Photographic element containing a cyclic azole coupler and an anti-fading agent containing a combination of functionalities

Abstract

Disclosed is a silver halide photographic element comprising a support bearing a light sensitive silver halide emulsion layer and a cyclic azole dye forming coupler associated with a stabilizer having the following Formula S: ##STR1## wherein: R.sub.1 represents an alkyl or cycloalkyl group, an alkenyl group or an aryl group;R.sub.2 and R.sub.3 each represents a hydrogen atom or a substituent;L represents a covalent bond or a divalent linking group;X represents O, S, SO, SO.sub.2, or NR.sub.4, or --O--X.sub.2 --O--;R.sub.4 represents H, alkyl, --CH.sub.2 CH(OH)CH.sub.2 OR.sub.5, or --COR.sub.6 ;R.sub.5 and R.sub.6 represent alkyl groups;Y represents a hydrogen bond donating group;X.sub.2 represents BR.sub.7, PR.sub.8, P(O)R.sub.9, SO, or SO.sub.2 ;R.sub.7 -R.sub.9 each represents phenoxy which may be substituted by 1 to 3 alkyl, alkoxy, or halogen groups;Z.sub.1 and Z.sub.2 each represents an alkylene group of 1 to 3 carbon atoms, which may be substituted, provided that the total number of carbon atoms in the ring is 3 to 6;p and q each represents an integer of 0 to 4.

Description

FIELD OF THE INVENTION

This invention relates to photographic elements containing particular dye forming couplers associated with compounds which reduce fading of the dyes formed from the couplers on processing of the photographic element.

BACKGROUND OF THE INVENTION

In a silver halide photographic element, a color image is formed when the element is exposed to light and then subjected to color development with a primary aromatic amine developer. Color development results in imagewise reduction of silver halide and production of oxidized developer. Oxidized developer reacts with one or more incorporated dye-forming couplers to form an imagewise distribution of dye.

The dyes that are formed by any color coupler during processing have a tendency to fade over time as a result of exposure to light, heat and humidity. As all three image dyes of a typical color element fade, this results in overall fading of the image over time. In addition, since the three image dyes may not fade at the same rate, an apparent change in image color may result. Such change is particularly noticable in the case of magenta image dye fading.

A variety of dye-forming coupler types have been used in photographic materials. Among the known dye-forming couplers are cyclic azoles such as pyrazolotriazoles, pyrazolobenzimidazoles, and imidazopyrazoles. These couplers contain bridgehead nitrogen 5,5 fused ring systems and include such couplers as pyrrolo[1,2-b]pyrazoles, pyrazolo[3,2-c][1,2,4]triazoles, pyrazolo[2,3-b][1,2,4]triazoles, imidazo[1,2-b]pyrazoles, imidazo[1,5-b]pyrazoles, imidazo[1,2-a]imidazoles, imidazo[1,2-b][1,2,4]triazoles, imidazo[2,1-c][1,2,4]triazoles, imidazo[5,1-c][1,2,4]triazoles and [1,2,4]triazolo[3,4-c][1,2,4]triazole. These couplers also contain bridgehead nitrogen 5,5,6 fused ring systems and include such as pyrazolo[3,2-b]benzimidazoles. These couplers may form magenta or cyan dyes, depending on the ring structure and substituents.

A significant disadvantage of pyrazoloazole couplers is fading of the dyes formed from them by photographic processing due to extended exposure to low levels of light. Compounds which are included in photographic elements to reduce image dye fading are known as stabilizers. Inclusion of stabilizers in color photographic materials can reduce the deterioration of the dye images which occurs over time as a result of the action of light, heat or humidity. This is true for dyes formed from pyrazoloazole couplers. U.S. Pat. Nos. 5,236,819 and 5,082,766 and German Published Patent Application DTOS 4,307,194 describe the use of certain stabilizers with pyrazoloazole couplers to improve their dye stability. However, it would be desirable to further improve the light stability of dyes derived from cyclic azole dye forming couplers, and thus retain the color rendition of the image for a longer period of time.

SUMMARY OF THE INVENTION

We have found that highly stable dye images formed from cyclic azole couplers can be obtained if there is associated with the coupler a stabilizer compound S, shown below, and optionally a combination of stabilizer compounds S and R, shown below, or a combination of stabilizer compounds S and I, shown below.

The present invention therefore provides a silver halide photographic element comprising a support bearing a light sensitive silver halide emulsion layer and a cyclic azole dye forming coupler associated with a stabilizer having the following Formula S: ##STR2## wherein: R.sub.1 represents an alkyl or cycloalkyl group, an alkenyl group or an aryl group;

R.sub.2 and R.sub.3 each represents a hydrogen atom or a substituent; L represents a covalent bond or a divalent linking group; X represents O, S, SO, SO.sub.2, or NR.sub.4, or --O--X.sub.2 --O--; R.sub.4 represents H, alkyl, --CH.sub.2 CH(OH)CH.sub.2 OR.sub.5, or --COR.sub.6 ; R.sub.5 and R.sub.6 represent alkyl groups;

Y represents a hydrogen bond donating group such as CONH, NHCO, NHCONH, SONH, SO.sub.2 NH, or NHSO.sub.2 ;

X.sub.2 represents BR.sub.7, PR.sub.8, P(O)R.sub.9, SO, or SO.sub.2 ; R.sub.7 -R.sub.9 each represents phenoxy which may be substituted by 1 to 3 alkyl, alkoxy, or halogen groups; Z.sub.1 and Z.sub.2 each represents an alkylene group of 1 to 3 carbon atoms, which may be substituted, provided that the total number of carbon atoms in the ring is 3 to 6; p and q each represents an integer of 0 to 4.

The invention also relates to a photographic element further comprising a compound having the following Formula R: ##STR3## wherein: each R.sub.10 independently represents a hydrogen atom, an alkyl or cycloalkyl group, an alkenyl group or an aryl group;

each R.sub.11 independently represents a halogen atom, an alkyl group, an alkenyl group, an alkoxy group, an aryl group, an aryloxy group, an alkylthio group, an aryl thio group, an acyl group, an acylamino group, a sulfonyl group, a sulfonamide group or a hydroxy group; each m is, individually an integer of 0 to 4; and

A represents an alkylene group having 1 to 10 carbon atoms in its linear structure.

