Light-sensitive silver halide color photographic material containing novel cyan coupler

BACKGROUND OF THE INVENTION
This invention relates to a light-sensitive silver halide color photographic material containing a novel cyan coupler.
By carrying out color developing processing of a light-sensitive silver halide color photographic material after giving exposure thereto, an aromatic primary amine developing agent reacts with a dye forming coupler (hereinafter merely called "coupler") to form a color image. In this method, color reproduction according to the subtractive color photography is effected, whereby yellow, magenta and cyan color images in complementary color relationships with blue, green and red, respectively, are formed.
As the cyan coupler, generally phenols or naphthols have been widely used, but the cyan coupler selected from phenols and naphthols of the prior art had some problems to be solved. For example, the color images obtained from 2,5-diacylaminophenol type cyan couplers as described in U.S. Pat. No. 2,367,531, No. 2,369,929, No. 2,423,730, No. 2,801,171, etc. are generally inferior in heat fastness, while the acylaminophenol type cyan couplers as described in U.S. Pat. No. 2,772,162, No. 2,895,826, etc. had the drawback that the light fastness of the color image obtained was generally bad. Also, 1-hydroxy-2-naphthoamide type cyan couplers are also insufficient in both light and heat (particularly humid heat) fastness.
SUMMARY OF THE INVENTION
Accordingly, an object of the present invention is to provide a novel cyan coupler which improves the drawbacks of the cyan couplers of the prior art and further gives a dye image which can stand storage for a long term. Another object of the present invention is to provide a light-sensitive silver halide color photographic material having at least one silver halide emulsion layer containing such a coupler.
The above objects of the present invention have been accomplished by a light-sensitive silver halide color photographic material having at least one silver halide emulsion layer on a support, characterized in that at least one layer of said silver halide emulsion layer contains at least one cyan coupler represented by the formula (I) shown below: ##STR2## wherein R.sub.1 and R.sub.2 each represent an alkyl group, an aryl group, a heterocyclic group, a dialkylamino group, an anilino group, an alkoxy group or an arloxy group; R.sub.3 represents a hydrogen atom or an alkyl group; R.sub.4 represents a hydrogen atom, an alkyl group, an aryl group, a R.sub.5 CO-- group or a R.sub.5 SO.sub.2 -- group; provided that R.sub.3 and R.sub.4 cannot be hydrogen atoms at the same time; R.sub.5 represents a hydrogen atom, an alkyl group, an aryl group, a dialkylamino group, an anilino group, an alkoxy group or an aryloxy group; and X represents a hydrogen atom or an eliminatable group through the reaction with the oxidized product of a color developing agent.

DESCRIPTION OF THE PREFERRED EMBODIMENTS
In the above formula (I), the alkyl group represented by R.sub.1 and R.sub.2 may be either straight chain, branched or cyclic, and includes those having substituents. Specific examples may include groups of methyl, ethyl, iso-propyl, t-butyl, cyclohexyl, undecyl, trifluoromethyl, trichloromethyl, perfluoropropyl, 2-methoxyethyl, hyroxymethyl, benzyl, phenethyl, 3-(2,5-di-t-amylphenoxy)propyl, 1-(4-butanesulfonamidophenoxy)tridecyl, 1-(2,4,6-trichlorophenoxy)-undecyl, and other groups. Among them, halosubstituted alkyl groups, subtituted aryloxy-substituted alkyl groups are preferred.
The aryl group represented by R.sub.1 and R.sub.2 includes also those having substituents, and preferable substituents may include halogen atoms, and each groups of alkyl, aryl, heterocyclic, alkoxy, aryloxy, acyl, ester, amide, imide, ureido, sulfonyl, alkoxycarbonyl, aryloxycarbonyl, hydroxy, carboxy, sulfo, cyano, nitro, etc.
Examples of the heterocyclic group represented by R.sub.1 and R.sub.2 may include 2-furyl, 2-imidazolyl, 2-thienyl, 2-pyridyl, 6-quinolyl and the like.
The dialkylamino group represented by R.sub.1 and R.sub.2 may be preferably an unsubstituted dialkylamino group, as exemplified by dimethylamino, diethylamino, methylbutylamino groups, etc.
The anilino group may have also substituents, and anilino groups substituted with, for example, halogen atoms, alkyl, alkoxy, amide, sulfonamide, cyano, nitro groups, etc. are preferred.
As the alkoxy group, preferred are non-substituted alkoxy groups such as methoxy, ethoxy, butoxy, octyloxy, dodecyloxy and the like, and also as the aryloxy group, preferred are non-substituted ones such as phenoxy group.
As the alkyl group represented by R.sub.3 and R.sub.4, substituted or unsubstituted alkyl groups having 1 to 22 carbon atoms may be included, preferably unsubstituted alkyl groups.
As the aryl group represented by R.sub.4, the same aryl groups as mentioned for R.sub.1 and R.sub.2 can be included.
The alkyl, aryl, dialkylamino, anilino, alkoxy and aryloxy groups represented by R.sub.5 have the same meanings as already mentioned for R.sub.1 and R.sub.2.
Among the groups represented by R.sub.3 and R.sub.4, the cases wherein R.sub.3 is a hydrogen atom or a lower alkyl group and R.sub.4 is an alkylcarbonyl or arylcarbonyl group (R.sub.5 CO--), an alkylsulfonyl or arylsulfonyl group (R.sub.5 SO.sub.2 --) are preferred.
As the group represented by X eliminatable by the reaction with the oxidized product of a color developing agent, the so-called split-off group conventionally used in the field of the art may be included.
Among the cyan couplers represented by the formula (I), preferred are those as shown by the following formulae (II), (III) and (IV): ##STR3##
In the above formulae (II) to (IV), R.sub.1, R.sub.2 and X have the same meanings as R.sub.1, R.sub.2 and X in the formula (I), respectively. R.sub.6 represents an alkyl group substituted by at least one halogen atom, R.sub.7 represents a substituted or unsubstituted amino group, an alkoxy group or an aryloxy group, R.sub.8 represents a substituted or unsubstituted phenyl group, and R.sub.9 represents a substituted or unsubstituted amino group, alkoxy group, alkyl group or aryl group.
Next, each compound is explained in more detail.
As R.sub.2 in the formula (II), preferred are a substituted or unsubstituted alkyl group, phenyl group or anilino group, more preferably a substituted alkyl group, particularly preferably an alkoxy group, a phenoxy group, an alkylsulfonyl group or a phenylsulfonyl-substituted alkyl group.
As R.sub.6, preferred are an alkyl group substituted by a chlorine atom or a bromine atom, more preferred are an alkyl group of which all the hydrogen atoms are substituted by chlorine atoms and/or fluorine atoms, particularly a perfluoroalkyl group is preferred.
As R.sub.7, preferred is an anilino group.
As X, preferred are a hydrogen atom, a chlorine atom, a substituted or unsubstituted alkoxy group and aryloxy group, and more preferably a chlorine atom, a substituted alkoxy group and a substituted aryloxy group.
As R.sub.2, R.sub.6 and X in the formula (III), preferred substituents may be mentioned those as specifically mentioned in the formula (II), respectively.
As R.sub.8, preferred is an unsubstituted phenyl group or a phenyl group substituted by a halogen atom, an alkoxy group or an acylamino group.
As R.sub.1 in the formula (IV), preferred are a substituted or unsubstituted alkyl group, a phenyl group and an anilino group, more preferably a substituted alkyl group.
As R.sub.6 and X, preferred substituents may be mentioned those as specifically mentioned in the formula (III), respectively.
As R.sub.9, preferred are a substituted or unsubstituted alkyl group, alkoxy group, aryl group and anilino group, and more preferably a substituted alkyl group.
Representative specific examples of the novel cyan coupler to be used in the present invention (called the cyan coupler of the present invention) are enumerated below, but the present invention is not limited to these.
