← Back to Patent Explorer
US4179291A Expired / Lapsed US ⏱️ 0.0 years remaining

Photographic dye diffusion transfer process

Assignee: Agfa Gevaert AG
•
Filing: 1977-10-04
•
Granted: 1979-12-18
•
Expires: 1997-10-04
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract In the dye diffusion transfer process for the production of colored images dye-providing compounds of the following formula give lower color fog values Dmin, as compared with known dye-providing compounds: ##STR1## X = dye or dye precursor Z = intermediate member n = 0 or 1 R 1 = --O--R 2 ; --S--R 2 or ##STR2## R 2 = hydrogen, alkyl, cycloalkyl or aryl R 3 = a group as defined under R 2 or acyl R 4 = hydrogen or alkyl Y = a residue to complete a condensed benzene ring and R 1 and/or a substituent on the condensed benzene ring is or contains a group that confers resistance to diffusion.

Inventors

  • 👤 Hans Vetter
  • 👤 Paul Marx

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-29 16:37
CPC Classifications
C; C07; C07D; C07D209/00; C07D209/02; C07D209/04; C07D209/30; C07D209/42; G; G03; G03C; G03C8/00; G03C8/02; G03C8/08; G03C8/10; Y; Y10; Y10S; Y10S430/00; Y10S430/156; Y10S430/159

Claims Analysis

Total Claims: 4
Claim 1
Independent Claim 308 words
The photographic dye diffusion transfer process for the production of colored images, in which a photographic material comprising at least one light-sensitive silver halide emulsion layer and, associated therewith, a non-diffusible dye-providing compound which in its oxidized form is capable of releasing a diffusible dye in an alkaline medium, is exposed imagewise and developed with a silver halide alkaline developer which in its oxidized form oxidizes the non-diffusible dye-providing compound and the latter is split by the developer alkali as a consequence of this oxidation, releasing a diffusible dye in image distribution, in which the improvement comprises the non-diffusible dye-providing compound is represented by the following formula: in which X represents the residue of a dye precursor which is attached to to the SO 2 group either directly or by way of an intermediate member Z; Z represents an alkylene group with 1 to 6 carbon atoms, arylene or a heterocyclic group which is attached to the residue X either directly or by way of an --O--, --S--, --SO 2 --, --NR-- (R=hydrogen or alkyl), --CO--, --CO--NH-- or --SO 2 --NH--group; n is 0 or 1; Y represents the residue to complete a condensed benzene ring; R 1 represents --OR 2 --, or ##STR12## R 2 represents hydrogen, an alkyl group having from 1 to 22 carbon atoms, or a cycloalkyl or aryl group; the said alkyl, cycloalkyl and aryl groups may in turn be substituted; R 3 represents one of the residues given under the definition for R 2 or an acyl group derived from aliphatic or aromatic carboxylic or sulphonic acids; R 4 represents hydrogen or a substituted or unsubstituted alkyl group having from 1 to 22 carbon atoms; and in which R 1 and/or a substituent on the condensed benzene ring which is completed by Y represents or contains a residue which confers diffusion resistance.
Claim 2
Dependent Claim 308 words
The photographic dye diffusion transfer process for the production of colored images, in which a photographic material comprising at least one light-sensitive silver halide emulsion layer and, associated therewith, a non-diffusible dye-providing compound which in its oxidized form is capable of releasing a diffusible dye in an alkaline medium, is exposed imagewise and developed with a silver halide alkaline developer which in its oxidized form oxidizes the non-diffusible dye-providing compound and the latter is split by the developer alkali as a consequence of this oxidation, releasing a diffusible dye in image distribution, in which the improvement comprises the non-diffusible dye-providing compound is represented by the following formula: in which X represents the residue of a dye precursor which is attached to to the SO 2 group either directly or by way of an intermediate member Z; Z represents an alkylene group with 1 to 6 carbon atoms, arylene or a heterocyclic group which is attached to the residue X either directly or by way of an --O--, --S--, --SO 2 --, --NR-- (R=hydrogen or alkyl), --CO--, --CO--NH-- or --SO 2 --NH--group; n is 0 or 1; Y represents the residue to complete a condensed benzene ring; R 1 represents --OR 2 --, or ##STR12## R 2 represents hydrogen, an alkyl group having from 1 to 22 carbon atoms, or a cycloalkyl or aryl group; the said alkyl, cycloalkyl and aryl groups may in turn be substituted; R 3 represents one of the residues given under the definition for R 2 or an acyl group derived from aliphatic or aromatic carboxylic or sulphonic acids; R 4 represents hydrogen or a substituted or unsubstituted alkyl group having from 1 to 22 carbon atoms; and in which R 1 and/or a substituent on the condensed benzene ring which is completed by Y represents or contains a residue which confers diffusion resistance.
Claim 3
Dependent Claim 64 words
The process as claimed in claim 1 in which the condensed benzene ring which is completed by Y contains one or more identical or different substituents selected from the group consisting of halogen, alkyl having up to 22 carbon atoms, aryl, aralkyl, cycloalkyl, alkoxy, aralkoxy, hydroxyl, dialkylamino, acylamino, acyl, cyano, sulfo, carboxyl, sulfamoyl, carbamoyl and residues for completing a condensed carbocyclic or heterocyclic ring.
Claim 4
Dependent Claim 24 words
The process as claimed in claim 2 in which the condensed benzene ring completed by Y is substituted by a methoxy or ethoxy group.

References Cited (Backward Citations)

DE2505248A1 Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1982-12-17 1983-06-18 1983-12-18 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1986-12-17 1987-06-18 1987-12-18 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1990-12-17 1991-06-18 1991-12-18 $7700.00 Window Closed / Lapsed

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag