USH567H - Silver halide color photographic light-sensitive materials containing cyan coupler and specific compound - Google Patents
Silver halide color photographic light-sensitive materials containing cyan coupler and specific compound Download PDFInfo
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- USH567H USH567H US06/932,875 US93287586A USH567H US H567 H USH567 H US H567H US 93287586 A US93287586 A US 93287586A US H567 H USH567 H US H567H
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/3003—Materials characterised by the use of combinations of photographic compounds known as such, or by a particular location in the photographic element
- G03C7/3005—Combinations of couplers and photographic additives
- G03C7/3006—Combinations of phenolic or naphtholic couplers and photographic additives
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- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/32—Colour coupling substances
- G03C7/34—Couplers containing phenols
- G03C7/344—Naphtholic couplers
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Abstract
A silver halide color photographic light sensitive material contains (i) at least one of cyan dye-forming coupler represented by formula (I) and cyan dye-forming couplers derived therefrom (ii) and at least one of compounds represented by formula (II), (III), (V), (VI), (VII) or (VIII) and compounds derived therefrom; ##STR1## wherein the symbols are defined as in claim 1.
Description
This invention relates to a silver halide color photographic light-sensitive material and more particularly to a silver halide color photographic light-sensitive material which does not cause the reduction of coloring density even in the case of processing using, in particular, a bleach or blix liquid fatigued or having weak oxidative power. The invention also produces a restrained occurrence of stain by the light exposure of the color photographic material for a long period of time after processing.
When a silver halide color photographic light-sensitive material is, after imagewise exposure, colordeveloped, the dye-forming coupler(s) (hereinafter, referred to as simply coupler) in the light-sensitive material reacts with the oxidation product of an aromatic primary amine developing agent to form color images.
Recently, couplers which are used for silver halide color photographic materials are required to have various properties. For example, the couplers are required to have properties such as excellent stability, processability, coloring property, and hue of the color images formed therefrom. The color images formed therefrom should be fast, able to be produced at low cost and excellent in production qualities, etc.
Hitherto, phenolic couplers and naphtholic couplers have been used as cyan couplers. In particular, 1-naphthol couplers are excellent in color reproduction since the colored dyes formed therefrom have an absorption maximum (λmax) at a long wavelength region and have less side absorption in the green region. In addition 1-naphthol couplers excellent in coloring property can be produced at a low cost and are excellent in production qualities. Thus, such cyan couplers have been widely used for color negative photographic materials.
However, conventional phenolic couplers and naphtholic couplers, in particular 2-alkylcarbamoyl-1-naphtholic couplers have a disadvantage that if a bleach liquid or blix liquid in a bleach step or blix step in a color photographic process is fatigued or has a weak oxidative power, color images having sufficient quality cannot be obtained. This phenomenon is considered to be caused by the reductive fading of cyan dyes by a ferrous ion formed in the bleach or blix step. Also, the cyan images formed from these couplers have a disadvantage of being low in color fastness.
The former disadvantage in naphtholic couplers can be eliminated by changing the substituent of the carbamoyl group at the 2-position from an alkyl group to an aryl group to convert the couplers to 2-arylcarbmoyl-1-naphtholic couplers (as described, for example, in U.S. Pat. No. 3,488,193). However, the latter disadvantage of the couplers has not yet been sufficiently solved and hence it is not always desired from the point of image stability to use only the naphthlic coupler as a cyan coupler in color photographic materials.
On the other hand, in regard to naphtholic couplers, the 1-naphtholic couplers having a specific substituent at the 5-position as disclosed in Japanese Patent Application (OPI) No. 237448/85, and European Patent 161626 (the term "OPI" as used herein means an "unexamined published application") have successfully eliminated the above-described two disadvantages and hence are excellent in performance but also have the following disadvantages. That is, one of the disadvantages is that when a color photographic material containing the coupler is exposed to light for a long period of time after processing, brown coloring or stain is formed. Another disadvantage is that the couplers are insufficient in coloring property and are lacking in aptitude for high-speed light-sensitive materials which have been required recently. In particular, the former disadvantage is a large problem since the stain formed causes the reduction in color reproducibility of the color photographic materials.
The first object of this invention is to provide a silver halide color photographic material having no reduction of cyan coloring density even when processed with a bleach or blix liquid fatigued or having a weak oxidative power.
The second object of this invention is to provide a silver halide color photographic material having a restrained occurrence of stain by a light-exposure of the color photographic material for a long period of time after processing.
It has now been discovered that the above-described objects can be attained by the silver halide color photographic material of this invention as set forth hereinbelow.
That is, the invention provides a silver halide color photographic light-sensitive material having on a support at least one light-sensitive silver halide emulsion layer, wherein the color photographic light-sensitive material contains (i) at least one cyan dye-forming coupler selected from the group consisting of compounds represented by following formula [I] and a compound having at least two coupler residue derived from the compound represented by formula [I] and (ii) at least one compound selected from the group consisting of compounds represented by formula [II], [III], [IV], [V], [VI], [VII] or VIII] and a compound having at least two residues derived from at least one compound selected from the same group: ##STR2## wherein, R1 represents --CONR6 R7, --NHCOR6, --NHCOOR8, --NHSO2 R8, --NHCONR6 R7, or --NHSO2 NR6 R7 (wherein, R6 and R7, which may be the same or different, each represents a hydrogen atom, an aliphatic group, an aromatic group, or a heterocyclic group and R8 represents an aliphatic group, an aromatic group, or a heterocyclic group), R2 represents a group capable of being substituted to a naphthalene ring; l represents an integer of from 0 to 3; R3 represents a mono-valent group: and X represents a hydrogen atom or a group capable of releasing by a coupling reaction with the oxidation product of an aromatic primary amine developing agent. When l is 2 or 3 the R2 groups may be the same or different or they may further combine with each other to form a ring when they are adjacent to each other. Also, said R2 and R3 groups or said R3 and X groups may combine with each other to form a ring when R2 is present at 6-position.
The compounds of formulae [II]-[V] are represented by the folowing structures: ##STR3## wherein
M represents Cu, Co, Ni, Pd, or Pt; R2, R3, R4, and R5 each represents a hydrogen atom, a halogen atom, a hydroxy group, a cyano group, an alkyl group, aryl group, cycloalkyl group, or heterocyclic group bonded to the carbon atom of the benzene ring directly or through a divalent linkage group, or a non-metallic atomic group necessary for forming a 6-membered ring by the combination of said R2 and R3, said R3 and R4, or said R4 and R5 with each other;
R6, R9, and R10 each represents a hydrogen atom, an alkyl group, or an aryl group;
R7 represents a hydrogen atom, an alkyl group, an aryl group, or a hydroxy group:
R8 represents an alkyl group, an aryl group, or a non-metallic atomic group necessary for forming a 5-membered to 8-membered ring by the combination of said R8 and R9 or R9 and R10 with each other; and
Y represents a non-metallic atomic group necessary for forming a 5-membered ring or a 6-membered ring.
The compounds of formulae [VI]- [VIII] are represented by the following structures: ##STR4## wherein,
R24 represents an aliphatic group, an aromatic group, a heterocyclic group an aliphatic oxy group, an aromatic oxy group, an aliphatic thio group, an aromatic thio group, an aliphatic carbonamido group, an aromatic carbonamido group, an aliphatic sulfonamido group, an aromatic sulfonamido group, a mono-substituted or disubstituted amino group with aliphatic or aronatic groups, and m represents an integer of 1 to 4. When said m is plural, said R24 groups may be the same or different or may combine with each other to form a ring when they are adjacent to each other. The two hydroxy groups are para-position or ortho-position relative to each other.
R25 represents an aliphatic group, an aromatic group, a heterocyclic group, or a substitued silyl group; R26 has the same significance as defined above for R24 in formula [VI]; n represents an integer of 1 to 3; and j represents an integer of 0 to 5, the sum of n and j being, however, 6 or less. When n is plural, said OR25 groups may be the same or different. When said j is plural, said R26 groups may be the same or different, and when said two OR25 groups, said two R26 groups, or said OR25 and R26 are in a ortho-position relative to each other, they may combine with each other to form a ring.
R27, R28, R29, and R30 each represents a hydrogen atom or an aliphatic group; Y represents a hydrogen atom, an aliphatic group, an acyl group, an aliphatic sulfonayl group, an aromatic sulfonyl group, an aliphatic sulfinyl group, an aromatic sulfinyl group, an aliphatic oxycarbonyl group, an aromatic oxycarbonyl group, an oxyradical group, or a hydroxy group; and Z represents a non-metallic atomic group necessary for forming a 5-membered to 7-membered ring with ##STR5## OR25 and R26 1 in formula VII may be present at any position on the benzene ring.
In the present invention an aliphatic group, an aromatic group and a heterocyclic group are defined as below unless they are defined specifically.
The aliphatic group preferably has from 1 to 32 carbon atoms and may be a saturated or unsaturated, substituted or unsubstituted, or straight chain, branched or cyclic alkyl, alkenyl or alkynyl group. Specific examples of an aliphatic group include a methyl group, an ethyl group, a butyl group, a cyclohexyl group, an allyl group, a t-butyl group, a 1,1-dimethylpropyl group, a 1,1-dimethylbutyl group, a 1,1,3,3-tetramethylbutyl group, a 2-hexyl group, a 2-decyl group, a 2-ethylhexyl group, a 3,5,5-trimethylhexyl group, a 2-dodecyl group, a 2-hexyl group, a 2-hexyldecyl group, a 9-octadecenyl group, a butoxy-ethyl group, a benzyl group, a phenetyl group, a 3-dodecyl-oxypropyl group, a 3-decyloxypropyl group, a 3-dodecylthiopropyl group, a propargyl group, a methoxyethyl group, an n-decyl group, an n-dodecyl group, an n-hexadecyl group, a trifluoromethyl group, a heptafluoropropyl group, a dodecyloxypropyl group, a 2,4-di-tert-amylphenoxypropyl group, a 2,4-di-tert-amylphenoxybutyl group, etc.
The aromatic group in this invention preferably has from 6 to 32 carbon atoms and may be a substituted or unsubstituted aromatic group and includes, for example, a phenyl group, a tolyl group, a 2-tetradecyloxyphenyl group, a pentafluorophenyl group, a 2-chloro-5-dodecyloxycarbonylphenyl group, a 4-chlorophenyl group, a 4-cyanophenyl group, a 4-hydroxyphenyl group, etc.
The heterocyclic group in this invention is a 5-7 membered heterocylcic group having at least one of N, O and S atom as a hetero atom and may be a substituted or unsubstituted. Examples of heterocyclic group include a 2-pyridyl group, a 4-pyridyl group, a 2-furyl group, a 4-thienyl group, a quinolinyl group, etc.
Examples of substituents for the above described aliphatic, aromatic and heterocyclic group are those which are commonly used for such a group, that is, a halogen atom, a nitro group, a cyano group, an acyl group, an acyloxy group, an alkyl or aryl sulfonyl group, a hydroxy group, an amido group, an amino group (may be mono- or di-substituted with an aliphatic or aromatic group), an alkyl group, an alkenyl group and aryl group (hereinafter these substituents are referred to as substituents A).
The substituents R1, R2, R3 and X in formula [I] described above are explained herein below in detail.
R1 in formula [I] represents --CONR6 R7, --NHCOR6, --NHCOOR8, --NHSO2 R8, --NHCONR6 R7, or --NHSO2 NR6 R7. Examples of R6, R7, and R8 groups include an aliphatic group having 1 to 30 carbon atoms, an aromatic group having 6 to 30 carbon atoms, and a heterocyclic group having 2 to 30 carbon atoms. The R6 and R7 groups each may be a hydrogen atom.
R2 represents a group or an atom substitutable to the naphthalene ring, such as a halogen atom, a hydroxy group, --NR6 'R7 ', a carboxy group, a sulfonic acid group, a cyano group, an aliphatic group, an aromatic group, a heterocyclic group, --NHCOR6 ', --NHSO2 R6 ', --CONR6 'R7 ', --SO2 NR6 'R7 ', --NHCONR6 'R7 ', --COR6 ', --OCR6 ',--OR8 ', --SR8 --SO2 R8 ', --NHSO2 NR6 R7, a nitro group, an acid imido group, etc., wherein R6 ', R7 ' and R8 ' have the same meaning as defined for R6, R7 and R8, respectively. The carbon number included in R2 is from 0 to 30. When l=2, as examples of a R2 group which forms a ring includes a dioxymethylene group, etc.
