Classifications

• • G—PHYSICS
  • G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
  • G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
  • G03C1/00—Photosensitive materials
  • G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
  • G03C1/485—Direct positive emulsions
  • G03C1/48538—Direct positive emulsions non-prefogged, i.e. fogged after imagewise exposure
• • 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
  • G03C7/305—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers
  • G03C7/30511—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers characterised by the releasing group
  • G03C7/30517—2-equivalent couplers, i.e. with a substitution on the coupling site being compulsory with the exception of halogen-substitution
  • G03C7/30529—2-equivalent couplers, i.e. with a substitution on the coupling site being compulsory with the exception of halogen-substitution having the coupling site in rings of cyclic compounds
• • 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
  • G03C7/36—Couplers containing compounds with active methylene groups
  • G03C7/38—Couplers containing compounds with active methylene groups in rings
  • G03C7/381—Heterocyclic compounds
  • G03C7/382—Heterocyclic compounds with two heterocyclic rings
  • G03C7/3825—Heterocyclic compounds with two heterocyclic rings the nuclei containing only nitrogen as hetero atoms

Definitions

• the present invention relates to a direct positive silver halide light-sensitive photographic material, and more particularly to a light-sensitive photographic material having an internal latent image-type silver halide emulsion layer which, after being imagewise exposed, is subjected to fogging treatment (such as an overall exposure or surface development treatment in the presence of a fogging agent), whereby a direct positive image can be obtained.
• fogging treatment such as an overall exposure or surface development treatment in the presence of a fogging agent
• Those conventionally known direct positive image-obtaining methods are broadly divided into two types.
• One type uses a silver halide emulsion provided with fogging nuclei.
• the emulsion is imagewise exposed to destroy the fogging nuclei or latent image in the exposed area by utilizing the solarization or Herschel effect. It is then developed, thereby giving a positive image.
• the other type uses an unprefogged internal latent image-type silver halide emulsion which, after being imagewise exposed, is subjected to fogging treatment (developing nuclei forming treatment) and then to surface development or which, after being imagewise exposed, is subjected to surface development while being subjected to fogging treatment (developing nuclei forming treatment), thereby giving a positive image.
• the above-mentioned fogging treatment may be carried out by an overall exposure, by using a chemical fogging agent, by using a high-energy developer solution, or by thermal treatment.
• an oxidized p-phenylenediamine color developing agent is reacted with dye image-forming couplers to form a color image.
• a color reproduction according to the subtractive color process is applied wherein a dye image is formed which is composed of cyan, magenta and yellow dyes corresponding to red, green and blue colors, respectively.
• a direct positive silver halide color photographic material a color image may be formed in similar manner. However, where a direct positive emulsion is used, since its development is performed along with its fogging treatment, the treatment generally tends to lower its sensitivity as well as increase its minimum density.
• DE-A-1 810 464 describes 1H-pyazolo[3,2- c ]-s-triazoles which act as magenta forming couplers when associated with photographic silver halide emulsions and subjected to chromogenic development.
• EP-A-0 278 986 belonging to the state of the art according to Article 54(3) EPC, describes direct positive photographic materials using internal latent image forming silver halide grains primarily for use in image transfer photographic systems.
• the materials may contain color forming couplers such as magenta forming couplers.
• an object of the present invention to provide a direct positive silver halide light-sensitive photographic material comprising an internal latent image-type silver halide emulsion whose maximum density is sufficiently large and whose minimum density is sufficiently small. It is also an object of this invention to provide such photographic material wherein the foot portion of the density/exposure curve exhibits high contrast, and the highlight portion shows little or no tendency toward magenta color.
• the material even if fixing or bleach-fixing solution is mixed by mistake into the color developer solution, the material will show no substantial soft gradation or increase in minimum density, and will not be affected by fogging treatment, thereby providing excellent reliability in the processing thereof.
• a direct positive silver halide light-sensitive photographic material comprising a support and a silver halide emulsion layer thereon containing direct positive silver halide emulsion grains adapted to form an internal latent image upon imagewise exposure and being unpre-fogged, characterised in that the material contains a magenta dye-forming coupler having one of the Formulas [I], [II], [III] or [IV] set out below: wherein X represents a hydrogen atom or a substituent capable of being split off upon reaction with an oxidization product of a color developing agent; and R1 , R2 and R3 each represent a halogen atom, an alkyl group, a cyclcalkyl group, an alkenyl group, a cycloalkenyl group, an alkynyl group, an aryl group, a heterocyclic group, an acyl group, a sulfonyl group, a sulfinyl group, a
• the alkyl, alkenyl, alkynyl, cycloalkyl and cycloalkenyl groups each may have a further substituent.
• Typical further substituents are an aryl group, cyano group, halogen atom, heterocyclic group, cycloalkyl group, cycloalkenyl group, spiro compound residue, cross-linked hydrocarbon compound residue, or a group substituting through a carbonyl group, such as acyl, carboxy, carbamoyl, alkoxycarbonyl or aryloxycarbonyl, or a group substituting through a hetero atom.
• Typical such groups are hydroxy, alkoxy, aryloxy, heterocyclic oxy, siloxy, acyloxy or carbamoyloxy group.
• the hetero atom is nitrogen, nitro, amino (including dialkylamino), sulfamoylamino, alkoxycarbonylamino, aryloxycarbonylamino, acylamino, sulfonamido, imido, or ureido group are typically suitable.
• hetero atom is sulfur, alkylthio, arylthio, heterocyclic thio, sulfonyl, sulfinyl, or sulfamoyl group
• hetero atom is phosphorus
• a phosphonyl group is among the useful radicals of suitable groups.
