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
  • 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
  • G03C7/34—Couplers containing phenols
  • G03C7/342—Combination of phenolic or naphtholic couplers

Definitions

• the present invention relates to silver halide color photographic materials and, more particularly, to silver halide color photographic materials which contain a specific combination of cyan couplers.
• a silver image is produced by means of an aromatic primary amino-type developer compound in the presence of color couplers which react with the oxidized developing substance to form a dye in the areas corresponding to the silver image.
• light sensitive color photographic materials which include, coated on a support, one or more red-sensitive silver halide emulsion layers, one or more green-sensitive silver halide emulsion layers, and one or more blue-sensitive silver halide emulsion layers, each layer comprising color couplers, wherein upon color development cyan, magenta and yellow dye images are respectively formed.
• the couplers used to produce cyan image dyes generally derive from phenols and naphthols (as described, for example, in US patents 2,367,351, 2,423,730, 2,474,293, 2,772,161, 2,772,162, 2,895,826, 2,920,961, 3,002,836, 3,466,622, 3,476,563, 3,880,661, 3,996,253, 3,758,308, in FR patents 1,478,188 and 1,479,043, and in GB patent 2,070,000).
• These types of couplers can be used either in photographic layers or in the processing baths. In the former case, when it is desired that they do not migrate from a layer into another, they can have ballasting substituents.
• couplers can bear also hydrophilic or hydrophobic substituents if they must be introduced into photographic layers, respectively, dissolved in water or in an organic solvent.
• such couplers Upon reaction with the oxidation products of the aromatic primary amino-type developing agents, such couplers give indoaniline dyes with consumption of four equivalents of silver ions per mole of dye and, preferably, two equivalents of silver ions per mole of dye when the reactive methine group (in the para position to the phenolic hydroxylic group) is substituted with atoms or groups which are split off during the coupling reaction.
• naphthol cyan couplers have been used in the red sensitive layers of silver halide photographic materials because they give a cyan dye, formed by the reaction with an oxidized product of a color developing agent, having absorptions at longer wavelength regions with respect to dyes given by phenol type couplers, that being preferred in connection with color reproduction.
• EP 102,821 describes a combination of 2-phenylureido-5-acylamino phenol couplers and naphthol couplers in a specific relative ratio to the purpose of having cyan dyes with a limited shift of absorption maximum towards shorter wavelengths in lower color density areas.
• a specific combination of cyan couplers for use in color photography comprising one cyan coupler having the following Formula (I) and one cyan coupler having the following Formula (II): wherein R 1 is an aryl group, R 2 is an alkyl group or an aryl group, R 3 is a hydrogen atom, a halogen atom, an alkyl group or an alkoxy group, and Z 1 is a hydrogen atom, a halogen atom or a group which can be split off by the reaction of said coupler with the oxidized product of an aromatic primary amine-type color developing agent, wherein, R 4 is a hydrogen atom or a lower alkyl group, R 5 is a ballasting group, and Z 2 is a hydrogen atom, a halogen atom or a group which can be split off by the reaction of said coupler with the oxidized product of an aromatic primary amine-type color developing agent (referred to in the art as a leaving group or splitting off
• Such a combination of cyan couplers when associated with silver halide color photographic materials, gives high sensitivity and, upon coupling with the oxidized aromatic primary amine-type color developing agents, provides cyan indoaniline dyes very stable to light, heat and humidity. They are also stable to bleaching solutions which have a weak oxidation power or are exhausted.