R3 represents a mono-valent group and is preferably shown by following formula [IX]:
R.sub.9 (Y.sub.1).sub.n -- [IX]
wherein, Y1 represents >NH,>Co, or >SO2, n represents 0 or 1; and R9 represents a hydrogen atom, an aliphatic group having 1 to 30 carbon atoms, an aromatic group having 6 to 30 carbon atoms, a heterocyclic group having 2 to 30 carbon atoms, --OR10, --COR10, ##STR6## --CO2 R12, --SO2 R12, or --SO2 OR12 (wherein, R10, R11, and R12 have the same meaning as defined above in R6, R7, and R8, respectively).
Also, R6 and R7 of ##STR7## in R1, R6 ' and R7 ' of ##STR8## in R2, and R10 and R11 of ##STR9## in R9 may combine with each other to form a nitrogen-containing heterocyclic ring (e.g., a morpholine ring, piperidine ring, pyrrolodine ring, etc.).
X in formula [I]described above represents a hydrogen atom or a coupling releasing group (including releasing atom). Specific examples of the coupling releasing group include a halogen atom, --OR13, --SR13, ##STR10## (wherein, R13 represents an aliphatic group having 1 to 30 carbon atoms, an aromatic group having 6 to 30 carbon atoms, or a heterocyclic group having 2 to 30 carobn atoms), an aromatic azo group having 6 to 30 carbon atoms, a heterocyclic group having 2 to 30 carbon atoms (e.g., succinic acid imido group, a phthalic acid imido group, a hydantoinyl group, a pyrazoline group, a 2-benzotriazolyl group, etc.) bonded to the coupling active position of the coupler by a nitrogen atom, etc.
Preferred substituents R1, R2, R3 and X for the cyan couplers shown in formula [I] described above are explained in detail hereinbelow.
R1 in formula [I] is preferably --CONR6 R7 and includes, preferably, a carbamoyl group, an ethylcarbamoyl group, a morpholinocarbonyl group, a dodecylcarbamoyl group, a hexadecylcarbamoyl group, a decyloxypropylcarbamoyl group, a dodecyloxypropylcarbamoyl group, a 2,4-di-tert-amylphenoxypropylcarbamoyl group, a 2,4-di-tert-amylphenoxybutylcarbamoyl group, etc.
Regarding R2 and l, it is most preferred that l is 0 and R2, if any, is preferably a halogen atom (F, Cl, Br or I), an aliphatic group, a carbonamido group, a sulfonamido group, etc.
Preferably R3 in formula [I] is when n in formula [IX] described above is 0 and also R9 in formula [IX] is --COR10 (such as a formyl group, an acetyl group, a trifluoroacetyl group, a chloroacetyl group, a benzoyl group, a pentafluorobenzyl group, a pchlorobenzoyl group, etc.), --COOR12 (e g., a methoxycarbonyl group, an ethoxycarbonyl group, a butoxycarbonyl group, a decyloxycarbonyl group, a methoxyethoxycarbonyl group, a phenoxycarbonyl group, etc.), --SO2 R12 (e.g., a methanesulfonyl group, an ethanesulfonyl group, a butanesulfonyl group, a hexadecanesulfonyl group, a benzenesulfonyl group, a toluenesulfonyl group, a p-chlorobenzenesulfonyl group, etc.), --CONR10 R11 (e.g., an N,N-dimethylcarbamoyl group, an N,N-diethylcarbamoyl group, an N,N-dibutylcarbamoyl group, a morpholinocarbonyl group, a piperidinocarbamoyl group, a 4-cyanophenylcarbamoyl group, a 3,4-dichlorophenylcarbamoyl group, a 4-methanesulfonylphenylcarbamoyl group, etc.), --SO2 NR10 OR11 (an N,N-dimethylsulfamoyl group, an N,N-diethylsulfamoyl group, an N,N-dipropylsulfamoyl group, etc.), etc. R3 in formula [I] is more preferably --COOR12, --COR10, or SO2 R12 and is most preferably --COOR12.
X in formula [I] is preferably a hydrogen atom, a chlorine atom, an aliphatic oxy group (e.g., a 2-hydroxyethoxy group, a 2-chloroethoxy group, a carboxymethyloxy group, a 1-carboxyethoxy group, a 2-methanesulfonylethoxy group, a 3-carboxypropyloxy group, a 2-methoxyethoxycarbamoylmethloxy group, a 1-carboxytridecyloxy group, a 2-(1-carboxytridecylthio)ethyloxy group, a 2-carboxymethylthioethyloxy group, a 2-methanesulfonamidoethyloxy group, etc.), an aromatic oxy group (e.g., a 4-acetamidophenoxy group, a 2-acetamidophenoxy group, a 4-(3-carboxypropaneamido)phenoxy group. etc.), or a carbamoyloxy group (e.g., an ethylcarbamoyloxy group, a phenylcarbamoyloxy group, etc.).
Examples of the compound having at least two coupler residues derived from the compound represented by formula [I] include bis-, tris-, tetrakis compound, an oligomer (polymerization degree: not more than 99) and a polymer (polymerization degree: at least 100). (Hereinafter the oligomer and the polymer are referred to as a polymer.)
The bis-, tris- and tetrakis compound may be formed by combining with each other through a divalent group or a group having a higher valent at said R1, R2, R3, or X. When the coupler of the present invention is a polymer, the polymer is a homopolymer or copolymer of an addition polymerizable ethylenically unsaturated compound (cyan-coloring monomer) having the cyan-dye forming coupler residue derived from the compound represented by formula [I]. In this case, the polymer may contain therein at least one type of recurring unit represented by formula [X] described below or may be a copolymer containing at least one type of cyan coloring recurring unit shown by formula [X] below and at least one type of non-coloring ethylenic monomer.
Formula X is represented by the following structure: ##STR11## wherein, R represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms or a chlorine atom; A represents --CONH--, --COO--, or a substituted or unsubstituted phenylene group; B represents a substituted or unsubstituted alkylene group (having preferably from 1 to 10 carbon atoms), a substituted or unsubstituted phenylene group, or a substituted or unsubstituted aralkylene group (having preferably from 7 to 20 carbon atoms); L represents --CONH--, --NHCONH--, --NHCOO--, --NHCO--, --OCONH--, --NH--, --COO--, --OCO--, --CO--, --O--, --SO2 --, --NHSO2 --, or --SO2 NH--; a, b, and c each represents 0 or 1; Q represents a cyan coupler residue formed by the release of a hydrogen atom other than the hydrogen atom of the hydroxy group at the 1-position of the compound shown by formula [I] described above or preferably a cyan coupler residue formed by the release of one hydrogen atom from the substituent R1, R2, R3, or X of the compound shown by formula [I]. Examples of substituents for above-described groups include the same as substituents A described hereinabove.
The preferred polymer is a copolymer of a cyan coloring monomer forming a coupler unit shown by formula [X] described above and the non-coloring ethylenical monomer described below.
That is, as the non-coloring ethylenical monomer which does not cause a coupling reaction with the oxidation product of an aromatic primary amine developing agent, there are acrylic acid, α-chloroacrylic acid, α-alkylacrylic acid (e.g., methacrylic acid, etc.). the esters or amides derived from these acrylic acids (e.g., acrylamide, methacrylamide, n-butylacrylamide, t-butylacrylamide, diacetoneacrylamide, methylacrylate, ethylacrylate, n-isobutyl acrylate, 2-ethylhexyl acrylate, n-octyl acrylate, lauryl acrylate, methyl methacrylate, ethyl methacrylate, n-butylmethacrylate, and β-hydroxy methacrylate), vinyl esters (e.g., vinylacetate, vinylpropionate, and vinyllaurate), acrylonitrile, methacrylonitrile, aromatic vinyl compounds (e.g., styrene and the derivatives thereof, such as vinyltoluene, divinylbenzene, vinylacetophenone, and sulfostyrene), itaconic acid, citraconic acid, crotonic acid, vinylidene chloride, vinyl alkyl ethers (e.g., vinyl ethyl ether, etc.), maleic acid esters, N-vinyl-2-pyrrolidone, N-vinylpyridine, and 2- and 4-vinylpyridines.
In the above-described monomers, acrylic acid esters, methacrylic acid esters, and maleic acid esters are particularly preferred. The above-described non-coloring ethylenical monomers may be used solely or as a mixture thereof, such as a mixture of methyl acrylate and butyl acrylate, butyl acrylate and styrene, butyl methacrylate and methacrylic acid, or methyl acrylate and diacetoneacrylamide.
The ethylenically unsaturated monomer to be copolymerized with the vinyl monomer corresponding to formula [X] described above may be selected so that, as is well known in the field of polymer couplers, the copolymer formed would have good chemical and/or physical properties such as solubility, compatibility with a binder for the photograpiic colloid compositions such as gelatin, flexibility of the binder, heat stability thereof, etc.
The cyan polymer coupler may be used in the present invention by dissolving an oleophilic polymer coupler obtained by polymerizing the vinyl monomer giving the coupler unit represented by formula [X] described above in an organic solvent and then dispersing in an aqueous gelatin solution to form a latex or it may be used by directly forming a latex by an emulsion polymerization of the vinyl monomer.
In this case, the oleophilic polymer coupler may be dispersed in an aqueous gelatin solution in the form of a latex by the method described in U.S. Pat. No. 3,451,820. Alternatively, the emulsion polymerization can be performed using the methods described in U.S. Pat. Nos. 4,080,211 and 3,370,952.
Specific examples of the cyan coupler represented by formula [I] are illustrated below, however, the invention is not limited to these specific compounds. In addition, (t)C5 H11 in the following formulae represents --C(CH3)2 C2 H5 and (t) C8 H17 represents --C(CH3)2 CH2 C(CH3)3. ##STR12##
The cyan couplers which are those represented by formula [I] described above and the above described derivatives thereof, can be preprared by the methods described, for example, in Japanese Patent Application (OPI) No. 237448/85 and European Pat. No. 161626.
The cyan coupler(s) are dissolved in a high-boiling organic solvent such as a phthalic acid ester having 16 to 32 carbon atoms or a phosphoric acid ester and, if desired, additionally using ethyl acetate, etc. The solution is dispersed by emulsification in an aqueous medium.
The cyan coupler used in the present invention may be added to a light-sensitive silver halide emulsion layer or a layer adjacent thereto, however it is preferable to add to a red-sensitive silver halide emulsion layer.
In this invention, the above described cyan coupler may be, if desired, used together with a conventional cyan coupler(s) in an amount preferably of not more than 40 mol %, more preferably of not more than 20 mol % based on the total amount of cyan couplers. The total amount added of the cyan coupler(s) is preferably from 0.002 to 0.3 mol pre mol of the light-sensitive silver halide in the photographic emulsion layer.
Metal complexes represented by formulae [II] to [V] described above are explained below in detail.
The halogen atom shown by R2, R3, R4, and R5 includes a fluorine atom, a chlorine atom, a bromine atom. and an iodine atom.
The alkyl group shown by R2, R3, R4, and R5 is preferably an alkyl group having 1 to 19 carbon atoms. The alkyl group may be a straight chain or branched alkyl group and also a substituted or unsubstituted alkyl group.
The aryl group shown by R2, R3, R4, and R5 is preferably an aryl group having 6 to 14 carbon atoms and may be substituted or unsubstituted.
The heterocyclic group shown by R2, R3, R4, and R5 is preferably a 5-membered or 6-membered heterocyclic ring and may be substituted or unsubstituted.
The cycloalkyl group shown by R2, R3, R4, and R5 is preferably a 5-membered or 6-membered cycloalkyl group and may be substituted or unsubstituted.
The 6-membered ring which is formed by the combination of said R2 and R3, said R3 and R4, or said R4 and R5 is preferably a benzene ring and may be substituted or unsubstituted or may be condensed.
