • developed restrainers such as chlorides, bromides, iodides, benzimidazoles, benzothiazoles and mercapto compounds and anti-fogging agents.
  • the color developing solutions may optionally contain preservatives such as hydroxylamine, diethylhydroxylamine, sulfites, hydrazine such as N,N-biscarboxymethylhydrazine, phenylsemicarbazides, triethanolamine, catecholsulfonic acids; organic solvents such as ethylene glycol and diethylene glycol; development accelerators such as benzyl alcohol, polyethylene glycol, quaternary ammonium salts and amines; color forming couplers, competitive couplers; auxiliary developing agents such as 1-phenyl-3-pyrazolidone; tackifiers; and chelating agents such as aminopolycarboxylic acids, aminopolyphosphonic acids, alkylphosphonic acids and phosphonocarboxylic acids, for example, ethylenediaminetetraacetic acid, nitrilotriacetic acid, diethylenetriaminepentaacetic acid, cyclohexanediaminetetraacetic acid, hydroxyeth
  • Black-and-white developing solutions may contain conventional developing agents such as dihydroxybenzenes (e.g., hydroquinone), 3-pyrazolidones (e.g., 1-phenyl-3-pyrazolidone) and aminophenols (e.g., N-methyl-p-aminophenol). These developing agents may be used either alone or in combination of two or more of them.
  • dihydroxybenzenes e.g., hydroquinone
  • 3-pyrazolidones e.g., 1-phenyl-3-pyrazolidone
  • aminophenols e.g., N-methyl-p-aminophenol
  • the pH of the color developing solutions and the black-and-white developing solutions is generally in the range of 9 to 12.
  • the replenishment rate of these developing solutions varies depending on the types of the color photographic materials, but is usually not more than 3 l per m 2 of the photographic material.
  • the replenishment rate can be reduced to 500 ml or less when the concentration of bromide ion in the replenisher is reduced.
  • the opening ratio is preferably not higher than 0.1, more preferably 0.001 to 0.05.
  • Methods for reducing the opening ratio include a method wherein a cover such as a floating lid is provided on the surface of the photographic processing solution in the processing tank; a method wherein a movable lid is used as described in JP-A-1-82033; and a slit development method described in JP-A-63-216050. It is preferred the opening ratio be reduced not only for color development and black and white development stages, but also all of the subsequent stages such as bleaching, bleaching-fixing, fixing, rinsing and stabilization stages. The replenishment rate can be reduced by inhibiting the accumulation of bromide ion in the developing solution.
  • Color development is usually 2 to 5 minutes. However, when a higher temperature and a higher pH are used and the color developing agents are used at a higher concentration, processing time can be shortened.
  • the photographic emulsion layer is generally bleached.
  • Bleaching may be carried out simultaneously with fixing (bleaching-fixing treatment) or separately carried out.
  • a bleaching-fixing treatment may be conducted to expedite processing. Processing may be conducted with a bleaching-fixing bath composed of two consecutive baths. Fixing may be conducted before the bleaching-fixing treatment.
  • bleaching may be conducted according to purpose. Examples of bleaching agents include compounds of polyvalent metals such as iron(III), peracids, quinones and nitro compounds.
  • Typical examples of the bleaching agents include organic complex salts of iron(III) such as complex salts of aminopolycarboxylic acids (e.g., ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, cyclohexanediaminetetraacetic acid, methyliminodiacetic acid, 1,3-diaminopropanetetraacetic acid, glycol ether diaminetetraacetic acid), citric acid, tartaric acid, and malic acid.
  • aminopolycarboxylic acids e.g., ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, cyclohexanediaminetetraacetic acid, methyliminodiacetic acid, 1,3-diaminopropanetetraacetic acid, glycol ether diaminetetraacetic acid
  • citric acid tartaric acid
  • malic acid e.g., citric acid, tartaric acid, and malic acid
  • iron(III) complex salts of aminopolycarboxylic acids such as (ethylenediaminetetraacetonato)-iron(III) complex and (1,3-diaminopropanetetraacetonato)iron(III) complex are preferred for rapid processing and prevention of environmental pollution.
  • iron(III) complex salts of aminopolycarboxylic acids are useful for bleaching solutions and bleaching-fixing solutions.
  • the pH of the bleaching solutions containing the iron(III) complex salts of aminopolycarboxylic acids and the bleaching-fixing solutions containing the iron(III) complex salts is generally in the range of 4.0 to 8. A lower pH may be used to expedite processing.
  • the bleaching solution, the bleaching-fixing solution and the pre-bath thereof may contain bleaching accelerators.
  • the bleaching accelerators include compounds having a mercapto group or disulfide group described in U.S. Patent 3,893,858, West German Patents 1,290,812 and 2,059,988, JP-A-53-32736, JP-A-53-57831, JP-A-53-37418, JP-A-53-72623, JP-A-53-95630, JP-A-53-95631, JP-A-53-104232, JP-A-53-124424, JP-A-53-141623, JP-A-53-28426 and Research Disclosure No.
  • the compounds having a mercapto group or disulfide group are preferred for their high accelerating effect.
  • Patent 3,893,858, West German Patent 1,290,812 and JP-A-53-95630 are preferred. Further, the compounds described in U.S. Patent 4,552,834 are preferred. These bleaching accelerators may be incorporated in the photographic materials. These bleaching accelerators are particularly effective in conducting bleaching-fixing of the color photographic materials for photographing.
  • the bleaching solution and the bleaching-fixing solution contain organic acids to prevent stain from being caused by bleaching.
  • organic acids are compounds having an acid dissociation constant (pKa) of 2 to 5.
  • the organic acids include acetic acid and propionic acid.
  • fixing agents used in the fixing solution and the bleaching-fixing solution include thiosulfates, thiocyanates, thioether compounds, thioureas and a large amount of an iodide.
  • the thiosulfates are widely used as the fixing agents. Particularly, ammonium thiosulfate is most widely used.
  • a combination of a thiosulfate with a thiocyanate, a thioether compound or a thiourea is also preferred.
  • Sulfites, bisulfites, carbonyl bisulfite adducts and sulfinic acid compounds described in European Patent 294769A are preferred as preservatives for the fixing solution and the bleaching-fixing solution. It is also preferred that aminopolycarboxylic acids or organic phosphonic acids are added to the fixing solution or the bleaching-fixing solution to stabilize the solution.
  • compounds having a pKa of 6.0 to 9.0 preferably imidazoles such as imidazole, 1-methylimidazole, 1-ethylimidazole and 2-methylimidazole, in an amount of 0.1 to 10 mol/l are added to the fixing solution or the bleaching-fixing solution to adjust the pH.
  • imidazoles such as imidazole, 1-methylimidazole, 1-ethylimidazole and 2-methylimidazole
  • Desilvering time is preferably 1 to 3 min, more preferably 1 to 2 min.
  • Processing temperature is 25 to 50°C, preferably 35 to 45°C.
  • agitation in the desilvering stage be intensified as much as possible.
  • Methods for intensifying agitation include a method wherein a jet of the processing solution collides with the surfaces of the emulsions of photographic materials as described in JP-A-62-183460; a method wherein stirring is improved by a rotating means as described in JP-A-62-183461; a method wherein a wiper blade provided in the solution is brought into contact with the surfaces of the emulsions, the photographic material is transferred to thereby form a turbulent flow, whereby a stirring effect is improved; and a method wherein the whole amount of the processing solution circulated is increased.
  • Such means for improving agitation are effectively applicable to any of the bleaching solution, the bleaching-fixing solution and the fixing solution. It is believed that an improvement agitation accelerates the feed of the bleaching solution and the fixing solution into the emulsion layers and as a result, the desilvering rate is enhanced.
  • the above-described means for improving agitation is more effective when the bleaching accelerators are used. The accelerating effect can be greatly increased and the problem of inhibiting fixation caused by the bleaching accelerators can be solved.
  • automatic processors for use in the processing of the photographic materials of the present invention be provided with photographic material conveying means described in JP-A-60-191257, JP-A-60-191258 and JP-A-60-191259.
  • the conveying means can greatly reduce the amount of the processing solution brought over from the previous bath to the subsequent bath so that preservation of the performance of the processing solution is very high. This is particularly effective in shortening the processing time in each stage or reducing the replenishment rate of the processing solution.
  • the silver halide color photographic materials of the present invention are subjected to washing and/or stabilization after desilvering.
  • the amount of rinsing water in the washing stage varies widely depending on the characteristics (e.g., depending on materials used such as couplers) of the photographic materials, their use, the temperature of rinsing water, the number of rinsing tanks (the number of stages), replenishing system (countercurrent, direct flow) and other conditions.
  • the relationship between the amount of water and the number of rinsing tanks in the multi-stage countercurrent system can be determined by the method described in Journal of the Society of Motion Picture and Television Engineers, Vol. 64, p. 248-253 (May 1955).
  • the amount of rinsing water can be greatly reduced.
