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
  • G03C7/327—Macromolecular coupling substances
• • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
  • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
  • Y10S534/00—Organic compounds -- part of the class 532-570 series
  • Y10S534/03—Polymeric azo compounds or azo compounds containing polymeric moieties

Definitions

• Our present invention relates to the manufac opment (chromogenic development) color pictures can be obtained photographically as described, for instance, in.U. S. Patent No. 1,102,028.
• amines for example, amines, phenols, aminophenols, 1 naphthols, aminonaphthols and bodies with the ticularly if the solubility in water is not suilicient.
• layers containing these bodies are suitable for formingthe required multi-layer material, since diffusion from one layer to another cannot occur.
• Suitable highly polymeric carboxylic acids and substances like polyglycuronic acids, prote'inaminc acids or synthetic compounds from unsaturated organic acids such as polyvinylcarboxylic acids (polyacrylic acid alone or as a mixed polymerizate with styrene, vinylchlorida'vinylether or nitrogeneous vinyl compounds such as vinylcarbazole or the like), polymerizates of maleic acid, fumaric acid, methylene-malonic acid, alone A or as mixed polymerizates with vinyl compounds.
• polycarboxylic acids are caused to react in the form of their acid chlorides or anhydrides or esters or other reactive derivatives with the aforesaid reactive amines, phenols and bodies with active methylene groups, for example with aminophenols, phenylenediamines, aminonaphthols,
• aminoacetic acid anhydrides aminobenzoylaceticacid esters, aminophenylmethylpyrazolones, hydroxynaphthoic acid aminoarylides, diazo-bodies, leuco-dyestuffs, or the like,
• Example 1 --l gram of a condensation product from metaaminophenylmethylpyrazolone and the mixed polymerizate from vinylchloride and maleic acid anhydride' are ground with 5 cc.,.oi caustic soda lye of 5 per centstrength and then dissolved in water. The solution is added to 100 cc. of silver bromide emulsion. A layer of this emulsion may be developed with para-amlnodimethylaniline to a picture which consists of a red dyestufl after the separation of the silver.
• Example-1 but instead of a pyrazolone and a condensation productv there is used. one made from 1.-5.-aminonaphthol and the mixed polymerizate namedin Example 1; the layer made yields a picture in a blue dyestufl.
• carboxylic acid derivative consisting of a carbon chain molecule wherein the color forming group recurs periodically in pairs, each group of a pair beingpnnited by an acid amide linkage to adjacent carbon atoms of said chain.

Landscapes

• Physics & Mathematics (AREA)
• Spectroscopy & Molecular Physics (AREA)
• General Physics & Mathematics (AREA)
• Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
• Silver Salt Photography Or Processing Solution Therefor (AREA)

Applications Claiming Priority (1)

Publications (1)

Family

ID=7193442

Family Applications (1)

Country Status (5)

Cited By (2)

Families Citing this family (6)

• 0
  • NL NL49641D patent/NL49641C/xx active
  • BE BE416339D patent/BE416339A/xx unknown
• 1936
  • 1936-06-11 GB GB16331/36A patent/GB479838A/en not_active Expired
  • 1936-07-02 FR FR807792D patent/FR807792A/fr not_active Expired
  • 1936-07-15 US US90726A patent/US2178612A/en not_active Expired - Lifetime

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