EP0430186A1 - Matériaux photographiques à l'halogénure d'argent sensibles à la lumière - Google Patents

Matériaux photographiques à l'halogénure d'argent sensibles à la lumière Download PDF

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Publication number
EP0430186A1
EP0430186A1 EP90122679A EP90122679A EP0430186A1 EP 0430186 A1 EP0430186 A1 EP 0430186A1 EP 90122679 A EP90122679 A EP 90122679A EP 90122679 A EP90122679 A EP 90122679A EP 0430186 A1 EP0430186 A1 EP 0430186A1
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Prior art keywords
group
dye
silver halide
layer
photographic
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EP90122679A
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German (de)
English (en)
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EP0430186B1 (fr
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Keiichi C/O Fuji Photo Film Co. Ltd. Adachi
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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
    • G03C1/00—Photosensitive materials
    • G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/825—Photosensitive materials characterised by the base or auxiliary layers characterised by antireflection means or visible-light filtering means, e.g. antihalation
    • G03C1/83—Organic dyestuffs therefor
    • G03C1/832—Methine or polymethine dyes

Definitions

  • This invention relates to silver halide photographic light-sensitive materials which have a colored hydrophilic colloid layer. More particularly, this invention relates to silver halide photographic light-sensitive materials which have a hydrophilic colloid layer which contains a dye which is inactive in terms of photographic chemistry and which is readily decolorized and/or washed out in photographic processing operations.
  • the coloring of photographic emulsion layers or other layers is often carried out in silver halide photographic light-sensitive materials in order to absorb light of a specified wavelength.
  • a colored layer is positioned on the side of a photographic emulsion layer that is farthest from the support in the photographic light-sensitive material.
  • a colored layer is known as a filter layer.
  • filter layers may also be located between these layers.
  • Colored layers can also be established between the photographic emulsion layer and the support or on the opposite side of the support from that of the photographic emulsion layer, in order to prevent image blurring which is caused by scattered light produced when passing through a photographic emulsion layer or transmitted reflected by the interface between the emulsion layer and the support or reflected at the surface of the light-sensitive material on the opposite side of the emulsion layer and redirected into the photographic emulsion layer, the above scattered light prevention thereby preventing halation.
  • Colored layers of this type are known as anti-halation layers.
  • Anti-halation layers can also be established between the various layers in the case of a multi-layer color light-sensitive material.
  • colored layers are also provided in X-ray light-sensitive materials as cross-over cut filters for reducing the amount of cross-over light in order to increase the level of sharpness.
  • the coloration of photographic emulsion layers is also carried out in order to prevent any reduction in image sharpness due to light scattering within the photographic emulsion layer (this phenomenon is known generally as irradiation).
  • These layers which are to be colored in many cases comprise a hydrophilic colloid layer and so dyes are normally included in the layers in order to achieve the desired coloration.
  • the dyes used must at least satisfy the following conditions:
  • Patent 2,865,752 arylidene dyes disclosed, for example, in U.S. Patents 2,538,009, 2,688,541 and 2,538,008, British Patents 584,609, 1,210,252, JP-A-50-40625, JP-A-51-3623, JP-A-51-10927, JP-A-54-118247, JP-B-48-3286 and JP-B-59-37303; styryl dyes disclosed, for example, in JP-B-28-3082, JP-B-44-16594 and JP-B-59-28898; triarylmethane dyes disclosed, for example, in British Patents 446,583 and 1,335,422, and JP-A-59-228250; merocyanine dyes disclosed, for example, in British Patents 1,075,653, 1,153,341, 1,284,730, 1,475,228 and 1,542,807; and cyanine dyes disclosed, for example, in U.S. Patent
  • oxonol dyes having two pyrazolone nuclei have the property of being decolorized in developers which contain sulfite, they have little adverse action on photographic emulsions and they have therefore been used as useful dyes for light-sensitive materials.
  • the colored layer is a filter layer or an anti-halation layer located on the same side of the support as the photographic emulsion layer, it is generally required that the layers be selectively colored and spreading of the coloration to other layers prevented. Failure to meet these requirements results in reduced efficiency of the colored layer as a filter layer or anti-halation layer and adverse spectral actions on the other photographic emulsion layers.
  • a hydrophilic polymer containing a portion oppositely charged to that of the dye ion, is included in a hydrophilic layer as a mordant.
  • Such polymers are included in specified emulsion layers having the dye localized by the interaction between the polymer and the dye molecule (due to an attraction by the charge and hydrophobic bonding).
  • dyes as disperse solids
  • JP-A-56-12639 JP-A-52-92716, JP-A-55-155350, JP-A-55-155351, JP-A-52-92716, JP-A-63-27838, JP-A-63-l97943, European Patents 0015601B1, 0276566A1, 274723, 276566 and 299435, and Published Unexamined International Application No. 1-502912.
  • one object of the present invention is to provide silver halide photographic light-sensitive materials having a hydrophilic colloid layer that is colored with a dye which is decolorized irreversibly by photographic processing and which has no adverse effect on the photographic and developing characteristics of the photographic emulsion.
  • Another object of the present invention is to provide silver halide photographic light-sensitive materials which have a hydrophilic colloid layer in which only the prescribed hydrophilic colloid layer is selectively dyed and which has excellent decolorizing properties upon photographic processing.
  • Still another object of the present invention is to provide silver halide photographic light-sensitive materials having a dyed hydrophilic colloid layer which has no adverse effect on the photographic character istics of the silver halide emulsion layer even when the dyed hydrophilic colloid layer is aged.
  • a silver halide photographic light-sensitive material comprising at least one dye represented by formula (I): wherein A represents an acidic nucleus; L1, L2 and L3 represent substituted or unsubstituted methine groups; z represents non-metal atoms which form a five membered heterocyclic ring; n represents 0 or 1; the dye comprises at least one group selected from a carboxyl group, a sulfonamido groups and a sulfamoyl group.
  • A represents an acidic nucleus
  • L1, L2 and L3 represent substituted or unsubstituted methine groups
  • z represents non-metal atoms which form a five membered heterocyclic ring
  • n represents 0 or 1
  • the dye comprises at least one group selected from a carboxyl group, a sulfonamido groups and a sulfamoyl group.
  • the above-mentioned objects are also met by a silver halide photographic light-sensitive material, wherein the material comprises at least one dye of formula (I) present in the form of a fine powder dispersion.
  • the above-mentioned objects of the present invention are further met by a silver halide photographic light-sensitive material wherein the acidic nucleus A of formula (I) is selected from the group consisting of a 5-pyrazolone, isooxazolone, barbituric acid, thiobarbituric acid, rhodanine, hydantoin, thiohydantoin, oxazolidindione, pyrazolidindione, indandione, pyrazolopyridone, l,2,3,4-tetrahydroquinolin-2,4-dione, 3-oxo-2,3-dihydrobenzo[d]thiophene-1,1-dioxide, or 3-dicyanomethine-2,3-dihydroxybenzo[d]--thiophene-1,1-dioxide nucleus.
