GB650631A - Diazotype photoprinting layers having organic esters and nitriles containing an active methylene group as azo coupling components - Google Patents
Diazotype photoprinting layers having organic esters and nitriles containing an active methylene group as azo coupling componentsInfo
- Publication number
- GB650631A GB650631A GB14501/48A GB1450148A GB650631A GB 650631 A GB650631 A GB 650631A GB 14501/48 A GB14501/48 A GB 14501/48A GB 1450148 A GB1450148 A GB 1450148A GB 650631 A GB650631 A GB 650631A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethyl
- zncl
- double salt
- methyl
- benzenediazonium 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
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
- G03C1/00—Photosensitive materials
- G03C1/52—Compositions containing diazo compounds as photosensitive substances
- G03C1/58—Coupling substances therefor
Abstract
650,631. Photographic diazotype material. GENERAL ANILINE & FILM CORPORATION. May 28, 1948, No. 14501. Convention date, Aug. 6, 1947. [Class 98 (ii)] Diazotype material comprises a light-sensitive diazonium salt of a p-diamine of the benzene series and an azo-coupling component which is an organic ester or nitrile of the general formula R-CH 2 -CO-R<SP>1</SP>, wherein R is an acyl, carbalkoxy, nitrile, or carbiminoalkoxy group and R<SP>1</SP> an alkoxy, carbalkoxy, aryl, or heterocyclic group, or is sodium ethyl oxalacetate. Other couplers specified are ethyl and methyl acetoacetate, ethyl malonate, ethyl benzoylacetate, ethyl cyanacetate, ethyl acetone dicarboxylate, methyl and ethyl acetone oxalate, methyl cyanpyruvate, # - cyanacetophenone, cyanacetylcoumarone, 1-cyanacetyl-2- naphthol methyl ether, 2-cyanacetyl-3-oxythionaphthene, and ethyl (#-ethoxy: #-imino)- propionate. Numerous diazo compounds are specified, and the sensitizing solution may contain other couplers, stabilizers such as citric and phosphoric acids and thiourea, swelling agents for cellulose ester (e.g. acetate) supports such as isopropanol, and shade intensifiers such as nickel sulphate. The support may be paper, transparentized paper, or cellulose acetate. In examples, transparentized paper is coated with an aqueous ethyl alcohol solution containing thiourea, citric acid, phosphoric acid, zinc chloride, and (1) ethyl acetoacetate and N- methyl: N - # - hydroxyethylamino - p - benzenediazonium chloride-ZnCl 2 double salt; (2) ethyl acetoacetate and N-phenylamino-p-benzenediazonium acid sulphate; (3) methyl acetoacetate and N: N-diethylamino-p-benzenediazonium chloride-ZnCl 2 double salt; (5) ethyl cyanacetate and 1-(N-ethylamino)-2-methyl-4- benzenediazonium chloride-ZnCl 2 double salt; (6) ethyl cyanacetate and 1-benzoylamino-2 :5- diethoxy - 4 - benzenediazonium chloride - ZnCl 2 double salt; (7) ethyl malonate and N-ethylamino - p - benzenediazonium chloride - CdCl 2 double salt; (8) ethyl acetoacetate, 2 : 3- dihydroxynaphthalene - 6 - sulphonic acid, 2 : 3 - dihydroxynaphthalene, and N : N - diethylamino - p - benzenediazonium chloride - ZnCl 2 double salt; (9) ethyl-(#-ethoxy: #-imino)- propionate and N - ethyl : N - # - hydroxyethylamino - p - benzenediazonium chloride- ZnCl 2 double salt; (10) ethyl sodium acetone oxalate and N'- methyl : N - # - hydroxyethylamino - p - benzenediazonium chloride - ZnCl 2 double salt; (11) #-cyanacetophenone and N: N - dimethylamino - p - benzenediazonium chloride - ZnCl 2 double salt ; and (12) 2 - w - cyanaceto - 3 - oxythionaphthene and 1 - (N - ethylamino) - 2 - methyl - 4 - benzenediazonium chloride-ZnCl 2 double salt.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US766874A US2552355A (en) | 1947-08-06 | 1947-08-06 | Diazotype layers having organic esters and nitriles containing an active methylene group as azo components |
Publications (1)
Publication Number | Publication Date |
---|---|
GB650631A true GB650631A (en) | 1951-02-28 |
Family
ID=25077785
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB14501/48A Expired GB650631A (en) | 1947-08-06 | 1948-05-28 | Diazotype photoprinting layers having organic esters and nitriles containing an active methylene group as azo coupling components |
Country Status (2)
Country | Link |
---|---|
US (1) | US2552355A (en) |
GB (1) | GB650631A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2658889A (en) * | 1950-08-22 | 1953-11-10 | Hoffmann La Roche | Substituted phenylazomalononitriles |
NL251055A (en) * | 1959-04-29 | |||
US3522048A (en) * | 1965-12-09 | 1970-07-28 | Gaf Corp | Two-component heat developing diazotypes |
US3971663A (en) * | 1974-04-11 | 1976-07-27 | Bialczak Edward C | Light-sensitive diazotype with yellow diazo couplers |
JPS50137721A (en) * | 1974-04-22 | 1975-11-01 | ||
US4743524A (en) * | 1986-10-17 | 1988-05-10 | Andrews Paper & Chemical Co., Inc. | Diazotype composition with a non-migrating yellow coupler of controlled coupling energy |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE343949A (en) * | 1926-07-09 | |||
GB310773A (en) * | 1928-01-30 | 1929-04-30 | British Celanese | Improvements in the production of pattern and like effects upon materials made of orcontaining cellulose esters |
NL35939C (en) * | 1932-07-02 | |||
US2113330A (en) * | 1935-02-27 | 1938-04-05 | Eastman Kodak Co | Color-forming developers |
GB478933A (en) * | 1936-04-23 | 1938-01-24 | Kodak Ltd | Improvements in and relating to colour forming developers and processes of colour development |
US2115394A (en) * | 1936-10-14 | 1938-04-26 | Eastman Kodak Co | Photographic color-forming compounds |
GB525765A (en) * | 1939-02-28 | 1940-09-04 | Kodak Ltd | Improvements in and relating to colour forming developers and processes of colour development |
US2436007A (en) * | 1944-05-12 | 1948-02-17 | Ilford Ltd | Dye intermediates for colour photography |
US2435661A (en) * | 1946-06-25 | 1948-02-10 | Carl C Weathers | Pencil sharpener |
-
1947
- 1947-08-06 US US766874A patent/US2552355A/en not_active Expired - Lifetime
-
1948
- 1948-05-28 GB GB14501/48A patent/GB650631A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
US2552355A (en) | 1951-05-08 |
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