GB945542A - Improvements in colour photography - Google Patents

Improvements in colour photography

Info

Publication number
GB945542A
GB945542A GB919759A GB919759A GB945542A GB 945542 A GB945542 A GB 945542A GB 919759 A GB919759 A GB 919759A GB 919759 A GB919759 A GB 919759A GB 945542 A GB945542 A GB 945542A
Authority
GB
United Kingdom
Prior art keywords
carbamoyl
chloride
reacting
dimethylaminostilbenzl
hydroxy
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
Application number
GB919759A
Inventor
James Anthony Carter
Hans Max Wagner
Miroslav Vasa Mijovic
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.)
Kodak Ltd
Original Assignee
Kodak Ltd
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 Kodak Ltd filed Critical Kodak Ltd
Priority to GB919759A priority Critical patent/GB945542A/en
Priority claimed from FR836957A external-priority patent/FR1266229A/en
Publication of GB945542A publication Critical patent/GB945542A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • 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
    • G03C1/00—Photosensitive materials
    • G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/815—Photosensitive materials characterised by the base or auxiliary layers characterised by means for filtering or absorbing ultraviolet light, e.g. optical bleaching
    • G03C1/8155—Organic compounds therefor
    • 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
    • G03C7/305—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers
    • G03C7/30541—Substances liberating photographically active agents, e.g. development-inhibiting releasing couplers characterised by the released group
    • G03C7/30547—Dyes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises compounds of the formula: <FORM:0945542/C2/1> where M represents the colour coupling portion of the molecule and R1 and R2 are substituents such as alkyl groups and any of the benzene rings may contain substituents. Such compounds are employed as photographic colour couplers (see Division G2). In examples 4-{3 - [4 - (4 - dimethylaminostilbenzl) carbamoyl] phenyl thio} -2- (2,4- di - t - amylphenoxybutylcarbamoyl) -1- naphthol is prepared by reacting 3(4-dimethyl-aminostilben -4- yl - carbamoyl) phenyl sulphenyl chloride with 1-hydroxy -N- [5-(2,4-di-t-amylphenoxy)butyl] -2-naphthamide; a -benzoyl -a - 3 -[4-(41-dimethylaminostilbenzylcarbamoyl) phenylthio] acetamilide is obtained by reacting the above sulphenyl chloride with a -benzoylacetanilide; and 4-{3-[4 - (41-dimethylaminostilbenzl) carbamoyl] phenylthio} 2-carbamoylcyclohexyl -1- naphthol is obtained by reacting 3(4-dimethylaminostilbenzl -4- carbamoyl) phenyl sulphenyl chloride with 2-carboxycyclohexylamide -1- hydroxynaphthalene. 3:31-Dithiobenzoyl chloride is obtained by treating 3:31-dithiobenzoic acid with thionyl chloride. Di -[3-(4-dimethylaminostilben -4- yl - carbamoyl disulphide is obtained by reacting 3:31-dithiobenzoyl chloride with 4-dimethylamino -4-aminostilbene in acetonitrile solution in the presence of trimethylamine. 2-carboxycyclohexamido -1- hydroxy - naphthalene is obtained by heating 1-hydroxy -2-phenylnaphthoate with cyclohexylamine.
GB919759A 1959-03-17 1959-03-17 Improvements in colour photography Expired GB945542A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB919759A GB945542A (en) 1959-03-17 1959-03-17 Improvements in colour photography

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB919759A GB945542A (en) 1959-03-17 1959-03-17 Improvements in colour photography
FR836957A FR1266229A (en) 1960-08-27 1960-08-27 New color photography process and new products for implementing this process

Publications (1)

Publication Number Publication Date
GB945542A true GB945542A (en) 1964-01-02

Family

ID=26187293

Family Applications (1)

Application Number Title Priority Date Filing Date
GB919759A Expired GB945542A (en) 1959-03-17 1959-03-17 Improvements in colour photography

Country Status (1)

Country Link
GB (1) GB945542A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2412872A1 (en) * 1977-12-23 1979-07-20 Eastman Kodak Co PHOTOGRAPHIC COUPLER RELEASING A USEFUL PHOTOGRAPHIC GROUPING, PHOTOGRAPHIC PRODUCT CONTAINING THIS COUPLER AND PROCESS FOR FORMING COLOR IMAGES
EP0253390A2 (en) 1986-07-17 1988-01-20 Fuji Photo Film Co., Ltd. Photographic support and color photosensitive material
EP0280252A2 (en) * 1987-02-26 1988-08-31 Fuji Photo Film Co., Ltd. Silver halide photographic material and method for forming super high contrast image therewith
US4774181A (en) * 1987-06-25 1988-09-27 Eastman Kodak Company Imaging element containing fluorescent dye-releasing coupler compound
EP0444933A1 (en) * 1990-02-28 1991-09-04 Konica Corporation Silver halide photographic light-sensitive material
WO2006134043A2 (en) * 2005-06-16 2006-12-21 Ciba Specialty Chemicals Holding Inc. Styryl sulfide dyes

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2412872A1 (en) * 1977-12-23 1979-07-20 Eastman Kodak Co PHOTOGRAPHIC COUPLER RELEASING A USEFUL PHOTOGRAPHIC GROUPING, PHOTOGRAPHIC PRODUCT CONTAINING THIS COUPLER AND PROCESS FOR FORMING COLOR IMAGES
EP0253390A2 (en) 1986-07-17 1988-01-20 Fuji Photo Film Co., Ltd. Photographic support and color photosensitive material
EP0280252A3 (en) * 1987-02-26 1989-12-13 Fuji Photo Film Co., Ltd. Silver halide photographic material and method for forming super high contrast image therewith
EP0280252A2 (en) * 1987-02-26 1988-08-31 Fuji Photo Film Co., Ltd. Silver halide photographic material and method for forming super high contrast image therewith
US4965170A (en) * 1987-02-26 1990-10-23 Fuji Photo Film Co., Ltd. Silver halide photographic material and method for forming super high contrast images therewith
US4774181A (en) * 1987-06-25 1988-09-27 Eastman Kodak Company Imaging element containing fluorescent dye-releasing coupler compound
EP0296794A3 (en) * 1987-06-25 1989-11-08 Eastman Kodak Company (A New Jersey Corporation) Imaging element containing fluorescent dye-releasing coupler compound
EP0296794A2 (en) * 1987-06-25 1988-12-28 EASTMAN KODAK COMPANY (a New Jersey corporation) Imaging element containing fluorescent dye-releasing coupler compound
EP0444933A1 (en) * 1990-02-28 1991-09-04 Konica Corporation Silver halide photographic light-sensitive material
US5236804A (en) * 1990-02-28 1993-08-17 Konica Corporation Silver halide photographic light-sensitive material containing a reducible fluorescent releasing compound
WO2006134043A2 (en) * 2005-06-16 2006-12-21 Ciba Specialty Chemicals Holding Inc. Styryl sulfide dyes
WO2006134043A3 (en) * 2005-06-16 2007-10-04 Ciba Sc Holding Ag Styryl sulfide dyes
US7811335B2 (en) 2005-06-16 2010-10-12 Ciba Specialty Chemicals Corp. Styryl sulfide dyes

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