Silver halide color photographic material

FIELD OF THE INVENTION
This invention relates to a silver halide color photographic material (hereinafter referred to simply as light-sensitive material), and more particularly to a light-sensitive material which gives a finished dye image by processing, said dye image being prevented from being faded or discolored.
BACKGROUND OF THE INVENTION
Generally, light-sensitive materials have silver halide emulsion layers sensitive to the three primary colors of red, green and blue, respectively, and a dye image is reproduced by a method wherein three kinds of color formers (couplers) contained in emulsion layers are developed to form colors having a relation of complementary colors to the light to which the emulsion layers are sensitive. Namely, a dye image is reproduced by subtractive color photography. A dye image obtained by photographically processing the light-sensitive material comprises generally an azomethine dye or an indoaniline dye formed by the reaction of the oxidants of aromatic primary amine color developing agents with couplers. The thus-obtained photographic color image is not always stable against light, heat and moisture, and when the color image is exposed to light over a long period of time or stored under high temperature and humidity conditions, the dye image is faded or discolored, and the image quality thereof is deteriorated.
The fading or discoloration of the image is a serious problem in recording materials. To eliminate this problem, there have been proposed the development of couplers giving a dye image having high fastness, the use of anti-fading agents, and the use of ultraviolet light absorbers to prevent the image from being deteriorated by ultraviolet light.
Examples of the anti-fading agents conventionally known include hydroquinones, hindered phenols, catechols, gallic esters, aminophenols, hindered amines, chromanols, indenes and ethers or esters obtained by silylating, acylating or alkylating the phenolic hydroxyl group of these compounds and metal complexes.
Further, sulfides having a specific structure, sulfoxides, sulfur-containing heterocyclic compounds and tetrahydrothiopyran compounds having a specific structure are proposed in U.S. Pat. Nos.4,540,658, 4,880,733, 4,704,350 and 5,104,781, U.K. Patent 1,410,846, JP-A-63-43146 (the term "JP-A" as used herein means an "unexamined published Japanese patent application"), JP-A-63-149644, JP-A-62-103642, European Patent Laid-Open Nos. 178,794, 310,551 and 310,552.
These compounds have certainly an effect of preventing dye images from being faded or discolored. However, these compounds are insufficient to cope with the demand of customers which require a higher image quality, and an excellent effect demanded by color photograph can not be obtained so far.
SUMMARY OF THE INVENTION
An object of the present invention is to provide a light-sensitive material which gives a dye image having greatly improved fastness to light.
Another object of the present invention is to provide a light-sensitive material which has improved fastness without any adverse effect on color developability, hue or photographic characteristics.
Still another object of the present invention is to provide a light-sensitive material which does not suffer from a change in color balance by the fading of the three colors of yellow, magenta and cyan colors.
Other object of the present invention is to provide a light-sensitive material which avoids formation of a yellow stain and a colored stain on white areas due to light, heat and temperature.
Still a further object of the present invention is to provide a light-sensitive material which is excellent in spectral absorption characteristics, has good color reproducibility, and gives a dye image having greatly improved fastness.
The present inventors have eagerly made studies and found that compounds represented by the following general formula (I), (II) or (III) have an excellent effect on preventing the fading of dye images.
Accordingly, the above-described objects of the present invention have been achieved by providing a silver halide color photographic material comprising a support having thereon at least one layer containing at least one compound represented by the following general formula (I), (II) or (III) ##STR2## wherein R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6, R.sub.11 and R.sub.12 may be the same or different and each represents a hydrogen atom, an alkyl group, an aryl group or a heterocyclic group; Y represents a group represented by following general formula ##STR3## R.sub.a, R.sub.b, R.sub.7, R.sub.8, R.sub.9, R.sub.10, R.sub.13, R.sub.14, R.sub.15 , R.sub.16, R.sub.17 and R.sub.18 may be the same or different and each represents a hydrogen atom or a substituent group, or R.sub.a and R.sub.b may be combined together to form a five-membered to seven-membered ring; R.sub.c represents an acyl group; R.sub.19 represents a substituent group; Z represents --S--, --SO--, --SO.sub.2 --, --O-- or --N(R.sub.20)--; R.sub.20 has the same meaning as R.sub.13 ; n represents 0 or an integer of 1 to 2; m represents 0 or an integer of 1 to 5; when m is 2 to 5, two or more R.sub.19 groups may be the same or different.
DETAILED DESCRIPTION OF THE INVENTION
Now, the present invention will be illustrated in more detail below.
The term "substituent group" as used herein refers to an alkyl group, an alkenyl group, an alkynyl group, an aryl group, a heterocyclic group, a halogen atom, a cyano group, a nitro group, a hydroxyl group, an alkoxy group, an aryloxy group, an alkylthio group, an arylthio group, an acyloxy group , a sulfonyloxy group, an unsubstituted amino group, an alkylamino group, an arylamino group, an acylamino group, a sulfonamido group, an oxycarbonylamino group, an oxysulfonylamino group, a ureido group, an acyl group, an oxycarbonyl group, a carbamoyl group, a sulfonyl group, a sulfinyl group, an oxysulfonyl group or a sulfamoyl group, unless otherwise stated. Of these, the acyloxy group includes an alkyl, aryl or heterocyclic acyloxy group, and similarly, the sulfonyloxy, acylamino, sulfonamido, oxycarbonylamino, oxysulfonylamino, ureido, acyl, oxycarbonyl, sulfonyl, sulfinyl and oxysulfonyl groups include alkyl, aryl or heterocyclic group-containing ones, respectively. These groups may be optionally substituted by one or more of organic groups capable of bonding through a carbon atom, an oxygen atom, a nitrogen atom or a sulfur atom or halogen atoms, so long as these groups can be substituted.
More specifically, examples of the substituent group include an alkyl group having 1 to 60 carbon atoms, preferably 1 to 30 carbon atoms (e.g., methyl, n-propyl, sec-butyl, n-dodecyl, n-octadodecyl, benzyl, cyclopropyl, cyclohexyl), an alkenyl group having 2 to 60 carbon atoms, preferably 2 to 30 carbon atoms (e.g., methylmethylene, ethylmethylene, isopropylmethylene), an alkynyl group having 2 to 60 carbon atoms, preferably 2 to 30 carbon atoms (e.g., methylmethine, isopropylmethine, phenylmethine), an aryl group having 6 to 60 carbon atoms, preferably 6 to 35 carbon atoms (e.g., phenyl, p-hexadecyloxyphenyl, 2,5-di-tert-amylphenyl, naphthyl), a saturated or unsaturated, optionally fused ring heterocyclic group having at least one hetero atom selected from the group consisting at O, S and N, and having 1 to 60 carbon atoms, preferably 1 to 30 carbon atoms (e.g., 2-furyl, 2-thienyl, 2-pyrimidinyl, 2-benzothiazolyl), a halogen atom (e.g., chlorine atom, bromine atom), a cyano group, a nitro group, a hydroxyl group, an alkoxy group having 1 to 60 carbon atoms, preferably 1 to 30 carbon atoms (e.g., methoxy, ethoxy, 2-methoxyethoxy, 2-dodecylethoxy, 2-methanesulfonylethoxy, an aryloxy group having 6 to 60 carbon atoms, preferably 6 to 35 carbon atoms (e.g., phenoxy, 2-methylphenoxy, 4-t-butylphenoxy, 3-nitrophenoxy, 3-t-butyloxycarbamoylphenoxy), an alkylthio group having 1 to 60 carbon atoms, preferably 1 to 30 carbon atoms (e.g., methylthio, octylthio, tetradecylthio, 2-phenoxyethylthio, 3-phenoxypropylthio, 3-(4-t-butylphenoxy)propylthio), an arylthio group having 6 to 60 carbon atoms, preferably 6 to 35 carbon atoms (e.g., phenylthio, 2-butoxy-5-t-octylphenylthio, 3-pentadecylphenylthio, 2-carboxyphenylthio, 4-tetradecaneamidophenylthio), an acyloxy group having 2 to 60 carbon atoms, preferably 2 to 35 carbon atoms (e.g., acetoxy), a sulfonyloxy group (e.g., sulfonyldioxy), an amino group, an alkylamino group having 1 to 60 carbon atoms, preferably 1 to 30 carbon atoms (e.g., methylamino, butylamino, dodecylamino, diethylamino, methylbutylamino), an arylamino group having 6 to 60 carbon atoms, preferably 6 to 35 carbon atoms (e.g., phenylamino), an acylamino group having 1 to 60 carbon atoms, preferably 1 to 35 carbon atoms (e.g., acetylamino, propanoylamino, sec-butanoylamino, n-dodecanoylamino), a sulfonamido group having 1 to 60 carbon atoms, preferably 1 to 35 carbon atoms (e.g., methanesulfonamido, hexadecanesulfonamido, benzenesulfonamido, p-toluenesulfonamido, octadecanesulfonamido, 2-methoxy-5-t-butylbenzenesulfonamido), an oxycarbonylamino group having 2 to 60 carbon atoms, preferably 2 to 35 carbon atoms (e.g., methoxycarbonylamino), an oxysulfonylamino group having 1 to 60 carbon atoms, preferably 1 to 35 carbon atoms (e.g., ethoxysulfonylamino), a ureido group having 1 to 60 carbon atoms, preferably 1 to 30 carbon atoms (e.g., phenylureido, methylureido, N,N-dibutylureido), an acyl group having 2 to 60 carbon atoms, preferably 2 to 35 carbon atoms (e.g., acetyl, benzoyl, pivaloyl, cyclopropionyl, .alpha.-(2,4-di-tert-amylphenoxy)butyryl, myristoyl, stearoyl, naphthoyl, m-pentadecylbenzoyl, isonicotinoyl), an oxycarbonyl group having 2 to 60 carbon atoms, preferably 2 to 35 carbon atoms (e.g., methoxycarbonyl, dodecyloxycarbonyl), a carbamoyl group having 1 to 60 carbon atoms, preferably 1 to 35 carbon atoms (e.g., N-ethylcarbamoyl, N-benzylcarbamoyl, N,N-dibutylcarbamoyl, N-phenylcarbamoyl , N-hexadecylcarbamoyl), a sulfonyl group having 1 to 60 carbon atoms, preferably 1 to 35 carbon atoms (e.g., methanesulfonyl, octanesulfonyl, benzenesulfonyl, toluenesulfonyl), a sulfinyl group having 1 to 60 carbon atoms, preferably 1 to 35 carbon atoms (e.g., dodecanesulfinyl, 3-pentadecylphenylsulfinyl, 3-phenoxypropylsulfinyl), an oxysulfonyl group having 1 to 60 carbon atoms, preferably 1 to 35 carbon atoms (e.g., methoxysulfonyl) and a sulfamoyl group having 0 to 60 carbon atoms, preferably 0 to 30 carbon atoms (e.g., N-ethylsulfamoyl, N,N-dipropylsulfamoyl, N-(2-dodecyloxyethyl)sulfamoyl, N-ethyl-N-dodecylsulfamoyl, N,N-diethylsulfamoyl). These groups may be optionally further substituted by one or more of the substituent groups described above, unless otherwise stated.