  • the residence time of water in the tanks is prolonged and as a result, bacteria are grown and the resulting suspended matter is deposited on the photographic material.
  • a method for reducing calcium ion and magnesium ion concentrations described in JP-A-62-288838 can be effectively used for the color photographic materials of the present invention to solve this problem.
  • isothiazolone compounds thiabendazole compounds
  • chlorine-containing germicides such as sodium chlorinated isocyanurate and benztriazole described in JP-A-57-8542 and germicides described in Chemistry of Germicidal Antifungal Agent, (1986) written by Hiroshi Horiguchi (Sankyo Shuppan), Sterilization, Disinfection, Antifungal Technique, edited by Sanitary Technique Society and Antibacterial and Antifungal Cyclopedie, (1986) edited by Nippon Antibacterial Antifungal Society, can be used.
  • the pH of rinsing water in the treatment of the photographic materials of the present invention is in the range of 4 to 9, preferably 5 to 8.
  • the temperature of rinsing water and washing time vary depending on the characteristics of the photographic materials and use, but the temperature and time of washing are generally 15 to 45°C for 20 seconds to 10 minutes, preferably 25 to 40°C for 30 seconds to 5 minutes.
  • the photographic materials of the present invention may be processed directly with stabilizing solutions in place of rinsing water. Such stabilizing treatment can be carried out by conventional methods described in JP-A-57-8543, JP-A-58-14834 and JP-A-60-220345.
  • a stabilizing treatment subsequent to rinsing may be conducted.
  • the stabilizing treatment may be used as the final bath for the color photographic materials for photographing.
  • An example thereof include a stabilizing bath containing a dye stabilizer and a surfactant.
  • the dye stabilizer include aldehydes such as formalin and glutaraldehyde, N-methylol compounds, hexamethylenetetramine and aldehydesulfite adducts.
  • the stabilizing bath may contain various chelating agents and antifungal agents.
  • Overflow solution from the replenishment of rinsing water and/or stabilizing can be reused in other stages such as desilvering stage.
  • the color developing agents may be incorporated in the silver halide color photographic materials of the present invention for the purpose of simplifying and expediting processing. It is preferred that precursors for the color developing agents are used for the incorporation thereof in the photographic materials. Examples of the precursors include indoaniline compounds described in U.S. Patent 3,342,597; Schiff base compounds described in U.S. Patent 3,342,599 Research Disclosure No. 14850 and ibid. , No. 15159; aldol compounds described in Research Disclosure No. 13924; metal complex salts described in U.S. Patent 3,719,492; and urethane compounds described in JP-A-53-135628.
  • 1-phenyl-3-pyrazolidones may be incorporated in the silver halide color photographic materials of the present invention for the purpose of accelerating color development.
  • Typical examples of the compounds include those described in JP-A-56-64339, JP-A-57-144547 and JP-A-58-115438.
  • various processing solutions are used at a temperature of 10 to 50°C. Generally, a temperature of 33 to 38°C is used. However, a higher temperature can be used to accelerate processing and to shorten processing time, while a lower temperature is used to improve image quality and to improve the stability of the processing solutions.
  • the silver halide photographic materials of the present invention include heat developable photo sensitive materials described in U.S. Patent 4,500,626, JP-A-60-133449, JP-A-59-218443, JP-A-61-238056 and European Patent 210,660A2.
  • the coating weights of silver halide and colloidal silver are represented by g/m 2 in terms of silver.
  • the coating weights of couplers, additives and gelatin are represented by g/m 2 .
  • the amounts of sensitizing dyes are represented by moles per mole of silver halide in the same layer.
  • First Layer Antihalation Layer Amount Black colloidal silver 0.15 Gelatin 1.20
  • Second Layer Interlayer Gelatin 1.45 UV-1 0.03 UV-2 0.06 UV-3 0.07 ExF-1 0.004 Solv-2 0.07
  • Third Layer Low-sensitivity Red-sensitive Emulsion Layer Silver iodobromide emulsion [AgI: 6 mol%, interior high AgI type, diameter (in terms of sphere): 0.3 ⁇ m, coefficient of variation in diameter (in terms of sphere): 20%, normal crystal-twin mixed grains, diameter/thickness ratio: 2.5]: coated silver 0.35 Gelatin 1.00 ExS-1 1.0 ⁇ 10 -4 ExS-2 3.0 ⁇ 10 -4 ExS-3 1.0 ⁇ 10 -5 ExC-3 0.22 ExC-4 0.006 Solv-1 0.007
  • Fourth Layer Medium-sensitivity Red-sensitive Emulsion Layer Silver iodobromide emulsion 0.75 [AgI: 10 mol%, interior high AgI type, diameter (in terms of sphere): 0.55 ⁇ m,
  • Each of Samples 102 and 103 was prepared in the same way as Sample 101, except that ExY-16 in an amount of twice by mol that of ExC-4 or ExM-17 in an amount of 1.4 times by mol that of ExC-4 was used in place of ExC-4 in each of the third and fourth layers of the Sample 101.
  • Each of Samples 104, 105 and 106 was prepared in the same way as Sample 101 except that Compound (5) in an amount of 4 times by mol that of ExC-4, Compound (7) in an amount of 3 times by mol that of ExC-4, or Compound (14) in an amount of 4 times by mol ExC-4 was used in place of ExC-4 in each of the third and fourth layers of Sample 101.
  • Each of Samples 107 to 124 was prepared by adding the yellow colored coupler (YC-26) in an amount of 0.025 g/m 2 and 0.008 g/m 2 to the fourth and fifth layers of each of the Samples 101 to 106, respectively. Similarly, (YC-32) and (YC-47) were added to prepare Samples 113 to 124.
  • Each of Samples 125 to 131 was prepared in the same way as Sample 101 except that each of (YC-3), (YC-24), (YC-25), (YC-1). )YC-85), (YC-86), and (YC-89) was used in place of (YC-26).
  • Sample 132 was prepared in the same way as Sample 110, except that ExM-9 in an amount of twice by weight that of the preferred Coupler (P-13) was used in place of Coupler (P-13) in each of the seventh and eighth layers of Sample 110, the amount of Solv-1 was increased to 1.8 times that used in Sample 110 and the amount of gelatin was increased to 1.5 times that used in Sample 110.
  • a sample 133 was prepared in the same way as Sample 132 except that an equimolar amount of ExM-11 was used in place of ExM-9.
  • Relative sensitivity was determined from the logarithm of the reciprocal of exposure amount giving a density of (Fog+0.2) under the Condition A.
  • Color turbidity was determined from a value obtained by subtracting the yellow density in the red unexposed area from the yellow density in an exposure amount giving a cyan density of (Fog+0.3) and (Fog+0.1) under the Conditions A and B.
  • Each processing solution used in each stage had the following composition. Color Developing Solution Sodium nitrilotriacetate 1.0 g Sodium sulfite 4.0 g Sodium carbonate 30.0 g Potassium bromide 1.3 g Hydroxylamine sulfate 2.4 g 4-(N-Ethyl-N- ⁇ -hydroxyethylamino)-2-methylaniline sulfate 4.5 g Add water to make 1 liter Bleaching Solution Ammonium bromide 160.0 g Ammonia water (28%) 25.0 ml Sodium iron salt of ethylenediaminetetraacetic acid 130 g Glacial acetic acid 14 ml Add water to make 1 liter Fixing Solution Sodium tetrapolyphosphate 2.0 g Sodium sulfite 4.0 g Ammonium thiosulfate (70% aqueous solution) 175.0 ml Sodium bisulfite 4.6 g Add water to make 1 liter Stabilizing Solution Formalin 2.0 ml
  • Sample 110 obtained by using the polymer coupler (P-13) is highly sensitive and has good sharpness and color reproducibility in comparison with Samples 132 and 133 obtained by using ExM-9 and ExM-11, respectively. Accordingly, it is clear that the use of the polymer coupler in the present invention is preferable.
  • a yellow colored coupler (YC-3) in an amount of 0.004 g/m 2 , 0.013 g/m 2 and 0.008 g/m 2 was added to the third layer, the fourth layer and the fifth layer of Sample 105 (Compound (26) being the same as Compound (4) and containing no any yellow colored cyan coupler) of JP-A-1-214849 to prepare Sample 201.
  • (YC-26), (YC-28) and (YC-59) were added to prepare Samples 202, 203 and 204.
  • Samples 201 to 204 of the present invention are highly sensitive, exhibit low color turbidity under any exposure conditions and are excellent in sharpness in comparison with Sample 105 of JP-A-1-214849.
  • Color development was conducted at 38°C with an automatic processor under the following conditions. Color development 3 min 15 sec Bleaching 1 min Bleaching-fixing 3 min 15 sec Rinse with water (1) 40 sec Rinse with water (2) 1 min Stabilization 40 sec Drying (50°C) 1 min 15 sec
  • the replenishment rate of each processing solution was such that the replenishment rate in the color development was 1200 ml per m 2 of photographic material and that in each of the other stages including rinse was 800 ml.
  • the amount of the processing solution brought over from the previous bath to the rinse stage was 50 ml per m 2 of photographic material.
  • Ethylenediaminetetraacetic acid iron(III) ammonium salt 50.0 g Disodium ethylenediaminetetraacetate 5.0 g Sodium sulfite 12.0 g
  • Aqueous solution of ammonium thiosulfate (70%) 240 ml Add ammonia water to make pH 7.3 Add water to make 1 liter
  • Drying temperature was 50°C.
  • the yellow colored cyan coupler (YC-31) in an amount of 0.012 g/m 2 and the compound (12) of formula (I) according to the present invention in an amount of 0.010 g/m 2 were added to the fourth layer of Sample 108 (containing no compound represented by formula (I) and yellow colored coupler of the present invention) of JP-A-61-51146.
  • the sample was processed in the same manner as in Example 1 of JP-A-61-51146.
  • the yellow color turbidity of the resulting sample was small in comparison with Sample 108 of JP-61-51146.

