[go: up one dir, main page]

US3199983A - 3-indazolone color couplers - Google Patents

3-indazolone color couplers Download PDF

Info

Publication number
US3199983A
US3199983A US167929A US16792962A US3199983A US 3199983 A US3199983 A US 3199983A US 167929 A US167929 A US 167929A US 16792962 A US16792962 A US 16792962A US 3199983 A US3199983 A US 3199983A
Authority
US
United States
Prior art keywords
color
indazolone
couplers
coupler
silver halide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US167929A
Inventor
Koepke Gunther
Pelz Willibald
Schellenberger Hans
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Agfa Gevaert NV
Original Assignee
Agfa AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Agfa AG filed Critical Agfa AG
Application granted granted Critical
Publication of US3199983A publication Critical patent/US3199983A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
    • C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
    • 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
    • G03C7/3231—Couplers containing an indazolone ring

Definitions

  • the present invention relates to indazolone color couplers in which the non-diifusing group comprises a long-aliphatic acyl radical substituted in the tat-position to the carbonyl group by a sulpho group, to silver halide emulsions containing such couplers and to the production of colored photographic images in the presence of such couplers.
  • the yellow coupler an open chain keto methylene compound such as benzoyl-acetanilide derivatives, as thecyan coupler a compound containing phenolic hydroxy groups such as a-naphthol derivatives and as the magenta coupler pyrazolone derivatives particularly those bearing an aryl radical on the nitrogen atom in the l-position of the pyrazolone ring.
  • an open chain keto methylene compound such as benzoyl-acetanilide derivatives
  • thecyan coupler a compound containing phenolic hydroxy groups such as a-naphthol derivatives
  • magenta coupler pyrazolone derivatives particularly those bearing an aryl radical on the nitrogen atom in the l-position of the pyrazolone ring.
  • color couplers have a similar coupling intensity and speed of coupling with respect to the oxidation products of color developers formed upon development so that they can tasily be employed for the production of multi-color images, for which purpose it is general practice to use multi-layer materials having three silver halide emulsion layers which are light-sensitive for different parts of the spectrum, the said emulsion layers having the said color couplers incorporated therein in a diifusion resistant form.
  • indazolone color couplers of the salt forming non-diffusing type in which a long aliphatic acyl radical contains the salt-forming function as a sulpho radical in u-position to the carbonyl group.
  • the acyl radical is linked in the manner of carbon amide to an amino group which is substituted in the 6-position of the indazolone ring.
  • R represents an alkyl radical having 618 carbon atoms, preferably 12-18 carbon atoms and X stands for a cation such as hydrogen, alkali metal, for example lithium, sodium and potassium, alkaline earth metal, such as magnesium and calcium, ammonium or ammoniurn substituted with at least one alkyl radical having up to 4 carbon atoms.
  • the amino derivatives according to the invention show an excellent solubility, even in the weakly acid range, and also a high coupling intensity, so that they can be used in conjunction with couplers which contain activated methylene groups or with a-naphthol derivatives, in single-layer or multi-layer materials.
  • the present couplers are resistant to digestion.