  • the acidic nucleus A of formula (I) is selected from the group consisting of a 5-pyrazolone, is
  • the above objects of the present invention are met by a silver halide photographic light-sensitive material wherein the dye according to formula (I) has formula (II): wherein R1 represents an alkyl, aryl, alkoxycarbonyl, aryloxycarbonyl, alkoxy, aryloxy, acyl, hydroxy, acylamino, cyano, ureido or amino group; L1 L2 and L3 represent substituted or unsubstituted methine groups; R2 represents an aryl or aryloxy group; R3 and R4 represent alkyl, aryl or alkoxycarbonyl groups or hydrogen atoms; Z1 represents non-metal atoms which form a five membered heterocyclic ring; the heterocyclic ring optionally comprising a condensed benzene ring; n represents 0 or 1; and the dye has at least one group selected from the group consisting of a carboxyl group, a sulfonamido
  • Still another embodiment meets the above objects of the present invention as a silver halide photographic light-sensitive material, comprising at least one fine powder dispersion of a dye represented by formula (II) and a fine powder dispersion of a dye represented by formula (III); wherein R1, R2, L1, L2 and L3 each are the same as R1, R2, L1, L2 and L3 in formula (II) above; two R1's or two R2 ⁇ s may be the same or different from each other; m represents 0, 1 or 2; and the dye comprises at least one group selected from the group consisting of a carboxyl group, a sulfonamido group and a sulfamoyl group.
  • a in formula (I) represents an acidic nucleus.
  • preferred acidic nuclei include 5-pyrazolone, isooxazolone, barbituric acid, thiobarbituric acid, rhodanine, hydantoin, thiohydantoin, oxazolidindione, pyrazolidindione, indandione, pyrazolopyridone, 1,2,3,4-tetrahydroquinolin-2,4-dione, 3-oxo-2,3-dihydrobenzo[d] thiophene-1,1-dioxide and 3-dicyanomethine-2,3-dihydrobenzo[d]thiophene-1,1-dioxide, and the acidic nucleus is preferably selected from the group consisting of 5-pyrazolone, isooxazolone, barbituric acid, oxazolidindione, pyrazolidindione, indandione and pyrazolopyridone
  • the acidic nucleus may have a substituent.
  • Heterocyclic rings formed by Z are selected from the group consisting of pyrrole, indole, pyrazole, pyrazolopyrimidone and benzindole rings.
  • n represents 0 or 1.
  • R1 preferably represents, for example, a substituted or unsubstituted alkyl group which has from 1 to 4 carbon atoms (for example, methyl, ethyl, butyl, t-butyl, 2-chloroethyl, methoxyethyl, 2-hydroxyethyl, trifluoromethyl), a substituted or unsubstituted aryl group which has from 6 to 10 carbon atoms (for example, phenyl, tolyl, methoxyphenyl, chlorophenyl, naphthyl, carboxyphenyl), a substituted or unsubstituted alkoxy group which has from 1 to 4 carbon atoms (for example, methoxy, ethoxy, butoxy, methoxyethoxy), a substituted or unsubstituted alkoxycarbonyl group which has from 2 to 5 carbon atoms (for example, methoxycarbonyl, ethoxycarbonyl, 2-meth
  • R2 preferably represents, for example, a substituted or unsubstituted aryl group which has from 6 to 12 carbon atoms (for example, phenyl, p-carboxyphenyl, 3,5-dicarboxyphenyl, o-carboxyphenyl, chlorophenyl, methoxyphenyl, methylphenyl), or a substituted or unsubstituted aralkyl group which has from 7 to 12 carbon atoms (for example, benzyl, 2-carboxybenzyl), and R3 and R4 preferably represent, for example, hydrogen atoms, substituted or unsubstituted alkyl groups which have from 1 to 10 carbon atoms (for example, methyl, ethyl, propyl, cyanoethyl, methoxyethyl, benzyl, carboxybenzyl), or substituted or unsubstituted aryl groups which have from 6 to 12 carbon atoms (for example, phenyl
  • the heterocyclic ring formed by Z1 is preferably, an indole, pyrrole or pyrazole ring, for example.
  • n represents 0 or 1.
  • the molecule contains at least one group selected from among carboxyl, sulfamoyl and sulfonamido groups. Furthermore, these groups are preferably bonded to an aryl group within the molecule. The carboxyl group is the most preferred of these groups.
  • Formula (III) is described as follows.
  • R1 and R2 have the same significance as R1 and R2 respectively in formula (II), and m represents 0, 1 or 2.
  • the compounds of formulae (I) and (II) as used in the present invention can be prepared using the methods disclosed, for example, in JP-A-63-l97943, JP-A-54-118247, JP-A-59-154439 and JP-A-56-12639 the contents of which are herein incorpoarated by reference. Examples of synthesis are indicated below.
  • dyes of formula (I) are used in a range of from about 1 to 1000 mg, and preferably in a range of from about 1 to 800 mg in all layers, per square meter surface area of light-sensitive material.
  • dyes represented by formula (I) are used as filter dyes or anti-halation dyes according to the present invention they can be used in any amount which is effective, but they are preferably used in an amount such that the optical density is within the range from about 0.05 to 3.5, and preferably from 0.1 to 3.0.
  • the dyes can be added at any stage prior to coating.
  • Dyes used in accordance with the present invention can be used in any emulsion layer or other hydrophilic colloid layer.
  • the dyes are preferably used in a light-insensitive layer.
  • Methods of dispersing dyes of the present invention as a fine powder dispersion include the dissolution of the dye in a weakly alkaline solution and addition to a hydrophilic colloid layer to form a fine crystalline dispersion by adjusting the pH to a weak acidic conditions.
  • fine powder disper sion of dyes are accomplished by known milling methods, for example ball milling, sand milling or colloid milling, used in the presence of a dispersing agent.
  • the dye may be dissolved in a suitable solvent, for example, an alcohol or a halogenated alcohol (e.g., as disclosed in JP-A-48-9715), acetone, water or pyridine, or in a mixture of these solvents, and a fine particle powder can be precipitated by adding a poor solvent to the solution.
  • a suitable solvent for example, an alcohol or a halogenated alcohol (e.g., as disclosed in JP-A-48-9715), acetone, water or pyridine, or in a mixture of these solvents, and a fine particle powder can be precipitated by adding a poor solvent to the solution.
  • Dye particles in the dispersion as used in the present invention have an average particle size of up to about 10 ⁇ m, preferably up to about 2 ⁇ m, and most desirably up to about 0.5 ⁇ m and, depending on the particular use, fine particles up to about 0.1 ⁇ m are especially desirable.
  • dispersing dyes into a hydrophilic colloid layer include dissolving dyes in an essentially water insoluble, high boiling point (above about 160°C) ester solvent and the dispersing the dye-solvent in a hydrophilic colloid solvent.
  • high boiling point solvents examples include phthalic acid alkyl esters (for example, dibutyl phthalate, dioctyl phthalate), phosphate esters (for example, diphenyl phosphate, triphenyl phosphate, tricresyl phosphate, dioctyl butyl phosphate), citric acid esters (for example, tributyl acetylcitrate), benzoic acid esters (for example, octyl benzoate), alkylamides (for example, diethyllaurylamide), fatty acid esters (for example, dibutoxyethyl succinate, diethyl azelate), trimesic acid esters (for example, tributyl trimesitate).
