GB598477A - Improvements in or relating to colour photography - Google Patents

Improvements in or relating to colour photography

Info

Publication number
GB598477A
GB598477A GB7372/45A GB737245A GB598477A GB 598477 A GB598477 A GB 598477A GB 7372/45 A GB7372/45 A GB 7372/45A GB 737245 A GB737245 A GB 737245A GB 598477 A GB598477 A GB 598477A
Authority
GB
United Kingdom
Prior art keywords
acetal
groups
dye intermediate
group
reaction product
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
GB7372/45A
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.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB598477A publication Critical patent/GB598477A/en
Expired legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C7/00Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
    • G03C7/30Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
    • G03C7/32Colour coupling substances
    • G03C7/327Macromolecular coupling substances
    • G03C7/3275Polymers obtained by reactions involving only carbon-to-carbon unsaturated bonds, e.g. vinyl polymers

Landscapes

  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Physics & Mathematics (AREA)
  • Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

Hydrophilic substantially colourless filmforming polymers and condensation products contain dye intermediate groups. They may contain a plurality of free hydroxyl groups and a plurality of dye intermediate groups, and the predominant hydrophilic groups may be nonphenolic hydroxyl groups. The dye intermediate groups may be attached either directly or indirectly to the chain, and may be connected by carbonamide, sulphonamide, amino, acetal, ester, or ether linkages to polymers such as hydrolysed polyvinyl esters (e.g. polyvinyl alcohols), hydrolysed interpolymers of vinyl esters (e.g. acetate, propionate, or butyrate), with olefines (e.g. ethylene, propylene, or butene-2), or other vinyl compounds (e.g. acrylic acid, acrylic acid alkyl esters, alkyl methacrylates, vinyl cyanide, vinyl chloride, or maleic anhydride), or the partial esters (e.g. acetate, propionate, or butyrate), ethers (e.g. methyl, ethyl, or hydroxyethyl), or acetals (e.g. formals, acetals, propionals, butyrals, or benzals) of such polymers. The change in solubility produced by the introduction of the dye intermediate groups may be balanced by the introduction of ester (e.g. acetate, propionate, benzoate, phthalate, or succinate), ether (e.g. from glycollic acid), or acetal (e.g. from phthalaldehydic acid, o-sulphobenzaldehyde, or acids of the type CHO. (CH2)X-COOH) before or after introduction of the dye intermediate groups, or by the use of dye intermediate groups containing such groups. A group or atom readily eliminated (e.g. a sulphonic or carboxylic acid group or a halogen atom) may be in the coupling reactive position. The dye intermediate group may contain a reactive acyclic or intracyclic methylene group or aromatic hydroxyl group and may be a phenol, naphthol, acylacetarylide, cyanoacetarylide, b -ketoester, pyrazolone, N-homophthalylamine, coumarone, indoxyl, or thioindoxyl. Light-sensitive silver salts may be precipitated therein, and allyl thiourea, allyl isothiocyanate, sodium thiosulphate, or cyanine dyes added. Polyvinyl alcholsalicylaldehyde condensation product; the acetal from polyvinyl alcohol, allylsalicylaldehyde, and phthalaldehydic acid; symmetrical bis-(m-1-phenyl-3-methyl-5-pyrazolone-1-yl)-urea-formaldehyde condensation product; the modified acetal of Example VI of Specification 535,341; the reaction product of 1-m-aminophenyl-3-methyl-5-pyrazolone and vinyl chloride-maleic anhydride interpolymer; the reaction product of 1 : 5-aminonaphthol and vinyl chloridemaleic anhydride interpolymer; the reaction product of oxynaphthoic acid and polyethylenemine; the reaction product of o-hydroxyphenylacetaldehyde and saponified polyglycerol; the reaction product of 1-p-carboxyphenyl-3-ethyl-5-pyrazolone and the m-aminobenzaldehyde acetal of polyvinyl alcohol; the reaction product of acetoacetaminophenylcarboxylic acid and the m-aminobenzaldehyde acetal of polyvinyl alcohol; the condensation product of m-cresol and p-cresol dialcohol; the condensation product of benzoylacet-p-hydroxyanilide and p-cresol dialcohol; and the salicylaldehyde acetal of hydrolysed ethylene vinyl acetate interpolymer are also referred to. A colourless or yellow-dyed interlayer may be of hardened polyvinyl alcohol or of a polyvinyl acetal from an aldehyde containing a sulphonic or carboxylic acid group. Specifications 479,838, [Group XX], 489,161, 521,169, 537,961, 578,666, 582,093 and 598,475 also are referred to.
GB7372/45A 1944-03-31 1945-03-23 Improvements in or relating to colour photography Expired GB598477A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US528942A US2397864A (en) 1944-03-31 1944-03-31 Color yielding photographic elements