The compounds of general formulas (I) and (II) according to the present invention will be illustrated below.
R.sub.1, R.sub.2, R.sub.3 and R.sub.4 in general formula (I) and R.sub.5, R.sub.6, R.sub.11 and R.sub.12 in general formula (II) may be the same or different, and each represents a hydrogen atom, an alkyl group having 1 to 60 carbon atoms, preferably 1 to 30 carbon atoms (e.g., methyl, n-propyl, sec-butyl, n-dodecyl, n-octadodecyl, benzyl, cyclopropyl, cyclohexyl), an aryl group having 6 to 60 carbon atoms, preferably 6 to 35 carbon atoms ( e.g., phenyl, p-hexadecyloxyphenyl, 2,5-di-tert-amylphenyl, naphthyl) or a saturated or unsaturated, optionally fused ring heterocyclic group having at least one hetero atom selected from the group consisting of O, S, and N, and having 1 to 60 carbon atoms, preferably 1 to 30 carbon atoms (e.g., furyl, 2-thienyl, 2-pyrimidinyl, 2-benzthiazolyl).
R.sub.a and R.sub.b in general formula (I) and R.sub.7, R.sub.8, R.sub.9 and R.sub.10 in general formula (II) may be the same or different, and each is preferably a hydrogen atom, a hydroxyl group, an acyloxy group having 2 to 60 carbon atoms, preferably 2 to 35 carbon atoms (e.g., acetyloxy, myristoyloxy, palmitoyloxy, .alpha.-(2,5-di-tert-amylphenoxy)butyloxy), an alkyl group having 1 to 60 carbon atoms, preferably 1 to 30 carbon atoms (e.g., methyl, n-propyl, sec-butyl, n-dodecyl, n-octadodecyl, benzyl, cyclopropyl, cyclohexyl), an aryl group having 6 to 60 carbon atoms, preferably 6 to 35 carbon atoms (e.g., phenyl, p-hexadecyloxyphenyl, 2,5-di-tert-amylphenyl, naphthyl), an alkoxy group having 1 to 60 carbon atoms, preferably 1 to 30 carbon atoms (e.g. , methoxy, ethoxy, 2-methoxyethoxy, 2-dodecylethoxy, 2-methanesulfonylethoxy), an aryloxy group having 6 to 60 carbon atoms, preferably 6 to 35 carbon atoms (e.g., phenoxy, 2-methylphenoxy, 4-t-butylphenoxy, 3-nitrophenoxy, 3-t-butyloxycarbamoylphenoxy), an alkylthio group having 1 to 60 carbon atoms, preferably 1 to 30 carbon atoms (e.g., methylthio, octylthio, tetradecylthio, 2-phenoxyethylthio, 3-phenoxypropylthio, 3-(4-t-butylphenoxy)propylthio), an arylthio group having 6 to 60 carbon atoms, preferably 6 to 35 carbon atoms (e.g., phenylthio, 2-butoxy-5-t-octylphenylthio, 3-pentadecylphenylthio, 2-carboxyphenylthio, 4-tetradecaneamidophenylthio), an alkylamino group having 1 to 60 carbon atoms, preferably 1 to 30 carbon atoms (e.g., methylamino, butylamino, dodecylamino, diethylamino, methylbutylamino), an arylamino group having 6 to 60 carbon atoms, preferably 6 to 35 carbon atoms (e.g., phenylamino), a carbamoyl group having 1 to 60 carbon atoms, preferably 1 to 35 carbon atoms (e.g., N-ethylcarbamoyl, N-benzylcarbamoyl, N,N-dibutylcarbamoyl, N-phenylcarbamoyl, N-hexadecylcarbamoyl), a sulfonamido group having 1 to 60 carbon atoms, preferably 1 to 35 carbon atoms (e.g., methanesulfonamido, hexadecanesulfonamido, benzenesulfonamido, p-toluenesulfonamido, octadecanesulfonamido, 2-methoxy-5-t-butylbenzenesulfonamido) or an acyl group having 2 to 60 carbon atoms, preferably 2 to 35 carbon atoms (e.g., acetyl, benzoyl, pivaloyl, cyclopropionyl, .alpha.-(2,4-di-tert-amylphenoxy)butyryl, myristoyl, stearoyl, naphthoyl, m-pentadecylbenzoyl, isonicotinoyl). R.sub.a and R.sub.b may be combined together to form a five-membered to seven-combined membered ring.
More preferably, R.sub.a and R.sub.b are each a hydrogen atom, an acyloxy group or an alkoxy group, and R.sub.7, R.sub.8, R.sub.9 and R.sub.10 are each a hydrogen atom, an acyloxy group, an alkyl group, an aryl group, an alkylthio group or an alkoxy group.
R.sub.c represents an acyl group having 2 to 60 carbon atoms, preferably 2 to 35 carbon atoms (e.g., acetyl, benzoyl, pivaloyl, cyclopropionyl, .alpha.-(2,4-di-tert-amylphenoxy)butyryl, myristoyl, stearoyl, naphthoyl, m-pentadecylbenzoyl, isonicotinoyl).
The compounds of general formula (I) where one of R.sub.1 and R.sub.2 is an aryl group and the other is a hydrogen atom, or where one of R.sub.3 and R.sub.4 is an aryl group and the other is a hydrogen atom, are preferred. Among the compounds of general formula (I), compounds represented by the following general formula (I-a) are more preferred. ##STR4## wherein n and Y are as defined in general formula (I); R.sub.21 and R.sub.22 may be the same or different and each represents a substituent group; k and k' each represents 0 or an integer of 1 to 5; when k and k' are each 2 or greater, two or more R.sub.21 and R.sub.22 groups may be the same or different; or when two or more R.sub.21 and R.sub.22 groups exist, the R.sub.21 or R.sub.22 groups at the ortho-position relative to each other may be combined together to form a five-membered to seven-membered ring.
Preferably, R.sub.21 and R.sub.22 are each an alkyl group, an aryl group, a saturated or unsaturated, optionally fused ring heterocyclic group, an alkoxy group, an aryloxy group, an alkylthio group, an arylthio group, an alkoxycarbonyl group, a carbamoyl group or an acyl group. More preferably, R.sub.21 and R.sub.22 are each an alkyl group, an aryl group, a heterocyclic group, an alkylthio group or an arylthio group.
Preferably, Y in formula (I) represents a group of the following general formula: ##STR5##
In general formulas (I) and (II), n is preferably 0 or 2, particularly preferably 0.
The compounds of general formula (II) where one of R.sub.5 and R.sub.6 is an aryl group and the other is a hydrogen atom or where one of R.sub.11 and R.sub.12 is an aryl group and the other is a hydrogen atom, are preferred. Among the compounds of general formula (II), compounds represented by the following general formula (II-a) are more preferred. ##STR6##
In general formula (II-a), R.sub.7, R.sub.8, R.sub.9, R.sub. 10 and n are the same as defined in general formula (II); R.sub.23 and R.sub.24 have the same meaning as R.sub.21 and R.sub.22 in general formula (I-a); and p and p' have the same meaning as k in general formula (I-a).
The compounds of general formula (III) will be illustrated in more detail below.