  • phthalic acid alkyl esters for example, dibutyl phthalate, dioctyl phthalate
  • phosphate esters for example, diphenyl phosphate, triphenyl phosphate, tric
  • organic solvents of boiling point from about 30°C to 150°C for example lower alkyl acetates such as ethyl acetate and butyl acetate, ethyl propionate, sec-butyl alcohol, methyl isobutyl ketone, ⁇ -ethoxyethyl acetate, methycellosolve acetate, and solvents which are readily dissolved in water, for example alcohols such as methanol and ethanol, can be used in the present invention.
  • lower alkyl acetates such as ethyl acetate and butyl acetate, ethyl propionate, sec-butyl alcohol, methyl isobutyl ketone, ⁇ -ethoxyethyl acetate, methycellosolve acetate
  • solvents which are readily dissolved in water for example alcohols such as methanol and ethanol, can be used in the present invention.
  • the ratio (by weight) in which the dye and the high boiling point solvent are used is preferably from about 10 to 1/10.
  • polyurethane polymers examples include, for example, polyurethane polymers and polymers obtained by polymerization from vinyl monomers
  • suitable vinyl monomers include acrylic acid esters (for example, methyl acrylate, ethyl acrylate, butyl acrylate, hexyl acrylate, octyl acrylate, dodecyl acrylate, glycidyl acrylate), ⁇ -substituted acrylic acid esters (for example, methyl methacrylate, butyl methacrylate, octyl methacrylate, glycidyl methacrylate), acrylamides (for example, butylacrylamide, hexylacrylamide), ⁇ -substituted acrylamides (for example, butyl methacrylamide, dibutylmethacrylamide), vinyl esters (for example, vinyl acetate, vinyl butyrate), vinyl halides (for example, vinyl chloride), vinylidene halides (
  • These filled polymer latexes can be prepared using the methods disclosed in JP-B-51-39853, JP-A-51-59943, JP-A--53-137131, JP-A-54-32552, JP-A-54-107941, JP-A-55-133465, JP-A-56-19043, JP-A-56-19047, JP-A-56-126830 and JP-A-58-149038, the contents of which are herein incorporated by reference.
  • the ratio of the amounts (by weight) of the dye (or additive) and polymer latex used is preferably from about 10 to 1/10.
  • methods in which the dye compounds are incorporated into hydrophilic colloid layers include dissolving the dye using a surfactant, according to another aspect of the present invention.
  • a surfactant may be oligomers or polymers. Details of these polymers have been disclosed in JP-A-60-158437, the contents of which are herein incorporated by reference.
  • hydrophilic polymers instead of the high boiling point solvent in the second method above, or in conjunction with these high boiling point solvents, can be used in the present invention to incorporated dyes into hydrophilic colloid layers. Disclosures have been made in connection with these methods in, for example, U.S. Patent 3,619,195 and West German Patent 1,957,467, the contents of which are herein incorporated by reference.
  • Microencapsulation methods can also be used to incorporate dyes into hydrophilic colloid layers with polymers which have carboxyl groups or sulfo groups, for example, in a side chain, as disclosed in JP-A-59-113434.
  • the lipophilic polymer hydrosols disclosed, for example, in JP-B-51-39835 may be added to the hydrophilic colloid dispersions obtained in the way described above.
  • Gelatin is a typical and preferred hydrophilic colloid, but any other known hydophilic colloids which can be used in photographic applications known can alternatively be used.
  • the first method and the second method are preferred
  • Silver halide emulsions which are used in silver halide photographic light-sensitive materials of the present invention and light-sensitive materials of the present invention are described in detail below.
  • Silver halide emulsions used in the present invention are preferably silver bromide, silver iodobromide, silver iodochlorobromide, silver chlorobromide or silver chloride emulsions.
  • Silver halide grains which are used in the present invention may have a regular crystalline form (such as a cubic or octahedral form); an irregular crystalline form (such as a spherical or tabular form); or a composite form comprised of combination of the above-mentioned crystalline forms.
  • emulsions comprised of mixtures of grains of various crystalline forms can also be used, but the use of grains which have a regular crystalline form is preferred.
  • Silver halide grains which are used in the present invention may be such that the interior part and the surface layer form different phases, each containing the grains, or the grains may consist of a uniform phase.
  • the grains may be of the type with which the latent image is formed principally on the surface (for example, negative type emulsions) or of the type with which the latent image is formed principally within the grains (for example, internal latent image type emulsions, pre-fogged direct reversal type emulsions). Grains of the type with which the latent image is formed principally on the surface are preferred.
  • Silver halide emulsions used in the present invention preferably comprise tabular grains emulsions in which grains of thickness of up to about 0.5 microns, and preferably up to about 0.3 microns, and of diameter preferably at least about 0.6 microns, and which have an average aspect ratio of at least about 5, account for at least about 50% of the total projected area.
  • tabular grain emulsions mono-disperse emulsions can be used, wherein the statistical variation coefficient (the value S/ d obtained by dividing the standard deviation S by the diameter d for a distribution represented by the diameters in cases where the projected areas are approximately circular) is up to about 20%.
  • two or more types of tabular grain emulsion and mono-disperse emulsion may be used in combination.
  • Photographic emulsions used in the present invention can be prepared using the methods described, for example, by P. Glafkides in Chimie et Physique Photographique, published by Paul Montel, 1967, by G.F. Duffin in Photographic Emulsion Chemistry, published by Focal Press, 1966, and by V.L. Zelikman et al. in Making and Coating Photographic Emulsions, published by Focal Press, 1964.
  • ammonia, potassium thiocyanate, ammonium thiocyanate, thioether compounds for example, those disclosed, for example, in U.S. Patents 3,271,157, 3,574,628, 3,704,130, 4,297,439 and 4,279,374), thione compounds (for example, those disclosed, for example, in JP-A-53-144319, JP-A-53-82408 and JP-A-55-77737), and amine compounds (for example, those disclosed in JP-A-54-100717) can be used as silver halide solvents for controlling grain growth during silver halide grain formation.
  • Cadmium salts, zinc salts, thallium salts, iridium salts or complex salts thereof, rhodium salts or complex salts thereof, or iron salts or complex salts thereof, for example, may be present during the formation or physical ripening processes of the silver halide grains used in the present invention.
  • Gelatin is useful as a binding agent or protective colloid which can be used in emulsion layers or intermediate layers of the light-sensitive materials of the present invention, but other hydophilic colloids can be used for this purpose.
  • gelatin hydrolyzates can also be used.
  • Light-sensitive materials of the present invention may contain inorganic or organic hardening agents in any of the hydrophilic colloid layers which form photographic light-sensitive layers or backing layers.
  • Chromium salts, aldehydes (for example, formaldehyde, glyoxal, glutaraldehyde) and N-methylol compounds (for example, dimethylolurea) are examples of such compounds.