• Suitable substituents for R1 include methyl, ethyl, isopropyl, t-butyl, pentadecyl, heptadecyl, 1-hexylnonyl, 1,1'-dipentylnonyl, 2-chloro-t-butyl, trifluoromethyl, 1-ethoxytridecyl, 1-methoxyisopropyl, methanesulfonylethyl, 2,4-di-t-amylphenoxymethyl, anilino, 1-phenylisopropyl, 3-m-butanesulfonaminophenoxypropyl, 3-4'- ⁇ -[4''(p-hydrorybenzenesulfonyl)phenoxy]dodecanoylamino ⁇ phenylpropyl, 3- ⁇ 4'-[ ⁇ -(2'',4''-di-t-amylphenoxy)-butaneamido]pheny
• the preferred aryl group represented by R1 is phenyl, which may have a substituent such as alkyl, alkoxy or acylamino.
• aryl group examples include phenyl, 4-t-butylphenyl, 2,4-di-t-amylphenyl, 4-tetradecaneamidophenyl, hexadecyloxyphenyl and 4'-[ ⁇ -(4''-t-butylphenoxy)-tetradecaneamido]-phenyl.
• the preferred heterocyclic group represented by R1 has 5 to 7 members, may have a substituent, or which may also be condensed.
• Examples of the group include 2-furyl, 2-thienyl, 2-pyrimidinyl and 2-benzothiazolyl.
• acyl group represented by R1 examples include alkylcarbonyl groups, such as acetyl, phenylacetyl, dodecanoyl and ⁇ -2,4-di-t-amylphenoxybutanoyl, and arylcarbonyl groups such as benzoyl, 3-pentadecyloxybenzoyl and p-chlorobenzoyl.
• Examples of the sulfonyl group represented by R1 include alkylsulfonyl groups such as methylsulfonyl and dodecylsulfonyl; and arylsulfonyl groups such as benzenesulfonyl and p-toluenesulfonyl.
• Examples of the sulfinyl group represented by R1 include alkylsulfinyl groups, such as ethylsulfinyl, octylsulfinyl and 3-phenoxybutylsulfinyl, and arylsulfinyl groups such as phenylsulfinyl and m-pentadecylphenylsulfinyl.
• Examples of the phosphonyl group represented by R1 include alkylphosphonyl groups such as butylphosphonyl; alkoxyphosphonyl groups such as octyloxyphosphonyl; aryloxy phosphonyl groups such as phenoxyphosphonyl; arylphosphonyl and groups such as phenylphosphonyl.
• the carbamoyl group represented by R1 may have a substituent such as alkyl or aryl (preferably phenyl) and examples of the carbamoyl group include N-methylcarbamoyl, N,N-dibutylcorbamoyl, N-(2-pentadecyloctylethyl)carbamoyl, N-ethyl-N-dodecylcarbamoyl and N-[3-(2,4-di-t-amylphenoxy)propyl]carbamoyl.
• the sulfamoyl group represented by R1 may have a substituent, such as alkyl and aryl (preferably phenyl), and examples of the sulfamoyl group include N-propylsulfamoyl, N,N-diethylsulfamoyl, N-(2-pentedecyloxyethyl)sulfamoyl, and N-ethyl-N-dodecylsulfamoyl and N-phenylsulfamoyl.
• a substituent such as alkyl and aryl (preferably phenyl)
• examples of the sulfamoyl group include N-propylsulfamoyl, N,N-diethylsulfamoyl, N-(2-pentedecyloxyethyl)sulfamoyl, and N-ethyl-N-dodecylsulfamoyl
• Examples of the spiro compound residue represented by R1 include spiro [3.3]heptane-1-yl.
• Examples of the cross-linked hydrocarbon compound residue represented by R1 include bicyclo[2.2.1]heptane-1-yl, tricyclo[3.3.1.1 3,7 ]decane-yl and 7,7-dimethyl-bicyclo[2.2.1]heptane-1-yl.
• the alkoxy group represented by R1 may have a further substituent such as one of those previously defined as a substituent for the foregoing alkyl group represented by R1.
• Examples of the alkoxy group include methoxy, propoxy, 2-ethoxyethoxy, pentadecyloxy, 2-dodecyloxyethoxy and phenethyloxyethoxy.
• the aryloxy group represented by R1 is preferably phenyl, and the nucleus may be substituted by one of those defined as the substituent for the aryl group represented by R1.
• Examples of the aryloxy group include phenoxy, p-t-butylphenoxy and m-pentadecylphenoxy.
• the heterocyclic oxy group represented by R1 preferably has a 5 to 7-member heterocyclic ring, and the heterocyclic ring may have a further substituent.
• Examples of the heterocyclic oxy group include 3,4,5,6-tetrahydropyranyl-2-oxy and 1-phenyltetrazole-5-oxy.
• the siloxy group represented by R1 may be further substituted by an alkyl group or the like, and examples of the siloxy group include trimethylsiloxy, triethylsiloxy and dimethylbutylsiloxy.
• the acyloxy group represented by R1 is, for example, alkylcarbonyloxy or arylcarbonyloxy, which may have a further substituent.
• Examples of the acyloxy group include acetyloxy, ⁇ -chloroacetyloxy and benzoyloxy,
• the carbamoyloxy group represented by R1 may be substituted by an alkyl or aryl group, and examples thereof include N-ethylcarbamoyloxy, N,N-diethylcarbamoyloxy and N-phenylcarbamoyloxy.
• the amino group represented by R1 may be substituted by alkyl or aryl (preferably phenyl) group, and examples thereof include ethylamino, anilino, m-chloroanilino, 3-pentadecyloxycorbonylanilino and 2-chloro-5-hexadecanenmidoanilino.
