EP0324476A2 - Matériaux photosensibles couleur à l'halogénure d'argent - Google Patents

Matériaux photosensibles couleur à l'halogénure d'argent Download PDF

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Publication number
EP0324476A2
EP0324476A2 EP89100484A EP89100484A EP0324476A2 EP 0324476 A2 EP0324476 A2 EP 0324476A2 EP 89100484 A EP89100484 A EP 89100484A EP 89100484 A EP89100484 A EP 89100484A EP 0324476 A2 EP0324476 A2 EP 0324476A2
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EP
European Patent Office
Prior art keywords
groups
group
silver halide
acid
photographic material
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EP89100484A
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German (de)
English (en)
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EP0324476A3 (en
EP0324476B1 (fr
Inventor
Osamu C/O Fuji Photo Film Co. Ltd. Takahashi
Tadahisa C/O Fuji Photo Film Co. Ltd. Sato
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Fujifilm Holdings Corp
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Fuji Photo Film Co Ltd
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    • 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
    • G03C7/388—Processes for the incorporation in the emulsion of substances liberating photographically active agents or colour-coupling substances; Solvents therefor
    • G03C7/3882—Processes for the incorporation in the emulsion of substances liberating photographically active agents or colour-coupling substances; Solvents therefor characterised by the use of a specific polymer or latex
    • 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
    • G03C7/392—Additives
    • G03C7/396—Macromolecular additives

Definitions

  • This invention concerns silver halide photographic materials which have excellent storage properties and, more precisely, the invention concerns silver halide color photographic materials of which the stability of the colored image with respect to light and heat during the storage of a color photograph is increased, and with which there is less coloration of the base (so-called staining) due to degradation of organic materials which have been included in the photosensitive materials, developing agents which are left behind in the photosensitive material after processing, and compounds derived therefrom.
  • the dye images of silver halide color photo­graphic materials are known to fade markedly, depending on the storage conditions, when they are stored for a long period of time in light, and also when they are exposed to light for short periods of time and stored for long periods of time in the dark.
  • the color fading in the former case is called light fading and that in the latter cases is called dark fading
  • when color photographic materials are stored semi-­permanently as records it is desirable that the extents of light fading and dark fading should be reduced to a minimum and that the overall color balance of the faded tricolor yellow, magenta and cyan dye images should be maintained in the initial state.
  • the extents of light and dark fading differ for each of the yellow, magenta and cyan dye images, and after long term storage the aforementioned overall faded color balance is inevitably destroyed and the picture quality of the dye image inevitably deteriorates.
  • the extents of light fading and dark fading differ according to the couplers which are used and other factors but, in many cases, dark fading arises most readily in the case of the cyan dye image, followed in order by the yellow dye image and the magenta dye image, and the extent of the dark fading of the cyan dye image is greater than that of the other dye images. Furthermore, in the case of light fading, the magenta dye image tends to fade most readily when a visible light source is used, followed in order by the cyan dye image and the yellow dye image.
  • a second important point in respect of the long term storage of color photographs involves the prevention of coloration of the white background which is to say the prevention of the occurrence of staining due to light and heat.
  • the occurrence of staining can be broadly classified as that which is caused by the degradation of organic materials which are present in the photosensitive material from the start and that which is due to development bath components, especially primary aromatic amine compounds which are the developing agents and compounds derived therefrom, which are left behind in the photosensitive material after development processing.
  • This staining not only causes coloration of the white base but also has a further disadvantage in that it reduces the image saturation of a color photograph.
  • Patent 4,540,654, JP-­A-61-65245, etc. which have a sharp spectral absorption without the subsidiary absorption in the vicinity of 430 nm, which is a major disadvantage of the existing 5-pyrazolone based couplers (JP-A-49-74027, JP-­A-49-111631, etc.), have been discovered and put to practical use.
  • the color reproduction in a silver halide color photograph is greatly improved by using these couplers, but the occurrence of staining during storage has become an even greater problem that it was in the past.
  • the first aim of the invention is to provide silver halide color photographic materials with which sharp color photographs with which an excellent tricolor balance is maintained even on long term storage, and with which there is little deterioration of the colored image, can be obtained.
  • the second aim of the invention is to provide silver halide color photographic materials with which it is possible to obtain color photographs with which there is very little coloration of the white background even on long term storage.
  • the aforementioned aims can be realized in the way indicated below.
  • the above mentioned aims can be realized by means of silver halide color photographic materials of which the distinguishing features are that, in a silver halide photographic material comprising a support having provided thereon a plurality of photographic constituting layers comprising a light-sensitive hydrophilic colloid layer and a cyan dye-forming coupler-containing silver halide emulsion layer, magenta dye-forming coupler containing silver halide emulsion layer and a yellow dye-forming coupler-­containing silver halide emulsion layer, wherein said magenta dye-forming coupler is represented by the formula (I) below, and a water insoluble but organic solvent soluble polymer is incorporated in at least one of said silver halide emulsion layers, and further an aliphatic ester solvent represented by the formula (II) or (III) below is incorporated in at least one of said light-insensitive hydrophilic colloid
  • R1 represents a hydrogen atom or a substituent group
  • X represents a hydrogen atom or a group which can be eliminated during a coupling reaction with the oxidized form of a developing agent.
  • R6 represents a substituent group.
  • m and n represent integer values of from 2 to 5
  • R2 and R5 represent alkylidene groups, alkylene groups, alkenylene groups, alkanetriyl groups, alkenetriyl groups, alkane­tetrayl groups, alkenetetrayl groups, alkanepentayl groups or alkenepentayl groups.
  • R3 and R4 represent alkyl groups, alkenyl groups or alkynyl groups which have not more the 20 carbon atoms.
  • the couplers of general formula (I) which can be represented by the general formulae (I-1), (I-2), (I-3), (I-4) and (I 5) are preferred.
  • R7, R8, R9, R10 and R11 represent hydrogen atoms, alkyl groups, aryl groups, heterocyclic groups, cyano groups, alkoxy groups, aryloxy groups, heterocyclic oxy groups, acyloxy groups, carbamoyloxy groups, silyloxy groups, sulfonyloxy groups, acylamino groups, anilino groups, ureido groups, imido groups, sulfamoylamino groups, carbamoylamino groups, alkylthio groups, arylthio groups, heterocyclic thio groups, alkoxycarbonylamino groups, aryloxycarbonylamino groups, sulfonamido groups, carbamoyl groups, acyl groups, sulfamoyl groups, sulfonyl groups, sulfinyl groups, alkoxycarbonyl groups or
  • X in general formulae (I-1) to (I-5) represents a hydrogen atom, halogen atom, carboxyl group or a group which is eliminated on coupling, being a group which is bonded to the carbon at the coupling position via an oxygen atom, nitrogen atom or sulfur atom, but it is preferably a halogen atom or a coupling leaving group which is bonded via a sulfur atom.
  • the coupler may take a polymeric form, and when, in such a case, the parts represented by the general formulae (I-1) to (I-5) are included in a vinyl monomer, R7, R8, R9, R10 or R11 represent a single bond or a linking group, and the vinyl group is bonded to the part represented by the general formula (I-1) to (I-5) via this group.
  • alkyl groups (moieties), aryl groups (moieties), and heterocyclic groups (moieties) among these groups include cases in which these groups are optionally substituted with substituent groups such as those listed as examples of R7 to R11, and the alkyl groups may be linear chain, branched or alicyclic alkyl groups.
  • the groups and atoms indicated below are included among the actual examples of the groups R7 to R11; hydrogen atom, halogen atoms (chlorine, bromine, etc.), alkyl groups (methyl, ethyl, propyl, iso-propyl, butyl, t-butyl, hexyl, cyclohexyl, trifluoromethyl, 2-­arylsulfonamidoethyl, 1-arylsulfonamidoethyl, alkyl­sulfonylethyl, arylsulfonylethyl, tridecyl, 3-(2,4-di-­tert-amylphenoxy)propyl, 2-dodecyloxyethyl, 3-phenoxy­propyl, cyclopentyl, benzyl, etc.), aryl groups (for example, phenyl, 4-tert-butylphenyl, 2,4-di-tert
  • X represents a hydrogen atom, a halogen atom (for example, chlorine, bromine, iodine, etc.), a carboxyl group, or a group which is linked via an oxygen atom (for example, acetoxy, propanoyloxy, benzoyloxy, 2,4-dichlorobenzoyl­oxy, ethoxyoxaloyloxy, pyruvinyloxy, cinnamoyloxy, phenoxy, 4-cyanophenoxy, 4-methanesulfonamidophenoxy, 4-­methanesulfonylphenoxy, ⁇ -naphthoxy, 3-pentadecyl­phenoxy, benzyloxycarbonyloxy, ethoxy, 2-cyanoethoxy, benzyloxy, 2-phenethyloxy, 2-phenoxyethoxy, 5-phenyl­tetrazolyloxy, 2-benzothiazolyloxy, etc
  • the divalent group is, more precisely, a substituted or unsubstituted alkylene group (for example, methylene, ethylene, 1-­ethylethylene, 1,10-decylene, -CH2CH2-O-CH2CH2-, etc.), a substituted or unsubstituted phenylene group (for example, 1,4-phenylene, 1,3-phenylene, etc.), and -NHCO-R12-CONH- group (where R12 represents a substituted or unsubstituted alkylene group or phenylene group).
