Heat-developable color photographic material

Claim 2

A heat-developable color photographic material, comprising a support having thereon a layer containing a light-sensitive silver halide, an organic silver salt oxidizing agent, a hydrophilic binder, a reducing agent for the substance selected from the group consisting of the silver halide and the organic silver salt oxidizing agent and a dye releasing compound, wherein the dye releasing compound releases a hydrophilic diffusible dye and is represented by the following general formula: C--L--D wherein C represents a moiety capable of bonding to an oxidized product which is formed by a reaction between a reducing agent and an organic silver salt oxidizing agent; D represents a dye portion for forming an image; and L represents a connection group between C and D and the bond between C and L is cleaved upon the reaction of C with the oxidized product of the reducing agent releasing the hydrophilic dye.

Claim 3

A heat-developable color photographic material as claimed in claim 1, wherein the moiety represented by C includes an active methylene residue, an active methine residue, a phenol residue or a naphthol residue.

Claim 4

A heat-developable color photographic material as claimed in claim 2, wherein the moiety represented by C is represented by the following general formula (I), (II), (III), (IV), (V), (VI) or (VII): ##STR16## wherein R 1 , R 2 , R 3 and R 4 , which may be the same or different, each represents hydrogen or a substituent selected from the group consisting of an alkyl group, a cycloalkyl group, an aryl group, an alkoxy group, an aryloxy group, an aralkyl group, an acyl group, an acylamino group, an alkoxyalkyl group, an aryloxyalkyl group, an N-substituted carbamoyl group, an alkylamino group, an arylamino group, a halogen atom, an acyloxy group, an acyloxyalkyl group and a cyano group, and these substituents may be further substituted with a hydroxyl group, a cyano group, a nitro group, an N-substituted sulfamoyl group, a carbamoyl group, an N-substituted carbamoyl group, an acylamino group, an alkylsulfonylamino group, an arylsulfonylamino group, an alkyl group, an aryl group, an alkoxy group, an aryloxy group, an aralkyl group or an acyl group, and the total number of the carbon atoms contained in the groups of R 1 , R 2 , R 3 and R 4 is from 12 to 40.

Claim 5

A heat-developable color photographic material as claimed in claim 1, wherein the moiety represented by C contains a ballast group.

Claim 6

A heat-developable color photographic material as claimed in claim 4, wherein the ballast group is a hydrophobic group selected from an alkyl group, an alkoxyalkyl group or an aryloxyalkyl group.

Claim 7

A heat-developable color photographic material as claimed in claim 4, wherein a total number of the carbon atoms contained in the ballast group is from 6 to 40.

Claim 8

A heat-developable color photographic material as claimed in claim 1, wherein a total number of the carbon atoms contained in the moiety C is from 12 to 40.

Claim 9

A heat-developable color photographic material as claimed in claim 1, wherein the connecting group represented by L is a divalent group connecting between the moiety C and the dye portion D with a covalent bond.

Claim 10

A heat-developable color photographic material as claimed in claim 8, wherein the divalent group is selected from the group represented by the following general formulae: ##STR17##

Claim 11

A heat-developable color photographic material as claimed in claim 8, wherein the divalent group is a group contains a total number of carbon atoms of not more than 12.

Claim 12

A heat-developable color photographic material as claimed in claim 1, wherein the dye portion represented by D includes an azo dye, an azomethine dye, an anthraquinone dye, a naphthoquinone dye, an indigoid dye, a carbonium ionic dye, a styryl dye, a quinoline dye, a nitro dye or a phthalocyanine dye.

Claim 13

A heat-developable color photographic material as claimed in claim 11, wherein the dye included in the dye portion represented by D is represented by the following general formulae: ##STR18## wherein R 11 to R 16 , which may be the same or different, each represents hydrogen or a substituent selected from the group consisting of an alkyl group, a cycloalkyl group, an aralkyl group, an alkoxy group, an aryloxy group, an aryl group, an acylamino group, an acyl group, a cyano group, a hydroxy group, an alkylsulfonylamino group, an arylsulfonylamino group, an alkylsulfonyl group, a hydroxyalkyl group, a cyanoalkyl group, an alkoxycarbonylalkyl group, an aryloxyalkyl group, a nitro group, a halogen atom, a sulfamoyl group, an N-substituted sulfamoyl group, a carbamoyl group, an N-substituted carbamoyl group, a sulfamido group, an N-substituted sulfamido group, a hydroxyalkoxy group, an alkoxyalkoxy group, a carboxy group, an amino group, a substituted amino group, an alkylthio group, an arylthio group, a hydroxamic acid group and an imido group, each having up to 25 carbon atoms.

Claim 14

A heat-developable color photographic material as claimed in claim 1, wherein the dye portion represented by D has a group which imparts hydrophilicity which is selected from a hydroxy group, a carboxy group, a sulfo group, a phosphoric acid group, an imido group, a hydroxamic acid group, a quaternary ammonium group, a carbamoyl group, a substituted carbamoyl group, a sulfamoyl group, a substituted sulfamoyl group, a sulfamoylamino group, a substituted sulfamoylamino group, a ureido group, a substituted ureido group, an alkoxy group, a hydroxyalkoxy group and an alkoxyalkoxy group.