• the acylamino group represented by R1 is alkylcarbonylamino, arylcarbonylamino (preferably phenylcarbonylamino) which may have a further substituent.
• Examples of the acylamino group include acetamido, ⁇ -ethylpropaneamido, N-phenylacetamido, dodecaneamido, 2,4-di-t-amylphenoxyacetamido and ⁇ -3-t-butyl-4-hydroxyphenoxybutaneamido.
• the sulfonamido group represented by R1 is alkylsulfonylamino or arylsulfonylamino which may have a further substituent.
• Examples of the sulfonamido group include methylsulfonylamino, pentadecylsulfonylamino, benzenesulfonamido, p-toluenesulfonamido and 2-methoxy-5-t-amylbenzenesulfonamido.
• the imido group represented by R1 may be either in the open-chain form or in the cyclic form, and may have a further substituent.
• Examples of the imido group include succinic acid imido, 3-heptadecyl-succinic acid imido, phthalimido and glutarimido.
• the ureido group represented by R1 may be substituted by alkyl or aryl (preferably phenyl), and examples of the ureido group include N-ethylureido, N-methyl-N-decylureido, N-phenylureido and N-p-tolylureido.
• the sulfamoylamino group represented by R1 may be substituted by alkyl or aryl (preferably phenyl), and examples of the sulfsmoylamino group include N,N-dibutylsulfamoylamino, N-methylsulfamoylamino and N-phenylsulfamoylamino.
• the alkoxycarbonylamino group represented by R1 may have a further substituent, and examples of the group include methoxycarbonylamino, methoxyethoxycarbonylamino and octadecyloxycarbonylamino.
• the aryloxycarbonylamino group represented by R1 may have a further substituent, and examples of the group include phenoxycarbonylamino and 4-methylphenoxycarbonylamino.
• the alkoxycarbonyl group represented by R1 may have a further substituent, and examples of the group include methoxycarbonyl, butyloxycarbonyl, dodecyloxycarbonyl, octadecyloxycarbonyl, ethoxymethoxycarbonyloxy and benzyloxycarbonyl.
• the aryloxycarbonyl group represented by R1 may have a further substituent, and examples of the group include phenoxycarbonyl, p-chlorophenoxycarbonyl and m-pentadecyloxyphenoxycarbonyl.
• the alkylthio group represented by R1 may have a further substituent, and examples of the group include ethylthio, dodecylthio, octadecylthio, phenethylthio and 3-phenoxypropylthio.
• the arylthio group represented by R1 is preferably a phenylthio, which may have a further substituent, and examples of the group include phenylthio, p-methoxyphenylthio, 2-t-octylphenylthio, 3-octadecylphenylthio, 2-carboxyphenylthio and p-acetaminophenylthio.
• the heterocyclic thio group represented by R1 is preferably one having 5 to 7 members, and may have a further condensed ring and may also have a further substituent.
• Examples of the group include 2-pyridylthio, 2-benzothiazolylthio and 2,4-diphenoxy-1,3,5-triazolo-6-thio.
• the substituent represented by X which can be split off by the reaction with the oxidized product of a color developing agent is preferably a hydrogen atom, a halogen atom, e.g. chlorine. bromine or fluorine. or an organic group having a carbon atom. an oxygen atom. a sulfur atom or a nitrogen atom through which said organic group is connected to the remainder of the compound.
• Examples of the group substituting through the carbon atom include carboxyl, hydroxymethyl group, triphenylmethyl group, and those groups having the general formula: wherein R2' and R3' each is hydrogen, aryl, alkyl, or a heterocyclic group.
• the group substituting through the above-mentioned oxygen group is alkoxy, aryloxy, heterocyclic oxy, acyloxy, sulfonyloxy, alkoxycarbonyloxy, aryloxycarbonyloxy, alkyloxalyloxy, or alkoxyoxalyloxy.
• the foregoing alkoxy group may have a further substituent, and examples of the group include ethoxy 2-phenoxyethoxy, 2-cyanoethoxy, phenethyloxy and p-chlorobenzyloxy.
• the foregoing aryloxy group is preferably phenoxy, and may have a further substituent.
• Examples of the group include phenoxy, 3-methylphenoxy, 3-dodecylphenoxy, 4-methanesulfonamidophenoxy, 4-[ -(3'pentadecylphenoxy)-butaneamido]phenoxy, hexydecylcarbamoylmethoxy, 4-cyanophenoxy, 4-methanesulfonylphenoxy, 1-naphthyloxy and p-methoxyphenoxy.
• the foregoing heterocyclic oxy group preferably has 5 to 7 members and may be a condensed ring and also may have a further substituent. Examples of this group include 1-phenyltetrazolyloxy and 2-benzothiazolyl.
• Examples of the foregoing acyloxy group include alkylcarbonyloxy groups such as acetoxy, butanoloxy, alkenylcarbonyloxy groups such as cinnamoyloxy; and arylcarbonyloxy groups such as benzoyloxy.
• Examples of the foregoing sulfonyloxy group include butanesulfonyloxy and methanesulfonyloxy.
• Examples of the foregoing alkoxycarbonyloxy group include ethoxycarbonyloxy and benzyloxycarbonyloxy.
• Examples of the foregoing aryloxycarbonyl group include phenoxycarbonyloxy.
• Examples of the foregoing alkyloxalyloxy group include methyloxalyloxy.
• Examples of the foregoing alkoxyoxalyloxy group include ethoxyoxalyloxy.