  • a substituted or unsubstituted alkylene group for example, methylene, ethylene, 1-­ethylethylene, 1,10-decylene, -CH2CH2-O-CH2CH2-, etc.
  • a substituted or unsubstituted phenylene group for example, 1,4-phenylene, 1,3-phenylene, etc.
  • -NHCO-R12-CONH- group where
  • Oligomers may also be formed at R7, R8, R9, R10, and R11 and here the term "oligomer” includes those which have two or more groups comprising any of those of general formulae (I-1) to (I-5) within a single molecule, and it includes bis forms and polymeric couplers.
  • a polymeric coupler may be a homo­polymer which has a part consisting only of monomers which can be represented by any one of the general formulae (I-1) to (I-5) (and preferably a monomer which has a vinyl group, referred to below as a vinyl monomer) or it may be a copolymer with a non-color forming ethylenic monomer which does not couple with the oxidation products of primary aromatic amine developing agents.
  • the linking groups represented by R7, R8, R9, R10, or R11 in the case of a vinyl monomer which incorporates a unit which can be represented by general formula (I-1) to (I-5) is an alkylene group (which may be a substituted or unsubstituted alkylene group, for example, methylene, ethylene, 1-methylethylene, 1,10-­ dodecylene, -CH2CH2-O-CH2CH2, etc.), a phenylene group (a substituted or unsubstituted phenylene group, for example, 1,4-phenylene, 1,3-phenylene, etc.) or a group which is made up of a combination of groups selected from among the -NHCO- group, -CONH- group, -O- group, -OCO- group and aralkylene groups (for example,
  • the vinyl groups in the vinyl monomers include those groups which have substituent groups other than those represented by the general formulae (I-1) to (I-5).
  • the preferred substituent groups are a hydrogen atom, a chlorine atom, and lower alkyl groups which have from 1 to 4 carbon atoms.
  • the non-color forming ethylenic monomers which do not couple with the oxidation products of primary aromatic amine developing agents include acrylic acid, ⁇ -chloroacrylic acid, ⁇ -alacrylic acids (for example, methacrylic acid, etc.) and esters and amides derived from these acrylic acids (for example, acrylamide, n-­ butylacrylamide, t-butylacrylamide, diacetoneacrylamide, methacrylamide, methyl acrylate, ethyl acrylate, n-­propyl acrylate, n-butyl acrylate, tert-butyl acrylate, iso-butyl acrylate, 2-ethylhexyl acrylate, n-octyl acrylate, lauryl acrylate, methyl methacrylate, ethyl methacrylate, n-butyl methacrylate, ⁇ -hydroxy methacrylate (sic), methylenebisacrylamide, vinyl est
  • Couplers which can be represented by the above mentioned general formulae (I-1) to (I-5) can be prepared using the methods of synthesis described in the literature indicated below.
  • compounds of general formula (I-1) can be prepared using the methods disclosed in JP-A-59 162548, etc.
  • compounds of general formula (I-2) can be prepared using the methods disclosed in JP-A-59-171956, etc.
  • compounds of general formula (I-3) can be prepared using the methods disclosed in U.S. Patent 3,725,067, etc.
  • compounds of general formula (I-4) can be prepared using the methods disclosed in JP-A-60-33552
  • compounds of general formula (I-5) can be prepared using the methods disclosed in U.S. Patents 3,061,432 and 3,369,897, etc.
  • the coupler represented by the general formula (I) is generally incorporated in a silver halide emulsion layer in an amount of from 0.1 to 1.0 mol, preferably from 0.1 to 0.5 mol per mol of silver halide.
  • ester based solvents which can be represented by general formulae (II) and (III) used in the invention are described in detail below.
  • R2 or R5 is an alkylidene group (for example, ethylidene, iso­propylidene, cyclohexylidene, etc.), an alkylene group for example, methylene, ethylene, ethylethylene, propylene, trimethylene, tetramethylene, pentamethylene, hexamethylene, heptamethylene, octamethylene, undeca­methylene, 2,2-dimethyltrimethylene, 1,2-cyclohexylene, 1,4-cyclohexylene, 3,4-epoxycyclohexan-1,2-ylene, 3,8-­tricyclo(5,2,1,0 2,6 )decylene, etc.), or an alkenylene group (e.g., vinylene, propenylene, 4-cyclohexen-1,2-­ylene, 2-pentenylene, 4-propen-2-octenylene, etc.), when m
  • n and n represent an integer value of from 2 to 5, preferably of value 2 or 3, and most desirably of value 2.
  • R2 and R4 represent alkyl groups, alkenyl groups or alkynyl groups which have not more than 20 carbon atoms, and they are preferably linear chain or branched chain alkyl groups, such as a methyl group, an ethyl group, an n-butyl group, a pentyl group, a neopentyl group, a hexyl group, a cyclohexyl group, an octyl group, a 2-ethylhexyl group, a decyl group, a dodecyl group, a hexadecyl group, an eicosanyl group, etc., alkenyl groups such as a 2-butenyl group, a 2-pentenyl group, a 2-nonyl-2-butenyl group, an 1,2-octadienyl group, etc., or alkynyl groups such as a 2-propynyl group,
  • R2, R3, R4 and R5 may have further substituent groups, and the preferred substituent groups are alkoxy groups, aryloxy groups, epoxy groups, a hydroxyl group, acyloxy groups, aryl groups, alkylthio groups, arylthio groups, acyl groups, acylamino groups, ketone groups, halogen atoms, etc., and most desirably the substituent groups are alkoxy groups (e.g., methoxy, butoxy, butoxyethoxy, etc.), epoxy groups, a hydroxyl group, acyloxy groups (acetyloxy group, propionyloxy group, cyclohexanoyloxy group, etc.), or halogen atoms (e.g., a fluorine atom, etc.).
  • the substituent groups are alkoxy groups (e.g., methoxy, butoxy, butoxyethoxy, etc.), epoxy groups, a hydroxyl group, acyloxy groups (acety
  • ester based solvents which can be represented by the general formulae (II) and (III) are indicated below, but the invention is not limited to these examples.
  • the water insoluble, organic solvent soluble polymers preferably used in this invention are non-­color-forming polymers and more preferably have a glass transition temperature of at least 60°C and, most desirably, they have a glass transition temperature of at least 90°C.
  • Preferred polymers are those having relative fluorescence quantum yield, K-value, of 0.2 or more, preferably 0.25 or more, and more preferably 0.3 or more. The polymers having higher K-value are more preferred.
  • the K-value is a relative fluorescence quantum yield, in polymers, of Compound A having the following structure, Compound A being one of the dyes which are often used as fluorescent probes.
  • the K-value was calculated using ⁇ a and ⁇ b , which were obtained by measuring at room temperature using thin films of polymers containing Compounds A at a concentration of 0.5 mmol/kg (note: the thin films were spin-coated on a slide glass in such a thickness that the absorbance of Compound A at ⁇ max was from 0.05 to 0.1).
  • the K-­value specified above was that obtained when poly(methylmethacrylate) with a number average molecular weight of 20,000 was used as polymer b.
  • G1 and G2 are polymers in which, in the polymers described in (3) above, one of G1 and G2 is a hydrogen atom and the other is a substituted or unsubstituted alkyl or aryl group which has from 3 to 12 carbon atoms.
  • Monomers which can be used to form vinyl polymers of this invention include acrylic acid esters, of which actual example include methyl acrylate, ethyl acrylate, n-propyl acrylate, iso-propyl acrylate, n-­butyl acrylate, iso-butyl acrylate, sec-butyl acrylate, tert-butyl acrylate, amyl acrylate, hexyl acrylate, 2-­ethylhexyl acrylate, octyl acrylate, tert-octyl acrylate, 2-chloroethyl acrylate, 2-bromoethyl acrylate, 4-chlorobutyl acrylate, cyanoethyl acrylate, 2-­acetoxyethyl acrylate, dimethylaminoethyl acrylate, benzyl acrylate, methoxybenzylacrylate, 2-chlorocyclo­hexyl
  • Methacrylic acid esters Actual example include methyl methacrylate, ethyl methacrylate, n-propyl methacrylate, iso-propyl methacrylate, n-butyl meth­acrylate, iso-butyl methacrylate, sec-butyl meth­acrylate, tert-butyl methacrylate, amyl methacrylate, hexyl methacrylate, cyclohexyl methacrylate, benzyl methacrylate, chlorobenzyl methacrylate, octyl methacrylate, stearyl methacrylate, sulfopropyl methacrylate, N-ethyl-N-phenylaminoethyl methacrylate, 2-(3-phenylpropyloxy)ethyl methacrylate, dimethylamino­ phenoxyethyl methacrylate, furfuryl methacrylate, tetrahydro
  • Vinyl esters Actual examples include vinyl acetate, vinyl propionate, vinyl butyrate, vinyl iso­butyrate, vinyl caproate, vinyl chloroacetate, vinyl methoxyacetate, vinyl phenylacetate, vinyl benzoate, vinyl salicylate, etc.
