GB1158627A - Photographic Systems - Google Patents
Photographic SystemsInfo
- Publication number
- GB1158627A GB1158627A GB35239/66A GB3523966A GB1158627A GB 1158627 A GB1158627 A GB 1158627A GB 35239/66 A GB35239/66 A GB 35239/66A GB 3523966 A GB3523966 A GB 3523966A GB 1158627 A GB1158627 A GB 1158627A
- Authority
- GB
- United Kingdom
- Prior art keywords
- bases
- substituted
- compound
- unsubstituted
- quinoline
- 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
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 4
- -1 isorosinduline Chemical compound 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 239000000460 chlorine Substances 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 150000002896 organic halogen compounds Chemical class 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- QGKMIGUHVLGJBR-UHFFFAOYSA-M (4z)-1-(3-methylbutyl)-4-[[1-(3-methylbutyl)quinolin-1-ium-4-yl]methylidene]quinoline;iodide Chemical compound [I-].C12=CC=CC=C2N(CCC(C)C)C=CC1=CC1=CC=[N+](CCC(C)C)C2=CC=CC=C12 QGKMIGUHVLGJBR-UHFFFAOYSA-M 0.000 abstract 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
- SIKJAQJRHWYJAI-UHFFFAOYSA-N Indole Chemical compound C1=CC=C2NC=CC2=C1 SIKJAQJRHWYJAI-UHFFFAOYSA-N 0.000 abstract 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 abstract 2
- DZBUGLKDJFMEHC-UHFFFAOYSA-N acridine Chemical compound C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
- 229910052794 bromium Inorganic materials 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 150000002391 heterocyclic compounds Chemical class 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000001624 naphthyl group Chemical group 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000005504 styryl group Chemical group 0.000 abstract 2
- BPDOAEIRGOPCCR-UHFFFAOYSA-N 1-ethyl-n-quinolin-4-ylquinolin-2-imine Chemical compound C1=CC=C2C(N=C3C=CC4=CC=CC=C4N3CC)=CC=NC2=C1 BPDOAEIRGOPCCR-UHFFFAOYSA-N 0.000 abstract 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- FIYBTMSBKCROIF-UHFFFAOYSA-N N-(1,3-benzothiazol-2-yl)-2-(3-ethyl-2H-1,3-benzothiazol-1-ylidene)ethanimine Chemical compound C(C)N1CS(C2=C1C=CC=C2)=CC=NC=2SC1=C(N2)C=CC=C1 FIYBTMSBKCROIF-UHFFFAOYSA-N 0.000 abstract 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 1
- 239000005864 Sulphur Substances 0.000 abstract 1
- 125000003435 aroyl group Chemical group 0.000 abstract 1
- 150000005840 aryl radicals Chemical group 0.000 abstract 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 1
- 239000012876 carrier material Substances 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- CMSRLFLXFXUENW-UHFFFAOYSA-L disodium;2-(3-oxido-1h-indol-2-yl)-1h-indol-3-olate Chemical compound [Na+].[Na+].N1C2=CC=CC=C2C([O-])=C1C1=C([O-])C2=CC=CC=C2N1 CMSRLFLXFXUENW-UHFFFAOYSA-L 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 abstract 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 abstract 1
- 229910052740 iodine Chemical group 0.000 abstract 1
- 239000011630 iodine Chemical group 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- KBENBTOTLFPADB-UHFFFAOYSA-N n,n-dimethyl-4-(quinolin-4-yldiazenyl)aniline Chemical compound C1=CC(N(C)C)=CC=C1N=NC1=CC=NC2=CC=CC=C12 KBENBTOTLFPADB-UHFFFAOYSA-N 0.000 abstract 1
- FMRXMCKJBASAKX-UHFFFAOYSA-N n-(4-ethoxyphenyl)naphthalen-1-amine Chemical compound C1=CC(OCC)=CC=C1NC1=CC=CC2=CC=CC=C12 FMRXMCKJBASAKX-UHFFFAOYSA-N 0.000 abstract 1
- KKFHAJHLJHVUDM-UHFFFAOYSA-N n-vinylcarbazole Chemical compound C1=CC=C2N(C=C)C3=CC=CC=C3C2=C1 KKFHAJHLJHVUDM-UHFFFAOYSA-N 0.000 abstract 1
- 239000001301 oxygen Substances 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 230000005855 radiation Effects 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 150000004961 triphenylmethanes Chemical class 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
- G03C1/675—Compositions containing polyhalogenated compounds as photosensitive substances
-
- 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
- G03C1/72—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705
- G03C1/73—Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705 containing organic compounds
- G03C1/732—Leuco dyes
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US48553565A | 1965-09-07 | 1965-09-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1158627A true GB1158627A (en) | 1969-07-16 |
Family
ID=23928536
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB35239/66A Expired GB1158627A (en) | 1965-09-07 | 1966-08-05 | Photographic Systems |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3486898A (cs) |
| BE (1) | BE686540A (cs) |
| DE (1) | DE1547946A1 (cs) |
| GB (1) | GB1158627A (cs) |
| NL (1) | NL6612323A (cs) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3650755A (en) * | 1963-05-06 | 1972-03-21 | Bell & Howell Co | Positive-mode photographic process and composition |
| JPS5152816A (en) * | 1974-09-03 | 1976-05-10 | Energy Conversion Devices Inc | Gazokeiseifuirumu oyobi gazokeiseihoho |
| KR20040083091A (ko) * | 2002-01-21 | 2004-09-30 | 히로세 엔지니어링 가부시키가이샤 | 나일 레드계 적색 발광 화합물, 그것의 제조 방법 및그것을 이용한 발광 소자 |
| CN106661337A (zh) * | 2014-07-04 | 2017-05-10 | 富士胶片株式会社 | 新型化合物、染色或印花用着色组合物、喷墨用油墨、布帛印花方法及被染色或印花布帛 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3102810A (en) * | 1961-04-05 | 1963-09-03 | Horizons Inc | Print-out cyanine and styryl dye bases and process of producing litho masters and the like therewith |
-
1965
- 1965-09-07 US US485535A patent/US3486898A/en not_active Expired - Lifetime
-
1966
- 1966-08-05 GB GB35239/66A patent/GB1158627A/en not_active Expired
- 1966-09-01 NL NL6612323A patent/NL6612323A/xx unknown
- 1966-09-06 DE DE19661547946 patent/DE1547946A1/de active Pending
- 1966-09-07 BE BE686540D patent/BE686540A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL6612323A (cs) | 1967-03-08 |
| BE686540A (cs) | 1967-02-15 |
| DE1547946A1 (de) | 1969-12-11 |
| US3486898A (en) | 1969-12-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US3102810A (en) | Print-out cyanine and styryl dye bases and process of producing litho masters and the like therewith | |
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| JPS57147656A (en) | Electrophotographic sensitive printing plate material | |
| GB1495317A (en) | Silver halide colour photographic materials | |
| GB1173328A (en) | Photosensitive Compositions | |
| GB1158627A (en) | Photographic Systems | |
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| IT1251083B (it) | Elementi fotografici agli alogenuri d'argento | |
| GB1466440A (en) | Styryl butadienyl dyes | |
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| JPS52117323A (en) | New 44*vvtriazolyl**styryl compound | |
| GB1198640A (en) | Light-Sensitive Organic Halogen Reproduction Material | |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |