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US4767698A Expired / Lapsed US ⏱️ 0.0 years remaining

Photographic material containing a pyridine azo or pyridazine azo cyan dye releasing compound

Assignee: Agfa Gevaert AG
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Filing: 1987-04-13
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Granted: 1988-08-30
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Expires: 2007-04-13
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Abstract

Abstract Cyan partial color images with increased light fastness and improved stability to moisture and heat may be produced by the dye diffusion process using cyan dyes corresponding to formula I released from dye releasing compounds. ##STR1## In the above formula, Q denotes a group for completing a pyridine or pyridazine ring optionally carrying a condensed aromatic ring; G denotes OH or NH--SO 2 --R 5 ; R 1 denotes H or one, two or three substituents; R 2 denotes H or a group with electron acceptor character preferably situated in an ortho-position to G; R 3 denotes H, acylamino or a group such as G; R 4 denotes H, SO 2 --NR 6 --R 7 or NH--SO 2 --R 5 ; R 5 denotes alkyl, aralkyl, aryl or NR 6 --R 7 ; R 6 , R 7 denote H, alkyl or aralkyl or together form a group for completing a cyclic amino group.

Inventors

  • 👤 Peter Bergthaller
  • 👤 Rudolf Stolzenburg
  • 👤 Paul Marx

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-30 10:02
CPC Classifications
C; C09; C09B; C09B29/00; C09B29/10; C09B29/103; C09B29/0025; C09B29/0029; C09B29/0048; C09B29/0051; C09B29/06; C09B29/095; G; G03; G03C; G03C8/00; G03C8/02; G03C8/08; G03C8/10

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 244 words
A colour photographic recording material for the production of colour images by the dye diffusion transfer process. comprising a non-diffusible, colour providing compound (dye releasing compound) associated with at least one light-sensitive silver halide emulsion layer, from which compound a diffusible azo dye is released under the conditions of alkaline development as a function of the development of the silver halide emulsion layer, wherein the azo dye corresponds to the following formula I wherein Q denotes a group for completing a pyridine or pyridazine ring on which a carbocyclic or heterocyclic aromatic ring may be condensed; G denotes OH or NH-SO 2 -R 5 ; R 1 denotes H or one, two or three substituents selected from halogen, alkyl, aryl, carboxyl, alkoxycarbonyl. carbamoyl, cyan, alkoxy, alkylthio, alkylsulphonyl, arylthio and arylsulphonyl; R 2 denotes H or a group with an electron acceptor character arranged in an ortho-position to G; R 3 denotes H, acylamine or a group G' having the same definition as G; R 4 denotes H, SO 2 -NR 6 -R 7 or NH-SO 2 -R 5 ; R 5 denotes alkyl, aralkyl, aryl or NR 6 -R 7 ; R 6 denotes H, alkyl, aralkyl or a group which together with R 7 and the nitrogen atom forms the residue of a cyclic amino group; R 7 denotes H, alkyl, aralkyl, aryl or a group which together with R 6 and the nitrogen atom forms the residue of a cyclic amino group.
Claim 2
Dependent Claim 244 words
A colour photographic recording material for the production of colour images by the dye diffusion transfer process. comprising a non-diffusible, colour providing compound (dye releasing compound) associated with at least one light-sensitive silver halide emulsion layer, from which compound a diffusible azo dye is released under the conditions of alkaline development as a function of the development of the silver halide emulsion layer, wherein the azo dye corresponds to the following formula I wherein Q denotes a group for completing a pyridine or pyridazine ring on which a carbocyclic or heterocyclic aromatic ring may be condensed; G denotes OH or NH-SO 2 -R 5 ; R 1 denotes H or one, two or three substituents selected from halogen, alkyl, aryl, carboxyl, alkoxycarbonyl. carbamoyl, cyan, alkoxy, alkylthio, alkylsulphonyl, arylthio and arylsulphonyl; R 2 denotes H or a group with an electron acceptor character arranged in an ortho-position to G; R 3 denotes H, acylamine or a group G' having the same definition as G; R 4 denotes H, SO 2 -NR 6 -R 7 or NH-SO 2 -R 5 ; R 5 denotes alkyl, aralkyl, aryl or NR 6 -R 7 ; R 6 denotes H, alkyl, aralkyl or a group which together with R 7 and the nitrogen atom forms the residue of a cyclic amino group; R 7 denotes H, alkyl, aralkyl, aryl or a group which together with R 6 and the nitrogen atom forms the residue of a cyclic amino group.
Claim 3
Dependent Claim 164 words
Recording material as claimed in claim 1, wherein the azo dye released corresponds to the following formula ##STR27## wherein Q denotes a group for completing a pyridine or pyridazine ring on which a carbocyclic or heterocyclic aromatic ring may be condensed; R 1 denotes H or one, two or three substituents selected from halogen, alkyl, aryl, carboxyl, alkoxycarbonyl, carbamoyl, cyano, alkoxy, alkylthio, alkylsulphonyl, arylthio and arylsulphonyl; R 2 denotes H, SO 2 -NR 6 -R 7 , CO-NR 6 -R 7 or Cl; R 4 denotes H, SO 2 -NR 6 -R 7 or NH-SO 2 -R 5 ; R 6 denotes H, alkyl, aralkyl or a group which together with R 7 and the nitrogen atom forms the residue of a cyclic amino group; R 7 denotes H, alkyl, aralkyl, aryl or a group which together with R 6 and the nitrogen atom forms the residue of a cyclic amino group and R 8 denotes alkyl, aralkyl, aryl or NR 6 -R 7
Claim 4
Dependent Claim 214 words
Recording material as claimed in claim 1, wherein at least one light-sensitive silver halide- emulsion layer has a compound corresponding to the following formula III associated therewith: ##STR28## wherein Q denotes a group for completing a pyridine or pyridazine ring on which a carbocyclic or heterocyclic aromatic ring may be condensed; G denotes OH or NH-SO 2 -R 5 ; R 1 denotes H or one, two or three substituents selected from halogen, alkyl, aryl, carboxyl, alkoxycarbonyl, carbamoyl, cyano, alkoxy, alkylthio, alkylsulphonyl, arylthio and arylsulphonyl; R 2 denotes H or a group with an electron acceptor character arranged in the ortho-position to G; R 3 denotes H, acylamino or a group G' having the same definition as G; R 4 denotes H, SO 2 -NR 6 -R 7 or NH-SO 2 -R 5 ; R 5 denotes alkyl, aralkyl, aryl or NR 6 -R 7 ; R 6 denotes H, alkyl, aralkyl, or a group which together with R 7 and the nitrogen atom forms the residue of a cyclic amino group; R 7 denotes H, alkyl, aralkyl, aryl or a group which together with R 6 and the nitrogen atom forms the residue of a cyclic amino group; and CAR denotes a carrier group containing at least one group which confers diffusion resistance.

References Cited (Backward Citations)

US3998640A Cited
US4529692A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1991-08-30 1992-02-29 1992-08-30 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1995-08-30 1996-02-29 1996-08-30 $3760.00 Window Closed / Lapsed
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