GB560082A - Improvements in sensitive photographic emulsions - Google Patents

Improvements in sensitive photographic emulsions

Info

Publication number
GB560082A
GB560082A GB5716/42A GB571642A GB560082A GB 560082 A GB560082 A GB 560082A GB 5716/42 A GB5716/42 A GB 5716/42A GB 571642 A GB571642 A GB 571642A GB 560082 A GB560082 A GB 560082A
Authority
GB
United Kingdom
Prior art keywords
bromide
nitrogen atom
ethyl
perchlorate
phenylethyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB5716/42A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kodak Ltd
Original Assignee
Kodak Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kodak Ltd filed Critical Kodak Ltd
Publication of GB560082A publication Critical patent/GB560082A/en
Expired legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/06Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/08Sensitivity-increasing substances
    • G03C1/10Organic substances
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/06Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/08Sensitivity-increasing substances
    • G03C1/10Organic substances
    • G03C1/12Methine and polymethine dyes

Landscapes

  • Physics & Mathematics (AREA)
  • Chemical & Material Sciences (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

A light-sensitive silver bromide, chlorobromide, bromiodide, or chloro-bromiodide emulsion is sensitized by incorporating in the emulsion up to 4 grams per gram-mole of silver halide of a non-surface-active cyclammonium quaternary salt which contains only carbon and nitrogen atoms in the heterocyclic nucleus embodying the cyclammonium nitrogen atom, and which contains not more than one quaternary nitrogen atom, and in which the heterocyclic nucleus does not bear a substituent containing an aliphatic unsaturated linkage conjugated through the nucleus with the quaternary nitrogen atom, or by incorporating in the emulsion a non-surface-active cyclammonium non-quaternary salt in which only one hydrogen atom is attached directly to the cyclammonium nitrogen atom and only two of the remaining valencies of the nitrogen atom are employed in the formation of the cyclic nucleus, and which contains only carbon and nitrogen atoms in the cyclic nucleus embodying the cyclammonium nitrogen atom and contains at the most only one quaternary nitrogen atom, which if present does not form part of a cyclic nucleus bearing a substituent containing an aliphatic unsaturated linkage conjugated through the nucleus with the quaternary nitrogen atom. The cyclammonium quaternary salt may be one in which the quaternary nitrogen atom is the nitrogen atom of a pyridine nucleus, e.g. pyridine, quinoline, isoquinoline, and benzoquinoline quaternary salts, or one in which the quaternary nitrogen atom is the nitrogen atom of a reduced pyridine nucleus, e.g. quaternary salts of N-alkyl piperidines, or one in which the quaternary nitrogen atom is the nitrogen atom of a benzimidazole or indazole nucleus. Aralkyl quaternary (e.g. b -phenylethyl and g -phenyl-n-propyl) salts are preferably employed, and may carry substituents, e.g. alkyl, alkoxy, arylmercapto, carboxyalkyl, halogen, carboxy, or thioalkyl, but usually not nitro, sulphonic acid, sulphonate, and like groups. The salt is incorporated in the emulsion in the form of an aqueous or methyl alcohol solution, e.g. in amount between about 0.2 and 4 grams of salt per gram-mole of silver halide. The salt may be incorporated in the emulsion before, simultaneously with, or after a sensitizing dye. Sensitizing dyes are incorporated in methyl or ethyl alcohol or acetone solution. The salts depress the sensitivity produced by acid sensitizing dyes (containing sulphonic, sulphinic, or carboxylic or like groups or salt forms thereof), and non-acid sensitizing dyes are preferably used. A supersensitizing combination (e.g. of 3 : 31-diethyl-9-methylthiacarbocyanines with 21-cyanines) of sensitizing dyes may be used. The use of merocyanine sensitizing dyes is referred to. The cyclammonium salts are preferably added after washing the emulsions and prior to coating. Examples specified are a -picoline-b -phenylethyl bromide, g -phenylmercaptopyridine ethiodide, 2-methylquinoline methiodide, 2-methoxyquinoline ethobromide, N-b -phenylethylpyridinium bromide, N - ethyl - 4 - phenylmercaptopyridinium iodide, N-g -phenyl-n-propyl-a -picolinium bromide, N-b -phenylethyl-a -picolinium iodide, N-b -phenylethyl-b -picolinium bromide, N - b - phenylethyl - g - picolinium bromide, N-ethyl-6-methylquinolinium iodide, N-ethyl-6-methoxyquinolinium bromide, N - b - phenylethylquinolinium bromide, N-ethylquinaldinium bromide, N - b - hydroxyethyllepidinium perchlorate, N - b - acetoxyethyllepidinium perchlorate, N - benzylpyridinium bromide, N - cinnamylpyridinium perchlorate, N - p - chlorobenzylpyridinium perchlorate, N - cinnamyl - a - picolinium perchlorate, N - b - phenylethyl - 3 - carbethoxypyridinium bromide, N - b - phenylethyl - quinaldinium bromide, N - b - phenylethylisoquinolinium bromide, N-benzyl-a -picolinium bromide, N-b -hydroxyethylquinaldinium perchlorate, N - b - phenoxyethylquinaldinium perchlorate, N-benzyllepidinium perchlorate, N-phenacyl-lepidinium perchlorate, N - o - chlorobenzylpyridinium bromide, 4 - methylmercapto - N - phenylpyridinium p - toluenesulphonate, N - benzylquinaldinium bromide, N-methyl - N-g -phenyl-n - propylpiperidinium bromide, N-b -phenylethyl - lepidinium bromide, N - p - chlorophenyl-pyridinium bromide, N-methyl-a -picolinium iodide, N - methyl. - a - picolinium p - toluenesulphonate, N - b - phenoxyethyl - a - picolinium bromide, N - ethyl - 2 - piperidylquinolinium iodide, N - ethyl - 2 - b - naphthoxyquinolinium iodide, N - ethyl - 2 - b - hydroxyethylquinolinium iodide, N-benzylquinaldinium perchlorate, N - phenylpyridinium bromide, N - ethyl - g - phenylmercaptopyridinium p - toluenesulphonate, N - b - phenylethylpiperidinium bromide, N - methyl - N - b - phenylethylpiperidinium bromide, N-ethyl-2 : 6-dimethylpyridinium iodide, N-ethyl-2 : 4 : 6-trimethylpyridinium iodide, N-ethyl-4-ethylpyridinium bromide, N - b - phenylethylbenzimidazolium bromide, g -phenylmercaptopyridine ethiodide, 2-methylquinoline methiodide, 2 - methoxyquinoline ethiobromide and, 1-methyl-b -phenylethylindazolium p-toluenesulphonate. Numerous sensitizing dyes are referred to. The silver halide emulsion may have a gelatine, cellulose derivative, or resin binder, and may be carried on a cellulose nitrate or acetate, polyvinyl acetal resin, glass, metal, or paper support. N - (b - phenylethyl) - piperidinium bromide is prepared by heating piperidine with b -phenylethyl bromide. Specifications 454,687, 498,290, [Group XX], 513,170, 514,375, 557,178 and 558,710 are referred to.
GB5716/42A 1942-02-02 1942-04-28 Improvements in sensitive photographic emulsions Expired GB560082A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US429282A US2334864A (en) 1942-02-02 1942-02-02 Photographic emulsion