• the group substituting through the foregoing sulfur atom is, for example, an alkylthio, arylthio, heterocyclic thio or alkyloxythiocarbonylthio.
• alkylthio group examples include butylthio, 2-cyanoethylthio, phenethylthio and benzylthio.
• arylthio group examples include phenylthio, 4-methanesulfonamidophenylthio, 4-dodecylphenethylthio, 4-nonafluoropentaneamidophenethylthio, 4-carboxyphenylthio and 2-ethoxy-5-t-butylphenylthio.
• heterocyclic thio group examples include 1-phenyl-1,2,3,4-tetrazolyl-5-thio and 2-benzothiazolylthio.
• alkyloxythiocarbonylthio group examples include dodecyloxythiocarbonylthio.
• R4' and R5' each is hydrogen, alkyl, aryl, heterocyclic, sulfamoyl, carbamoyl, acyl, sulfonyl, aryloxycarbonyl, or alkoxycarbonyl; provided that R4' and R5' may combine with each other to form a heterocyclic ring, but are not both hydrogen atoms at the same time.
• the alkyl group represented by R4' and R5' may be either straight-chain or branched-chain, and is preferably one having from 1 to 22 carbon atoms.
• the alkyl group may have a substituent such as aryl, alkoxy, aryloxy, alkylthio, arylthio, alkylamino, arylamino, acylamino, sulfonamido, imino, acyl, alkylsulfonyl, arylsulfonyl, carbamoyl, sulfamoyl, alkoxycarbonyl, aryloxycarbonyl, alkyloxycarbonylamino, aryloxycarbonylamino, hydroxyl, carboxyl, cyano or halogen.
• Examples of the above alkyl group include ethyl, octyl, 2-ethylhexyl and 2-chloroethyl.
• the aryl group represented by R4' or R5' has 6 to 32 carbon atoms, and is preferably phenyl or naphthyl.
• the aryl group may have a substituent such as one represented by R4' or R5' or an alkyl group. Examples of the aryl group include phenyl, 1-naphthyl, and 4-methylsulfonylphenyl.
• the heterocyclic group represented by R4' or R5' has 5 to 6 members, may be a condensed ring, and may also have a substituent.
• Examples of the group include 2-furyl, 2-quinolyl, 2-pyrimidyl, 2-benzothiazolyl and 2-pyridyl.
• the sulfamoyl group represented by R4' or R5' is a N-alkylsulfamoyl, N, N-dialkylsulfamoyl, N-arylsulfamoyl or N,N-diarylsulfamoyl, and these alkyl and aryl groups each may have one of those substituents as defined in the above-mentioned alkyl and aryl groups represented by R4' or R5'.
• sulfamoyl group examples include N-diethylsulfamoyl, N-methylsulfamoyl, N-dodecylsulfamoyl, and N-p-tolylsulfamoyl.
• the carbamoyl group represented by the R4' or R5' is N-alkylcarbamoyl, N,N-dialkylcarbamoyl, N-arylcarbamoyl or N,N-diarylcarbamoyl; and these alkyl and aryl groups each may have one of those substituents as defined in the foregoing alkyl and aryl groups represented by R4' and R5'.
• Examples of the carbamoyl group include N,N-diethylcarbamoyl, N-methylcarbamoyl, dodecylcarbamoyl, N-p-cyanophenylcarbamoyl, and N-p-tolylcarbamoyl.
• the acyl group represented by R4' or R5' is, for example, alkylcarbonyl, arylcarbonyl, or heterocyclic carbonyl, and these alkyl, aryl and heterocyclic groups each may have a substituent.
• Examples of the acyl group include hexafluorobutanoyl, 2,3,4,5,6-pentafluorobenzoyl, acetyl, benzoyl, naphthoyl, 2-furylcarbonyl.
• the sulfonyl group represented by R4' or R5' is alkylsulfonyl, arylsulfonyl or heterocyclic sulfonyl, and may have a substituent.
• Examples of the group include ethanesulfonyl, benzenesulfonyl, octanesulfonyl, naphthalenesulfonyl and p-chlorobenzenesulfonyl.
• the aryloxycarbonyl group represented by the R4' or R5' may have one of those substituents as defined in the above aryl group represented by R4' and R5', and is, for example, phenoxycarbonyl.
• the alkoxycarbonyl group represented by R4' and R5' may have one of those substituents as defined in the above alkyl group, and examples of the group include methoxycarbonyl, dodecyloxycarbonyl and benzyloxycarbonyl.
• the heterocyclic group formed by the combination of the R4' and R5' preferably has 5 to 6 members, which may be either saturated or unsaturated, may or may not be aromatic, and also may be a condensed ring.
• the heterocyclic group include N-phthalimido, N-succinic acid imido, 4-N-urazolyl, 1-N-hydantoinyl, 3-N-2,4-dioxooxazolidinyl, 2-N-1,1-dioxo-3-(2II)-oxo-1,2-benzothiazolyl, 1-pyrrolyl, 1-pyrrolidinyl, 1-pyrazolyl, 1-pyrazolidinyl, 1-piperidinyl, 1-pyrrolinyl, 1-imidazolyl, 1-imidazolinyl, 1-indolyl, 1-isoindolinyl, 2-isoindolyl, 2-isoindolinyl, 1-benzotriazolyl, 1-benzimi
• heterocyclic groups each may have a substituent such as an alkyl, aryl, alkyloxy, aryloxy, acyl, sulfonyl, alkylamino, arylamino, acylamino, sulfonamino, carbamoyl, sulfamoyl, alkylthio, arylthio, ureido, alkoxycarbonyl, aryloxycarbonyl, imido, nitro, cyano or carboxyl, or halogen.