  • the silver halide emulsions to which these couplers are added can be kept for a relatively long time in a molten condition without any precipitation of the coupler, which would lead to a change in the viscosity and the pH-value of the emulsion, a flattening of the gradation and a matting of the layers produced from these emulsions, as Well as a decrease in the coupling intensity and thus a color tone displacement upon development of a multi-layer material.
  • the couplers thus render possible the production of color materials with uniform and high-grade properties.
  • photographic silver halide emulsions containing these color couplers can also be cast in the acid pH-range, so that improved keeping properties are guaranteed in the layers so produced. Furthermore, these layers have the advantage that even after relatively long storage, they do not show any change in color tone and color intensity of the developed image, by comparison with layers developed immediately after manufacture, whereas with layers having known indazolone derivatives, occur a displacement of the color tone from magenta-red to magenta-blue shades and a decrease in the color intensity.
  • indazolone derivatives according to the invention by contrast with corresponding known indazoline derivatives, are not transformed into yellow dyestuffs by the action of potassium ferricyanide solutions, which are used for the bleaching of photographic color materials being developed by means of color-forming developers. Consequently, the present color couplers can also be used for the production of those multi-layer films or papers which are employed for the production or" positive color images by the use of potassium ferricyanide bleaching baths.
  • the color couplers to be used according to the invention are advantageously added to the silver halide emulsions in quantities of about 5 to 20 g./kg.
  • Gelatine is preferably used as binder for the emulsion, but other binders known per se can also be used.
  • the color couplers it is also possible for the color couplers to be introduced into layers of multi-layer materials which are not sensitive to light, the said materials containing silver halide emulsion layers in addition to the said layers which are not light-sensitive.
  • the conventional color developers in particular aromatic color developers with primary amino groups, can be used for the development of the present color materials.
  • the present color couplers can be obtained by reaction of 6-amino indazolone with the mono-alkali metal salts of ot-sulpho fatty acids using phosphorus trichloride in the presence of tertiary amines, for example pyridine.
  • Example 1 22.2 g. of 6-amino-indazolone, 2 H01 and 35.8 g. of the mono-sodium salt of sulphopalmitic acid are suspended in 260 cc. ofpyridine. From this mixture, 100 cc. of pyridine are distilled off with stirring, the suspension then being cooled to room temperature and a solution of 4.5
  • Example 2 The preparation is carried out in a manner similar to ,that indicated in Example 1,. except that 38.4 g. of the mono-sodium salt of a-sulphostearic acid are used instead of 35.8 g. of mono-sodium salt of sulphopalmitic acid.
  • Suitable salts of said compound are obtained by reaction with carbonates or hydroxides of alkali metals or alkaline .earth metals, ammonia or amines containing at least one alkyl radical having up to 4 carbon atoms.
  • Example 3 14.8 g. of the coupler described in Example 1 are formed into a paste with 20 g. of methanol and dissolved ,by adding 40 cc. of 5 n-sodium hydroxide solution and 150 cc. of water with heating to 65 C. The clear solu- -tion is added to 1 kg. of green sensitized silver halide emulsion. After addition of hardeners and wetting agents,
  • the pH-value of the emulsion is adjusted by means of citric acid to pH 5.5.
  • a photographic material produced .With this emulsion mixture is exposed and then developed in a color developer containing N,N-diethyl-p-phenylene diamine, bleached and fixed or bleach-fixed.