The invention also relates to a photographic element further comprising a compound having the following Formula I: ##STR4## wherein: R.sub.14 is an alkyl, alkenyl, or aryl group;

R.sub.15 is a substituent; and m is an integer of 0 to 5.

Photographic elements of the present invention yield dye images that have low fading when exposed to light.

DETAILED DESCRIPTION OF THE INVENTION

As used herein, unless otherwise indicated the alkyl and aryl groups, and the alkyl and aryl portions of groups, can be unsubstituted or substituted. Typical alkyl groups have 1 to 32 carbon atoms and typical aryl groups have 6 to 32 carbon atoms. Other groups identified below which contain a replacable hydrogen atom can be substituted or not, depending on the particular structure and properties desired.

The dye forming couplers of this invention can be based on any cyclic zole coupler, especially any of the bridgehead nitrogen 5,5 fused ring systems or 5,5,6 fused ring systems identified above. Preferred couplers are pyrazolotriazoles represented by Formula M: ##STR5## wherein: R.sub.12 is hydrogen, a substituent group or a ballast group;

R.sub.13 is a ballast group or a fused benzene ring; and X is hydrogen or a coupling-off-group, provided that X, R.sub.12 and R.sub.13 contain a number of carbon atoms sufficient to immobilize the coupler in the emulsion layer; and Z.sub.a, Z.sub.b, and Z.sub.c are independently a substituted or unsubstituted methine group, .dbd.N--, ##STR6## or --NH--, provided that one of either the Z.sub.a -Z.sub.b bond or the Z.sub.b -Z.sub.c bond is a double bond and the other is a single bond, and when the Z.sub.b -Z.sub.c bond is a carbon-carbon double bond, it can be part of an aromatic ring and at least one of Z.sub.a, Z.sub.b, and Z.sub.c represents a methine group connected to R.sub.13. These couplers generally form magenta dyes when R.sub.12 and R.sub.13 are electron donating groups, and cyan dyes when R.sub.12 and R.sub.13 are electron withdrawing groups.

Preferred pyrazolotriazole couplers of this invention are compounds represented by Formula MI: ##STR7## wherein R.sub.12 is hydrogen or a substituent group; R.sub.13 is a ballast group; and X is hydrogen or a coupling-off-group.

Preferably, in formula MI, R.sub.12 represents a tertiary alkyl group of 4 to 12 carbon atoms. Most preferably it represents t-butyl.

Other preferred pyrazolotriazole couplers of this invention compounds represented by Formula MII: ##STR8## wherein R.sub.12 is hydrogen or a substituent group; R.sub.13 is a ballast group; and X is hydrogen or a coupling-off-group.

Preferably, in formula MII, R.sub.12 represents a tertiary alkyl group of 4 to 12 carbon atoms. Most preferably it represents t-butyl.

Other preferred couplers are couplers represented by Formula MIII ##STR9## wherein R.sub.12 and R.sub.14 each is hydrogen, a substituent group or a ballast group; X is hydrogen or a coupling-off-group, provided that X, R.sub.12 and R.sub.14 together contain a number of carbon sufficient to immobilize the coupler in the emulsion layer.

Preferably, in formula MIII, R.sub.12 represents an alkoxy group of 1 to 30 carbon atoms, and R.sub.14 is hydrogen.

Examples of suitable R.sub.12 and R.sub.14 substituent groups are alkyl, which can be straight or branched, such as methyl, ethyl, n-propyl, n-butyl, t-butyl, trifluoromethyl, tridecyl or 3-(2,4-di-t-amylphenoxy)propyl; alkoxy, such as methoxy or ethoxy; alkylthio, such as methylthio or octylthio; aryl, aryloxy or arylthio, such as phenyl, 4-t-butylphenyl, 2,4,6-trimethylphenyl, phenoxy, 2-methylphenoxy, phenylthio or 2-butoxy-5-t-octylphenylthio; heterocyclyl, heterocyclyloxy or heterocyclylthio, each of which contain a 3 to 7 membered heterocyclic ring composed of carbon atoms and at least one hetero atom selected from oxygen, nitrogen and sulfur, such as 2-furyl, 2-thienyl, 2-benzimidazolyloxy or 2-benzothiazolyl; cyano; acyloxy, such as acetoxy or hexadecanoyloxy; carbamoyloxy, such as N-phenylcarbamoyloxy or N-ethylcarbamoyloxy; silyloxy, such as trimethylsilyloxy; sulfonyloxy, such as dodecylsulfonyloxy; acylamino, such as acetamido or benzamido; anilino, such as phenylanilino or 2-chloroanilino; ureido, such as phenylureido or methylureido; imido, such as N-succinimido or 3-benzylhydantoinyl; sulfamoylamino, such as N,N-dipropyl-sulfamoylamino or N-methyl-N-decylsulfamoylamino; carbamoylamino, such as N-butylcarbamoylamino or N,N-dimethylcarbamoylamino; alkoxycarbonylamino, such as methoxycarbonylamino or tetradecyloxycarbonylamino; aryloxycarbonylamino, such as phenoxycaronylamino, 2,4-di-t-butylphenoxycarbonylamino; sulfonamido, such as methanesulfonamido or hexadecanesulfonamido; carbamoyl group, such as N-ethylcarbamoyl or N,N-dibutylcarbamoyl; acyl, such as acetyl or (2,4-di-t-amylphenoxy)acetyl; sulfamoyl, such as N-ethylsulfamoyl or N,N-dipropylsulfamoyl; sulfonyl, such as methanesulfonyl or octanesulfonyl; sulfinyl, such as octanesulfinyl or dodecylsulfinyl; alkoxycarbonyl, such as methoxycarbonyl or butyloxycarbonyl; aryloxycarbonyl, such as phenyloxycarbonyl or 3-pentadecyloxycarbonyl; alkenyl; hydroxyl; amino; and carbonamido groups.