• the nitrogen containing heterocyclic ring represented by Z is pyrazole, imidazole, triazole, or tetrazole, and the substituent which the above ring may have includes those as defined in the previously mentioned R.
• the substituents (e.g., R1, R2, and R3 ) on the heterocyclic rings of Formulae [I] through [IV] may form bis-type couplers, which are included in the materials of the present invention.
• R2 and R3 in Formula [III] and in Formula [IV] may combine with each other to form rings such as 5 to 7 member cycloalkene and benzene, respectively.
• magenta color image forming couplers used in the materials of the invention are represented by the general Formulae [I] to [IV]
• the particularly preferred magenta color image forming coupler is represented by Formula [ I ].
• R1 preferably should satisfy Condition 1, more desirably should satisfy Conditions 1 and 2, and most desirably should satisfy Conditions 1, 2 and 3.
• R9, R10 and R11 is hydrogen, halogen, alkyl, cycloalkyl, alkenyl, cycloalkenyl, alkynyl, aryl, heterocyclic, acyl, sulfonyl, sulfinyl, phosphonyl, carbamoyl, sulfamoyl, cyano, spiro compound residue, cross-linked hydrocarbon compound residue, alkoxy, aryloxy, heterocyclic oxy, siloxy, acyloxy, carbamoyloxy, amino, acylamino, sulfonamido, imido, ureido, sulfamoylamino, alkoxycarbonylamino, aryloxycarbonylamino, alkoxycarbonyl, aryloxycarbonyl, alkylthio, arylthio or heterocycl
• R9, R10 and R11 may combine with each other to form a saturated or unsaturated ring (e.g., cycloalkane, cycloalkene or heterocyclic), and further the third (e.g. R11) may combine with this ring to form a cross-linked hydrocarbon compound residue.
• a saturated or unsaturated ring e.g., cycloalkane, cycloalkene or heterocyclic
• R11 may combine with this ring to form a cross-linked hydrocarbon compound residue.
• any of the groups represented by R9 through R11 may have a substituent, and specific examples of the groups represented by R9 through R11 and of the substituent which they may have are the same as those examples of the groups represented by R1 and of the substituents thereon.
• examples of the ring formed by the combination of, e.g., R9 and R10, and of the cross-linked hydrocarbon compound residue formed by R9 through R11, and of the substituents which they may have, are the same as those examples of the cycloalkyl, cycloalkenyl and heterocyclic cross-linked hydrocarbon compound residue represented by R1 of the Formulae [I] to [IV] and the substituents thereon.
• Particularly preferred among (i) are those groups in which two of R9 through R11 are alkyl and the third is hydrogen or alkyl.
• the alkyl and the cycloalkyl herein each may have a further substituent. Examples of the alkyl, cycloalkyl and substituent thereto are the same as those examples of the alkyl and cycloalkyl represented by R1 of Formulas [I] to [IV] and of the substituents thereon.
• R2 or R3 of Formulas [I] through [IV] are: Formula [X] -R12-SO2-R13 wherein R12 is alkylene, and R13 is alkyl, cycloalkyl or aryl.
• the alkylene represented by R12 has a straight chain portion preferably having not less than two carbon atoms, and more preferably from 3 to 6 carbon atoms, and may be in the straight-chain or branched-chain form, and also may have a further substituent. Examples of the substituent are the same as those exemplified for the substituent which may be carried by the alkyl represented by R1.
• the substituent is preferably a phenyl group.
• the preferred examples of the alkylene represented by the R12 are as follows: -CH2CH2CH2- , -CH2CH2CH2CH2-
• the alkyl group represented by R13 may be either straight or branched chain. Examples include methyl, ethyl, propyl, iso-propyl, butyl, 2-ethylhexyl, octyl, dodecyl, tetradecyl, hexadecyl, octadecyl and 2-hexyldecyl.
• the cycloalkyl group represented by R13 preferably has 5 to 6 members, e.g. cyclohexyl.
• the alkyl or cycloalkyl group represented by R13 may have a substituent, examples of which are the same as those exemplified as the substituent on R1.
• Examples of the aryl group represented by R13 include phenyl and naphthyl and may have a substituent such as straight or branched chain alkyl groups as well as those exemplified as substituents on R12. In addition, where the group has two or more substituents, these substituents may be either the same or different.
• the most preferred compounds of Formula [I] are: The following are non-limiting examples representative of the magenta dye image forming couplers according to the invention.
• known internal latent image-type silver halide emulsions may be used as the emulsion for use in forming the emulsion layer. These include conversion-type silver halide emulsions described in U.S. Patent No. 2,592,250, stratified structure-type silver halide emulsions described in Japanese Patent Examined Publication No. 1412/1983, internally chemically sensitized core/shell-type silver halide emulsions described in Japanese Patent Examined Publications 34213/1977 and 55821/1985, core/shell-type emulsions described in Japanese Examined Publication 55820/1985, and the like.
• the core/shell type emulsions are preferably used in the present invention.
• the silver halide composition of the internal latent image-type silver halide to be used in the present invention is discretionary; for example, any of silver chloride, silver chlorobromide, silver chloroiodobromide, silver bromide, silver iodobromide, and silver chloroiodide may be used alone or in combination.
• the silver chloride content of the silver halide is preferably not less than 5 mole %, and more preferably not less than 30 mole %.
• the grains of the silver halides may be in any form such as cubic, regular octahedral, or dodecahedral, or mixtures thereof; or may also be spherical, tabular, or irregular.