Landscapes

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

Claims (16)

  1. Matériau photographique couleur à l'halogénure d'argent, comportant un support portant au moins une couche d'émulsion d'halogénure d'argent sensible au rouge contenant un copulant du cyan, au moins une couche d'émulsion d'halogénure d'argent sensible au vert contenant un copulant du magenta et au moins une couche d'émulsion d'halogénure d'argent sensible au bleu contenant un copulant du jaune, dans lequel ledit matériau photographique contient au moins un composé représenté par la formule générale (I) qui suit, en quantité de 1 x 10-6 à 1 x 10-3 mole/m2:

            A-(L1)v-B-(L2)w-DI     (I)

    dans laquelle A représente un groupe qui est séparé de (L1)v-B-(L2)w-DI par une réaction du composé de formule (I) avec un produit d'oxydation d'un agent de développement; L1 représente un groupe de liaison qui est séparé de B après la rupture de la liaison entre L1 et A; B représente un groupe qui réagit avec un produit d'oxydation d'un agent de développement pour libérer (L2)w-DI; L2 est un groupe qui est séparé de DI après la rupture de la liaison entre B et L2; DI représente un inhibiteur de développement; v et w représentent chacun un entier de 0 à 2; et, lorsque v ou w vaut 2, les deux groupes L1 ou les deux groupes L2 peuvent être des groupes identiques ou différents,
    et au moins un copulant du cyan, coloré en jaune, présentant un maximum d'absorption entre 400 nm et 500 nm, qui forme un colorant cyan présentant un maximum d'absorption entre 630 nm et 750 nm, par copulation avec le produit d'oxydation d'un agent de développement amine aromatique primaire,
    avec la condition que le composé de la formule I n'est pas
    Figure imgb0390
  2. Matériau photographique couleur à l'halogénure d'argent selon la revendication 1, dans lequel le composé représenté par la formule (I) et le copulant du cyan coloré en jaune sont chacun incorporés dans au moins l'une desdites couches d'émulsion d'halogénure d'argent et dans au moins une couche intermédiaire insensible à la lumière qui lui est contiguë.
  3. Matériau photographique couleur à l'halogénure d'argent selon la revendication 1, dans lequel le composé représenté par la formule (I) est incorporé dans la couche présentant la même sensibilité chromatique que celle de la couche contenant le copulant du cyan coloré en jaune.
  4. Matériau photographique couleur à l'halogénure d'argent selon la revendication 1, dans lequel la couche contenant le composé représenté par la formule (I) est une couche sensible au rouge.
  5. Matériau photographique couleur à l'halogénure d'argent selon la revendication 1, dans lequel le copulant du cyan coloré en jaune est contenu dans la couche sensible au rouge.
  6. Matériau photographique couleur à l'halogénure d'argent selon la revendication 1, dans lequel le composé représenté par la formule générale (I) et le copulant du cyan coloré en jaune sont contenus dans la même couche d'émulsion d'halogénure d'argent sensible au rouge.
  7. Matériau photographique couleur à l'halogénure d'argent selon la revendication 1, dans lequel un copulant polymère du magenta est contenu dans la couche d'émulsion d'halogénure d'argent sensible au vert ou dans une couche insensible à la lumière qui lui est contiguë.
  8. Matériau photographique couleur à l'halogénure d'argent selon la revendication 1 dans lequel, à partir du support, les couches d'émulsion d'halogénure d'argent sont disposées dans l'ordre d'une couche sensible au rouge, une couche sensible au vert et une couche sensible au bleu, et un copulant polymère du magenta est contenu dans la couche d'émulsion d'halogénure d'argent sensible au vert.
  9. Matériau photographique couleur à l'halogénure d'argent selon la revendication 1, dans lequel la quantité du copulant du cyan coloré en jaune est de 0,05 à 0,30 g/m2.
  10. Matériau photographique couleur à l'halogénure d'argent selon la revendication 1, dans lequel ledit copulant du cyan coloré en jaune est apte à libérer un fragment d'un colorant soluble dans l'eau, présentant un groupe choisi dans l'ensemble constitué d'un groupe 6-hydroxy-2-pyridone-5-ylazo, d'un groupe pyrazolone-4-ylazo, d'un groupe 2-acylaminophénylazo, d'un groupe 2-sulfonamido-phénylazo et d'un groupe 5-aminopyrazole-4-ylazo, par une réaction de couplage avec un produit d'oxydation d'un agent de développement amine aromatique primaire.
  11. Matériau photographique couleur à l'halogénure d'argent selon la revendication 1, dans lequel ledit copulant du cyan coloré en jaune est choisi dans le groupe constitué des copulants représentés par les formules (CI) à (CIV):
    Figure imgb0391
    Figure imgb0392
    Figure imgb0393
    Figure imgb0394
    dans lesquelles Cp représente un fragment de copulant du cyan (T est lié au site de couplage de celui-ci); T représente un groupe de temporisation; k représente 0 ou 1; X représente un groupe bivalent contenant N-, O- ou S-, qui est lié à (T)k par l'atome de N, de O ou de S, et qui est également lié à Q;
    Q représente un groupe arylène ou un groupe hétérocyclique bivalent; R1 et R2 représentent chacun un atome d'hydrogène, un groupe carboxyle, un groupe sulfo, un groupe cyano, un groupe hydrocarboné à chaîne droite ou ramifiée qui peut contenir des liaisons insaturées et qui peut présenter un ou plusieurs groupes de substitution, un cycle comptant de 3 à 8 chaînons qui peut présenter des groupes de réticulation, des liaisons insaturées ou des groupes de substitution,
    un groupe phényle ou naphtyle, substitué ou non substitué, un cycle comptant de 3 à 8 chaînons, présentant comme hétéroatome au moins l'un parmi les atomes de N, de O et de S, un groupe carbamoyle substitué ou non substitué, un groupe sulfamoyle substitué ou non substitué, un groupe carbonamido substitué ou non substitué, un groupe sulfonamido aliphatique ou aromatique ou un groupe alkylsulfonyle;
    R3 est un atome d'hydrogène, un groupe hydrocarboné à chaîne droite ou ramifiée, qui peut contenir des liaisons insaturées et qui peut présenter un ou plusieurs groupes de substitution, un cycle comptant de 3 à 8 chaînons qui peut présenter des groupes de réticulation, des liaisons insaturées ou des groupes de substitution,