  • a negative magenta image is obtained with an absorption maximum of 560 me, which shows pure whites, even after being bleached and fixed.
  • Example 4 A cellulose acetate film support is cast with a redsensitized silver halide emulsion containing, per kg. of
  • emulsion containing 15 g. of the color coupler described in Example 2 per kg. of emulsion.
  • a gelatine solution containing a yellow filter dyestuff a bluesensitive silver halide emulsion is applied which contains, per kg. of emulsion 15 kg. of the color coupler 4-stearoylamido benzoyl-3',5'-dicarboxy acetanilide.
  • a protective layer consisting of a 3 percent gelatine solution, the film is dried.
  • the film After exposure, the film is developed in a color developer containing N,N-diethyl-p-phenylene diamine, and is then bleached and fixed.
  • a negative color image is obtained.
  • color developer it is for example possible to use the following solution: 7
  • a suitable bath for fixing the bleached layers has the following composition:
  • the color couplers can be used in any color photographic material such as mono-layer or multi-layer
  • the non-diffusing color couplers according to the invention can be used in combination with any sensitizers, anti-fog agents, stabilizers or the like which are known to be employed incolor photographic material.
  • the layer arrangement or sensitization-colorrelationship are not especially critical.
  • the binding agent of the layers in which the color couplers are to be used is preferably gelatine, other layer forming vhydrophilic agents can be used such as carboxy cellulose,
  • the processing of the exposed color material, containing in one layer a magenta coupler according to the invention, is accomplished in a manner well known by first developing the material with a developer composition containing a color forming developer.
  • Said developers generally spoken are characterised by a content of a primary amino group or a substituted amino group, the substituent of which being split 'ofi during the development, e.g., as described in German -butyl-p-phenylene-diamine, N-ethyl-N-methyl sulfoaminoethyl-p-phenylene-diamine, or derivatives thereof being substituted in the phenylene nucleus, furthermore,
  • the developer composition may be alkaiised by alkali carbonates,
  • a photographic material containing at least one silver halide emulsion layer and developing the said exposed silver halide emulsion layer with a primary aromatic amine developer in the presence of a substituted indazolinone color coupler that is capable of forming a colored image with the oxidation product of a primary aromatic amine developer and has the following formula:
  • R is an alkyl radical having between 12 and 18 carbon atoms
  • X is a cation of the group consisting of hydrogen, alkali metals, alkaline-earth metals, ammonium, and alkyl-substituted ammonium radicals, the alkyl radicals of which contain between 1 and 4 carbon atoms.
  • R stands for an alkyl radical having from 12 to 18 carbon atoms, said coupler being capable of forming a colored image upon reaction with the oxidation product of said primary amine developer
  • X is a cation selected from the group consisting of hydrogen, alkali metals, alkaline-earth metals, ammonium, and alkylsubstituted ammonium radicals the alkyl radicals of which contain between 1 and 4 carbon atoms.
  • a photographic element according to claim 7, wherein said color coupler has the following formula 9.
  • a photographic element according to claim 7, wherein said color coupler has the following formula 0:0 Si aH NH 1:1 3?) 1% C 1% g References Cited by the Examiner UNITED STATES PATENTS 2,186,045 1/40 Schneider 96100 2,823,998 2/58 Jennen 96100 2,902,366 9/59 Sprung et a1 9655 3,043,694 7/62 Barr et al. 96-55 NORMAN G. TORCHIN, Primary Examiner.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Developing Agents For Electrophotography (AREA)