In general formula (III), R.sub.13, R.sub.14, R.sub.15, R.sub.16, R.sub.17 and R.sub.18 may be the same or different, and each is preferably a hydrogen atom, an alkyl group (e.g., methyl, n-propyl, sec-butyl, n-dodecyl, n-octadodecyl, benzyl, cyclopropyl, cyclohexyl ), an alkenyl group (e.g., methylmethylene, ethylmethylene, isopropylmethylene), an alkynyl group (e.g., methylmethine, isopropylmethine, phenylmethine), an aryl group (e.g., phenyl, p-hexadecyloxyphenyl, 2,5-di-tert-amylphenyl, naphthyl), a saturated or unsaturated, optionally fused ring heterocyclic group (e.g., 2-furyl, 2-thienyl, 2-pyrimidinyl, 2-benzothiazolyl), a halogen atom (e.g., chlorine atom, bromine atom), a cyano group, a nitro group, a hydroxy group, an alkoxy group (e.g., methoxy, ethoxy, 2-methoxyethoxy, 2-dodecylethoxy, 2-methanesulfonylethoxy), an aryloxy group (e.g., phenoxy, 2-methylphenoxy, 4-t-butylphenoxy, 3-nitrophenoxy, 3-t-butyloxycarbamoylphenoxy), an alkylthio group (e.g., methylthio, octylthio, tetradecylthio, 2-phenoxyethylthio, 3-phenoxypropylthio, 3-(4-t-butylphenoxy)propylthio), an arylthio group (e.g., phenylthio, 2-butoxy-5-t-octylphenylthio, 3-pentadecylphenylthio, 3-carboxyphenylthio, 4-tetradecaneamidophenylthio), an acyloxy group (e.g., acetoxy), a sulfonyloxy group (e.g., sulfonyldioxy), an unsubstituted amino group, an alkylamino group (e.g., methylamino, butylamino, dodecylamino, diethylamino, methylbutylamino), an arylamino group (e.g., phenylamino), an acylamino group (e.g., acetylamino, propanoylamino, sec-butanoylamino, n-dodecanoylamino), a sulfonamido group (e.g., methanesulfonamido, hexadecanesulfonamido, benzenesulfonamido, p-toluenesulfonamido, octadecanesulfonamido, 2-methoxy-5-t-butylbenzenesulfonamido), an oxycarbonylamino group (e.g., methoxycarbonylamino), an oxysulfonylamino group (e.g., ethoxysulfonylamino), a ureido group (e.g., phenylureido, methylureido, N,N-dibutylureido), an acyl group (e.g., acetyl, benzoyl, pivaloyl, cyclopropionyl, .alpha.-(2,4-di-tert-amylphenoxy)butyryl, myristoyl, stearoyl, naphthoyl, m-pentadecylbenzoyl, isonicotinoyl), an oxycarbonyl group (e.g., methoxycarbonyl, dodecyloxycarbonyl), a carbamoyl group (e.g., N-ethylcarbamoyl, N-benzylcarbamoyl, N,N-dibutylcarbamoyl, N-phenylcarbamoyl, N-hexadecylcarbamoyl), a sulfonyl group (e.g., methanesulfonyl, octanesulfonyl, benzenesulfonyl, toluenesulfonyl), a sulfinyl group (e.g., dodecanesulfinyl, 3-pentadecylphenylsulfinyl, 3-phenoxypropylsulfinyl), an oxysulfonyl group (e.g., methoxysulfonyl) or a sulfamoyl group (e.g., N-ethylsulfamoyl, N,N-dipropylsulfamoyl, N-(2-dodecyloxyethyl)sulfamoyl, N-ethyl-N-dodecylsulfamoyl, N,N-diethylsulfamoyl).
Preferably, R.sub.13, R.sub.14, R.sub.17 and R.sub.18 are each a hydrogen atom, an alkyl group, an aryl group, an alkoxy group, an aryloxy group, an alkylthio group, a ureido group, an oxycarbonylamino group or an acylamino group. More preferred are a hydrogen atom, an alkyl group, an aryl group and an alkoxy group.
Preferably, R.sub.15 and R.sub.16 are each a hydrogen atom, a halogen atom, an alkyl group, an aryl group or an alkoxy group. More preferably, R.sub.15 is an aryl group, and R.sub.16 is hydrogen atom.
Examples of the substituent group represented by R.sub.19 include those already described above in the definition of the substituent group for R.sub.21 in general formula (I-a). Preferably, R.sub.19 is an alkyl group, an aryl group, a heterocyclic group, an alkoxy group, an aryloxy group, an alkylthio group, an arylthio group, an alkoxycarbonyl group, a carbamoyl group or an acyl group. More preferably, R.sub.19 is an alkyl group, an aryl group, a heterocyclic group, an alkylthio group or an arylthio group.
In general formula (III), n is an integer of 0 to 2, preferably 0 or 2, more preferably 0.
Preferably, Z is --S--, --SO--, --SO.sub.2 -- or --O--.
More preferably, Z is --S-- or --SO.sub.2 --.
Specific examples of the compounds of general formulas (I), (II) and (III) include, but are not limited to, the following compounds. ##STR7##
Preferred examples of the compounds of general formulas (I), (II) and (III) include (I-a-l), (I-a-7), (I-a-10), (I-a-12), (I-a-16), (II-a-1), (II-a-3), (II-a-7), (II-a-9), (II-a-10), (II-a-17), (III-3), (III-5) and (III-24).
The compounds of general formulas (I) to (III) can be easily synthesized, for example, by the methods described in Chem. & Ind., 450 (1963), J. Am. Chem. Soc., 93, 676 (1971), J. AM. Chem. Soc., 59, 707 (1937) or J. Pharm. Soc. Japan, 77,359 (1957).
A synthesis example of a typical compound is illustrated below.
Synthesis of Compound (I-a-11)
To 50 ml of ethanol, there was added 6.0 g of sodium sulfite. An ethanol solution of 1,3-dichloro-1,3-diphenylpropane was slowly added dropwise thereto under reflux. After the resulting mixture was stirred for 6 hours, the reaction mixture (solution) was poured into water and extracted with 100 ml of ethyl acetate. The extract was washed with 50 ml of brine twice and dried over anhydrous magnesium sulfate. After magnesium sulfate was recovered by filtration, ethyl acetate was distilled off under reduced pressure to obtain a crystal. Mass spectrum, NMR spectrum and infrared absorption spectrum showed that the crystal was compound (I-a-11). Yield: 4.05 g (79%).
It is preferred that the compound of general formula (I), (II) or (III) according to the present invention is used in combination with a cyan coupler, a magenta coupler or a yellow coupler in the same layer, said couplers being coupled with the oxidation product of a primary aromatic amine color developing agent to form cyan color, magenta color and yellow color, respectively.
The couplers used in combination with the compounds may be a four equivalent type or a two equivalent type for silver ion. The couplers may be in the form of a polymer or an oligomer or may be used either alone or as a mixture of two or more of them.
The couplers which can be preferably used in the present invention will be illustrated below.
It is preferred from the viewpoint of the effect of the present invention that the compounds of general formula (I), (II) or (III) are used together with yellow couplers or cyan couplers, particularly together with yellow couplers. When the compounds of the present invention are used together with magenta couplers, the compounds have the excellent effect of improving fastness to light in the region of a further lower color density in comparison with conventional anti-fading agents such as diethers of hydroquinone derivatives, diethers of resorcin derivatives, diethers of catechol derivatives, tetraalkoxy-spirobiindane derivatives, aniline derivatives and ethers of aminophenol derivatives.
Examples of the yellow couplers include those described in U.S. Pat. Nos. 3,933,501, 4,022,620, 4,326,024, 4,401,752 and 4,248,961, JP-B-58-10739 (the term "JP-B" as used herein means an "examined Japanese patent publication"), U.K. Patents 1,425,020 and 1,476,760, U.S. Pat. Nos. 3,973,968, 4,314,023 and 4,511,649, European Patents 249,473A, 446,863A and 447,969, JP-A-63-23145, JP-A-63-123047, JP-A-1-250944, JP-A-1-213648, JP-A-2-139544 and Japanese Patent Application Nos. 3-179042 and 3-203545.
Yellow couplers which can be preferably used in the present invention are compounds represented by the following general formula (Y). ##STR8##
In general formula (Y), R.sub.1y represents a tertiary alkyl group, an aryl group or --N(R.sub.x)(R.sub.y); R.sub.2y represents hydrogen atom, a halogen atom, an alkoxy group, an aryloxy group, an alkyl group or a dialkylamino group; R.sub.3y represents a group which can be attached to the benzene ring; X represents hydrogen atom or a group (eliminatable group) which is eliminated by the coupling reaction with the oxidant of an aromatic primary amine developing agent; Q represents 0 or an integer of 1 to 4 and when Q is 2 or greater, two or more R.sub.3Y groups may be the same or different; and R.sub.x and R.sub.y may be the same or different and each represents an alkyl group, an alkenyl group, an aryl group or a heterocyclic group, or R.sub.x and R.sub.y may be combined together to form a five-membered or six-membered ring which may be optionally substituted or fused together with an aromatic ring, an alicyclic ring or a heterocyclic ring.
Examples of the group represented by R.sub.3Y include a halogen atom, an alkyl group, an aryl group, an alkoxy group, an aryloxy group, an alkoxycarbonyl group, an aryloxycarbonyl group, a carboxamido group, a sulfonamido group, a carbamoyl group, a sulfamoyl group, a sulfonyl group, a sulfonylsulfamoyl group, a sulfonylcarbamoyl group, a ureido group, an acylcarbamoylamino group, an acylsulfamoylamino group, a sulfamoylamino group, an alkoxycarbonylamino group, an acylsulfamoyl group, an acylcarbamoyl group, a nitro group, a heterocyclic group, a cyano group, an acyl group, an acyloxy group, an alkylsulfonyloxy group and an arylsulfonyloxy group. Examples of the eliminatable group include a heterocyclic group attached to the coupling active site through a nitrogen atom, an aryloxy group, an arylthio group, an acyloxy group, an alkylsulfonyloxy group, a heterocyclic oxy group and a halogen atom.
In general formula (Y), R.sub.1Y is preferably a t-butyl group, a cyclopropyl group wherein the 1-position is substituted by an alkyl group, a phenyl group, a phenyl group substituted by one or more halogen atoms, an alkyl group and an alkoxy group, a dialkylamino group, an alkylarylamino group or an indolinyl group; R.sub.2Y is preferably a halogen atom, a trifluoromethyl group, an alkoxy group or an aryloxy group; R.sub.3Y is preferably a halogen atom, an alkoxy group, an alkoxycarbonyl group, a carboxamido group, a sulfonamido group, a carbamoyl group or a sulfamoyl group; X is preferably an aryloxy group or a five-membered to seven-membered ring which is attached to the coupling active site through nitrogen atom and may be a heterocyclic group containing further one or more atoms of N, S, O and P; Q is preferably an integer of 0 to 2.
The couplers of general formula (Y) may be in the form of a dimer or a higher polymer coupler wherein the substituent group R.sub.1Y, X, R.sub.2Y or R.sub.3Y contains a mother nucleus or a main chain of a homopolymer or a copolymer having a non-color forming polymerized unit.
Examples of the couplers of general formula (Y) include the following compounds. ##STR9##
Preferred examples of the couplers of general formula (Y) include (Y-1), (Y-3) and (Y-4).