    un groupe phényle ou naphtyle substitué ou non substitué, un cycle comptant de 3 à 8 chaînons, présentant comme hétéroatome au moins l'un parmi les atomes de N, de O et de S; le groupe
    Figure imgb0395
     peut se trouver sous la forme d'au moins l'une de ses autres formes tautomères;
    R4 est un groupe acyle aliphatique ou aromatique ou un groupe sulfonyle aliphatique ou aromatique; R5 est un groupe qui peut être fixé au cycle de benzène; j est un entier de 0 à 4; lorsque j vaut 2 ou plus, les deux ou plusieurs groupes R5 peuvent être identiques ou différents; R9 est un atome d'hydrogène, un groupe carboxyle, un groupe sulfo, un groupe cyano, un groupe hydrocarboné à chaîne droite ou ramifiée qui peut contenir des liaisons insaturées et qui peut présenter un ou plusieurs groupes de substitution, un cycle comptant de 3 à 8 chaînons, qui peut présenter des groupes de réticulation, des liaisons insaturées ou des groupes de substitution, un groupe phényle ou naphtyle substitué ou non substitué, un groupe alcoxy, un groupe cycloalkyloxy, un groupe aryloxy, un cycle comptant de 3 à 8 chaînons, présentant comme hétéroatome au moins l'un parmi les atomes de N, de O et de S, un groupe carbamoyle substitué ou non substitué, un groupe sulfamoyle substitué ou non substitué, un groupe carbonamido, un groupe sulfonamido aliphatique ou aromatique, un groupe alkylsulfonyle, un groupe arylsulfonyle, un groupe alcoxycarbonyle ou un groupe aryloxycarbonyle;
    R10 est un atome d'hydrogène, un groupe hydrocarboné à chaîne droite ou ramifiée qui peut contenir des liaisons insaturées et qui peut présenter un ou plusieurs groupes de substitution; un cycle comptant de 3 à 8 chaînons, qui peut présenter des groupes de réticulation, des liaisons insaturées ou des groupes de substitution;
    un groupe phényle ou naphtyle substitué on non substitué ou un cycle comptant de 3 à 8 chaînons et présentant comme hétéroatome au moins l'un parmi les atomes de N, de O et de S; le groupe
    Figure imgb0396
     peut se présenter sous sa forme tautomère; et
       ledit copulant présente au moins un groupe de solubilisation dans l'eau en T, X, Q, R1, R2, R3, R4, R5, R9 et R10.
  12. Matériau photographique couleur à l'halogénure d'argent selon la revendication 1, dans lequel ledit copulant du cyan coloré en jaune est ajouté à une couche d'émulsion d'halogénure d'argent ou à une couche intermédiaire insensible à la lumière qui lui est contiguë.
  13. Matériau photographique couleur à l'halogénure d'argent selon la revendication 7, dans lequel le copulant polymère du magenta est un polymère dérivé d'au moins un monomère choisi dans le groupe constitué de monomères représentés par la formule (P):
    Figure imgb0397
    dans laquelle R121 représente un atome d'hydrogène, un groupe alkyle comptant de 1 à 4 atomes de carbone ou un atome de chlore; -D- représente -COO-, -CONR122- ou un groupe phénylène substitué ou non substitué; -E- représente un groupe alkylène, phénylène ou aralkylène, substitué ou non substitué; -F- représente -CONR122-, -NR122CONR122-,-NR122COO-, -NR122CO-, -OCONR122-, -NR122-, -COO-, -OCO-, -CO-,-O-, -S-, -SO2-; -NR122SO2- ou -SO2NR122-; R122 représente un atome d'hydrogène ou un groupe aliphatique substitué ou non substitué, saturé ou non saturé ou un groupe aryle substitué ou non substitué et, lorsqu'il existe deux ou plusieurs groupes R122 par molécule, ils peuvent être des groupes identiques ou différents; et chacun parmi p, q et r représente 0 ou 1, avec la condition qu'il n'existe pas de cas dans lequel p, q et r valent 0 simultanément;
    T représente un fragment (qui est lié à (̵F)̵r- en un site quelconque de Ar, Z et R133) d'un copulant du magenta représenté par la formule (Q)
    Figure imgb0398
    dans laquelle Ar représente un groupe alkyle substitué ou non substitué, un groupe hétérocyclique substitué ou non substitué, un groupe aryle substitué ou non substitué, un groupe alcoxy, un groupe aryloxy, un groupe alcoxycarbonyle, un groupe acylamino, un groupe carbamoyle, un groupe alkylcarbamoyle, un groupe dialkylcarbamoyle, un groupe arylcarbamoyle, un groupe alkylsulfonyle, un groupe arylsulfonyle, un groupe alkylsulfonamido, un groupe arylsulfonamido, un groupe sulfamoyle, un groupe alkylsulfamoyle, un groupe dialkylsulfamoyle, un groupe alkylthio, un groupe arylthio, un groupe cyano, un groupe nitro ou un atome d'halogène;
    R133 représente un groupe anilino, un groupe acylamino, un groupe uréido ou un groupe sulfonamido, lesdits groupes pouvant être substitués;
    Z représente un atome d'halogène, et un groupe qui est lié par l'intermédiaire d'un atome d'oxygène, d'un atome d'azote ou d'un atome de soufre et éliminé par une réaction de couplage.
  14. Matériau photographique couleur à l'halogénure d'argent selon la revendication 13, dans lequel le polymère est un copolymère avec un monomère éthylénique non chromogène.
  15. Matériau photographique couleur à l'halogénure d'argent selon la revendication 7, dans lequel le copulant polymère du magenta est utilisé dans la couche d'émulsion d'halogénure d'argent sensible au vert, en quantité de 0,005 à 0,5 mole par mole d'argent utilisée dans la même couche.
  16. Matériau photographique couleur à l'halogénure d'argent selon la revendication 7, dans lequel le copulant polymère du magenta est utilisé dans la couche insensible à la lumière en quantité de 0,01 à 1,0 g/m2.
EP90125708A 1989-12-29 1990-12-28 Produit photographique couleur à l'halogénure d'argent contenant un coupleur cyan coloré en jaune Expired - Lifetime EP0435334B1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP34358689 1989-12-29
JP343586/89 1989-12-29
JP272024/90 1990-10-09
JP27202490A JPH03223751A (ja) 1989-12-29 1990-10-09 ハロゲン化銀カラー写真感光材料

Publications (3)

Publication Number Publication Date
EP0435334A2 EP0435334A2 (fr) 1991-07-03
EP0435334A3 EP0435334A3 (en) 1991-09-04
EP0435334B1 true EP0435334B1 (fr) 1997-11-05

Family

ID=26549997

Family Applications (1)

Application Number Title Priority Date Filing Date
EP90125708A Expired - Lifetime EP0435334B1 (fr) 1989-12-29 1990-12-28 Produit photographique couleur à l'halogénure d'argent contenant un coupleur cyan coloré en jaune

Country Status (2)

