Silver halide color photographic lightsensitive material

Radiation imagery chemistry: process – composition – or product th – Radiation sensitive product – Two or more radiation-sensitive layers containing other than...

Reexamination Certificate

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C430S558000, C430S553000, C430S506000, C430S544000

Reexamination Certificate

active

06322959

ABSTRACT:

BACKGROUND OF THE INVENTION
The present invention relates to a silver halide color photographic lightsensitive material. More particularly, the present invention relates to a silver halide color photographic lightsensitive material improved in color reproducibility.
It is important to improve the hue of the dye which forms images in the improvement of the color reproducibility of the silver halide color photographic lightsensitive material. In the field of, for example, the silver halide color reversal photographic lightsensitive material, a 5-pyrazolone magenta coupler is commonly employed as a magenta color-forming coupler and a 2,5-diamidophenol coupler as a cyan color-forming coupler. However, the hue of the image forming dye produced from these couplers has not been fully satisfactory because of intense secondary absorption or sub-absorption.
In this situation, the use of various pyrazoloazole couplers leading to excellent hue has been proposed as a magenta coupler. Further, the use of naphthol couplers having the property of undergoing an association to thereby realize shorter wave leading to desirable absorption and the use of pyrroloazole couplers capable of producing excellent hue have been proposed as a cyan coupler.
For attaining the further improvement of the color reproducibility, it has been proposed to employ an associable naphthol coupler in combination with pyrazolo-[5,1-c]-1,2,4-triazole magenta coupler having a phenylene group at its 3- or 6-position as disclosed in, for example, Jpn. Pat. Appln. KOKAI Publication No. (hereinafter referred to as JP-A-) 4-37747 and to employ a pyrroloazole coupler in combination with a pyrazoloazole magenta coupler as disclosed in JP-A-5-150418. Specifically, it is described to employ such a cyan coupler leading to excellent hue in combination with a two-equivalent pyrazoloazole magenta coupler. However, as a result of the inventors' testing of the use of the pyrroloazole and associable cyan coupler in combination with two-equivalent pyrazoloazole magenta coupler, it has been found that the combined use involves difficulty because of the problems such that color mixing between a green-sensitive layer and a red-sensitive layer is aggravated to thereby deteriorate the color reproducibility and such that, when the image is stored in a highly humid atmosphere, magenta stain occurs.
BRIEF SUMMARY OF THE INVENTION
An object of the present invention is to provide a silver halide color photosensitive lightsensitive material which is excellent in color reproducibility and image preservability. Especially, it is intended to apply the present invention to a color reversal photographic lightsensitive material that is sequentially subjected to black-and-white development, reversal processing and color development.
DETAILED DESCRIPTION OF THE INVENTION
The object of the present invention has been attained by a following silver halide color photographic light-sensitive material:
(1) a silver halide color photographic lightsensitive material comprising a support and, superimposed thereon, a yellow color-forming blue-sensitive emulsion layer comprising at least one lightsensitive emulsion sub-layer, a magenta color-forming green-sensitive emulsion layer comprising at least one lightsensitive emulsion sub-layer and a cyan color-forming red-sensitive emulsion layer comprising at least one lightsensitive emulsion sub-layer, wherein said at least one sub-layer in said green-sensitive emulsion layer contains at least one magenta coupler represented by a general formula (MC-1):
wherein R
1
represents a hydrogen atom or a substituent; and each of G
1
and G
2
represents a nitrogen atom or a carbon atom, provided that G
2
is a carbon atom when G
1
is a nitrogen atom, G
1
is a carbon atom when G
2
is a nitrogen atom; and R
2
binds to G
1
or G
2