Examples of yellow couplers which can be used in addition to the above-described yellow couplers in the present invention and the synthesis methods of these yellow couplers are described in U.S. Pat. Nos. 3,227,554, 3,408,194, 3,894,875, 3,933,501, 3,973,968, 4,022,620, 4,057,432, 4,115,121, 4,203,768, 4,248,961, 4,266,019, 4,314,023, 4,327,175, 4,401,752, 4,404,274, 4,420,556, 4,711,837 and 4,729,944, European Patents 30,747A, 284,081A, 296,793A, 313,308A and 447,964, West German Patent 3,107,173C, JP-A-58-42044, JP-A-59-174839, JP-A-62-276547, JP-A-63-123047 and Japanese Patent Application Nos. 3-179042 and 3-203545.
Cyan couplers include phenol couplers and naphthol couplers. Examples of cyan couplers which can be preferably used in the present invention include those described in U.S. Pat. Nos. 4,052,212, 4,146,396, 4,228,233, 4,296,200, 2,269,929, 2,801,171, 2,772,162, 2,895,862, 3,772,002, 3,758,308, 4,334,011 and 4,327,173, West German Patent Laid-Open No. 3,329,729, European Patents 121,365A, 249,453A and 333,185A2, U.S. Pat. Nos. 3,446,622, 4,333,999, 4,775,616, 4,451,559, 4,427,767, 4,690,889, 4,254,212 and 4,296,199 and JP-A-1-42658. Further, there can be used azole couplers described in JP-A-64-553, JP-A-64-554, JP-A-64-555, JP-A-64-556 and Japanese Patent Application Nos. 3-280964 and 3-335916, imidazole couplers described in U.S. Pat. No. 4,818,672 and JP-A-2-33144 and cyclic active methylene type cyan couplers described in JP-A-64-32260.
Particularly preferred cyan couplers include couplers of general formulas (C-I) and (C-II) described in JP-A-2-139544 (left lower column of page 17 to left lower column of page 20).
Magenta couplers which can be preferably used in the present invention include 5-pyrazolone compounds and pyrazoloazole compounds. Examples of the magenta couplers which can be more preferably used in the present invention include those described in U.S. Pat. Nos. 4,310,619 and 4,351,897, European Patent 73,636, U.S. Pat. Nos. 3,061,432 and 3,725,067, Research Disclosure No. 24220 (June 1984), JP-A-60-33552, Research Disclosure No. 24230 (June 1984), JP-A-60-43659, JP-A-61-72238, JP-A-60-35730, JP-A-55-118034, JP-A-60-185951, U.S. Pat. Nos. 4,500,630, 4,540,654 and 4,556,630 and (PCT) WO 88/04795.
Particularly preferred magenta couplers include pyrazoloazole magenta couplers of general formula (I) described in JP-A-2-139544 (right lower column of page 3 to right lower column of page 10) and 5-pyrazolone magenta couplers of general formula (M-1) described in JP-A-2-139544 (left lower column of page 17 to left upper column of page 21). Most preferred are the above-described pyrazoloazole magenta couplers.
Typical examples of the magenta couplers and cyan couplers which can be used in the present invention include the following compounds. ##STR10##
Preferred examples of the magenta couplers include (M-1), (M-5) and (M-8).
Preferred examples of the cyan couplers include (C-1), (C-5) and (c-6).
Couplers which release a photographically useful residue with coupling can be used in the present invention. Preferred examples of DIR coupler which release a restrainer include those described in patent specifications cited in Research Disclosure (RD) No. 17643, Item VII-F, JP-A-57-151944, JP-A-57-154234, JP-A-60-184248, JP-A-63-37346, U.S. Pat. Nos. 4,248,962 and 4,782,012.
Preferred examples of couplers which imagewise release a nucleating agent or a development accelerator during development include those described in U.K. Patents 2,097,140 and 2,131,188, JP-A-59-157638 and JP-A-59-170840.
Examples of other couplers which can be used in the light-sensitive materials of the present invention include competitive couplers described in U.S. Pat. No. 4,130,427; polyequivalent type couplers described in U.S. Pat. Nos. 4,284,472, 4,338,393 and 4,310,618; DIR redox compound-releasing couplers, DIR coupler-releasing couplers, DIR coupler-releasing redox compounds and DIR redox-releasing redox compounds described in JP-A-60-185950 and JP-A-62-24252; couplers which release a dye whose color is restored after elimination as described in European Patent 173,302A; bleach-accelerating agent-releasing couplers described in RD No. 11449, RD No. 24241 and JP-A-61-201247; ligand-releasing couplers described in U.S. Pat. No. 4,553,477; leuco dye-releasing couplers described in JP-A-63-75747; and fluorescent dye-releasing couplers described in U.S. Pat. No. 4,774,181.
These couplers are generally used in an amount of 0.001 to 1 mol per mol of the light-sensitive silver halide in the present invention. Preferably, yellow couplers are used in amount of 0.01 to 0.5 mol, magenta couplers are used in an amount of 0.003 to 0.3 mol, and cyan couplers are used in an amount of 0.002 to 0.3 mol.
The amounts of the compounds of general formula (I), (II) or (III) according to the present invention vary depending on the types of couplers to be used, but are generally used in an amount of preferably 0.5 to 300 mol % more preferably 1 to 200 mol % most preferably 5 to 150 mol % based on the amount of the coupler used in the same layer.
The compounds of the present invention may be used together with conventional anti-fading agents. When the compounds of the present invention are used in combination with conventional anti-fading agents, the fading prevention effect can be further increased. If desired, the compounds of general formulas (I) to (III) may be used in combination of two or more of them.
Examples of organic anti-fading agents for cyan, magenta and/or yellow images include hydroquinones, 6-hydroxychromans, 5-hydroxycoumarans, spirochromans, p-alkoxyphenols, hindered phenols such as bisphenols gallic acid derivatives, methylenedioxybenzenes, aminophenols, hindered amines and ethers or ester derivatives obtained by silylating or alkylating the phenolic hydroxyl group of the above-described compounds. Further, metal complexes such as (bissalicylaldoximato)nickel complex and ( bis-N,N-dialkyldithiocarbamato)nickel complex can also be used.
Examples of the organic anti-fading agents include hydroquinones, described in U. S. Pat. Nos. 2,360,290, 2,418,613, 2,700,453, 2,701,197, 2,728,659, 2,732,300, 2,735,765, 3,982,944 and 4,430,425, U.K. Patent 1,363,921, U.S. Pat. Nos. 2,710,801 and 2,816,028; 6-hydroxychromans, 5-hydroxychromans, and spiro-chromans described U.S. Pat. Nos. 3,432,300, 3,573,050, 3,574,627, 3,698,909 and 3,764,337 and JP-A-52-152225; spiroindanes described in U.S. Pat. No. 4,360,589; p-alkoxyphenols described in U.S. Pat. No. 2,735,765, U.K. Patent 2,066,975, JP-A-59-10539 and JP-B-57-19765; hindered phenols described in U.S. Pat. Nos. 3,700,455 and 4,228,235, JP-A-52-72224 and JP-B-52-6623; gallic acid derivatives, described in U.S. Pat. No. 3,457,079, methylenedioxybenzenes described in U.S. Pat. No. 4,332,886; aminophenols described in JP-B-56-21144; hindered amines described in U.S. Pat. Nos. 3,336,135 and 4,268,593, U.K. Patents 1,326,889, 1,354,313 and 1,410,846, JP-B-51-1420, JP-A-58-114036, JP-A-59-53846 and JP-A-59-78344; and metal complexes described in U.S. Pat. Nos. 4,050,938 and 4,241,155 and U.K. Patent 2,027,731(A). These compounds are used in an amount of generally 5 to 100% by weight based on the amount of the corresponding coupler. These compounds are co-emulsified with the couplers and added to the light-sensitive layers.
The photographic materials of the present invention may contain hydroquinone derivatives, aminophenol derivatives, gallic acid derivatives and ascorbic acid derivatives as color fogging inhibitors (antifogging agents).
It is more effective to introduce ultraviolet light absorbers into the cyan color forming layer and both layers adjacent thereto to prevent the cyan dye image from being deteriorated by heat and particularly light.
Examples of the ultraviolet light absorbers include aryl group-substituted benzotriazole compounds described in U.S. Pat. No. 3,533,794; 4-thiazotidone compounds described in U.S. Pat. Nos. 3,314,794 and 3,352,681; benzophenone compounds described in JP-A-46-2784; silicic ester compounds described in U.S. Pat. Nos. 3,705,805 and 3,707,395; butadiene compounds described in U.S. Pat. No. 4,045,229; and benzoxazole compounds described in U.S. Pat. Nos. 3,406,070 and 4,271,307; and triazine compounds described in JP-A-46-3335. If desired, ultraviolet absorbing couplers (e.g., .alpha.-naphthol cyan color forming couplers) and ultraviolet light absorbing polymers may be used. These ultraviolet light absorbers may be mordanted in specific layers. Among them, the aryl group-substituted benzotriazole compounds are preferred.
The compounds of general formulas (I), (II) or (III) according to the present invention and the couplers can be introduced into the light-sensitive materials by various conventional dispersion methods. There are preferred oil-in-water dispersion methods wherein they are dissolved in a high-boiling organic solvent (optionally together with organic a low-boiling organic solvent), the resulting solution is emulsified and in dispersed an aqueous gelatin solution, and the resulting emulsified dispersion is added to a silver halide emulsion.
Examples of the high-boiling organic solvent which can be used in the oil-in-water dispersion methods are described in U.S. Pat. No. 2,322,027. The stages and effects of latex dispersion methods as a type of a polymer dispersion method and examples of impregnating latex are described in U.S. Pat. No. 4,199,363, West German Patent Laid-Open (OLS) Nos. 2,541,274 and 2,541,230, JP-B-53-41091 and European Patent Laid-Open No. 029104. A dispersion method using organic solvent-soluble polymers is described in (PCT) WO 88/00723.