The straight chain or branched alkyl group shown by R2, R3, R4, and R5 includes, for example, a methyl group, an ethyl group, a propyl group, a butyl group, a hexyl group, an octyl group, a decyl group, a dodecyl group, a tetradecyl group, a hexadecyl group, an octadecyl group, etc.
The aryl group shown by R2, R3, R4, and R5 includes a phenyl group, a naphthyl group, etc.
The heterocyclic group shown by R2, R3, R4, and R5 is a 5-membered or 6-membered heterocyclic ring having at least one nitrogen atom, oxygen atom, or sulfur atom in the ring as a hetero atom and includes, for example, a furyl group, a hydrofuryl group, a thienyl group, a pyrrolyl group, a pyrrolidyl group, a pyridyl group, an imidazolyl group, a pyrazolyl group, a quinolyl group, an indolyl group, an oxazolyl group, a thiazolyl group, etc.
The cycloalkyl group shown by R2, R3, R4, and R5 includes, for example, a cyclopentyl group, a cyclohexyl group, a cyclohexenyl group, a cyclohexadienyl group, etc.
The 6-membered ring formed by the combination of said R2 and R3, said R3 and R4, or said R4 and R5 with each other includes, for example, a benzene ring, a naphthalene ring, an isobenzthiophene ring, an isobenzofuran ring, an isoindoline ring, etc.
The alkyl group, cycloalkyl group, aryl group or heterocyclic group shown by said R2, R3, R4, and R5 may bonded to a carbon atom of the benzene ring through a divalent linkage group such as, for example, an oxy group (--O--), a thio group (--S--), an --NH--, an oxycarbonyl group, a carbonyl group, --NHCO--, --NHSO2 --, a carbonylamino group, a sulfonyl group, or a carbonyloxy group.
Examples of an alkyl group shown by said R2, R3. R4, and R5 which is bonded to a carbon atom of the benzene ring through a divalent linkage group include an alkoxy group (e.g., a methoxy group, an ethoxy group, a butoxy group, a propoxy group, an n-decyloxy group, an n-dodecyloxy group, an n-hexadecyloxy group, etc.), an alkoxycarbonyl group (e.g., a methoxycarbonyl group, an ethoxycarbonyl group, a butoxycarbonyl group, an n-decyloxycarbonyl group, an n-hexadecyloxycarbonyl group, etc.), an acyl group (e.g., an acetyl group, a valeryl group, a stearoyl group, a benzoyl group, a toluoyl group, etc.), an acyloxy group (e.g., an acetoxy group, a hexadecylcarbonyloxy group, etc.), an alkylamino group (e.g.. an n-butylamino group, an N,N-diethylamino group, an N,N-didecylamino group, etc.), an alkylcarbamoyl group (e.g., a butylcarbamoyl group, an N,N-diethylcarbamoyl group, an n-dodecylcarbamoyl group, etc.), an alkylsulfamoyl group (e.g., a butylsulfamoyl group, an N,N-diethylsulfamoyl group, an n-dodecylsulfamoyl group, etc.,), an alkylsulfonylamino group (e.g., methylsulfonylamino group, a butylsulfonylamino group, etc.), an alkyl sulfonyl group (e.g., a mesyl group, an ethanesulfonyl group, etc.), an acylamino group (e.g., an acetylamino group, a valerylamino group, a palmitoylamino group, etc.), etc.
Examples of a cycloalkyl group shown by said R2, R3, R4, and R5 which is bonded to a carbon atom of the benzene ring through the above-described divalent linkage group include a cyclohexyloxy group, a cyclohexylcarbonyl group, a cyclohexyloxycarbonyl group, a cyclohexylamino group, a cyclohexenylcarbonyl group, a cyclohexenyloxy group, etc.
Also, examples of an aryl group shown by said R2, R3, R4 and R5 which is bonded to a carbon atom of the benzene ring through the above-described divalent linkage group include an aryloxy group (e.g., a phenoxy group, a naphthoxy group, etc.), an aryloxycarbonyl group (e.g., a phenoxycarbonyl group, a naphthoxycarbonyl group, etc.), an acyl group (e.g., a benzoyl group, a naphthoyl group, etc.), an anilino group (e.g., a phenylamino group, an N-methylanilino group, an N-acetylanilino group, etc.), an acyloxy group (e.g., a benzoyloxy group, a toluoyloxy group, etc.), an arylcarbamoyl group (e.g., a phenylcarbamoyl group, etc.), an arylsulfamoyl group (e.g., a phenylsulfamoyl group, etc.), an arylsulfonylamino group (a phenylsulfonylamino group, a p-tolylsulfonylamino group, etc.), an arylsulfonyl group (a benzenesulfonyl group, a tosyl group, etc.), an acylamino group (e.g., a benzoylamino group, a toluoylamino group, etc.), etc.
Furthermore, the alkyl group, the aryl group, the heterocyclic group, the cycloalkyl group shown by aforesaid R2, R3, R4, and R5 or the 6-membered ring formed by the combination of said R2 and R3, said R3 and R4, or said R4 and R5 may be substituted by a substituent. Examples of substituents are described below (these substituents may be further substituted with substituents A shown herein above).
The Examples include a halogen atom (e.g., chlorine atom, bromine atom, fluorine atom, etc.), a cyano group, a straight chain or branched substituted or unsubstituted alkyl group (e.g., a methyl group, an ethyl group, a propyl group, a butyl group, a hexyl group, an octyl group, a decyl group, a dodecyl group, a tetradecyl group, a hexadecyl group, a heptadecyl group, an octadecyl group, a methoxyethoxyethyl group, etc.), an aryl group (e.g., a phenyl group, a tolyl group, a naphthyl group, a chlorophenyl group, a methoxyphenyl group, an acetylphenyl group, etc.), an alkoxy group (e.g., a methoxy group, an ethoxy group, a butoxy group, a propoxy group, a methoxyethoxy group, etc.), an aryloxy group (e.g., a phenoxy group, a tolyloxy group, a naphthoxy group, a methoxyphenoxy group, etc.), an alkoxycarbonyl group (e.g., a methoxycarbonyl group, a butoxycarbonyl group, a phenoxymethoxycarbanoyl group, etc.), an aryloxycarbonyl group (e.g., a phenoxycarbonyl group, a tolyloxycarbonyl group, a methoxyphenoxycarbonyl group, etc.), an acyl group (e.g., a formyl group, an acetyl group, a valeryl group, a stearoyl group, a benzoyl group, a toluoyl group, a naphthoyl group, a p-methoxybenzoyl group, etc.), an acyloxy group (e.g., an acetoxy group, a benzyloxy group, etc.), an acylamino group (e.g., an acetamido group, a benzamido group, a methoxyamido group, etc.), an anilino group (e.g., a phenylamino group, an N-methylanilino group, an N-phenylanilino group, an N-acetylanilino group, etc.), an alkylamino group (e.g., an n-butylamino group, an N,N-diethylamino group, a 4-methoxy-n-butylamino group, etc.), a carbamoyl group (e.g., an n-butylcarbamoyl group, an N,N-diethylcarbamoyl group, etc.), a sulfamoyl group (e.g., an n-butylsulfamoyl group, an N,N-diethylsulfamoyl group, an n-dodecylsulfamoyl group, an N-(4-methoxy-n-butyl)- sulfamoyl group, etc.), a sulfonylamino group (e.g., a methylsulfonylamino group, a phenylsulfonylamino group, a methoxymethylsulfonylamino group, etc.), a sulfonyl group (e.g., a mesyl group, a tosyl group, a methoxymethanesulfonyl group, etc.), etc.
The alkyl group shown by R6, R7, R8, R9, or R10 in formulae [II] [V] described above may be a substituted or unsubstituted alkyl group, or may be a straight chain or a branched alkyl group. The number of carbon atoms of the alkyl group excluding the carbon atom(s) of the substituent is 1 to 20 and examples thereof include a methyl group, an ethyl group, a propyl group, a butyl group. a hexyl group, an octyl group, a decyl group, a dodecyl group, a tetradecyl group, a hexadecyl group, a heptadecyl group, an octadecyl group, etc.
Also, the aryl group shown by said R6, R7, R8, R9, or R10 includes a substituted or unsubstituted aryl group. The number of carbon atoms in the acyl group excluding the carbon atom(s) of the substituent is preferably from 6 to 14, and examples thereof include a phenyl group, a tolyl group, a naphthyl group, etc.
The non-metallic atomic group shown by Y in formula [III] or [V] described above which is necessary for forming a 5-membered or a 6-membered ring includes a non-metallic atomic group represented by formula (a), (b) (c) (d) or (e) described below: ##STR13## wherein, R15 represents a hydrogen atom or an alkyl group. The alkyl group shown by said R15 is a substituted or unsubstituted alkyl group. The number of carbon atoms of the alkyl group excluding the carbon atom (s) of the substituent is preferably from 1 to 20. Also, the alkyl group may be a straight chain or a branched alkyl group. Specific examples of the alkyl group include the substituents illustrated above for R2, R3, R4, and R5.
In the metal complexes represented in formula [II], [III], [IV], or [V] described above, preferred complexes are those represented by following formula [IIa], [IIb], [IIIa], [IVa], [IVb], or [Va], respectively. ##STR14## wherein R2 to R10 and M are defined as defined hereinabove in the definition for formulae [II] to [V], n represents 2 or 3 and R17 represents an alkyl group or an aryl group.
In the complexes shown by formulae [IIa], [IIb], [IIIa], [IVa], [IVb], and [Va] described above, particularly preferred complexes are those shown by formuIae [IIa], [IIb] and [IIIa]. Also, the more preferred complexes shown by formula [IIa], [IIb], or [IIIa] described above is when R2 is a group capable of causing hydrogen bonding, at least one of R3, R4, or R5 is a hydrogen atom, a hydroxy group, an alkyl group, or an alkoxy group, and the sum of carbon atoms of the group shown by R2, R3, R4, R5, R6, or R7 is at least 4.
The group shown by R2 which is capable of forming a hydrogen bond includes a group containing --O-- (e.g., a methoxy group, an ethoxy group, a propoxy group, a butoxy group, an n-octyloxy group, a 2-ethylhexyloxy group, a decyloxy group, an n-dodecyloxy group, a 2-hexyldecyloxy group, an isostearyloxy group, a benzyloxy group, a piperonyloxy group, a phenoxy group, a trimethylsilyloxy group, etc.), a group containing --S-- (e.g., a methylthio group, an ethylthio group, a propylthio group, a butylthio group, a 2-ethylhexylthio group, an n-dodecylthio group, a 2-hexyldecylthio group, an isostearylthio group, a substituted or unsubstituted phenylthio group, etc.), a group containing carbonyl group (e.g., an acetyl group, a propionyl group, a butyryl group, a hexanoyl group, an octanoyl group, a stearoyl group, a benzoyl group, etc.), a group containing oxycarbonyl group (e.g., a methoxycarbonyl group, an ethoxycarbonyl group, a butoxycarbonyl group an n-decyloxycarbonyl group, a stearyloxycarbonyl group, a phenoxycarbonyl group, etc.), a carbamoyl group (e.g., a methylcarbamoyl group, an ethylcarbamoyl group, a butylcarbamoyl group, an N,N-diethylcarbamoyl group, an n-dodecylcarbamoyl group, a phenylcarbamoyl group, etc.), a sulfamoyl group (e.g., a methylsulfamoyl group, an N,N-diethylsulfamoyl group, a butylsulfamoyl group, an n-dodecylsulfamoyl group, a phenylsulfamoyl group, etc.), a group having a sulfonyl group (e.g., a mesyl group, an ethanesulfonyl group, a benzenesulfonyl group, a tosyl group, etc.), a group having a sulfonylamino group (e.g., a methylsulfonylamino group, a butylsulfonylamino group, etc.), an acylamino group (e.g., an acetylamino group, a benzoylamino group, etc.), a group having a carbonyloxy group (e.g., an acetyloxy group, a butyryloxy group, a benzyloxy group, etc.), an amino group (e.g., --NH2 group, a methylamino group, a diethylamino group, a dibutylamino group, a hexylamino group, a benzylamino group, an anilino group, etc.), a hydroxy group, a nitro group, a cyano group, a carboxylic acid group, a sulfonic acid group, and a halogen atom.
