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US4200466A Expired / Lapsed US ⏱️ 0.0 years remaining

Light-sensitive silver halide photographic materials

Assignee: Konica Minolta Inc
•
Filing: 1978-02-01
•
Granted: 1980-04-29
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Expires: 1998-02-01
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Abstract

Abstract A light-sensitive silver halide photographic material comprising a m-aminophenol type coupler of the structure particularly defined therein is disclosed, which can successfully yield an excellent image stable against oxidation.

Inventors

  • 👤 Mitsuto Fujiwhara
  • 👤 Syunji Matsuo
  • 👤 Mikio Kawasaki
  • 👤 Toyoaki Masukawa
  • 👤 Yutaka Kaneko

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-10-26 07:18
CPC Classifications
C; C07; C07D; C07D207/00; C07D207/02; C07D207/30; C07D207/34; C07D207/36; C07D207/40; C07D207/404; C07D207/408; C07D207/412; C07D209/00; C07D209/02; C07D209/44; C07D209/48; C07D257/00; C07D257/02; C07D257/04; G; G03; G03C; G03C7/00; G03C7/30; G03C7/305; G03C7/30511; G03C7/30517; G03C7/30523; G03C7/32; G03C7/34; G03C7/346

Claims Analysis

Total Claims: 5
Claim 1
Independent Claim 269 words
A light-sensitive silver halide photographic material comprising an m-aminophenol type coupler represented by the formula, ##STR133## wherein R 1 and R 2 individually represent a hydrogen atom, an alkyl group, an aryl group, an alkenyl group, or an aralkyl group; R 3 and R 4 individually represent a hydrogen atom, a halogen atom, a hydroxyl, an alkyl group, an alkoxy group, an alkylamido group, an arylamido group, an alkylsulfonamido group or an arylsulfonamido group; and X and Y individually represent a hydrogen atom, halogen atom or a group capable of being split off on the coupling reaction with an oxidation product of a primary amine type color developing agent, said group selected from the group consisting of sulfo and its salts, carboxyl and its salts, an alkoxy group, an aryloxy group, an alkylcarbonyloxy group, an alkylsulfonyloxy group, an arylcarbonyloxy group, an arylsulfonyloxy group, an alkylcarbamoyloxy group, an arylcarbamoyloxy group, a halogen-substituted alkylamido group, a halogen-substituted arylamido group, an alkylsulfonamido group, an arylsulfonamido grou, 5- or 6-membered imido-group, an arylthio group, an arylseleno group, an arylsulfonyl group, an arylazo group, or a 5- or 6-membered heterocyclic thio group containing in the molecular structure 1 to 4 nitrogen atoms, or one of X and Y is hydroxyl, mercapto, amino, an alkylamino group or an arylamino group, and the other is hydrogen atom, a halogen atom or a split-off group as defined above, said coupler not containing a color developing agent moiety in its molecular structure, whereby said coupler reacts with two molecules of an oxidation product of an aromatic primary amino color developing agent to form a neutral black dye image.
Claim 2
Dependent Claim 269 words
A light-sensitive silver halide photographic material comprising an m-aminophenol type coupler represented by the formula, ##STR133## wherein R 1 and R 2 individually represent a hydrogen atom, an alkyl group, an aryl group, an alkenyl group, or an aralkyl group; R 3 and R 4 individually represent a hydrogen atom, a halogen atom, a hydroxyl, an alkyl group, an alkoxy group, an alkylamido group, an arylamido group, an alkylsulfonamido group or an arylsulfonamido group; and X and Y individually represent a hydrogen atom, halogen atom or a group capable of being split