__________________________________________________________________________ ##STR4## (I)No. R.sub.1 R.sub.2 R.sub.3 R.sub.4 X__________________________________________________________________________I-1 ##STR5## ##STR6## H COCH.sub.3 ClI-2 ##STR7## ##STR8## H COC.sub.2 H.sub.5 ClI-3 ##STR9## ##STR10## H ##STR11## ClI-4 C.sub.3 F.sub.7 ##STR12## H COC.sub.3 H.sub.7 HI-5 C.sub.2 F.sub.5 ##STR13## H COCH.sub.3 HI-6 ##STR14## ##STR15## H ##STR16## ClI-7 C.sub.4 H.sub.9 (t) ##STR17## H SO.sub.2 C.sub.4 H.sub.9 ClI-8 (CF.sub.2).sub.4 H ##STR18## H ##STR19## HI-9 ##STR20## ##STR21## H COC.sub.3 H.sub.7 HI-10 ##STR22## ##STR23## H COC.sub.3 H.sub.7 OCH.sub.2 COCOOC.sub.2 H.sub.5I-11 ##STR24## ##STR25## H COC.sub.3 H.sub.7 ##STR26##__________________________________________________________________________ ##STR27##No. R.sub.6 R.sub.2 R.sub.7 X__________________________________________________________________________II-1 (CF.sub.2).sub.3 OH CH.sub.3 ##STR28## ClII-2 CF.sub.3 C.sub.12 H.sub.25 OC.sub.4 H.sub.9 (i) ClII-3 CCl.sub.3 ##STR29## ##STR30## HII-4 C.sub.2 F.sub.5 ##STR31## ##STR32## ClII-5 C.sub.2 F.sub.5 ##STR33## ##STR34## ##STR35##II-6 C.sub.3 F.sub.7 ##STR36## ##STR37## ClII-7 C.sub.3 F.sub.7 ##STR38## ##STR39## ClII-8 C.sub.4 F.sub.9 CH.sub.2 CH.sub.2 OCH.sub.3 ##STR40## ClII-9 (CF.sub.2).sub.4 H C.sub.12 H.sub.25 ##STR41## OCH.sub.2 CONH(CH.sub.2).sub.2 OCH.sub.3II-10 C.sub.7 H.sub.15 CH.sub.2 CH.sub.2 SO.sub.2 C.sub.12 H.sub.25 ##STR42## Cl__________________________________________________________________________ ##STR43##No. R.sub.8 R.sub.2 R.sub.6 X__________________________________________________________________________III-1 ##STR44## ##STR45## CF.sub.3 HIII-2 ##STR46## C.sub.12 H.sub.25 CCl.sub.3 ##STR47##III-3 ##STR48## CH.sub.2 CH.sub.2 SO.sub.2 C.sub. CHCl.sub.25 ##STR49##III-4 ##STR50## ##STR51## C.sub.2 F.sub.5 ClIII-5 ##STR52## ##STR53## C.sub.2 F.sub.5 ClIII-6 ##STR54## ##STR55## C.sub.3 F.sub.7 OCH.sub.2 COOC.sub.2 H.sub.5III-7 ##STR56## ##STR57## C.sub.3 F.sub.7 ##STR58##III-8 ##STR59## ##STR60## C.sub.4 F.sub.9 ClIII-9 ##STR61## ##STR62## (CF.sub.2).sub.4 H OCH.sub.2 CONH(CH.sub.2).sub. 2 OCH.sub.3III-10 ##STR63## ##STR64## C.sub.5 F.sub.11 Cl__________________________________________________________________________ ##STR65##No. R.sub.1 R.sub.6 R.sub.9 X__________________________________________________________________________IV-1 C.sub.12 H.sub.25 CF.sub.3 OC.sub.4 H.sub.9 (i) ClIV-2 CH.sub.2 CH.sub.2 SO.sub.2 C.sub.12 H.sub.25 CCl.sub.3 ##STR66## HIV-3 ##STR67## CHCl.sub.2 ##STR68## ClIV-4 ##STR69## C.sub.2 F.sub.5 ##STR70## ClIV-5 ##STR71## C.sub.2 F.sub.5 C.sub.2 F.sub.5 ClIV-6 ##STR72## C.sub.3 F.sub.7 C.sub.3 F.sub.7 ClIV-7 C.sub.3 F.sub.7 C.sub.3 F.sub.7 ##STR73## ##STR74##IV-8 ##STR75## C.sub.4 H.sub.9 ##STR76## OCH.sub.2 CONH(CH.sub.2).sub.2 OCH.sub.3IV-9 ##STR77## (CF.sub.2).sub.4 H CH.sub.3 ClIV-10 ##STR78## C.sub.5 F.sub.11 C.sub.12 H.sub.25 ##STR79##__________________________________________________________________________
In the following, synthesis examples of the cyan coupler of the present invention are shown.
Synthesis example 1 (synthesis of the exemplary compound I--1)
Synthesis of 2-pentafluorobenzamido-4-chloro-5-{2-(2,4-di-t-amylphenoxy)-3-methylbutaneamido}-6-nitrophenol
An amount of 5 g (7.3.times.10.sup.-3 mole) of 2-pentafluorobenzamido-4-chloro-5-{2-(2,4-di-t-amylphenoxy)-3-methylbutaneamido}phenol was dissolved in 25 ml of acetone and 25 ml of acetic acid, and cooled in a salt-ice bath. To this solution was added dropwise 0.55 ml (one equivalent) of a 61% nitric acid (specific gravity: 1.38) diluted with 2 ml of acetic acid slowly so that the liquid temperature might not exceed 3.degree. C. Further, the mixture was cooled to -5.degree. C. and after addition of 0.3 ml of conc. sulfuric acid, the mixture was gradually returned to room temperature (the solution became colored in orange). The reaction mixture was poured into water, and the yellow solids precipitated were filtered and washed with water. The crude product (5.1 g) was used as such for the subsequent reaction.
Synthesis of 2-pentafluorobenzamido-4-chloro-5-{2-(2,4-di-t-amylphenoxy)-3-methylbutaneamido}-6-aminophenol
The above nitro derivative (4.1 g, 5.7.times.10.sup.-3 mole) was dissolved in 100 ml of ethanol and 2 ml (tetra equivalents) of conc. hydrochloric acid was added thereto. Hydrogenation was effected with the use of 0.4 g of Pd-C (palladium-carbon) as the catalyst. The color of the nitro derivative disappeared in 2 hours, and the Pd-C was removed by filtration and ethanol was evaporated from the filtrate, followed by extraction of the residue with ethyl acetate. The ethyl acetate layer was washed with an aqueous sodium hydrogen carbonate solution and then with water, and after drying over magnesium sulfate, ethyl acetate was evaporated. The residue was purified by separation according to column chromatography to give 3.1 g of an amorphous solid.
Synthesis of 2-pentafluorobenzamido-4-chloro-5-{2-(2,4-di-t-amylphenoxy)-3-methylbutaneamido}-6-acetamidophenol (Compound I--1)
The above amino derivative (1.01 g, 1.48.times.10.sup.-3 mole) was dissolved in 10 ml of acetonitrile, and refluxed under heating with addition of 0.2 ml (1.3 equivalents) of acetic anhydride for 4 hours. The reaction mixture was applied to silica gel column chromatography (toluene.fwdarw.toluene/acetone=50/1) to separate the desired product, which was recrystallized from a solvent mixture of hexaneethanol (20/1) to give 0.64 g of the Compound I--1. melting point: 196.degree. to 198.degree. C.
Synthesis example 2 (synthesis of the exemplary compound II--4)
Synthesis of 2-pentafluoropropylamido-4-chloro-5-nitrophenol
In 100 ml of acetonitrile was dissolved 11 g (58.times.10.sup.-3 mole) of 2-amino-4-chloro-5-nitrophenol. To the solution was added 19.9 g of pentafluoropropionic acid anhydride at room temperature and then the mixture was heated under reflux for 2 hours. After the reaction, a solvent was evaporated under reduced pressure and the residue was recrystallized from hexane to obtain products. Yield: 17 g (87%).
Synthesis of 2-pentafluoropropylamido-4-chloro-5-aminophenol
In 150 ml of ethanol was dissolved 13.7 g (41.times.10.sup.-3 mole) of 2-pentafluoropropylamido-4-chloro-5-nitrophenol and hydrogenation was effected by using 0.9 g of Pd-C as a catalyst. The color of the nitro derivative disappeared in 2 hours, and the Pd-C was removed by filtration and ethanol was evaporated from the filtrate, followed by extraction of the residue with ethyl acetate. The ethyl acetate layer was washed with an aqueous sodium hydrogen carbonate solution and then with water, and after drying over magnesium sulfate, ethyl acetate was evaporated. 12.1 g of a crude product was used as such for the subsequent reaction.
Synthesis of 2-pentafluoropropylamido-4-chloro-5-{2-(2,4-di-t-amylphenoxy)butaneamido}phenol
In 100 ml of ethyl acetate was dissolved 12 g (39.times.10.sup.-3 mole) of 2-pentafluoropropylamido-4-chloro-5-aminophenol and then 15 g (43.times.10.sup.-3 mole) of 2-(2,4-di-t-amylphenoxy)butanoic acid chloride and 3.5 g (43.times.10.sup.-3 mole) of pyridine were added to the solution, and the mixture was stirred at room temperature for 3 hours. After the reaction, a solvent was removed by evaporation, the residue was separated and purified through a column chromatography, and recrystallized from n-hexane to obtain the title compound. Yield: 9.0 g, FD-Mass 608, melting point: 167.degree. to 168.degree. C.
Synthesis of 2-pentafluoropropylamido-4-chloro-5-{2-(2,4-di-t-amylphenoxy)butanamido}-6-nitrophenol
In 100 ml of acetic acid and 40 ml of dimethylformamide was dissolved 9 g (15.times.10.sup.-3 mole) of 2-pentafluoropropylamido-4-chloro-5-{2-(2,4-di-t-amylphenoxy)butanamido}phenol. To the solution was added dropwise slowly a solution of 1.2 g (18.times.10.sup.-3 mole) of sodium nitrite dissolved in 5 ml of a distilled water at room temperature, and then the mixture was stirred for one hour. The reaction mixture was poured into ice-cold water and precipitated yellow solids were collected by filtration and washed with water. Yield: 8 g.
Synthesis of 2-pentafluoropropylamido-4-chloro-5-{2-(2,4-di-t-amylphenoxy)butanamido}-6-aminophenol
In 30 ml of tetrahydrofuran and 30 ml of ethanol was dissolved 8.3 g (13.times.10.sup.-3 mole) of 2-pentafluoropropylamido-4-chloro-5-{2-(2,4-di-t-amylphenoxy)butanamido}-6-nitrophenol and hydrogenation was effected by using 0.6 g of Pd-C as a catalyst. The color of the nitro derivative disappeared in 4 hours, and the Pd-C was removed by filtration and a solvent was evaporated therefrom under reduced pressure, followed by extraction of the residue with ethyl acetate. The ethyl acetate layer was washed with an aqueous sodium hydrogen carbonate solution and then with water, and after drying over magnesium sulfate, ethyl acetate was evaporated. Yield: 7.9 g.
Synthesis of phenyl-[2-{2-(2,4-di-t-amylphenoxy)butanamido}-3-chloro-5-pentafluoropropylamido-6-hydroxyphenyl]urea
In 100 ml of ethyl acetate was dissolved 3.6 g (5.8.times.10.sup.-3 mole) of 2-pentafluoropropylamido-4-chloro-5-{2-(2,4-di-t-amylphenoxy)butanamido}-6-aminophenol, and 0.69 g (5.8.times.10.sup.-3 mole) of phenylisocyanate was added to the solution and the mixture was refluxed under heating for 2 hours. After the reaction, a solvent was distilled off, and the residue was separated and purified through column chromatography and recrystallized from hexane. Yield: 2.4 g (60%), FD-Mass: 741, melting point: 127.degree. to 128.degree. C.
Synthesis example 3 (synthesis of the exemplary compound III--4)
Synthesis of 2-benzamido-4-chloro-5-nitrophenol
In 100 ml of ethyl acetate was dissolved 40 g (210.times.10.sup.-3 mole) of 2-amino-4-chloro-5-nitrophenol, and 33 g of benzoyl chloride was added at room temperature and then the mixture was refluxed under heating for 2 hours. After the reaction, a solvent was distilled off under reduced pressure and the residue was recrystallized from hexane to obtain products. Yield: 60 g.