The metal complexes shown by formulae [II], [III], [IV] or [V] described above which are particularly effective for the practice of this invention include the compounds shown by following structural formulae although the complexes of this invention are not limited to these compounds. ##STR15##
The metal complexes of formulae [II] to [V] for use in this invention can be synthesized by the methods described, for example. in U.S. Pat. Nos. 4,246,330, 4,241,154, 4,229,843, 4,246,329 and 4,248,949 and Japanese Patent Application (OPI) No. 12,129/80.
In formula [VI] described above, R24 represents an aliphatic group having 1 to 30 carbon atoms, an aromatic group having 6 to 30 carbon atoms, a heterocyclic group having 2 to 30 carbon atoms, an aliphatic oxy group having 1 to 30 carbon atoms, an aromatic oxy group having 6 to 30 carbon atoms, an aliphatic thio group having 1 to 30 carbon atoms, an aromatic thio group having 6 to 30 carbon atoms, a carbonamido group having 2 to 30 carbon atoms, a sulfonamido group having 1 to 30 carbon atoms, a monosubstituted amino group having 1 to 30 carbon atoms, or a di-substituted amino group having 2 to 30 carbon atoms and m represents an integer of 1 to 4. When m is 2 to 4, said R24 groups may be the same or different and also may be combined with each other to form a ring.
The two hydroxy groups in formula [VI] are in a para-position or an ortho-position relative to each other. The hydroquinone derivatives or cathecohl derivatives represented by formula [VI] may form a bis-, tris- or tetrakis compound or a polymer by bonding the substituents R24 groups thereof and in this case, the number of carbon atoms of R24 may not be in the above-described range.
In formula [VII] described above, R25 represents an aliphatic group having 1 to 30 carbon atoms, an aromatic group having 6 to 30 carbon atoms, a heterocyclic group haivng 2 to 30 carbon atoms, or a substituted silyl group having 3 to 30 carbon atoms; R26 has the same significance as defined for R24 in formula [VI]; n represents an integer of 1 to 3: j represents an integer of 0 to 5; and the sum of n and j is 6 or less. When n is plural, said OR25 groups may be the same or different. Also, when said two OR25 groups, said two R26 groups, or said OR25 and R26 are in an ortho-position relative to each other, they may combine with each other to form a ring. Examples of such a ring are substituted or unsubstituted methylenedioxy group, a substituted or unsubstituted ethylenedioxy group, a substituted or unsubstituted trimethylene group, a substituted or unsubstituted tetramethylene group, a substituted or unsubstituted trimethyleneoxy group, etc. Examples of substituents for these substituted groups are the same as substituents A shown hereinabove.
The substituted oxybenzene derivatives shown by formula [VlI] may combine with each other at R25 or R26 to form a bis-, tris- and tetrakis compound and a polymer and in this case the number of carbon atoms of said R25 or R26 may not be in the above-defined range.
In formula [VIII] described above. R27, R28, R29, and R30 each represents a hydrogen atom or an aliphatic group having 1 to 30 carbon atoms; Y represents a hydrogen atom, an aliphatic group having 1 to 30 carbon atoms, an acyl group having 1 to 30 carbon atoms, an aliphatic sulfonyl group having 1 to 30 carbon atoms, an aromatic sulfonyl group having 6 to 30 carbon atoms, an aliphatic oxycarbonyl group having 2 to 31 carbon atoms, an aromatic oxycarbonyl group having 6 to 31 carbon atoms, an oxyradical group or a hydroxy group; and Z represents a non-metallic atomic group necessary for forming a 5-membered to 7-membered ring together with ##STR16##
The heterocyclic ring formed by Z and ##STR17## may further contain at least one of N, O and S atoms as heteroatoms, >C=0 group and >SO2 group. Examples of the ring include piperidine, pyrrolidine, morpholine, 4-thiapiperidine, piperazine, 4-thiapiperidine-4-oxide, 4-thiapiperidine-4,4-dioxide, piperidine-4-one, etc. These heterocyclic rings may further have a substituent in addition to R27, R28, R29, R30, and Y. Examples of such a substituent include an aliphatic group having 1 to 30 carbon atoms, an aliphatic oxy group having 1 to 31 carbon atoms preferably 2 to 31 carbon atoms, an aliphatic and aromatic carbonamido group having 2 to 30 carbon atoms, an acyloxy group having 2 to 30 carbon atoms, an aliphatic oxycarbonyl group having 2 to 31 carbon atoms, etc.
The heterocyclic rings shown by formula [VIII] described above may combine with each other at said substituent R27, R28, R29, R30, Y or Z to form a bis-, tris- or tetrakis compound or a polymer. In this case, the number of carbon atoms of said R27, R28, R29, R30, Y or Z may not be in the above-defined range.
In formula [VI] described above, R24 is preferably an aliphatic group, an aliphatic and aromatic carbonamido group, an aliphatic and aromatic sulfonamido group, an aliphatic oxy group, or an aliphatic thio group and is more preferably an aliphatic group. Also, m is preferably 1 to 3 and is more preferably 2. The two hydroxy groups are preferably in a para-position relative to each other.
The most preferred compound of the compounds shown by formula [VI], described above is represented by following formula [VI-a] ##STR18## wherein R39 and R40, which may be the same or different, each represents an aliphatic group having 1 to 30 carbon atoms. Preferable examples of the aliphatic group include a methyl group, an ethyl group, an isopropyl group, a t-butyl group, a 1,1-dimethylpropyl group, a 1,1-dimethylbutyl group, a cyclopentyl group, a cyclohexyl group, a 2-hexyl group, a 1,1,3,3-tetramethylbutyl group, a 2-dodecyl group, an n-pentadecyl group, a 2-hexadecyl group, a 1-ethyl-1,5,9-trimethyldecyl group, a 4-hexyloxycarbonyl-1,1-dimethylbutyl group, etc.
In formula [VII] described above, R25 is preferably an aliphatic group or a substituted silyl group and R26 is preferably an aliphatic group. Also, n is preferably 2 or 3 and j is preferably 1 to 3. Preferable positions for OR25 and R26 on the benzene ring are ortho- and para-positions relative to each other.
The most preferred compound of the compounds shown by formula [VII] is represented by following formula [VII-a], [VII-b], [VII-c], [VII-d], or [VII-e]; ##STR19##
In formulae, [VII-a], [VII-b], [VII-c], [VII-d] and, [VII-e], R41 and R42, which may be the same or different, each represents an aliphatic group having 1 to 30 carbon atoms (specific examples thereof are same as those described above in regard to R39 of formula [VI-a]) or a substituted silyl group having 3 to 30 carbon atoms (e.g., a trimethylsily group, a dimethylpropylsily group, et.); R43 represents an aliphatic group having 1 to 30 carbon atoms (specific examples thereof are the same as those described above in regard to R39), an aliphatic oxy group having 1 to 30 carbon atoms (e.g., a methoxy group. an ethoxy group. an n-propyloxy group, an n-butoxy group,a 2-methoxyethoxy group, an n-dodecyloxy group, etc.), an aliphatic thio group having 1 to 30 carbon atoms (e.g., a methylthio group, an n-butylthio group, an n-dodecylthio group. etc.), or a carbon amido group having 2 to 30 carbon atoms (e.g., an acetamido group, a tetradecanamido group, a benzamido group, etc.); R44 represents an aliphatic group having 1 to 30 carbon atoms (specific examples thereof are same as those described above in regard to R39) or an aromatic group having 6 to 30 carbon atoms (e.g., a phenyl group, a tolyl group, a 4-hydroxyphenyl group, a 2,5-dimethoxy-3-methylphenyl group, etc.); R45, R46, R47, and R48 , which may be the same or different, each represents a hydrogen atom or an aliphatic group having 1 to 12 carbon atoms (e.g., a methyl group, an ethyl group. an n-propyl group, etc.); q represents an integer of 1 to 4; r represents an integer of 0 to 3; s represents an integer of 0 to 6: t represents an integer of 1 to 4; u represents an integer of 0 to 3; and v represents an integer of 0 to 2. When said q, r, s, t, or u are plural, said plural R43 groups or R44 groups may be the same or different.
In formuIa [VIII] described above, R27, R28, R29, and R30 are preferably a hydrogen atom or an aliphatic group having 1 to 12 carbon atoms (e.g., a methyl group, an ethyl group, etc.) and are more preferably a methyl group. Y in the formula is preferably a hydrogen atom, an aliphatic group having 1 to 12 carbon atoms (e.g., a methyl group, an ethyl group, an n-butyl group, etc.), an acyl group having 1 to 12 carbon atoms (e.g., an acetyl group. a butanoyl group, an acryloyl group, a benzoyl group, etc.), or an oxyradical group. The heterocyclic ring formed by Z and ##STR20## is preferably a piperidine.
The most preferred example of the compounds shown by formula [VIII-a]. described above is shown by following fo formula [VIII-a]. ##STR21## wherein, Y has the same significance as defined above and V represents an acyloxy group having 2 to 30 carbon atoms (e.g., an acetoxy group, a benzoyloxy group, an n-dodecanoyloxy group, etc.), or an aliphatic and aromatic carbonamido group having 2 to 30 carbon atoms (e.g., a 2-ethylhexaneamido group, an n-tetradecaneamido group, etc.).
A compound which is formed by combining two or more residues of at least two different compounds represented by formulae [VI], [VII] and [VIII] may also be used.
The piperidine derivatives shown by formula [VIII-a] above may combine with each other at said Y or V to form a bis-, tris-, tetrakis compound or a polymer and in this case, the number of carbon atoms defined above may not be the above-defined range.
Specific examples of the compound represented by formulae [VI], [VII] and [VIII] and derivatives thereof described above are illustrated below but the compounds for use in this invention are not limited to these compounds. pounds. ##STR22##
The compounds shown by formulae [VI], [VII], and [VIII] described above can be synthesized by the methods described in British Pat. Nos. 1,326,889, 1,347,556, 1,354,313, 1,410,846, 2,062,888, 2,066,975, and 2,077,455, U.S. Pat. Nos. 3,336,135, 3,432,300, 3,573,050, 3,574,627, 3,700,455, 3,764,337, 3,935,016, 3,982,944, 4,254,216, 4,268,593, and 4,279,990, Japanese Patent Application (OPI) Nos. 97353/85, 1024/76, 146,234/77, 147,434/77, 152,225/77, 9528/78, 17,729/78, 20, 327/78, 55,121/78, 145,530/79, 6321/80, 69,141/80, 89,835/80, 89,826/80, 125,141/80, 21,004/80, 52,747/81, 129,644/81, 25,141/83, 114,026/83, 5,246/84, and 10,539/84, Japanese Patent Publication Nos. 20,977/67, 21,625/73, 1,420/76, 6,623/77, 27,534/77 and 12,337/79.
The amounts added of the compounds of formulae [II] to [VIII] and derivatives thereof for use in this invention is preferably from 0.01 mol to 1 mol, more preferably from 0.05 mol to 0.8 mol per mol of the cyan coupler defined in this invention. When the amount exceeds 1 mol it is not preferable because stain tends to form or density tends to decrease.
The compounds of formulae [II] to [VIII] and derivatives thereof for use in this ivnention exist in the same layer containing the cyan coupler of formula [I] described above or in an adjacent layer thereto. However, it is preferred that said compounds and said cyan couplers are present in the some layers. More preferabIy, the compounds of formulae [II] to [VIII] and derivatives thereof are coemulsified with the cyan coupler of formula [I] and the emulsion is coated as a layer.
In this invention. various color couplers can be used together with the cyan coupIers and the compounds described above in the color photographic light-sensitive materials. Specific examples of these cyan dye forming couplers, magenta dye forming couplers, and yellow dye forming couplers are described in Research Disclosure. 1978 Dec. (17643), Paragraph VII-D and also in the patents cited in Research Disclosure, 1979, Nov. (18717). It is preferred that each of these couplers is rendered non-diffusile by the introduction of a ballast group or by forming a bis-, tris or tetrakis compound or a polymer thereof. The couplers may be of two equivalent or four equivalent. Furthermore, couplers wherein the formed dyes of which properly diffuse to improve the graininess of the color photographic materials, DIR couplers capable of releasing a development inhibitor with a coupling reaction for giving an edge effect or double layer effect, or colored couplers for giving a color correction can be used in this invention.
