GB726755A - Improvements in or relating to photographic diazotype materials - Google Patents
Improvements in or relating to photographic diazotype materialsInfo
- Publication number
- GB726755A GB726755A GB21183/53A GB2118353A GB726755A GB 726755 A GB726755 A GB 726755A GB 21183/53 A GB21183/53 A GB 21183/53A GB 2118353 A GB2118353 A GB 2118353A GB 726755 A GB726755 A GB 726755A
- Authority
- GB
- United Kingdom
- Prior art keywords
- diazo
- type
- compounds
- chlorobenzene
- rays
- 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
- 239000000463 material Substances 0.000 title abstract 8
- 150000008049 diazo compounds Chemical class 0.000 abstract 24
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 abstract 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 5
- 150000003839 salts Chemical class 0.000 abstract 5
- 239000011592 zinc chloride Substances 0.000 abstract 4
- 235000005074 zinc chloride Nutrition 0.000 abstract 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- PNPCRKVUWYDDST-UHFFFAOYSA-N 3-chloroaniline Chemical compound NC1=CC=CC(Cl)=C1 PNPCRKVUWYDDST-UHFFFAOYSA-N 0.000 abstract 2
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 abstract 2
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 abstract 2
- 159000000000 sodium salts Chemical class 0.000 abstract 2
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 abstract 2
- DHJKHOVAFCEJMP-UHFFFAOYSA-N (4e)-2-chloro-4-diazo-n,n-diethylcyclohexa-1,5-dien-1-amine Chemical compound CCN(CC)C1=C(Cl)CC(=[N+]=[N-])C=C1 DHJKHOVAFCEJMP-UHFFFAOYSA-N 0.000 abstract 1
- YYZRXNIZXRJETP-UHFFFAOYSA-N (4e)-4-diazo-n-phenylcyclohexa-1,5-dien-1-amine Chemical compound C1=CC(=[N+]=[N-])CC=C1NC1=CC=CC=C1 YYZRXNIZXRJETP-UHFFFAOYSA-N 0.000 abstract 1
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-naphthoquinone Chemical compound C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 abstract 1
- IKQCSJBQLWJEPU-UHFFFAOYSA-N 2,5-dihydroxybenzenesulfonic acid Chemical compound OC1=CC=C(O)C(S(O)(=O)=O)=C1 IKQCSJBQLWJEPU-UHFFFAOYSA-N 0.000 abstract 1
- OFUXYBDYXIXULD-UHFFFAOYSA-N 2-chloro-4-diazo-N-ethylcyclohexa-1,5-dien-1-amine Chemical class [N+](=[N-])=C1CC(=C(C=C1)NCC)Cl OFUXYBDYXIXULD-UHFFFAOYSA-N 0.000 abstract 1
- YRYHSOVHYUPBHZ-UHFFFAOYSA-N 2-chloro-N-cyclohexyl-4-diazocyclohexa-1,5-dien-1-amine Chemical compound [N+](=[N-])=C1CC(=C(C=C1)NC1CCCCC1)Cl YRYHSOVHYUPBHZ-UHFFFAOYSA-N 0.000 abstract 1
- ZTFYJIXFKGPCHV-UHFFFAOYSA-N 2-propan-2-ylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(C(C)C)=CC=C21 ZTFYJIXFKGPCHV-UHFFFAOYSA-N 0.000 abstract 1
- AMEFXYVDFUUOMG-UHFFFAOYSA-N 4-diazo-N,N-diethyl-2-iodocyclohexa-1,5-dien-1-amine Chemical compound [N+](=[N-])=C1CC(=C(N(CC)CC)C=C1)I AMEFXYVDFUUOMG-UHFFFAOYSA-N 0.000 abstract 1
- XCKSVXOZXKLPGS-UHFFFAOYSA-N 4-diazo-N-ethyl-2-(trifluoromethyl)cyclohexa-1,5-dien-1-amine Chemical class [N+](=[N-])=C1CC(=C(C=C1)NCC)C(F)(F)F XCKSVXOZXKLPGS-UHFFFAOYSA-N 0.000 abstract 1
- FZLSTQYXGUDVAL-UHFFFAOYSA-N 4-diazo-n,n-diethyl-2-methylcyclohexa-1,5-dien-1-amine Chemical compound CCN(CC)C1=C(C)CC(=[N+]=[N-])C=C1 FZLSTQYXGUDVAL-UHFFFAOYSA-N 0.000 abstract 1
- YZYFPMLAGIGAJJ-UHFFFAOYSA-N 4-diazo-n,n-diethylcyclohexa-1,5-dien-1-amine Chemical compound CCN(CC)C1=CCC(=[N+]=[N-])C=C1 YZYFPMLAGIGAJJ-UHFFFAOYSA-N 0.000 abstract 1
- HVLAFPUUUISBRV-UHFFFAOYSA-N 4-diazo-n-ethyl-2-methylcyclohexa-1,5-dien-1-amine Chemical compound CCNC1=C(C)CC(=[N+]=[N-])C=C1 HVLAFPUUUISBRV-UHFFFAOYSA-N 0.000 abstract 1
- VKHOVLYIOYFOPD-UHFFFAOYSA-N 6-diazo-n,n-diethylcyclohexa-2,4-dien-1-amine Chemical compound CCN(CC)C1C=CC=CC1=[N+]=[N-] VKHOVLYIOYFOPD-UHFFFAOYSA-N 0.000 abstract 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 abstract 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 abstract 1
