US2380809A - Color couplers for photographic color development - Google Patents

Color couplers for photographic color development Download PDF

Info

Publication number
US2380809A
US2380809A US389222A US38922241A US2380809A US 2380809 A US2380809 A US 2380809A US 389222 A US389222 A US 389222A US 38922241 A US38922241 A US 38922241A US 2380809 A US2380809 A US 2380809A
Authority
US
United States
Prior art keywords
color
photographic
development
developing
couplers
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
US389222A
Other languages
English (en)
Inventor
Verkinderen Honore
Vankeirabilek Norbert
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Application granted granted Critical
Publication of US2380809A publication Critical patent/US2380809A/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • G03C7/36Couplers containing compounds with active methylene groups

Definitions

  • This invention relates to photographic color development and to processes of color development for use in connection with color photography.
  • Y-rCHri-B where Y is one of the electro-negative groups CR- or 2.00- (wherexis anelhior aryl group, substituted or unsubstitimd) while B is an arylor hctcrocyclo-substitutcd amino roup.
  • the invention are compounds having the general formula: "Ii "if --on
  • the invention comprises the process of poration, in the photographic emulsion, before or after coating, of a color coupler as above deiineii and, further. the process of developing a latent photographic image by means of a color developer comprising in addition to an aromatic amino developing agent a color. coupler as above defined.
  • the invention includes the method of color development which comprises developing a latent photographic image by means 01' an aromatic amino developer in the presence of color couplers as above defined, and eliminating the silver image which is formed during development so that a clear and transparent color image remains.
  • the invention also consists in new or improved color iorming developers comprising, in addition to an aromatic amino developing agent, color couplers as above, defined.
  • the present invention includesphoto- 2 l s,sso,soc
  • graphic elements having at least one layer con- B essentially of the product resulting from the taining maker and transparent image composed cm-C c-N coupling in situ during development of color couplers as above defined, with the oxidation 5 K Cnhco product of an aromatic amino developing agent.
  • the aromatic amino compounds which may be uethmol' "com" 100 used as developing asents in the present inventlon include the mono-, diand tri-amino-aryl- For m B to compounds.
  • the mono-amino developing Rosanna 4 agents may be mentioned amino-phenols and amlno-cresols and their halogen derivatives and 4 amino-naphthols.
  • the developing agents preferably used and g pan phenylened e g 3 having hitherto given the best results in connecl5 s u tion with the present invention are the aromatic fi fi fi g zgfl'i "g" :3 orthoand para-diamines. such as para-phenyl- 7 sodium hydroxide 2 enedlamine and its substitution products.
  • These water h" 1000 developing agents may be substituted in one aminogroup'orintheringorinbothJormingzo 3 compounds such as: NR diethyl-para-phenylenedlamine.
  • the invention is in no way limited to the use oi the color couplers in the developing solution itself.
  • the color coupler which during the development forms the dye, can also be added to the photographic emulsion (for instance by adsorption upon the silver salts) before or after coating.
  • the other ingredients of the color forming baths containing chiefly the aromatic amino developer, may be applied later, during the developing process. as a bath.
  • the present invention may be utilized in the formation of colored photographic images on plates or papers as well as on films, employing gelatine or some other carrier substance :lor the silver halide.
  • the developing process may be used for developing photographic material, provided with one or more sensitive layers, which are, applied on one side or on both sides of the support.
  • the silver formed during the developing process may be eliminated.
  • a bath should be used, however, which does not destroy the dye.
  • a bath consisting of a solution in water of potassium ferricyanide and sodium thiosulphateeasily eliminates the silver without destroying the dye, leaving a pure dye image.
  • the process of developing a colored image in a. gelatin-silver halide photographic layer which comprises coupling the development product of a primary aromatic amino developing compound with the coupler compound, 3 benzyl-5 acetonyll,2,4-oxodiazole 2.
  • the process of developing a colored image in a gelatin-silver halide photographic layer which comprises coupling the development productof a primary aromatic amino developing compound with the color coupler compound of the general formula wherein X is an electro-negative organic radicalselected from the class consisting of acyl and cyano, while Y is an organic radical of the class consisting of substituted alkyl.