The yellow couplers which are preferred for use in this invention include the α-pivaloyl or the α-benzoyl acetanilide couplers which release the dye at an oxygen atom or at a nitrogen atom. Particularly preferred examples of these two-equivalent yellow couplers include the yellow couplers of the type which release dyes at the oxygen atom as described in U.S. Pat. Nos. 3,408,191, 3,417,928, 3,933,501, 4,022,620, etc., and the yellow couplers of the type which release dyes at the nitrogen atom as described in U.S. Pat. Nos. 3,973,968, 4.311,023, Japanese Patent Publication No. 10,739/83, Japanese Patent Application (OPI) No. 132,926/75. West German Patent Application (OLS) Nos. 2,219,917, 2,261,361. 2,329,587, 2,433,812, etc.
The magenta coupIers which can be used in this invention include, for example, 5-pyrazolone coupler and, pyrazolo[5.1-C.][1,2.4] triazoles which are described in U.S. Pat. No. 3,725,067, etc., and pyrazolo [5,1-b][1,2,4]-triazoles which are described in European Patent 119.860, etc. Magenta couplers which are formed into two equivalent matenta couplers by a releasable group bond to the coupling active position with a nitrogen atom or a sulfur atom are preferably used in this invention. Additional couplers which have resistance or fastness to humidity and temperature can be used together with the cyan couplers of formula [I] or derivatives thereof described above. Specific examples of these additional couplers are phenolic couplers described in U.S. Pat. No. 3,772,002, etc., 2,5-diacylaminophenolic couplers described in Japanese Patent Application (OPI) Nos. 31,953/84, 166,956/84, 166,956/84, etc., and phenolic couplers having a phenylureido group at the 2-position thereof and an acylamino group at the 5-position thereof described in U.S. Pat. No. 4,333,999, etc.
Each of the dye-forming couplers which are used together with the cyan couplers of formula [I] and derivatives thereof described above in this invention are dissolved in high-boiling organic solvent such as a phthalic acid ester having 16 to 32 carbon atoms or a phosphoric acid ester. If desired, a low-boiling organic solvent such as ethyl acetate, etc. is also used to dissolve the couplers. The dissolved couplers are then dispersed by emulsification in an aqueous medium. The standard amount for each of the main or major couplers which are used includes preferably from 0.01 to 0.5 mol of yellow coupler. from 0.003 to 0.3 mol of magenta coupIer. and from 0.002 to 0.3 mol of cyan coupler per mol of the light-sensitive silver halide in the silver halide emulsion layer in which the coupler is incorporated.
The photographic emulsion layers of the color photographic materials of this invention use silver bromide, silver iodobromide, silver iodochlorobromide, silver chlorobromide, or silver chloride. Silver iodobromide or silver iodochlorobromide containing at most 30 mol % silver iodide is preferred. Silver iodobromide containing from 2 mol % to 25 mol % silver iodide is particularly preferrred.
There is no particular restriction regarding the form of silver halide grains in the photographic emulsions in this invention. That is, the silver halide grains may include the so-called regular grains such as cube shaped. octahedron shaped, tetradecahedron shaped. etc., or the grains may be irregular shaped (e.g., sphere shaped, etc.) Furthermore, the silver halide grains may have a crystal defect such as twinning, etc., or may be a composite form thereof.
Also, as to the grain size, the silver halide grains may be fine grains having a grain size of less than about 0.1 micron or they may be large grains having a projected area diameter of up to about 10 microns. The silver halide emulsion for use in this invention may be a mono-dispersed emulsion having a narrow silver halide grain size distribution. Alternatively, the silver halide emulsion for use in this invention may be a poly-dispersed emulsion having a broad silver halide grain distribution.
The silver halide emulsions for use in this invention can be prepared by the methods described, for example, in P. Grafkides, Chimie et Physique Photographique, Paul Montel, 1967, G. F. Duffin. Photographic Bmulsion Chemistry. Focal Press, 1966, V.L. Zelikman et al, Making and Coating Photographic Emulsion, Focal Press. 1964, etc. Thus. an acid method, a neutralization method, an ammonia method, etc., may be used for preparing the photographic emulsions. Also, the methods for reacting a soluble silver salt and a soluble halide which may be used include a single jet method, a double jet method, or a combination thereof. Furthermore, a back mixing method for forming silver halide grains in the presence of excessive silver ion may be used. One type of system of the double jet method which may be used includes a so-called controlled double jet method which maintains a constant pAg in a liquid phase for forming silver halide grains. In this method the silver halide in the silver halide emulsion has a regular crystal form and the grain size thereof is almost uniform.
Two or more types of silver halide emulsions separately prepared may be used as a mixture thereof.
Also, tabular silver halide grains having an asp act ratio of at least 5 can be used in this invention. Tabular silver halide grains can be easily prepared by the methods described in Cleve Gutoff, Photographic Theory and Practice, (1930), p 131, Photographic Science and Engineering, Vol.14, 248-257 (1970), U.S. Pat. Nos. 4,434,226, 4,414,310, 4,433,048. British Patent No. 2,112.157. etc. Advantages obtained when using tabular silver halide grains include an increased covering power and also an increased efficiency in color sensitizing by the sensitizing dyes as described in U.S. Pat. No. 4,434,226 previously cited above.
The crystal structure of the silver halide for use in this invention may have a uniform halide composition throughout the whole grain. Alternatively the crystal structure may have a different halogen composition between the inside portion and the outside portion thereof, it may have a layer structure. These silver halide grains are disclosed in British Patent No. 1,027,146, U.S. Pat. Nos. 3,505,068, 4,444,877, Japanese Patent Application (OPI) No. 143,331/85, etc. Also, silver halides each having a different composition may be combined with each other by an epitaxial junction. Furthermore, a silver halide may be combined with a compound other than silver halide, such as silver rhodanate, lead oxide, etc. These silver halide grains are disclosed in U.S. Pat. Nos. 4,094,684, 4,142,900, 4,459,353, British Patent No. 2,038,792, U.S. Pat. Nos. 4,349,622, 4,395,478, 4,433,501, 4,463,087, 3,656,962, 3,852,067, Japanese Patent Application (OPI) No. 162,540/84, etc.
The silver halide photographic emulsions for use in this invention may be spectrally sensitized by sensitizing dyes which are known in the field of photography. Also, for the purpose of preventing the occurrence of fog during production, storage and photographic processing of the color photographic materials, antifoggants or stabilizers may be used. Specific examples and methods of using antifoggants and stabilizers are described, for example, in U.S. Pat. Nos. 3,954,474, 3,982,947, Japanese Patent Publication No. 28,660/77, Research Disclosure, 17643 (1978, Dec.). VlA and VIM, B. J. Birr, Stabilization of Photographic Silver Halide Emulsions, Focal Press, 1974, etc.
The color photographic light-sensitive materials of this invention may further contain hydroquinones, aminophenols, sulfonamidophenols, etc., as color fogging preventing agents or color mixing preventing agents.
The color photographic materials of this invention may further contain ultraviolet absorbents such as benzotriazoles, etc., and specific benzotriazoles are described in Research Disclosure, 24239 (1984, June).
The color photographic materials of this invention may further contain water-soluble dyes in the hydrophilic colloid layers as filter dyes or for irradiation prevention, antihalation, etc.
The binder for the hydrophilic colloid layers and backing layers of the color photographic materials of this invention which may be used include gelatin, modified gelatin, synthetic hydrophilic polyemrs. etc. Furthermore, the hydrophilic colloid layers of the color photographic materials of this invention may contain a hardening agent such as vinylsulfone derivatives. A vinyl polymer having a sulfinate at the side chain may be used as a hardening accelerator.
The color photographic materials of this invention may further contain one or more types of surface active agents which are useful as coating aids and for static prevention, improving slidability, improving dispersibility, sticking prevention, and improving photographic characteristics such as development acceleration, increasing contrast, sensitization, etc.
The color photographic materials of this invention may further contain various types of stabilizers, stain preventing agents, developing agents or the precursors therefor, development accelerators or the precursors therefor, lubricants, mordants, matting agents, antistatic agents, plasticizers, and other additives useful for photographic light-sensitive materials in addition to the above-described additives. Specific examples of these additives are described in Research Disclosure, 17643 (1978. Dec.) and ibid, 18716 (1979, Nov.).
This invention may preferably be applied to a high speed color photographic film for photography having at least two silver halide emulsion layers of the same color sensitivity but each having a different sensitivity on a support. The typical order of the emulsion layers are a red sensitive emulsion layer, a green-sensitive emulsion layer, and a blue-sensitive emulsion layer from support side. However a reverse layer order such that a high-speed emulsion layer is disposed between enulsion layers having different color sensitivity may also be employed.
The color photographic material of this invention is, after imagewise exposure, processed by a color developer containing an aromatic primary amine color developing agent as the main component and thereafter processed by a bleach liquid and a fix liquid, a blix (bleach-fix) liquid, or a combination of them for removing developed silver.
The color developing solution to be used in the development of the present light-sensitive material is preferably an alkali aqueous solution mainly comprising an aromatic primary amine color-developing agent. As such a color-developing agent, a p-phenylene diamine compound is preferably used. Typical examples of such a compound include 3-methyl-4-amino-N,N-diethylaniline, 3-methyl-4-amino-N-ethyl-N-β-hydroxylethylaniline, 3-methyl-4-amino-N-ethyl-N-β-methanesulfonamide ethylaniline, 3-methyl-4-amino-N-ethyl-N-β-methoxyethylaniline, and sulfates, hydrochlorides, and p-toluenesulfonates thereof.
As bleaching agent there may be used a compound of a polyvalent metal such as iron (III), cobalt (III), chromium (VI), and copper (II), a peroxide a quinone, and nitroso compound. Typical exmaples of such a bleaching agent include ferricyanides, dichromates, organic complex salts of iron (III) or cobalt (III), aminopolycarboxylic acids such as ethylenediamine tetraacetic acid, diethylene triamine pentaacetic acid, nitrilo triacetic acid, 1,3-diamino-2-propanol tetraacetic acid; complex salts of organic acids such as citric acid, tartaric acid, and malic acid; persulfates; manganates; and nitrosophenol. Among these bleaching agents, iron (III) ethylene diamine tetraacetate and persulfates are preferably used in view of rapidness of processing and pollution consideration. Furthermore, ethylene diamine tetraacetic acid-iron (III) complex salt is useful in single bleaching bath, particularly in combined blix bath.
If desired, bleach accelerators such as iodine ion, thiourea, or thiol series compounds, etc., may be used together with a bleaching agent or a blixing agent.
After blixing or fixing, wash (or water washing) is frequently applied. It is preferred to employ a counter-currentwash system using two or mroe wash baths to save water. A multistage countercurrent stabilization process as described in Japanese Patent Application (OPI) No. 8,543/82 may be employed. For the stabilization process, a ph controlling buffer or formulin may be used and further an ammonium salt is a preferred additive for the process.
The invention is further explained below in detail by the following examples but the invention is not limited thereby.
Samples 101 to 107 of color photogrpahic materials were prepared by forming the following two layers on a cellulose triacetate film.
______________________________________
Layer 1: Red-Sensitive Emulsion Layer
Silver Iodobromide Emulsion (Silver
1.9 g/m.sup.2
iodide 5 mol %, mean grain size 0.6 μm)
as silver
Sensitizing Dye I: 4.2 × 10.sup.-4 mol
per mol of Ag
Sensitizing Dye II: 1.4 × 10.sup.-4 mol
per mol of Ag
Gelatin 1.8 g/m.sup.2
Coupler Shown in Table 1
below
Metal Complex Shown in Table 1
Coupler Dispersing Oil (Oil-1)
0.4 g/m.sup.2
Layer 2: Protective Layer
Gelatin layer containing polymethyl
methacrylate particles (diameter of about
1.5 μm)
Gelatin 1.1 g/m.sup.2
______________________________________
Each layer further Contained gelatin hardening agent H and a surface active agent in addition to the above-described components.