  • active halogen compounds for example, 2,4-dichloro-6-hydroxy-1,3,5-triazine and its sodium salt
  • active vinyl compounds for example, 1,3-bis-vinylsulfonyl-2-propanol, 1,2-bis-(vinylsulfonylacetamido)ethane, bis(vinylsulfonylmethyl) ether or vinyl based polymers which have vinyl groups in side chains
  • active halogen compounds for example, 2,4-dichloro-6-hydroxy-1,3,5-triazine and its sodium salt
  • active vinyl compounds for example, 1,3-bis-vinylsulfonyl-2-propanol, 1,2-bis-(vinylsulfonylacetamido)ethane, bis(vinylsulfonylmethyl) ether or vinyl based polymers which have vinyl groups in side chains
  • N-Carbamoyl-pyridinium salts for example, (1-morpholinocarbonyl-3-pyridino)methanesulfonate
  • haloamidinium salts for example, 1-(1-chloro-1-pyridinomethylene)pyrrolidinium-2-naphthalenesulfonate
  • Silver halide photographic emulsions used in the present invention may be spectrally sensitized using methine dyes or by other known means.
  • Dyes which can thus be used include cyanine dyes, merocyanine dyes, complex cyanine dyes, complex merocyanine dyes, holopolar cyanine dyes, hemi-cyanine dyes, styryl dyes and hemi-oxonol dyes. Dyes classified as cyanine dyes, merocyanine dyes and complex merocyanine dye are preferred.
  • the nucleus may be a pyrroline nucleus, an oxazoline nucleus, a thiazoline nucleus, a pyrrole nucleus, an oxazole nucleus, a thiazole nucleus, a selenazole nucleus, an imidazole nucleus, a tetrazole nucleus or a pyridine nucleus; a nucleus in which one of these nuclei is fused with an alicyclic hydrocarbyl ring, or nucleus in which one of these nuclei is fused with an aromatic hydrocarbyl ring, for example, an indolenine nucleus, a benzindolenine nucleus, an indole nucleus, a benzoxazole nucleus, a
  • a nucleus which has a ketomethylene structure in merocyanine dyes or complex merocyanine dyes, may be a five or six membered heterocyclic nucleus, for example, a pyrazolin-5-one nucleus, a thiohydantoin nucleus, a 2-thio-oxazolidin-2,4-dione nucleus, a thiazolidin-2,4-dione nucleus, a rhodanine nucleus or a thiobarbituric acid nucleus.
  • sensitizing dyes may be used individually or in combination, and combinations of such sensitizing dyes may be used to achieve supersensitization.
  • Substances which provide for supersensitization being dyes with substantially no spectrally sensitizing action or substances which do not substantially absorb visible light, can be included in emulsions together with sensitizing dyes.
  • substituted aminostilbene compounds with a nitrogen containing heterocyclic group for example, those disclosed in U.S. Patents 2,933,390 and 3,635,721
  • aromatic organic acid/formaldehyde condensates for example, those disclosed in U.S. Patent 3,743,510
  • cadmium salts and azaindene compounds for example.
  • Such combinations disclosed in U.S. Patents 3,615,613, 3,615,641, 3,617,295 and 3,635,721 are especially useful.
  • Various compounds can be included in silver halide photographic emulsions of the present invention in order, e.g., to prevent fogging during manufacture, storage or photographic processing of the light-sensitive material, or stabilize photographic performance.
  • many compounds which are known as anti-fogging agents or stabilizers can be added to emulsions of the present invention, for example, azoles (for example, benzothiazolium salts, nitroimidazoles, nitrobenzimidazoles, chlorobenzimidazoles, bromobenzimidazoles, mercaptothiazoles, mercaptobenzothiazoles, mercaptobenzimidazoles, mercaptothiadiazoles, aminotriazoles, benzotriazoles, nitrobenzotriazoles), mercaptotetrazoles (especially 1-phenyl-5-mercaptotetrazole); mercaptopyrimidines; mercaptotriazines; thioketo compounds such as oxazolinethione
  • One or more types of surfactants may be included in light-sensitive materials of the present invention for various purposes, for example, as coating aids, anti-static agents, for improving slip properties, for emulsification and dispersion purposes, for preventing adhesion or for improving photographic characteristics (for example, for accelerating development, increasing contrast or increasing sensitivity).
  • Light-sensitive materials of the present invention may contain water soluble dyes (in hydrophilic colloid layers) as filter dyes, for the prevention of irradiation or halation, or for various other purposes.
  • Oxonol dyes, hemi-oxonol dyes, styryl dyes, merocyanine dyes, anthraquinone dyes, and azo dyes are preferably used as dyes of this type, but cyanine dyes, azomethine dyes, triarylmethane dyes and phthalocyanine dyes are also useful.
  • Oil soluble dyes can be emulsified using oil in water dispersion methods and added to hydrophilic colloid layers.
  • Multi-layer natural color photographic materials generally have, on a support, at least one red sensitive emulsion layer, at least one green sensitive emulsion layer and at least one blue sensitive emulsion layer.
  • the order of these layers can be changed arbitrarily, as required.
  • Preferred layer arrangements are (beginning with the layer closest to the support) red-sensitive layer, green-sensitive layer, blue-sensitive layer; blue-sensitive layer, green-sensitive layer, red-sensitive layer or, from the support side, blue-sensitive layer, red-sensitive layer, green-sensitive layer.
  • any emulsion layers of the same color sensitivity may be comprised of two or more emulsion layers which have different photographic sensitivity to improve the sensitivity achieved, and graininess of the developed film can be reduced by using triple layer structures.
  • light-insensitive layers may be present between two or more emulsion layers which have the same color sensitivity. Structures in which an emulsion layer having a different color sensitivity is introduced between certain emulsion layers which have the same color sensitivity can also be used.
  • the establishment of a reflecting layer, such as a fine grained silver halide layer, below the highest sensitivity layer, and especially below the highest sensitivity blue-sensitive layer, may be used to increase photographic sensitivity.
  • Cyan forming couplers can be generally included in red-sensitive emulsion layers, magenta forming couplers can be generally included in green-sensitive emulsion layers, and yellow forming couplers can be generally included in blue-sensitive emulsion layers, but different combinations can be used, depending on the desired results. For example, with the incorporation of an infrared-sensitive layer, the materials can be used for making false color photographs or for use with semiconductor laser exposures.
  • Photographic emulsion layers and other layers in the photographic materials of the present invention can be coated onto a flexible support (such as, a plastic film, paper or cloth) or onto a rigid support (such as glass, porcelain or metal) of types generally used for photographic light-sensitive materials.
  • a flexible support such as, a plastic film, paper or cloth
  • a rigid support such as glass, porcelain or metal
  • Useful flexible supports include, for example, films made of semi-synthetic or synthetic polymers (for example, cellulose nitrate, cellulose acetate, cellulose acetate butyrate, polystyrene, poly(vinyl chloride), poly(ethylene tere phthalate) or polycarbonate) and papers which have been coated or laminated with a baryta layer or an ⁇ -olefin polymer (for example, polyethylene, polypropylene, ethylene/butene copolymer).
  • the support may be colored using dyes or pigments.
  • the support may also be colored black for light shielding purposes.
  • the surface of the support can be generally undercoated in order, e.g., to improve adhesion with the photographic emulsion layer.
  • the surface of the support may be subjected, e.g., to glow discharge treatment, corona discharge treatment, ultraviolet irradiation or a flame treatment, before or after undercoating treatment.
  • Coating of photographic emulsion layers and other hydrophilic colloid layers used in the present invention can be achieved using a variety of known coating methods, for example using dip coating, roller coating, curtain coating, or extrusion coating methods.
  • Multi-layers can be coated simultaneously using methods disclosed, for example, in U.S. Patents 2,681,294, 2,761,791, 3,526,528 and 3,508,947, as required.
  • the present invention can be applied to various color, and black-and-white light-sensitive materials. Typical applications include color negative films (for general and cinematographic purposes), color reversal films (for slides and television purposes), color pages, color positive films and color reversal papers, color diffusion transfer type light-sensitive materials, and heat-developable type color light-sensitive materials.
  • the present invention can also be applied to black-and-white light-sensitive materials, intended for X-ray purposes, in which the mixtures of three color couplers are used (e.g., as disclosed, for example, in Research Disclosure, No. 17123 [published July 1978]) or in which black colored couplers are used (e.g., as disclosed, for example, in U.S. Patent 4,126,461 and British Patent 2,102,136).
  • the present invention can also be applied to printing plate making films (such as lith films and scanner films); X-ray films (intended for use, e.g., in direct or indirect medical or industrial applications), camera black-and-white negative films, black-and-white printing papers, microfilms for COM or general purposes, and print-out type light-sensitive materials.
  • Various exposure means can be used with light-sensitive materials of the present invention.
  • Any light source which emits radiation with a band width corresponding to sensitive wavelengths of light-sensitive materials can be used as an exposing light source or write-in light source.
  • natural light unsunlight
  • incandescent electric lamps sealed halogen lamps
  • mercury lamps mercury lamps
  • fluorescent lamps or flash lamps such as strobes and burning metal flash lamps
  • gas, dye solution or semiconductor lasers which emit light in wavelength regions from the ultraviolet region through to the infrared region
  • light emitting diodes, and plasma light sources can also be used as light sources for recording purposes.
  • exposing devices such as fluorescent screens which release light from phosphors which have been excited by an electron beam (e.g., a CRT) or one in which a line type or surface type light source is combined with a micro-shutter array (such as a liquid crystal display (LCD) or a lead titanium zirconate doped with lanthanum (PLZT) device), can also be used.
  • Spectral distributions of light which is used to make exposures can be adjusted, as required, using color filters.
  • Color developers used for development processing of light-sensitive materials of the present invention are preferably aqueous alkaline solutions preferably having pH of 10 to 12 which contain primary aromatic amine-based color developing agents as the principal component.
  • Aminophenol based compounds are also useful, but the use of p-phenylenediamine based compounds as color developing agents is preferred.
  • Typical examples of these compounds include 3-methyl-4-amino-N,N-diethyl-aniline, 3-methyl-4-amino-N-ethyl-N-ß-hydroxyethyl-aniline, 3-methyl-4-amino-N-ethyl-N-ß-methanesulfonamidoethylaniline, 3-methyl-4-amino-N-ethyl-N-ß-methoxyethylaniline, and the sulfate, hydrochloride and p-toluenesulfonate salts, for example, of these compounds.
  • These diamines are generally more stable in the form of salts than in their free state, and the use of the salts is preferred.
  • pH buffers such as alkali metal carbonates, borates or phosphates, and development inhibitors or anti-foggants (such as bromide, iodide, benzimidazoles, benzothiazoles or mercapto compounds) can be generally included in color developers used with the present invention.
  • Preservatives such as hydroxylamine or sulfite
  • organic solvents such as triethanolamine and diethylene glycol
  • development accelerators such as benzyl alcohol, polyethylene glycol
  • quaternary ammonium salts and amines dye forming couplers, competitive couplers
  • nucleating agents such as sodium borohydride
  • auxiliary developing agents such as 1-phenyl-3-pyrazolidone
  • viscosity imparting agents such as aminopolycarboxylic acids, aminopolyphosphonic acids, alkylphosphonic acids and phosphonocarboxylic acids
  • antioxidants e.g., as disclosed in West German Patent Application (OLS) 2,622,950
  • OLS West German Patent Application
  • Color development of photographic materials of the present invention is carried out after normal black-and-white development in the development processing of reversal color light-sensitive materials.
  • black-and-white developing agents for example, dihydroxybenzenes [such as hydroquinone], 3-pyrazolidones [such as 1-phenyl-3-pyrazolidone], or aminophenols [such as N-methyl-p-aminophenol]
  • dihydroxybenzenes such as hydroquinone
  • 3-pyrazolidones such as 1-phenyl-3-pyrazolidone
  • aminophenols such as N-methyl-p-aminophenol
  • Color developed photographic emulsion layers are normally subjected to bleaching processes.
  • Bleaching processes can be carried out at the same time as fixing processes, or may be carried out separately.
  • a method of processing in which bleach-fixing is carried out after a bleaching process can be used in order to speed up processing.
  • Compounds of multi-valent metals such as iron(III), cobalt(III), chromium(IV) and copper(II)
  • peracids such as iron(III), cobalt(III), chromium(IV) and copper(II)
  • 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, nitrilotriacetic acid, and 1,3-diamino-2-propanol tetra-acetic acid] or organic acids [such as citric acid, tartaric acid or malic acid]); persulfates; manganates; and nitrosophenol can be used as bleaching agents.
  • aminopolycarboxylic acids such as ethylenediamine tetra-acetic acid, diethylenetriamine penta-acetic acid, nitrilotriacetic acid, and 1,3-diamino-2-propanol tetra-acetic acid
  • organic acids such as citric acid, tartaric acid or malic acid
  • persulfates manganates
  • manganates
  • ethylenediamine tetra-acetic acid iron(III) salts diethylenetriamine penta-acetic acid iron(III) salts and persulfate
  • ethylenediamine tetra-acetic acid iron(III) complex salts are especially useful in both independent bleach baths and single bath bleach-fix baths.
  • the pH of bleach bath is preferably from 2 to 8.
  • Bleaching accelerators can be used, as required, in bleach baths, bleach-fix baths and bleach or bleach-fix pre-baths used for developing materials of the present invention.
  • useful bleach accelerators have been disclosed in the following specifications; compounds which have a mercapto group or a disulfide group (as disclosed, for example, 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-53-37148, JP-A-53-65732, JP-A-53-72623, JP-A-53-95630, JP-A-53-95631, JP-A-53-10432, JP-A-53-124424, JP-A-53-141623, JP-A-53-28426, and Research Disclosure, No.
  • iodide e.g., as disclosed in West German Patent 1,127,715 and JP-A-58-16235
  • polyethylene oxides e.g., as disclosed in West German Patents 966,410 and 2,748,430
  • polyamine compounds e.g., as disclosed in JP-B-45
  • bleach accelerating compounds disclosed, e.g., in U.S. Patent 3,893,858, West German Patent 1,290,812 and JP-A-53-95630 are especially preferred, as are accelerating compounds disclosed in U.S. Patent 4,552,834.
  • bleach accelerators may also be included in light-sensitive materials, and are especially effective when bleach-fixing color light-sensitive materials used in cameras.
  • Thiosulfate, thiocyanate, thioether based compounds, thioureas and large amounts of iodide can be used, for example, as fixing agents, but thiosulfates are preferred.
  • the pH of fixer bath is preferably from 4 to 8. Sulfites, bisulfites, or carbonyl/bisulfite addition compounds are preferred as examples of preservatives for bleach-fix baths and fixer baths.