  • Acrylamides For example, acrylamide, methyl­acrylamide, ethylacrylamide, propylacrylamide, butyl­acrylamide, tert-butylacrylamide, cyclohexylacrylamide, benzylacrylamide, hydroxymethylacrylamide, methoxyethyl­acrylamide, dimethylaminoethylacrylamide, phenylacryl­ amide, dimethylacrylamide, diethylacrylamide, ⁇ -cyano­ethylacrylamide, N-(2-acetoacetoxyethyl)acrylamide, di­acetoneacrylamide, tert-octylacrylamide, etc.
  • Methacrylamides For example, methacrylamide, methylmethacrylamide, ethylmethacrylamide, propylmeth­acrylamide, butylmethacrylamide, tert-butylmethacryl­amide, cyclohexylmethacrylamide, benzylmethacrylamide, hydroxymethylmethacrylamide, methoxyethylmethacrylamide, dimethylaminoethylmethacrylamide, phenylmethacrylamide, dimethylmethacrylamide, diethylmethacrylamide, ⁇ -cyano­ethylmethacrylamide, N-(2-acetoacetoxyethyl)methacryl­amide, etc.
  • Olefins For example, dicyclopentadiene, ethyl­ene, propylene, 1-butene, 1-pentene, vinyl chloride, vinylidene chloride, isoprene, chloroprene, butadiene, 2,3-dimethylbutadiene, etc.; styrenes, for example, styrene, methylstyrene, dimethylstyrene, trimethyl­styrene, ethylstyrene, iso-propylstyrene, chloromethyl­styrene, methoxystyrene, acetoxystyrene, chlorostyrene, dichlorostyrene, bromostyrene, methyl vinylbenzoate, etc.
  • styrenes for example, styrene, methylstyrene, dimethylstyrene, trimethyl­styrene, ethylsty
  • Vinyl ethers For example, methyl vinyl ether, butyl vinyl ether, hexyl vinyl ether, methoxyethyl vinyl ether, dimethylaminoethyl vinyl ether, etc.
  • Two or more of the monomers can be used as co-monomers for various purposes (for example, for improving solubil­ity).
  • monomers which have acid groups such as those indicated below can also be used as co-monomers for the adjustment of coloring properties and solubility provided that the copolymer remains insoluble in water.
  • hydrophilic monomer here, this signifies a monomer which forms a water soluble homopolymer
  • vinyl monomers indicated here or other vinyl monomers which can be used in the invention no particular limitation is imposed on the proportion of hydrophilic monomer in the copolymer, provided that the copolymer does not become water soluble, but normally such monomers are used in an amount not exceeding 40 mol%, preferably not exceeding 20 mol% and, most desirably, in an amount not exceeding 10 mol%.
  • the proportion in the copolymer of the co-monomer which has acid groups is normally not more than 20 mol%, and preferably not more than 10 mol%, from the point of view of the image storage properties as mentioned earlier, and the absence of copolymers of this type is most desirable.
  • the monomers in the polymers in this invention are preferably methacrylate based, acrylamide based or methacrylamide based monomers.
  • the acrylamide and methacrylamide based monomers are especially desirable.
  • Polyesters formed from polyhydric alcohols and polybasic acids and polyamides formed from diamines and dibasic acids, and from ⁇ -amino- ⁇ ′-carboxylic acids, are generally known as condensation polymers, and polymers such as the polyurethanes which are formed from diisocyanates and dihydric alcohols are known as polymers which have been formed by means of a polyaddition reaction.
  • Glycols which have an OH-R1-OH structure (where R1 is a hydrocarbon chain, especially an aliphatic hydrocarbon chain, which has from 2 to about 12 carbon atoms), and polyalkyleneglycols are effective as polyhydric alcohols, and acids which have an HOOC-R2- COOH structure (where R2 represents a single bond or a hydrocarbon chain which has from 1 to about 12 carbon atoms) are effective as polybasic acids.
  • polyhydric alcohols include ethyleneglycol, diethyleneglycol, triethyleneglycol, 1,2-propyleneglycol, 1,3-propylene glycol, trimethylol­propane, 1,4-butanediol, iso-butylenediol, 1,5-pentane­diol, neopentylglycol, 1,6-hexanediol, 1,7-heptanediol, 1,8-octanediol, 1,9-nonanediol, 1,10-decanediool, 1,11-­undecanediol, 1,12-dodecanediol, 1,13-tridecanediol, glycerine, diglycerine, triglycerine, 1-methylglycerine, erythritol, mannitol, sorbitol, etc.
  • polybasic acids include oxalic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, azelaic acid, sebacic acid, nonanedicarboxylic acid, decanedicarboxylic acid, undecanedicarboxylic acid, dodecanedicarboxylic acid, fumaric acid, maleic acid, itaconic acid, citraconic acid,phthalic acid, isophthalic acid, terephthalic acid, tetrachlorophthalic acid, metaconic acid, isopymelic acid, cyclopendadiene-maleic anhydride adduct, rosin­maleic anhydride adduct, etc.
  • diamines examples include hydrazine, methylenediamine, ethylenediamine, trimethylenediamine, tetramethylenediamine, hexamethylenediamine, dodeca­methylenediamine, 1,4-diaminocyolohexane, 1,4-diamino­methylcyclohexane, o-aminoaniline, p-aminoaniline, 1,4-­diaminomethylbenzene, (4-aminophenyl)ether, etc.
  • ⁇ -amino- ⁇ -carboxylic acids examples include glycine, ⁇ -alanine, 3-aminopropanoic acid, 4-amino­butanoic acid, 5-aminopentanoic acid, 11-aminododecanoic acid, 4-aminobenzoic acid, 4-(2-aminoethyl)benzoic acid, 4-(4-aminophenyl)butanoic acid, etc.
  • diisocyanates examples include ethylene­diisocyanate, hexamethylenediisocyanate, m-phenylenedi­isocyanate, p-phenylenediisocyanate, p-xylenediiso­cyanate, 1,5-naphthyldiisocyanate, etc.
  • polyesters and polyamides which can be obtained by ring opening polymerization can be used.
  • X in this equation represents an -O- group or an -NH- group, and m represents an integer of value 4 to 7.
  • the -CH2- groups may be branched.
  • Monomers of this type include ⁇ -propiolactone, ⁇ -caprolactone, dimethylpropiolactone, ⁇ -pyrrolidone, ⁇ -­piperidone, ⁇ -caprolactam and ⁇ -methyl- ⁇ -caprolactam, etc.
  • the molecular weight and degree of polymer­ization of the polymer of this invention have no great effect in practice on the effect of the invention, but problems arise with long time taken to dissolve in an auxiliary solvent as the molecular weight increases, and emulsification and dispersion become difficult because of the high solution viscosity, coarse particles are formed, and this can have an adverse effect on the color forming properties and it is also liable to give rise to problems such as failure of the coating properties. Reduction of the viscosity of the solution using large amounts of auxiliary solvent to overcome this problem gives rise to problems with a coating process.
  • the viscosity on dissolving 30 grams of the polymer in 100 cc of the auxiliary solvent which is being used is preferably not more than 5000 cps, and most desirably it is not more than 2000 cps.
  • the molecular weights of the polymers which can be used in the invention are preferably not more than 150,000, and most desirably they are not more than 100,000.
  • a water insoluble polymer is a polymer of which the solubility is not more than 3 grams, and preferably not more than 1 gram, in 100 grams of distilled water.
  • the proportion with respect to the auxiliary solvent of the polymer of this invention differs according to the type of polymer which is being used, and varies over a wide range depending on solubility in the auxiliary solvent, the degree of polymerization, the solubility of the coupler, etc.
  • the amount of auxiliary solvent used is that which is required to provide a solution on dissolving at least the coupler, the high boiling point coupler solvent and the polymer in the auxiliary solvent which has a sufficiently low viscosity for easy dispersion in water or in an aqueous hydrophilic colloid solution.
  • the viscosity of the solution increases as the degree of polymerization of the polymer increases and so the proportion with respect to the auxiliary solvent of the polymer is not dependent just on the type of polymer and it is difficult to formulate a general rule, but normally a proportion (by weight) of from about 1:1 to 1:50 is preferred.
  • the proportion (by weight) with respect to the coupler of the polymer of this invention is preferably from 1:20 to 20:1, and most desirably it is from 1:10 to 10:1.
  • Methyl methacrylate (50.0 grams), 0.5 gram of poly(sodium acrylate) and 200 ml of distilled water were introduced into a 500 ml three necked flask and the mixture was heated to 80°C with stirring under a blanket of nitrogen. Dimethyl azobisisobutyrate (500 mg) was added as a polymerization initiator and polymerization started.
  • the reaction mixture was cooled after polymerizing for a period of 2 hours and 48.7 grams of the polymer P-3 was obtained by recovering by filtration and washing with water the polymer which had been formed in the form of beads.
  • t-Butylacrylamide (50.0 grams) and 250 ml of toluene were introduced into a 500 ml three necked flask and heated to 80°C with stirring under a blanket of nitrogen.