Synthesis of 2-benzamido-4-chloro-5-aminophenol
In 100 ml of ethanol was dissolved 28 g (96.times.10.sup.-3 mole) of 2-benzamido-4-chloro-5-nitrophenol and hydrogenation was effected by using 1.5 g of Pd-C as a catalyst. The color of the nitro derivative disappeared in 2 hours, and the Pd-C was removed by filtration and ethanol was evaporated from the filtrate, followed by extraction of the residue with ethyl acetate. The ethyl acetate layer was washed with an aqueous sodium hydrogen carbonate solution and then with water, and after drying over magnesium sulfate, ethyl acetate was evaporated. 26 g of the crude product was used as such for the following reaction.
Synthesis of 2-benzamido-4-chloro-5-{2-(2,4-di-t-amylphenoxy)butanamido}phenol
In 100 of ethyl acetate was dissolved 15 g (57.times.10.sup.-3 mole) of 2-benzamido-4-chloro-5-aminophenol, and then 21 g of 2-(2,4-di-t-amylphenoxy)butanoic acid chloride and 5 g of pyridine were added thereto and the mixture was stirred at room temperature for 3 hours. After the reaction, a solvent was distilled off, and the residue was separated and purified through column chromatography and recrystallized from n-hexane to obtain the title compound. Yield: 14.1 g, FD-Mass: 564, melting point: 190.degree. to 191.degree. C.
synthesis of 2-nitro-3-{2-(2,4-di-t-amylphenoxy)butanamido}-4-chloro-6-benzamidophenol
In 100 ml of acetic acid and 100 ml of dimethylformamide was dissolved 20 g (35.times.10.sup.-3 mole) of 2-benzamido-4-chloro-5-{2-(2,4-di-t-amylphenoxy)butanamido}phenol. To the solution was added dropwise slowly a solution of 2.7 g of sodium nitrite dissolved in 5 ml of a distilled water at room temperature, and then the mixture was stirred for 2 hours. The reaction mixture was poured into ice-cold water, and precipitated yellow solids were collected by filtration and washed with water. Yield: 21 g.
Synthesis of 2-amino-3-{2-(2,4-di-t-amylphenoxy)butanamido}-4-chloro-6-benzamidophenol
In 50 ml of tetrahydrofuran and 100 ml of ethanol was dissolved 21 g (13.times.10.sup.-3 mole) of 2-nitro-3-{2-(2,4-di-t-amylphenoxy)butanamido}-4-chloro-6-benzamidophenol and hydrogenation was effected by using 1.2 g of Pd-C as a catalyst. The color of the nitro derivative disappeared in 4 hours, and the Pd-C was removed by filtration and a solvent was evaporated therefrom under reduced pressure, followed by extraction of the residue with ethyl acetate. The ethyl acetate layer was washed with an aqueous sodium hydrogen carbonate solution and then with water, and after drying over magnesium sulfate, ethyl acetate was evaporated. Yield: 20 g.
Synthesis of 2-pentafluoropropylamido-3-{2-(2,4-di-t-amylphenoxy)butanamido}-4-chloro-6-benzaminophenol
In 50 ml of ethyl acetate was dissolved 4 g (6.9.times.10.sup.-3 mole) of 2-amino-3-{2-(2,4-di-t-amylphenoxy)butanamido}-4-chloro-6-benzamindophenol, and 2.4 g of pentafluoropropionic acid anhydride was added to the solution and the mixture was stirred at room temperature for 2 hours. After the reaction, a solvent was evaporated and the residue was separated and purified through colomn chromatography and recrystallized from hexane. Yield: 1.8 g, FD-Mass: 724, melting point: 197.degree. to 198.degree. C.
Synthesis example 4 (synthesis of the exemplary compound IV--5)
Synthesis of 2-{2-(2,4-di-t-amylphenoxy)butanamido}-4-chloro-5-nitrophenol
In 100 ml of ethyl acetate was dissolved 25 g (133.times.10.sup.-3 mole) of 2-amino-4-chloro-5-nitrophenol. To the solution was added 50 g of 2-(2,4-di-t-amylphenoxy)butanoic acid chloride at room temperature, and then the mixture was refluxed under heating for 2 hours. After the reaction, a solvent was evaporated under reduced pressure and the residue was recrystallized from hexane to obtain products. Yield: 61 g.
Synthesis of 2-{2-(2,4-di-t-amylphenoxy)butanamido}-4-chloro-5-aminophenol
In 100 ml of ethanol was dissolved 30 g (61.times.10.sup.-3 mole) of 2-{2-(2,4-di-t-amylphenoxy)butanamido}-4-chloro-5-nitrophenol and hydrogenation was effected by using 1.5 g of Pd-C as a catalyst. The color of the nitro derivative disappeared in 2 hours, and the Pd-C was removed by filtration and ethanol was evaporated from the filtrate, followed by extraction of the residue with ethyl acetate. The ethyl acetate layer was washed with an aqueous sodium hydrogen carbonate solution and then with water, and after drying over magnesium sulfate, ethyl acetate was evaporated. 28 g of the crude product was used as such for the following reaction.
Synthesis of 2-{2-(2,4-di-t-amylphenoxy)butanamido}-4-chloro-5-pentafluoropropylamidophenol
In 100 ml of ethyl acetate was dissolved 20 g (43.times.10.sup.-3 mole) of 2-{2-(2,4-di-t-amylphenoxy)butanamido}-4-chloro-5-aminophenol, and 15 g of pentafluoropropionic acid anhydride was added to the solution and the mixture was stirred at room temperature for 2 hours. After the reaction, a solvent was evaporated and the residue was separated and purified through column chromatography and recrystallized from n-hexane to obtain the title compound. Yield: 14 g, FD-Mass: 606, melting point: 175.degree. to 176.degree. C.
Synthesis of 2-nitro-3-pentafluoropropylamido-4-chloro-6-{2-(2,4-di-t-amylphenoxy)butanamino}phenol
In 100 ml of acetic acid and 20 ml of dimethylformamide was dissolved 13.4 g (22.times.10.sup.-3 mole) of 2-{2-(2,4-di-t-amylphenoxy)butanamido}-4-chloro-5-pentafluoropropylamidophenol. To the solution was added dropwise slowly a solution of 1.7 g of sodium nitrite dissolved in 5 ml of distilled water at room temperature, and then the mixture was stirred for one hour. The reaction mixture was poured into ice-cold water and precipitated yellow solid was collected by filtration and washed with water. Yield: 13 g.
Synthesis of 2-amino-3-pentafluoropropylamido-4-chloro-6-{2-(2,4-di-t-amylphenoxy)butanamido}phenol
In 40 ml of tetrahydrofuran and 60 ml of ethanol was dissolved 13 g (20.times.10.sup.-3 mole) of 2-nitro-3-pentafluoropropylamido-4-chloro-6-{2-(2,4-di-t-amylphenoxy)butanamido}phenol, and hydrogenation was effected by using 1.3 g of Pd-C as a catalyst. The color of the nitro derivative disappeared in 5 hours, and the Pd-C was removed by filtration and a solvent was evaporated therefrom under reduced pressure, followed by extraction of the residue with ethyl acetate. The ethyl acetate layer was washed with an aqueous sodium hydrogen carbonate solution and then with water, and after drying over magnesium sulfate, ethyl acetate was evaporated. Yield: 12.5 g.
Synthesis of 2,3-dipentafluoropropylamido-4-chloro-6-{2-(2,4-di-t-amylphenoxy)butanamido}phenol
In 50 ml of ethyl acetate was dissolved 4 g (6.4.times.10.sup.-3 mole) of 2-amino-3-pentafluoropropylamido-4-chloro-6-{2-(2,4-di-t-amylphenoxy)butanamido}phenol, and 2.2 g of pentafluoropropionic acid anhydride was added to the solution and the mixture was refluxed under heating for 3 hours. After the reaction, a solvent was evaporated and the residue was separated and purified through column chromatography. Yield: 3.6 g (amorphous solid), FD-Mass: 768.
The cyan coupler of the present invention is used in a silver halide emulsion layer, primary in a red-sensitive emulsion layer, and its amount added may be in the range of 2.times.10.sup.-3 to 8.times.10.sup.-1 mole, preferably 1.times.10.sup.-2 to 5.times.10.sup.-1 mole, per one mole of silver halide.
As the method for incorporating the cyan coupler of the present invention in the silver halide emulsion layer, various methods may be employed. For example, it may be dissolved in a high boiling point organic solvent having a boiling point of 150.degree. C. or higher such as alkyl phthalates (dibutyl phthalate, dioctyl phthalate, etc.), phosphates (diphenyl phosphate, triphenyl phosphate, tricresyl phosphate, dioctylbutyl phosphate), phenol derivatives (2,4-di-t-butylphenol, etc.), etc. and/or a low boiling point organic solvent having a boiling point of 30.degree. to 150.degree. C. (e.g., ethyl acetate, butyl acetate, ethyl propionate, sec-butyl alcohol, methyl isobutyl ketone, methyl cello-solve acetate, etc.) before dispersed in a hydrophilic colloid. Ordinarily, it is preferable to use a mixture of a high boiling point organic solvent and a low boiling point solvent.
The silver halide grains to be used in the silver halide emilsion layer of the light-sensitive silver haldie photographic material are not particularly limited, but silver iodobromide, silver bromide, silver halide, silver chlorobromide, silver chloroiodobromide or the like is preferred.
Crystals of these silver halide grains may be of regular crystals, twin crystals or others, and these can be used those having any ratio of {100} face to {111} face. Further, crystal structure of these silver halide grains may be uniform through inside to outside, or may be of layered structure comprising an inside and outside of different nature (a core-shell type). These silver halide grains may be also of the type such that a latent image is chiefly formed on the surface, or of the type wherein it is formed in the inside of a grain. Furthermore, plate-like silver halide grains (see Japanese Provisional Patent Publications No. 113934/1983 and No. 47959/1986) can also be used.