Claim 15

A heat-developable color photographic material as claimed in claim 1, wherein the dye portion represented by D has a group selected from a phenolic hydroxy group, a carboxy group, a sulfo group, a phosphoric acid group, an imido group, a hydroxamic acid group, a substituted or unsubstituted sulfamoyl group and a substituted or unsubstituted sulfamoylamino group.

Claim 16

A heat-developable color photographic material as claimed in claim 1, wherein the dye releasing compound is present in an amount of from 0.01 mol to 4 mols per mol of the organic silver salt oxidizing agent.

Claim 17

A heat-developable color photographic material as claimed in claim 1, wherein the light-sensitive silver halide is selected from the group consisting of silver chloride, silver chlorobromide, silver chloroiodide, silver bromide, silver iodobromide, silver chloroiodobromide and silver iodide.

Claim 18

A heat-developable color photographic material as claimed in claim 1, wherein the light-sensitive silver halide is present in a range of from 0.005 mol to 5 mols per mol of the organic silver salt oxidizing agent.

Claim 19

A heat-developable color photographic material as claimed in claim 1, wherein the particle size of the silver halide is from 0.001 μm to 2 μm.

Claim 20

A heat-developable color photographic material as claimed in claim 1, wherein the organic silver salt oxidizing agent is a silver salt which forms silver by reacting with the reducing agent, when it is heated to a temperature of above 80° C. in the presence of exposed silver halide.

Claim 21

A heat-developable color photographic material as claimed in claim 1, wherein the organic silver salt oxidizing agent is a silver salt of an organic compound having a carboxy group, a silver salt of a compound containing a mercapto group or a thione group or a silver salt of a compound containing an imino group.

Claim 22

A heat-developable color photographic material as claimed in claim 20, wherein the organic silver salt oxidizing agent is a silver salt of a carboxylic acid derivative or an N-containing heterocyclic compound.

Claim 23

A heat-developable color photographic material as claimed in claim 1, wherein the light-sensitive silver halide and the organic silver salt oxidizing agent are present in the same layer.

Claim 24

A heat-developable color photographic material as claimed in claim 1, wherein the hydrophilic binder is gelatin or a gelatin derivative.

Claim 25

A heat-developable color photographic material as claimed in claim 1, wherein the reducing agent is a compound which is oxidized by the organic silver salt oxidizing agent to form an oxidized product capable of reacting with the dye releasing compound and releasing a dye.

Claim 26

A heat-developable color photographic material as claimed in claim 24, wherein the reducing agent is a color developing agent which is capable of forming an image upon oxidative coupling.

Claim 27

A heat-developable color photographic material as claimed in claim 24, wherein the reducing agent is selected from the group consisting of a p-phenylenediamine type color developing agent, an aminophenol compound, an aminonaphthol compound, an aminohydroxypyrazole compound, an aminopyrazoline compound and a hydrazone compound.

Claim 28

A heat-developable color photographic material as claimed in claim 24, wherein the reducing agent is selected from the group consisting of a p-aminophenol, a p-phenylenediamine, a hydrazone and derivatives thereof.

Claim 29

A heat-developable color photographic material as claimed in claim 1, wherein the color photographic material further contains an auxiliary developing agent.

Claim 30

A heat-developable color photographic material as claimed in claim 1, wherein the reducing agent is present in an amount of from 0.1 mol to 20 mols per mol of the oxidizing agent.

Claim 31

A heat-developable color photographic material as claimed in claim 1, wherein a color photographic material further contains a base or a base releasing agent.

Claim 32

A heat-developable color photographic material as claimed in claim 30, wherein the base releasing agent is a salt of a carboxylic acid and an organic base.

Claim 33

A heat-developable color photographic material as claimed in claim 30, wherein the base releasing agent is guanidine trichloroacetate.

Claim 34

A heat-developable color photographic material as claimed in claim 1, wherein the color photographic material further contains a thermal solvent.

Claim 35

A heat-developable color photographic material as claimed in claim 1, wherein the color photographic material further comprises an image receiving layer capable of receiving the hydrophilic diffusible dye.

Claim 36

A heat-developable color photographic material as claimed in claim 34, wherein the image receiving layer contains a dye mordant.

Claim 37

A heat-developable color photographic material as claimed in claim 34, wherein the image receiving layer contains a polymer mordant and gelatin.

Claim 38

A heat-developable color photographic material as claimed in claim 1, wherein the color photographic material further contains a transfer solvent.

Claim 39

A heat-developable color photographic material as claimed in claim 37, wherein the transfer solvent is selected from the group consisting of water and an alkaline aqueous solution.

Claim 40

A method of forming a color image which comprises imagewise exposing the heat-developable color photographic material as claimed in claim 1, developing the exposed color photographic material by uniformly heating to release a hydrophilic diffusible dye and transferring the diffusible dye into an image receiving material.

Claim 41

A method of forming a color image as claimed in claim 39, wherein the heating is carried out at a temperature ranging from 80° C. to 250° C.

Claim 42

A method of forming a color image as claimed in claim 39, wherein the transferring of the diffusible dye is carried out using a transfer solvent.

Claim 43

A method of forming a color image as claimed in claim 40, wherein the transfer solvent is selected from the group consisting of water and an alkaline aqueous solution.

Claim 44

A method of forming a color image as claimed in claim 39, wherein the image receiving material contains a mordant for the diffusible dye.