Country Link
EP (1) EP0435334B1 (fr)
DE (1) DE69031679T2 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5364745A (en) * 1990-12-19 1994-11-15 Eastman Kodak Company Azoaniline masking couplers for photographic materials
JP2709226B2 (ja) * 1991-06-06 1998-02-04 富士写真フイルム株式会社 ハロゲン化銀カラー写真感光材料
US5656418A (en) 1994-09-12 1997-08-12 Fuji Photo Film Co., Ltd. Silver halide color photographic material
CN113866303B (zh) * 2021-09-28 2023-08-08 中国农业科学院农业质量标准与检测技术研究所 一种甲氧基丙烯酸酯类物质的检测方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0423727A2 (fr) * 1989-10-16 1991-04-24 Fuji Photo Film Co., Ltd. Matériau photographique couleur à l'halogénure d'argent contenant un coupleur coloré
EP0436938A2 (fr) * 1989-12-29 1991-07-17 Fuji Photo Film Co., Ltd. Produit photographique couleur à l'halogénure d'argent contenant un coupleur cyan coloré en jaune
JPH06254260A (ja) * 1993-03-04 1994-09-13 Sega Enterp Ltd 家庭用ゲーム機を用いた自動デモシステム

Family Cites Families (217)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE470936A (fr) 1940-02-24
US2369929A (en) 1943-03-18 1945-02-20 Eastman Kodak Co Acylamino phenol couplers
BE528764A (fr) 1953-05-13
US2772162A (en) 1954-11-03 1956-11-27 Eastman Kodak Co Diacylaminophenol couplers
BE543745A (fr) 1954-12-20
US2895826A (en) 1956-10-08 1959-07-21 Eastman Kodak Co Photographic color couplers containing fluoroalkylcarbonamido groups
DE1070030B (fr) 1958-06-21 1959-11-26
BE601636A (fr) 1960-03-23
BE606193A (fr) 1960-07-16
US3342597A (en) 1964-06-08 1967-09-19 Eastman Kodak Co Color developer precursor
DE1570672C3 (de) 1964-06-23 1975-02-06 Gevaert Photo-Producten N.V., Mortsel, Antwerpen (Belgien) Verfahren zur Herstellung von farbphotographischen Silberhalogenidemulsionen
US3370952A (en) 1964-09-23 1968-02-27 Du Pont Color formers
USB342599I5 (fr) 1965-06-07
DE1290812B (de) 1965-06-11 1969-03-13 Agfa Gevaert Ag Verfahren zum Bleichfixieren von photographischen Silberbildern
GB1156193A (en) 1965-10-21 1969-06-25 Eastman Kodak Co Photographic Silver Halide Emulsions
US3426010A (en) 1965-12-01 1969-02-04 Du Pont Thiazole-pyrazolone azo yellow dyes
US3446622A (en) 1966-01-11 1969-05-27 Ferrania Spa Process for the preparation of color images using 2 - ureido phenolic couplers
DE1643988C3 (de) 1966-07-25 1978-04-06 Fuji Shashin Film K.K., Ashigara, Kanagawa (Japan) Verwendung eines maskierenden Cyankupplers zum Herstellen von maskierten Farbbildern in farbphotographischen SiIberhalogenidemulsionen
US3574628A (en) 1968-01-29 1971-04-13 Eastman Kodak Co Novel monodispersed silver halide emulsions and processes for preparing same
JPS4915495B1 (fr) 1969-04-17 1974-04-15
GB1334515A (en) 1970-01-15 1973-10-17 Kodak Ltd Pyrazolo-triazoles
US3706561A (en) 1970-03-23 1972-12-19 Eastman Kodak Co Compositions for making blixes
DE2059988A1 (de) 1970-12-05 1972-06-15 Schranz Karl Heinz Dr Fotografisches Farbentwicklungsverfahren Agfa-Gevaert AG,5090 Leverkusen
US3674478A (en) 1970-12-17 1972-07-04 Polaroid Corp Novel products and processes
CA972353A (en) 1970-12-22 1975-08-05 Ciba-Geigy Ag Azo compounds, their manufacture and use
US3758308A (en) 1971-02-18 1973-09-11 Eastman Kodak Co Silver halide emulsion containing para fluoro phenols
US3719492A (en) 1971-03-05 1973-03-06 Eastman Kodak Co Complexed p-phenylenediamine containing photographic element and development process therefor
JPS5110783B2 (fr) 1971-04-26 1976-04-06
US3763170A (en) 1971-09-20 1973-10-02 Ici Ltd 1 or 4 sulphoaryl-6-hydroxy-2-pyridones
US3772002A (en) 1971-10-14 1973-11-13 Minnesota Mining & Mfg Phenolic couplers
GB1425020A (en) 1971-12-17 1976-02-18 Konishiroku Photo Ind Photographic yellow coupler
BE795745A (fr) 1972-02-21 1973-08-21 Eastman Kodak Co Procede de preparation d'une emulsion photographique aux halogenures d'argent homodispersee
US3932480A (en) 1972-02-28 1976-01-13 Polaroid Corporation Benzylthiosulfuric acid salts
JPS4940943A (fr) 1972-08-24 1974-04-17
FR2202088B1 (fr) 1972-10-05 1976-10-01 Ciba Geigy Ag
JPS5128227B2 (fr) 1972-10-05 1976-08-18
US3893858A (en) 1973-03-26 1975-07-08 Eastman Kodak Co Photographic bleach accelerators
JPS541175B2 (fr) 1973-04-21 1979-01-22
US4009029A (en) 1973-06-05 1977-02-22 Eastman Kodak Company Cyanoethyl-containing blocked development restrainers
DE2329587C2 (de) 1973-06-09 1984-06-20 Agfa-Gevaert Ag, 5090 Leverkusen Farbphotographisches Aufzeichnungsmaterial
US3933501A (en) 1973-11-28 1976-01-20 Eastman Kodak Company Photographic elements containing color-forming couplers having and inhibiting effect upon the reactivity of competing couplers
JPS5437822B2 (fr) 1974-02-08 1979-11-17
US4004929A (en) 1974-03-04 1977-01-25 Eastman Kodak Company Color corrected photographic elements
JPS51102636A (en) 1974-04-03 1976-09-10 Fuji Photo Film Co Ltd Karaashashingazo no keiseihoho
JPS50140219A (fr) 1974-04-26 1975-11-10
GB1500497A (en) 1974-07-09 1978-02-08 Kodak Ltd Photographic silver halide multilayer colour materials
US4138258A (en) 1974-08-28 1979-02-06 Fuji Photo Film Co., Ltd. Multi-layered color photographic materials
JPS586939B2 (ja) 1974-08-28 1983-02-07 富士写真フイルム株式会社 カラ−シヤシンカンコウザイリヨウ
GB1504949A (en) 1974-09-17 1978-03-22 Eastman Kodak Co Aqueous polymer latexes containing hydrophobic materials
BE833512A (fr) 1974-09-17 1976-03-17 Nouvelle composition de latex charge par un compose hydrophobe, sa preparation et son application photographique
CA1079432A (fr) 1974-09-17 1980-06-10 Tsang J. Chen Distribution uniforme et efficace de matieres hydrophobes a travers des couches colloides hydrophiles, et produits utiles a ces fins
US3993681A (en) 1975-04-04 1976-11-23 W. R. Grace & Co. Process for preparing iminodiacetonitrile
JPS5220832A (en) 1975-08-09 1977-02-17 Konishiroku Photo Ind Co Ltd Color photography processing method
JPS5242121A (en) 1975-09-30 1977-04-01 Fuji Photo Film Co Ltd Color photographic light sensitive material
JPS5943736B2 (ja) 1976-01-26 1984-10-24 富士写真フイルム株式会社 カラ−写真画像の形成方法
GB1579722A (en) 1976-06-09 1980-11-26 Agfa Gavaert Two equivalent colour coupler for yellow
JPS604980B2 (ja) 1976-08-27 1985-02-07 富士写真フイルム株式会社 カラ−写真処理法
JPS609255B2 (ja) 1976-09-07 1985-03-08 コニカ株式会社 ハロゲン化銀カラ−写真感光材料の処理方法
JPS606506B2 (ja) 1976-09-07 1985-02-19 コニカ株式会社 ハロゲン化銀カラ−写真感光材料の処理方法
JPS5337418A (en) 1976-09-17 1978-04-06 Konishiroku Photo Ind Co Ltd Processing method for silver halide color photographic light sensitive material
JPS606508B2 (ja) 1976-11-05 1985-02-19 コニカ株式会社 ハロゲン化銀カラ−写真感光材料の処理方法
JPS609257B2 (ja) 1976-12-10 1985-03-08 コニカ株式会社 カラ−写真処理方法
CH628161A5 (de) 1976-12-24 1982-02-15 Ciba Geigy Ag Farbphotographisches material.
JPS5394927A (en) 1977-01-28 1978-08-19 Fuji Photo Film Co Ltd Color photographic processing method
JPS5395631A (en) 1977-02-01 1978-08-22 Fuji Photo Film Co Ltd Color photograph processing method
JPS5395630A (en) 1977-02-01 1978-08-22 Fuji Photo Film Co Ltd Color photograph processing method
DE2707489C2 (de) 1977-02-21 1983-10-06 Agfa-Gevaert Ag, 5090 Leverkusen Farbphotographisches Aufzeichnungsmaterial
JPS6016616B2 (ja) 1977-02-23 1985-04-26 コニカ株式会社 ハロゲン化銀カラ−写真感光材料の処理方法