The above silver halide grains may be substantially monodispersed or polydispersed.
As an emulsion for color negative, silver iodobromide is generally employed and a content of the silver iodobromide is preferably 10 mole % or less.
In light-sensitive materials for which particularly rapid developability is demanded such as printing papers for color, etc., they may be preferably silver chloride, silver chlorobromide or silver iodobromide containing silver chloride.
Particularly preferred as such silver halide grains are silver halide grains for rapid processing containing 90 mole % or more of silver chloride.
Such silver halide grains for rapid processing contain 90 mole % or more of silver chloride, with the silver bromide content being preferably 5 mole % or less and the silver iodide content being preferably 0.5 mole % or less. More preferably, silver chloribromide with a silver bromide content of 0.1 to 1.0 mole % may be employed.
The silver halide grains for rapid processing may be used either alone or as a mixture with other silver halide grains having different compositions. Also, they can be used as a mixture with silver halide grains containing less than 10 mole % of silver chloride.
In the silver halide emulsion containing the silver halide grains for rapid processing, the proportion of the silver halide grains for rapid processing occupied in the total silver halide grains contained in these emulsion layers may be preferably 60% by weight or more, more preferably 80% by weight or more.
The silver halide to be used in the present invention may be also a polydisperse emulsion in which average grain sizes are distributed in wide range, but preferably a monodisperse emulsion.
The emulsion containing these silver halides may be chemically sensitized with an active gelatin, a sulfur sensitizer, a selenium sensitizer, a reductive sensitizer, a noble metal sensitizer, etc.
The silver halide to be used in the present invention may be optically sensitized with addition of an apropriate sensitizing dye in order to impart sensitivity to the respective desired light-sensitive wavelength regions.
The light-sensitive silver halide photographic material of the present invention comprising the above composition can be, for example, negative and positive films of color negative, and also a color printing paper.
The light-sensitive silver halide photographic material of the present invention, typically such color printing paper, is a light-sensitive silver halide photographic material for multi-color, and since color reproduction by the subtractive color photography is effected, it has ordinarily a structure having silver halide emulsion layers containing the respective couplers of magenta, yellow and cyan as the couplers for photography laminated in appropriate layer number and layer order on a support, but said layer number and layer order may be appropriately changed depending on the important performance, the purpose of use.
As a specific layer constitution of the light-sensitive silver halide photographic material to be used in the present invention, in case of a color printing paper, one having a yellow dye image forming layer, an intermediate layer, a magenta dye image forming layer, an intermediate layer, a cyan dye image forming layer, an intermediate layer and a protective layer arranged on a support successively from the support side is particularly preferred.
In the light-sensitive silver halide photographic material of the present invention, color fog preventives, image stabilizers, hardeners, plasticizers, polymer latices, UV-ray absorbers, formalin scavengers, mordants, development accelerators, development retarders, fluorescent brighteners, matting agents, lubricants, antistatic agents, surfactants, etc. can be used as desired.
For developing processing of the light-sensitive silver halide photographic material of the present invention, various color developing processings can be applied.
The light-sensitive silver halide photographic material of the present invention, by containing the cyan coupler of the present invention, has good sensitivity and color forming characteristic, and moreover, the cyan image formed became to have excellent fastness to light and heat.
EXAMPLES
The present invention is described in detail by referring to Examples, but the present invention is not limited thereto.
Example 1
On a paper support laminated on both surfaces with polyethylene, the respective layers shown below were successively provided by coating from the support side to prepare a silver halide color photographic material sample 1. The amounts of the compound added are shown per 1 m.sup.2 (silver halide is calculated on silver) unless otherwise specifically noted.
Layer 1 . . . a layer containing 1.2 g of gelatin, 0.32 g of blue-sensitive silver chlorobromide emulsion (containing 98 mole % of silver chloride) and 0.80 g of the yellow coupler (Y--1) shown below dissolved in 0.50 g of dioctyl phthalate.
Layer 2 . . . an intermediate layer comprising 0.70 g of gelatin, 8 mg of the irradiation dyes (AI--1) shown below and 4 mg of (AI--2) shown below.
Layer 3 . . . a layer containing 1.25 g of gelatin, 0.20 g of a green-sensitive silver chlorobromide emulsion (containing 99 mole % of silver chloride) and 0.62 g of the magenta coupler (M--1) dissolved in 0.30 g of dioctyl phthalate.
Layer 4 . . . an intermediate layer comprising 1.20 g of gelatin.
Layer 5 . . . a layer containing 1.20 g of gelatin, 0.30 g of a red-sensitive silver chlorobromide emulsion (containing 99 mole % of silver chloride) and 0.45 g of the cyan coupler (C--1) dissolved in 0.20 g of dioctyl phthalate.
Layer 6 . . . a layer containing 1.00 g of gelatin and 0.30 g of the UV-ray absorber (UV--1) dissolved in 0.20 g of dioctyl phthalate.
Layer 7 . . . a layer containing 0.50 g of gelatin. ##STR80##
As the hardener, 2,4-dichloro-6-hydroxy-s-triazine sodium was added in the layers 2, 4 and 7, each to an amount of 0.017 g per 1 g of gelatin.
Also, samples 2 to 5 were prepared in the same manner as the above sample 1, except for replacing the cyan coupler (C--1) in the layer 5 in the above sample 1 with the Control couplers and the couplers of the present invention as shown in Table 1. The cyan couplers were added each in the amount equimolar to the cyan coupler (C--1).
Each of the above light-sensitive samples 1 to 5 was exposed to light through an optical wedge and then processed according to the following steps.
Processing steps
______________________________________Color developing 35.degree. C. 45 sec.Bleach-fixing 35.degree. C. 45 sec.Stabilizing 35.degree. C. 1 min. 30 sec.Drying 60 to 80.degree. C. 2 min.______________________________________
The respective processing solutions had the following compositions.
______________________________________[Color developing solution]______________________________________Water 800 mlTriethanol amine 11 mlN,N--diethylhydroxylamine (85% aqueous solution) 6 mlPotassium chloride 2.3 gPotassium sulfite 0.3 gPotassium carbonate 30 gSodium tetrapolyphosphate 2.0 gN--ethyl-N--.beta.-methanesulfonamidoethyl-3-ethyl- 5.2 g4-aminoaniline sulfate______________________________________
Made up to one liter with addition of water, and adjusted to pH=10.1 with a 20% potassium hydroxide or a 10% diluted sulfuric acid.
______________________________________[Bleach-fixing solution]______________________________________Water 800 mlIron (III) ammonium ethylenediaminetetraacetate 65 g2-Sodium ethylenediaminetetraacetate 5 gAmmonium thiosulfate 60 gSodium hydrogen sulfite 10 gSodium metabisulfite 2 gSodium chloride 10 g______________________________________
Made up to one liter with addition of water, and adjusted to pH=5.6 with diluted sulfuric acid.
______________________________________[Stabilizing solution]______________________________________5-Chloro-2-methyl-4-isothiazolin-3-one 1.0 g1-Hydroxyethylidene-1,1-diphosphonic acid 2.0 g______________________________________
Made up to one liter with addition of water, and adjusted to pH=7.0 with sulfuric acid or potassium hydroxide.
Each sample after the above processing was subjected to sensitometry to determine the maximum density (D.sub.max) and the sensitivity of the red-sensitive emulsion layer.
Also, the above processed sample was irradiated by xenon fadometer for 5 days for examination of light resistance of the cyan image.
The storage stability (dark fading characteristic) of the cyan image was also examined by storing the above processed sample under high temperature and high humidity of 80.degree. C., 90% RH (relative humidity) for 2 weeks. The results are shown in Table 1.
TABLE 1______________________________________ *2 *3 *1 Light Image Sensi- Maximum resist- stora-Sample No. Coupler tivity density ance bility______________________________________1 (Control) C-1 100 2.28 0.89 0.812 (Control) C-2 85 1.78 0.85 0.963 (This I-1 102 2.31 0.90 0.96invention)4 (This I-2 104 2.35 0.88 0.97invention)5 (This I-6 101 2.32 0.91 0.98invention)______________________________________ *1 relative value to sensitivity of sample 1 as 100. *2 density afer deterioration of the portion with initial density of 1.0. *3 density after deterioration of the portion with initial density of 1.0 ##STR81##
As is apparent from the results shown in Table 1, the sample 1 by use of the Control coupler C--1 is insufficient in image storage stability (dark fading characteristic), while the sample 2 by use of the Control coupler C--2 is insufficient in sensitivity and color forming characteristic (maximum density).
In contrast, the samples 3, 4 and 5 by use of the cyan couplers of the present invention have good sensitivity and color forming characteristic (maximum density), and yet also excellent in light resistance, image storability (dark fading characteristic).
Example 2
The coupler C--3 shown below (10 g), 10 g of dioctyl phthalate and 20 ml of ethyl acetate were completely dissolved by heating to 50.degree. C., and the resultant solution was mixed and stirred with 10 g of gelatin and 100 ml of an aqueous solution containing 0.4 g of Alkanol XC (sodium diisopropylnaphthalene sulfonate, produced by Du Pont), and then finely emulsified by sonication. The coupler dispersion was added into 400 g of a photographic emulsion containing 35 g of silver chlorobromide (containing 99% of silver chloride) and 40 g of gelatin and, after addition of 40 ml of a 2% aqueous solution of 2,4-dichloro-6-hydroxy-s-triazine sodium as the hardener, with adjustment of the pH to 6.0, the mixture was uniformly applied on a triacetylcellulose film base subjected to subbing to provide a sample 6.
Next, samples 7, 8 and 9 were prepared similarly as sample 6, except for using equal moles of the cyan coupler I--4, 5 or 8 of the present invention in place of the coupler C--3.
These samples were exposed by use of a wedge for sensitometry, and then subjeccted to the same color developing, bleach-fixing and stabilizing processing as in Example 1, followed by determination of sensitivity and maximum density.