Publications (1)

Publication Number Publication Date
GB598477A true GB598477A (en) 1948-02-19

Family

ID=24107858

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7372/45A Expired GB598477A (en) 1944-03-31 1945-03-23 Improvements in or relating to colour photography

Country Status (3)

Country Link
US (1) US2397864A (en)
FR (1) FR927414A (en)
GB (1) GB598477A (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2476988A (en) * 1946-07-08 1949-07-26 Du Pont 5-acyloxypyrazole amidoacetals
US2551133A (en) * 1946-08-29 1951-05-01 Du Pont Photographic light-sensitive diazo element
US2513190A (en) * 1948-02-18 1950-06-27 Du Pont Polymeric color formers
US2562528A (en) * 1949-01-21 1951-07-31 Du Pont Color former acetals of polyvinyl alcohol and substituted carbalkoxyacetamidobenzaldehydes
US2754286A (en) * 1951-10-15 1956-07-10 Du Pont Aldehydes and their acetals
US2758029A (en) * 1953-04-10 1956-08-07 Du Pont Process of making colored pictures
US4335197A (en) * 1980-11-25 1982-06-15 E. I. Du Pont De Nemours And Company Photoimaging process
US4520093A (en) * 1984-01-30 1985-05-28 E. I. Du Pont De Nemours And Company Photosensitive composition and method for forming a neutral black image
US4576894A (en) * 1984-09-24 1986-03-18 E. I. Du Pont De Nemours And Company Tanning development in low silver photoimaging using polymeric couplers

Also Published As

Publication number Publication date
US2397864A (en) 1946-04-02
FR927414A (en) 1947-10-29

Similar Documents

Publication Publication Date Title
US2310943A (en) Polyvinyl acetals
GB598477A (en) Improvements in or relating to colour photography
GB786346A (en) Process for gelling hydroxyl polymers
US2945006A (en) Reaction products of carbonyl containing polymers and aminoguanidine that are usefulas mordants
ES366943A1 (en) Procedure for the preparation of derivatives of 1-etil-3, 3-dimethyl-cyclohexane. (Machine-translation by Google Translate, not legally binding)
GB531579A (en) Improvements in or relating to photographic products
GB600023A (en) Improvements in photographic light-sensitive materials
US2473403A (en) Hydrophilic dye intermediates
US2489655A (en) Polymeric color formers
FI802189A (en) ACETYLACETOXYALKYL-ALLYLETER DERAS FRAMSTAELLNING OCH ANVAENDNING
GB629631A (en) Improvements in or relating to colour photography
GB478357A (en) Improvements in and relating to photographic films
FR1181578A (en) Antistatic photographic film
US2361936A (en) Photographic materials and process of manufacturing same
US2513190A (en) Polymeric color formers
US2421971A (en) Hydrolyzed vinyl ester interpolymers
US2622026A (en) Photographic element and tinted film base
GB651625A (en) Diazotype photoprinting material
US2606835A (en) Light-sensitive photographic element
GB600039A (en) Photographic elements containing hydrophilic colloid layers
GB537952A (en) Improvements in and relating to colour-forming developers and processes of colour development
GB809340A (en) Polymers and photographic emulsions containing them
Abramovitch et al. A General Method for the Synthesis of t-Butyl Esters
US2562528A (en) Color former acetals of polyvinyl alcohol and substituted carbalkoxyacetamidobenzaldehydes
GB418745A (en) Improvements in the sensitisation of photographic emulsions