Description

United States Patent 3,199,983 3-INDAZOLONE COLQR CUUPLERS Giinther Koepke, Leverlrusen, Willibald Pelz, ()piadcn,
and Hans Scheilenberger, Leverlrusen, Germany, assignors to Ag'r'a Alstiengeselischaft, Leverkusen, Germany,
a corporation of Germany No Drawing. Filed .Fan. 22, 1962, Ser. No. 167,929
Claims priority, application G9ermany, Feb. 1, 1%
6 62 9 Claims. in. sis-es The present invention relates to indazolone color couplers in which the non-diifusing group comprises a long-aliphatic acyl radical substituted in the tat-position to the carbonyl group by a sulpho group, to silver halide emulsions containing such couplers and to the production of colored photographic images in the presence of such couplers.
In the production of dyestutf images by color-forming development it is the practice to employ color formers containing non-diffusing groups such as a long aliphatic chain, the purpose of which is to prevent diffusion of the coupler in the silver halide emulsion. It is likewise common practice to provide such couplers with certain acid radicals such as a carboxy or sulpho radical, the alkali or ammonium salts of which are soluble in water or aqueous solutions such as photographic emulsions. It is, furthermore, customary to employ as the yellow coupler an open chain keto methylene compound such as benzoyl-acetanilide derivatives, as thecyan coupler a compound containing phenolic hydroxy groups such as a-naphthol derivatives and as the magenta coupler pyrazolone derivatives particularly those bearing an aryl radical on the nitrogen atom in the l-position of the pyrazolone ring. These color couplers have a similar coupling intensity and speed of coupling with respect to the oxidation products of color developers formed upon development so that they can tasily be employed for the production of multi-color images, for which purpose it is general practice to use multi-layer materials having three silver halide emulsion layers which are light-sensitive for different parts of the spectrum, the said emulsion layers having the said color couplers incorporated therein in a diifusion resistant form.
Since the pyrazolone derivatives do not meet all practical requirements as regards the absorption properties and stability, attempts have already been made to replace the pyrazolone derivatives by indazolone derivatives for the production of magenta color images. The indazolone derivatives and more especially those which are made diffusion-resistant by introduction of relatively long alkyl radicals, have, however, the disadavantage that the coupling intensity and the solubility thereof are too low. This refers also to octadecenyl succinoyl amino indazolone described in German Patent No. 814,996. These couplers precipitate on casting whereby matting of the resulting layers and flattening of the color gradation occur.
It is not possible to increase the solubility of such indazolone derivatives by introduction of sulpho groups into the benzene nucleaus, because this is associated with an unacceptable displacement of the absorption maxima of the dyestuffs produced from these couplers towards longer wave lengths.
It is among the objects of the present invention to avoid the disadvantages described above.
We have now discovered a class of indazolone color couplers of the salt forming non-diffusing type in which a long aliphatic acyl radical contains the salt-forming function as a sulpho radical in u-position to the carbonyl group. The acyl radical is linked in the manner of carbon amide to an amino group which is substituted in the 6-position of the indazolone ring. Such indazolone 3,19%383 Patented Aug. 10, 1965 "ice derivatives are characterized by the following general formula:
in which R represents an alkyl radical having 618 carbon atoms, preferably 12-18 carbon atoms and X stands for a cation such as hydrogen, alkali metal, for example lithium, sodium and potassium, alkaline earth metal, such as magnesium and calcium, ammonium or ammoniurn substituted with at least one alkyl radical having up to 4 carbon atoms.
These color couplers have extremely useful and valuable photographic properties. The amino derivatives according to the invention show an excellent solubility, even in the weakly acid range, and also a high coupling intensity, so that they can be used in conjunction with couplers which contain activated methylene groups or with a-naphthol derivatives, in single-layer or multi-layer materials. In contrast to known indazolone derivatives, the present couplers are resistant to digestion. The silver halide emulsions to which these couplers are added can be kept for a relatively long time in a molten condition without any precipitation of the coupler, which would lead to a change in the viscosity and the pH-value of the emulsion, a flattening of the gradation and a matting of the layers produced from these emulsions, as Well as a decrease in the coupling intensity and thus a color tone displacement upon development of a multi-layer material. The couplers thus render possible the production of color materials with uniform and high-grade properties.