• the present invention relates to a silver halide color photographic material comprising a support having coated thereon one or more silver halide emulsion layers, wherein at least one of said layers comprises in combination one cyan coupler having the following Formula (I) and one cyan coupler having the following Formula (II): wherein R 1 is an aryl group, R 2 is an alkyl group of up to 20 carbon atoms (such as methyl, ethyl, butyl, dodecyl, etc.) or an aryl group of up to 20 carbopn atoms, R 3 is a hydrogen atom, a halogen atom (such as fluorine, bromine, chlorine, etc.), an alkyl group of up to 20 carbon atoms (such as methyl, ethyl, butyl, dodecyl, etc.) or an alkoxy group of up to 20 carbpn atoms (such as methoxy, ethoxy, etc.), and Z 1 is a hydrogen atom
• ballasting group represented by R 5 in Formula (II) is an organic radical of such size and configuration as to confer to the coupler sufficient bulk to render it substantially non-diffusible from a layer in which is introduced of the photographic material.
• Representative ballasting groups include substituted or unsubstituted alkyl or aryl groups containing up to 20 carbon atoms.
• substituents include alkyl, aryl, alkoxy, aryloxy, alkylthio, arylthio, hydroxy, halogen, alkoxycarbonyl, aryloxycarbonyl, carboxy, acyl, acyloxy, carbonamido, carbamoyl, alkylsulfonyl, arylsulfonyl, sulfonamido, and sulfamoyl groups.
• the aryl group represented by R 1 of Formula (I) is, e.g., a phenyl group, a naphthyl group, or other aryl group of up to 30 carbon atoms, and preferably is a phenyl group.
• This group is allowed to have a single substituent or a plurality of substituents; for example, typical substituents introducible to the aryl group include halogen atoms (such as fluorine, chlorine, bromine, etc.), alkyl groups (such as methyl, ethyl, propyl, butyl, dodecyl, etc.), hydroxyl group, cyano group, nitro group, alkoxy groups (such as methoxy, ethoxy, etc.), alkylsulfonamido groups (such as methylsulfonamido, octylsulfonamido, etc.), arylsulfonamido groups (such as phenylsulfonamido, naphthylsulfonamido, etc.), alkylsulfamoyl groups (such as butylsulfamoyl), arylsulfamoyl (such as phenylsulfam
• the preferred group represented by R 1 is a phenyl group, the more preferred is a phenyl group having one or more substituents including halogen atoms and cyano groups.
• alkyl group includes not only alkyl moieties as methyl, ethyl, octyl, dodecyl, etc., but also such moieties bearing sustituent groups such as halogen, cyano, hydroxyl, nitro, amine, carboxylate, etc.
• alkyl moiety includes only methyl, ethyl, octyl, dodecyl, etc.
• the preferred cyan couplers having Formula (I) are the compounds having the following Formula (III): wherein X 1 is a hydrogen atom, a halogen atom or a monovalent organic group, R 6 is a hydrogen atom or a substituent exemplified by a halogen atom (such as fluorine, bromine, chlorine, etc.), a hydroxyl group, a nitro group, an alkyl group of up to 20 carbon atoms (such as methyl, ethyl, iso-propyl, tert.-butyl, n-octyl, n-dodecyl, etc.), an alkyloxycarbonyl group (such as methyloxycarbonyl), an aryloxycarbonyl group (such as phenyloxycarbonyl), an alkoxy group of up to 20 carbon atoms (such as methoxy, ethoxy, etc.), an aryloxy group (such as phenoxy), an al
• Examples of monovalent organic group represented by X 1 include a halogen atom (such as fluorine, chlorine, bromine, etc.), a nitro group, an amino group, a cyano group, a hydroxy group, a carboxy group, an alkyl group (such as methyl, ethyl, propyl, isopropyl, t-butyl, octyl, etc.), an aralkyl group (such as benzyl, phenethyl, etc.), an alkoxy group (such as methoxy, ethoxy, benzyloxy, etc.), an aryloxy group (such as phenoxy, p-nitrophenoxy, etc.), an acylamino group (such as acetylamino, propionylamino, benzoylamino, phenoxyacetylamino, etc.), a carbamoyl group (such as methylcarbamoyl, dimethylcarbamoyl
• the more preferred cyan couplers having Formula (I) are the compounds having the following formula (V): wherein X 2 is a hydrogen atom or a halogen atom (such as fluorine, chlorine, bromine, etc.), R 8 is a hydrogen atom or an alkyl group of up to 20 carbon atoms (such as methyl, ethyl, propyl, butyl, octyl, dodecyl, etc.), Rg and R 10 may be either the same or different and each is a hydrogen atom, an alkyl group of up to 20 carbon atoms (such as methyl, ethyl, butyl, dodecyl, etc.) or an alkoxy group of up to 20 carbon atoms (such as methoxy, ethoxy, etc.), provided that the sum of carbon atoms of Rg, Rg and R10 is from 8 to 20, p is an integer of 0 to 2, and Z 4 is a hydrogen atom or a chlorine
