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US4052212A Expired / Lapsed US ⏱️ 0.0 years remaining

Photographic silver halide emulsion containing 2-equivalent cyan coupler

Assignee: Konica Minolta Inc
•
Filing: 1975-02-05
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Granted: 1977-10-04
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Expires: 1995-02-05
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Abstract

Abstract Cyan couplers of the 2-equivalent type, useful in photography are described. These compounds are characterized in that they have at least one divalent group of the formula, --OCH 2 CO--, in the molecule with a split-off group at the methoxy site of said divalent radical. Photographic materials and color developers incorporating these couplers are also described.

Inventors

  • 👤 Hidetaka Deguchi
  • 👤 Hajime Wada
  • 👤 Takaya Endo
  • 👤 Shoji Kikuchi
  • 👤 Haruo Hori

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-28 08:30
CPC Classifications
C; C07; C07D; C07D295/00; C07D295/16; C07D295/18; C07D295/182; C07D295/192; G; G03; G03C; G03C7/00; G03C7/30; G03C7/305; G03C7/30511; G03C7/30517; G03C7/30523

Claims Analysis

Total Claims: 6
Claim 1
Independent Claim 336 words
A process for forming a cyan dye image, which comprises bringing a 2-equivalent type cyan coupler into contact with exposed silver halide crystals in the presence of a phenylenediamine type developing agent for said silver halide crystals, said 2-equivalent cyan coupler having the general formula: A (OCH.sub.2 CO -- Y).sub.n or (A' -- OCH.sub.2 CO).sub.m --Y' wherein A and A' each represent, at the active point of the cyan coupler, a cyan coupler residue, which has the general formula: ##STR68## wherein R 1 represents a hydrogen atom, a halogen atom, a saturated or unsaturated, aliphatic or cycloaliphatic hydrocarbon group, --O--R 4 or --S-R 4 (where R 4 represents a said hydrocarbon group), r is 1 to 3 and q is 1 to 5 and if r or q is more than 1 the R 1 groups may be the same or different; and each of R 2 and R 3 independently represents a saturated or unsaturated, aliphatic or cycloaliphatic hydrocarbon group, an aryl group, a heterocyclic group or hydrogen atom or R 2 and R 3 together with the nitrogen atom to which they are attached form a heterocyclic group; Y represents a heterocyclic group, an alkoxy group, a phenoxy group, a naphthoxy group, an aliphatic hydrocarbon amino group, a heterocyclic amino group and a mercapto group, which groups also include those having substituents which are selected from halogen, nitro, hydroxyl, carboxyl, amino, sulfo, alkyl, alkenyl, aryl, heterocyclic, alkoxy, aryloxy, arylthio, arylazo, acylamino, carbamoyl, ester, acyl, acyloxy, sulfonamide, sulfamoyl, sulfonyl, morpholino, piperazyl and imidazolyl groups; Y' is an m-valent group selected from the group consisting of a heterocyclic group, an alkylenedioxy group, an arylenedioxy group, an alkylenediamino group, an arylenediamino group and a heterocyclic diamino group; wherein said Y' groups also include those having substituents which are selected from halogen, nitro, hydroxyl, carboxyl, amino, sulfo, alkyl, alkenyl, aryl, heterocyclic, alkoxy, aryloxy, arylthio, arylazo, acylamino, carbamoyl, ester, acyl, acyloxy, sulfonamide, sulfamoyl, sulfonyl, morpholino, piperazyl and imidazolyl groups; and n is 1 or 2 and m is 2.
Claim 2
Dependent Claim 336 words
A process for forming a cyan dye image, which comprises bringing a 2-equivalent type cyan coupler into contact with exposed silver halide crystals in the presence of a phenylenediamine type developing agent for said silver halide crystals, said 2-equivalent cyan coupler having the general formula: A (OCH.sub.2 CO -- Y).sub.n or (A' -- OCH.sub.2 CO).sub.m --Y' wherein A and A' each represent, at the active point of the cyan coupler, a cyan coupler residue, which has the general formula: ##STR68## wherein R 1 represents a hydrogen atom, a halogen atom, a saturated or unsaturated, aliphatic or cycloaliphatic hydrocarbon group, --O--R 4 or --S-R 4 (where R 4 represents a said hydrocarbon group), r is 1 to 3 and q is 1 to 5 and if r or q is more than 1 the R 1 groups may be the same or different; and each of R 2 and R 3 independently represents a saturated or unsaturated, aliphatic or cycloaliphatic hydrocarbon group, an aryl group, a heterocyclic group or hydrogen atom or R 2 and R 3 together with the nitrogen atom to which they are attached form a heterocyclic group; Y represents a heterocyclic group, an alkoxy group, a phenoxy group, a naphthoxy group, an aliphatic hydrocarbon amino group, a heterocyclic amino group and a mercapto group, which groups also include those having substituents which are selected from halogen, nitro, hydroxyl, carboxyl, amino, sulfo, alkyl, alkenyl, aryl, heterocyclic, alkoxy, aryloxy, arylthio, arylazo, acylamino, carbamoyl, ester, acyl, acyloxy, sulfonamide, sulfamoyl, sulfonyl, morpholino, piperazyl and imidazolyl groups; Y' is an m-valent group selected from the group consisting of a heterocyclic group, an alkylenedioxy group, an arylenedioxy group, an alkylenediamino group, an arylenediamino group and a heterocyclic diamino group; wherein said Y' groups also include those having substituents which are selected from halogen, nitro, hydroxyl, carboxyl, amino, sulfo, alkyl, alkenyl, aryl, heterocyclic, alkoxy, aryloxy, arylthio, arylazo, acylamino, carbamoyl, ester, acyl, acyloxy, sulfonamide, sulfamoyl, sulfonyl, morpholino, piperazyl and imidazolyl groups; and n is 1 or 2 and m is 2.
Claim 3
Dependent Claim 28 words
A process as claimed in claim 1, wherein the cyan coupler is present in the exposed light-sensitive silver halide photographic emulsion layer of a light-sensitive color photographic material.
Claim 4
Dependent Claim 24 words
A process as claimed in claim 1, wherein the cyan coupler is present in a color developer containing the phenylenediamine type color developing agent.
Claim 5
Dependent Claim 27 words
A light-sensitive silver halide color photographic material having a support and thereon a light-sensitive silver halide emulsion layer containing the photographic 2-equivalent cyan coupler of claim 1.
Claim 6
Dependent Claim 28 words
A color developer for developing exposed light-sensitive silver halide color photographic material, which comprises a phenylenediamine type developing agent and the photographic 2-equivalent cyan coupler of claim 1.

References Cited (Backward Citations)

US2772161A Cited
US3432521A Cited
US3516831A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1980-10-03 1981-04-04 1981-10-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1984-10-03 1985-04-04 1985-10-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1988-10-03 1989-04-04 1989-10-04 $7700.00 Window Closed / Lapsed

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