off on the coupling reaction with an oxidation product of a primary amine type color developing agent, said group selected from the group consisting of sulfo and its salts, carboxyl and its salts, an alkoxy group, an aryloxy group, an alkylcarbonyloxy group, an alkylsulfonyloxy group, an arylcarbonyloxy group, an arylsulfonyloxy group, an alkylcarbamoyloxy group, an arylcarbamoyloxy group, a halogen-substituted alkylamido group, a halogen-substituted arylamido group, an alkylsulfonamido group, an arylsulfonamido grou, 5- or 6-membered imido-group, an arylthio group, an arylseleno group, an arylsulfonyl group, an arylazo group, or a 5- or 6-membered heterocyclic thio group containing in the molecular structure 1 to 4 nitrogen atoms, or one of X and Y is hydroxyl, mercapto, amino, an alkylamino group or an arylamino group, and the other is hydrogen atom, a halogen atom or a split-off group as defined above, said coupler not containing a color developing agent moiety in its molecular structure, whereby said coupler reacts with two molecules of an oxidation product of an aromatic primary amino color developing agent to form a neutral black dye image.
Claim 3
Dependent Claim 24 words
A light-sensitive silver halide photographic material according to claim 1 wherein R 1 , R 2 and R 3 individually represent a hydrogen atom.
Claim 4
Dependent Claim 24 words
A light-sensitive silver halide photographic material according to claim 2 wherein the primary amine type color developing agent is a p-phenylenediamine-type color developing agent.
Claim 5
Dependent Claim 188 words
A light-sensitive silver halide photographic material according to claim 1 comprising an m-amino phenol type coupler selected from the group consisting of N-Decyl-m-aminophenol ##STR134## N-Dodecyl-m-aminophenol ##STR135## N-Octadecenyl-m-aminophenol ##STR136## N-Octadecyl-m-aminophenol ##STR137## 3-(p-Dodecylbenzylamino)phenol ##STR138## 3-[4-(2,4-di-tert-Aminophenoxyacetamido)anilino]phenol ##STR139## 3-{[α-(Hexadecyloxycarbonyl)ethyl]amino}phenol ##STR140## N-[α-(Dodecylcarbamoyl)ethyl]-m-aminophenol ##STR141## N-[β-(Dodecylcarbamoyl)ethyl]-m-aminophenol ##STR142## N-{β-[2-Chloro-5-(2,4-di-tert-amylphenoxybutylamido)phenylcarbamoyl]ethyl}-m-aminophenol ##STR143## N-(4-Lauroylamidophenethyl)-m-aminophenol ##STR144## N-{4-[α-(2,4-di-tert-Amylphenoxy)propionamido]phenethyl}-m-aminopheno ##STR145## 4-Chloro-N-octadecyl-m-aminophenol ##STR146## 4-Sulfo-N-octadecyl-m-aminophenol ##STR147## N,N-Didodecyl-m-aminophenol ##STR148## N-Methyl-N-octadecyl-m-aminophenol ##STR149## N-{α-Carboxytridecyl}-m-aminophenol ##STR150## N-{β-[2-sulfo-5-(N-methyl-N-octadecylamino)phenylcarbamoyl]ethyl}-m-aminophenol ##STR151## 6-Chloro-N-octadecyl-m-aminophenol ##STR152## 5-Ethoxy-3-hexadecyl-m-aminophenol ##STR153## 5-Dodecyloxy-m-ethylaminophenol ##STR154## 5-Hydroxy-3-{N-[α-(hexadecyloxycarbonylethyl]amino}phenol ##STR155## 5-Benzoylamido-3-{α-(dodecylcarbamoyl)ethylamino}phenol ##STR156## 2-Acetamido-3-{α-(hexadecyloxycarbonyl)ethylamino}phenol ##STR157## 2-Benzensulfonylamido-3-dodecylaminophenol ##STR158## 2-Palmiticacidamido-3-N-ethylaminophenol ##STR159## 2,5-Dimethyl-3-N-oxtadecylaminophenol ##STR160## 2-Hydroxy-4-chloro-5-N-octadecylaminophenol ##STR161## 2,4,6-Trichloro-3-N-octadecylaminophenol ##STR162## 2,4-Disulfo-5-N-hexadecylaminophenol ##STR163## 4-Phenylthio-3-N-octadecylaminophenol ##STR164## 6-Phenylthio-3-N-octadecylaminophenol ##STR165## 2,4-Diphenylthio-5-{4-(2,4-di-tert-amylphenoxyacetamido)anilino}phenol ##STR166## 