TABLE 1
______________________________________
Metal Complex
Sample Coupler (Amount)*1
(Amount)*2
______________________________________
101 EX - 1 (0.05) --
102 I - 3 (0.05) --
103 I - 3 (0.05) M - 13 (0.2)
104 I - 3 (0.05) M - 27 (0.2)
105 I - 13 (0.05) --
106 I - 13 (0.05) M - 7 (0.2)
107 I - 13 (0.05) M - 26 (0.2)
______________________________________
*1: Mol amount per mol of silver
*2: Mol amount per mol of coupler
The compounds used for preparing the above samples were as follows.
Sensitizing Dye I: Anhydro-5,5,'-dichloro-3,3,'-di- (γ-sulfopropyl)-9-ethyl-thiacarbocyanine hydroxide piridiniium salt.
Sensitizing Dye II: Anhydro-9-ethyl-3,3,'-di-(γ-sulfopropyl)-4,5,4',5'-dibenzothiacarbocyanine hydroxide triethylamine salt. ##STR23##
After applying a sensitometric light exposure to each of Samples 101 to 107 thus prepared, the sample was subjected to the following processing steps (A) at 38° C.
______________________________________ 1. Color Development 3 min. 15 sec. 2. Bleach 6 min. 30 sec. 3. Wash with water 3 min. 15 sec. 4. Fix 4 min. 20 sec. 5. Wash with water 3 min. 15 sec. 6. Stabilization 1 min. 5 sec. ______________________________________
The compositions of the processing liquids used in the above-described steps were as follows.
______________________________________
Color Development
Sodium Nitrilotriacetate
1.0 g
Sodium Sulfite 4.0 g
Sodium Carbonate 30.0 g
Potassium Bromide 1.4 g
Hydroxylamine Sulfate
2.4 g
4-(N--Ethyl-N--β-hydroxyethyl-
4.5 g
amino)-2-methylaniline Sulfate
Water to make 1 liter
Bleach Liquid
Ammonium Bromide 160.0 g
Aqueous Ammonia (28%)
14.0 ml
Ethylenediamine tetraacetic Acid
130.0 g
Sodium Iron Salt
Glacial Acetic Acid 14.0 ml
Water to make 1 liter
Fix Liquid
Sodium Tetrapolyphosphate
2.0 g
Sodium Sulfite 4.0 g
Ammonium Thiosulfate (70%)
175.0 ml
Sodium Biphosphite 4.6 g
Water to make 1 liter
Stabilization Liquid
Formalin 8.0 ml
Water to make 1 liter
______________________________________
Then, another set of samples were subjected to Processing Step (B) in the same manner as above except that the composition of the bleach liquid in Processing Step (A) is changed as follows. The bleach l-quid imitates a fatigued state of bleach liquid after the processing of a large quantity of color photographic materials.
______________________________________
Bleach Liquid:
______________________________________
(B - 1):
Ammonium Bromide 160.0 g
Aqueous Ammonia (28%)
7.1 ml
Ethylenediamine-tetraacetic
117 g
Acid Sodium Iron Salt
Glacial Acetic Acid 14 ml
Water to make 1 liter
(B - 2):
Ethylenediamine-tetraacetic
130 g
Acid Sodium Iron Salt
Water to make 1 liter
______________________________________
After addiing steel wool to bleach liquid (B - 2) closing the container holding the bleach liquid (B - 2) and allowing the bleach liquid (B - 2) to stand in the system to convert Fe(111)-BDTA into Fe(II)-BDTA,100 ml of bleach liquid (B - 1) was added to bleach liquid (B - 2) to provide the bleach liquid for Processing Step (B). The density is then measured on each sample thus processed. The relative cyan color density, that is, the value obtained by dividing the cyan color density in Processing Step (B) at the exposure level which produces the cyan coloring density of 1.5 in Processing Step (A) by 1.5 is shown in Table 2 below for each sample.
TABLE 2
______________________________________
Sample Relative Cyan Coloring Density
______________________________________
101 (Comparative)
0.64
102 (Comparative)
1.00
103 (Invention)
0.99
104 (Invention)
1.00
105 (Comparative)
0.99
106 (Invention)
0.99
107 (Invention)
0.99
______________________________________
From the results shown in Table 2 above, it can be seen that Samples (102 to 107) which use the cyan coupler defined in this invention show almost no reduction in color density even when processed in the fatigued bleach liquid. However, Sample (101) using a comparison cyan coupler shows a reduction in color density.
Samples 101 to 107 which were processed in Processing Step (A) were then subjected to a color image stabiity test wherein the emulsion layer side of each sample was exposed for 7 days using a fluorescent lamp fade meter (10,000 lux). The results obtained are shown in Table 3 below.
TABLE 3
______________________________________
Fluorescent Lamp (10,000 lux)
Exposure for 7 Days
Sample D.sub.B *
Color Image Residue(%)**
______________________________________
101 (Comparative)
0.04 89
102 (Comparative)
0.11 98
103 (Invention)
0.03 97
104 (Invention)
0.04 98
105 (Comparative)
0.10 98
106 (Invention)
0.04 99
107 (Invention)
0.03 98
______________________________________
*The value obtained by subtracting the yellow density at the unexposed
portion before the light exposure from the yellow density at the unexpose
portion after exposing the sample to the fluorescent lamp (10,000 lux) fo
7 days.
**Color image residue at a portion having an initial density of 1.5.
From the results shown in Table 3, it can be seen that Comparison Samples 102 and 105 show a large amount of yellow stain as a result of the light exposure. In contrast, Samples 103, 104, 106, and 107 of this invention which contain the metal complex of this invention show a very small amount of yellow stain.
From the results described above, it becomes clear that the samples based on this invention are excellent and they do not indicate a reduction of cyan color density even when processed in a fatigued bleach liquid. In addition the samples of the present invention indicate less formation of yellow stain even after light exposure for a long period of time.
Multilayer color photographic materials 201 to 207 were prepared by fomring 14 layers having the composition shown below on a cellulose triacetate support.
______________________________________
Layer 1: Antihalation Layer
Gelatin layer containing black colloid silver
Gelatin 1.1 g/m.sup.2
Layer 2: Interlayer
Gelatin layer containing an emulsified disper-
sion of 2,5-di-t-pentadecylhydroquinone and
Coupler EX - 2, and silver iodobromide
(silver iodide 1 mol %, mean grain size 0.07
μm).
Gelatin 1.2 g/m.sup.2
Coupler Dispersing Oil Oil-1
0.2 g/m.sup.2
Coupler Dispersing Oil Oil-2
0.02 g/m.sup.2
Layer 3: 1st Red-Sensitive Emulsion Layer
Silver Iodobromide Emulsion
1.6 g/m.sup.2 as Ag
(Silver iodide: 5 mol %, mean
grain side: 0.7 μm)
Sensitizing Dye I 4.2 × 10.sup.-4 mol
per mol of silver
halide
Sensitizing Dye II 1.4 × 10.sup.-4 mol
per mol of silver
halide
Coupler Shown in Table 4
Metal Complex Shown in Table 4
Gelatin 1.2 g/m.sup.2
Coupler Dispersing Oil,Oil-1
0.3 g/m.sup.2
Layer 4: 2nd Red-Sensitive Emulsion Layer
Silver Iodobromide Emulsion
1.9 g/m.sup.2 as Ag
(silver iodide: 10 mol %, mean
grain size: 1.5 μm)
Sensitizing Dye I 3.0 × 10.sup.-4 mol
per mol of silver
halide
Sensitizing Dye II 1.0 × 10.sup.-4 mol
per mol of silver
halide
Coupler Shown in Table 5
Metal Complex Shown in Table 5
Gelatin 1.3 g/m.sup.2
Coupler Dispersing Oil,Oil-1
0.3 g/m.sup.2
Layer 5: Interlayer
Gelatin Layer
Gelatin 0.9 g/m.sup.2
Layer 6: 1st Green-Sensitive Emulsion Layer
Silver Iodobromide Emulsion
0.6 g/m.sup.2 as Ag
(silver iodide: 5 mol %, mean
grain size: 0.8 μm)
Sensitizing Dye III: 4.5 × 10.sup.-4 mol
per mol of silver
halide
Sensitizing Dye IV: 1.8 × 10.sup.-4 mol
per mol of silver
halide
Coupler EX - 6 0.071 mol per mol
of silver halide
Coupler EX - 7 0.015 mol per mol
of silver halide
Coupler EX - 8 0.006 mol per mol
of silver halide
Gelatin 0.5 g/m.sup.2
Coupler Dispersing Oil,Oil-1
0.15 g/m.sup.2
Layer 7: 2nd Green-Sensitive Emulsion Layer
Silver Iodobromide Emulsion
1.6 g/m.sup.2 as Ag
(silver iodide: 6 mol %, mean
grain size: 0.85 μm)
Sensitizing Dye III 4.0 × 10.sup.-4 mol
per mol of silver
halide
Sensitizing Dye IV 1.6 × 10.sup.-4 mol
per mol of silver
halide
Coupler EX - 9 0.020 mol per mol
of silver halide
Coupler EX - 7 0.002 mol per mol
of silver halide
Coupler EX - 8 0.001 mol per mol
of silver halide
Gelatin 1.8 g/m.sup.2
Coupler Dispersing Oil,Oil-1
0.45 g/m.sup.2
Oil-2 0.1 g/m.sup.2
Layer 8: 3rd Green-Sensitive Emulsion Layer
Silver Iodobromide Emulsion
2.1 g/m.sup.2 as Ag
(silver iodide: 10 mol %, mean
grain size: 1,5 μm)
Sensitizing Dye III 3.0 × 10.sup.-4 mol
per mol of silver
halide
Sensitizing Dye IV 1.2 × 10.sup.-4 mol
per mol of silver
halide
Coupler EX - 9 0.009 mol per mol
of silver halide
Coupler EX - 2 0.001 mol per mol
of silver halide
Gelatin 2.1 g/m.sup.2
Coupler Dispersing Oil,Oil-1
0.7 g/m.sup.2
Coupler Dispersing Oil,Oil-2
0.1 g/m.sup. 2
Layer 9: Yellow Filter Layer
Gelatin layer formed by coating an emulsified
dispersion of yellow colloid silver and 2,5-di-t-
pentadecylhydroquinone in an aqueous gelatin
solution.
Gelatin 0.9 g/m.sup.2
Layer 10: 1st Blue-Sensitive Emulsion Layer
Silver Iodobromide Emulsion
0.4 g/m.sup.2 as Ag
(silver iodide: 6 mol %, mean
grain size: 0.6 μm)
Coupler EX - 10 0.27 mol per mol
of silver halide
Coupler EX - 11 0.005 mol per mol
of silver halide
Gelatin 1.3 g/m.sup.2
Coupler Dispersing Oil,Oil-1
0.3 g/m.sup.2
Layer 11: 2nd Blue-Sensitive Emulsion Layer
Silver Iodobromide Emulsion
0.6 g/m.sup.2 as Ag
(silver iodide: 10 mol %, mean
grain size: 1.0 μm)
Coupler EX - 10 0.045 mol per mol
of silver halide
Gelatin 0.5 g/m.sup.2
Coupler Dispersing Oil,Oil-1
0.05 g/m.sup.2
Layer 12: 3rd Blue-Sensitive Emulsion Layer
Silver Iodobromide Emulsion
0.8 g/m.sup.2 as Ag
(silver iodide: 10 mol %, mean
grain size: 1.8 μm)
Sensitizing Dye V 2.0 × 10.sup.-4 per mol
of silver halide
Coupler EX - 10 0.036 mol per mol
of silver halide
Gelatin 0.4 g/m.sup.2
Coupler Dispersing Oil,Oil-1
0.1 g/m.sup.2
Layer 13: 1st Protective Layer
Gelatin Layer
Gelatin 0.7 g/m.sup.2
Layer 14: 2nd Protective Layer
Gelatin Layer containing silver iodobromide
(silver iodide: 1 mol %, mean grain size: 0.07
μm) and polymethyl methacrylate particles
(diameter: about 1.5 μm).