  • the reaction mixture was cooled after polymerizing for a period of 3 hours and 47.9 grams of the polymer P-57 was obtained on recovering by filtration the solid which precipitated out on pouring the mixture into 1 liter of hexane, washing the solid with hexane, and drying the product by heating under reduced pressure.
  • magenta coupler which can be represented by the general formula (I) of this invention is used alone, and this is desirable from the point of view of color reproduction and from the point of view of the prevention of staining due to light but, where desired, mixtures with pyrazolone based magenta couplers which can be represented by the general formula (M-I) indicated below can also be used.
  • R12 represents an alkyl group, aryl group, acyl group or carbamoyl group.
  • Ar represents a phenyl group or a phenyl group which is substituted with at least one halogen atom, alkyl group, cyano group, alkoxy group, alkoxycarbonyl group or acyl­amino group.
  • Z c represents a hydrogen atom or a group which can be eliminated in a reaction with the oxidized form of a primary aromatic amine developing agent.
  • the alkyl group of R12 in general formula (M-I) is preferably an alkyl group which has from 1 to 42 carbon atoms, and these may be substituted with halogen atoms, alkoxy groups, aryl groups, alkoxycarbonyl groups, aryloxycarbonyl groups, acylamido groups, sulfonamido groups, sulfamoyl groups, carbamoyl groups, aryloxy groups, alkylthio groups, arylthio groups, sulfonyl groups, cyano groups, acyloxy groups, aryloxy groups, imido groups, etc.
  • the aryl groups of R12 are preferably aryl groups which have from 6 to 46 carbon atoms, and these may be substituted with the same substituent groups as the alkyl groups of R12.
  • the acyl groups of R12 are preferably aliphatic acyl groups which have from 2 to 32 carbon atoms, and aromatic acyl groups which have from 7 to 46 carbon atoms. These acyl groups may be substituted with the same substituent groups as the alkyl groups of R12.
  • the carbamoyl groups of R12 are preferably aliphatic carbamoyl groups which have from 2 to 32 carbon atoms or aromatic carbamoyl groups which have from 7 to 46 carbon atoms, and these may be substituted with the same groups as the alkyl groups of R12.
  • Z c represents a hydrogen atom or a coupling leaving group, and examples of such groups include halogen atoms, alkoxy groups, aryloxy groups, acyloxy groups, sulfonyloxy groups, amido groups, alkoxycarbonyl groups, aryloxycarbonyl groups, aliphatic or aromatic thio groups, imido groups, N-heterocyclic groups, aromatic azo groups, etc.
  • These leaving groups may contain photographically useful groups.
  • Dimers or larger oligomers may be formed via R12, Ar or Z c in the general formula (M-I)
  • Typical examples of pyrazolone based magenta couplers which can be represented by the general formula (M-I) are indicated below, but they are not limited to these examples.
  • magenta dye-forming coupler represented by the formula (I), water insoluble but organic solvent soluble polymer, and aliphatic ester solvent represented by the formula (II) or (III) may be incorporated in the same layer or in the different layers.
  • the magenta dye-forming coupler is preferably incorporated in a green sensitive layer, the polymer is preferably incorporated in a red sensitive layer and/or blue sensitive layer, and the solvent of the formula (II) or (III) is preferably incorporated in a red sensitive layer and/or blue sensitive layer, or light-­insensitive hydrophilic colloid layer.
  • the aliphatic ester solvent of formula (II) or (III) is effective in preventing stain when it is incorporated in the light-­insensitive hydrophilic colloid layer, especially using together with magenta dye-forming coupler of formula (I).
  • ester based solvents which can be represented by the general formulae (II) and (III) of this invention may be used as high boiling point coupler solvents, and they can be used in all the layers or they may be used in only one layer for providing the effect of this invention, and especially the anti-staining effect of the invention. Their effect is most pronounced when they are used, preferably, in the layers other than the green sensitive layer.
  • the amount of the solvent used varies over a wide range, depending on the type and amount of polymer and coupler, but a ratio by weight of high boiling point coupler solvent/coupler of from 0.05 to 20 is preferred, and a ratio of from 0.1 to 10 is most desirable, while the ratio of high boiling point solvent/polymer is preferably from 0.02 to 40, and most desirably from 0.05 to 20.
  • the ester based organic solvents of this invention can be used individually or as complex mixtures.
  • any high boiling point organic solvents such as phosphate ester based solvents, phthalate ester based solvents, monoester based solvents, ether based solvents, alcohol based solvents or phenol based solvents, can be used in the layers in which ester based solvents of this invention are not used.
  • ester based solvents of this invention can be used in admixture with these solvents.
  • Actual examples of the above mentioned high boiling point solvents other than the ester based solvents of this invention which can be used are indicated below, but these solvents are not limited to the examples.
  • the water insoluble, organic solvent soluble polymer of this invention is normally dissolved in an appropriate organic auxiliary solvent for use, but the proportion with respect to the auxiliary solvent differs according to the type of polymer which is being used, and it varies over a wide range according to the solubility in the auxiliary solvent and the degree of polymerization, or the solubility of the coupler, etc.
  • the amount of auxiliary solvent required to provide a sufficiently low viscosity such that the solution obtained by dissolving at least the coupler, the high boiling point coupler solvent and the polymer in the auxiliary solvent can be dispersed easily in water or in an aqueous hydrophilic colloid solution is used.
  • the proportion with respect to the coupler of. the polymer of this invention is preferably from 1:20 to 20:1, and most desirably from 1:10 to 10:1.
  • the polymers of this invention improve image stability, the effect of the invention, in whichever layer they are used, but the resulting effect is especially pronounced when they are used in the red sensitive layer, and they provide a marked improvement in the extent dark heat fading and light fading of the cyan image which, as described in the background of the invention, was a problem in the past.
  • the oil protected type naphthol based and phenol based couplers can be used as cyan couplers in this invention, and typical examples of naphthol based couplers include those disclosed in U.S. Patent 2,474,293, and the preferred two equivalent naphthol based couplers of the oxygen atom elimination type disclosed in U.S. Patents 4,052,212, 4,146,396, 4,228,233 and 4,296,200. Actual examples of phenol based couplers have been disclosed in U.S. Patents 2,369,929, 2,801,171, 2,772,162, 2,895,826, etc.
  • the use of the phenol based cyan couplers which have an alkyl group consisting of an ethyl or larger group in the meta position of the phenol ring disclosed in U.S. Patent 3,772,002, the 2,5-diacylamino substituted phenol based couplers disclosed in U.S. Patents 2,772,162, 3,758,308, 4,126,396, 4,334,011 and 4,327,173, in West German Patent Laid Open No. 3,329,729, and in Japanese Patent Application No. 42,671/83, etc., and the phenol based couplers which have a phenylureido group in the 2-position and an acylamino group in the 5-position disclosed in U.S. Patents 3,446,622, 4,333,999, 4,451,559 and 4,427,767, etc. is preferred in this invention.
  • cyan couplers for use in the invention are those which can be represented by the general formulae (C-I) and (C-II) which are indicated below.
  • R13 represents an alkyl group, aryl group, amino group or heterocyclic group.
  • R14 represents an acylamino group or an alkyl group.
  • R15 represents a hydrogen atom, halogen atom, alkyl group or an alkoxy group. Furthermore, R15 and R14 may be joined together to form a ring.
  • Z d represents a hydrogen atom or a group which can be eliminated in a reaction with the oxidized form of a primary aromatic amine color developing agent.
  • the alkyl groups represented by R13 in general formula (C-I) are preferably linear chain, branched chain or cyclo alkyl groups which have from 1 to 32 carbon atoms, and the aryl groups represented by R13 are preferably aryl groups which have from 6 to 42 Carbon atoms.
  • R13 represents an amino group it may be an alkyl amino or aryl amino group, but it is preferably a phenylamino group which may have substituent groups.
  • the alkyl groups, aryl groups and phenylamino groups represented by R13 may have substituent groups selected from among the alkyl groups, aryl groups, alkyloxy or aryloxy groups, carboxyl group, alkyl or aryl carbonyl groups, alkyl or aryl oxycarbonyl groups, acyloxy groups, sulfamoyl groups, carbamoyl groups, sulfonamido group, acylamino groups, imido groups, sulfonyl groups, hydroxyl group, cyano group and the halogen atoms.
  • the ring so formed is a five to seven membered ring, and oxyindole rings, 2-oxobenzoimidazoline rings or carbostyril rings etc. are preferred.
  • Z d represents a hydrogen atom or a coupling leaving group.
  • coupling leaving groups include halogen atoms, alkoxy groups, aryloxy groups, acyloxy groups, sulfonyloxy groups, amido groups, alkoxycarbonyloxy groups, aryloxycarbonyloxy groups, aliphatic, aromatic or heterocyclic thio groups, imido groups, N-heterocyclic groups, aromatic azo groups, etc.
  • These leaving groups may contain photographically useful groups.
  • Dimers or larger oligomers may be formed via R13, R14 or Z d in the general formula (C-I).