  • a water washing process and a stabilization process are generally carried out after the bleach-fixing process or fixing process.
  • Various known compounds can be added to the solutions used in water washing and stabilizing processes to prevent sedimentation and also to economize water usage.
  • hard water softening agents such as inorganic phosphoric acid, aminopolycarboxylic acids, organic aminopolyphosphonic acid and organic phosphoric acids
  • disinfectants and biocides for preventing the growth of various bacteria, algae and fungi
  • metal salts as typified by magnesium salts, aluminum salts and bismuth salts
  • Surfactants and various hardening agent can also be added, as required, to reduce the drying load and to prevent unevenness.
  • compounds disclosed, e.g., by L.E. West in Phot. Sci Eng. , Vol. 6, pages 344 to 359 (1965) may be added.
  • the addition of chelating agents and biocides is especially preferred.
  • Counter-current washing with two or more tanks can be generally employed in water washing processes to economize on water.
  • a multi-stage counter-current stabilization process (such as that disclosed, e.g., in JP-A-57-8543) can be used in place of water washing processes.
  • a counter-current system which has from two to nine tanks is required.
  • Various compounds for image stabilization may be added to the stabilizing bath, in addition to the aforementioned additives.
  • various buffers can be used to control pH (e.g., from about 3 to 9), for example, combinations of borates, metaborates, borax, phosphates, carbonates, potassium hydroxide, sodium hydroxide, aqueous ammonia, monocarboxylic acids, dicarboxylic acids, and polycarboxylic acids, and aldehydes (such as formalin).
  • additives can be used, as required, such as chelating agents (for example, inorganic phosphoric acid, aminopolycarboxylic acids, organophosphonic acids, organophosphonic acids, aminopolyphosphonic acids and phosphonocarboxylic acids), disinfectants (for example, benzoisothiazolinone, isothiazolone, 4-thiazolinbenz-imidazole, halogenated phenols, sulfanilamide and benzotriazole), surfactants, brightening agents and hardening agents.
  • chelating agents for example, inorganic phosphoric acid, aminopolycarboxylic acids, organophosphonic acids, organophosphonic acids, aminopolyphosphonic acids and phosphonocarboxylic acids
  • disinfectants for example, benzoisothiazolinone, isothiazolone, 4-thiazolinbenz-imidazole, halogenated phenols, sulfanilamide and benzotriazole
  • surfactants for example, benzois
  • ammonium salts such as ammonium chloride, ammonium nitrate, ammonium sulfate, ammonium phosphate, ammonium sulfite and ammonium thiosulfate, are preferably added as post-processing adjusting agents for film pH.
  • post fixing (water washing - stabilization) processes which can be generally used with camera color light-sensitive materials, can also be replaced with the aforementioned stabilization processes and water washing processes (processing reduced water usage).
  • water washing processes processing reduced water usage.
  • formalin should be removed from the stabilizing bath.
  • Water washing and stabilization processing times used in the present invention differ according to the type of light-sensitive materials and processing conditions, but the time is preferably in the range of about 20 seconds to about 10 minutes, and more preferably in the range from about 20 seconds to about 5 minutes.
  • Color developing agents can be incorporated into a silver halide color light-sensitive material of the present invention to simplify and speed up processing.
  • the incorporation of various color developing agent precursors is preferred.
  • indoaniline based compounds as disclosed, e .g., in U.S. Patent 3,342,597
  • Schiff's base type compounds e.g., as disclosed in U.S. Patent 3,342,599 and Research Disclosure, No. 14850, and ibid, No. 15159
  • aldol compounds e.g., as disclosed in Research Disclosure, No. 13924
  • metal complex salts e.g., as disclosed in U.S.
  • various salt type precursors e.g., as disclosed in JP-A-56-6235, JP-A-56-16133, JP-A-56-59232, JP-A-56-67842, JP-A-56-8
  • Various 1-phenyl-3-pyrazolidones can be incorporated, as required, into silver halide color light-sensitive materials of the present invention to accelerate color development.
  • Typical examples of such compounds have been disclosed, for example, in JP-A-56-64339, JP-A-57-144547, JP-A-57-211147, JP-A-58-50532, JP-A-58-50536, JP-A-58-50533, JP-A-58-50534, JP-A-58-50535 and JP-A-58-115438.
  • Various processing baths used in the present invention can be preferably maintained at a temperature of from about 10°C to 50°C.
  • the temperature can be generally from about 33°C to 38°C, but accelerated processing and shorter processing times can be realized at higher temperatures while increased picture quality and improved processing bath stability can be achieved at lower temperatures.
  • processes using cobalt intensification or hydrogen peroxide intensification e.g., as disclosed in West German Patent 2,226,770 or U.S. Patent 3,674,499), can be used in order to economize on the amount of silver used in light-sensitive materials of the present invention.
  • Heaters, temperature sensors, liquid level sensors, circulating pumps, filters, floating lids and squeegees and other desired processing equipment may be provided, as required, in each of the various processing baths used for developing photographic materials of the present invention.
  • replenishers can be used for various processing baths when continuous processing is being carried out, and a constant level of development can be obtained by preventing fluctuation in bath composition in this way. Replenishment can be made at half, or less than half, the standard replenishment rate in order to reduce costs.
  • Bleach-fix processes can be used when light-sensitive material of the present invention is a color paper, and such bleach-fix processes can be used as required in the case of camera color photographic materials.
  • Dyes in a dye layer of silver halide photographic light-sensitive materials of the present invention have the appropriate spectral absorbances, dye the dye layer specifically, and do not diffuse into other layers of the photographic material, resulting in superior quality developed photographic material.
  • Silver halide photographic light-sensitive materials of the present invention which contain compounds that are decolorized or washed out easily by photographic processing provide the effect that a low D min is obtained without loss of photographic sensitivity, and decrease in photographic sensitivity on storage is minimized.
  • the silver halide photographic light-sensitive materials of the present invention provide images which have increased sharpness. Furthermore, photographs obtained from silver halide photographic light-sensitive materials of the present invention are resistant to staining and exhibit no loss of photographic performance, due to retention of stability even during long term storage.
  • UV Ultraviolet absorber
  • solv High boiling point organic solvent
  • ExF Dye
  • ExS Sensitizing dye
  • ExC Cyan coupler
  • ExM Magenta coupler
  • ExY Yellow coupler
  • Cpd Additive.
  • An aqueous solution of silver nitrate and an aqueous solution of sodium chloride which contained 0.5x10 ⁇ 4 mol/mol ⁇ Ag of ammonium hexachlororhodium(III) were mixed using a controlled double jet method in a gelatin solution at 35°C with a control in such a way that the pH was 6.5 and a monodisperse silver chloride emulsion of average grain size 0.07 ⁇ m was obtained.
  • nucleating agents and nucleation accelerators were added to the aforementioned emulsion A, and then 300 mg/m2 of poly(ethyl acrylate) latex and 2,4-dichloro-6-hydroxy-1,3,5-triazine sodium salt (as a hardening agent) were added and a silver halide emulsion layer was coated on a transparent poly(ethylene terephthalate) support in such a way as to provide a coated silver weight of 3.5 grams per square meter.
