GB519208A - Improvements in or relating to colour photography - Google Patents
Improvements in or relating to colour photographyInfo
- Publication number
- GB519208A GB519208A GB2716638A GB2716638A GB519208A GB 519208 A GB519208 A GB 519208A GB 2716638 A GB2716638 A GB 2716638A GB 2716638 A GB2716638 A GB 2716638A GB 519208 A GB519208 A GB 519208A
- Authority
- GB
- United Kingdom
- Prior art keywords
- groups
- amino
- substituted
- hydroxy
- atoms
- 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
- 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
- G03C7/00—Multicolour photographic processes or agents therefor; Regeneration of such processing agents; Photosensitive materials for multicolour processes
- G03C7/30—Colour processes using colour-coupling substances; Materials therefor; Preparing or processing such materials
- G03C7/32—Colour coupling substances
- G03C7/34—Couplers containing phenols
- G03C7/344—Naphtholic couplers
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Cosmetics (AREA)
Abstract
519,208. 1 - Hydroxy - 2 - napthoylanhilides. KENDALL, J. D.,' and COLLINS, R. B. Sept. 17, 1938, No. 27166. Drawings to Specification. [Class 2 (iii)] [Also in Group XX] Compound of the general formula where R is a phenyl group substituted by one chlorine atom, two chlorine atoms, one bromine atom, two bromine atoms, or one chlorine atom and one bromine atom,.and where X is hydrogen, chlorine, or bromine, are prepared by condensing a 1-hydroxy-2-naphthoylhalide (which may be unsubstituted or substituted in the 4- position by a chlorine or bromine atom) with a chloraniline, dichloraniline, bromaniline, dibromaniline, or chlorbromaniline. The compounds prepared from o- and p-chlor-and bromanilines and 2:4-dichloraniline are referred to. The Provisional Specification refers to colour formers of the general formula while R1 and R2represent either the same or different atoms or groups consisting of hydrogen atoms, alky groups such as methyl, ethyl, or propyl, aryl groups such as phenyl, aralkyl groups such as benzyl, heterocyclic groups such as thiazole, thiazoline, oxazole, oxazoline, selenazole, selenazoline, pyridine, quinoline, indolenine, diazole or diazine such as pyrimidine, thiodiazole, or quinazoline, benzthiazole, naphthathiazole, and anthrathiazole, or a single cyclic grouping such as piperidine, pyrazole, indole, or N-alkyldihydrobenzthiazole and X represents hydrogen or a halogen atom. The groups R1 and R2may be substituted by halogen atoms or amino, substituted, amino, nitro, hydroxy, alkoxy, or oxyalkyl groups. The naphthalene nucleus may be substituted in any of the 3-, 5-, 6-, 7-, or 8- positions with halogen atoms or alkyl, aryl, amino, substituted amino, nitro, hydroxy, alkoxy, carbalkoxy, or oxyalkyl groups. 1-hydroxy-2-naphthoylchloride may be condensed with ammonia, aniline, monomethylaniline, p-nitroaniline, oc- or #-naphthylamine, ethyloc-naphthylamine, o- or p-anisidine, p-aminophenol, p-amino-. benzoic acid, 2:6-dibrom-4-aminophenol, maminoacetophenone, m - aminobenzaldehyde, ethyl - p -aminobenzoate, 1 - amino - 5 -ethoxybenzthiazole, 1-iminodihydrobenzthiazole, or 2-imino-1-methyl-dihydroquinoline.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2716638A GB519208A (en) | 1938-09-17 | 1938-09-17 | Improvements in or relating to colour photography |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2716638A GB519208A (en) | 1938-09-17 | 1938-09-17 | Improvements in or relating to colour photography |
Publications (1)
Publication Number | Publication Date |
---|---|
GB519208A true GB519208A (en) | 1940-03-19 |
Family
ID=10255274
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2716638A Expired GB519208A (en) | 1938-09-17 | 1938-09-17 | Improvements in or relating to colour photography |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB519208A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2521908A (en) * | 1947-03-13 | 1950-09-12 | Eastman Kodak Co | 1-hydroxy-2-naphthamide colored couplers |
US3005709A (en) * | 1958-01-13 | 1961-10-24 | Gen Aniline & Film Corp | Photographic couplers containing acylamino groups |
US4178183A (en) * | 1978-07-27 | 1979-12-11 | Eastman Kodak Company | Thiazolyl coupler compositions and photographic elements suited to forming integral sound tracks |
US4208210A (en) * | 1974-12-19 | 1980-06-17 | Fuji Photo Film Co., Ltd. | Process for forming an optical soundtrack |
US5030544A (en) * | 1984-09-28 | 1991-07-09 | Agfa-Gevaert, N.V. | Photographic elements comprising thiazolyl couplers capable of forming infrared-absorbing dyes for integral sound track |
-
1938
- 1938-09-17 GB GB2716638A patent/GB519208A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2521908A (en) * | 1947-03-13 | 1950-09-12 | Eastman Kodak Co | 1-hydroxy-2-naphthamide colored couplers |
US3005709A (en) * | 1958-01-13 | 1961-10-24 | Gen Aniline & Film Corp | Photographic couplers containing acylamino groups |
US4208210A (en) * | 1974-12-19 | 1980-06-17 | Fuji Photo Film Co., Ltd. | Process for forming an optical soundtrack |
US4178183A (en) * | 1978-07-27 | 1979-12-11 | Eastman Kodak Company | Thiazolyl coupler compositions and photographic elements suited to forming integral sound tracks |
US5030544A (en) * | 1984-09-28 | 1991-07-09 | Agfa-Gevaert, N.V. | Photographic elements comprising thiazolyl couplers capable of forming infrared-absorbing dyes for integral sound track |
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