The respective processed samples were also irradiated by a xenon fadometer for 5 days for examination of light stability of the cyan image. The results obtained are shown in Table 2.
TABLE 2______________________________________ *5 *4 Light Sensi- Maximum stabi-Sample No. Coupler tivity density lity______________________________________6 (Control) C-3 100 1.25 0.487 (This I-4 103 1.28 0.77invention)8 (This I-5 101 1.30 0.75invention)9 (This I-8 104 1.32 0.78invention)______________________________________ *4 relative value to sensitivity of sample 6 as 100. *5 density after deterioration of the portion with initial density of 1.0 ##STR82##
As is apparent from the results shown in Table 2, also in this Example in which a tetra-equivalent cyan coupler is employed, the light-sensitive silver halide photographic material exhibits excellent effects.
Also, the present invention exhibits good effects in a light-sensitive silver halide photographic material constituted of a single layer similarly as in the case of a light-sensitive silver halide photographic material constituted of multiple layers.
Example 3
(Preparation of silver halide emulsion)
Six kinds of silver halide emulsions as shown in Table 3 were prepared according to the neutral method or simultaneous mixing method.
TABLE 3______________________________________Emul- Average Chemical Spectralsion AgCl AgBr grain dia- sensiti- sensitiz-No. % % meter (.mu.m) zer ing dye______________________________________Em-1 99.5 0.5 0.67 Sodium SD-1*.sup.3Em-2 99.5 0.5 0.46 thiosul- SD-2*.sup.4 fate*.sup.1Em-3 99.5 0.5 0.43 Chloro- SD-3*.sup.5 platinic acid*.sup.2Em-4 10 90 0.67 Sodium SD-1*.sup.3Em-5 30 70 0.46 thiosul- SD-2*.sup.4Em-6 30 70 0.43 fate*.sup.1 SD-3*.sup.5______________________________________ *.sup.1 added 2 mg per one mole of silver halide *.sup.2 added 5 .times. 10.sup.-5 mole per one mole of silver halide *.sup.3 added 0.9 .times. 10.sup.-3 mole per one mole of silver halide *.sup.4 added 0.7 .times. 10.sup.-3 mole per one mole of silver halide *.sup.5 added 0.2 .times. 10.sup.-3 mole per one mole of silver halide
Each silver halide emulsion was added STB--1 as shown below as an emulsion stabilizer with an amount of 5.times.10.sup.-3 mole per one mole of silver halide after completion of the chemical sensitization. ##STR83##
(Preparation of sample of silver halide color photographic material)
Then, the following layers 1 to 7 were successively coated (simultaneous coating) on a paper support coated both surfaces thereof with a polyethylene to prepare silver halide color photographic materials 10 to 15 (in the following, added amounts are all shown by an amount per 1 m.sup.2 of the light-sensitive material.).
Layer 1 . . . a layer containing gelatin (1.2 g), 0.29 g (in terms of silver, hereinafter the same) of a blue-sensitive silver halide emulsion (Em--1) and 0.3 g of dinonylphthalate (DNP) dissolved 0.75 g of yellow coupler (Y--1), 0.3 g of light stabilizer ST--1 and 0.015 g of 2,5-dioctylhydroquinone (HQ--1) therein.
Layer 2 . . . a layer containing gelatin (0.9 g), and 0.2 g of dioctylphthalate (DOP) dissolved 0.04 g of HQ--1 therein.
Layer 3 . . . a layer containing gelatin (1.4 g), 0.2 g of a green-sensitive silver halide emulsion (Em--2), 0.50 g of magenta coupler (M--2), 0.25 g of light stabilizer (ST-2), 0.3 g of DOP dissolved 0.01 g of HQ--1, and 6 mg of the filter dye (AI--2).
Layer 4 . . . a layer containing gelatin (1.2 g) and 0.3 g of DNP dissolved 0.6 g of the ultraviolet-ray absorber (UV--1) and 0.05 g of HQ--1 therein.
Layer 5 . . . a layer containing gelatin (1.4 g), 0.20 g of a red-sensitive silver halide emulsion (Em--3) and 0.3 g of DOP dissolved 0.9 mmole of the cyan coupler as shown in Table 4 and 0.01 g of HQ--1 therein.
Layer 6 . . . a layer containing gelatin (1.1 g), 0.2 g of DOP dissolved 0.2 g of UV--1 therein, and 5 mg of the filter dye (AI--1).
Layer 7 . . . a layer containing gelatin (1.0 g) and 0.05 g of sodium 2,4-dichloro-6-hydroxytriazine. ##STR84##
After processings were carried out according to the color developing processing steps, sensitivity of the red-sensitive emulsion layer (inverse number of exposed amount providing a density of fog+0.1) and the maximum density (D.sub.max) by using a photodensitometer (available from KONICA CORPORATION).
Also, the resulting samples were preserved at 85.degree. C. and 60% relative humidity for 25 days, and by measuring a density after deterioration of the dye image at an initial density of 1.0, dark color fading property was evaluated. The results are shown in Table 4.
______________________________________[Processing steps] Temperature Time______________________________________Color developing 34.7 .+-. 0.3.degree. C. 45 sec.Bleach-fixing 34.7 .+-. 0.5.degree. C. 50 sec.Stabilizing 30 to 34.degree. C. 90 sec.Drying 60 to 80.degree. C. 60 sec.______________________________________
The respective processing solutions had the following compositions.
______________________________________[Color developing solution]______________________________________Water 800 mlTriethanol amine 8 gN,N--diethylhydroxylamine 5 gPotassium chloride 2 gN--ethyl-N--.beta.-methanesulfonamidoethyl-3-ethyl- 5 g4-aminoaniline sulfateSodium tetrapolyphosphate 2 gPotassium carbonate 30 gPotassium sulfite 0.2 gFluorescent brightener (4,4'-diaminostylbene- 1 gdisulfonic acid derivative)______________________________________
Made up to one liter with addition of water, and adjusted to pH 10.2.
______________________________________[Bleach-fixing solution]______________________________________Ferric ammonium ethylenediaminetetraacetate 60 gdihydrateEthylenediaminetetraacetic acid 3 gAmmonium thiosulfate (70% aqueous solution) 100 mlAmmonium sulfite (40% aqueous solution) 27.5 ml______________________________________
Made up to one liter with addition of water, and adjusted to pH 5.7 with glacial acetic acid.
______________________________________[Stabilizing solution]______________________________________5-Chloro-2-methyl-4-isothiazolin-3-one 1 g1-Hydroxyethylidene-1,1-diphosphonic acid 2 g______________________________________
Made up to one liter with addition of water, and adjusted to pH 7.0 with sulfuric acid or potassium hydroxide.
On the other hand, 5 g of sodium hydrosulfite was added to the bleach-fixing solution to decrease bleaching power and it was used as a fatigue bleach-fixing solution (hereinafter referred to as "fatigue BF") to examine color reproducibility.
That is, after color developing processing, two kinds of bleach-fixing processings using a new solution of the bleach-fixing solution (hereinafter referred to as "new BF") and a fatigue bleach-fixing solution were applied, and by comparing the maximum density of the resulting cyan dye, color reproducibility (%) was calculated due to the following equation. ##EQU1##
TABLE 4______________________________________ Image Color Sensi- stora- repro-Sample No. Coupler tivity* D.sub.max bility ducibility (%)______________________________________10 (Control) C - 1 100 2.56 0.71 6511 (Control) C - 4 98 2.52 0.83 7012 (This II - 4 105 2.62 0.91 93 invention)13 (This II - 5 102 2.63 0.90 92 invention)14 (This II - 7 103 2.59 0.89 90 invention)15 (This II - 9 100 2.57 0.88 91 invention)______________________________________ *sensitivity is shown by a relative value when sensitivity of sample 10 a 100.
As seen from Table 4, it can be understood that when the cyan coupler of the present invention is used, high maximum density and sensitivity can be obtained and heat resistivity of the obtained cyan image is good.
Further, with respect to color reproducibility which is an important point for rapid processing, it can be also understood that the coupler of the present invention is positioned at extremely higher level as compared with the conventional couplers.
Also, with respect to these samples 10 to 15, color reproducibility of these samples when printings were effected under the conditions of which color negative and neutral were combined and photographying a color checker (produced by Macbeth Co.) with Konica color GX-100 was evaluated with eyes.
As compared with the sample No. 10, each of Samples 12 to 15 of the present invention is extremely improved in discrimination of blue and cyan as well as color reproducibility of green color and red to magenta.
From the facts as mentioned above, it can be understood that the compound represented by the formula (II) is a cyan coupler particularly suitable for a color paper.
Example 4
Samples No. 16 to 21 of light-sensitive silver halide color photographic materials were prepared in the same manner as in Example 3 except that the blue-sensitive silver halide emulsion in layer 1 of the light-sensitive silver halide color photographic material prepared in Example 3 was replaced by Em--4 in Table 3, the green-sensitive silver halide emulsion in layer 3 by Em--5 of the same, and the red-sensitive silver halide emulsion in layer 5 by Em--6, respectively.
The samples obtained were subjected to wedge-exposure with use of the photosensitometer KS--7 type (produced by KONICA CORPORATION), followed by processing with the following color developing processing step and measurements were carried out in the same manner as in Example 3.
The results are shown in Table 5.
______________________________________[Processing steps]______________________________________Color developing 3 min 30 sec temperature 33.degree. C.Bleach-fixing 1 min 30 sec temperature 33.degree. C.Washing 3 min temperature 33.degree. C.______________________________________
Color developing solution prescription
______________________________________N--ethyl-N--.beta.-methanesulfonamidoethyl-3-methyl- 4.9 g4-aminoaniline sulfateHydroxylamine sulfate 2.0 gPotassium carbonate 25.0 gPotassium bromide 0.6 gAnhydrous sodium sulfite 2.0 gBenzyl alcohol 13 mlPolyethylene glycol (average polymerization 3.0 mldegree: 400)______________________________________
Made up to one liter with addition of water, and adjusted to pH 10.0 with sodium hydroxide.