• the average grain size and the grain size distribution thereof can vary widely according to the photographic characteristics required, but it is desirable to have the grain size distribution as narrow as possible: That is, the silver halide grains used in this invention preferably contain silver halide grains whose sizes are plus or minus 20% of the average grain size thereof and which account for not less than 60% by weight of the total silver halide grains, and more preferably not less than 70% by weight.
• the silver halide emulsion of the present invention may be one comprising a mixture of silver halide grains of different average grain size.
• Such emulsions are produced by blending two or more individual emulsions, each of which has an average grain size substantially different from the others.
• the 'difference in the average grain size' herein means that the average grain size of smaller-size grains is not more than 80% of the average grain size of larger-size grains, and preferably not more than 70%.
• the grains of larger average size and the grains of smaller average size may be either the same or different in silver halide composition as well as grain form. The proportion of the larger grains to the smaller grains may be quite freely selected. In this instance, two or three or more different size silver halide grains may be mixed.
• the internal latent image-type silver halide of this invention in order to widen the exposure latitude thereof, may be used in the form of superposed emulsion layers different in sensitivity or may be mixed to be used in an emulsion layer. In this instance, the proportions of the amounts of silver in the respective emulsion layers is determined according to the photographic characteristics required.
• unprefogged internal latent image-type silver halide grains are used as the internal latent image-type silver halide.
• the term 'unprefogged' i.e., the grain surface is not prefogged
• 'unprefogged' means that, when an unexposed test piece made by coating an emulsion on a transparent film support so that the amount of silver coated is 35 mg Ag/cm2, is developed in the following surface developer solution A at 20°C for 10 minutes, the density obtained does not exceed 0.6, and preferably does not exceed 0.4.
• the silver halide emulsion of this invention provides an adequate density when the test piece prepared in the above manner, after being exposed, is developed in the following internal developer solution B.
• part of the above test piece when part of the above test piece is subjected to a light-intensity scale exposure over a given period of time up to about 1 second, and then developed in Internal Developer Solution B at 20°C for 10 minutes, the part shows a maximum density at least 5 times, and preferably at least 10 times, the maximum density obtained when the other part is exposed under the same conditions and is developed in Surface Developer Solution A at 20°C for 10 minutes.
• the silver halide emulsion of this invention may be optically sensitized by the usual sensitizing dyes.
• sensitizing dyes Such combinations of these sensitizing dyes as are used for supersensitization of internal latent image-type silver halide emulsions, negative-type silver halide emulsions, and the like, are useful also for the silver halide emulsion of this invention.
• sensitizing dyes reference can be made to Research Disclosures 15162 and 17643.
• a direct positive image can be easily obtained by surface development of an imagewise exposed (photographed) light-sensitive material of this invention.
• the primary process of making a direct positive image is such that a photgraphic light-sensitive material comprising the unprefogged internal latent image-type silver halide emulsion layer of this invention is imagewise exposed and then subjected to a treatment for producing fog nuclei chemically or optically.
• the imagewise exposed light-sensitive material is surface-developed after and/or during a fogging treatment.
• the fogging treatment may be carried out either by giving an overall exposure (by exposing the entire area of the light-sensitive material) or by using a fog nucleus-producing compound; i.e., a fogging agent.
• the overall exposure is carried out so that the imagewise exposed light-sensitive material is immersed in or wetted by a developer or other solution and then uniformly exposed.
• the light source for the overall exposure may be any light, as long as it is in the wavelength region to which the light-sensitive material is sensitive. It may be a short-period-emitting high-intensity light like an electronic flash, or may also be a weak light exposed over a long period of time. The time may be widely varied according to the photographic light-sensitive material, developing conditions, type of the light source, and the like, to obtain the best-quality positive image. It is most desirable that the exposure required for the overall exposure be given in a certain specific range in combination with the light-sensitive material.
• the use of excessive exposure increases or decreases the maximum density, thus resulting in deterioration of the resulting image quality.
• the light-sensitive material of this invention it reduces the degree of deterioration of the image quality to thereby produce a stable image.
• a large variety of compounds may be used as the fogging agents of this invention.
• the fogging agent needs only to be present at the time of development; for example, the agent may be present in the nonsupport component layers of the photographic material (the silver halide emulsion layer is especially preferred), or may be contained in a developer or in a processing solution used prior to the developer.
• the amount of agent used may be varied widely according to known parameters.
• the preferred amount of fogging agent, when incorporated into the silver halide emulsion layer is from 1 to 1,500 mg per mole of silver halide, and preferably from 10 to 1,000 mg, and, when incorporated into a processing solution such as a developer solution, is from 0.01 to 5 g/liter, and more preferably from 0.05 to 1 g/liter.
• Compounds usable as the fogging agents of this invention include those hydrazines described in U.S. Patents 2,563,785 and 2,588,982, or those hydrazides or hydrazine compounds described in U.S. Patent 3,227,552; those heterocyclic quaternary nitrogen salt compounds described in U.S. Patents 3,615,615; 3,718,479; 3,719,494; 3,734,738; and 3,759,901; and compounds having a group adsorbable onto the silver halide surface such as those acylhydrazinophenylthioureas described in U.S. Patent 4,030,925. These fogging agents may be used in combination.
• Research Disclosure 15162 describes the combined use of a nonadsorption-type fogging agent and an adsorption-type fogging agent; this combined-use technique is useful also in this invention.
• the invention allows the use of both nonadsorption-type and adsorption-type fogging agents and also their combined use.