Specific examples of the high-boiling organic solvent which can be used in the oil-in-water dispersion methods include phthalic esters (e.g., dibutyl phthalate, dioctyl phthalate, dicyclohexyl phthalate, di-2-ethylhexyl phthalate, decyl phthalate, bis(2,4-di-tert-amylphenyl) isophthalate, bis(1,1-diethylpropyl) phthalate), phosphoric or phosphonic esters (e.g., diphenyl phosphate, triphenyl phosphate, tricresyl phosphate, 2-ethylhexyl diphenyl phosphate, dioctyl butyl phosphate, tricyclohexyl phosphate, tri-2-ethylhexyl phosphate, tridodecyl phosphate, di-2-ethylhexyl phenyl phosphate), benzoic esters (e.g., 2-ethylhexyl benzoate, 2,4-di-chlorobenzoate, dodecyl benzoate, 2-ethylhexyl-p-hydroxybenzoate), amides (e.g., N,N-diethyldodecaneamide, N,N-diethyllaurylamide), alcohols and phenols (e.g., isostearyl alcohol, 2,4-di-tert-amylphenol), aliphatic esters (e.g., dibutoxyethyl succinate, di-2-ethylhexyl succinate, 2-hexyldecyl tetradecanoate, tributyl citrate, diethyl azelate, isostearyl lactate, trioctyl citrate), aniline derivatives (e.g., N,N-dibutyl-2-butoxy-5-tert-octylaniline), chlorinated paraffins (e.g., paraffins having a chlorine content of 10 to 80%), trimesic ester (e.g., tributyl ester of trimesic acid), dodecylbenzene, diisopropylnaphthalene, phenols (e.g., 2,4-di-tert-amylphenol, 4-dodecyloxyphenol, 4-dodecyloxycarbonylphenol, 4-(4-dodecyloxyphenylsulfonyl)phenol), carboxylic acids (e.g., 2-(2,4-di-tert-amylphenoxybutyric acid, 2-ethoxyoctanedecanoic acid) and alkylphosphoric acids (e.g., di-2-ethylhexylphosphoric acid, diphenylphosphoric acid). Organic solvents having a boiling point of not lower than 30.degree. C., but not higher than about 160.degree. C. may be used as auxiliary solvents together with the high-boiling organic solvents. Examples of the auxiliary solvents include ethyl acetate, butyl acetate, ethyl propionate, methyl ethyl ketone, 2-ethoxyethyl acetate and dimethylformamide.
The high-boiling organic solvents are used in an amount of 0 to 10.0 times, preferably 0 to 6.0 times the weight of the couplers.
The light-sensitive material of the present invention comprises a support having thereon at least one layer containing at least one member of the compounds of general formula (I), (II) or (III). Generally, the light-sensitive material comprises a support having thereon at least one blue-sensitive silver halide emulsion layer, at least one green-sensitive silver halide emulsion layer and at least one red-sensitive silver halide emulsion layer in this order. However, the arrangement of the layers may be made in the reverse order to that described above. If desired, an infrared-sensitive silver halide emulsion layer may be used in place of at least one of the above light-sensitive emulsion layers. Color reproduction by subtractive color photography can be made by supplying color couplers to the light-sensitive emulsion layers. These color couplers form dyes having the relation of complementary colors to the light to which silver halide emulsions, having sensitivity to respective wavelength regions are sensitive. The light-sensitive layers may not correspond to the hue of developed color as described above.
The compounds of the present invention can be applied to, for example, color papers, color reversal papers, direct positive color light-sensitive materials, color negative films, color positive films and reversal color films. It is preferred that the compounds of the present invention are applied to color light-sensitive materials having a reflection support (e.g., color paper, reversal color paper) and color light-sensitive materials which form a positive image (e.g., direct positive color light-sensitive materials, color positive films, reversal color films). It is particularly preferred that the compounds of the present invention are applied to the color light-sensitive materials having a reflection support.
Examples of silver halide which can be used in the present invention include silver chloride, silver bromide, silver chlorobromide, silver iodochlorobromide and silver iodobromide. For the purpose of rapid processing, silver chlorobromide containing substantially no silver iodide and having a silver chloride content of preferably at least 90 mol %, more preferably at least 95 mol %, particularly preferably at least 98 mol %, or pure silver chloride emulsion is preferred.
It is preferred that dyes decolorizable by processing (particularly oxonol dyes) as described in EP0,337,490A2 (pages 27 to 76) are added to the hydrophilic colloid layers of the present invention in such an amount as to give an optical reflection density of at least 0.70 at 680 nm to improve the sharpness of the image; or at least 12 wt % (more preferably at least 14 wt %) of titanium oxide having a surface treated with a bihydric to tetrahydric alcohol (e.g., trimethylol ethane) is contained in the water-resistant resin layer of the support to improve the sharpness of image.
It is preferred that the light-sensitive materials of the present invention contain dye image preservability improving compounds described in EP0,277,589A2 together with the couplers, particularly pyrazoloazole magenta couplers.
Namely, a compound (F) described in EP 0,277,589 A2 and/or a compound (G) described in EP 0,277,589 A2 are/is contained in the light-sensitive materials of the present invention, said compound (F) being chemically bonded to the aromatic amine color developing agent left behind after color development to form a compound which is chemically inert and substantially colorless, and said compound (G) being chemically bonded to the oxidant of the aromatic amine color developing agent left behind to form a compound which is chemically inert and substantially colorless. Accordingly, the use of the compound (F) and/or the compound (G) is preferred from the viewpoint of preventing the formation of a stain caused by the formation of developed dye formed by the reaction of the couplers with the color developing agent or the oxidant thereof left behind in the layers or preventing other side effects from being caused.
It is preferred that the light-sensitive materials of the present invention contain antifungal agents described in JP-A-63-271247 to prevent the image from being deteriorated by the growth of various molds or bacteria in the hydrophilic colloid layers.
Examples of supports which can be used for the light-sensitive materials of the present invention include white polyester supports for display and supports having a white pigment-containing layer on the silver halide emulsion layer side thereof. It is preferred that an antihalation layer is coated on the silver halide emulsion layer-coated side of the support or on the back side thereof. It is particularly preferred that the transmission density of the support is set to a value in the range of 0.35 to 0.8 so as to allow display to be enjoyed by reflected light as well as transmitted light.
The light-sensitive materials of the present invention may be exposed to visible light or infrared light. The exposure method may be a low-illumination exposure or a high-illumination exposure. In the latter case, a laser beam scanning exposure system wherein exposure time per one pixel is shorter than 10.sup.-4 seconds is preferred.
It is preferred that a band stop filter described in U.S. Pat. No. 4,880,726 is used when exposure is conducted, whereby light color mixing can be eliminated and color reproducibility can be greatly improved.
The light-sensitive materials of the present invention can be processed by conventional methods described in RD No. 17643, pp. 28-29 and RD No. 18716 (left column to right column of page 615). For example, a color development stage, a desilverization stage and a rinsing stage are carried out. In the desilverization stage, a bleaching-fixing stage may be carried out, instead of conducting separately a bleaching stage using a bleaching solution and a fixing stage using a fixing solution. A bleaching stage, a fixing stage and a bleaching-fixing stage may be arbitrarily arranged. A stabilization stage may be used in place of the rinsing stage. After the rinsing stage, the stabilization stage may be carried out. A monobath processing stage using a monobath developer bleaching fixer may be used in which color development, bleaching and-fixing are carried out by one bath. In combination with these stages, a prehardening stage, a neutralization stage therefor, a stop fixing stage, an after-hardening stage, a compensating stage and an intensification stage may be optionally used. An intermediate rinsing stage may be used between the above stages. An activator processing stage may be used in place of the color development stage in the processing described above.
Silver halide emulsions, other materials (e.g., additives), photographic constituent layers (e.g., layer arrangement), processing methods and processing additives described in the following patent publications, particularly EP 0,355,660A2 can be preferably applied to the present invention.