  • R16 represents an alkyl group, an aryl group or a heterocyclic group
  • R17 represents an acyl group, sulfonyl group, alkoxycarbonyl group, or an alkoxysulfonyl group
  • R18 represents a hydrogen atom, halogen atom, alkyl group, alkoxy group, aryloxy group, amido group, imido group, alkylthio group, arylthio group, ureido group, alkylsulfonyl group or an arylsulfonyl group
  • p represents 0 or 1.
  • Z e represents a hydrogen atom or a group which can be eliminated in a reaction with the oxidized form of a primary aromatic amine color developing agent.
  • the alkyl groups represented by R16 in general formula (C-II) are preferably linear chain, branched chain or cyclo alkyl groups which have from 1 to 32 carbon atoms
  • the aryl groups represented by R16 are preferably aryl groups which have from 6 to 42 carbon atoms
  • heterocyclic groups are four to seven membered rings which contain at least one oxygen atom, nitrogen atom or sulfur atom, and these may be substituted with the substituent groups described for the alkyl groups of R13 in general formula (C-I).
  • Z e represents a hydrogen atom or a coupling leaving group, and it represents the same leaving groups as Zd in general formula (C-I). Dimers or larger oligomers can be formed via R16, R17, R18 or Z e in general formula (C-­II).
  • the oil protected type acylacetamide based couplers are typical of the yellow couplers which can be used in the invention. Actual examples have been disclosed in U.S. Patents 2,407,210, 2, 875,057, 3,265,506, etc.
  • the use of two-equivalent yellow couplers is preferred in this invention, and typical examples include the yellow couplers of the oxygen atom elimination type disclosed in U.S. Patents 3,408,194, 3,447,928, 3,933,501, 4,022,620, etc. and the nitrogen atom elimination type yellow couplers disclosed in JP-B-­58-10739, in U.S. Patents 4,401,752 and 4,326,024, in Research Disclosure 18053 (April 1979), in British Patent No.
  • the ⁇ -pivaloylacetanilide based couplers are excellent in terms of the fastness, especially the light fastness, of the colored dye, while the ⁇ -benzoylacetanilide based couplers provide high color densities.
  • yellow couplers for use in the invention are those which can be represented by the general formulae (Y-I) and (Y-II) which are indicated below.
  • R19 represents a substituted or unsubstituted N-phenylcarbamoyl group
  • Z f represents a group which can be eliminated in a reaction with the oxidized form of a primary aromatic amine developing agent.
  • the substituent groups on the phenyl ring of the N-phenylcarbamoyl group represented by R19 in general formula (Y-I) are aliphatic groups, heterocyclic groups, aliphatic oxy groups, aromatic oxy groups, acyl groups, ester groups, amido groups, imido groups, ureido groups, aliphatic or aromatic sulfonyl groups, or aliphatic or aromatic thio groups, and when there are two or more groups they may be the same or different.
  • Z f in general formula (Y-I) represents a coupling leaving group, and examples include halogen atoms, alkoxy groups, aryloxy groups, acyloxy groups, sulfonyloxy groups, amido groups, alkoxycarbonyloxy groups, aryloxycarbonyloxy groups, aliphatic or aromatic thio groups, imido groups, N-heterocyclic groups, aromatic azo groups, etc., but the N-heterocyclic groups are preferred from the point of view of high activity.
  • These leaving groups may contain photographically useful groups.
  • Dimers or larger oligomers can be formed via R19 or Z f in general formula (Y-I).
  • R20 represents a substituted or unsubstituted N-phenylcarbamoyl group
  • Z g represents a group which can be eliminated in a reaction with the oxidized form of a primary aromatic amine color developing agent
  • R21 represents a hydrogen atom or a substituent group
  • s represents an integer of value from 1 to 5.
  • R20 and Z g in general formula (Y-II) have the same significance as R19 and Z f in general formula (Y-I), and the substituent groups represented by R21 are the same as those defined for the phenyl group of the N-­phenylcarbamoyl group of R19 in general formula (Y-I).
  • Dimers or larger oligomers can be formed via R20, Z g or R21 in general formula (Y-II).
  • Dispersions of fine lipophilic particles which contain coupler, high boiling point coupler solvent and polymer of this invention are typically prepared in the way indicated below.
  • the polymer of this invention which is a so­called linear polymer which is uncrosslinked and which has been prepared by solution polymerization, emulsion polymerization or suspension polymerization, etc., the high boiling point coupler solvent and the coupler are formed into a complete solution, together with an auxiliary solvent, after which the solution is dispersed, with the aid of a dispersing agent, with ultrasonic waves or in a colloid mill, in water, preferably in an aqueous solution of a hydrophilic colloid, and most desirably in an aqueous gelatin solution, to form fine particles, and this is included in the silver halide emulsion.
  • water or an aqueous hydrophilic colloid solution such as a gelatin solution may be added to an auxiliary organic solvent which contains a dispersion promotor such as a surfactant, the polymer of this invention, the high boiling point coupler solvent and the coupler, and an oil in water dispersion may be formed by phase reversal.
  • a dispersion promotor such as a surfactant
  • the polymer of this invention the high boiling point coupler solvent and the coupler
  • an oil in water dispersion may be formed by phase reversal.
  • the auxiliary organic solvent is then removed by volatalization, noodle washing or ultrafiltration, etc. from the dispersion which has been prepared in this way, after which the dispersion may be mixed with the photographic emulsion.
  • auxiliary organic solvent signifies an organic solvent which is useful at the time of emulsification and dispersion, being a low boiling point organic solvent which is ultimately eliminated from the photosensitive material in practice during the course of drying at the time of coating or in the ways indicated above, or a solvent which has a certain degree of solubility in water and which can be removed by washing with water.
  • the auxiliary solvent may be a lower alcohol acetate such as ethyl acetate or butyl acetate, ethyl propionate, sec-butyl alcohol, methyl ethyl ketone, methyl isobutyl ketone, ⁇ -ethoxyethyl acetate, methylcellosolve acetate, methylcarbitol acetate, methylcarbitol propionate, cyclohexanone, etc.
  • a lower alcohol acetate such as ethyl acetate or butyl acetate, ethyl propionate, sec-butyl alcohol, methyl ethyl ketone, methyl isobutyl ketone, ⁇ -ethoxyethyl acetate, methylcellosolve acetate, methylcarbitol acetate, methylcarbitol propionate, cyclohexanone, etc.
  • organic solvent which is completely miscible with water, for example, methyl alcohol, ethyl alcohol, acetone, tetrahydrofuran, etc., can be used conjointly, as desired.
  • anionic surfactants such as alkyl­benzene sulfonic acids and alkylnaphthalene sulfonic acids and/or non-ionic surfactants such as sorbitane sesquioleic acid esters and sorbitane monolauric acid esters etc. as the above mentioned surfactants is preferred.
  • the average particle size of the fine lipophilic particles obtained in this way is preferably within the range from 0.04 ⁇ to 2 ⁇ and, most desirably, the average particle size is within the range from 0.06 ⁇ to 0.4 ⁇ .
  • the particle diameter of the fine lipophilic particles can be measured with a measuring device such as the "Nanosizer" made by the British Coal Tar Co.
  • Silver bromide, silver iodobromide, silver iodochlorobromide, silver chlorobromide and silver chloride can all be used as the silver halide in this invention.
  • the use of silver chlorobromides of which the silver chloride content is at least 90 mol% (and preferably at least 98 mol%) is especially desirable in cases where rapid processing is intended.
  • the silver chlorobromide may contain a little silver iodide, but the absence of silver iodide is preferred.
  • the average grain size (the grain diameter in the case of spherical grains or grains which approach a spherical form or the length of an edge in the case of cubic grains is taken for the grain size, the average being expressed on the basis of the projected areas) of the silver halide grains in the photographic emulsion is of no particular importance, but it is preferably not more than 2 ⁇ m and, most desirably, it is within the range from 0.2 to 1.5 ⁇ m.
  • the silver halide grains in the photographic emulsion layer may have a regular crystalline form, such as a cubic, tetradecahedral or octahedral form, (being a regular crystalline emulsion), or they may have an irregular crystalline form, such as a spherical or plate like form, or they may have a composite form consisting of these crystalline forms. They may also take the form of mixtures of grains of various crystalline forms. Of these, the use of the aforementioned regular emulsions is preferred.
  • Emulsions in which tabular silver halide grains of which the diameter is at least 5 times the thickness account for at least 50 mol% of the total projected area can also be used.
  • the silver halide emulsion which is included in at least one photosensitive layer is preferably a mono-­disperse emulsion of which the coefficient of variation (the value obtained by dividing the statistical standard deviation by the average grain size expressed as a percentage) is not more than 15%, and most desirably not more than 10%.
  • Mono-disperse emulsions of this type may be independent emulsions which have a coefficient of variation as mentioned above, but they may be emulsions in which two or more mono-disperse emulsions which have been prepared separately and of which the average grain size in each case has a coefficient of variation of not more than 15%, and preferably not more than 10%, are mixed together.
  • the difference in grain size and the mixing ratio is not limited, but the use of emulsions of which the average grain size difference is within the range from at least 0.2 ⁇ m but not more than 1.0 ⁇ m is preferred.