- PZWFZJVVWCXOFE-UHFFFAOYSA-N N,N-dibutyl-2-chloro-4-diazocyclohexa-1,5-dien-1-amine Chemical compound [N+](=[N-])=C1CC(=C(C=C1)N(CCCC)CCCC)Cl PZWFZJVVWCXOFE-UHFFFAOYSA-N 0.000 abstract 1
- ROGOAQTWKUPPPT-UHFFFAOYSA-N N-[5-diazo-2-(diethylamino)cyclohexa-1,3-dien-1-yl]benzamide Chemical compound [N+](=[N-])=C1CC(=C(C=C1)N(CC)CC)NC(C1=CC=CC=C1)=O ROGOAQTWKUPPPT-UHFFFAOYSA-N 0.000 abstract 1
- PWQSSKCMYLGPDP-UHFFFAOYSA-N N-benzyl-2-chloro-4-diazocyclohexa-1,5-dien-1-amine Chemical compound [N+](=[N-])=C1CC(=C(C=C1)NCC1=CC=CC=C1)Cl PWQSSKCMYLGPDP-UHFFFAOYSA-N 0.000 abstract 1
- GDCPABOBRZJPPK-UHFFFAOYSA-N N-cyclohexyl-4-diazo-2-(trifluoromethyl)cyclohexa-1,5-dien-1-amine Chemical compound [N+](=[N-])=C1CC(=C(C=C1)NC1CCCCC1)C(F)(F)F GDCPABOBRZJPPK-UHFFFAOYSA-N 0.000 abstract 1
- ODAIAUIHDNVGLV-UHFFFAOYSA-N O.O.O.O.O.[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-] Chemical compound O.O.O.O.O.[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[K+].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-].[O-]B([O-])[O-] ODAIAUIHDNVGLV-UHFFFAOYSA-N 0.000 abstract 1
- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 abstract 1
- 229910021627 Tin(IV) chloride Inorganic materials 0.000 abstract 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 1
- YUDRVAHLXDBKSR-UHFFFAOYSA-N [CH]1CCCCC1 Chemical group [CH]1CCCCC1 YUDRVAHLXDBKSR-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- -1 alkyl radical Chemical class 0.000 abstract 1
- 150000001450 anions Chemical class 0.000 abstract 1
- 230000008033 biological extinction Effects 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 230000008878 coupling Effects 0.000 abstract 1
- 238000010168 coupling process Methods 0.000 abstract 1
- 238000005859 coupling reaction Methods 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 229920000609 methyl cellulose Polymers 0.000 abstract 1
- 239000001923 methylcellulose Substances 0.000 abstract 1
- 235000010981 methylcellulose Nutrition 0.000 abstract 1
- 230000007935 neutral effect Effects 0.000 abstract 1
- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 abstract 1
- 229960001553 phloroglucinol Drugs 0.000 abstract 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 abstract 1
- 230000001235 sensitizing effect Effects 0.000 abstract 1
- 239000000600 sorbitol Substances 0.000 abstract 1
- 239000010902 straw Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 239000010409 thin film Substances 0.000 abstract 1
- HPGGPRDJHPYFRM-UHFFFAOYSA-J tin(iv) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 abstract 1
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
- G03C1/54—Diazonium salts or diazo anhydrides
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL171784 | 1952-08-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB726755A true GB726755A (en) | 1955-03-23 |
Family
ID=19750576
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB21183/53A Expired GB726755A (en) | 1952-08-13 | 1953-07-30 | Improvements in or relating to photographic diazotype materials |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US2793118A (en(2012)) |
| BE (1) | BE521426A (en(2012)) |
| CH (1) | CH327756A (en(2012)) |
| DE (1) | DE1015679B (en(2012)) |
| FR (1) | FR1090494A (en(2012)) |
| GB (1) | GB726755A (en(2012)) |
| NL (2) | NL171784B (en(2012)) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4427500A (en) | 1982-03-15 | 1984-01-24 | American Hoechst Corporation | Method for producing an aluminum support useful for lithography |
| US4540648A (en) * | 1983-03-02 | 1985-09-10 | Hoechst Aktiengesellschaft | Two-component diazotype material with ultraviolet light-absorbing dye salt of a benzothiazole |
| US4581996A (en) * | 1982-03-15 | 1986-04-15 | American Hoechst Corporation | Aluminum support useful for lithography |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE543608A (en(2012)) * | 1954-12-15 | |||
| BE561008A (en(2012)) * | 1956-09-26 | |||
| US3450536A (en) * | 1961-03-24 | 1969-06-17 | Eg & G Inc | Silver halide photographic film having increased exposure-response characteristics |
| NL275942A (en(2012)) * | 1962-03-14 | |||
| SE335474B (en(2012)) * | 1963-04-18 | 1971-05-24 | R Landau | |
| NL299034A (en(2012)) * | 1963-10-09 | |||
| US3382070A (en) * | 1964-01-02 | 1968-05-07 | Gen Aniline & Film Corp | Black-line moist diazotype process |
| US3331690A (en) * | 1964-06-08 | 1967-07-18 | Ibm | Development of diazotype papers without a coupler |
| US3484241A (en) * | 1967-01-16 | 1969-12-16 | Ibm | Diazo type films with extended linear latitude |
| ZA6801453B (en(2012)) * | 1967-03-08 | |||
| US3622325A (en) * | 1968-03-07 | 1971-11-23 | Ricoh Kk | Diazotype photographic copying material adapted for wet development and for producing copied image in black color |
| JPS5280118A (en) * | 1975-12-26 | 1977-07-05 | Mitsubishi Paper Mills Ltd | Diazo photosensitive material for intermediates |
| JPS5297725A (en) * | 1976-02-13 | 1977-08-16 | Mitsubishi Paper Mills Ltd | Diazo photosensitive material for intermediates |
| US4148646A (en) * | 1977-06-13 | 1979-04-10 | Trans World Technology Laboratories, Inc. | Continuous tone diazotype process |
| US4224397A (en) * | 1979-01-26 | 1980-09-23 | Trans World Technology Laboratories Inc. (Twt Labs, Inc.) | Continuous tone diazo material |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1967371A (en) * | 1931-03-28 | 1934-07-24 | Kalle & Co Ag | Process of preparing copies |
| BE474743A (en(2012)) * | 1946-07-23 | |||
| US2532126A (en) * | 1946-12-16 | 1950-11-28 | Gen Aniline & Film Corp | Diazotype photographic material |
| GB644493A (en) * | 1948-01-09 | 1950-10-11 | Hall Harding Ltd | Improvements relating to the production of diazotype photo printing materials |
-
0
- NL NL80603D patent/NL80603C/xx active
- BE BE521426D patent/BE521426A/xx unknown
- NL NLAANVRAGE7710330,A patent/NL171784B/xx unknown
-
1953
- 1953-07-29 US US371022A patent/US2793118A/en not_active Expired - Lifetime
- 1953-07-30 CH CH327756D patent/CH327756A/de unknown
- 1953-07-30 GB GB21183/53A patent/GB726755A/en not_active Expired
- 1953-08-01 DE DEC7988A patent/DE1015679B/de active Pending
- 1953-08-06 FR FR1090494D patent/FR1090494A/fr not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4427500A (en) | 1982-03-15 | 1984-01-24 | American Hoechst Corporation | Method for producing an aluminum support useful for lithography |
| US4581996A (en) * | 1982-03-15 | 1986-04-15 | American Hoechst Corporation | Aluminum support useful for lithography |
| US4540648A (en) * | 1983-03-02 | 1985-09-10 | Hoechst Aktiengesellschaft | Two-component diazotype material with ultraviolet light-absorbing dye salt of a benzothiazole |
| EP0118086A3 (en) * | 1983-03-02 | 1987-05-27 | Hoechst Aktiengesellschaft | Two-component diazo type material |
Also Published As
| Publication number | Publication date |
|---|---|
| CH327756A (de) | 1958-02-15 |
| BE521426A (en(2012)) | |
| NL171784B (nl) | |
| FR1090494A (fr) | 1955-03-30 |
| US2793118A (en) | 1957-05-21 |
| DE1015679B (de) | 1957-09-12 |
| NL80603C (en(2012)) |
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