  • a protective layer which contained 1.3 g/m2 of gelatin, 0.1 g/m2 of Compound 8 of the present invention, three surfactants indicated below as coating promotors) and the stabilizer and matting agent indicated below were coated over the aforementioned layer and dried.
  • Liquid I was added gradually while stirring liquid II at 40°C.
  • Example 1 The four samples (Sample 1 and Comparative Samples 1-A, 1-B and 1-C) were exposed through a flat halftone screen using the printer mentioned above and then were developed and processed as described in (1) above.
  • Comparative Samples 1-B and 1-C exhibited good tone variability.
  • Liquid 1, Liquid 2 and water were mixed in the proportions of 100 parts to 5 parts to 100 parts, respectively.
  • the sample of the present invention was good in terms of decolorizing properties, tone variability and reduction properties.
  • Example 2 As in Example 1, the results for Example 2 indicated good decolorizing properties, good tone variability and good reducing properties, as compared to Comparative Samples 1-A, 1-B and 1-C.
  • a fine crystal dispersion prepared in the same way as described in the aforementioned examples was coated as a dye layer, with the emulsion and the surface protective layer, all as indicated below, on both sides of an undercoated poly(ethylene terephthalate) film which had been dyed blue of thickness 175 ⁇ m to provide photographic material Control Sample 3-1, Comparative Samples 3-2 and 3-3 and, Samples 3-4 to 3-6 as shown in Table 2, below.
  • Potassium bromide (5 grams), 0.05 gram of potassium iodide, 30 grams of gelatin and 2.5 cc of a 5% aqueous solution of the thioether HO(CH2)2S(CH2)2S- (CH2)2OH were added to 1 liter of water and an aqueous solution containing 8.33 grams of silver nitrate and an aqueous solution containing 5.98 grams of potassium bromide and 0.726 gram of potassium iodide were added over a period of 45 seconds using the double jet method while stirring the mixture and maintaining a temperature of 75°C.
  • an aqueous solution which contained 8.33 grams of silver nitrate was added over a period of 7 minutes 30 seconds in such a way that the flow rate at the end of the addition was twice that at the start of the addition.
  • an aqueous solution containing 153.34 grams of silver nitrate and an aqueous solution of potassium bromide were added over a period of 25 minutes using the controlled double jet method in such a way that the potential was maintained at pAg 8.1.
  • the flow rate at this time was increased in such a way that the flow rate at the end of the addition was eight times that at the start of the addition.
  • the emulsion obtained was such that 93% of the total projected area of all the grains was accounted for by grains of which the aspect ratio was at least 3, and of all the grains of aspect ratio at least 2 the average projected area diameter was 0.83 ⁇ m, the standard deviation was 18.5%, the average thickness was 0.161 ⁇ m and the aspect ratio was 5.16.
  • 1,2-Bis(sulfonylacetamido)ethane was coated as a hardening agent in an amount of 57 mg/m2 per side.
  • a G-4 Grenex series screen (available from Fuji Photographic film Co.) was used as a screen for exposing the photographic material samples (Control Sample 3-1, Comparative Samples 3-2 and 3-3, and Samples 3-4 to 3-6).
  • the photographic material samples 3-1 to 3-6 were sandwiched between two G-4 screens in intimate contact with the screens in the usual way and subjected to an X-ray exposure through a 10 cm water phantom.
  • Photographic sensitivities were indicated as relative sensitivities taking the sensitivity of photographic material Sample 3-1 to be 100.
  • MTF values were measured using the combination of G4 screens and automatic processor processing described earlier. The measurements were made with a 30 ⁇ m x 500 ⁇ m aperture, and the evaluation was made in a region of optical density 1.0 using the MTF value for a spatial frequency of 1.0 cycle/mm.
  • Paper support samples A, B and C were obtained using a gelatin under-layer or the dye dispersion indicated below after carrying out a corona discharge treatment on a paper support which had been laminated on both sides with polyethylene.
  • Crystals of the dye indicated below were milled and finely pulverized in a sand mill. This was then dispersed in 25 ml of a 10% aqueous lime-treated gelatin solution in which 0.5 gram of citric acid had been dissolved and, after removing the sand with a glass filter, the dye which was attached to the sand on the glass filter was removed and 100 ml of a 7% gelatin solution was added (the average particle size of the fine dye particles was 0.15 ⁇ m)
  • Multi-layer color printing paper samples 4-1 to 4-4 of which the layer structure is indicated below were obtained on paper support Samples A, B and C.
  • the coating liquids were prepared as described below.
  • the blue-sensitive sensitizing dyes indicated below were added to a silver chlorobromide emulsion (a 3 : 7 (Ag mol ratio) mixture of cubic emulsions of average grain size 0.88 ⁇ m and 0.70 ⁇ m; the variation coefficients of the grain size distributions were 0.08 and 0.10, and each emulsion had 0.2 mol% silver bromide included locally on the surface of the grains) in amounts of 2.0x10 ⁇ 4 mol of each per mol of silver for the emulsion which had large grains and in amounts of 2.5x10 ⁇ 4 mol of each per mol of silver halide for the emulsion which had small grains, after which the emulsion was sulfur sensitized.
  • This emulsion was mixed with the aforementioned emulsified dispersion to prepare the first layer coating liquid of which the composition is indicated below.
  • the coating liquids for the second to the seventh layers were prepared using the same procedure as for the first layer coating liquid.
  • 1-Oxy-3,5-dichloro-s-triazine sodium salt was used as a gelatin hardening agent in each layer.
  • Blue-Sensitive Emulsion Layer (2.0x10 ⁇ 4 mol of each per mol of silver halide for the large size emulsion and 2.5x10 ⁇ 4 mol of each per mol of silver halide for the small size emulsion)
  • Green-Sensitive Emulsion Layer (4.0x10 ⁇ 4 mol per mol of silver halide for the large size emulsion and 5.6x10 ⁇ 4 mol per mol of silver halide for the small size emulsion) and
  • Red-Sensitive Emulsion Layer (0.9x10 ⁇ 4 mol per mol of silver halide for the large size emulsion and 1.1x10 ⁇ 4 mol per mol of silver halide for the small size emulsion)
  • the compound indicated below was added in an amount of 2.6x10 ⁇ 3 mol per mol of silver halide to the red-sensitive emulsion layer.
  • 1-(5-methylureidophenyl)-5-mercaptotetrazole was added to the blue, green and red-sensitive emulsion layers in amounts, per mol of silver halide, of 8.5x10 ⁇ 5 mol, 7.7x10 ⁇ 4 mol and 2.5x10 ⁇ 4 mol respectively.
  • the comparative dyes indicated below were added to the emulsion layer on one of the paper support A samples.
  • composition of each layer is indicated below.
  • the numerical values indicate coated weights as g/m2. In the case of silver halide emulsions the coated weight is shown as the calculated coated weight of silver.
  • Samples 4-1 to 4-4 obtained were subjected to a stepwise exposure for sensitometric purposes through blue, green and red filters using an actinometer (model FWH available from Fuji Photo Film Co., Ltd. light source color temperature 3200°K). Additionally, exposures were made for measuring resolution (CTF) and then they were developed and processed as indicated below. The results of density measurements of the samples obtained are shown in Table 3.
