GB615431A - Improvements in and relating to colour sensitised silver-halide emulsions and photographic materials coated therewith - Google Patents

Improvements in and relating to colour sensitised silver-halide emulsions and photographic materials coated therewith

Info

Publication number
GB615431A
GB615431A GB25125/45A GB2512545A GB615431A GB 615431 A GB615431 A GB 615431A GB 25125/45 A GB25125/45 A GB 25125/45A GB 2512545 A GB2512545 A GB 2512545A GB 615431 A GB615431 A GB 615431A
Authority
GB
United Kingdom
Prior art keywords
carboxybenzyl
prepared
bromide
chloro
chloride
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
GB25125/45A
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.)
Gevaert Photo Producten NV
Original Assignee
Gevaert Photo Producten NV
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 Gevaert Photo Producten NV filed Critical Gevaert Photo Producten NV
Publication of GB615431A publication Critical patent/GB615431A/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
    • G03C1/12Methine and polymethine dyes
    • G03C1/24Styryl dyes

Abstract

3-Chloro-4-methylbenzoyl chloride is prepared by heating together 3-chloro-p-methylbenzoic acid and thionyl chloride. 3-Chloro-4-chloromethylbenzoyl chloride is prepared by chlorinating 3-chloro-4-methylbenzoyl chloride in sunlight. 0-Chloro-p-carboxybenzylchloride is prepared by refluxing 3-chloro-4-chloromethylbenzoyl chloride with water. 2-Methylbenzoxazole-p-carboxybenzyl bromide is prepared by heating together 2-methylbenzoxazole and p-carboxybenzyl bromide. 2 : 4-Dimethylthiazole - p - carboxybenzyl bromide and 2 - methylbenzthiazole - p - carboxybenzyl bromide are similarly prepared. 2-b -Anilinovinylbenzoxazole-p-carboxybenzyl bromide is prepared by heating together 2-methylbenzoxazole - p - carboxybenzyl bromide and dipenylformamidine. 2-b -Anilinovinylbenzoxazole benzyl bromide is similarly prepared.ALSO:In a cyanine or styryl dye, the nitrogen atom of at least one heterocyclic nucleus has attached thereto substituted in m- or p-position an aralkyl group substituted by one or more carboxyl groups. The dyes may be formed from quaternary salts derived from a heterocyclic nitrogen base and m-carboxybenzyl chloride, or o-chloro-p-carboxybenzyl chloride. In example (1), a carbocyanine is obtained by reacting in acetic anhydride 2-methylbenzoxazole p-carboxybenzyl bromide and ethyl orthoformate. In example (2), a carbocyanine is prepared by reacting 2 : 4-dimethylthiazole p-carboxybenzyl bromide with 2-b -anilinovinylbenzoxazole p-carboxybenzyl bromide. In example (3), a pseudocyanine is prepared by reacting 2 - methylmercaptoquinoline ethobromide with 2-methylbenzthiazole p-carboxybenzyl bromide. In example (4), a styryl dye is prepared by reacting p-dimethylaminobenzaldehyde with 2 : 4-dimethylthiazole p-carboxybenzyl bromide. In example (5), a carbocyanine is prepared by reacting 2-methylbenzoxazole p-carboxybenzyl bromide with 2-b -anilinovinylbenzoxazole benzyl bromide.
GB25125/45A 1942-06-06 1945-09-27 Improvements in and relating to colour sensitised silver-halide emulsions and photographic materials coated therewith Expired GB615431A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE238344X 1942-06-06

Publications (1)

Publication Number Publication Date
GB615431A true GB615431A (en) 1949-01-06

Family

ID=5903524

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25125/45A Expired GB615431A (en) 1942-06-06 1945-09-27 Improvements in and relating to colour sensitised silver-halide emulsions and photographic materials coated therewith

Country Status (5)

Country Link
BE (1) BE450888A (en)
CH (1) CH238344A (en)
FR (1) FR895151A (en)
GB (1) GB615431A (en)
NL (1) NL60086C (en)

Also Published As

Publication number Publication date
NL60086C (en) 1947-10-15
CH238344A (en) 1945-07-15
BE450888A (en) 1943-07-31
FR895151A (en) 1945-01-17

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