• the groups that can be split off by the reaction of these couplers with the oxidized product of the aromatic primary amine-type color developing agents represented by Z 1 and Z 3 are all known to those skilled in the art. Any of these groups changes the reactivity of the coupler or is split from the coupler to fulfill its development-inhibiting and bleach-inhibiting functions to thereby advantageously act in the coupler-containing layers or other layers of the silver halide color photographic material.
• Typical examples os such groups include, for example, alkoxy groups, aryloxy groups, thioether, car- bamoyloxy groups, acyloxy groups, imido groups, sulfonamido groups, thiocyano group or heterocyclic groups (such as oxazolyl, diazolyl, triazolyl, tetrazolyl, etc.), and the like.
• the particularly preferred examples represented by Z are a hydrogen atom or a chlorine atom.
• the cyan couplers used in combination according to the present invention are incorporated in a silver halide emulsion layer of the color photographic material.
• the skilled in the art knows that, if the cyan couplers are incorporated into the silver halide emusion layer, they are, in most instances, required not to diffuse within the layers themselves.
• a group bearing a ballasting group such as a hydrophobic residue with 8 to 20 carbon atoms is introduced into the coupler molecules in order to avoid said diffusing process.
• ballasting group is linked, directly or through one or more of imino, ether, carbonamido, sulfonamido, ureido, ester, imido, carbamoyl, sulfamoyl, phenylene, etc. groups, to the coupler molecule.
• ballasting group is preferably comprised by the group R 2 of Formula (I) and R 5 of Formula (II).
• ballasting groups are illustrated in US patent 4,009,038, in European patents 87,930, 84,100, 87,931, 73,146, 88,563, in German patents 3,300,412, 3,351,012, in Japanese patents J5 8033248, J5 8033250, J58031334, J5 8106539.
• ballasting groups comprise alkyl chains, the total carbon atoms of which are from 8 to 20.
• cyan couplers of Formula (I) and (II) can readily be synthesized by use of methods well known in the art such as described, for example, in US Patents 3,758,308, 4,333,999 and 4,451,559 for couplers of Formula (I) and in the Journal of the American Chemical Society Vol. 64, p. 798 (1942) for couplers of Formula (II).
• cyan couplers represented by the Formulas (I) and (II) are illustrated below, but the present invention is not limited thereby.
• the silver halide color photographic materials of the present invention comprise at least one blue-sensitive silver silver halide emulsion layer, at least one green-sensitive silver halide emulsion layer and at least one silver-halide red-sensitive silver halide emulsion layer, said layers being associated with yellow, magenta and cyan dye-forming couplers.
• the word "associated" means that the cyan dye-forming couplers according to the present invention and the silver halide emulsions are positioned in such a way as to image-wise produce in the photographic layers upon coupling with the oxidized aromatic primary amine-type developing agents very stable cyan indoaniline dyes.
• Such cyan couplers may be incorporated in the silver halide emulsion layers, in an adjacent layer or in the processing solutions. In a preferred form, the cyan couplers are incorporated in the silver halide emulsion layer.
• the silver halide emulsion layer comprising the combination of cyan couplers of general Formula (I) and (II) described above is a red-sensitive silver halide emulsion layer.
• the couplers of Formula (II) should be used in an amount of from 0.005 to 0.15 mole, and preferably from 0.01 to 0.05 mole per mole of the cyan couplers of formula (I) contained in the entire silver halide photographic element.
• said cyan couplers of Formula (I) and (II) are present in a total amount of from about 6.5x10- 3 to about 80x10- 3 mole per mole of silver halide contained in said silver halide emulsion layer, and preferably from about 13.5x10- 3 to about 53.5x10- 3 mol per mol of silver halide.
• the couplers of the present invention can be incorporated into the silver halide emulsion layer by the dispersion technique, which consists of dissolving the coupler in a water-immiscible high-boiling organic solvent and then dispersing such a solution in a hydrophilic colloidal binder under the form of very small droplets.