JPS6024464B2 (ja) 1977-04-06 1985-06-13 コニカ株式会社 ハロゲン化銀カラ−写真感光材料の処理方法
JPS5814671B2 (ja) 1977-05-02 1983-03-22 富士写真フイルム株式会社 カラ−写真感光材料
JPS6026210B2 (ja) 1977-05-16 1985-06-22 コニカ株式会社 ハロゲン化銀カラ−写真材料の処理方法
DE2729213C2 (de) 1977-06-29 1985-09-12 Agfa-Gevaert Ag, 5090 Leverkusen Farbfotografisches Aufzeichnungsmaterial
JPS5944626B2 (ja) 1977-08-25 1984-10-31 富士写真フイルム株式会社 カラ−写真処理法
JPS5448237A (en) 1977-09-22 1979-04-16 Fuji Photo Film Co Ltd Cyan coupler for photography
DE2748430A1 (de) 1977-10-28 1979-05-03 Agfa Gevaert Ag Photographische bleichzusammensetzungen mit bleichungsbeschleunigenden verbindungen
US4248962A (en) 1977-12-23 1981-02-03 Eastman Kodak Company Photographic emulsions, elements and processes utilizing release compounds
US4283331A (en) 1978-01-25 1981-08-11 Ciba-Geigy Corporation Azo dyes, their preparation and use
JPS5526506A (en) 1978-08-14 1980-02-26 Fuji Photo Film Co Ltd Bleaching method of color photographic material
JPS5930261B2 (ja) 1978-08-29 1984-07-26 富士写真フイルム株式会社 ハロゲン化銀写真感光材料
US4310612A (en) 1978-10-10 1982-01-12 Eastman Kodak Company Blocked photographically useful compounds in photographic compositions, elements and processes employing them
JPS55118034A (en) 1979-03-05 1980-09-10 Fuji Photo Film Co Ltd Color image forming method
JPS5926016B2 (ja) 1979-05-31 1984-06-23 富士写真フイルム株式会社 黄色カプラ−
JPS5810739B2 (ja) 1979-06-06 1983-02-26 富士写真フイルム株式会社 ハロゲン化銀カラ−写真感光材料
JPS5930263B2 (ja) 1979-06-19 1984-07-26 富士写真フイルム株式会社 ハロゲン化銀写真感光材料
JPS565543A (en) 1979-06-26 1981-01-21 Fuji Photo Film Co Ltd Silver halide color photosensitive material
JPS5612369A (en) 1979-07-12 1981-02-06 Nippon Kayaku Co Ltd Preparation of 6-hydroxy-pyrido-2-one compound
JPS5625738A (en) 1979-08-07 1981-03-12 Fuji Photo Film Co Ltd Multilayered color photosensitive material
JPS5930264B2 (ja) 1979-08-13 1984-07-26 富士写真フイルム株式会社 ハロゲン化銀写真感光材料
US4333999A (en) 1979-10-15 1982-06-08 Eastman Kodak Company Cyan dye-forming couplers
JPS5664339A (en) 1979-10-29 1981-06-01 Konishiroku Photo Ind Co Ltd Silver halide color phtographic material
JPS6038695B2 (ja) 1979-12-05 1985-09-02 富士写真フイルム株式会社 カラ−写真感光材料
JPS56104333A (en) 1980-01-23 1981-08-20 Fuji Photo Film Co Ltd Color photographic sensitive material
US4338393A (en) 1980-02-26 1982-07-06 Eastman Kodak Company Heterocyclic magenta dye-forming couplers
US4283472A (en) 1980-02-26 1981-08-11 Eastman Kodak Company Silver halide elements containing blocked pyrazolone magenta dye-forming couplers
US4310618A (en) 1980-05-30 1982-01-12 Eastman Kodak Company Silver halide photographic material and process utilizing blocked dye-forming couplers
JPS578542A (en) 1980-06-18 1982-01-16 Konishiroku Photo Ind Co Ltd Processing method for photographic sensitive silver halide material
JPS578543A (en) 1980-06-18 1982-01-16 Konishiroku Photo Ind Co Ltd Processing method for color photographic sensitive silver halide material
JPS5912169B2 (ja) 1980-07-04 1984-03-21 富士写真フイルム株式会社 ハロゲン化銀カラ−感光材料
JPS5735858A (en) 1980-08-12 1982-02-26 Fuji Photo Film Co Ltd Color photographic sensitive material
JPS5943728B2 (ja) 1980-10-30 1984-10-24 三菱製紙株式会社 ハロゲン化銀写真材料
JPS5794752A (en) 1980-12-05 1982-06-12 Fuji Photo Film Co Ltd Color photographic sensitive silver halide material
JPS57112751A (en) 1980-12-29 1982-07-13 Fuji Photo Film Co Ltd Multilayered photosnsitive color reversal material
JPS57144547A (en) 1981-03-03 1982-09-07 Fuji Photo Film Co Ltd Silver halide color photosensitive material and its processing method
US4363865A (en) 1981-03-04 1982-12-14 Eastman Kodak Company Imido methyl blocked photographic dyes and dye releasing compounds
JPS57150845A (en) 1981-03-13 1982-09-17 Fuji Photo Film Co Ltd Silver halide photographic material
JPS57151944A (en) 1981-03-16 1982-09-20 Fuji Photo Film Co Ltd Color photosensitive silver halide material
JPS57154234A (en) 1981-03-19 1982-09-24 Konishiroku Photo Ind Co Ltd Phtotographic sensitive silver halide material
JPS57176038A (en) 1981-04-21 1982-10-29 Fuji Photo Film Co Ltd Silver halide color photographic material
JPS5828745A (ja) 1981-05-08 1983-02-19 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS57204038A (en) 1981-06-10 1982-12-14 Fuji Photo Film Co Ltd Color photosensitive silver halide material
EP0148536B1 (fr) 1981-06-11 1989-09-06 Konica Corporation Matériaux photosensibles à l'halogénure d'argent pour la photographie en couleurs
JPS5810738A (ja) 1981-07-13 1983-01-21 Fuji Photo Film Co Ltd ハロゲン化銀カラ−感光材料
JPS5814834A (ja) 1981-07-21 1983-01-27 Konishiroku Photo Ind Co Ltd ハロゲン化銀カラ−写真感光材料の安定化処理方法
JPS5816235A (ja) 1981-07-23 1983-01-29 Konishiroku Photo Ind Co Ltd 撮影用透過型ハロゲン化銀カラー写真感光材料の処理方法
EP0073636B2 (fr) 1981-08-25 1992-09-09 EASTMAN KODAK COMPANY (a New Jersey corporation) Eléments photographiques contenant des coupleurs lestés
JPS5842044A (ja) 1981-09-07 1983-03-11 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS5858543A (ja) 1981-10-02 1983-04-07 Fuji Photo Film Co Ltd 熱現像カラ−感光材料およびそれを用いたカラ−画像形成方法
JPS5879248A (ja) 1981-11-06 1983-05-13 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
US4433048A (en) 1981-11-12 1984-02-21 Eastman Kodak Company Radiation-sensitive silver bromoiodide emulsions, photographic elements, and processes for their use
US4414310A (en) 1981-11-12 1983-11-08 Eastman Kodak Company Process for the preparation of high aspect ratio silver bromoiodide emulsions
US4434226A (en) 1981-11-12 1984-02-28 Eastman Kodak Company High aspect ratio silver bromoiodide emulsions and processes for their preparation
US4439520A (en) 1981-11-12 1984-03-27 Eastman Kodak Company Sensitized high aspect ratio silver halide emulsions and photographic elements
US4401752A (en) 1981-11-23 1983-08-30 Eastman Kodak Company Aryloxy substituted photographic couplers and photographic elements and processes employing same
JPS5898731A (ja) 1981-12-07 1983-06-11 Fuji Photo Film Co Ltd カラ−写真感光材料
JPS58111941A (ja) 1981-12-16 1983-07-04 Konishiroku Photo Ind Co Ltd ハロゲン化銀カラ−写真感光材料
JPS58115438A (ja) 1981-12-28 1983-07-09 Fuji Photo Film Co Ltd ハロゲン化銀カラ−感光材料の処理方法
JPS58145944A (ja) 1982-02-25 1983-08-31 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS58163940A (ja) 1982-03-25 1983-09-28 Fuji Photo Film Co Ltd カラ−写真感光材料の処理法
JPS58205151A (ja) 1982-05-24 1983-11-30 Fuji Photo Film Co Ltd ハロゲン化銀カラ−感光材料
EP0096570B1 (fr) 1982-06-05 1988-08-24 Olympus Optical Co., Ltd. Dispositif optique de détection d'écart de focalisation
US4410618A (en) 1982-06-11 1983-10-18 Eastman Kodak Company Blocked photographic reagents
JPS599657A (ja) 1982-07-07 1984-01-19 Fuji Photo Film Co Ltd ハロゲン化銀カラ−感光材料
US4463086A (en) 1982-08-17 1984-07-31 Konishiroku Photo Industry Co., Ltd. Light-sensitive silver halide color photographic material
JPS5950439A (ja) 1982-09-16 1984-03-23 Fuji Photo Film Co Ltd ハロゲン化銀写真感光材料
JPS5999437A (ja) 1982-10-28 1984-06-08 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS59113440A (ja) 1982-12-20 1984-06-30 Konishiroku Photo Ind Co Ltd ハロゲン化銀写真感光材料
JPS59113438A (ja) 1982-12-18 1984-06-30 Konishiroku Photo Ind Co Ltd ハロゲン化銀写真感光材料