The ballast group is a group of such size and configuration that, in combination with the remainder of the molecule, it provides the coupler, and the dye formed from it, with sufficient bulk that it is substantially non-diffusible from the layer in which it is coated in the photographic element. Representative ballast groups include alkyl or aryl groups containing 6 to 32 carbon atoms. Other ballast groups include alkoxy, aryloxy, arylthio, alkylthio, alkoxycarbonyl, aryloxycarbonyl, carboxy, acyl, acyloxy, carbonamido, carbamoyl, alkylcarbonyl, arylcarbonyl, alkysulfonyl, arylsulfonyl, sulfamoyl, sulfenamoyl, alkylsulfinyl, arylsulfinyl, alkylphosphonyl, arylphosphonyl, alkoxyphosphonyl, and arylphosphonyl. In formula MI, preferably R.sub.13 is an alkyl group of 6 to 32 carbon atoms

Possible substituents for R.sub.12, R.sub.13 and R.sub.14 include halogen, alkyl, aryl, aryloxy, heterocyclyl, cyano, alkoxy, acyloxy, carbamoyloxy, silyloxy, sulfonyloxy, acylamino, anilino, ureido, imido, sulfonylamino, carbamoylamino, alkylthio, arylthio, heterocyclylthio, alkoxycarbonylamino, aryloxycarbonylamino, sulfonamido, carbamoyl, acyl, sulfamoyl, sulfonyl, sulfinyl, alkoxycarbonyl, aryloxycarbonyl, alkenyl, carboxyl, sulfo, hydroxyl, amino and carbonamido groups.

The coupling off group represented by X can be a hydrogen atom or any of the coupling-off groups known in the art. Coupling-off groups can determine the equivalency of the coupler, can modify the reactivity of the coupler, or can advantageously affect the layer in which the coupler is coated or other layers in the element by performing, after the release from the coupler, such functions as development inhibition, development acceleration, bleach inhibition, bleach acceleration, color correction, and the like. Representative classes of coupling-off groups include halogen, particularly chlorine, bromine, or fluorine, alkoxy, aryloxy, heterocyclyloxy, heterocyclic, such as hydantoin and pyrazolo groups, sulfonyloxy, acyloxy, carbonamido, imido, acyl, heterocyclythio, sulfonamido, alkylthio, arylthio, heterocyclythio, sulfonamido, phosphonyloxy, and arylazo.

Preferably, X is hydrogen or halogen. Most preferably, X is chlorine.

Specific couplers within the scope of the present invention have the following structures: ##STR10##

The compounds that have the Formula S above are believe to stabilize by acting as singlet oxygen quenchers. In this formula rings "A" and "B" can be substituted with substituent groups described above, as can be the alkylene groups represented by Z.sub.1 and Z.sub.2.

Preferred compounds represented by Formula S, are those having the following Formula SI: ##STR11## wherein L represents a covalent bond or a divalent linking group; and R.sub.1, R.sub.2, R.sub.3, p and q are as described above.

The most preferred compounds represented by Formula S are those having the formula SI wherein L has the structure O--L.sub.l ; L.sub.l is an alkylene or heteroalkylene group; R.sub.1 is an alkyl group, p and q are each 0 (i.e., R.sub.2 and R.sub.3 are absent); L is attached to Ring "B" at a position para to Ring "C"; and the sulfonamido group is attached to Ring "A" is at a position para to L.

Representative examples of stabilizer having the Formula S are: ##STR12##

The stabilizers that have the Formula R above are believed to stabilize the dye image by scavenging free radicals. In this formula, the group represented by A is a straight, branched or cyclic alkylene group, the linear portion of which has 1 to 10 carbon atoms, which can be substituted with one or more aryl, cyano, halogen, heterocyclyl, cycloalkyl, alkoxy, hydroxy, and aryloxy groups. The alkylene group can form a cycloalkyl ring, such as ##STR13##

Preferred compounds represented by Formula R, are those in which:

each R.sub.1 independently is hydrogen, alkyl or cycloalkyl of 1 to 8 carbon atoms; each R.sub.2 is independently halogen, hydroxy, alkyl or alkoxy of 1 to 8 carbon atoms; each m is an integer of 0 to 2; and A is an alkylene group of 1 to 6 carbon atoms in its linear structure.

Representative examples of stabilizer compounds which satisfy Formula R are: ##STR14##

The stabilizers that have the formula I above are more particularly described as compounds of formula I wherein:

R.sub.14 is an alkyl, alkenyl, or aryl group; R.sub.15 is a substituent, and if m is greater than 1, two or more R4 groups may join to form a carbocyclic or heterocyclic ring, which may in turn be substituted; m is an integer of 0 to 5, preferably 1 or 2.

Preferred stabilizers of formula I are those wherein:

R.sub.14 is an alkyl, alkenyl, or aryl group which together with substituents contains 1 to 30 carbon atoms; most preferably, R.sub.14 is an alkyl group of 2 to 30 carbon atoms; R.sub.15 is an alkyl or alkoxy group which together with substituents contains 1 to 30 carbon atoms; and m is 1.

Particularly useful are stabilizers of formula I in which R.sub.15 is an alkoxy group substituted at the alpha position by an alkoxycarbonyl group. Representative examples of the stabilizers of formula I are: ##STR15##

The stabilizer compounds of formulas R and I of the present invention can be prepared by techinque known to those skilled in the art. The preparation of the compounds of formula R is described in U.S. Pat. No. 5,236,819 and references cited therein. The preparation of the compounds of formula I is described in U.S. Pat. No. 4,124,396, in connection with the synthesis of intermediate D as shown in columns 5, 6, 9 and 10.

The preparation of stabilizer compounds of formula S of the invention is illustrated by the following synthesis of Stabilizer S-3. ##STR16## A mixture of para-aminophenol (25 g, 229 mmol) and divinylsulfone (32.5 g, 275 mmol) was heated at reflux in ethanol (100 ml) for two days. The reaction mixture was cooled and poured into ice water (1 l). The mixture was made acidic with the addition of acetic acid and the resulting tan solid was isolated by filtration and washed with water. Recrystallization from methanol afforded the desired 4-(1',1'-dioxothiomorpholino)phenol as a light tan crystalline solid (35 g, 67%). Mp. 149-151.degree. C.