______________________________________
Each layer further contains Gelation Hardening Agent H and a surface active agent in addition to the above-described components.
The compounds used for preparing the above samples are shown below. However, Sensitizing Dyes I and II, Coupler EX - 1, Oil - 1, and Gelatin Hardening Agent H - 1 are same as in Example 1.
Sensitizing Dye III: Anhydro-9-ethyl-5,5'-dichloro-3,3'-di-(γ-sulfopropyl)oxacarbocyanine Sodium Salt.
Sensitizing Dye IV: Anhydro-5,6,5',6'-tetrachloro-1,1'-diethyl-3,3'-di-{β{β-(γ-sulfopropoxy)ethoxy}ethyl}-imidazolocarbocyanine Hydroxide Sodium Salt.
Sensitizing Dye V: Anhydro-5,5'-dichloro-3,3'-di-(γ-sulfobutyl)thiacyanineethyl Ammonium Salt. ##STR24##
TABLE 4
______________________________________
Metal Complex
Sample Coupler(Amount)*1 (Amount)*2
______________________________________
201 EX-3(0.002),EX-4(0.002),EX-1(0.05)
--
201 EX-3(0.002),EX-4(0.002),I-3(0.05)
--
203 EX-3(0.002),EX-4(0.002),I-3(0.05)
M-3(0.2)
204 EX-3(0.002),EX-4(0.002),I-3(0.05)
M-3(0.2)
205 EX-3(0.002),EX-4(0.002),I-13(0.05)
--
206 EX-3(0.002),EX-4(0.002),I-13(0.05)
M-12(0.2)
207 EX-3(0.002),EX-4(0.002),I-13(0.05)
M-22(0.2)
______________________________________
TABLE 5
______________________________________
Metal Complex
Sample Coupler (Amount)*1
(Amount)*2
______________________________________
201 EX-5 (0.02) --
202 I-18 (0.02) --
203 I-18 (0.02) --
204 I-18 (0.02) M-8 (0.2)
205 I-14 (0.02) --
206 I-14 (0.02) --
207 I-14 (0.02) --
______________________________________
*1Amount added per mol of the silver halide in the emulsion layer
containing it.
*2Amount added per mol of the coupler in the emulsion layer containing it
Samples 201 to 207 thus obtained were subjected o the same test as in Example 1 and the results obtained re shown in Table 6 below.
TABLE 6
______________________________________
Fluorescent Lamp (10,000
lux) for 7 days
Relative Cyan Color Image
Sample Coloring Density
D.sub.B *1
Residue (%)*2
______________________________________
201 (Comparison)
0.75 0.03 95
202 (Comparison)
0.99 0.10 99
203 (Invention)
0.99 0.04 100
204 (Invention)
1.00 0.02 99
205 (Comparison)
0.99 0.09 99
206 (Invention)
1.00 0.03 99
207 (Invention)
0.99 0.03 100
______________________________________
*1Exposed from the support side.
*2Color image residue at the portion having a cyan initial density of 1.5
From the results shown in Table 6, it can be seen hat the Samples of this invention (203, 204, 206, and 207) are excellent because they do not indicate a reduction in cyan color density even when processed in a fatigued leach liquid. Furthermore, the samples of the present invention show less stain even after light exposure for a long period of time.
Samples 301 to 307 of color photographic materials were prepared in the same manner as Example 1 except that couplers and compounds shown in Table 7 were used and Coupler Dispersing Oil (Oil-1) in layher 1 was used in an amount of 0.5 g/m2.
TABLE 7
______________________________________
Sample Coupler (Amount)*1
Compound (Amount)*2
______________________________________
301 EX - 1 (0.05) --
302 I - 3 (0.05) --
303 I - 3 (0.05) (1) (0.3)
304 I - 3 (0.05) (20) (0.3)
305 I - 13 (0.05) --
306 I - 13 (0.05) (7) (0.3)
307 I - 13 (0.05) (21) (0.3)
______________________________________
*1Mol amount per mol of silver
*2Mol amount per mol of coupler
Relative Cyan Coloring Density obtained in the same manner as in Example 1 are shown in Table 8 below.
TABLE 8
______________________________________
Relative Cyan
Sample Coloring Density
______________________________________
301 (Comparison)
0.65
302 (Comparison)
0.99
303 (Invention)
1.00
304 (Invention)
1.00
305 (Comparison)
1.00
306 (Invention)
0.99
307 (Invention)
1.00
______________________________________
From the results shown in Table 8 above, it can be seen that Samples (302 to 307) which use the cyan coupler defined in this invention show almost no reduction in color density even when processed in the fatigued bleach liquid. However, Sample (301) using a comparison cyan coupler shows a reduction in color density.
Samples 301 to 307 which were processed in Processing Step (A) were then subjected to a color image stability test in the same manner as in Example 1. The results obtained are shown in Table 9 below.
TABLE 9
______________________________________
Fluorescent Lamp (10,000 lux.)
Exposure for 7 Days
Sample D.sub.B
Color Image Residue (%)
______________________________________
301 (Comparison)
0.04 88
302 (Comparison)
0.11 99
303 (Invention)
0.03 96
304 (Invention)
0.03 98
305 (Comparison)
0.10 99
306 (Invention)
0.03 98
307 (Invention)
0.04 97
______________________________________
From the results shown in Table 9. it can be seen that Comparison Samples 302 and 305 show a large amount of yellow stain as a result of the light exposure. In contrast. Samples 303, 304, 306, and 307 of this invention which contain the compound of this invention show a very small amount of yellow stain.
From the results described above. it becomes clear that the samples based on this invention are excellent and they do not indicate reduction of cyan color density even when processed in a fatigued bleach liquid. In addition, the samples of the present invention indicate less formation of yellow stain even after light exposure for a long period of time.
Multilayer color photographic materials 401 to 407 were prepared in the same manner as in Example 2 except that the couplers and the compounds (defined in the present invention) shown in Tables 10 and 11 were used in layers 3 and 4, respectively.
TABLE 10
______________________________________
Compound
Sample Coupler (Amount) (Amount)
______________________________________
401 EX-3(0.002),EX-4(0.002),EX-1(0.05)
--
402 EX-3(0.002),EX-4(0.002),I-3(0.05)
--
403 EX-3(0.002),EX-4(0.002),I-3(0.05)
(17) (0.2)
404 EX-3(0.002),EX-4(0.002),I-3(0.05)
(17) (0.2)
405 EX-3(0.002),EX-4(0.002),I-13(0.05)
--
406 EX-3(0.002),EX-4(0.002),I-13(0.05)
(30) (0.2)
407 EX-3(0.002),EX-4(0.002),I-13(0.05)
(33) (0.2)
______________________________________
TABLE 11
______________________________________
Sample Coupler (Amount)
Compound (Amount)
______________________________________
401 EX-5 (0.02) --
402 I-18 (0.02) --
403 I-18 (0.02) --
404 I-18 (0.02) (17) (0.2)
405 I-14 (0.02) --
406 I-14 (0.02) --
407 I-14 (0.02) --
______________________________________
Samples 401 to 407 thus obtained were subjected to the same test as in Example 1 and the results obtained are shown in Table 12 below.
TABLE 12
______________________________________
Fluorescent Lamp (10,000
lux.) for 7 Days
Relative Cyan Color Image
Sample Coloring Density
D.sub.B Residue (%)
______________________________________
401 (Comparison)
0.74 0.04 95
402 (Comparison)
1.00 0.11 99
403 (Invention)
0.99 0.04 98
404 (Invention)
0.98 0.03 97
405 (Comparison)
0.98 0.10 98
406 (Invention)
0.99 0.04 97
407 (Invention)
0.99 0.04 98
______________________________________
From the results shown in Table 12, it can be seen that Samples of this invention (403, 404, 406 and 407) are excellent and they do not indicate a reduction of cyan coloring density even when processed in a fatigued bleach liquid. In addition, the samples of the present invention indicate less stain even after light exposure for a long period of time.
While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skilled in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.
Claims (20)
1. A silver halide color photographic light-sensitive material having at least one light-sensitive silver halide emulsion layer on a support, wherein said silver halide color photographic light-sensitive material contains (i) at least one cyan dye-forming coupler selected from the group consisting of compounds represented by formula (I) and a compound having at least two coupler residues derived from the compound represented by formula (I) and ii) at least one compound selected from the group consisting of compounds represented by formulas (II), (III), (IV), (V), (VI), (VII), (VIII) and a compound having at least two residues derived from at least one compound selected from the group consisting of compounds represented by formulas (VI), (VII) and (VIII); ##STR25## wherein R1 represents --CONR6 R7, --NHCOR6, --NHCOOR8, --NHSO2 R8, --NHCONR6 R7, or --NHSO2 NR6 R7, wherein R6 and R7 each represents a hydrogen atom, an aliphatic group, an aromatic group, or a heterocyclic group and R8 represents an aliphatic group, an aromatic group, or a heterocyclic group, or R6 and R7 in ##STR26## combine with each other to form a nitrogen-containing heterocyclic ring, R2 represents a group capable of being substituted to a naphthalene ring; l represents an integer of from 0 to 3; R3 represents a mono-valent organic group; and X represents a hydrogen atom or a group capable of releasing by a coupling reaction with the oxidation product of an aromatic primary amine developing agent, when l is 2 or 3, the R2 groups are the same or different, or they combine with each other to form a ring when they are adjacent to each other, or R2 and R3 groups when R2 is present at 6-position or R3 and X groups combine with each other to form a ring ##STR27## wherein M represents Cu, Co, Ni, Pd, or Pt; R2, R3, R4, and R5 each represents a hydrogen atom, a halogen atom, a hydroxy group, a cyano group; a substituted or unsubstituted alkyl group, aryl group, cycloalkyl group, or heterocyclic group bonded to the carbon atom of the benzene ring directly or through a divalent linkage group; or non-metallic atomic group necessary for forming a 6-membered ring by the combination of said R2 and R3, said R3 and R4, or said R4 and R5 with each other, R6, R9, and R10 each represents a hydrogen atom, a substituted or unsubstituted alkyl group or aryl group; R7 represents a hydrogen atom, a substituted or unsubstituted alkyl group or aryl group, or a hydroxy group; R8 represents a substituted or unsubstituted alkyl group, or aryl group, or a non-metallic atomic group necessary for forming a 5-membered to 8-membered ring by the combination of said R8 and R9 or R9 and R10 with each other; and Y represents a non-metallic atomic group necessary for forming a 5-membered ring or a 6-membered ring: ##STR28## wherein R24 represents an aliphatic group, an aromatic group, a heterocyclic group, an aliphatic oxy group, an aromatic oxy group, an aliphatic thio group, an aromatic thio group, an aliphatic carbonamido group, an aromatic carbonamido group, an aliphatic sulfonamido group, an aromatic sulfonamido group, a mono-substituted or disubstituted amino group with aliphatic or aromatic groups, and m represents an integer of 1 to 4 when m is plural, R24 groups are the same or different or combine with each other to form a ring when they are adjacent to each other, the two hydroxy groups are para-position or ortho-position relative to each other, R25 represents an aliphatic group, an aromatic group, a heterocyclic group, or a substituted silyl group, R26 has the same significance as defined above for R24 in formula (VI); n represents an integer of 1 to 3; and j represents an integer of 0 to 5, the sum of n and j being 6 or less; when n is plural, said OR25 groups are the same or different; when said j is plural, said R26 groups are the same or different, or when two OR25 groups, said two R26 groups, or said OR25 and R26 are in an ortho-position relative to each other, they are not combined or combined with each other to form a ring; R27, R28, R29, and R30 each represents a hydrogen atom or an aliphatic group; Y represents a hydrogen atom, an aliphatic group, an acyl group, an aliphatic sulfonyl group, an aromatic sulfonyl group, an aliphatic sulfinyl group, an aromatic sulfinyl group, an aliphatic oxycarbonyl group, an aromatic oxycarbonyl group, an oxyradical group, or a hydroxy group; and Z represents a non-metallic group necessary for forming a 5-membered to 7-membered ring with ##STR29##
2. The silver halide color photographic light-sensitive material as in claim 1, wherein R2 represents a halogen atom, a hydroxy gorup, --NR'6 R'7, a carboxy group, a sulfonic acid group, a cyano group, an aliphatic group, an aromatic group, a heterocyclic group, --NHCOR'6, --NHSO2 R'6, --CONR'6 R'7, --SO2 NR'6 R'7, --NHCONR'6 R'7, --COR'6, --OCOR'6, --OR'8, --SR'8, --SO2 R'8, --NHSO2 NR'6 R'7, a nitro group, an acid imido group, wherein R'6, R'7 and R'8 each represents an aliphatic group, an aromatic group, and a heterocyclic group or R'6 and R'7 each is a hydrogen atom, or R'6 and R'7 combine with each other to form a nitrogen-containing heterocyclic ring.