Bleach-fixing solution prescription
______________________________________Iron sodium ethylenediaminetetraacetate 6.0 gAmmonium thiosulfate 100 gSodium bisulfite 10 gSodium metabisulfite 3 g______________________________________
Made up to one liter with addition of water, and adjusted to pH 7.0 with aqueous ammonia.
TABLE 5______________________________________ ImageSample No. Coupler Sensitivity* D.sub.max storability______________________________________16 (Control) C - 1 100 2.58 0.7517 (Control) C - 4 100 2.60 0.9118 (This II - 4 115 2.71 0.96 invention)19 (This II - 5 110 2.62 0.93 invention)20 (This II - 7 113 2.63 0.93 invention)21 (This II - 9 105 2.65 0.94 invention______________________________________ * sensitivity is shown in the same manner as in Example 3 by a relative value when sensitivity of sample 16 as 100.
As described above, substantially the same results can be obtained as in Example 3.
Example 5
The following emulsions were prepared.
Preparation of emulsion S
To 750 ml of 2.0% inactive gelatin solution maintained at 50.degree. C. were added the following A1 and B solutions simultaneously while stirring and injected over 3 minutes. After ripenning for 25 minutes, excessive salts were removed by the precipitation washing method and then redispersed and the following C1 and D1 solutions were added. After 10 minutes, excessive water-soluble salts were again removed and silver halide grains were dispersed by adding a small amount of gelatin.
Preparation of emulsion L
To 750 ml of 1.5% inactive gelatin solution maintained at 60.degree. C. were added the following A2 and B solutions simultaneously while stirring and injected over 15 minutes. After ripenning for 40 minutes, excessive salts were removed by the precipitation washing method and then redispersed and 10 mg of hypo was added thereto, and the following C2 and D2 solutions were added. After 10 minutes, excessive water-soluble salts were again removed and silver halide grains were dispersed by adding a small amount of gelatin.
Preparation of emulsion M
To 750 ml of 2.0% inactive gelatin solution maintained at 50.degree. C. were added the following A3 and B solutions simultaneously while stirring and injected over 5 minutes. After ripenning for 25 minutes, excessive salts were removed by the precipitation washing method and then redispersed and the following C1 and D2 solutions were added. After 10 minutes, excessive water-soluble salts were again removed and silver halide grains were dispersed by adding a small amount of gelatin.
______________________________________ Water 2000 ml NaCl 35 gAl solution NH.sub.4 Br 109.6 g KI 0.8 g Water 1000 ml NaCl 26.3 gA2 solution NH.sub.4 Br 109.6 g KI 0.8 g Water 1000 mlA3 solution NaCl 33.8 g KBr 12 g Water 1200 mlB solution AgNO.sub.3 170 g Water 1000 mlC1 solution NaCl 60 g NH.sub.4 Br 6.9 g Water 1000 mlC2 solution NaCl 31.6 g Water 1000 mlD1 solution AgN0.sub.3 70 g Water 1000 mlD2 solution AgN0.sub.3 80 g______________________________________
To the three kinds of emulsions, the following sensitizing dyes, couplers, etc. are added and they are coated on a support to form a multi-layer light-sensitive color material.
Red-sensitive emulsion layer (first layer)
To the emulsion S and the emulsion M was added a coupler solution which is protect dispersed containing sensitizing dyes (SD--6) and (SD--7), stabilizers (STB--1) and (STB--2), a surfactant (S--2), and further added dibutyl phthalate, ethyl acetate, a surfactant (S--2), 2,5-dioctylhydroquinone and cyan couplers (C--1) and (C--2), respectively.
Gelatin was added to the mixture and each of emulsions was mixed to coat so as to become the gamma value being 1.5.
First intermediate layer (second layer)
A gelatin solution containing a protect dispersed solution containing dioctyl phthalate, 2,5-dioctylhydroquinone, a UV absorber Tinuvin 328 (trade name, produced by Chiba Geigy AG) and surfactant (S--1) was prepared and coated so as to become a Tinuvin coated amount being 0.15 g/m.sup.2.
Green-sensitive emulsion layer (third layer)
To the emulsion S and the emulsion M was added a coupler solution which is protect dispersed containing a sensitizing dye (SD--5), stabilizers (STB--1) and (STB--2), a surfactant (S--2), and further dibutyl phthalate, ethyl acetate, 2,5-dioctylhydroquinone, a surfactant (S--1) and a magenta coupler (M--3).
Gelatin was added and a hardener (H--1) was further added and coated so as to become the gamma value of the resulting emulsion being 1.5.
Second intermediate layer (fourth layer)
The same prescription as in the first intermediate layer and coated so as to become a Tinuvin 328 coated amount being 0.2 g/m.sup.2.
Yellow filter layer (fifth layer)
By adding a yellow colloidal silver prepared by oxidizing in the presence of an alkaline weak reducing agent (the weak reducing agent was removed by the nudel washing method after neutralization) as well as dioctyl phthalate, ethyl acetate, a surfactant (S--1), 2,5-dioctylhydroquinone solution, a surfactant (S--2) and a hardener (H-1), it was coated so as to become a colloidal silver coated amount being 0.15 g/m.sup.2.
Third intermediate layer (sixth layer)
The same as in the first intermediate layer.
Blue-sensitive emulsion layer (seventh layer)
To the emulsion L, the emulsion S and the emulsion M was added a coupler solution which is protect dispersed containing a sensitizing dye (SD--4), stabilizers (STB--1) and (STB--3), a surfactant (S--2), and further dibutyl phthalate, ethyl acetate, 2,5-dioctylhydroquinone, a surfactant (S--1) and a yellow coupler (Y--2).
Gelatin was added and a hardener (H--1) was further added and coated so as to become the gamma value of the resulting emulsion being 1.5.
Fourth intermediate layer (eighth layer)
The same prescription as in the first intermediate layer and coated so as to become a Tinuvin 328 coated amount being 0.35 g/m.sup.2.
Protective layer (ninth layer)
By using a gelatin solution containing a colloidal silica, a surfactant (S--2), hardeners (H--2) and (H--3), and coated so as to become a gelatin coated amount being 1.0 g/m.sup.2.
On a polyethylene laminated paper which was surface treated were coated the first layer to the ninth layer according to the simultaneous coating method and then dried (Sample 22).
Further, in the same manner as in the above except that the cyan coupler in the red-sensitive emulsion layer (first layer) was replaced as shown in Table 6 by an equimolar amount of a coupler of the present invention, samples No. 23 to No. 27 were prepared. ##STR85##
To the light-sensitive materials prepared by the above procedures, white wedge exposure was effected and then the developing processing was effected following the steps as shown below to obtain a neutral positive wedge.
A density of a cyan image at a density of 1.0 after preservation at 85.degree. C., under 60% relative humidity for 20 days was measured as well as D.sub.max of a cyan image thereof was measured. The results are shown in Table 6.
In the table, an emulsion composition in the respective light-sensitive layer shows parts by weight.
Processing steps (processing temperature and processing time)
______________________________________[1] Impregnation (in color 38.degree. 8 sec developing solution)[2] Fog exposure -- 10 sec at 1 lux[3] Color developing 38.degree. 2 min[4] Bleach-fixing 35.degree. 60 sec[5] Stabilizing processing 25 to 30.degree. C. 1 min 30 sec[6] Drying 75 to 80.degree. C. 1 min______________________________________
Composition of processing solutions
(Color developing solution)
______________________________________Benzyl alcohol 10 mlEthylene glycol 15 mlPotassium sulfite 2.0 gPotassium bromide 1.5 gSodium chloride 0.2 gPotassium carbonate 30.0 gHydroxylamine sulfate 3.0 gPolyphosphoric acid (TPPS) 2.5 g3-Methyl-4-amino-N--ethyl-N--(.beta.-methane-sulfonamidoethyl)aniline sulfate 5.5 gFluorescent brightener (4,4'-diamino-styrbenedisulfonic acid derivative) 1.0 gPotassium hydroxide 2.0 g______________________________________
Made up to one liter with addition of water and adjusted to pH 10.20.
(Bleach-fixing solution)
______________________________________Ferric ammonium ethylenediaminetetraacetate 60 gdihydrateEthylenediaminepentaacetic acid 3 gAmmonium thiosulfate (70% solution) 100 mlAmmonium sulfite (40% solution) 27.5 ml______________________________________
Made up to one liter with addition of water and adjusted to pH 7.1 with potassium carbonate or glacial acetic acid.
(Stabilizing solution)
______________________________________5-Chloro-2-methyl-4-isothiazolin-3-one 1.0 gEthylene glycol 10 g1-Hydroxyethyliden-1,1'-diphosphonic acid 2.5 gBismuth chloride 0.2 gMagnesium chloride 0.1 gAmmonium hydroxide (28% aqueous solution) 2.0 gSodium nitrilotriacetate 1.0 g______________________________________
Made up to one liter with addition of water and adjusted to pH 7.0 with ammonium hydroxide or sulfuric acid.
Provided that the stabilizing processing is made a counter-current system of two tanks constitution.
TABLE 6______________________________________Sample No. Coupler D.sub.max Image storability______________________________________22 (control) C - 1 2.19 0.87 C - 223 (This II - 4 2.30 0.93 invention)24 (This II - 5 2.31 0.92 invention)25 (This IV - 4 2.45 0.95 invention)26 (This IV - 5 2.48 0.97 invention)27 (This IV - 6 2.50 0.96 invention)______________________________________
As described above, it can be understood that the couplers represented by the formulae (II) and (IV) of the present invention are suitable for a direct positive emulsion since they are excellent in coloring property and also good in heat resistance. Also, by setting the light-sensitive material in KONICA Color 7 (trade name) and scanning exposure was carried out with a constant rate of 5 cm/sec from a rectangular slit having 1.times.20 cm to effect copying a color checker (produced by Macbeth Co.). As results, with respect to samples No. 23 to 27, hue difference of cyan and blue can be clearly understood as compared with control salme No. 22 whereby color reproduction of red to magenta has improved.