A mixture of 4-(1',1'-dioxothiomorpholino)phenol (10 g, 44 mmol), 1,4-diiodobutane (40.9 g, 132 mmol) and cesium carbonate (42.9 g, 132 mmol) was heated at 50.degree. C. in acetonitrile (400 ml). After 4 hours, the reaction mixture was cooled, filtered and the solid salts washed with acetonitrile. The filtrate was poured into dilute HCl/ice water (1.2 l) and the resultant cream colored solid was isolated by filtration and washed with water. Chromatography on silica gel, with 97:3; dichloromethane:ether, afforded 1-iodo-4-[4'-(1,1-dioxothiomorpholino)phenoxy] butane, II (13.4 g, 74%). Mp. 119-121.degree. C.

A mixture of the above iodo-compound (6 g, 14.6 mmol), acid I (6.68 g, 14.6 mmol) and cesium carbonate (4.75 g, 14.6 mmol) was heated in dimethylformamide (100 ml) at 75.degree. for 3 hours. After cooling, the reaction was poured into dilute HCl/ice water (700 ml) and the water decanted from a tan semi-solid. The semi-solid solidified upon air drying and was then chromatographed on silica gel, with 95:5; dichloromethane:ether. The resulting material was recrystallized from isopropanol to afford the desired product, S-3, as a white solid (7.5 g, 69.8%). Mp. 73-75.degree. C.

Typically, the couplers and the stabilizers with which they are associated are dispersed in the same layer of the photographic element in a high boiling organic compound known in the art as a coupler solvent. Representative coupler solvents include phthalic acid alkyl esters such as dibutyl phthalate, dioctyl phthalate, and diundecyl phtalate; phosphoric acid esters such as tricresyl phosphate, diphenyl phosphate, tris-2-ethylhexyl phosphate, and tris-3,5,5-trimethylhexyl phosphate; citric acid esters such as tributyl citrate and tributyl acetylcitrate; benzoic acid esters such as octyl benzoate;, aliphatic amides such as N,N-diethyl lauramide and N,N-dibutyl lauramide; aliphatic alcohols such as oleyl alcohol; and alkyl phenols such as 2,4-di-t-butyl phenol. Preferred coupler solvents are the phthalate esters and aliphatic alcohols, which can be used alone or in combination with one another or with other coupler solvents. Selection of the correct coupler solvent has been found to influence the coupling efficiency of the coupler, as well as the hue and stability of the dye formed on coupling.

Throughout this application a reference to any type of chemical "group" includes both the unsubstituted and substituted forms of the group described. Generally, unless otherwise specifically stated, substituent groups usable on molecules herein include any groups, whether substituted or unsubstituted, which do not destroy properties necessary for the photographic utility. It will also be understood throughout this application that reference to a compound of a particular general formula includes those compounds of other more specific formula which specific formula falls within the general formula definition. Examples of substituents on any of the mentioned groups can include known substituents, such as: halogen, for example, chloro, fluoro, bromo, iodo; alkoxy, particularly those with 1 to 6 carbon atoms (for example, methoxy, ethoxy); substituted or unsubstituted alkyl, particularly lower alkyl (for example, methyl, trifluoromethyl); alkenyl or thioalkyl (for example, methylthio or ethylthio), particularly either of those with 1 to 6 carbon atoms; substituted and unsubstituted aryl, particularly those having from 6 to 20 carbon atoms (for example, phenyl); and substituted or unsubstituted heteroaryl, particularly those having a 5 or 6-membered ring containing 1 to 3 heteroatoms selected from N, O, or S (for example, pyridyl, thienyl, furyl, pyrrolyl); and others known in the art. Alkyl substituents may specifically include "lower alkyl", that is having from 1 to 6 carbon atoms, for example, methyl, ethyl, and the like. Further, with regard to any alkyl group, alkylene group or alkenyl group, it will be understood that these can be branched or unbranched and include ring structures.

The coupler and stabilizer compounds of the present invention are known compounds and can be prepared by techniques known to those skilled in the art. References which describe the preparation of the dye forming couplers are the patents and published applications referred to above as describing these compounds, and references cited therein. The preparation of Stabilizer Compounds R and S is described in U.S. Pat. No. 5,236,819 and references cited therein. The synthesis of Stabilizer Compound I is described in U.S. Pat. No. 4,124,396, in connection with the synthesis of intermediate D as shown in columns 5, 6, 9 and 10.

Typically the amount of each of compound S, compound I and compound R will range from about 0.2 to about 2.0 moles stabilizer per mole of coupler, preferably from about 0.5 to 1.0 moles stabilizer per mole of coupler.

The pyrazoloazole coupler is typically coated in the element at a coverage of from 0.25 mmol/m.sup.2 to 1.01 mmol/m.sup.2, and preferably at a coverage of from 0.40 to 0.70 mmol/m.sup.2. When a coupler solvent is employed, it typically is present in an amount of 0.50 to 5.0 mg. per mg. coupler, and preferably in an amount of 1.0 to 3.0 mg. per mg. coupler.

The photographic elements of this invention can be black and white elements (for example, using magenta, cyan and yellow dye forming couplers), single color elements or multicolor elements. Multicolor elements contain dye image-forming units sensitive to each of the three primary regions of the spectrum. Each unit can be comprised of a single emulsion layer or of multiple emulsion layers sensitive to a given region of the spectrum. The layers of the element, including the layers of the image-forming units, can be arranged in various orders as known in the art. In an alternative format, the emulsions sensitive to each of the three primary regions of the spectrum can be disposed as a single segmented layer.