• the preferred colloidal binder is gelatin, even if some other kinds of binders can be used.
• Another type of introduction of the couplers into the silver halide emulsion layer consists of the so-called "loaded-latex technique".
• a detailed description of such technique can be found in BE patents 853,512 and 869,816, in US patents 4,214,047 and 4,199,363 and in EP patent 14,921. It consists of mixing a solution of the couplers in a water-miscible organic solvent with a polymeric latex consisting of water as a continous phase and of polymeric particles having a mean diameter ranging from 0.02 to 0.2 micrometers as a dispersed phase.
• couplers having a water-soluble group such as a carboxyl group, a hydroxy group, a sulfonic group or a sulfonamido group, can be added to the photographic layer for example by dissolving them in an alkaline water solution.
• the cyan couplers of the combination of the present invention are generally incorporated into a red-sensitive silver halide emulsion layer to form one of the differently sensitized silver halide emulsion layers of a multilayer color photographic material.
• Such material generally comprises a support base having coated thereon one or more red-sensitive silver halide emulsion layers, one or more green-sensitive silver halide emulsion layers, one or more blue-sensitive silver halide emulsion layers and additionally filter layers, interlayers, protective layers and sub-layers.
• the layer units can be coated in any conventional order, but in a preferred layer arrangement the red-sensitive layes are coated nearest the support and are overcoated by the green-sensitive layers, a yellow filter layer and the blue-sensitive layers.
• the red-sensitive silver halide emulsion layer associated according to this invention with the combination of the cyan couplers of Formulae (I) and (II), is composed of two or more silver halide emulsion layers sensitized to the same spectral region of the visible spectrum, the uppermost silver halide emulsion layer of which having the highest sensitivity and the lowermost silver halide emulsion layer having the lowest sensitivity, as described in GB patent 923,045, in FR patent 2,043,433 and in US patent 4,582,780.
• the uppermost red-sensitive silver halide emulsion layer having the highest sensitivity comprises the combination of the cyan couplers of Formulae (I) and (II), the other red-sensitive silver halide emulsion layers comprising the cyan couplers of Formula (I).
• the sensitive layers are each associated with at least one image dye forming compound.
• Incorporated dye forming couplers constitute exemplary preferred image-dye providing compounds.
• the blue, green and red-responsive layers preferably contain yellow, magenta and cyan image-dye providing couplers, respectively.
• yellow-forming couplers are conventional open-chain ketomethylene type couplers. Particular examples of such couplers are benzoylacetanilide type and pivaloyl acetanilide type compounds. Yellow-forming couplers that can be used are specifically described in US patents 2,875,057, 3,265,506, 3,408,194, 3,551,151, 3,682,322, 3,725,072 and 3,891,445, in DE patents 2,219,917, 2,261,361 and 2,414,006, in GB patent 1,425,020, in JP patent 10,783/76 and in JP patent applications 26,133/72, 73,147/73, 102,636/76, 6,341/75, 123,342/75, 130,442/75, 1,827/76, 87,650/75, 82,424/77 and 115,219/77.
• magenta-forming couplers are conventional pyrazolone type compounds, indazolone type compounds, cyanoacetyl compounds, pyrazoletriazole type compounds, etc, and particularly preferred couplers are pyrazolone type compounds.
• Magenta-forming couplers are described for example in US patents 2,600,788, 2,983,608, 3,062,653, 3,127,269, 3,311,476, 3,419,391, 3,519,429, 3,558,319, 3,582,322, 3,615,506, 3,834,908 and 3,891,445,in DE patent 1,810,464, in DE patent applications 2,408,665, 2,417,945, 2,418,959 and 2,424,467 and in JP patent applications 20,826/76, 58,922/77, 129,538/74, 74,027/74, 159,336/75, 42,121/77, 74,028/74, 60,233/75, 26,541/76 and 55,122/78.