Example 6
On a triacetylcellulose film support which had been carried out a subbing treatment with a copolymer of maleic acid anhydride and vinyl acetate after carried out antistatic treatment to a back surface, each layer having the following composition was coated successively from the support side to form a multi-layer light-sensitive color material sample No. 28. An amount added shows per one mole of silver halide otherwise described particularly.
<Back surface antistatic treatment>
______________________________________Back surface Stearic acid 20 mg/m.sup.2first layer: Diacetylcellulose 10 mg/m.sup.2 Alumina sol 1 g/m.sup.2Back surface Diacetylcellulose 50 mg/m.sup.2second layer: Stearic acid 10 mg/m.sup.2 Silica matting agent 50 mg/m.sup.2 (average grain diameter: 3 .mu.m)______________________________________
<On the support>
First layer: an antihalation layer
0.3 g/m.sup.2 of a ultraviolet-ray absorber UV--2, 0.4 g/m.sup.2 of a ultraviolet-ray absorber UV--3, 0.24 g/m.sup.2 of black colloidal silver and 2.7 g/m.sup.2 of gelatin.
Second layer: an intermediate layer
0.1 g/m.sup.2 of 2,5-di-t-octylhydroquinone and 1.0 g/m.sup.2 of gelatin.
Third layer: Low-sensitivity red-sensitive silver halide emulsion layer
Monodispersed emulsion (emulsion I) comprising AgBrI containing 2.5 mole % of AgI having an average grain diameter of 0.35 .mu.m . . . silver amount: 0.5 g/m.sup.2, SD--8 . . . 7.6.times.10.sup.-4 mole, Coupler C--3 . . . 0.1 mole and 0.9 g/m.sup.2 of gelatin.
Fourth layer: High-sensitivity red-sensitive silver halide emulsion layer
Monodispersed emulsion (emulsion II) comprising AgBrI containing 2.5 mole % of AgI having an average grain diameter of 0.75 .mu.m . . . silver amount: 0.8 g/m.sup.2, SD--8 . . . 3.2.times.10.sup.-4 mole, Coupler C--3 . . . 0.2 mole and 1.75 g/m.sup.2 of gelatin.
Fifth layer: Intermediate layer
0.1 g/m.sup.2 of 2,5-di-t-octylhydroquinone and 0.9 g/m.sup.2 of gelatin.
Sixth layer: Low-sensitivity green-sensitive silver halide emulsion layer
Emusion I . . . silver amount: 1.0 g/m.sup.2,
SD--9 . . . 6.6.times.10.sup.-4 mole,
SD--10 . . . 0.6.times.10.sup.-4 mole,
Coupler M--4 . . . 0.05 mole and 0.8 g/m.sup.2 of gelatin.
Seventh layer: High-sensitivity green-sensitive silver halide emulsion layer
Emulsion II . . . silver amount: 1.0 g/m.sup.2,
SD--9 . . . 2.76.times.10.sup.-4 mole,
SD--10 . . . 0.23.times.10.sup.-4 mole,
Coupler M--4 . . . 0.15 mole and 1.5 g/m.sup.2 of gelatin.
Eighth layer: Intermediate layer
The same as in the fifth layer.
Ninth layer: Yellow filter layer
0.1 g/m.sup.2 of yellow colloidal silverr, 0.9 g/m.sup.2 of gelatin and 0.1 g/m.sup.2 of 2,5-di-t-octylhydroquinone.
Tenth layer: Low-sensitivity blue-sensitive silver halide emulsion layer
Monodispersed emulsion (emulsion III) comprising AgBrI containing 2.5 mole % of AgI having an average grain diameter of 0.6 .mu.m . . . silver amount: 0.4 g/m.sup.2,
SD--11 . . . 2.65.times.10.sup.-4 mole,
Coupler Y--3 . . . 0.3 mole and 1.3 g/m.sup.2 of gelatin.
Eleventh layer: High-sensitivity blue-sensitive silver halide emulsion layer
Monodispersed emulsion (emulsion IV) comprising AgBrI containing 2.5 mole % of AgI having an average grain diameter of 1.0 .mu.m . . . silver amount: 0.8 g/m.sup.2,
SD--11 . . . 1.59.times.10.sup.-4 mole,
Coupler Y--3 . . . 0.3 mole and 2.1 g/m.sup.2 of gelatin.
Twelfth layer: First protective layer
0.3 g/m.sup.2 of UV--2, 0.4 g/m.sup.2 of UV--3, 1.2 g/m.sup.2 of gelatin and 0.1 g/m.sup.2 of 2,5-di-t-octylhydroquinone.
Thirteenth layer: Second protective layer
Non-light-sensitive fine particle silver halide emulsion comprising AgBrI containing 1 mole % of AgI having an average grain diameter of 0.06 .mu.m . . . silver amount: 0.3 g/m.sup.2, a polyethylmethacrylate particle (diameter: 1.5 .mu.m), 0.7 g/m.sup.2 of gelatin and a surfactant S--3.
In the respective layer, in addition to the above composition, H--1 or a surfactant was added thereto. Also, as a solvent for a coupler, tricresylphosphate was employed.
All the emulsions used are monodisperse octahedral emulsions and are those prepared by the double jet method in which seed grains having 0.095 .mu.m or 0.25 .mu.m (average silver iodide content of 2 mole %) are grown at 45.degree. C. in the presence of ammonia while controlling pAg and pH. Silver iodide contents in a core, an intermediate layer and a shell were varied by changing a composition of silver halide to be added.
For growth of a core/sheel type silver halide emulsion, the methods as disclosed in Japanese Provisional Patent Publications No. 52238/1984, No. 138538/1985, No. 49938/-1983 and No. 122935/1985 have been used.
(Compounds used for preparing samples)
Ultraviolet-ray absorber UV--2 ##STR86##
Ultraviolet-ray absorber UV--3 ##STR87##
Next, by replacing the cyan coupler C--3 in the third layer and the fourth layer of the sample No. 28 with couplers of the present invention as shown in Table 7, samples No. 29 to No. 33 were prepared.
After samples No. 28 to No. 33 were subjected to wedge exposure and then the following reversal process was subjected to, D.sub.max of the cyan image was measured by a red light. Also, color checker (produced by Macbeth Co.) was photographed by actually using the samples No. 28 to No. 33, and after subjected to reverse treatment, color reproducibility was evaluated with eyes.
The results are shown in Table 7.
______________________________________Processing steps Processing time Processing temperature______________________________________First developing 6 min 38.degree. C. (.+-.0.3)Washing 2 min 38.degree. C. (.+-.0.3)Reversing 2 min 38.degree. C. (.+-.0.3)Color developing 6 min 38.degree. C. (.+-.0.3)Adjustment 2 min 38.degree. C. (.+-.0.3)Bleaching 6 min 38.degree. C. (.+-.0.3)Fixing 4 min 38.degree. C. (.+-.0.3)Washing 4 min 38.degree. C. (.+-.0.3)Stabilizing 1 min normal temperatureDrying______________________________________
______________________________________First developing solutionWater 700 mlSodium tetrapolyphosphonic acid 2 gSodium sulfite 20 gHydroquinone monosulfonate 30 gSodium carbonate (monohydrate) 30 g1-Phenyl-4-methyl-4-hydroxymethyl- 2 g3-pyrazolidonePotassium bromide 2.5 gPotassium thiocyanate 1.2 gPotassium iodide (0.1% solution) 2 mlMade up to 1000 ml with addition of water.Reverse solutionWater 700 mlHexasodium nitrilotrimethylenephosphonate 3 gStannous chloride (dihydrate) 1 gp-Aminophenol 0.1 gSodium hydroxide 8 gGlacial acetic acid 15 mlMade up to 1000 ml with addition of water.Color developing solutionSodium tetrapolyphosphonate 2 gSodium sulfite 7 gSodium tert-phosphate (dihydrate) 36 gPotassium bromide 1 gPotassium iodide (0.1% solution) 90 mlSodium hydroxide 3 gCitrazinic acid 1.5 gN--Methyl-N--(.beta.-methanesulfonamidoethyl)- 11 g3-methyl-4-aminoaniline sulfateEthylenediamine 3 gMade up to 1000 ml with addition of water.Adjustment solutionWater 700 mlSodium sulfite 12 gSodium ethylenediaminetetraacetate (dihydrate) 8 gThioglycerin 0.4 mlGlacial acetic acid 3 mlMade up to 1000 ml with addition of water.Bleaching solutionSodium ethylenediaminetetraacetate (dihydrate) 2 gIron (III) ammonium ethylenediamine- 120.0 gtetraacetate (dihydrate)Ammonium bromide 100.0 gMade up to 1000 ml with addition of water.Fixing solutionWater 800 mlAmmonium thiosulfate 80.0 gSodium sulfite 5.0 gSodium bisulfite 5.0 gMade up to 1000 ml with addition of water.Stabilizing solutionWater 800 mlFormalin (37% by weight) 5.0 mlKonidax (produced by KONICA CORPORATION) 5.0 mlMade up to 1000 ml with addition of water.______________________________________
TABLE 7______________________________________Sample No. Coupler D.sub.max (red)______________________________________28 (Control) C-3 3.1829 (This in- II-4 3.28 vention)30 (This in- II-5 3.30 vention)31 (This in- IV-4 3.45 vention)32 (This in- IV-5 3.52 vention)33 (This in- IV-6 3.49 vention)______________________________________
As can be seen from the above results, the samples using the cyan coupler represented by the formula (II) or (IV) of the present invention are suitable for a reversal light-sensitive material since they are hing in D.sub.max.
Also, as long as the evaluation with eyes of the samples photographed a color checker practically, the samples No. 29 to No. 33 of the present invention are excellent in discrimination of cyan and blue which is one of the characteristic feature of the present invention as compared with the control sample No. 28, whereby color reproducibility of green and red has been improved.
Example 7
To a silver halide emulsion prepared according to the method as described in Japanese Patent Application No. 31330/1986, that is, a core/shell silver iodobromide emulsion having a polyshell structure in which an iodide content becomes lower from a higher iodide shell at the inner portion of the grain toward the outer side, was applied a chemical sensitization according to the conventional manner, and each coating solution to which the following additives had been added was coated on a triacetylcellulose film support from the support side successively to prepare a light-sensitive color material sample No. 34 comprising 13 layers.