Photographic elements of this invention can have the structures and components shown on Research Disclosure, February 1995, Item 37038, pages 79-114. Research Disclosure is published by Kenneth Mason Publications, Ltd., Dudley Annex, 12a North Street, Emsworth, Hampshire P010 7DQ, ENGLAND. Specific elements can be those shown on pages 96-98 of this Research Disclosure item as Color Paper Elements 1 and 2, in which is employed in the magenta dye forming layers the stabilizer combinations of the present invention instead of the stabilizers shown there. A typical multicolor photographic element of this invention comprises a support bearing a cyan dye image-forming unit comprised of at least one red-sensitive silver halide emulsion layer having associated therewith at least one cyan dye-forming coupler, a magenta dye image-forming unit comprising at least one green-sensitive silver halide emulsion layer having associated therewith at least one magenta dye-forming coupler, and a yellow dye image-forming unit comprising at least one blue-sensitive silver halide emulsion layer having associated therewith at least one yellow dye-forming coupler. The element can contain additional layers, such as filter layers, interlayers, overcoat layers, subbing layers, and the like. All of these can be coated on a support which can be transparent or reflective (for example, a paper support). Photographic elements of the present invention may also usefully include a magnetic recording material as described in Research Disclosure, Item 34390, November 1992, or a transparent magnetic recording layer such as a layer containing magnetic particles on the underside of a transparent support as in U.S. Pat. No. 4,279,945 and U.S. Pat. No. 4,302,523. The element typically will have a total thickness (excluding the support) of from 5 to 30 microns. While the order of the color sensitive layers can be varied, they will normally be red-sensitive, green-sensitive and blue-sensitive, in that order on a transparent support, (that is, blue sensitive furthest from the support) and the reverse order on a reflective support being typical.

This invention also contemplates the use of photographic elements of the present invention in what are often referred to as single use cameras (or "film with lens" units). These cameras are sold with film preloaded in them and the entire camera is returned to a processor with the exposed film remaining inside the camera. Such cameras may have glass or plastic lenses through which the photographic element is exposed.

In the following discussion of suitable materials for use in elements of this invention, reference will be made to Research Disclosure, September 1994, Number 365, Item 36544, which will be identified hereafter by the term "Research Disclosure I." The Sections hereafter referred to are Sections of the Research Disclosure I.

The silver halide emulsions employed in the elements of this invention can be either negative-working, such as surface-sensitive emulsions or unfogged internal latent image forming emulsions, or direct positive emulsions of the unfogged, internal latent image forming type which are positive working when development is conducted with uniform light exposure or in the presence of a nucleating agent. Suitable emulsions and their preparation as well as methods of chemical and spectral sensitization are described in Sections I through V. Color materials and development modifiers are described in Sections V through XX. Vehicles which can be used in the elements of the present invention are described in Section II, and various additives such as brighteners, antifoggants, stabilizers, light absorbing and scattering materials, hardeners, coating aids, plasticizers, lubricants and matting agents are described, for example, in Sections VI through X and XI through XIV. Manufacturing methods are described in all of the sections, other layers and supports in Sections XI and XIV, processing methods and agents in Sections XIX and XX, and exposure alternatives in Section XVI.

With negative working silver halide a negative image can be formed. Optionally a positive (or reversal) image can be formed although a negative image is typically first formed.

The photographic elements of the present invention may also use colored couplers (e.g. to adjust levels of interlayer correction) and masking couplers such as those described in EP 213 490; Japanese Published Application 58-172,647; U.S. Pat. No. 2,983,608; German Application DE 2,706,117; UK Patent 1,530,272; Japanese Application A-113935; U.S. Pat. No. 4,070,191 and German Application DE 2,643,965. The masking couplers may be shifted or blocked.

The photographic elements may also contain materials that accelerate or otherwise modify the processing steps of bleaching or fixing to improve the quality of the image. Bleach accelerators described in EP 193 389; EP 301 477; U.S. Pat. No. 4,163,669; U.S. Pat. No. 4,865,956; and U.S. Pat. No. 4,923,784 are particularly useful. Also contemplated is the use of nucleating agents, development accelerators or their precursors (UK Patent 2,097,140; UK Patent 2,131,188); electron transfer agents (U.S. Pat. No. 4,859,578; U.S. Pat. No. 4,912,025); antifogging and anti color-mixing agents such as derivatives of hydroquinones, aminophenols, amines, gallic acid; catechol; ascorbic acid; hydrazides; sulfonamidophenols; and non color-forming couplers.

The elements may also contain filter dye layers comprising colloidal silver sol or yellow and/or magenta filter dyes and/or antihalation dyes (particularly in an undercoat beneath all light sensitive layers or in the side of the support opposite that on which all light sensitive layers are located) either as oil-in-water dispersions, latex dispersions or as solid particle dispersions. Additionally, they may be used with "smearing" couplers (e.g. as described in U.S. Pat. No. 4,366,237; EP 096 570; U.S. Pat. No. 4,420,556; and U.S. Pat. No. 4,543,323.) Also, the couplers may be blocked or coated in protected form as described, for example, in Japanese Application 61/258,249 or U.S. Pat. No. 5,019,492.

The photographic elements may further contain other image-modifying compounds such as developer inhibitor releasing compounds (DIR's).

The elements of the present invention may be employed to obtain reflection color prints as described in Research Disclosure, November 1979, Item 18716, available from Kenneth Mason Publications, Ltd, Dudley Annex, 12a North Street, Emsworth, Hampshire P0101 7DQ, England, incorporated herein by reference. The emulsions and materials to form elements of the present invention, may be coated on pH adjusted support as described in U.S. Pat. No. 4,917,994; with epoxy solvents (EP 0 164 961); with additional stabilizers (as described, for example, in U.S. Pat. No. 4,346,165; U.S. Pat. No. 4,540,653 and U.S. Pat. No. 4,906,559); with ballasted chelating agents such as those in U.S. Pat. No. 4,994,359 to reduce sensitivity to polyvalent cations such as calcium; and with stain reducing compounds such as described in U.S. Pat. No. 5,068,171 and U.S. Pat. No. 5,096,805. Other compounds useful in the elements of the invention are disclosed in Japanese Published Patent Applications 83/09,959; 83/62,586; 90/072,629, 90/072,630; 90/072,632; 90/072,633; 90/072,634; 90/077,822; 90/078,229; 90/078,230; 90/079,336; 90/079,338; 90/079,690; 90/079,691; 90/080,487; 90/080,489; 90/080,490; 90/080,491; 90/080,492; 90/080,494; 90/085,928; 90/086,669; 90/086,670; 90/087,361; 90/087,362; 90/087,363; 90/087,364; 90/088,096; 90/088,097; 90/093,662; 90/093,663; 90/093,664; 90/093,665; 90/093,666; 90/093,668; 90/094,055; 90/094,056; 90/101,937; 90/103,409; 90/151,577.

