US4200466A
Expired / Lapsed
US
⏱️ 0.0 years remaining
Light-sensitive silver halide photographic materials
Assignee: Konica Minolta Inc
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Filing: 1978-02-01
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Granted: 1980-04-29
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Expires: 1998-02-01
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##
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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 |