• Colored couplers can be used which include those described for example in US patents 3,476,560, 2,521,908 and 3,034,892, in JP patent publications 2,016/69, 22,335/63, 11,304/67 and 32,461/69, in JP patent applications 26,034/76 and 42,121/77 and in DE patent application 2,418,959.
• DIR (Development Inhibitor Releasing) couplers can be used which include those described for example in US patents 3,227,554, 3,617,291, 3,701,783, 3,790,384 and 3,632,345, in DE patent applications 2,414,006, 2,454,301 and 2,454,329, in GB patent 953,454, in JP patent applications 69,624/77, 122,335/74 and 16,141/76.
• DIR couplers In addition to DIR couplers, some other compounds which release development inhibitors upon development can also be present in the light-sensitive material. Such kind of DIR compounds is described for example in US patents 3,297,445 and 3,379,529, in DE patent application 2,417,914, in JP patent applications 15,271/77 and 9,116/78.
• Couplers described above can be incorporated in the same layer, or the same coupler can also be present in two or more layers.
• Said couplers can be introduced into the silver halide emulsion layers of the photographic materials by using some of the methods described above. Moreover, said couplers are made non-diffusing by means of the above described ballasting groups.
• the present invention is not limited to photographic materials with a particular type of emulsion or silver halides. It can therefore find an application with photographic materials containing different types of emulsions or silver halides, such as for example those described in Research Disclosure 17643, I, December 1978.
• the emulsions which can be used in the present invention can be chemically and optically sensitized as described in Research Disclosure 17643, III and IV, December 1978. They can contain optical brighteners, antifogging agents and stabilizers, filtering and antihalo dyes, hardeners, coating aids, plasticizers and lubricants and other auxiliary substances as described for example in Research Disclosure 17643, V, VI, VIII, X, XI and XII, December 1978.
• the layers of the photographic material can contain various colloids, alone or in combination, such as binding materials, as for example described in Research Disclosure 17643, IX, December 1978.
• the photographic materials which can be used in the present invention can contain orthochromatic or panchromatic emulsions, as well as unsensitized emulsions. In particular and more preferably, they can be emulsions for color photography as described in Research Disclosure 17643, VII, December 1978. Such photographic materials, in particular, can be of the negative color print type or of the reversal type, of the color paper type or of the movie positive type. Of course, unconventional photographic materials of the transfer type, which make use of negative or direct positive emulsions, such as for example those described in US patents 3,277,550 and 3,227,551, can use the couplers of the present invention.
• emulsions can be coated onto several support bases (cellulose triacetate, paper, resin-coated paper, polyester, and the like) by adopting various methods, as described in Research Disclosure 17643, XV and XVI, December 1978.
• the silver halide emulsion layers exposed to light radiation to form a latent image are developed with a compound of the aromatic amine type in the presence of the color couplers.
• Suitable developing compounds are in particular the p-phenylenediamine derivatives, for example 2-amino-5-di-ethylamino-toluene chlorydrate (called CD2), 2-amino-N-ethyl-N-(#-methanesulfonamido)-m-toluidine sesquisulfate monohydrate (called CD3), 4-amino-3-methyl-N-ethyl-N-(#-hydroxyethyl)-aniline sulfate (called CD4).
• CD2 2-amino-5-di-ethylamino-toluene chlorydrate
• CD3 2-amino-N-ethyl-N-(#-methanesulfonamido)-m-toluidine sesqui
• the bleaching bath is a water solution having a pH equal to 5.60 and containing an oxidizing agent, normally a complex salt on an alkali metal or of ammonium and of trivalent iron with an organic acid, e. g. EDTA.Fe.NH 4 , wherein EDTA is the ethylenediaminotetracetic acid.
• an oxidizing agent normally a complex salt on an alkali metal or of ammonium and of trivalent iron with an organic acid, e. g. EDTA.Fe.NH 4 , wherein EDTA is the ethylenediaminotetracetic acid.
• this bath is con- tinously aired to oxidize the divalent iron which forms while bleching the silver image and regenerated, as known in the art, to maintain the bleach effectiveness.