JPS59162548A (ja) 1983-02-15 1984-09-13 Fuji Photo Film Co Ltd 色画像形成方法
JPS59157638A (ja) 1983-02-25 1984-09-07 Fuji Photo Film Co Ltd ハロゲン化銀カラ−感光材料
JPS59170840A (ja) 1983-02-25 1984-09-27 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS59166956A (ja) 1983-03-14 1984-09-20 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS59171956A (ja) 1983-03-18 1984-09-28 Fuji Photo Film Co Ltd カラ−画像形成方法
JPS59202464A (ja) 1983-04-30 1984-11-16 Konishiroku Photo Ind Co Ltd ハロゲン化銀写真感光材料
JPS59214854A (ja) 1983-05-20 1984-12-04 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS59218443A (ja) 1983-05-26 1984-12-08 Fuji Photo Film Co Ltd 画像形成方法
JPS602953A (ja) 1983-06-20 1985-01-09 Fuji Photo Film Co Ltd カラ−写真感光材料
JPS6033552A (ja) 1983-08-04 1985-02-20 Fuji Photo Film Co Ltd カラ−画像形成方法
JPS6035730A (ja) 1983-08-08 1985-02-23 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS6043659A (ja) 1983-08-19 1985-03-08 Fuji Photo Film Co Ltd カラ−画像形成方法
JPS60133449A (ja) 1983-12-22 1985-07-16 Konishiroku Photo Ind Co Ltd 熱現像カラ−感光材料
JPS60185951A (ja) 1984-02-07 1985-09-21 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS60185950A (ja) 1984-02-23 1985-09-21 Fuji Photo Film Co Ltd ハロゲン化銀カラ−感光材料
JPS60184248A (ja) 1984-03-01 1985-09-19 Fuji Photo Film Co Ltd ハロゲン化銀写真感光材料
JPS60191259A (ja) 1984-03-13 1985-09-28 Fuji Photo Film Co Ltd 現像装置用フイルム蛇行防止機構
JPS60191258A (ja) 1984-03-13 1985-09-28 Fuji Photo Film Co Ltd 現像装置用フイルムリ−ダの搬送機構
JPS60191257A (ja) 1984-03-13 1985-09-28 Fuji Photo Film Co Ltd 現像装置用フイルム搬送機構
JPS60220345A (ja) 1984-04-17 1985-11-05 Konishiroku Photo Ind Co Ltd ハロゲン化銀カラ−写真感光材料の処理方法
DE3580785D1 (de) 1984-05-10 1991-01-17 Fuji Photo Film Co Ltd Farbphotographisches lichtempfindliches silberhalogenidmaterial.
JPS6134541A (ja) 1984-07-06 1986-02-18 Fuji Photo Film Co Ltd カラ−写真感光材料
JPH0614176B2 (ja) 1984-07-09 1994-02-23 コニカ株式会社 ハロゲン化銀カラ−写真感光材料
JPS6120038A (ja) 1984-07-09 1986-01-28 Konishiroku Photo Ind Co Ltd ハロゲン化銀カラ−写真感光材料
JPS6142658A (ja) 1984-08-03 1986-03-01 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
US4552834A (en) 1984-08-06 1985-11-12 Eastman Kodak Company Enhanced bleaching of photographic elements containing silver halide and adsorbed dye
JPS6143748A (ja) 1984-08-08 1986-03-03 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS6151146A (ja) 1984-08-21 1986-03-13 Fuji Photo Film Co Ltd 高感度ハロゲン化銀カラ−写真感光材料
JPS61184541A (ja) 1984-08-27 1986-08-18 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS6172238A (ja) 1984-09-14 1986-04-14 Konishiroku Photo Ind Co Ltd ハロゲン化銀カラ−写真感光材料
JPS6172244A (ja) 1984-09-17 1986-04-14 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS61107245A (ja) 1984-10-30 1986-05-26 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
US4555477A (en) 1985-01-02 1985-11-26 Eastman Kodak Company Photographic element and process utilizing metal complex color masking dyes
JPH0690461B2 (ja) 1985-02-28 1994-11-14 富士写真フイルム株式会社 カラ−写真感光材料
CA1287765C (fr) 1985-02-28 1991-08-20 Eastman Kodak Company Materiau photographique colorant et methode englobant un compose a decharge d'agent accelerateur de blanchiment
JPS61201245A (ja) 1985-03-04 1986-09-05 Fuji Photo Film Co Ltd カラ−写真感光材料
JPH0680458B2 (ja) 1985-04-05 1994-10-12 富士写真フイルム株式会社 ハロゲン化銀カラ−写真感光材料
JPS61238056A (ja) 1985-04-15 1986-10-23 Fuji Photo Film Co Ltd 画像形成方法
JPS6254260A (ja) * 1985-05-27 1987-03-09 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS61273543A (ja) 1985-05-29 1986-12-03 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPH083621B2 (ja) 1985-07-31 1996-01-17 富士写真フイルム株式会社 画像形成方法
JPH0610754B2 (ja) 1985-09-14 1994-02-09 コニカ株式会社 多色写真要素
JPH071382B2 (ja) 1985-10-09 1995-01-11 富士写真フイルム株式会社 ハロゲン化銀写真感光材料
JPS62151850A (ja) 1985-12-26 1987-07-06 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPH0690463B2 (ja) 1986-01-08 1994-11-14 富士写真フイルム株式会社 カラ−写真感光材料
JP2534227B2 (ja) 1986-02-07 1996-09-11 富士写真フイルム株式会社 ハロゲン化銀カラ−写真感光材料の処理方法
JPH0715575B2 (ja) 1986-02-07 1995-02-22 富士写真フイルム株式会社 ハロゲン化銀カラ−写真感光材料の処理方法
JPS62200350A (ja) 1986-02-28 1987-09-04 Konishiroku Photo Ind Co Ltd 新規な層構成のハロゲン化銀カラ−写真感光材料
JPS62206543A (ja) 1986-03-07 1987-09-11 Konishiroku Photo Ind Co Ltd 新規な層構成のハロゲン化銀カラ−写真感光材料
JPH0623831B2 (ja) 1986-03-07 1994-03-30 コニカ株式会社 新規な層構成のハロゲン化銀カラ−写真感光材料
JPS62272248A (ja) 1986-05-20 1987-11-26 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料の処理方法
JP2648911B2 (ja) 1986-06-06 1997-09-03 富士写真フイルム株式会社 ハロゲン化銀カラー写真感光材料の処理方法及び装置
GB8614213D0 (en) 1986-06-11 1986-07-16 Kodak Ltd Photographic acetanilide couplers
US4818672A (en) 1986-06-13 1989-04-04 Konishiroku Photo Industry Co., Ltd. Silver halide color photographic light-sensitive material improved in cyan image characteristics
JPS6323152A (ja) 1986-06-16 1988-01-30 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
CA1324609C (fr) 1986-07-30 1993-11-23 Eastman Kodak Company Element et processus photographiques
JPH07122738B2 (ja) 1986-08-01 1995-12-25 コニカ株式会社 ハロゲン化銀カラ−写真感光材料
US4749641A (en) 1986-09-15 1988-06-07 Eastman Kodak Company Imaging element containing dye masking coupler
JPH0614177B2 (ja) 1986-10-03 1994-02-23 富士写真フイルム株式会社 ハロゲン化銀カラ−写真感光材料
US4775616A (en) 1986-12-12 1988-10-04 Eastman Kodak Company Cyan dye-forming couplers and photographic materials containing same
US4853319A (en) 1986-12-22 1989-08-01 Eastman Kodak Company Photographic silver halide element and process
JPH0690470B2 (ja) 1986-12-26 1994-11-14 富士写真フイルム株式会社 ハロゲン化銀カラ−写真感光材料
JPS63216050A (ja) 1987-03-05 1988-09-08 Fuji Photo Film Co Ltd ハロゲン化銀感光材料の水洗・安定化処理方法及びその装置
JPH0664315B2 (ja) 1987-04-15 1994-08-22 富士写真フイルム株式会社 ハロゲン化銀写真感光材料
JPS63281160A (ja) 1987-05-14 1988-11-17 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPH0627119B2 (ja) 1987-05-15 1994-04-13 富士写真フイルム株式会社 チオエ−テル基を有するカテコ−ル類の合成方法
US4777120A (en) 1987-05-18 1988-10-11 Eastman Kodak Company Photographic element and process comprising a masking coupler
JPS63304242A (ja) * 1987-06-04 1988-12-12 Fuji Photo Film Co Ltd 熱現像カラ−感光材料
JPH07119981B2 (ja) 1987-06-08 1995-12-20 富士写真フイルム株式会社 ハロゲン化銀カラー写真感光材料の処理方法
US4774181A (en) 1987-06-25 1988-09-27 Eastman Kodak Company Imaging element containing fluorescent dye-releasing coupler compound
JPH0797208B2 (ja) 1987-07-08 1995-10-18 コニカ株式会社 新規なカプラ−を含有するハロゲン化銀カラ−写真感光材料
US4782012A (en) 1987-07-17 1988-11-01 Eastman Kodak Company Photographic material containing a novel dir-compound
JPH0754403B2 (ja) 1987-09-16 1995-06-07 コニカ株式会社 新規なカプラーを含有するハロゲン化銀カラー写真感光材料
JPS6480941A (en) 1987-09-22 1989-03-27 Fuji Photo Film Co Ltd Silver halide photographic sensitive material
JPH0664324B2 (ja) 1987-09-25 1994-08-22 富士写真フイルム株式会社 感光材料処理装置
US4840884A (en) 1987-10-19 1989-06-20 Eastman Kodak Company Photographic element and process comprising a dye releasing group
JPH026945A (ja) * 1987-12-01 1990-01-11 Fuji Photo Film Co Ltd ハロゲン化銀カラー写真感光材料
JPH0753830B2 (ja) 1988-02-02 1995-06-07 富士写真フイルム株式会社 アゾ化合物の製造方法
JPH01214849A (ja) 1988-02-23 1989-08-29 Fuji Photo Film Co Ltd ハロゲン化銀カラー写真感光材料の処理方法
DE3815469C2 (de) * 1988-05-06 1993-12-09 Agfa Gevaert Ag Farbfotografisches Aufzeichnungsmaterial mit neuen farbigen Blaugrünkupplern