that is a carbon atom, wherein R
2
represents a substituent;
and said at least one sub-layer in said red-sensitive emulsion layer contains at least one cyan coupler represented by a general formula (PC-1):
wherein X represents a hydrogen atom or a group capable of dissociating by a coupling reaction with an aromatic primary amine color developing agent;
A represents a substituent; m is an integer of 0 to 4;
Q represents a divalent group selected from —O—, —COO—, —SO
2
—, —OC(O)—, —NR
18
CO—, —CONR
18
—, —NR
18
SO
2
—, —SO
2
NR
18
—, —NR
18
COO— and —NR
18
CONR
19
—, wherein each of R
18
and R
19
independently represents a hydrogen atom or an alkyl group; R
12
represents a substituent having a moiety of an aryl group or alkyl group each having at least 6 total carbon atoms; n is 1 or 2, provided that, when n is 1, R
12
has at least one dissociating group and that, when n is 2, two —Q—R
12
groups may be the same or different from each other and may contain a dissociating group; each of R
13
and R
14
independently represents an alkyl group; each of R
15
, R
16
and R
17
independently represents a hydrogen atom or an alkyl group; and Z represents a group of nonmetallic atoms forming a 5 to 8-membered carbocyclic or heterocyclic ring, with which a saturated or unsaturated carbocyclic or heterocyclic ring may be condensed; and
(2) a silver halide color photographic lightsensitive material comprising a support and, superimposed thereon, a yellow color-forming blue-sensitive emulsion layer comprising at least one lightsensitive emulsion sub-layer, a magenta color-forming green-sensitive emulsion layer comprising at least one lightsensitive emulsion sub-layer and a cyan color-forming red-sensitive emulsion layer comprising at least one lightsensitive emulsion sub-layer, wherein said at least one sub-layer in said green-sensitive emulsion layer contains at least one magenta coupler represented by the general formula (MC-1) set forth in item (1) above, and said at least one sub-layer in said red-sensitive emulsion layer contains at least one cyan coupler represented by a general formula (NC-1):
wherein M has the same meaning as X of the above general formula (PC-1); Y represents a hydrogen atom or a substituent, provided that, when Y is a substituent, Y binds to any one of 5 to 8-positions of the naphthol ring; L represents a divalent group; U represents a substituent containing at least one —NH— therein; j is an integer of 1 to 3; k is 0 or 1; B represents a substituent; and b is an integer of 0 to 4.
The present invention will be described in detail below.
First, the general formula (MC-1) will be described.
In the general formula (MC-1), R
1
represents a hydrogen atom or a substituent. The substituent is, for example, a halogen atom, an alkyl group, an aryl group, a heterocyclic group, a cyano group, a hydroxyl group, a nitro group, a carboxyl group, an amino group, an alkoxy group, an aryloxy group, an acylamino group, an alkylamino group, an anilino group, a ureido group, a sulfamoylamino group, an alkylthio group, an arylthio group, an alkoxycarbonylamino group, a sulfonamido group, a carbamoyl group, a sulfamoyl group, a sulfonyl group, an alkoxycarbonyl group, a heterocyclic oxy group, an acyloxy group, a carbamoyloxy group, a silyloxy group, an aryloxycarbonylamino group, an imido group, a heterocyclic thio group, a sulfinyl group, a phosphonyl group, an aryloxycarbonyl group or an acyl group.
In the following description, the term “total carbon atoms” of each substituent means the number of all carbon atoms possessed by the substituent which, when the substituent is substituted with a group, include carbon atoms of the substitution group.
More specifically, R
1
, when being a substituent, represents a halogen atom (e.g., a chlorine atom or a bromine atom), an alkyl group (e.g., a linear or branched alkyl group, aralkyl group, alkenyl group, alkynyl group, cycloalkyl group or cycloalkenyl group, each having 1 to 32 total carbon atoms, such as methyl, ethyl, propyl, isopropyl, t-butyl, tridecyl, 2-methanesulfonylethyl, 3-(3-pentadecylphenoxy)propyl, 3-{4-{2-[4-(4-hydroxyphenylsulfonyl)phenoxy]dodecanamido}phenyl}propyl, 2-ethoxytridecyl, trifluoro

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