On account of the good stability of the present color couplers, photographic silver halide emulsions containing these color couplers can also be cast in the acid pH-range, so that improved keeping properties are guaranteed in the layers so produced. Furthermore, these layers have the advantage that even after relatively long storage, they do not show any change in color tone and color intensity of the developed image, by comparison with layers developed immediately after manufacture, whereas with layers having known indazolone derivatives, occur a displacement of the color tone from magenta-red to magenta-blue shades and a decrease in the color intensity. It is also surprising that the indazolone derivatives according to the invention by contrast with corresponding known indazoline derivatives, are not transformed into yellow dyestuffs by the action of potassium ferricyanide solutions, which are used for the bleaching of photographic color materials being developed by means of color-forming developers. Consequently, the present color couplers can also be used for the production of those multi-layer films or papers which are employed for the production or" positive color images by the use of potassium ferricyanide bleaching baths.
The color couplers to be used according to the invention are advantageously added to the silver halide emulsions in quantities of about 5 to 20 g./kg. Gelatine is preferably used as binder for the emulsion, but other binders known per se can also be used. Furthermore, it is also possible for the color couplers to be introduced into layers of multi-layer materials which are not sensitive to light, the said materials containing silver halide emulsion layers in addition to the said layers which are not light-sensitive.
The conventional color developers, in particular aromatic color developers with primary amino groups, can be used for the development of the present color materials.
The present color couplers can be obtained by reaction of 6-amino indazolone with the mono-alkali metal salts of ot-sulpho fatty acids using phosphorus trichloride in the presence of tertiary amines, for example pyridine.
Example 1 22.2 g. of 6-amino-indazolone, 2 H01 and 35.8 g. of the mono-sodium salt of sulphopalmitic acid are suspended in 260 cc. ofpyridine. From this mixture, 100 cc. of pyridine are distilled off with stirring, the suspension then being cooled to room temperature and a solution of 4.5
occasion, and then suction-filtered. About 47 g. of crude product are obtained after drying, which product can be purified by dissolving it at about 60 C. in 220 cc. of water and about'45 cc. of 10 percent sodium hydroxide solution, followed by filtration and precipitation by introduction .of the solution dropwise into a mixture of 570 cc. of water and 65 cc. of concentrated hydrochloric acid. It is then washed with dilute hydrochloric acid and thereafter with about 3 percent sodium chloride solution and dried.
37 to 40 g. of the compound of the following formula are obtained:
By. neutralization with sodium hydroxide or potassium hydroxide the corresponding salts are formed.
Example 2 The preparation is carried out in a manner similar to ,that indicated in Example 1,. except that 38.4 g. of the mono-sodium salt of a-sulphostearic acid are used instead of 35.8 g. of mono-sodium salt of sulphopalmitic acid.
The following indazolone derivative is obtained:
Suitable salts of said compound are obtained by reaction with carbonates or hydroxides of alkali metals or alkaline .earth metals, ammonia or amines containing at least one alkyl radical having up to 4 carbon atoms.
Example 3 14.8 g. of the coupler described in Example 1 are formed into a paste with 20 g. of methanol and dissolved ,by adding 40 cc. of 5 n-sodium hydroxide solution and 150 cc. of water with heating to 65 C. The clear solu- -tion is added to 1 kg. of green sensitized silver halide emulsion. After addition of hardeners and wetting agents,
the pH-value of the emulsion is adjusted by means of citric acid to pH 5.5. A photographic material produced .With this emulsion mixture is exposed and then developed in a color developer containing N,N-diethyl-p-phenylene diamine, bleached and fixed or bleach-fixed. A negative magenta image is obtained with an absorption maximum of 560 me, which shows pure whites, even after being bleached and fixed.
Example 4 A cellulose acetate film support is cast with a redsensitized silver halide emulsion containing, per kg. of
emulsion, 15 g. of the color coupler l-hydroxy-Z-naphthoyl-3'-sulpho-6'-N-methyl N octadecylamino anilide. A separation layer of 3 percent gelatine solution is then cast thereon and above is a green-sensitized silver halide positive or negative material or reversal color films.
emulsion, containing 15 g. of the color coupler described in Example 2 per kg. of emulsion. After casting a gelatine solution containing a yellow filter dyestuff a bluesensitive silver halide emulsion is applied which contains, per kg. of emulsion 15 kg. of the color coupler 4-stearoylamido benzoyl-3',5'-dicarboxy acetanilide. After casting a protective layer consisting of a 3 percent gelatine solution, the film is dried.
' After exposure, the film is developed in a color developer containing N,N-diethyl-p-phenylene diamine, and is then bleached and fixed.