• the bad working of these operations may cause the drawback of the loss of cyan density of the dyes.
• the blix bath contains known fixing agents, such as for example ammonium or alkali metal thiosulfates.
• Both bleaching and fixing baths can contain other additives, e. g. polyalkyleneoxide derivatives, as described in GB patent 933,008 in order to increase the effectiveness of the bath, or thioethers known as bleach accelerators.
• Film A was prepared by coating a cellulose triacetate support base, subbed with gelatin, with the following layers in the following order:
• Film B was prepared by coating a cellulose triacetate support base, subbed with gelatin, with the following layers in the following order:
• Film C was prepared by coating a cellulose triacetate support base, subbed with gelatin, with the following layers in the following order:
• Film D was prepared by coating a cellulose triacetate support base, subbed with gelatin, with the following layers in the following order:
• Film E was prepared by coating a cellulose triacetate support base, subbed with gelatin, with the following layers in the following order:
• the couplers used are as follows:
• Samples of the five films were exposed to 5500° K light through a grey step wedge, then subjected to a standard Kodak C41 process for color negative films.
• Table 1 reports the amount of naphthol coupler 11-1 versus the total amount of the phenol coupler 1-19, the wavelengths of the absorption maxima of the spectrophotometric curves of the cyan dyes formed in the coupling reaction read at density 2.0 ( ⁇ max 2 . 0 ) and 0.5 (Xmax o . 5 ), Dmin, sensitivity (log exposure corresponding to a density 0.2 above Dmin) and maximum density (Dmax) values of the cyan sensitometric HD curves.
• the spectrophotometric and sensitometric curves of the developed cyan images show how the combination of couplers according to the present invention has absorption maxima shifted towards higher wavelengths in the lower density areas and higher sensitivity, as desired.
• a Film F was prepared similar to Film A of example 1, having in the high-sensitivity red-sensitive emulsion layer the cyan dye-forming coupler I-19.
• a Film G was prepared similar to Film B of Example 1, having in the high-sensitivity red-sensitive emulsion layer 0.045 mole of cyan dye-forming coupler 11-7 per mole of cyan dye-forming coupler 1-19 in the film.
• a Film H was prepared similar to Film E of Example 1, having in the high-sensitivity red-sensitive emulsion layer 0.115 mole of cyan dye-forming coupler 11-7 per mole of cyan dye-forming coupler 1-19 in the film.
• a Film I was prepared similar to Film B of Example 1, having in the high-sensitivity red-sensitive emulsion layer 0.045 mole of cyan dye-forming coupler 11-6 per mole of cyan dye-forming coupler 1-19 in the film.
• a Film L was prepared similar to Film E of Example 1, having in the high-sensitivity red-sensitive emulsion layer 0.115 mole of cyan dye-forming coupler 11-6 per mole of cyan dye-forming coupler 1-19 in the film.
• a Film M was prepared similar to Film B of Example 1, having in the high-sensitivity red-sensitive emulsion layer 0.045 mole of comparison cyan dye-forming coupler C per mole of cyan dye-forming coupler 1-19 in the film.
• the sensitometric results show how the combination of couplers according to the present invention has higher sensitivity, as desired.

Landscapes

• Physics & Mathematics (AREA)
• General Physics & Mathematics (AREA)
• Silver Salt Photography Or Processing Solution Therefor (AREA)

Applications Claiming Priority (2)

Related Parent Applications (1)

Publications (1)

Family

ID=11160542

Family Applications (2)

Family Applications After (1)

Country Status (4)

Cited By (1)

Families Citing this family (3)

Citations (5)

Family Cites Families (2)

• 1989
  • 1989-03-09 IT IT8919706A patent/IT1229993B/it active
• 1990
  • 1990-03-01 EP EP91117859A patent/EP0476710A1/de not_active Withdrawn
  • 1990-03-01 EP EP90103931A patent/EP0389817A1/de not_active Withdrawn
  • 1990-03-08 CA CA002011730A patent/CA2011730A1/en not_active Abandoned
  • 1990-03-08 JP JP2057816A patent/JPH02272541A/ja active Pending

Patent Citations (5)

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events