First layer: Halation preventive layer
a gelatin layer containing black colloidal silver.
gelatin: 2.2 g/m.sup.2.
Second layer: Intermediate layer
a gelatin layer containing an emulsified dispersion of 2,5-di-t-octylhydroquinone.
gelatin: 1.2 g/m.sup.2.
Third layer: Low-sensitivity red-sensitive silver halide emulsion layer
Monodispersed emulsion (emulsion V) comprising octahedral silver iodobromide containing an average iodide content of 7.84% (weight ratio) and having an average grain diameter of 0.38 .mu.m . . . silver coated amount: 1.8 g/m.sup.2,
SD--12 . . . 6.times.10.sup.-5 mole per one mole of silver,
SD--13 . . . 1.0.times.10.sup.-5 mole per one mole of silver,
SD--14 . . . 1.0.times.10.sup.-5 mole per one mole of silver,
Cyan coupler (C--5) . . . 0.06 mole per one mole of silver,
Colored cyan coupler (CC--1) . . . 0.003 mole per one mole of silver,
DIR compound (D--1) . . . 0.0015 mole per one mole of silver,
DIR compound (D--2) . . . 0.002 mole per one mole of silver, and
1.4 g/m.sup.2 of gelatin.
Fourth layer: High-sensitivity red-sensitive silver halide emulsion layer
Monodispersed emulsion (emulsion VI) comprising octahedral silver iodobromide containing an average iodide content of 7.37% (weight ratio) and having an average grain diameter of 0.65 .mu.m . . . silver coated amount: 1.3 g/m.sup.2,
SD--12 . . . 3.times.10.sup.-5 mole per one mole of silver,
SD--13 . . . 1.0.times.10.sup.-5 mole per one mole of silver,
SD--14 . . . 1.0.times.10.sup.-5 mole per one mole of silver,
Cyan coupler (C--5) . . . 0.02 mole per one mole of silver,
Colored cyan coupler (CC--1) . . . 0.0015 mole per one mole of silver,
DIR compound (D--2) . . . 0.001 mole per one mole of silver, and
1.0 g/m.sup.2 of gelatin.
Fifth layer: Intermediate layer
a gelatin layer which is the same as the second layer.
gelatin: 1.0 g/m.sup.2.
Sixth layer: Low-sensitivity green-sensitive silver halide emulsion layer
Emulsion V . . . coated silver amount: 1.5 g/m.sup.2,
SD--15 . . . 2.5.times.10.sup.-5 mole per one mole of silver,
SD--16 . . . 1.2.times.10.sup.-5 mole per one mole of silver,
SD--17 . . . 1.0.times.10.sup.-5 mole per one mole of silver,
Magenta coupler (M--5) . . . 0.05 mole per one mole of silver,
Colored magenta coupler (CM--1) . . . 0.009 mole per one mole of silver,
DIR compound (D--1) . . . 0.0010 mole per one mole of silver,
DIR compound (D--3) . . . 0.0030 mole per one mole of silver, and
2.0 g/m.sup.2 of gelatin.
Seventh layer: High-sensitivity green-sensitive silver halide emulsion layer
Emulsion VI . . . coated silver amount: 1.4 g/m.sup.2,
SD--15 . . . 1.5.times.10.sup.-5 mole per one mole of silver,
SD--16 . . . 1.0.times.10.sup.-5 mole per one mole of silver,
SD--17 . . . 7.0.times.10.sup.-6 mole per one mole of silver,
Magenta coupler (M--5) . . . 0.020 mole per one mole of silver,
Colored magenta coupler (CM--1) . . . 0.002 mole per one mole of silver,
DIR compound (D--3) . . . 0.0010 mole per one mole of silver, and
1.8 g/m.sup.2 of gelatin.
Eighth layer: Intermediate layer
a gelatin layer which is the same as the second layer.
gelatin: 1.0 g/m.sup.2.
Ninth layer: Yellow filter layer
a gelatin layer containing an emulsified dispersion of yellow collidal silver and 2,5-di-t-octylhydroquinone.
gelatin: 1.5 g/m.sup.2.
Tenth layer: Low-sensitivity blue-sensitive silver halide emulsion layer
Monodispersed emulsion (Emulsion V) . . . coated silver amount: 0.9 g/m.sup.2,
SD--18 . . . 1.3.times.10.sup.-5 mole per one mole of silver,
Yellow coupler (Y--4) . . . 0.29 mole per one mole of silver, and
1.9 g/m.sup.2 of gelatin.
Eleventh layer: High-sensitivity blue-sensitive silver halide emulsion layer
Monodispersed emulsion (Emulsion VI) . . . coated silver amount: 0.5 g/m.sup.2,
SD--18 . . . 1.0.times.10.sup.-5 mole per one mole of silver,
Yellow coupler (Y--4) . . . 0.08 mole per one mole of silver,
DIR compound (D--2) . . . 0.0015 mole per one mole of silver, and
1.6 g/m.sup.2 of gelatin.
Twelfth layer: First protective layer
a gelatin layer containing silver iodobromide (AgI: 1 mole %, average grain diameter: 0.07 .mu.m) . . . coated silver amount: 0.5 g/m.sup.2,
and ultraviolet-ray absorbers UV--2 and UV--3.
1.2 g/m.sup.2 of gelatin.
Thirteenth layer: Second protective layer (Pro--2)
a gelatin layer containing polymethyl methacrylate particles (diameter: 1.5 .mu.m), copolymer particles of ethyl methacrylate: methyl methacrylate: methacrylic acid (avearge grain diameter: 2.5 .mu.m),
5 mg/m.sup.2 of polydimethylsiloxane, 10 mg/m.sup.2 of ##STR88## and formalin scavenger (HS--1).
1.2 g/m.sup.2 of gelatin.
In each layer, in addition to the above compositions, a gelatin hardener (H--1) and a surfactant were added thereto. ##STR89##
Also, those in which the cyan couplers C--5's in the third layer and the fourth layer were replaced with those as shown in Table 8 are made samples No. 35 to 40.
Each sample thus prepared was subjected to wedge exposure with white light and was carried out the following developing processing to obtain sensitivity and fog of a panchromatic layer. The sensitivity was shown by a reverse number of an exposed dosage providing a density of fog+0.5 and shown by a relative value to the sensitivity of the sample No. 34 as 100. Also, the color reproducibility of the cyan dye was evaluated in the same manner as in Example 3. Further, with respect to the cyan image, light resistance test was carried out by a xenon fade meter for 20 days and the light resistance was shown by a density after deterioration at a density of 1.0. The results are shown in Table 8 all together.
Processing steps (38.degree. C.)
______________________________________Color developing 3 min 15 secBleaching 6 min 30 secWashing 3 min 15 secFixing 6 min 30 secWashing 3 min 15 secStabilizing 1 min 30 secDrying______________________________________
Compositions of the processing solutions used in each of processing steps are as follows:
______________________________________[Color developing solution]______________________________________4-Amino-3-methyl-N--ethyl-N--(.beta.-hydroxy- 4.75 gethyl)aniline.sulfateAnhydrous sodium sulfite 4.25 gHydroxylamine.1/2sulfate 2.0 gAnhydrous potassium carbonate 37.5 gSodium bromide 1.3 gTrisodium nitrilotriacetate (monohydrate) 2.5 gPotassium hydroxide 1.0 g______________________________________
Made up to one liter with addition of water.
______________________________________[Bleaching solution]______________________________________Ferric ammonium ethylenediaminetetraacetate 100.0 gDiammonium ethylenediaminetetraacetate 10.0 gAmmonium bromide 150.0 gGlacial acetic acid 10.0 ml______________________________________
Made up to one liter with addition of water and adjusted to pH=6.0 with aqueous ammonia.
______________________________________[Fixing solution]______________________________________Ammonium thiosulfate 175.0 gAnhydrous sodium sulfite 8.5 gSodium metasulfite 2.3 g______________________________________
Made up to one liter with addition of water and adjusted to pH=6.0 with acetic acid.
______________________________________[Stabilizing solution]______________________________________Formalin (37% aqueous solution) 1.5 mlKonidax (produced by KONICA CORPORATION) 7.5 mlMade up to one liter with addition of water.______________________________________
Made up to one liter with addition of water.
TABLE 8______________________________________ Color repro- Light Sensi-* ducibi- resis- maxSample No. Coupler tivity lity (%) tance (nm)______________________________________34 (Control) C-5 100 75 0.75 70035 (Control) C-6 78 97 0.78 69236 (Control) C-3 69 95 0.80 66837 (This III-2 102 96 0.94 700 invention)38 (This III-4 105 97 0.95 695 invention)39 (This III-5 103 98 0.92 703 invention)40 (This III-7 159 99 0.93 703 invention)______________________________________
As seen from the results of Table 8, it can be understood that the cyan couplers of the formula (III) of the present invention have high sensitivity and are excellent in color reproducibility and light resistance. Heretofore, a naphthol type cyan coupler such as C--5 has conventionally been employed for a color negative film in an aspect of wavelength but a coupler of C--6 type has also been employed since the former is bad in color reproducibility.
On the other hand, since the C--6 type coupler has become longer wavelength due to their association so that absorption wavelength is broad and yet main wavelength thereof is slightly a short wave, and also there is a problem in light resistance.
The cyan coupler C--3 which has partially similar structure to that of the present invention is extremely a short wave in absorption wavelength as in a phenol type cyan coupler which is conventionally known, thus it is clear that it is basically different from the coupler of the present invention.
That is, it can be understood from the present Examples that the coupler represented by the formula (III) of the present invention is a epoch-making cyan coupler which can solve various problems as mentioned above.

Number	Name	Date
3311476	Loria	Mar 1967
4513081	Okazaki et al.	Apr 1985
4621047	Kishimoto et al.	Nov 1986
4696893	Umemoto et al.	Sep 1987

Light-sensitive silver halide color photographic material containing novel cyan coupler

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