A negative color imageis obtained. As color developer, it is for example possible to use the following solution: 7
N,N-diethyl-p-phenylene-diamine sulphate 3 Potassium carbonate Anhydrous sodium sulphite 2 Potassium bromide 1 Water to make 1000 cc.
The following baths can be used for bleaching the developed layers:
(1) K Fe(CN) g KBr g 15 Water to make 1000 cc.
(2) KBr g 20 I ZCI207 g.. 5 KA1(SO4)2 a -.----g-- 21 CH .COO.Na g 2.5 Glacial acetic acid cc 30 Water to make 1000 cc.
A suitable bath for fixing the bleached layers has the following composition:
N21 S O .5H O
'Na SO 'Na B O .10H O 25 Sodium hexaphosphate l Water to make 1000 cc. 0
For bleach-fixing, i.e., for simultaneously bleaching and fixing the layers, it is possible to use baths according to German patent No. 866,605.
Having thus described our invention, we now state that our invention is. capable of numerous variation. It will be clear to those skilled in the art thatthe color couplers, according to our invention, can be used in any color photographic material such as mono-layer or multi-layer The non-diffusing color couplers according to the invention can be used in combination with any sensitizers, anti-fog agents, stabilizers or the like which are known to be employed incolor photographic material. With regard to the utility for multi layer color films it should be pointed out that the layer arrangement or sensitization-colorrelationship are not especially critical. Although the binding agent of the layers in which the color couplers are to be used is preferably gelatine, other layer forming vhydrophilic agents can be used such as carboxy cellulose,
polyvinyl alcohol or the like. The processing of the exposed color material, containing in one layer a magenta coupler according to the invention, is accomplished in a manner well known by first developing the material with a developer composition containing a color forming developer. Said developers generally spoken are characterised by a content of a primary amino group or a substituted amino group, the substituent of which being split 'ofi during the development, e.g., as described in German -butyl-p-phenylene-diamine, N-ethyl-N-methyl sulfoaminoethyl-p-phenylene-diamine, or derivatives thereof being substituted in the phenylene nucleus, furthermore,
4-aminopyrazolone and derivatives thereof. The developer composition may be alkaiised by alkali carbonates,
colored image which comprises exposing to an object to.
be reproduced a photographic material containing at least one silver halide emulsion layer and developing the said exposed silver halide emulsion layer with a primary aromatic amine developer in the presence of a substituted indazolinone color coupler that is capable of forming a colored image with the oxidation product of a primary aromatic amine developer and has the following formula:
in which R is an alkyl radical having between 12 and 18 carbon atoms, X is a cation of the group consisting of hydrogen, alkali metals, alkaline-earth metals, ammonium, and alkyl-substituted ammonium radicals, the alkyl radicals of which contain between 1 and 4 carbon atoms. 2. A process according to claim 1, wherein said color coupler is a compound having the following formula -C=O soarr I 3. A process according to claim 1, wherein said color coupler is a compound having the following formula 4. A light-sensitive silver halide emulsion containing a color coupler of the following general formula R A? CONH SOaX H wherein R stands for an alkyl radical having from 12 to 18 carbon atoms, said coupler being capable of forming a colored image upon reaction with the oxidation product of said primary amine developer, and X is a cation selected from the group consisting of hydrogen, alkali metals, alkaline-earth metals, ammonium, and alkylsubstituted ammonium radicals the alkyl radicals of which contain between 1 and 4 carbon atoms.
5. A light-sensitive silver halide emulsion according to claim 4 containing a color coupler having the following formula 6. A light-sensitive silver halide emulsion according to claim 4 containing a color coupler having the following formula 7. A photographic element having superimposed silver halide emulsion layers sensitive to different regions of the visible spectrum, one of said layers containing a color coupler capable of reacting with the oxidation product of a primary amine developer to form a dyestutf image, said coupler having the following general formula in which R is an alkyl radical having between 12 and 18 carbon atoms and X is a cation of the group consisting of hydrogen, alkali metals, alkaline-earth metals, ammonium, and alkyl-substituted ammonium radicals the alkyl radicals of which contain between 1 and 4 carbon atoms.
8. A photographic element according to claim 7, wherein said color coupler has the following formula 9. A photographic element according to claim 7, wherein said color coupler has the following formula 0:0 Si aH NH 1:1 3?) 1% C 1% g References Cited by the Examiner UNITED STATES PATENTS 2,186,045 1/40 Schneider 96100 2,823,998 2/58 Jennen 96100 2,902,366 9/59 Sprung et a1 9655 3,043,694 7/62 Barr et al. 96-55 NORMAN G. TORCHIN, Primary Examiner.
LOUISE P. QUAST, Examiner.

