Heat-developable color light-sensitive material with alkyl carboxylic acid base precursor containing triple bond

Claim 2

A heat-developable color light-sensitive material comprising a support having thereon at least a light-sensitive silver halide, a binder, a dye releasing redox compound which is capable of reducing the light-sensitive silver halide and is capable of reacting with the light-sensitive silver halide by heating to release a hydrophilic dye and a salt of an alkylcarboxylic acid having a triple bond between the α-position carbon atom and the β-position carbon atom with an organic base as a base precursor.

Claim 3

A heat-developable color light-sensitive material as claimed in claim 1, wherein the base precursor is a compound represented by the following general formula (I) or (II): (R--C.tbd.C--CO.sub.2 H).sub.x.B (I) R--C.tbd.C--CO.sub.2 H).sub.2.B.sub.y (II) wherein R represents a monovalent residue selected from a hydrogen atom, an alkyl group, a substituted alkyl group, a cycloalkyl group, an alkenyl group, an alkynyl group, an aryl group, a substituted aryl group, a heterocyclic group, a substituted heterocyclic group, an aralkyl group, a substituted aralkyl group, an acyl group, an alkoxycarbonyl group, a carbamoyl group, a substituted carbamoyl group, --CO 2 M (wherein M represents an alkali metal) and --CO 2 H.B or a divalent residue selected from an alkylene group, an arylene group and a heterocyclic divalent residue and these groups may be further substituted; B represents an organic base; x represents 1 when B represents a monoacidic base or 2 when B represents a diacidic base; and y represents 1 when B represents a diacidic base or 2 when B represents a monoacidic base.

Claim 4

A heat-developable color light-sensitive material as claimed in claim 2, wherein R represents a hydrogen atom, an alkyl group having from 1 to 5 carbon atoms, a substituted alkyl group having from 1 to 5 carbon atoms, a cycloalkyl group having from 5 to 8 carbon atoms, an alkenyl group having from 2 to 5 carbon atoms, an alkynyl group having from 2 to 5 carbon atoms, a phenyl group, a substituted phenyl group, a naphthyl group, a substituted naphthyl group, an anthryl group, a pyridyl group, a substituted pyridyl group, a thienyl group, a substituted thienyl group, a thiazolyl group, a benzoxazolyl group, a benzothiazolyl group, an imidazolyl group, a benzimidazolyl group, a quinolyl group, a furyl group, a pyrrolyl group, an aralkyl group having from 7 to 10 carbon atoms, an acyl group having from 2 to 12 carbon atoms, an alkoxycarbonyl group having from 2 to 9 carbon atoms, a carbamoyl group, a substituted carbamoyl group having from 2 to 9 carbon atoms, --CO 2 Na, --CO 2 K, --CO 2 CS, --CO 2 H.B (wherein B represents a base component as described above), a 1,3-phenylene group, a 1,4-phenylene group, a 1,5-naphthylene group, a 2,5-thienylene group or a 9,10-anthrylene group.

Claim 5

A heat-developable color light-sensitive material as claimed in claim 2, wherein R represents an alkenyl group, an alkynyl group, a phenyl group, a substituted phenyl group, a naphthyl group, a substituted naphthyl group, an anthryl group, a pyridyl group, a substituted pyridyl group, a thienyl group, a substituted thienyl group, a benzoxazolyl group, a benzothiazolyl group, an acyl group, an alkoxycarbonyl group, a carbamoyl group, a substituted carbamoyl group, --CO 2 M, --CO 2 H.B, a phenylene group, a naphthylene group, a thienylene group or an anthrylene group.

Claim 6

A heat-developable color light-sensitive material as claimed in claim 2, wherein the base precursor is a compound represented by the following general formula (III) or (IV): (Ar--C.tbd.C--CO.sub.2 H).sub.x. B (III) Ar--C.tbd.C--CO.sub.2 H).sub.2.B.sub.y (IV) wherein Ar represents a phenyl group, a substituted phenyl group, a naphthyl group, a substituted naphthyl group, an anthryl group, a pyridyl group, a substituted pyridyl group, a thienyl group, a substituted thienyl group or a divalent group selected from these groups; and B, x and y each has the same meaning as defined in claim 2.

Claim 7

A heat-developable color light-sensitive material as claimed in claim 5, wherein B represents an organic base having a pKa of 9 or more and a boiling point of 100° C. or higher.

Claim 8

A heat-developable color light-sensitive material as claimed in claim 5, wherein the organic base represented by B is a guanidine, a cyclic guanidine, an amidine or a cyclic amidine.

Claim 9

A heat-developable color light-sensitive material as claimed in claim 1, wherein the base precursor is incorporated in a layer of the material and present in that layer in an amount of 50% by weight or less based on the coated amount of the layer.

Claim 10

A heat-developable color light-sensitive material as claimed in claim 8, wherein the base precursor is present in the layer in an amount of 0.01% by weight to 40% by weight based on the coated amount of the layer.

Claim 11

A heat-developable color light-sensitive material as claimed in claim 1, wherein the material further contains a dye releasing activator.

Claim 12

A heat-developable color light-sensitive material as claimed in claim 1, wherein the material further contains an organic silver salt oxidizing agent.

Claim 15

A method of forming a color image as claimed in claim 12, wherein the heating of the light-sensitive material is carried out at a temperature of at least 80° C.

Claim 16

A method of forming a color image as claimed in claim 12, wherein the mobile dye released is then transferred into a dye fixing layer.