The silver halide used in the photographic elements of the present invention may be silver iodobromide, silver bromide, silver chloride, silver chlorobromide, silver chloroiodobromide, and the like. The type of silver halide grains preferably include polymorphic, cubic, and octahedral. The grain size of the silver halide may have any distribution known to be useful in photographic compositions, and may be ether polydipersed or monodispersed. Particularly useful in this invention are tabular grain silver halide emulsions. Specifically contemplated tabular grain emulsions are those in which greater than 50 percent of the total projected area of the emulsion grains are accounted for by tabular grains having a thickness of less than 0.3 micron (0.5 micron for blue sensitive emulsion) and an average tabularity (T) of greater than 25 (preferably greater than 100), where the term "tabularity" is employed in its art recognized usage as

T=ECD/t.sup.2 where ECD is the average equivalent circular diameter of the tabular grains in microns and t is the average thickness in microns of the tabular grains.

The average useful ECD of photographic emulsions can range up to about 10 microns, although in practice emulsion ECD's seldom exceed about 4 microns. Since both photographic speed and granularity increase with increasing ECD's, it is generally preferred to employ the smallest tabular grain ECD's compatible with achieving aim speed requirements.

Emulsion tabularity increases markedly with reductions in tabular grain thickness. It is generally preferred that aim tabular grain projected areas be satisfied by thin (t>0.2 micron) tabular grains. To achieve the lowest levels of granularity it is preferred to that aim tabular grain projected areas be satisfied with ultrathin (t>0.06 micron) tabular grains. Tabular grain thicknesses typically range down to about 0.02 micron. However, still lower tabular grain thicknesses are contemplated. For example, Daubendiek et al. U.S. Pat. No. 4,672,027 reports a 3 mole percent iodide tabular grain silver bromoiodide emulsion having a grain thickness of 0.017 micron.

As noted above tabular grains of less than the specified thickness account for at least 50 percent of the total grain projected area of the emulsion. To maximize the advantages of high tabularity it is generally preferred that tabular grains satisfying the stated thickness criterion account for the highest conveniently attainable percentage of the total grain projected area of the emulsion. For example, in preferred emulsions tabular grains satisfying the stated thickness criteria above account for at least 70 percent of the total grain projected area. In the highest performance tabular grain emulsions tabular grains satisfying the thickness criteria above account for at least 90 percent of total grain projected area.

Suitable tabular grain emulsions can be selected from among a variety of conventional teachings, such as those of the following:

Research Disclosure, Item 22534, January 1983, published by Kenneth Mason Publications, Ltd., Emsworth, Hampshire P010 7DD, England; U.S. Pat. Nos. 4,439,520; 4,414,310; 4,433,048; 4,643,966; 4,647,528; 4,665,012; 4,672,027; 4,678,745; 4,693,964; 4,713,320; 4,722,886; 4,755,456; 4,775,617; 4,797,354; 4,801,522; 4,806,461; 4,835,095; 4,853,322; 4,914,014; 4,962,015; 4,985,350; 5,061,069 and 5,061,616.

The silver halide grains to be used in the invention may be prepared according to methods known in the art, such as those described in Research Disclosure I and James, The Theory of the Photographic Process. These include methods such as ammoniacal emulsion making, neutral or acidic emulsion making, and others known in the art. These methods generally involve mixing a water soluble silver salt with a water soluble halide salt in the presence of a protective colloid, and controlling the temperature, pAg, pH values, etc, at suitable values during formation of the silver halide by precipitation.

The silver halide to be used in the invention may be advantageously subjected to chemical sensitization with noble metal (for example, gold) sensitizers, middle chalcogen (for example, sulfur) sensitizers, reduction sensitizers and others known in the art. Compounds and techniques useful for chemical sensitization of silver halide are known in the art and described in Research Disclosure I and the references cited therein.

The photographic elements of the present invention, as is typical, provide the silver halide in the form of an emulsion. Photographic emulsions generally include a vehicle for coating the emulsion as a layer of a photographic element. Useful vehicles include both naturally occurring substances such as proteins, protein derivatives, cellulose derivatives (e.g., cellulose esters), gelatin (e.g., alkali-treated gelatin such as cattle bone or hide gelatin, or acid treated gelatin such as pigskin gelatin), gelatin derivatives (e.g., acetylated gelatin, phthalated gelatin, and the like), and others as described in Research Disclosure I. Also useful as vehicles or vehicle extenders are hydrophilic water-permeable colloids. These include synthetic polymeric peptizers, carriers, and/or binders such as poly(vinyl alcohol), poly(vinyl lactams), acrylamide polymers, polyvinyl acetals, polymers of alkyl and sulfoalkyl acrylates and methacrylates, hydrolyzed polyvinyl acetates, polyamides, polyvinyl pyridine, methacrylamide copolymers, and the like, as described in Research Disclosure I. The vehicle can be present in the emulsion in any amount useful in photographic emulsions. The emulsion can also include any of the addenda known to be useful in photographic emulsions. These include chemical sensitizers, such as active gelatin, sulfur, selenium, tellurium, gold, platinum, palladium, iridium, osmium, rhenium, phosphorous, or combinations thereof. Chemical sensitization is generally carried out at pAg levels of from 5 to 10, pH levels of from 5 to 8, and temperatures of from 30 to 80.degree. C., as illustrated in Research Disclosure, June 1975, item 13452 and U.S. Pat. No. 3,772,031.

The silver halide may be sensitized by sensitizing dyes by any method known in the art, such as described in Research Disclosure I. The dye may be added to an emulsion of the silver halide grains and a hydrophilic colloid at any time prior to (e.g., during or after chemical sensitization) or simultaneous with the coating of the emulsion on a photographic element. The dye/silver halide emulsion may be mixed with a dispersion of color image-forming coupler immediately before coating or in advance of coating (for example, 2 hours).

Photographic elements of the present invention are preferably imagewise exposed using any of the known techniques, including those described in Research Disclosure I, section XVI. This typically involves exposure to light in the visible region of the spectrum, and typically such exposure is of a live image through a lens, although exposure can also be exposure to a stored image (such as a computer stored image) by means of light emitting devices (such as light emitting diodes, CRT and the like).

