GB402458A - Improvements in photographic sensitisers - Google Patents
Improvements in photographic sensitisersInfo
- Publication number
- GB402458A GB402458A GB15678/32A GB1567832A GB402458A GB 402458 A GB402458 A GB 402458A GB 15678/32 A GB15678/32 A GB 15678/32A GB 1567832 A GB1567832 A GB 1567832A GB 402458 A GB402458 A GB 402458A
- Authority
- GB
- United Kingdom
- Prior art keywords
- dyestuffs
- methyl
- naphthothio
- naphthothiazoles
- naphthothiazole
- 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
Links
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01K—MEASURING TEMPERATURE; MEASURING QUANTITY OF HEAT; THERMALLY-SENSITIVE ELEMENTS NOT OTHERWISE PROVIDED FOR
- G01K5/00—Measuring temperature based on the expansion or contraction of a material
- G01K5/28—Measuring temperature based on the expansion or contraction of a material the material being a gas
- G01K5/30—Measuring temperature based on the expansion or contraction of a material the material being a gas the gas displacing a liquid column
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/08—Sensitivity-increasing substances
- G03C1/10—Organic substances
- G03C1/12—Methine and polymethine dyes
- G03C1/14—Methine and polymethine dyes with an odd number of CH groups
- G03C1/18—Methine and polymethine dyes with an odd number of CH groups with three CH groups
Landscapes
- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- General Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Abstract
Carbocyanine dyestuffs suitable for sensitizing silver halide emulsions are obtained by condensing a quaternary salt of a 2-methyl -a -naphthothiazole containing a nuclear alkyloxy group with an alkyl ester of ortho acetic acid. The dyestuffs may be added to the emulsion at any step of its production in alcoholic solution. In an example 1 - methyl - 6 - methoxy - a - naphthothiazole ethyliodide is condensed with ethyl orthoacetate. The halides, perchlorates, para toluenesulphonates, alkylosulphates and nitrates of the dyestuffs are mentioned. The naphthothiazoles used as starting materials may be prepared by the known methods for the preparation of unsubstituted naphthothiazoles. The Specification as open to inspection under Sect. 91 comprises also the production and use as photographic sensitizers of carbocyanine dyestuffs derived from a 2-methyl derivative of any substituted a or b naphthothiazole quaternary salt. The nuclear substituted alkyl, halogen, amino and substituted amino, e.g., alkyl, aryl and acyl amino, derivatives of the naphthothiazoles are mentioned. In further examples the following dyestuffs are prepared: 1 : 1<1>-diethyl - 5 : 5<1> - diethoxy - b - naphthothio - meso-ethylcarbocyanine-bromide, 1 : 1<1> : 5 : 5<1> - tetramethyl - a - naphthothio - meso - methyl - carbocyaninebromide, 1 : 1<1> - dimethyl - 5 : 5<1> - diethoxy - a - naphthothio - meso - methylcarbocyaninebromide, 1 : 1<1> - diethyl - 5 : 5<1> - dimethoxy - a - naphthothiocarbocyaninebromide and 1 : 1<1> - diethyl - 6 : 6<1> - dimethoxy - a - naphthothiocarbocyanine. This subject-matter does not appear in the Specification as accepted.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE402458X | 1931-06-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB402458A true GB402458A (en) | 1933-12-04 |
Family
ID=6411538
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB15678/32A Expired GB402458A (en) | 1931-06-05 | 1932-06-02 | Improvements in photographic sensitisers |
Country Status (3)
Country | Link |
---|---|
BE (1) | BE388884A (en) |
FR (2) | FR402458A (en) |
GB (1) | GB402458A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2447332A (en) * | 1944-05-18 | 1948-08-17 | Eastman Kodak Co | Trimethine cyanine dyes |
US2476669A (en) * | 1944-05-18 | 1949-07-19 | Eastman Kodak Co | Production of thiazoles and selenazoles with fused-on rings |
US2694716A (en) * | 1951-10-17 | 1954-11-16 | Eastman Kodak Co | Polymethylene-bis-benzothiazolium salts |
-
0
- BE BE388884D patent/BE388884A/xx unknown
-
1909
- 1909-04-27 FR FR402458D patent/FR402458A/en not_active Expired
-
1932
- 1932-06-02 GB GB15678/32A patent/GB402458A/en not_active Expired
- 1932-06-03 FR FR738121D patent/FR738121A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2447332A (en) * | 1944-05-18 | 1948-08-17 | Eastman Kodak Co | Trimethine cyanine dyes |
US2476669A (en) * | 1944-05-18 | 1949-07-19 | Eastman Kodak Co | Production of thiazoles and selenazoles with fused-on rings |
US2694716A (en) * | 1951-10-17 | 1954-11-16 | Eastman Kodak Co | Polymethylene-bis-benzothiazolium salts |
Also Published As
Publication number | Publication date |
---|---|
FR402458A (en) | 1909-10-09 |
FR738121A (en) | 1932-12-21 |
BE388884A (en) |
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