Publications (1)

Publication Number Publication Date
GB560082A true GB560082A (en) 1944-03-20

Family

ID=9801290

Family Applications (1)

Application Number Title Priority Date Filing Date
GB5716/42A Expired GB560082A (en) 1942-02-02 1942-04-28 Improvements in sensitive photographic emulsions

Country Status (5)

Country Link
US (1) US2334864A (en)
BE (1) BE467068A (en)
DE (1) DE857308C (en)
FR (1) FR942831A (en)
GB (1) GB560082A (en)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB615880A (en) * 1946-08-20 1949-01-12 John David Kendall Improvements in or relating to silver halide photographic emulsions
BE486662A (en) * 1948-01-13
US2784090A (en) * 1952-11-08 1957-03-05 Eastman Kodak Co Stabilization of emulsions sensitized with onium compounds
US3146102A (en) * 1960-08-22 1964-08-25 Eastman Kodak Co Photographic multicolor diffusion transfer process using dye developers
US3260597A (en) * 1960-12-02 1966-07-12 Eastman Kodak Co Photographic multicolor diffusion transfer process using dye developers and development arrestors
CA685877A (en) * 1961-03-27 1964-05-05 Canadian Kodak Co. Limited Photographic multicolor diffusion transfer process using dye developers
DE1240399B (en) * 1963-12-17 1967-05-11 Agfa Ag Non-spectrally sensitized silver halide emulsion with non-sensitizing quaternary cycloammonium salts
JPS51120223A (en) * 1975-04-14 1976-10-21 Konishiroku Photo Ind Co Ltd Halogenized silver color photosensitive materials
JPS59191032A (en) * 1983-04-13 1984-10-30 Fuji Photo Film Co Ltd Silver halide photosensitive material

Also Published As

Publication number Publication date
US2334864A (en) 1943-11-23
DE857308C (en) 1952-11-27
BE467068A (en)
FR942831A (en) 1949-02-18

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