Photographic elements comprising the composition of the invention can be processed in any of a number of well-known photographic processes utilizing any of a number of well-known processing compositions, described, for example, in Research Disclosure I, or in T. H. James, editor, The Theory of the Photographic Process, 4th Edition, Macmillan, New York, 1977. In the case of processing a negative working element, the element is treated with a color developer (that is one which will form the colored image dyes with the coloi couplers), and then with a oxidizer and a solvent to remove silver and silver halide. In the case of processing a reversal color element, the element is first treated with a black and white developer (that is, a developer which does not form colored dyes with the coupler compounds) followed by a treatment to fog unexposed silver halide (usually chemical or light fogging), followed by treatment with a color developer. Preferred color developing agents are p-phenylenediamines. Especially preferred are: 4-amino N,N-diethylaniline hydrochloride, 4-amino-3-methyl-N,N-diethylaniline hydrochloride, 4-amino-3-methyl-N-ethyl-N-(b-(methanesulfonamido) ethylaniline sesquisulfate hydrate, 4-amino-3-methyl-N-ethyl-N-(b-hydroxyethyl)aniline sulfate, 4-amino-3-b-(methanesulfonamido)ethyl-N,N-diethylaniline hydrochloride and 4-amino-N-ethyl-N-(2-methoxyethyl)-m-toluidine di-p-toluene sulfonic acid.

Development is followed by bleach-fixing, to remove silver or silver halide, washing and drying. Bleaching and fixing can be performed with any of the materials known to be used for that purpose. Bleach baths generally comprise an aqueous solution of an oxidizing agent such as water soluble salts and complexes of iron (III)(e.g., potassium ferricyanide, ferric chloride, ammonium or potassium salts of ferric ethylenediaminetetraacetic acid), water-soluble persulfates (e.g., potassium, sodium, or ammonium persulfate), water-soluble dichromates (e.g., potassium, sodium, and lithium dichromate), and the like. Fixing baths generally comprise an aqueous solution of compounds that form soluble salts with silver ions, such as sodium thiosulfate. ammonium thiosulfate, potassium thiocyanate, sodium thiocyanate, thiourea, and the like.

The stabilizers of this invention can be used in photographic elements that are intended to be processed in amplification processes that use developer/amplifier solutions described in U.S. Pat. No. 5,324,624, for example. When processed in this way, the low volume, thin tank processing system and apparatus described in U.S. patent application 08/221,711, filed Mar. 31, 1994, preferably is employed.

The following examples further illustrate this invention.

EXAMPLES

Preparation of Photographic Elements

Coupler M-9, comparison stabilizer CS-1, and coupler solvent diundecyl phthalate were dispersed in aqueous gelatin in the following manner. Coupler M-9 (0.406 g, 8.58.times.10.sup.-4 mole) and stabilizer CS-1 (0.137 g, 4.03.times.10.sup.-4 mole) were dissolved in a mixture of diundecyl phthalate (0.645 g) and ethyl acetate (1.144 g). The mixture was heated to effect solution. After adding a solution of aqueous gelatin (20.18 g, 11.69%), diisopropylnaphthalene sulfonic acid (sodium salt) (2.36 g 10% solution), and water to make a total of 47.19 grams, the mixture was dispersed by passing it three times through a Gaulin homogenizer. This dispersion was used in the preparation of photographic element 101.

Dispersions containing the stabilizers shown for elements 102-104 in Table 1 were prepared in a similar manner. The amount of coupler in each dispersion was 8.05.times.10.sup.-4 mole, the amount of each stabilizer was as listed (in moles per mole coupler), and other components were the same as in Example 101. ##STR17##

The photographic elements were prepared as follows:

On a gel-subbed, polyethylene-coated paper support were coated the following layers: First Layer

An underlayer containing 3.23 grams gelatin per square meter.

Second Layer

A photosensitive layer containing (per square meter) 2.15 grams total gelatin, an amount of green-sensitized silver chloride emulsion containing 0.172 grams silver; the dispersion containing 5.38.times.10.sup.-4 mole of the coupler indicated in Table 1; and 0.043 gram surfactant diisopropylnaphthalene sulfonic acid (sodium salt) (in addition to the surfactant used to prepare the coupler dispersion

Third Layer

A protective layer containing (per square meter) 1.40 grams gelatin, 0.15 gram bis(vinylsulfonyl)methyl ether, 0.043 gram Alkanol XC, and 4.40.times.10.sup.-6 gram tetraethylammonium perfluorooctanesulfonate.

Preparation of Processed Photographic Examples

Processed samples were prepared by exposing the coatings through a step wedge and processing as follows:

______________________________________Process Step Time (min) Temp. (C.)______________________________________Developer 0.75 35.0 Bleach-Fix 0.75 35.0 Water wash 1.50 35.0______________________________________

The processing solutions used in the above process had the following compositions (amounts per liter of solution):

______________________________________Developer Triethanolamine 12.41 g Blankophor REU (trademark of Mobay Corp.) 2.30 g Lithium polystyrene sulfonate 0.09 g N,N-Diethylhydroxylamine 4.59 g Lithium sulfate 2.70 g 4-amino-3-methyl-N-ethyl-N- 5.00 g (2-methansulfonamidoethyl)aniline sesquisulfate hydrate 1-Hydroxyethyl-1,1-diphosphonic acid 0.49 g Potassium carbonate, anhydrous 21.16 g Potassium chloride 1.60 g Potassium bromide 7.00 mg pH adjusted to 10.4 at 26.7 C. Bleach-Fix Solution of ammonium thiosulfate 71.85 g Ammonium sulfite 5.10 g Sodium metabisulfite 10.00 g Acetic acid 10.20 g Ammonium ferric ethylenediaminetetra acetate 48.58 g Ethylenediaminetetraacetic acid 3.86 g pH adjusted to 6.7 at 26.7 C.______________________________________

The density of each step of each strip was measured. The strips were then covered by UV-absorbing filters (in lieu of coating a similar filter layer over the photosensitive layer of the photographic element) and subjected to irradiation by the light of a xenon arc lamp at an intensity of 50,000 lux for 2 weeks. The light stability of the dye ("Dye Stab"), expressed as the percent of the density to green light remaining from initial densities of 1.0 and 1.7, is shown in Table 1.