Claims (1)

  1. 4. A LIGHT-SENSITIVE SILVER HALIDE EMULSION CONTAINING A COLOR COUPLER OF THE FOLLOWING GENERAL FORMULA
US167929A 1961-02-01 1962-01-22 3-indazolone color couplers Expired - Lifetime US3199983A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEA36629A DE1130287B (en) 1961-02-01 1961-02-01 Process for the production of color photographic images by the process of color development and material for carrying out the process

Publications (1)

Publication Number Publication Date
US3199983A true US3199983A (en) 1965-08-10

Family

ID=6929745

Family Applications (1)

Application Number Title Priority Date Filing Date
US167929A Expired - Lifetime US3199983A (en) 1961-02-01 1962-01-22 3-indazolone color couplers

Country Status (5)

Country Link
US (1) US3199983A (en)
BE (1) BE613328A (en)
CH (1) CH412567A (en)
DE (1) DE1130287B (en)
GB (1) GB935205A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3770447A (en) * 1970-12-29 1973-11-06 Agfa Gevaert Ag Light-sensitive silver halide color photographic material containing indazolone couplers
US4500630A (en) * 1983-02-15 1985-02-19 Fuji Photo Film Co., Ltd. Method for forming magenta color image

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2186045A (en) * 1938-02-05 1940-01-09 Agfa Ansco Corp Production of color photographic pictures
US2823998A (en) * 1949-12-13 1958-02-18 Gevaert Photo Prod Nv Process and material for producing photographic multi-color images
US2902366A (en) * 1956-10-23 1959-09-01 Gen Aniline & Film Corp Acylated 3-aminopyrazolone couplers
US3043694A (en) * 1960-05-23 1962-07-10 Eastman Kodak Co Novel class of 3-indazolinone developing agent

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL80779C (en) * 1948-11-23

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2186045A (en) * 1938-02-05 1940-01-09 Agfa Ansco Corp Production of color photographic pictures
US2823998A (en) * 1949-12-13 1958-02-18 Gevaert Photo Prod Nv Process and material for producing photographic multi-color images
US2902366A (en) * 1956-10-23 1959-09-01 Gen Aniline & Film Corp Acylated 3-aminopyrazolone couplers
US3043694A (en) * 1960-05-23 1962-07-10 Eastman Kodak Co Novel class of 3-indazolinone developing agent

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3770447A (en) * 1970-12-29 1973-11-06 Agfa Gevaert Ag Light-sensitive silver halide color photographic material containing indazolone couplers
US4500630A (en) * 1983-02-15 1985-02-19 Fuji Photo Film Co., Ltd. Method for forming magenta color image

Also Published As

Publication number Publication date
BE613328A (en) 1962-07-31
CH412567A (en) 1966-04-30
GB935205A (en) 1963-08-28
DE1130287B (en) 1962-05-24

Similar Documents

Publication Publication Date Title
US3061432A (en) Pyrazolino benzimidazole color coupler
US2342546A (en) Production and use of dyestuffs
GB1571506A (en) 4-phenyl azo - 2 - pyrazolin - 5 - one colour coupler and their use in photography
US3615505A (en) Silver halide emulsion containing 2-pyrazolin-5-one color coupler
US3013879A (en) Production of color photographic images
US2846307A (en) Isoxazolone couplers in color photography
US3222176A (en) Photographic colour images from amino substituted phenols
US3677764A (en) Silver halide emulsion containing purple coupler for color photography and process of making the same
US3684514A (en) Light-sensitive silver halide color photographic emulsions
US3199983A (en) 3-indazolone color couplers
US2673801A (en) Production of color photographic images
US3656953A (en) Silver dyestuff bleaching process using quinoxaline catalyst
US2902366A (en) Acylated 3-aminopyrazolone couplers
US3337344A (en) Color photographic silver halide emulsion
US3419390A (en) Elements and developers for color photography utilizing phenolic couplers containingan aminoalkyl group on the coupling position
DE69020431T2 (en) Photographic material with a cyan dye-forming coupler.
US4204867A (en) Process for the production of color photographic images using new white coupler substances
US3649278A (en) Process for forming a photographic image
US3892576A (en) Photographic water-insoluble compounds having a hydrophobic diffusion-fast substituent
US2448939A (en) Thioglycolic amide couplers
US2756149A (en) Mordanting basic dyes in photography
US2688541A (en) Light-sensitive color photographic material
US2710802A (en) Dialkyl-5-(oxanilamido) isophthalate couplers for color photography
US2500487A (en) Yellow diffusion-fast color formers of the benzimidazole class
US3910790A (en) Color photographic materials processed in the presence of anti-color fogging agents