Landscapes

  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
US389222A 1939-12-11 1941-04-18 Color couplers for photographic color development Expired - Lifetime US2380809A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB31978/39A GB540760A (en) 1939-12-11 1939-12-11 Improvements in and relating to colour couplers for photographic colour development
GB22002/48A GB645043A (en) 1939-12-11 1948-08-20 Improvements in or relating to the production of colour photographic images

Publications (1)

Publication Number Publication Date
US2380809A true US2380809A (en) 1945-07-31

Family

ID=26255644

Family Applications (1)

Application Number Title Priority Date Filing Date
US389222A Expired - Lifetime US2380809A (en) 1939-12-11 1941-04-18 Color couplers for photographic color development

Country Status (6)

Country Link
US (1) US2380809A (it)
BE (2) BE490600A (it)
DE (1) DE870947C (it)
FR (2) FR869169A (it)
GB (2) GB540760A (it)
IT (1) IT390064A (it)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2441491A (en) * 1944-05-12 1948-05-11 Ilford Ltd Cyanacetylamino phenol color formers for color photography
US2531004A (en) * 1947-11-26 1950-11-21 Gen Aniline & Film Corp Acetonitriles as azo components in diazotypes
DE1045230B (de) * 1956-03-23 1958-11-27 Gevaert Photo Prod Nv Verfahren zur Herstellung photographischer Farbbilder nach dem Farbentwicklungsverfahren
US3189452A (en) * 1961-12-05 1965-06-15 Eastman Kodak Co Color-forming photographic process utilizing a bleach-fix followed by a bleach
US4871652A (en) * 1988-09-07 1989-10-03 Eastman Kodak Company Photographic silver halide material and process
US5066576A (en) * 1989-10-03 1991-11-19 Fuji Photo Film Co., Ltd. Silver halide color photographic material
US5162196A (en) * 1989-11-20 1992-11-10 Fuji Photo Film Co., Ltd. Color coupler for photography and silver halide photographic material comprising the same
WO2017062523A2 (en) 2015-10-05 2017-04-13 Dsm Ip Assets B.V. Oil compositions and methods of making

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE589419A (it) * 1959-04-06
CH627562A5 (de) 1977-04-29 1982-01-15 Ciba Geigy Ag Farbphotographisches material.

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2441491A (en) * 1944-05-12 1948-05-11 Ilford Ltd Cyanacetylamino phenol color formers for color photography
US2531004A (en) * 1947-11-26 1950-11-21 Gen Aniline & Film Corp Acetonitriles as azo components in diazotypes
DE1045230B (de) * 1956-03-23 1958-11-27 Gevaert Photo Prod Nv Verfahren zur Herstellung photographischer Farbbilder nach dem Farbentwicklungsverfahren
US2897079A (en) * 1956-03-23 1959-07-28 Gevaert Photo Prod Nv Production of colored photographic images with oxodiazole couplers
US3189452A (en) * 1961-12-05 1965-06-15 Eastman Kodak Co Color-forming photographic process utilizing a bleach-fix followed by a bleach
US4871652A (en) * 1988-09-07 1989-10-03 Eastman Kodak Company Photographic silver halide material and process
US5066576A (en) * 1989-10-03 1991-11-19 Fuji Photo Film Co., Ltd. Silver halide color photographic material
US5162196A (en) * 1989-11-20 1992-11-10 Fuji Photo Film Co., Ltd. Color coupler for photography and silver halide photographic material comprising the same
WO2017062523A2 (en) 2015-10-05 2017-04-13 Dsm Ip Assets B.V. Oil compositions and methods of making

Also Published As

Publication number Publication date
BE490600A (it)
BE440012A (it)
IT390064A (it)
DE870947C (de) 1953-03-19
FR59472E (fr) 1954-05-25
GB540760A (en) 1941-10-29
FR869169A (fr) 1942-01-26
GB645043A (en) 1950-10-25

Similar Documents

Publication Publication Date Title
US2108602A (en) Photographic color-forming compounds
US2367531A (en) Acylaminophenol photographic couplers
US2313586A (en) Hydroxynaphthoic acid amide coupler
GB1578408A (en) Coupler containing silver halide colour photo sensitive materials
US3295976A (en) Novel inhibitors for use in the black and white development of color reversal film
US2380809A (en) Color couplers for photographic color development
US2296306A (en) Nondiffusing metallic salt coupler compound
US3482971A (en) Scavengers for oxidized developing agent
US3222176A (en) Photographic colour images from amino substituted phenols
US2186736A (en) Coupling compounds for color forming development
US2334495A (en) Color photography
US2350138A (en) Nondiffusing acylacetyl sulphonamide coupler
US2113330A (en) Color-forming developers
GB1324374A (en) Photographic dye developer diffusion transfer process
US2357395A (en) Photographic emulsion
US3622328A (en) Process for producing photographic color images
US1807761A (en) of wiesbaden-biebrich
US3376310A (en) Substituted 1-phenyl-5-mercapto-tetrazoles
US2295008A (en) Photographic color forming compound
US2039730A (en) Color-forming developer
US2289805A (en) Sulphonic ester coupler
US2728660A (en) Salicylic acid ester and amide photographic coupler compounds
US2527476A (en) Cyanoacetylhydrazones as photographic color couplers
US2418624A (en) Azo dyes for color photography
US3447923A (en) Color photographic process