  • composition of each processing bath is indicated below.
  • Sample 501 a multi-layer color photographic material of which the layer structure is indicated below was prepared on an undercoated cellulose triacetate film support.
  • the coated weights are the amounts indicated in units of grams of silver per square meter in the case of silver halides and colloidal silver, in units of g/m2 in the case of couplers, additives and gelatin, an in units of mol per mol of silver halide in the same layer in the case of sensitizing dyes.
  • the symbols which indicate additives have the significance indicated hereinbelow. However, in cases where an additive has a plurality of effects it is indicated only once in a typical application.
  • UV Ultraviolet absorber
  • solv High boiling point organic solvent
  • ExF Dye
  • ExS Sensitizing dye
  • ExC Cyan coupler
  • ExM Magenta coupler
  • ExY Yellow coupler
  • Cpd Additive.
  • Cpd-2 in the eleventh layer was dissolved by heating to 60°C in ethyl acetate together with Cpd-1 and Solv-1 and the solution was emulsified and dispersed using a domestic mixer in an aqueous gelatin solution which contained sodium dodecylbenzenesulfonate and mixed with the silver halide emulsion.
  • Liquid I was introduced into the barrel of a hypodermic syringe and jetted into liquid II through a nozzle of mouth diameter 0.2 mm and a fine dispersion of Compound I was obtained.
  • the methyl ethyl ketone and sodium dodecylbenzenesulfonate were removed from this dispersion using an ultra-filtration membrane.
  • Sample 503 was prepared in the same way as sample 502 except that Compound 3 of the present invention was used instead of Compound 1 of the present invention in the eleventh layer of Sample 502.
  • Sample 504 was prepared in the same way as sample 502 except that Cpd-8 was used instead of Compound 1 of the present invention in the eleventh layer of Sample 502.
  • composition of the processing baths in indicated below.
  • Town water was passed through a mixed bed type column which had been packed with an H-type strongly acidic cation exchange resin (Amberlite IR-120B, available from Rohm and Haas Co.) and an OH-type anion exchange resin (Amberlite IR-400, available from Rohm & Haas Co.) and treated in such a way that the calcium and magnesium ion concentrations were up to 3 mg/liter, after which 20 mg/liter of sodium cyanurate dichloride and 1.5 g/liter of sodium sulfate were added. The pH of this liquid was within the range from 6.5 to 7.5.
  • H-type strongly acidic cation exchange resin Amberlite IR-120B, available from Rohm and Haas Co.
  • Amberlite IR-400 available from Rohm & Haas Co.
  • the dyes of the present invention When used as filter dyes, the dyes of the present invention (Samples 502 and 503) produced little loss of photographic sensitivity and it was possible to obtain color photographic light-sensitive materials with which there was little residual coloration. In contrast, Comparative Samples 501 and 504 had significantly higher residual coloration.

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EP0566063A1 (fr) * 1992-04-14 1993-10-20 Fuji Photo Film Co., Ltd. Matériau photographique à l'halogénure d'argent
EP0583004A1 (fr) * 1992-08-12 1994-02-16 Fuji Photo Film Co., Ltd. Matériau photographique à l'halogénure d'argent
EP0554834A3 (en) * 1992-02-03 1995-03-22 Fuji Photo Film Co Ltd Process for dispersing dyestuff and silver halide photographic material containing dyestuff
EP0600518A3 (fr) * 1992-12-03 1995-03-29 Fuji Photo Film Co Ltd Produit photographique couleur à l'halogénure d'argent sensible à la lumière.
EP0762198A1 (fr) 1995-08-02 1997-03-12 Eastman Kodak Company Colorants filtres pour éléments photographiques
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EP0460550B1 (fr) * 1990-06-04 1997-08-06 Fuji Photo Film Co., Ltd. Matériau photographique à l'halogénure d'argent
US5834173A (en) * 1995-12-22 1998-11-10 Eastman Kodak Company Filter dyes for photographic elements
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US7060822B1 (en) 1999-07-30 2006-06-13 Abbott Gmbh & Co. Kg 2-pyrazolin-5-ones
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JP2887718B2 (ja) * 1992-08-17 1999-04-26 富士写真フイルム株式会社 ハロゲン化銀写真感光材料
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EP0460550B1 (fr) * 1990-06-04 1997-08-06 Fuji Photo Film Co., Ltd. Matériau photographique à l'halogénure d'argent
US5296344A (en) * 1991-06-11 1994-03-22 Fuji Photo Film Co., Ltd. Silver halide photographic light-sensitive material
EP0519306A1 (fr) * 1991-06-11 1992-12-23 Fuji Photo Film Co., Ltd. Colorants pour filtres jaunes en dispersion d'huile
EP0554834A3 (en) * 1992-02-03 1995-03-22 Fuji Photo Film Co Ltd Process for dispersing dyestuff and silver halide photographic material containing dyestuff
EP0566063A1 (fr) * 1992-04-14 1993-10-20 Fuji Photo Film Co., Ltd. Matériau photographique à l'halogénure d'argent
EP0583004A1 (fr) * 1992-08-12 1994-02-16 Fuji Photo Film Co., Ltd. Matériau photographique à l'halogénure d'argent
EP0600518A3 (fr) * 1992-12-03 1995-03-29 Fuji Photo Film Co Ltd Produit photographique couleur à l'halogénure d'argent sensible à la lumière.
US5449594A (en) * 1992-12-03 1995-09-12 Fuji Photo Film Co., Ltd. Silver halide color photographic light-sensitive material
EP0762198A1 (fr) 1995-08-02 1997-03-12 Eastman Kodak Company Colorants filtres pour éléments photographiques
US5695917A (en) * 1995-11-22 1997-12-09 Eastman Kodak Company Combination of yellow filter dye and 4-equivalent pyrazolone magenta coupler
EP0775938A1 (fr) * 1995-11-22 1997-05-28 Eastman Kodak Company Combinaison de colorant filtre jaune et copulant magenta pyrazolone à 4 équivalents
US5834173A (en) * 1995-12-22 1998-11-10 Eastman Kodak Company Filter dyes for photographic elements
US5834172A (en) * 1996-02-23 1998-11-10 Eastman Kodak Company Photographic coating compositions and photographic elements made therefrom
US7060822B1 (en) 1999-07-30 2006-06-13 Abbott Gmbh & Co. Kg 2-pyrazolin-5-ones
US7772271B2 (en) 2004-07-14 2010-08-10 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US7781478B2 (en) 2004-07-14 2010-08-24 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US7868037B2 (en) 2004-07-14 2011-01-11 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US7973069B2 (en) 2004-07-14 2011-07-05 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US8013006B2 (en) 2004-07-14 2011-09-06 Ptc Therapeutics, Inc. Methods for treating hepatitis C
US7645881B2 (en) 2004-07-22 2010-01-12 Ptc Therapeutics, Inc. Methods for treating hepatitis C

Also Published As

Publication number Publication date
EP0430186B1 (fr) 1995-11-22
DE69023744D1 (de) 1996-01-04
JP2649980B2 (ja) 1997-09-03
DE69023744T2 (de) 1996-03-28
JPH03167546A (ja) 1991-07-19

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