__________________________________________________________________________Photographicconstituent layer JP-A-62-215272 JP-A-2-33144 EP0,355,660A2__________________________________________________________________________Silver halide The 6th line of right The 16th line of right upper The 53th line of pageemulsion upper column of page 10 column of page 28 to the 45 to the 3rd line of to the 5th line of left 11th line of right lower page 47; and the 20th lower column of page 12; column of page 29; and line to the 22nd line and the 4th line from the 2nd line to the 5th of page 47 the bottom of right line of page 30 lower column of page 12 to the 17th line of left upper column of page 13Solvents for The 6th line to the 14th -- --silver halide line of left lower column of page 12; and the third line from the bottom of left upper column of page 13 to the bottom of left lower column of page 18Chemical The 3rd line from the The 12th line to the bottom The 4th line to thesensitizing bottom of left lower of right lower column 9th line of page 47agent column of page 12 of page 29 to the 5th line from the bottom of page 12; and the first line of right lower column of page 18 to the 9th line from the bottom of right upper column of page 22Spectral The 8th line from the The first line to the 13th The 10th line to thesensitizing bottom of right upper line of left upper column 15th line of page 47agent (spectral column of page 22 to of page 30sensitization the bottom of page 38method)Emulsion The 1st line of left upper The 14th line of left upper The 16th line to thestabilizer column of page 39 to the column of page 30 to the 19th line of page 47 bottom of right upper first line of right upper column of page 72 column of page 30Development The 1st line of left lower -- --accelerator column of page 72 to the 3rd line of right upper column of page 91Color coupler The 4th line of right The 14th line of right The 15th line to the(cyan, magenta upper column of page 91 upper column of page 3 27th line of page 4;and yellow to the 6th line of to the bottom of left the 30th line of pagecouplers) left upper column of upper column of page 18; 5 to the bottom of page 121 and the 6th line of right page 28; the 29th line upper column of page 30 to the 31st line of to the 11th line of page 45; and the 23rd right lower column of line of page 47 to the page 35 50th line of page 63Supersensitizing The 7th line of left upper -- --agent column of page 121 to the first line of right upper column of page 125Ultraviolet The 2nd line of right The 14th line of right The 22nd line to thelight upper column of page 125 lower column of page 37 31st line of page 65absorber to the bottom of left to the 11th line of left lower column of page 127 upper column of page 38Anti-fading The 1st line of right The 12th line of right The 30th line of pageagent (image lower column of page 127 upper column of page 36 to 4 to the 23rd line ofstabilizer) to the 8th line of left the 19th line of left page 5; the 1st line lower column of page 137 upper column of page 37 of page 29 to the 25th line of page 45; the 33rd line to the 40th line of page 45; and the 2nd line to the 21st line of page 65High-boiling The 9th line of left lower The 14th line of right lower The 1st line to theand/or low- column of page 137 to the column of page 35 to the 51st line of page 64boiling organic bottom of right upper 4th line from the bottomsolvent column of page 144 of left upper column of page 36Dispersion The 1st line of left lower The 10th line of right lower The 51st line ofmethod of column of page 144 to column of page 27 to the page 63 to the 56thphotographic the 7th line of right bottom of left upper column line of page 64additive upper column of page 146 of page 28; and the 12th line of right lower column of page 35 to the 7th line of right upper column of page 36Hardening The 8th line of right -- --agent upper column of page 146 to the 4th line of left lower column of page 155Developing The 5th line of left lower -- --agent column of page 155 to theprecursor 2nd line of right lower column of page 155Restrainer The 3rd line to the 9th -- --releasing line of right lower columncompound of page 155Support The 19th line of right The 18th line of right The 29th line of page lower column of page 155 upper column of page 38 to 66 to the 13th line to the 14th line of left the 3rd line of left upper of page 67 upper column of page 156 column of page 39Layer structure the 15th line of left The 1st line to the 15th The 41st line to the upper column of page 156 line of right upper column 52nd line of page 45 to the 14th line of right of page 28 lower column of page 156Dye The 15th line of right The 12th line of left The 18th line to the lower column of page 156 upper column of page 38 22nd line of page 66 to the bottom of right to the 7th line of right lower column of page 184 upper column of page 38Color mixing The 1st line of left The 8th line to the 11th The 57th line of pageinhibitor upper column of page 185 line of right upper column 64 to the 1st line of to the 3rd line of right of page 36 page 65 lower column of page 188Gradation The 4th line to the 8th -- --controller line of right lower column of page 188Stain The 9th line of right The bottom of left upper The 32nd line of pageinhibitor lower column of page 188 column of page 37 to the 65 to the 17th line of to the 10th line of right 13th line of right lower page 66 lower column of page 193 column of page 37Surfactant The 1st line of left lower The 1st line of right upper -- column of page 201 to column of page 18 to the the bottom of right upper bottom of right lower column column of page 210 of page 24; and the 10th line from the bottom of left lower column of page 27 to the 9th line of right lower column of page 27Fluorine- The 1st line of left The 1st line of left upper --containing lower column of page 210 column of page 25 to the 9thcompound to the 5th line of left line of right lower column(antistatic lower column of page 222 of page 27agent, coatingaid, lubricant,anti-stickingagent, etc.)Binder The 6th line of left The 8th line to the 18th The 23rd line to the(hydrophilic lower column of page 222 line of right upper 28th line of page 66colloid) to the bottom of left column of page 38 upper column of page 225Thickener The 1st line of right -- -- upper column of page 225 to the 2nd line of right upper column of page 227Antistatic the 3rd line of right -- --agent upper column of page 227 to the 1st line of left upper column of page 230Polymer latex The 2nd line of left upper -- -- column of page 230 to the bottom of page 239Matting agent The 1st line of left -- -- upper column of page 240 to the bottom of right upper column of page 240Photographic The 7th line of right The 4th line of left upper The 14th line of pageprocessing upper column of page 3 column of page 39 to the 67 to the 28th line ofmethod to the 5th line of right bottom of left upper column page 69(processing upper column of page 10 of page 42stage,additive, etc.)__________________________________________________________________________ Note The cited places of JPA-62-215272 include an amendment dated March 16, 1987 attached to the end of this publication. Among the abovedescribed couplers, short wave type yellow couplers described in JPA-63-231451, JPA-63-123047, JPA-63-241547, JPA-1-173499, JPA-1-213648, and JPA-1-250944 can be preferably used as the yellow couplers.

EXAMPLE
The present invention is now illustrated in greater detail by reference to the following examples which, however, are not to be construed as limiting the present invention in any way.
Example 1
There was weighed 16.1 g of yellow coupler Y-1, and 11.5 g of high-boiling organic solvent dibutyl phthalate was added thereto. Further, 24 ml of ethyl acetate was added thereto to dissolve them. The resulting solution was emulsified and dispersed in 200 g of a 10 wt % aqueous gelatin solution containing 1.5 g of sodium dodecylbenzenesulfonate.
The whole amount of the resulting emulsified dispersion was added to 247 g of a high silver chloride emulsion (silver content: 70.0 g/kg of emulsion, silver bromide content: 0.5 mol %), and the resulting emulsion was coated on an undercoated triacetate film base in such an amount as to give a coating weight of 1.73 g/m.sup.2 in terms of silver. Further, a gelatin layer as a protective layer was coated on the coated layer in such an amount as to give a dry thickness of 1.0 .mu., thus preparing a sample 101. Sodium salt of 1-oxy-3,5-di-chloro-s-triazine was used as a hardening agent for gelatin.
Emulsified dispersions were prepared in the same manner as in the preparation of the emulsified dispersion used in the preparation of the sample 101 except that couplers and dye image stabilizers (used in an amount of 100 mol % based on the amount of the coupler) were co-emulsified as indicated in Table A. In the same manner as in Example 1, emulsions were prepared by using each of the resulting emulsified dispersions, and coated to prepare samples 102 to 138.
Each of the thus-prepared samples was exposed to light through a wedge, and processed in the following processing stages.
______________________________________ Temperature TimeProcessing stage (.degree.C.) (sec.)______________________________________Color development 35 45Bleaching-fixing 30-35 45Rinse (1) 30-35 20Rinse (2) 30-35 20Rinse (3) 30-35 20Drying 70-80 60______________________________________
Each processing solution had the following composition.
______________________________________Color developing solutionWater 800 mlEthylenediamine-N,N,N',N'-tetramethyl- 1.5 gene phosphonic acidPotassium bromide 0.015 gTriethanolamine 8.0 gSodium chloride 1.4 gPotassium carbonate 25 gN-Ethyl-N-(.beta.-methanesulfonamidoethyl)- 5.0 g3-methyl-4-aminoaniline sulfateDisodium N,N-bis(sulfonatoethyl)- 5.5 ghydroxylamineFluorescent brightener 1.0 g(WHITEX 4B manufactured by SumitomoChemical Co., Ltd.)Water to make 1000 mlpH (25.degree. C.) 10.05Bleaching-fixing solutionWater 400 mlAmmonium thiosulfate (700 g/l) 100 mlSodium sulfite 17 gAmmonium (ethylenediaminetetraacetato) 55 giron (III)Disodium ethylenediaminetetraacetate 5 gAmmonium bromide 40 gWater to make 1000 mlpH (25.degree. C.) 6.0Rinsing solutionIon-exchanged water(The concentration of each of calcium ion andmagnesium ion being reduced to not higher than 3 ppm)______________________________________
Each of the samples 101 to 138 having a dye image formed thereon was exposed to light through an ultraviolet light absorbing filter (manufactured by Fuji Photo Film Co., Ltd.) which cut light having a wave-length of not longer than 400 nm for 8 days by using a xenon tester (illuminance: 200,000 lx). The yellow density (stain) of the unexposed area of each sample was measured, and the residual ratio of the density at an initial density of 1.0 was determined.
The measurement was made by using Fuji automatic recording densitometer.
The results are shown in Table A.
TABLE A______________________________________ Residual ratio of yellow density (initial density: 1.0, Xe: 200,000 1x Cou- Dye image for 8 days)Sample pler stabilizer Stain (%) Remarks______________________________________101 Y-1 -- 0.16 46 Comp. Ex.102 " Comparative 0.17 49 " compound 1103 " Comparative 0.20 48 " compound 2104 " Comparative 0.17 42 " compound 3105 " Comparative 0.18 44 " compound 4106 " Comparative 0.19 47 " compound 5107 " Comparative 0.19 42 " compound 6108 " Comparative 0.23 38 " compound 7109 " Comparative 0.21 29 " compound 8110 " Comparative 0.20 28 " compound 9111 " Comparative 0.18 39 " compound 11112 " Comparative 0.16 55 " compound 12113 " I-a-1 0.14 75 Invention114 " I-a-10 0.12 82 "115 " I-a-14 0.13 78 "116 " II-a-3 0.11 84 "117 " II-a-9 0.12 80 "118 " II-a-15 0.11 85 "119 " III-3 0.12 76 "120 Y-1 III-10 0.13 78 Invention121 " III-14 0.12 82 "122 " III-17 0.11 81 "123 Y-3 -- 0.16 45 Comp. Ex.124 " Comparative 0.17 48 " compound 4125 " Comparative 0.19 42 " compound 11126 " Comparative 0.17 49 " compound 12127 " I-a-10 0.11 82 Invention128 " II-a-9 0.11 80 "129 " III-3 0.11 84 "130 " III-14 0.11 83 "131 Y-6 -- 0.16 42 Comp. Ex.132 " Comparative 0.16 46 " compound 4133 " Comparative 0.17 47 " compound 11134 " Comparative 0.16 48 " compound 12135 " I-a-10 0.12 86 Invention136 " II-a-9 0.11 82 "137 " III-3 0.11 85 "138 " III-14 0.11 84 "______________________________________ ##STR11##
It can be seen from the above results that the compounds of the present invention are effective in preventing dye images from being faded by light and are also effective in preventing unexposed areas from being yellowed. The results show that the compounds of the present invention have an excellent effect which cannot be expected from conventional compounds.
Example 2
A sample 201 was prepared in the same manner as in the preparation of the sample 101 of Example 1 except that 16.1 g of magenta coupler (M-1) was used in place of yellow coupler used in the sample 101 of Example 1.