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0423727A2 (fr) * 1989-10-16 1991-04-24 Fuji Photo Film Co., Ltd. Matériau photographique couleur à l'halogénure d'argent contenant un coupleur coloré
EP0436938A2 (fr) * 1989-12-29 1991-07-17 Fuji Photo Film Co., Ltd. Produit photographique couleur à l'halogénure d'argent contenant un coupleur cyan coloré en jaune
JPH06254260A (ja) * 1993-03-04 1994-09-13 Sega Enterp Ltd 家庭用ゲーム機を用いた自動デモシステム

Also Published As

Publication number Publication date
EP0435334A3 (en) 1991-09-04
DE69031679T2 (de) 1998-06-04
EP0435334A2 (fr) 1991-07-03
DE69031679D1 (de) 1997-12-11

Similar Documents

Publication Publication Date Title
EP0464612B1 (fr) Matériaux photographiques à l'halogénure d'argent
EP0502424B1 (fr) Matériau photographique couleur à l'halogénure d'argent
US5071735A (en) Silver halide color photographic material containing a compound releasing a dir command upon reaction with an oxidized developing agent
US5306609A (en) Silver halide color photographic material
US5112730A (en) Silver halide color photographic material comprising a yellow-colored cyan coupler
US5631122A (en) Silver halide color photographic material
EP0456257A1 (fr) Matériau photographique couleur à l'halogénure d'argent
EP0435334B1 (fr) Produit photographique couleur à l'halogénure d'argent contenant un coupleur cyan coloré en jaune
EP0456181B1 (fr) Produit photographique couleur à l'halogénure d'argent et méthode pour son traitement
US5534399A (en) Silver halide color photographic photosensitive material
EP0451526B1 (fr) Produits photographiques couleur à l'halogénure d'argent
EP0446863B1 (fr) Produit photographique couleur à l'halogénure d'argent
EP0436938B1 (fr) Produit photographique couleur à l'halogénure d'argent contenant un coupleur cyan coloré en jaune
US5063145A (en) Silver halide color photographic material
US5376513A (en) Silver halide color photographic light-sensitive materials
EP0423727B1 (fr) Matériau photographique couleur à l'halogénure d'argent contenant un coupleur coloré
JP2729690B2 (ja) ハロゲン化銀カラー写真感光材料
JP2699218B2 (ja) ハロゲン化銀カラー写真感光材料
US5476759A (en) Silver halide color photographic material
JP2903091B2 (ja) カラー画像形成方法
JP2926418B2 (ja) ハロゲン化銀カラー写真感光材料
EP0583004A1 (fr) Matériau photographique à l'halogénure d'argent
EP0428902B1 (fr) Matériaux photographiques couleur à l'halogénure d'argent
EP0421453A1 (fr) Matériau photographique couleur à l'halogénure d'argent
EP0517214A1 (fr) Matériau photographique couleur à l'halogénure d'argent sensible à la lumière et procédé pour son traitement

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): DE FR GB NL

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

Designated state(s): DE FR GB NL

17P Request for examination filed

Effective date: 19911121

17Q First examination report despatched

Effective date: 19941220

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

RBV Designated contracting states (corrected)

Designated state(s): DE GB

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE GB

REF Corresponds to:

Ref document number: 69031679

Country of ref document: DE

Date of ref document: 19971211

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

REG Reference to a national code

Ref country code: GB

Ref legal event code: 732E

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20071227

Year of fee payment: 18

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20071220

Year of fee payment: 18

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20081228

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20090701

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20081228