  • the silver halide grains may have different phases for the internal part and the surface layer. Furthermore, they may be of the type with which the latent image is formed principally at the surface of the grains or of the type with which the latent image is formed principally within the grains. Grains of the latter type are especially useful for direct positive emulsions.
  • Cadmium salts, zinc salts, thallium salts, lead salts, iridium salts or complex salts thereof, rhodium salts or complex salts thereof, iron salts or complex salts thereof, etc. may also be present during the formation or physical ripening process of the silver halide grains.
  • Silver halide emulsions are normally subjected to chemical sensitization.
  • the usual methods of chemical sensitization can be used, and details have been disclosed from line 18 of the lower left hand column of page 12 to line 16 on the lower right hand column on page 12 of the specification of JP-A-62-­215272.
  • the silver halide emulsions are normally subjected to spectral sensitization.
  • the usual methine dyes can be used for the spectral sensitization, and details have been disclosed between line 3 from the bottom of the upper right hand column on page 22 and page 38 of the specification of JP-A-62-215272, and on separate page (B) of the Procedural Amendment dated 16th March 1987 attached thereto.
  • Various compounds can be included in the photographic emulsions which are used in the invention with a view to preventing the occurrence of fogging during the manufacture, storage or photographic process­ing of the photosensitive material, or with a view to stabilizing photographic performance.
  • anti-fogging agents or stabilizers such as azoles, for example, benzo­thiazolium salts, nitroimidazoles, nitrobenzimidazoles, chlorobenzimidazoles, bromobenzimidazoles, mercapto­thiazoles, mercaptobenzothiazoles, mercaptobenz­imidazoles, mercaptothiadiazoles, aminotriazoles, benzo­triazoles, nitrobenzotriazoles, mercaptotetrazoles (especially 1-phenyl-5-mercaptotetrazole, etc.), mercaptopyrimidines; mercaptotriazines, etc.; thioketo compounds such as, for example, o
  • the photosensitive materials of this invention may contain hydroquinone derivatives, aminophenol derivatives, amines, gallic acid derivatives, catechol derivatives, ascorbic acid derivatives, colorless couplers, sulfonamidophenol derivatives, etc. as anti-­color fogging agents or anti-color mixing agents.
  • anti-color fading agents can also be used in the photosensitive materials of this invention. That is to say, typical examples of organic anti-color fading agents which can be used for cyan, magenta and/or yellow images include hydroquinones, 6-hydroxychromans, 5-hydroxycoumarans, spirochromans, p-alkoxyphenols, hindered phenols centered on the bisphenols, gallic acid derivatives, methylenedioxybenzenes, aminophenols, and hindered amines, and ether and ester derivatives in which the phenolic hydroxyl groups of these compounds have been silylated or alkylated. Furthermore, metal complexes typified by the (bis salicylaldoxymato)nickel complex and the (bis-N,N-dialkyldithiocarbamato)nickel complex can be used for this purpose.
  • Patent 4,360,589 p-alkoxyphenols have been disclosed in U.S. Patent 2,735,765, in British Patent No. 2,066,975, in JP-A-59-10539, and in JP-B-57-19764, etc.
  • hindered phenols have been disclosed in U.S. Patent 3,700,455, in JP-A-52-72225, in U.S. Patent 4,225,235, and in JP-B-52-­6623, etc.
  • gallic acid derivatives, methylenedioxy­benzenes and aminophenols have been disclosed in U.S. Patents 3,457,079 and 4,332,556, and in JP-B-56-21144, respectively, hindered amines have been disclosed in U.S.
  • Patent 4,279,990, and in JP-B-53-3263, etc., and metal complexes have been disclosed in U.S. Patents 4,050,935 and 4,241,155, and in British Patent No. 2,027,731(A), etc. These compounds can be used to achieve the intended purpose by coemulsification with the couplers and addition to the photosensitive layer, normally at a rate of from 5 to 100 wt% with respect to the corresponding coupler.
  • the introduction of ultraviolet absorbers into layers on either side adjacent to the cyan color forming layer is more effective for preventing deterioration of the cyan dye image by heat and, more especially, by light.
  • the spiroindanes and the hindered amines are especially effective among the above mentioned anti-­color fading agents. Furthermore, the use of compounds of the type indicated below, together with the afore­mentioned couplers, and especially together with the pyrazoloazole couplers, is desirable in this invention.
  • a compound (A) which bonds chemically with aromatic amine based developing agents which are left behind after color development processing and which forms a compound which is chemically inert and which is essentially colorless, and/or a compound (B) which bonds chemically with the oxidized form of aromatic amine based color developing agents which are left behind after the color development process and which forms a compound which is chemically inert and which is essentially colorless is desirable for preventing the occurrence of staining and other side effects due to colored dye formation resulting from reaction between the coupler and the color developing agent or the oxidized form thereof which is left behind in the film during the storage of the material after processing for example.
  • the preferred compounds (A) are those which react with p-anisidine in such a way that the second order reaction rate constant k2 (in trioctyl phosphate at 80°C) is within the range from 1.0 to 1 ⁇ 10 ⁇ 5 l/mol sec.
  • the second order reaction rate constant k2 is obtained by a method disclosed in JP-A-63-158545.
  • R22 and R23 each represent an aliphatic group, an aromatic group or a heterocyclic group.
  • n represents a value of 1 or 0.
  • A represents a group forming a chemical bond by reacting with an aromatic amino developing agent;
  • X represents a group being released by reacting with an aromatic amino developing agent;
  • B represents a hydrogen atom, aliphatic group, aromatic group, heterocyclic group, acyl group or a sulfonyl group, and
  • Y represents a group accelerating the addition of an aromatic amino developing agent to the compound of formula (A II ).
  • Said R22 and X, or said Y and R23 or B may be conbined with each other to form a cyclic structure.
  • a typical system is a substitution reaction and an addition reaction.
  • the compound (B) forming a chemically inactive and colorless compound by causing chemical bonding with the oxidation product of an aromatic amino developing agent remaining after color development is more preferably shown by following formula (B I ); R - Z (B I ) wherein R represents an alipahtic group, an aromatic group or a heterocyclic group and Z represents a nucleophilic group or a group releasing a nucleophilic group by being decomposed in the photographic material.
  • Z is preferably a group having the Pearson's nucleophilic nCH3I value (R.G. Pearson, et al., Journal of Americal Chemical Society , 90 , 319 (1968)) of at least 5 or a group induced from such a group.
  • Ultraviolet absorbers can be included in the hydrophilic colloid layers of the photosensitive materials of this invention.
  • use can be made of the benzotriazole compounds substituted with aryl groups (for example, those disclosed in U.S. Patent 3,533,794), 4-thiazolidone compounds (for example, those disclosed in U.S. Patents 3,314,794 and 3,352,681), benzophenone compounds (for example, those disclosed in JP-A-46-2784), cinnamic acid ester compounds (for example, those disclosed in U.S. Patents 3,705,805 and 3,707,375), butadiene compounds (for example, those disclosed in U.S.
  • Patent 4,045,229) or benzo-oxidol compounds (for example, those disclosed in U.S. Patent 3,700,455).
  • Ultraviolet absorbing couplers for example, the ⁇ -naphthol based cyan dye forming couplers
  • ultraviolet absorbing polymers, etc. can also be used for this purpose. These ultraviolet absorbers may be mordanted into a specified layer.
  • Water soluble dyes can be included in the hydrophilic colloid layers of the photosensitive materials of this invention as filter dyes or for anti-­irradiation and various other purposes.
  • Dyes of this type include oxonol dyes, hemi-oxonol dyes, styryl dyes, merocyanine dyes, cyanine dyes and azo dyes. Of these dyes, the oxonol dyes, hemi-oxonol dyes and merocyanine dyes are useful. Details of useful oxonol dyes have been described from the upper right column on page 158 to page 163 of the specification of JP-A-62-215272.
  • gelatin is convenient as the binding agent or protective colloid in the emulsion layers of photosensitive materials of this invention, but other hydrophilic colloids can be used either independently or in conjunction with gelatin.
  • the gelatin used in the invention may be a lime treated gelatin, or a gelatin which has been treated with acid can be used. Details of the manufacture of gelatin have been described by Arthur Wiese in "The Macromolecular Chemistry of Gelatin” (published by Academic Press, 1964).
  • the cellulose nitrate films, cellulose acetate films, cellulose acetate butyrate films, cellulose acetate propionate films, polystyrene films, polyethylene-terephthalate films, polycarbonate films, laminates of these films with other materials, thin glass films, paper, etc. normally used in photographic materials can be used for the support which is used in this invention.
  • Supports such as papers which have been coated or laminated with baryta or an ⁇ -olefin polymer, especially a polymer made from an ⁇ -olefin which has from 2 to 10 carbon atoms, for example, polyethylene, polypropylene, ethylene/butene copolymer etc., vinyl chloride resins which contain reflecting substances such as TiO2, and plastic films of which the adhesion with other polymeric materials has been improved by surface roughening as described in JP-B-47-19068 provide good results. Furthermore, ultraviolet curable resins can be used for this purpose.
  • a transparent support or a non-transparent support can be selected according to the intended purpose of the photosensitive material. Furthermore, the supports can be rendered colored and transparent by the addition of dyes or pigments.