3. The silver halide color photographic light-sensitive material as in claim 1, wherein R3 represents a group represented by formula (IX)
R.sub.9 (Y.sub.1).sub.n - (IX)
wherein Y1 represents >NH,>CO, or >SO2, n represents 0 or 1; and R9 represents a hydrogen atom, an aliphatic group having 1 to 30 carbon atoms, an aromatic group having 6 to 30 carbon atoms, a heterocyclic group having 2 to 30 carbon atoms, 13 OR10, --COR10, ##STR30## --CO2 R12, --SO2 R12, or --SO2 OR12 wherein R10, R11, and R12 each represents an aliphatic group, an aromatic group, and a heterocyclic group, or R10, R11 and R12 each is a hydrogen atom, or R10 and R11 combine with each other to form a nitrogen-containing heterocyclic ring.
4. The silver halide color photographic light sensitive material as in claim 1, wherein X in formula (I) represents a hydrogen atom or a coupling releasing group (including releasing atom) selected from the group consisting of a halogen atom, --OR13, --SR13, ##STR31## (wherein R13 represents an aliphatic group having from 1 to 30 arbon atoms, an aromatic group having from 6 to 30 carbon atoms, or a heterocyclic group having from 2 to 30 carbon atoms), an aromatic azo group having from 6 to 30 carbon atoms, a heterocyclic group having from 2 to 30 carbon atoms bonded to the coupling active position of the coupler by a nitrogen atom.
5. The silver halide color photographic light sensitive material as in claim 1, wherein said divalent linkage group is a group selected from the group consisting of --O--, --S--, --NH--, an oxycarbonyl group, a carbonyl group, --HNCO--, --HNSO2 --, a carbonylamino group, a sulfonyl group and a carbonyloxy group.
6. The silver halide color photographic light sensitive material as in claim 1, wherein said non-metallic atomic group shown by Y in formulas (III) or (v) nessary for forming a 5- or 6-membered ring is selected from the group consisting of (a), (b), (c), (d) or (e) ##STR32## wherein R15 represents a hydrogen atom or a substituted or unsubstituted alkyl group.
7. The silver halide color photographic light sensitive material as in claim 1, wherein said compounds represented by formulae (II), (III), (IV) or (V) are those represented by formulae (IIa), (IIb), (IIIa), (IVa) (IVb) or (Va) ##STR33## wherein R2 to R10 and M are defined in claim 1 in the definition for formulae (II) to (V), n represents 2 or 3, and R17 represents a substituted or unsubstituted alkyl group or aryl group.
8. The silver halide color photographic light sensitive material as in claim 1, wherein said compound represented by formula (VI) is a compound represented by formula (VI-a) ##STR34## wherein R39 and R40 each represents an aliphatic group.
9. The silver halide color photographic light sensitive material as in claim 1, wherein said compound represented by formula (VII) is a compound represented by formulae (VII-a), (VII-b), (VII-c), (VII-d) or (VII-e) ##STR35## wherein R41 and R42 each represents an aliphatic group having 1 to 30 carbon atoms or a substituted silyl group having 3 to 30 carbon atoms, R43 represents an aliphatic group having 1 to 30 carbon atoms, an aliphatic oxy group having 1 to 30 carbon atoms, an aliphatic thio group having 1 to 30 carbon atoms, or a carbon amido group having 2 to 30 carbon atoms; R44 represents an aliphatic group having 1 to 30 carbon atoms or an aromatic group having 6 to 30 carbon atoms; R45, R46, R47, and R48 each represents a hydrogen atom or an aliphatic group having 1 to 12 carbon atoms; q represents an integer of 1 to 4; r represents an integer of 0 to 3; s represents an integer of 0 to 6; t represents an integer of 1 to 4; u represents an integer of 0 to 3; and v represents an integer of 0 to 2.
10. The silver halide color photographic light sensitive material as in claim 1, wherein said compound represented by formula (VIII) and derivatives thereof are compounds represented by formulae (VIII-a) and a bis-, tris-, or tetrakis compounds and a polymer which are derived by combining the compounds at Y or V; ##STR36## wherein Y has the same definition as in claim 1 and V represents an acyloxy group having from 2 to 30 carbon atoms, or an aliphatic and aromatic carbonamide group having from 2 to 30 carbon atoms.
11. The silver halide color photographic light sensitive material as in claim 1, wherein said compound of (ii) is a compound which is derived by combining two or more residues of at least two different compounds selected from the group consisting of compounds represented by formulae (VI), (VII) or (VIII).
12. The silver halide color photographic light sensitive material as in claim 1, wherein the total amount of a cyan coupler(s) is from 0.002 to 0.3 mol per mol of the light sensitive silver halide in the silver halide emulsion layer, wherein the amount of a cyan coupler other than the cyan coupler of (i) is not more than 40 mol %.
13. The silver halide color photographic light sensitive material as in claim 1, wherein the amount of the compound of (ii) is from 0.01 to 1 mol per mol of the cyan coupler of (i).
14. The silver halide color photographic light sensitive material as in claim 1, wherein said cyan coupler of (i) is incorporated to the light-sensitive silver halide emulsion layer or a layer adjacent thereto.
15. The silver halide color photographic light sensitive material as in claim 14, wherein said light-sensitive silver halide emulsion layer is red-sensitive.
16. The silver halide color photographic light sensitive material as in claim 1, wherein said compound of (ii) is incorporated to the same layer containing the cyan coupler of (i) or to a layer adjacent thereto.
17. The silver halide color photographic light sensitive material as in claim 1, wherein said compound of (i) having at least two coupler residues is in a form selected from the group consisting of a bis-, tris- and tetrakis compounds, an oligomer and a polymer.
18. The silver halide color photographic light sensitive material as in claim 1, wherein said compound of (ii) having at least two residues is in a form selected from the group consisting of a bis-, tris- and tetrakis compound, an oligomer and a polymer.
19. The silver halide color photographic light sensitive material as in claim 1, wherein the substituent which can be substituted to any one of groups contained in compounds (i) and (ii) is a substituent selected from the group consisting of a halogen atom, a nitro group, a cyano group, an acyl group, an alyloxy group, an alkyl- or arylsulphonyl group, a hydroxy group, an amido group, an amino group including NH2 and mono- and disubstituted with an aliphatic or aromatic group, an alkyl group, an alkenyl group and a aryl group.
20. A method for producing a color image which comprises (1) developing an exposed silver halide color photographic light-sensitive material using developing solution containing an aromatic primary amino-developing agent, (2) bleaching and then fixing, or blixing, said light-sensitive material which comprises at least one light-sensitive silver halide emulsion layer on a support, wherein said silver halide color photographic light-sensitive material contains (i) at least one cyan dye-forming coupler selected from the group consisting of compounds represented by following formula (I) and a compound having at least two coupler residues derived from the compound represented by formula (I), and (ii) at least one compound selected from the group consisting of compounds represented by formulas (II), (III), (IV), (V), (VI), (VII), (VIII) and a compound having at least two residues derived from at least one compound selected from the group consisting of compounds represented by formulas (VI), (VII), and (VIII): ##STR37## wherein R1 represents --CONR6 R7, --NHCOR6, --NHCOOR8, --NHSO2 R8, --NHCONR6 R7, or --NHSO2 NR6 R7, wherein R6 and R7 each represents a hydrogen atom, an aliphatic group, an aromatic group, or a heterocyclic group and R8 represents an aliphatic group, an aromatic group, or a heterocyclic group, or R6 and R7 in ##STR38## combine with each other to form a nitrogen-containing heterocyclic ring, R2 represents a group capable of being substituted to a naphthalene ring; l represents an integer of from 0 to 3; R3 represents a mono-valent organic group; and X represents a hydrogen atom or a group capable of releasing by a coupling reaction with the oxidation product of an aromatic primary amine developing agent, when l is 2 or 3, the R2 groups are the same or different, or they combine with each other to form a ring when they are adjacent to each other, or R2 and R3 groups when R2 is present at the 6-position or R3 and X groups combine with each other to form a ring ##STR39## wherein M represent Cu, Co, Ni, Pd, or Pt; R2, R3, R4, and R5 each represents a hydrogen atom, a halogen atom, a hydroxy group, a cyano group; a substituted or unsubstituted alkyl group, aryl group, cycloalkyl group, or heterocyclic group bonded to the carbon atom of the benzene ring directly or through a divalent linkage group; or a non-metallic atomic group necessary for forming a 6-membered ring by the combinaton of said R2 and R3, said R3 and R4, or said R4 and R5 with each other, R6 R9, and R10 each represents a hydrogen atom, a substituted or unsubstituted alkyl group or aryl group; R7 represents a hydrogen atom, a substituted or unsubstituted alkyl group or aryl group, or a hydroxy group; R8 represents a substituted or unsubstituted alkyl group, or aryl group, or a non-metallic atomic group necessary for forming a 5-membered to 8-membered ring by the combination of said R8 and R9 or R.sup. 9 and R10 with each other; and Y represents a non-metallic atomic group necessary for forming a 5-membered ring or a 6-membered ring: ##STR40## wherein R24 represents an aliphatic group, an aromatic group, a heterocyclic group, an aliphatic oxy group, an aromatic oxy group, an aliphatic thio group, an aromatic thio group, an aliphatic carbonamido group, an aromatic carbonamido group, an aliphatic sulfonamido group, an aromatic sulfonamido group, a mono-substituted or disubstituted amino group with an aliphatic or aromatic groups and m represents an integer of 1 to 4 when m is plural, R24 groups are the same or different or combine with each other to form a ring when they are adjacent to each other, the two hydroxy groups are para-position or ortho-position relative to each other, R25 represents an aliphatic group, an aromatic group, a heterocyclic group, or a substituted silyl group, R26 has the same significance as defined above for R24 in formula (VI); n represents a integer of 1 to 3; and j represents an integer of 0 to 5, the sum of n and j being 6 or less; when n is plural, said OR25 groups are the same or different; when said j is plural, said R26 groups are the same or different, or when two OR25 groups, said two R26 groups, or said OR25 and R26 are in an orthoposition relative to each other, they are not combined or combined with each other to form a ring; R27, R28, R29, and R30 each represents a hydrogen atom or an aliphatic group; Y represents a hydrogen atom, an aliphatic group; and acyl group; an aliphatic sulfonyl group, an aromatic sulfonyl group, an aliphatic sulfinyl group, an aromatic sulfinyl group, an aliphatic oxycarbonyl group, an aromatic oxycarbonyl group, an oxyradical group, or a hydroxy group; and Z represents a non-metallic group necessary for forming a 5-membered to 7-membered ring with ##STR41##
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60-259810 | 1985-11-21 | ||
| JP60-259809 | 1985-11-21 | ||
| JP25981085A JPS62121457A (en) | 1985-11-21 | 1985-11-21 | Silver halide color photographic sensitive material |
| JP25980985A JPS62121456A (en) | 1985-11-21 | 1985-11-21 | Silver halide color photographic sensitive material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USH567H true USH567H (en) | 1989-01-03 |
Family
ID=26544291
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/932,875 Abandoned USH567H (en) | 1985-11-21 | 1986-11-20 | Silver halide color photographic light-sensitive materials containing cyan coupler and specific compound |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USH567H (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0377910A2 (en) * | 1989-01-12 | 1990-07-18 | Agfa-Gevaert AG | Colour-photographic negative-recording material |
| EP0413204A2 (en) * | 1989-08-15 | 1991-02-20 | Agfa-Gevaert AG | Colour photographic silver halide material |
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