TABLE 1______________________________________ Dye Stab (% remaining)Element Comp/Inv Stabilizer from 1.0 from 1.7______________________________________101 Comparison CS-1 76 82 102 Invention S-1 86 84 103 Invention S-2 80 84 104 Invention S-3 81 85______________________________________

The data in Table 1 show that elements 102-104 of our invention all have better light stability than element 101, containing comparison coupler CS-1, which is similar to the stabilizers of Formula S but lacks the required Ring "A" with its sulfonamido substituent.

Claims

1. A silver halide photographic element comprising a support bearing a light sensitive silver halide emulsion layer and a cyclic azole dye forming coupler associated with a stabilizer comprising rings "A", "B", and "C" and having the following Formula S: ##STR18## wherein R.sub.1 represents an alkyl or cycloalkyl group, an alkenyl group or an aryl group;

R.sub.2 and R.sub.3 each represents a hydrogen atom or a substituent;

L represents a covalent bond or a divalent linking group;

X represents O, S, SO, SO.sub.2, or NR.sub.4, or --O--X.sub.2 --O--;

R.sub.4 represents H, alkyl, --CH.sub.2 CH(OH)CH.sub.2 OR.sub.5, or --COR.sub.6 ;

R.sub.5 and R.sub.6 represent alkyl groups;

Y is SO.sub.2 NH;

X.sub.2 represents BR.sub.7, PR.sub.8, P(O)R.sub.9, SO, or SO.sub.2 ;

R.sub.7 -R.sub.9 each represents phenoxy which may be substituted by 1 to 3 alkyl, alkoxy, or halogen groups;

Z.sub.1 and Z.sub.2 each represents an alkylene group of 1 to 3 carbon atoms, which may be substituted, provided that the total number of carbon atoms in the ring is 3 to 6;

p and q each represents an integer of 0 to 4.

2. The photographic element of claim 1, wherein the stabilizer combination further comprises a compound having the following Formula R: ##STR19## wherein: each R.sub.10 independently represents a hydrogen atom, an alkyl or cycloalkyl group, an alkenyl group or an aryl group;

each R.sub.11 independently represents a halogen atom, an alkyl group, an alkenyl group, an alkoxy group, an aryl group, an aryloxy group, an alkylthio group, an aryl thio group, an acyl group, an an acylamino group, a sulfonyl group, a sulfonamide group or a hydroxy group;

each m is, individually an integer of 0 to 4; and

A represents an alkylene group having 1 to 10 carbon atoms in its linear structure.

3. The photographic element of claim 1, wherein the stabilizer combination further comprises a compound having the following Formula I: ##STR20## wherein: R.sub.14 is an alkyl, alkenyl, or aryl group;

R.sub.15 is a substituent; and

m is an integer of 0 to 5.

4. The photographic element of claim 1, wherein the dye forming coupler has the following structure M: ##STR21## wherein: R.sub.12 is hydrogen, a substituent group or a ballast group;

R.sub.13 is a ballast group or a fused benzene ring; and

X is hydrogen or a coupling-off-group, provided that X, R.sub.12 and R.sub.13 contain a number of carbon sufficient to immobilize the coupler in the emulsion layer; and

Z.sub.a, Z.sub.b, and Z.sub.c are independently a substituted or unsubstituted methine group, .dbd.N--, ##STR22## or --NH--, provided that one of either the Z.sub.a -Z.sub.b bond or the Z.sub.b -Z.sub.c bond is a double bond and the other is a single bond, and when the Z.sub.b -Z.sub.c bond is a carbon-carbon double bond, it can be part of the aromatic ring and at least one of Z.sub.a, Z.sub.b, and Z.sub.c represents a methine group connected to R.sub.13.

5. The photographic element of claim 4, wherein the dye forming coupler has the following structure MI: ##STR23## wherein: R.sub.12 is hydrogen or a substituent group;

R.sub.13 is a ballast group; and

X is hydrogen or a coupling-off-group.

6. The photographic element of claim 4, wherein the dye forming coupler has the following structure MII: ##STR24## wherein: R.sub.12 is hydrogen or a substituent group

R.sub.13 is a ballast group; and

X is hydrogen or a coupling-off-group.

7. The photographic element of claim 4, wherein the dye forming coupler has the following structure MIII: ##STR25## wherein: R.sub.12 and R.sub.14 each is hydrogen, a substituent group or a ballast group;

X is hydrogen or a coupling-off-group, provided that X, R.sub.12 and R.sub.14 together contain a number of carbon sufficient to immobilize the coupler in the emulsion layer.

8. The photographic element of claim 5, wherein R.sub.12 is a t-alkyl group.

9. The photographic element of claim 6, wherein R.sub.12 is a t-alkyl group.

10. The photographic element of claim 7, wherein R.sub.12 is an alkoxy group.

11. The photographic element of claim 1, wherein the coupler is a magenta dye forming coupler.

12. The photographic element of claim 1, wherein ring "C" of compound S has the following structure: ##STR26##

13. The photographic element of claim 1, wherein L has the structure OL.sub.1, and L.sub.1 is an alkylene or heteroalkylene group.

14. The photographic element of claim 1, wherein compound S has the following structure SII: wherein:

R.sub.1 represents an alkyl or cycloalkyl group, an alkenyl group or an aryl group; and

L.sub.1 is an alkylene or heteroalkylene group.

15. The photographic element of claim 1, wherein compound S is present in a range of about 0.2 to 2.0 moles compound per mole dye forming coupler.

16. The photographic element of claim 2, wherein each of compounds S and R is present in a range of about 0.2 to 2.0 moles compound per mole dye forming coupler.

17. The photographic element of claim 3, wherein each of compounds S and I is present in a range of about 0.2 to 2.0 moles compound per mole dye forming coupler.

18. The photographic element of claim 1, further comprising a phthalate ester coupler solvent.

19. The photographic element of claim 1, further comprising an aliphatic alcohol coupler solvent.

20. The photographic element of claim 1, wherein the support is opaque.