Emulsified dispersions were prepared in the same manner as in the preparation of the emulsified dispersion used in the preparation of the sample 201 except that couplers and dye image stabilizers (used in an amount of 100 mol % based on the amount of the coupler) were co-emulsified as indicated in Table B. In the same manner as in the preparation of the sample 201, emulsions were prepared by using each of the resulting emulsified dispersions and coated to prepare samples 202 to 222.
The same comparative compounds as those used in Example 1 were used.
In the same manner as in Example 1, each of the thus-prepared samples was exposed and processed. Each of the samples 201 to 222 having a dye image formed thereon was exposed to light though an ultraviolet light absorbing filter (manufactured by Fuji Photo Film Co., Ltd.) which cut light having a wavelength of not longer than 400 nm for 10 days by using a xenon tester (illuminance: 200,000 lx). The yellow density (stain) of the unexposed area of each sample was measured, and the residual ratio of the density at an initial density of 1.0 was determined.
The measurement was made by using Fuji automatic recording densitometer.
The results are shown in Table B.
TABLE B______________________________________ Residual ratio of magenta density (initial density: 1.0, Xe: 200,000 1x Cou- Dye image for 10 days)Sample pler stabilizer Stain (%) Remarks______________________________________201 M-1 -- 0.14 6 Comp. Ex.202 " Comparative 0.15 49 " compound 2203 " Comparative 0.16 48 " compound 5204 " Comparative 0.15 42 " compound 12205 " I-a-10 0.12 80 Invention206 " II-a-9 0.11 82 "207 " III-3 0.11 85 "208 " III-14 0.12 84 "209 M-4 -- 0.15 12 Comp. Ex.210 " Comparative 0.15 55 " compound 2211 " Comparative 0.15 39 " compound 12212 " I-a-1 0.12 87 Invention213 " I-a-10 0.13 88 "214 " II-a-10 0.12 86 "215 " III-3 0.12 85 "216 " III-10 0.13 84 "217 M-8 -- 0.20 5 Comp. Ex.218 " Comparative 0.20 42 " compound 5219 " I-a-10 0.17 82 Invention220 " II-a-10 0.18 78 "221 " III-3 0.17 86 "222 " III-17 0.17 85 "______________________________________
It can be seen from the above results that when magenta couplers are used, the compounds of the present invention have an excellent anti-fading effect, and the effect obtained thereby is very superior in comparison with comparative compounds.
Example 3
A sample 301 was prepared in the same manner as in the preparation of the sample 101 of Example 1 except that 9.8 g of cyan coupler (C-1) was used in place of yellow coupler used in the sample 101 of Example 1.
Emulsified dispersions were prepared in the same manner as in the preparation of the emulsified dispersion used in the preparation of the sample 101 of Example 1 except that couplers and dye image stabilizers (used in an amount of 100 mol % based on the amount of the coupler) were co-emulsified as indicated in Table C. In the same manner as in the preparation of the sample 101 of Example 1, emulsions were prepared by using each of the resulting emulsified dispersions and coated to prepare samples 301 to 312.
In the same manner as in Example 1, each of the thus-obtained samples was exposed and processed. Each of the samples 301 to 312 having a dye image formed thereon was exposed to light through an ultraviolet light absorbing filter (manufactured by Fuji Photo Film Co., Ltd.) which cut light having a wavelength of not longer than 400 nm for 8 days by using a xenon tester (illuminance: 200,000 lx). The yellow density (stain) of the unexposed area of each sample was measured, and the residual ratio of the density at an initial density of 1.0 was determined.
The measurement was made by using Fuji automatic recording densitometer.
The results are shown in Table C.
TABLE C______________________________________ Residual ratio of cyan density (initial density: 1.0, Xe: 200,000 1x Cou- Dye image for 8 days)Sample pler stabilizer Stain (%) Remarks______________________________________301 C-1 -- 0.18 48 Comp. Ex.302 " Comparative 0.20 50 " compound 6303 " Comparative 0.19 48 " compound 8304 " Comparative 0.18 49 " compound 11305 " I-a-1 0.11 78 Invention306 " II-a-10 0.15 80 "307 " III-3 0.16 84 "308 " III-10 0.17 82 "309 C-5 -- 0.22 32 Comp. Ex.310 " Comparative 0.24 30 " compound 12311 " I-a-10 0.20 78 Invention312 " II-a-9 0.18 80 "______________________________________
It can be seen from the above results that when cyan couplers are used, the compounds of the present invention have an excellent anti-fading effect and the effect obtained thereby is very superior in comparison with comparative compounds.
Example 4
Both sides of a paper support were laminated with polyethylene. The surface of the polyethylene-laminated paper support was subjected to a corona discharge treatment, and then coated with a gelatin undercoat layer containing sodium dodecylbenzenesulfonate. Further, various photographic constituent layers were coated thereon to prepare a multi-layer color photographic paper having the following layer structure (sample 101). Coating solutions were prepared in the following manner.
Preparation of Coating Solution for First Layer
There was dissolved 153.0 g of yellow coupler (ExY) in 25 g of solvent (Solv-1), 25 g of solvent (Solv-2) and 180 cc of ethyl acetate. The resulting solution was emulsified and dispersed in 1,000 g of a 10% aqueous gelatin solution containing 60 cc of 10% sodium dodecylbenzenesulfonate and 10 g of citric acid to prepare an emulsified dispersion A. Separately, a silver chlorobromide emulsion A (cubic; a 3:7 (by mol of Ag) mixture of a larger-size emulsion A having an average grain size of 0.88 .mu.m and a smaller-size emulsion A having a mean grain size of 0.70 .mu.m; a coefficient of variation in a grain size distribution: 0.08 and 0.10, respectively; 0.3 mol % of silver bromide being localized on a part of the surface of the grain in each size emulsion) was prepared. The following blue-sensitive sensitizing dyes A and B were added to the emulsion (2.0.times.10.sup.-4 mol of each of the dyes A and B was added to the larger-size emulsion A, and 2.5.times.10.sup.-4 mol of each of them was added to the smaller-size emulsion A). The chemical ripening of the emulsion was carried out by adding a sulfur sensitizing agent and a gold sensitizing agent. The above emulsified dispersion A and the silver chlorobromide emulsion A were mixed and dissolved, and a coating solution for the first layer was prepared so as to give the following composition.
Coating solutions for the second layer through the seventh layer were prepared in the same manner as in the preparation of the coating solution for the first layer. Sodium salt of 1-oxy-3,5-dichloro-s-triazine was used as the hardening agent for gelatin in each layer.
Further, Cpd-10 and Cpd-11 were added to each layer in such an amount as to give the total weights of 25.0 mg/m.sup.2 and 50.0 mg/m.sup.2, respectively.
The following spectral sensitizing dyes were used for the silver chlorobromide emulsion in each light-sensitive emulsion layer. ##STR12##
Further, 8.5.times.10.sup.-5 mol, 7.7.times.10.sup.-4 mol and 2.5.times.10.sup.-4 mol of 1-(5-methylureidophenyl)-5-mercaptoethanol were added to the blue-sensitive emulsion layer, the green-sensitive emulsion layer and the red-sensitive emulsion layer, respectively, each amount being per mol of silver halide.
Further, 1.times.10.sup.-4 mol and 2.times.10.sup.-4 mol of 4-hydroxy-6-methyl-1,3,3a,7-tetrazaindene were added to the blue-sensitive emulsion layer and the green-sensitive emulsion layer, respectively, each amount being per mol of silver halide.
The following dyes (parenthesized numerals being coating weights) were added to the emulsion layers to prevent irradiation. ##STR13##
Layer Structure
Each layer had the following composition. Numerals represent coating weight (g/m.sup.2). The amounts of the silver halide emulsions are represented by coating weight in terms of silver.
