GB898706A - Azo dyes derived from dihydroxyphenyl ketones and their use in photography - Google Patents

Azo dyes derived from dihydroxyphenyl ketones and their use in photography

Info

Publication number
GB898706A
GB898706A GB28756/58A GB2875658A GB898706A GB 898706 A GB898706 A GB 898706A GB 28756/58 A GB28756/58 A GB 28756/58A GB 2875658 A GB2875658 A GB 2875658A GB 898706 A GB898706 A GB 898706A
Authority
GB
United Kingdom
Prior art keywords
dyes
indicated
propionyl
methoxy
coupling
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
GB28756/58A
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.)
Polaroid Corp
Original Assignee
Polaroid Corp
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 Polaroid Corp filed Critical Polaroid Corp
Publication of GB898706A publication Critical patent/GB898706A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B39/00Other azo dyes prepared by diazotising and coupling
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09BORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B31/00Disazo and polyazo dyes of the type A->B->C, A->B->C->D, or the like, prepared by diazotising and coupling
    • C09B31/02Disazo dyes
    • 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
    • G03C8/00Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
    • G03C8/02Photosensitive materials characterised by the image-forming section
    • G03C8/08Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds
    • G03C8/10Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds of dyes or their precursors
    • G03C8/12Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds of dyes or their precursors characterised by the releasing mechanism
    • G03C8/14Oxidation of the chromogenic substances
    • G03C8/16Oxidation of the chromogenic substances initially diffusible in alkaline environment
    • G03C8/18Dye developers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Heat Sensitive Colour Forming Recording (AREA)
  • Coloring (AREA)

Abstract

The invention comprises dyes of formula <FORM:0898706/IV (c)/1> where Ar is an aryl nucleus, Z is OH, Hlg, Alk or AlkO, m 0 or 1, n 0 or 1-4, q 1 or 2, R alkylene, Y o- or p-dihydroxyphenyl or an alkyl or halogen substituted derivative thereof and Xa and Xb are coupling component residues. The dyes are made by conventional diazotization and coupling processes and the hydroxy groups in Y may be protected during these processes by using, e.g. in the form of o-acetyl derivatives. Benzene and naphthalene nuclei are indicated for Ar. Preferred alkyl and alkoxy groups for Z are those containing 1-5 carbon atoms. Preferred dyes are those in which Ar is a benzene residue and where R is an ethylene group. Representative of indicated coupling components are phenol, anilines, naphthols, anthrols, naphthylamines, pyrazolones, pyrroles, 1,3-diketones and beta-ketonic acid arylamides. The coupling components may contain substituents such as alkyl, sulpho, alkoxy, aryl, aryloxy, amino, keto, alkylamino, arylamino, hydroxy, cyano, alkylamido, arylamido, carbalkoxy, carboxamido and sulphonamido groups. Preferred diazo components are 2 - [gamma - (21, 51 - dimethoxy - 31 - aminophenyl) - propionyl and beta - methyl - propionyl - ] - and 2 - (gamma - [21, 51 - di - methoxy - 31 - (211, 511 - dimethoxy 311 - amino - phenylazo) - phenyl] - propionyl) - hydroquinones. Amongst coupling components indicated or specified are 4-methyl, methoxy- and benzyl-1-naphthols, 4-methoxy- and -aectamido-a -naphthylamines, 1,5-naphtholenediamine, 1-hydroxy-2-naphthanilide, phenol, p-cresol, aniline, 2,5-dimethoxyaniline, 1-hydroxyanthracene, diketohydrindene, malonitrile, acetoacetanilide and 1-phenyl - 3 - methyl - 5 - pyrazolone. Indicated coupling components for use in compounds where p is Z are 1,6-dihydroxynaphthalene and 1-naphthol. A further indicated value for R is isopropylene. The dyes are developers and are of particular use in colour photography. Examples are provided of the preparation of the dyes and thie use in photographic processes and compositions. Specifications 804,971, 804,972, 811,579, 853,478, 853,479 and 898,707 are referred to.
GB28756/58A 1957-09-20 1958-09-08 Azo dyes derived from dihydroxyphenyl ketones and their use in photography Expired GB898706A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US68506657A 1957-09-20 1957-09-20
US68508157A 1957-09-20 1957-09-20
US222702A US3208991A (en) 1957-09-20 1962-09-10 Azo dye developers

Publications (1)

Publication Number Publication Date
GB898706A true GB898706A (en) 1962-06-14

Family

ID=27397130

Family Applications (2)

Application Number Title Priority Date Filing Date
GB28756/58A Expired GB898706A (en) 1957-09-20 1958-09-08 Azo dyes derived from dihydroxyphenyl ketones and their use in photography
GB19820/61A Expired GB898707A (en) 1957-09-20 1958-09-08 Dihydroxyphenylketonic compounds and their use in photography

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB19820/61A Expired GB898707A (en) 1957-09-20 1958-09-08 Dihydroxyphenylketonic compounds and their use in photography

Country Status (5)

Country Link
US (1) US3208991A (en)
BE (1) BE571336A (en)
DE (2) DE1419866A1 (en)
FR (1) FR1215651A (en)
GB (2) GB898706A (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4247455A (en) * 1978-08-02 1981-01-27 Polaroid Corporation Yellow 2:1 azo-azo or azo-azomethine chrome complexed dye developers
WO2005118551A2 (en) * 2004-05-28 2005-12-15 Ligand Pharmaceuticals Inc. Thrombopoietin activity modulating compounds and methods
NZ554662A (en) * 2004-10-25 2008-11-28 Ligand Pharm Inc Thrombopoietin activity modulating compounds and methods

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL293714A (en) * 1956-02-13 1900-01-01
US2997390A (en) * 1956-09-04 1961-08-22 Polaroid Corp Novel color processes and products
US3009958A (en) * 1957-06-06 1961-11-21 Polaroid Corp Hydroquinonyl derivatives and their synthesis

Also Published As

Publication number Publication date
US3208991A (en) 1965-09-28
DE1419866A1 (en) 1968-11-21
GB898707A (en) 1962-06-14
FR1215651A (en) 1960-04-20
DE1129371B (en) 1962-05-10
BE571336A (en) 1959-03-19

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