2-Chloro-4-phenylthio-5-[{β-(dodecylcarbamoyl)ethyl}amino]phenol ##STR167## 4-(1-Phenyltetrazolium-5-thio)-3-[β-(m-pentadecylphenoxy)ethylamino]phenol ##STR168## 2-Mercapto-5-N-octadecylaminophenol ##STR169## 4-Phenylseleno-3-N-octadecylaminophenol ##STR170## 4-Ethoxy-3-N-octadecylaminophenol ##STR171## 2-Chloroethoxy-5-N-octadecylaminophenol ##STR172## 2-Chloro-4-(iso-propylcarbamoylmethoxy)-5-N-octadecylaminophenol ##STR173## 4-(iso-Propylcarbamoylmethoxy)-3-N-octadecylaminophenol ##STR174## 2,4-Dichloro-3-methoxy-5-N-hexadecylaminophenol ##STR175## 4-Butoxycarbonylmethoxy-3-{[α-(hexadecyloxycarbonyl)ethyl]amino}phenol ##STR176## 4-(p-Carboxyphenoxy)-3-{[α-(p-dodecylphenylcarbamoyl)ethyl]amino}phenol ##STR177## 4-Benzoyloxy-3-N-dodecylaminophenol ##STR178## 4-Acetoxy-3-[(O-hexadecyloxyphenylcarbamoyl)methylamino]phenol ##STR179## 4-Perfluoropropyl-3-[(O-hexadecyloxyphenylcarbamoyl)methylamino]phenol ##STR180## 2-Phenoxy-5-N-octadecylaminophenol ##STR181## 4-Benzensulfonyloxy-3-N-octadecylaminophenol ##STR182## 2-Chloro-4-benzensulfonyloxy-5-N-octadecylaminophenol ##STR183## 2-Succimido-5-N-hexadecylaminophenol ##STR184## 4-Phthalimido-5-N-hexadecylaminophenol ##STR185## 4-(p-Benzensulfonylphenoxy)-3-N-octadecylaminophenol ##STR186## 4-Phenylsulfonylamido-3-N-octadecylaminophenol ##STR187## 4-Methanesulfonylamido-3-N-octadecylaminophenol ##STR188## 2-Phenylsulfonylamido-4-chloro-3-N-octadecylaminophenol ##STR189## 4-Trifluoroacetamido-3-N-dodecylaminophenol ##STR190## 2-Amino-5-N-hexadecylaminophenol ##STR191## 2-Anilino-5-N-octadecylaminophenol ##STR192## 2-Ethylamino-5-N-hexadecylaminophenol ##STR193## 4-Phenylsulfonyl-3-N-octadecylaminophenol ##STR194## 2-Octadecylsuccimido-5-γ-sulfopropylaminophenol sodium salt ##STR195## 4-Dodecylcarbamoylmethoxy-3-N-ethylaminophenol ##STR196## 4-Dodecylcarbamoylmethoxy-3-N-(ω-sulfopropylamino)phenol sodium salt ##STR197## 4-(p-Dodecylbenzensulfonyloxy)-3-N-(ω-sulfopropylamino)phenol sodium salt ##STR198## 2-Chloro-4-(o-dodecylphenyl)carbamoylmethoxy-5-N-carboxymethylaminophenol ##STR199## 2-(m-Palmiticacidamidophenylsulfonamido)-5-(N-methoxycarbonylmethylamino)phenol ##STR200## 4-[2-Chloro-{5-[d-dodecyloxycarbonyl)ethoxy]carbonyl}phenylazo]-3-(N-.gamma.-sulfopropylamino)phenol ##STR201## 4-Dodecylcarbamoylmethoxy-3-aminophenol ##STR202## 4-(p-Dodecylbenzensulfonyloxy)-3-N-ethylaminophenol ##STR203## 4-p-Methoxyphenylcarbamoyloxy-3-N-octadecylaminophenol ##STR204## N-[β-(Dodecylcarbamoyl)ethyl]-m-aminophenol ##STR205## N-(4-Lauroylamidophenethyl)-m-aminophenol ##STR206## 4-Chloro-3-(N,N-di-n-octadecylamino)phenol ##STR207## 4-{(3-Lauroylamidophenyl)carbamoyloxy}-3-(N-γ-sulfopropyl)aminophenol ##STR208## 4-{(3-Lauroylamidophenyl)carbamoylmethoxy}-m-aminophenol ##STR209## 4-(Dodecylbenzensulfonyloxy)-m-aminophenol ##STR210## 4-(Dodecylbenzensulfonylamino)-m-aminophenol ##STR211## 4-(Dodecylcarbamoylmethoxy)-3-(N-carboxymethyl)aminophenol ##STR212## 4-(Dodecylcarbamoylmethoxy)-3-(ethyloxycarbonylmethyl)-aminophenol ##STR213##

References Cited (Backward Citations)

US2181944A Cited
US2728660A Cited
US3222176A Cited
US3516831A Cited
US3622629A Cited
US3674490A Cited
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USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1983-04-29 1983-10-29 1984-04-29 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1987-04-29 1987-10-29 1988-04-29 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1991-04-29 1991-10-29 1992-04-29 $7700.00 Window Closed / Lapsed

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