Support
Polyethylene-laminated paper [Polyethylene on the first layer side contained white pigment (TiO.sub.2) and bluish dye (ultramarine)]
______________________________________First layer (blue-sensitive emulsion layer)The above silver chlorobromide 0.27emulsion AGelatin 1.36Yellow coupler (ExY) 0.79Solvent (Solv-1) 0.13Solvent (Solv-2) 0.13Second layer (color mixing inhibiting layer)Gelatin 1.00Color mixing inhibitor (Cpd-4) 0.06Solvent (Solv-7) 0.03Solvent (Solv-2) 0.25Solvent (Solv-3) 0.25Third layer (green-sensitive emulsion layer)Silver chlorobromide emulsion B 0.13(cubic; a 1:3 (by mol of Ag) mixtureof a larger-size emulsion B having amean grain size of 0.55 .mu.m anda smaller-size emulsion B havinga mean grain size of 0.39 .mu.m;a coefficient of variationin a grain size distribution:0.10 and 0.08, respectively;0.8 mol % of AgBr being localizedon a part of the surface ofthe grain in each size emulsion)Gelatin 1.45Magenta coupler (ExM) 0.16Dye image stabilizer (Cpd-5) 0.15Dye image stabilizer (Cpd-2) 0.03Dye image stabilizer (Cpd-6) 0.01Dye image stabilizer (Cpd-7) 0.01Dye image stabilizer (Cpd-8) 0.08Solvent (Solv-3) 0.50Solvent (Solv-4) 0.15Solvent (Solv-5) 0.15Fourth layer (color mixing inhibiting layer)Gelatin 0.70Color mixing inhibitor (Cpd-4) 0.04Solvent (Solv-7) 0.02Solvent (Solv-2) 0.18Solvent (Solv-3) 0.18Fifth layer (red-sensitive emulsion layer)Silver chlorobromide emulsion C 0.18(Cubic; a 1:3 (by mol of Ag) mixtureof a larger-size emulsion C having amean grain size of 0.50 .mu.m anda smaller-size emulsion C havinga mean grain size of 0.41 .mu.m;a coefficient of variarionin a grain size of distribution:0.09 and 0.11, respectively;0.8 mol % of AgBr being localizedon a part of the surface ofthe grain in each size emulsion)Gelatin 0.85Cyan coupler (ExC) 0.25Ultraviolet light absorber (UV-2) 0.18Dye image stabilizer (Cpd-1) 0.25Dye image stabilizer (Cpd-6) 0.01Dye image stabilizer (Cpd-7) 0.01Dye image stabilizer (Cpd-8) 0.03Dye image stabilizer (Cpd-9) 0.01Dye image stabilizer (Cpd-10) 0.01Solvent (Solv-6) 0.20Solvent (Solv-1) 0.01Sixth layer (ultraviolet light absorbing layer)Gelatin 0.55Ultraviolet light absorber (UV-1) 0.38Dye image stabilizer (Cpd-12) 0.15Dye image stabilizer (Cpd-5) 0.02Seventh layer (protective layer)Gelatin 1.13Acrylic-modified copolymer of polyvinyl 0.05alcohol (a degree of modification: 17%)Liquid paraffin 0.02Dye image stabilizer (Cpd-13) 0.01(ExY) Yellow coupler ##STR14## ##STR15##and1:1 mixture (by mol) ##STR16##(ExM) Magenta coupler ##STR17##(ExC) Cyan coupler ##STR18## ##STR19##(Cpd-4) Color mixing inhibitor ##STR20##(Cpd-5) Dye image stabilizer ##STR21##(Cpd-6) ##STR22##(Cpd-7) ##STR23##(Cpd-8) Dye image stabilizer ##STR24##(Cpd-9) Dye image stabilizer ##STR25##(Cpd-10) Dye image stabilizer ##STR26##(Cpd-11) ##STR27##(Cpd-12) ##STR28##(Cpd-13) ##STR29##(Cpd-14) Antiseptic ##STR30##(Cpd-15) Antiseptic ##STR31##(UV-1) Ultraviolet light absorber ##STR32## ##STR33## ##STR34## ##STR35##(UV-2) Ultraviolet light absorber ##STR36## ##STR37## ##STR38##(Solv-1) Solvent ##STR39##(Solv-2) Solvent ##STR40##(Solv-3) Solvent ##STR41##(Solv-4) Solvent ##STR42##(Solv-5) Solvent ##STR43##(Solv-6) Solvent ##STR44##(Solv-7) Solvent ##STR45##______________________________________
Each sample was subjected to gradation exposure through a three-color separation filter for sensitometry by using a sensitometer (FWH type, color temperature of light source: 3,200.degree. K. manufactured by Fuji Photo Film Co., Ltd.). The exposure time was 0.1 second, and the exposure amount was 250 MSC.
The exposed sample was subjected to continuous processing (running test) by using a paper processor until the replenishment rate reached twice the tank capacity of the color developing solution. The following processing stages and the following processing solutions were used.
______________________________________ Replenish- TankProcessing stage Temp. Time ment rate* capacity______________________________________Color 35.degree. C. 45 sec 161 ml 17 ldevelopmentBleaching-fixing 30-35.degree. C. 45 sec 215 ml 17 lRinse 30.degree. C. 90 sec 350 ml 10 lDrying 70-80.degree. C. 60 sec______________________________________ *Replenishment rate being per m.sup.2 of lightsensitive material
Each processing solution had the following composition.
______________________________________ Tank Re-Color developing solution Solution plenisher______________________________________Water 800 ml 800 mlEthylenediamine-N,N,N',N'- 1.5 g 2.0 gtetramethylenephosphonic acidPotassium bromide 0.015 gTriethanolamine 8.0 g 12.0 gSodium chloride 1.4 gPotassium carbonate 25 g 25 gN-Ethyl-N-(.beta.-methanesulfon- 5.0 g 7.0 gamidoethyl)-3-methyl-4-aminoaniline sulfateN,N-Bis(carboxymethyl)- 4.0 g 5.0 ghydrazineMonosodium salt of N,N-bis- 4.0 g 5.0 g(sulfoethyl)hydroxylamineFluorescent brightener 1.0 g 2.0 g(WHITEX 4B manufacture bySumitomo Chemical Co., Ltd.)Water to make 1000 ml 1000 mlpH (25.degree. C.) 10.05 10.45______________________________________Bleaching-fixing solutionTank solution and replenisher being the same.______________________________________Water 400 mlAmmonium thiosulfate (700 g/l) 100 mlSodium sulfite 17 gAmmonium (ethylenediaminetetraacetato) 55 giron (III)Disodium ethylenediaminetetraacetate 5 gAmmonium bromide 40 gWater to make 1000 mlpH (25.degree. C.) 6.0______________________________________Rinsing waterTank solution and replenisher being the same.______________________________________Ion-exchanged water(The concentration of each of calcium ion andmagnesium ion was reduced to not higher than 3 ppm).______________________________________
The thus-obtained sample was referred to as sample 1A. Samples 2A to 8A were prepared in the same manner as in the preparation of the sampler 1A except that the yellow coupler used in the first layer was co-emulsified with dye image stabilizer as indicated in Table D. An equimolar amount of each compound was used.
The same comparative compounds as those used in Example 1 were used.
Each of the samples having a dye image formed thereon was subjected to a fading test. The evaluation of an anti-fading effect was made by determining the residual ratio of yellow density at an initial density of 2.0 after the samples were exposed to light for 10 days by using a xenon tester (illuminance: 200,000 lx).
The results are shown in Table D.
TABLE D______________________________________ Residual ratio of yellow density (initial density: 2.0, Xe: 200,000 1x Cou- Dye image for 10 days)Sample pler stabilizer Stain (%) Remarks______________________________________1A ExY -- 0.14 66 Comp. Ex.2A " Comparative 0.17 64 " compound 113A " Comparative 0.18 70 " compound 124A " I-a-10 0.11 85 Invention5A " I-a-9 0.11 84 "6A Y-10 -- 0.16 51 Comp. Ex.7A " III-3 0.12 82 Invention8A " III-14 0.2 80 "______________________________________
It can be seen form Table 5 that the samples of the present invention which contain the compounds of the present invention have an excellent effect as in Example 1 even when the samples are multi-layer light-sensitive materials.
Example 5
Samples were prepared in the same manner as in the preparation of the sample 101 of Example 1 of JP-A-2-854 except that the compound (I-a-l),. (I-a-10), (II-a-12), (III-10) or (III-18) of the present invention in an amount of 25 mol % based on the amount of the coupler was added to the third layer, the fourth layer and the fifth layer of the sample 101.
Further, samples were prepared in the same manner as in the preparation of the sample 101 except that the compound (I-a-16), (I-a-21), (II-a-3), (III-18) or (III-21) of the present invention in an amount of 25 mol % based on the amount of the coupler was added to the 12th layer and the 13th layer of the sample 101.
In the same manner as in Example 1 of JP-A-2-854, the samples were exposed, processed and subjected to a fading test. It was found that the compounds of the present invention had an excellent anti-fading effect a good effect on photographic characteristics.
Accordingly, it was found that the compounds of the present invention have an excellent effect, even when used in the above light-sensitive material.
Example 6
Samples were prepared in the same manner as in the preparation of the color photographic material of Example 2 of U.S. Pat. No. 5,079,132 except that an equimolar amount of the compound (I-a-10), (I-a-16), (II-a-6), (III-10) or (III-15) of the present invention was used in place of Cpd-9 used in the 6th layer and the 7th layer of the color photographic material of Example 2 of U.S. Pat. No. 5,079,132.
Further, samples were prepared in the same manner as in the preparation of the color photographic material of Example 2 of U.S. Pat. No. 5,079,132 except that an equimolar amount of the compound (I-a-16), (I-a-21), (II-a-3), (III-18) or (III-21) of the present invention was used in place of Cpd-6 used in the 11th layer and 12th layer of the color photographic material of Example 2 of U.S. Pat. No. 5,079,132.
In the same manner as in Example 2 of U.S. Pat. No. 5,079,132, these samples were exposed, processed and subjected to a fading test to examine photographic characteristics. It was found that the samples of the present invention had an excellent anti-fading effect and good photographic characteristics.
Accordingly, it was found that the compounds of the present invention had an excellent effect even when used in the above light-sensitive material.
Example 7
Samples were prepared in the same manner as in the preparation of the sample 101 of Example 1 of U.S. Pat. No. 5,071,736 except that the compound (I-a-l), (I-a-10), (II-a-12), (III-10) or (III-18) of the present invention in an amount of 25 mol % based on the amount of the coupler was used in each of the 12th layer and the 13th layer of the sample 101.
In the same manner as in Example 1 of U.S. Pat. No. 5,071,736, these samples were exposed, processed and subjected to a fading test. It was found that the samples of the present invention had an excellent anti-fading effect and good photographic characteristics.
Accordingly, it was found that the compounds of the present invention had an excellent effect even when used in the above light-sensitive material.
It will be understood from the above disclosure that according to the present invention there can be obtained a silver halide color photographic material which gives a dye image with good color reproducibility after processing and is greatly improved in fastness to light in comparison with conventional anti-fading agents, and moreover which scarcely suffers from the formation of stain in the unexposed area and gives well-balanced color in connection with fading.
While the present invention has been described in detail and with reference to specific embodiments thereof, it is apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and the scope of the present invention.

Number	Name	Date
4540658	Sasaki et al.	Sep 1985
4704350	Morigaki et al.	Nov 1987
4880733	Kaneko	Nov 1989
5082766	Nishijima et al.	Jan 1992
5104781	Seto et al.	Apr 1992
5232821	Merkel et al.	Aug 1993

Number	Date	Country
0178794	Apr 1986	EPX
0310551	Sep 1988	EPX
0310552	Sep 1988	EPX
0510576	Oct 1992	EPX
62-103642	May 1987	JPX
63-43146	Feb 1988	JPX
63-149644	Jun 1988	JPX
1410846	Oct 1975	GBX

Silver halide color photographic material

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

Priority Claims (1)

US Referenced Citations (6)

Foreign Referenced Citations (8)