  • non-transparent supports also include those made by adding dyes or organic pigments, such as titanium oxide, to a transparent film, and plastic films which have been surface treated using methods such as those described in JP-B-47-19068, etc.
  • An underlayer is normally established on the support.
  • Preliminary surface treatments such as corona discharge treatments, ultraviolet irradiation and flame treatments, etc. can also be used with these supports in order to improve their adhesion properties.
  • the color photosensitive materials which can be used for making color photographs of this invention may be any of the usual types of color photographic materials, for example, color negative films, color papers, reversal color papers, color reversal films etc, and they are especially suitable for color photo­sensitive materials intended for printing purposes.
  • a color development bath preferably consists of an aqueous alkaline solution which contains a primary aromatic amine based color developing agents, as the principal component. Aminophenol based compounds are also useful as color developing agents, but the use of p-phenylenediamine based compounds is preferred.
  • Typical examples of these compounds 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 the sulfate, hydro chloride and p-toluenesulfonate salts of these compounds. Two or more of these compounds can be used conjointly, depending on the intended purpose.
  • the color development baths generally contain pH buffers such as alkali metal carbonates, borates or phosphates, and development inhibitors or anti-fogging agents such as bromides, iodides, benzimidazoles, benzo­thiazoles or mercapto compounds.
  • pH buffers such as alkali metal carbonates, borates or phosphates
  • development inhibitors or anti-fogging agents such as bromides, iodides, benzimidazoles, benzo­thiazoles or mercapto compounds.
  • They may also contain, as required, various preservatives such as hydroxyl­amine, diethylhydroxylamine, sulfites, hydrazines, phenylsemicarbazides, triethanolamine, catechol sulfonic acids, triethylenediamine(1,4-diazabicyclo[2,2,2]­octane), etc., organic solvents such as ethyleneglycol and diethyleneglycol, development accelerators such as benzyl alcohol, poly(ethyleneglycol), quaternary ammonium salts and amines, dye forming couplers, competitive couplers, fogging agents such as sodium borohydride, auxiliary developing agents such as 1-­phenyl-3-pyrazolidone, viscosity imparting agents, and various chelating agents as typified by the aminopolycarboxylic acids, aminopolyphosphonic acids, alkylphosphonic acids and phosphonocarboxylic acids, typical examples of which include ethylenediamine tetra­acetic
  • Color development is carried out after a normal black and white development in the case of reversal processing.
  • the known black and white developing agents for example, dihydroxybenzenes such as hydroquinone, etc., 3-pyrazolidones such as 1-phenyl-3-­pyrazolidone, etc., and aminophenols such as N-methyl-p-­aminophenol, etc., can be used individually or in combinations for the black and white development bath.
  • the pH of these color development and black and white development baths is generally within the range from 9 to 12. Furthermore, the replenishment rate of these development baths depends on the color photographic material which is being processed, but it is generally not more than 3 liters per square meter of photosensitive material and it is possible, by reducing the bromide ion concentration in the replenisher, to use a replenishment rate of not more than 500 ml per square meter of photosensitive material. Prevention of the loss of liquid by evaporation, and aerial oxidation, by minimizing the contact area with the air in the processing tank is desirable in cases where the replenishment rate is low. Furthermore, the replenis­hment rate can be reduced by using a means of suppressing the accumulation of bromide ion in the developer.
  • the photographic emulsion layers are subjected to a normal bleaching process after color development.
  • the bleaching process may be carried out at the same time as the fixing process (in a bleach-fix process) or it may be carried out as a separate process.
  • a bleach-fix process can be carried out after a bleaching process in order to speed-up processing.
  • processing can be carried out in two connected bleach-fix baths, a fixing process can be carried out before carrying out a bleach-fix process, or a bleaching process can be carried out after a bleach-fix process, according to the intended purpose of the processing.
  • bleaching agents include ferricyanides; dichromates; organic complex salts of iron(III) or cobalt(III), for example, complex salts with amino­polycarboxylic acids such as ethylenediamine tetra-­acetic acid, diethylenetriamine penta-acetic acid, cyclohexanediamine tetra-acetic acid, methylimino diacetic acid, 1,3-diaminopropane tetra-acetic acid, glycol ether diamine tetra-acetic acid, etc., or citric acid, tartaric acid, malic acid, etc.; persulfates; bromates; permanaganates; and nitrobenzenes, etc.
  • amino­polycarboxylic acids such as ethylenediamine tetra-­acetic acid, diethylenetriamine penta-acetic acid, cyclohexanediamine tetra-acetic acid, methylimino diacetic acid, 1,3-di
  • aminopolycarboxylic acid iron(III) complex salts principally ethylenediamine tetra-acetic acid iron(III) complex salts, and per­sulfates, is preferred from the points of view of both rapid processing and the prevention of environmental pollution.
  • the amino polycarboxylic acid iron(III) complex salts are especially useful in both bleach baths and bleach-fix baths.
  • the pH of a bleach or bleach-fix bath in which aminopolycarboxylic acid iron(III) complex salts are being used is normally from 5.5 to 8, but processing can be carried. out at lower pH values in order to speed-up processing.
  • Bleach accelerators can be used, as required, in the bleach baths, bleach-fix baths, or bleach or bleach-­fix pre-baths. Actual examples of useful bleach accelerators have been disclosed in the following specifications: Thus there are the compounds which have a mercapto group or a disulfide group disclosed in U.S. Patent 3,893,858, West German Patent Nos.
  • 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 and JP-A-53-­28426, and in Research Disclosure No.
  • Thiosulfates, thiocyanates, thioether based compounds, thioureas and large quantities of iodides, etc. can be used as fixing agents, but thiosulfates are generally used for this purpose, and ammonium thiosulfate in particular can be used in the widest range of applications. Sulfites or bisulfites, or carbonyl-bisulfite addition compounds, are preferred as preservatives for bleach-fix baths.
  • the silver halide color photographic materials of this invention are generally subjected to a water washing and/or stabilizing process after the desilvering process.
  • the quantity of water used in the water washing process can be established within a wide range according to the nature of the photosensitive material (for example, the materials, such as the couplers, which are being used), the wash water temperature, the number of washing tanks (the number of washing stages), the replenishment system, i.e. whether a counter-flow or a sequential-flow system is used, and various other conditions.
  • the relationship between the quantity of water used and the number of water washing tanks in a multi-stage counter-flow system can be obtained using the method outlined on pages 248-253 of Journal of the Society of Motion Picture and Television Engineers, Volume 64 (May 1955).
  • the amount of wash water can be greatly reduced by using the multi-stage counter-flow system noted in the aforementioned literature, but bacteria proliferate due to the increased residence time of the water in the tanks and problems arise as a result of the sediments which are formed becoming attached to the photosensitive material.
  • the method in which the calcium ion and manganese ion concentrations are reduced as disclosed in Japanese Patent Application No. 61-131632 can be used very effectively to overcome problems of this sort in the processing of color photosensitive materials of this invention.
  • the pH value of the wash water used when processing photosensitive materials of invention is within the range from 4 to 9, and preferably within the range from 5 to 8.
  • the wash water temperature and the washing time can be set variously according to the nature of the photosensitive material and the application, etc. but, in general, washing conditions of from 20 seconds to 10 minutes at a temperature of from 15 to 45°C, and preferably of from 30 seconds to 5 minutes at a temperature of from 25 to 40°C, are selected.
  • the photosensitive materials of this invention can be processed directly in a stabilizing bath instead of being subjected to a water washing process as described above.
  • the known methods disclosed in JP-A-57-8543, JP-A-58-14834 and JP-A-60-­220345 can all be used for this purpose.
  • stabilizing baths which contain formalin and surfactant which are used as a final bath for camera color photosensitive materials are an example of such a process.
  • Various chelating agents, biocides, etc. can be added to these stabilizing baths.
  • the overflow which accompanies replenishment of the abovementioned wash water and/or stabilizer can be re-used in other processes such as the desilvering process, etc.
  • a color developing agent may also be incorporated into the silver halide color photosensitive materials of this invention in order to simplify and speed-up processing.
  • the incorporation of various color developing agent precursors is preferred.
  • the indoaniline based compounds disclosed in U.S. Patent 3,342,597, the Schiff's base type compounds disclosed in U.S. Patent 3,342,599 and in Research Disclosure Nos. 14,850 and 15,159 the aldol compounds disclosed in Research Disclosure No. 13,924, the metal salt complexes disclosed in U.S. Patent 3,719,492, and the urethane based compounds disclosed in JP-A-53-135628 can be used for this purpose.
  • the various processing baths are used at a temperature of from 10 to 50°C in this invention.
  • the standard temperature is normally from 33 to 38°C, but processing is accelerated and the processing time is shortened at higher temperatures and, conversely, increased picture quality and improved stability of the processing baths can be achieved at lower temperature.
  • processes using hydrogen peroxide intensification or cobalt intensification as disclosed in West German Patent No. 2,226,770 or U.S. Patent 3,674,499 can be carried out in order to economize on silver in the photosensitive material.
  • the multi-layer silver halide photosensitive material 101 of which the layer structure is indicated below was prepared on a paper support which had been laminated on both sides with polyethylene. Moreover, ethyl acetate was used as an auxiliary solvent together with the high boiling point solvent in the coupler solvents mentioned below.
  • composition of each layer is indicated below.
  • the numerical values indicate coated weights (in grams per square meter). In the case of the silver halide emulsions the weight coated is indicated after calculation as silver.
  • Polyethylene laminated paper White pigment (TiO2) and ultramarine dye were included in the polyethylene on the first layer side.
  • Mono-disperse silver chlorobromide emulsion (EM5) which had been spectrally sensitized with the sensitizing dye (ExS-4, 5) 0.07 Mono-disperse silver chlorobromide emulsion (EM6) which had been spectrally sensitized with the sensitizing dye (ExS-4, 5) 0.16 Gelatin 0.92 Cyan coupler (C-4) 0.17 Cyan coupler (C-5) 0.15 Colored image stabilizer (Cpd-1) 0.03 Colored image stabilizer (Cpd-5) 0.01 Colored image stabilizer (Cpd-6) 0.01 Ultraviolet absorber (Cpd-7/Cpd-9/Cpd-10 3/4/2 by weight) 0.17 Solvent (S-16) 0.20
  • Cpd-11 and Cpd-12 were used at this time as anti-irradiation compounds.
  • "Alcanol XC” (made by DuPont), sodium alkylbenzenesulfonate, succinic acid ester and "Magafao F-120” (made by Dainippon Ink) were used as emulsification and dispersion, and coating, promotors in each layer.
  • Cpd-­13 and Cpd-14 were used as silver halide stabilizers.
  • 1-oxy-3,5-dichloro-s-triazine, sodium salt was used as a gelatin hardening agent in each layer, and Cpd-2 was used as a viscosity increasing agent.
  • Samples 102 to 113 were prepared in the same way as the above mentioned sample 101 except that the magenta coupler and the high boiling point solvent in each layer in the above mentioned photosensitive material Sample 101 were changed, and polymers of this invention were added, as indicated in Table 1 below.
  • each processing bath was as indicated below. Color Development Bath Tank Soln.
  • Replenisher Water 800 ml 800 ml Diethylenetriamine pentaacetic acid 1.0 l 1.0 g Nitrilotriacetic acid 2.0 l 2.0 g 1-Hydroxyethylidene-1,1-diphosphonic acid 2.0 l 2.0 g Benzyl alcohol 16 ml 22 ml Diethyleneglycol 10 ml 10 ml Sodium sulfite 2.0 g 2.5 g Potassium bromide 0.5 g Potassium carbonate 30 g 30 g n-Ethyl-N-( ⁇ -methanesulfonamidoethyl)-3-methyl-4-aminoaniline sulfate 5.5 g 7.5 g Hydroxylamine sulfate 2.0 g 2.5 g Fluorescent whitener (Whitex4B, made by Sumitomo Chemicals) 1.5 g 2.0 g Water to make up to 1000 ml 1000 m
  • Ion exchanged water (Calcium and magnesium both not more than 3 ppm)
  • the fractional reduction in density from an initial density of 1.5 on storing the samples for 7 days in the dark at 100°C was used to represent heat fading and the fractional reduction in density from an initial value of 1.5 on storing for 7 days in a xenon fadometer (80,000 lux) was used to represent light fading.
  • M-staining was evaluated in terms of the difference in magenta density of the white background (unexposed part) immediately after processing and after storing the samples for 7 days at 100°C. (Table 2)
  • the invention provided overall excellent results in respect of the storage properties of the image form both the point of view of the colored image fastness and from the point of view of staining. More precisely, the colored image fastness showed an excellent fading balance between the three colors yellow, magenta and cyan, a point which is great practical importance, and with little increase in staining.
  • Photosensitive materials 201 to 213 were prepared in the same way as in Example 1 except that the silver halide emulsions used in Example 1 were changed as indicated below.
  • EM-1 and EM-2 were changed to EM-7
  • EM-3 and EM-4 were changed to EM 8
  • EM-5 and EM-6 were changed to EM-9.
  • composition of each processing bath was as indicated below.
  • Formalin (37%) 0.1 g Formalin/sulfurous acid adduct 0.7 g 5-Chloro-2-methyl-4-isothiazolin-3-one 0.02 g 2-Methyl-4-isothiazolin-3-one 0.01 g Copper sulfate 0.005 g Water to make up to 1000 ml pH (25°C) 4.0
  • the coating emulsions for each layer were prepared as is disclosed in a case of, for example, material 102.
  • the coating emulsion for red sensitive layer was prepared by dissolving the cyan couplers (C-4) and (C-5), and (II-5) and (P-57) together with ethylacetate, dispersing the solution to aqueous gelatin solution to form a dispersion, and then adding the emulsion thus obtained to a mixture of emulsion EM5 and EM6 to form a coating emulsion for red sensitive layer.
  • the coating emulsion for blue sensitive layer was prepared by dissolving the yellow coupler (Y-2), and (II-8) and (P-57) together with ethylacetate and processing in the same way as in the coating emulsion of red sensitive layer.
  • the coating emulsion for green sensitive layer was prepared by dissolving the magenta coupler (I-1) into the solvents thereof (S-16) and (S-8) and processing in the same way as in the coating emulsion of red sensitive layer.

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  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
EP19890100484 1988-01-12 1989-01-12 Matériaux photosensibles couleur à l'halogénure d'argent Expired - Lifetime EP0324476B1 (fr)

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JP63003171A JP2896437B2 (ja) 1988-01-12 1988-01-12 ハロゲン化銀カラー感光材料

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Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0638844A1 (fr) * 1993-08-10 1995-02-15 Fuji Photo Film Co., Ltd. Matériau photographique couleur à l'halogénure d'argent sensible à la lumière
US5436124A (en) * 1993-04-02 1995-07-25 Eastman Kodak Company Photographic elements containing particular color couplers in combination with polymeric stabilizers
EP0672948A3 (fr) * 1994-03-14 1995-11-02 Agfa Gevaert Ag
US5582960A (en) * 1995-02-17 1996-12-10 Eastman Kodak Company Photographic print material
US5594047A (en) * 1995-02-17 1997-01-14 Eastman Kodak Company Method for forming photographic dispersions comprising loaded latex polymers
BE1009540A5 (fr) * 1995-02-07 1997-05-06 Agfa Gevaert Ag Materiau pour photographie en couleurs.

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JP2665614B2 (ja) * 1989-10-30 1997-10-22 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

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JPS5312378B2 (fr) * 1973-07-03 1978-04-28
JPS5139853A (ja) * 1974-09-28 1976-04-03 Aikoku Kogyo Kk Aamusojugatakureen
JPS52102722A (en) * 1976-02-24 1977-08-29 Fuji Photo Film Co Ltd Photosensitive material for color photography
JPS53137131A (en) * 1977-05-06 1978-11-30 Mitsubishi Paper Mills Ltd Photo drain filling plug polymeratex dispersion
JPS58149038A (ja) * 1982-03-01 1983-09-05 Konishiroku Photo Ind Co Ltd 写真用添加剤の分散方法
JPS60140344A (ja) * 1983-12-28 1985-07-25 Konishiroku Photo Ind Co Ltd 疎水性写真用添加剤の分散方法及びハロゲン化銀写真感光材料
JPS6147957A (ja) * 1984-08-14 1986-03-08 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS6292946A (ja) * 1985-10-19 1987-04-28 Fuji Photo Film Co Ltd ハロゲン化銀カラ−写真感光材料
JPS62178952A (ja) * 1986-02-03 1987-08-06 Konishiroku Photo Ind Co Ltd ハロゲン化銀写真感光材料
JPS62194252A (ja) * 1986-02-20 1987-08-26 Fuji Photo Film Co Ltd カラ−画像形成方法
WO1988000723A1 (fr) * 1986-07-10 1988-01-28 Fuji Photo Film Company Limited Materiau photographique en couleurs a halogenure d'argent
JP2542852B2 (ja) * 1987-02-23 1996-10-09 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

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5436124A (en) * 1993-04-02 1995-07-25 Eastman Kodak Company Photographic elements containing particular color couplers in combination with polymeric stabilizers
EP0638844A1 (fr) * 1993-08-10 1995-02-15 Fuji Photo Film Co., Ltd. Matériau photographique couleur à l'halogénure d'argent sensible à la lumière
EP0672948A3 (fr) * 1994-03-14 1995-11-02 Agfa Gevaert Ag
BE1009540A5 (fr) * 1995-02-07 1997-05-06 Agfa Gevaert Ag Materiau pour photographie en couleurs.
US5582960A (en) * 1995-02-17 1996-12-10 Eastman Kodak Company Photographic print material
US5594047A (en) * 1995-02-17 1997-01-14 Eastman Kodak Company Method for forming photographic dispersions comprising loaded latex polymers

Also Published As

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DE68923097D1 (de) 1995-07-27
JP2896437B2 (ja) 1999-05-31
EP0324476A3 (en) 1990-06-13
DE68923097T2 (de) 1995-10-26
EP0324476B1 (fr) 1995-06-21
JPH01179945A (ja) 1989-07-18

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