• hydrazine compounds such as hydrazine hydrochloride, phenylhydrazine hydrochloride, 4-methylphenylhydrazine hydrochloride, 1-formyl-2-(4-methylphenyl)hydrazine, 1-acetyl-2-phenylhydrazine, 1-acetyl-2-(4-acetamidophenyl)hydrazine, 1-methylsulfonyl-2-phenylhydrazine, 1-benzoyl-2-phenylhydrazine, 1-methylsulfonyl-2-(3-phenylsulfonamidophenyl)-hydrazine, formaldehydophenyl-hydrazine, etc.; N-substituted quaternary cycloammonium salts such as 3-(2-formylethyl)-2-methylbenzothiazolium bromide, 3-(2-formylethyl)-2-propylbenzo
• the photographic light-sensitive material comprising the silver halide emulsion layer of this invention provides a direct positive image which is formed so that the material, after being imagewise exposed, is either overall-exposed and then surface-developed or surface-developed in the presence of a fogging agent.
• Surface-developed implies that the light-sensitive material is processed in a developer solution substantially free of silver halide solvent.
• Developing agents usable in the surface developer of the present invention include ordinary silver halide developing agents; e.g., polyhydroxybenzenes such as hydroquinone, aminophenols, 3-pyrazolidones, ascorbic acid and derivatives thereof, reductones, phenylenediamines, and mixtures thereof.
• polyhydroxybenzenes such as hydroquinone, aminophenols, 3-pyrazolidones, ascorbic acid and derivatives thereof, reductones, phenylenediamines, and mixtures thereof.
• Examples include hydroquinone, aminophenol, N-methylaminophenol, 1-phenyl-3-pyrazolidone, 1-phenyl-4,4-dimethyl-3-pyrazolidone, 1-phenyl-4-methyl-4-hydroxymethyl-3-pyrazolidone, ascorbic acid, N,N-diethyl-p-phenylenediamine, diethylamino-o-toluidine, 4-amino-3-methyl-N-ethyl-N-( ⁇ -methanesulfonamidoethyl)aniline, 4-amino-3-methyl-N-ethyl-N-( ⁇ -hydroxyethyl)aniline, and the like. Any of these developing agents may be incorporated into the emulsion in advance, and the photographic material immersed in a high-pH aqueous solution to make the emulsion react with the agent.
• the developer solution of this invention may contain further specific fogging agents and development restraining agents; alternatively these additives may be incorporated into the constituent layer of the photographic material.
• the direct positive silver halide photographic material of this invention due to the addition of the magenta color image forming coupler having one of the Formulas [I] to [IV] therein, even if a fixing or bleach-fixing solution is mixed by mistake into the color developer solution, almost no noticeable softening of the gradation at the foot of the density/exposure curve appears and increase in the minimum density is kept to a minimum. Accordingly, even if fixing or bleach-fixing solution is mixed accidentally into the color developer solution due to some operational error, or, for example, when pulling a jammed paper out of the processor, or during the belt-transport-type automatic processor operation, as long as the above-mentioned light-sensitive material is used, the processing can be reliably carried out. Therefore, the use of the light-sensitive material of this invention makes it unnecessary to renew the color developer solution each time accidental mixing occurs, thus reducing costs and saving time.
• the light-sensitive material of this invention is also useful for rapid processing which is carried out at a high temperature exceeding 35°C.
• the silver halide emulsion of this invention may contain the usual photographic additives such as wetting agents, physical property improving agents for the layers and coating aids.
• wetting agent are dihydroxyalkanes.
• Physical property improving agents include water-dispersed particulate high-molecular materials obtained by emulsion polymerization, such as copolymers of alkyl acrylates or alkyl methacrylates with acrylic acid or methacrylic acid, styrene-maleic acid copolymers and styrene-maleic anhydride-half alkyl ester copolymers.
• Coating aids include saponin and polyethylene glycol-lauryl ether.
• photographic additives may also be used which include gelatin plasticizers, surface active agents, ultraviolet absorbing agents, pH control agents, oxidation inhibitors, antistatic agents, viscosity increasing agents, graininess improving agents, dyes, mordants, brightening agents, developing speed control agents, matting agents, developing speed control agents and matting agents.
• the above-prepared silver halide emulsion is coated, if necessary, through a subbing layer, antihalation layer, filter layer, on a support, whereby the direct positive silver halide photographic material of this invention is obtained.
• the photographic material of this invention is useful in color photographic processing.
• the couplers can be those ordinarily used.
• an ultraviolet absorbing agent such as thiazolidone, benzotriazole, acrylonitrile, or a benzophenone-type compound, particularly Tinuvin PS, Tinuvin 320, Tinuvin 326, Tinuvin 327 and Tinuvin 328 (all manufactured by Ciba Geigy).
• Materials suitable as the support of the photographic material of this invention include polyethylene terephthalate film, polycarbonate film, polystyrene film, polypropylene film, cellulose acetate film, glass plates, baryta paper and polyethylene-laminated paper. These may be subbed if needed.
• the silver halide emulsion layer used in this invention may contain appropriate gelatin derivatives in addition to gelatin as the protective colloid or binder thereof.
• appropriate gelatin derivates include acylated gelatin, guanidylated gelatin, carbamylated gelatin, cyano-ethanolated gelatin and esterified gelatin.
• the silver halide emulsion layer of this invention may contain other hydrophilic binder materials, such as colloidal albumin, agar-agar, gum arabic, dextran, alginic acid, cellulose derivatives such as cellulose acetate hydrolyzed to 19 to 20% acetyl content, polyacrylamide, imidated polyacrylamide, casein, vinyl alcohol, vinyl alcohol polymers containing a urethanecarboxylic acid group or cyanoacetyl group such as vinylaminoacetate copolymer, polyvinyl alcohol, polyvinyl pyrolidone, hydrolyzed polyvinyl acetate, polymers obtained by the polymerization of protein or saturated acylated protein with monomers having vinyl groups, polyvinyl pyridine, polyvinyl amine, polyaminoethyl methacrylate and polyethyleneamine.
• hydrophilic binder materials such as colloidal albumin, agar-agar, gum arabic, dextran, alginic acid,
• the constituent layers of the photographic material e.g. the emulsion layer, intermediate layer, protective layer, filter layer and subbing layer.
• the above-mentioned hydrophilic binder may contain appropriate plasticizers and wetting agents.
• constituent layers of the photographic material of this invention may be hardened by using any appropriate hardening agent.
• hardening agent examples include chromium salts, zirconiums, aldehyde-type compounds such as formaldehyde and mucohalogenic acid and halotriazine-type, polyepoxy compound-type, ethyleneimine-type, vinyl-sulfone-type and acryloyl-type hardening agents.
• the photographic material of this invention may have on the support various photographic constituent layers such as filter layers, intermediate layers, protective layers, subbing layers, backing layers, antihalation layers, and the like in addition to at least one light-sensitive emulsion layer containing the internal latent image-type silver halide grains of this invention.
• the photographic material of this invention is for full-color use
• on the support thereof are coated at least one red-sensitive silver halide emulsion layer, at least one green-sensitive silver halide emulsion layer and at least one blue-sensitive silver halide emulsion layer.
• at least one light-sensitive silver halide emulsion layer must contain the internal latent image-type silver halide grains according to this invention. It is desirable, however, that all the light-sensitive silver halide layers contain the internal latent image-type silver halide grains according to this invention.
• Each of these light-sensitive silver halide emulsion layers may be separated into two or more layers having the same color sensitivity but differing in the speed.
• At least one layer having the same color sensitivity but different in speed must contain the internal latent image-type silver halide grains according to this invention. It is desirable, however, that all the emulsion layers contain the internal latent image-type silver halide grains according to the present invention.
• the photographic material of this invention may be effectively applied to various uses, such as black-and-white general use, X-ray, color photography, false-color, graphic arts, infrared photography, micrographics and silver-dye bleach process. It may also be applied to the colloid transfer process, silver salt diffusion transfer process, and those color image transfer processes and color transfer processes described in Rodgers' U.S. Patents 3,087,817; 3,185,567; and 2,983,606; Weyerts' U.S. Patent 3,253,915; Whitmore's U.S. Patent 3,227,550; Barr's U.S. Patent 3,227,551; Whitmore's U.S. Patent 3,227,552,; and Land's U.S. Patents 3,415,644; 3,415,645; and 3,415,646.
• magenta color image forming coupler (Exemplified Compound (3) ) dissolved in dioctyl phthalate, and a coating aid and hardening agent were also added.
• This liquid mixture was coated on a support and dried, whereby Sample 1 was obtained.
• the coated amount of the above internal latent image-type emulsion on the support of Sample 1 was 1.0 g/m2 in silver equivalent.
• the above magenta color image forming coupler was incorporated into the above emulson so that the coating amount thereof was 1.8 g/m2.
• Samples 2 to 8 were prepared in the same manner as Sample 1 except that the magenta color image forming coupler was replaced by those compounds described in Table 1.
• the photographic material in this example was formed by preparing and coating the emulsions of the respective constituent layers thereof as follows:
• a mixed green-sensitive emulsion in a molar ratio of 1:1 made green-sensitive by using a green-sensitizing dye and a mixed red-sensitive emulsion in a molar ratio of 1:1 made red-sensitive by using a red-sensitizing dye were similarly prepared.
• a red-sensitive emulsion layer comprising 0.4 g/m2 of the above red-sensitive emulsion, 0.8 g/m2 of oil-protect-dispersed cyan coupler C-1, and 1.5 g/m2 of gelatin.
• a green-sensitive layer comprising 0.4 g/m2 of the above green-sensitive emulsion, 0.8 g/m2 of oil-protected Exemplified Compound (7) as a magenta color image forming coupler, and 1.5 g/m2 of gelatin.
• a blue-sensitive emulsion layer comprising 0.5 g/m2 of the above blue-sensitive emulsion, 0.7 g/m2 of oil-protected yellow coupler Y-1, and 1.5 g/m2 of gelatin.
• Samples 10 through 16 were prepared in the same manner as Sample 9 except that the magenta color image forming coupler in the green-sensitive emulsion layer was replaced as shown in Table 2.
• Samples 9 through 16 were exposed through an optical wedge and then processed in the following procedure using the same processing solutions as in Example 1.
• Procedure (at 38°C) Color developing 2 minutes and 30 seconds Bleach-fix 1 minute and 30 seconds Stabilizing 1 minute and 30 seconds
• Processing 1 The entire area of each sample was exposed to 2 luxes of white light for a period of 10 seconds between 10 seconds and 20 seconds after the commencement of the color developing process. This processing was regarded as Processing 1.
• Processing 2 a similar processing to Processing 1 was performed and this was regarded as Processing 2.
• Processing 2 a color developer solution having 0.1% of bleach-fix solution was used.
• Samples 9, 11, and 16 of the samples obtained in Example 2 were used and Processing 1 was repeated. In addition to Processing 1, Processing 3 and Processing 4 were performed with respect to Samples 9, 11, and 16.
• Processing 3 was carried out in the same manner as Processing 1 except that the illumination in the overall exposure was 4 luxes and Processing 4 was performed in the same manner as Processing 1 except that the illumination in the overall exposure light was 8 luxes.
• Samples 9 and 11 (the present invention) produce a satisfactory image stable to change in the developer composition, particularly change in the fogging agent.

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