GB1465184A - Photographic silver halide elements useful in colour diffusion transfer processes and chemical compounds useful in said elements - Google Patents
Photographic silver halide elements useful in colour diffusion transfer processes and chemical compounds useful in said elementsInfo
- Publication number
- GB1465184A GB1465184A GB624974A GB624974A GB1465184A GB 1465184 A GB1465184 A GB 1465184A GB 624974 A GB624974 A GB 624974A GB 624974 A GB624974 A GB 624974A GB 1465184 A GB1465184 A GB 1465184A
- Authority
- GB
- United Kingdom
- Prior art keywords
- compound
- hydroxy
- formula
- alkyl
- prepared
- 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
- 150000001875 compounds Chemical class 0.000 title abstract 17
- -1 silver halide Chemical class 0.000 title abstract 5
- 238000000034 method Methods 0.000 title abstract 2
- 238000009792 diffusion process Methods 0.000 title 1
- 229910052709 silver Inorganic materials 0.000 title 1
- 239000004332 silver Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 4
- 230000008878 coupling Effects 0.000 abstract 4
- 238000010168 coupling process Methods 0.000 abstract 4
- 238000005859 coupling reaction Methods 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 125000001118 alkylidene group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 238000006193 diazotization reaction Methods 0.000 abstract 2
- 239000000543 intermediate Substances 0.000 abstract 2
- OENHRRVNRZBNNS-UHFFFAOYSA-N naphthalene-1,8-diol Chemical compound C1=CC(O)=C2C(O)=CC=CC2=C1 OENHRRVNRZBNNS-UHFFFAOYSA-N 0.000 abstract 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N naphthalene-acid Natural products C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 abstract 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 2
- MYQNLKLVSGDHNB-UHFFFAOYSA-M sodium 4-acetamido-5-hydroxy-8-[(4-sulfamoylphenyl)diazenyl]naphthalene-1-sulfonate Chemical compound [Na+].C1=CC(O)=C2C(NC(=O)C)=CC=C(S([O-])(=O)=O)C2=C1N=NC1=CC=C(S(N)(=O)=O)C=C1 MYQNLKLVSGDHNB-UHFFFAOYSA-M 0.000 abstract 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 abstract 2
- GYVABUSMWJYZKN-UHFFFAOYSA-N 4-[(3-aminophenyl)sulfonylamino]-n-[4-[2,4-bis(2-methylbutan-2-yl)phenoxy]butyl]-1-hydroxynaphthalene-2-carboxamide Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=CC=C1OCCCCNC(=O)C1=CC(NS(=O)(=O)C=2C=C(N)C=CC=2)=C(C=CC=C2)C2=C1O GYVABUSMWJYZKN-UHFFFAOYSA-N 0.000 abstract 1
- IARLJPWFLRVFST-UHFFFAOYSA-N 4-acetamido-5-acetyloxynaphthalene-1-sulfonic acid pyridine Chemical compound C1=CC=NC=C1.CC(=O)NC1=C2C(OC(C)=O)=CC=CC2=C(C=C1)S(O)(=O)=O IARLJPWFLRVFST-UHFFFAOYSA-N 0.000 abstract 1
- OADVKRWKQAOOAE-UHFFFAOYSA-N 4-acetamido-8-[(4-chlorosulfonylphenyl)diazenyl]-5-hydroxynaphthalene-1-sulfonyl chloride Chemical compound C1=CC(O)=C2C(NC(=O)C)=CC=C(S(Cl)(=O)=O)C2=C1N=NC1=CC=C(S(Cl)(=O)=O)C=C1 OADVKRWKQAOOAE-UHFFFAOYSA-N 0.000 abstract 1
- LQPYPLBCZNOKKA-UHFFFAOYSA-N 4-amino-n-[4-[2,4-bis(2-methylbutan-2-yl)phenoxy]butyl]-1-hydroxynaphthalene-2-carboxamide Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=CC=C1OCCCCNC(=O)C1=CC(N)=C(C=CC=C2)C2=C1O LQPYPLBCZNOKKA-UHFFFAOYSA-N 0.000 abstract 1
- HVBSAKJJOYLTQU-UHFFFAOYSA-N 4-aminobenzenesulfonic acid Chemical compound NC1=CC=C(S(O)(=O)=O)C=C1 HVBSAKJJOYLTQU-UHFFFAOYSA-N 0.000 abstract 1
- AAJOTUBGWZPIHV-UHFFFAOYSA-N 4-benzamido-8-[[4-(benzenesulfonylsulfamoyl)phenyl]diazenyl]-5-hydroxynaphthalene-1-sulfonyl chloride Chemical compound C(C1=CC=CC=C1)(=O)NC1=CC=C(C2=C(C=CC(=C12)O)N=NC1=CC=C(C=C1)S(NS(=O)(=O)C1=CC=CC=C1)(=O)=O)S(=O)(=O)Cl AAJOTUBGWZPIHV-UHFFFAOYSA-N 0.000 abstract 1
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 abstract 1
- NHCUYZJWKREOHS-UHFFFAOYSA-N [4-[(3-chlorosulfonylphenyl)diazenyl]-5-(methanesulfonamido)naphthalen-1-yl] ethyl carbonate Chemical compound C12=C(NS(C)(=O)=O)C=CC=C2C(OC(=O)OCC)=CC=C1N=NC1=CC=CC(S(Cl)(=O)=O)=C1 NHCUYZJWKREOHS-UHFFFAOYSA-N 0.000 abstract 1
- 235000011054 acetic acid Nutrition 0.000 abstract 1
- 150000001243 acetic acids Chemical class 0.000 abstract 1
- 125000003668 acetyloxy group Chemical group [H]C([H])([H])C(=O)O[*] 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000005099 aryl alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000005129 aryl carbonyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 abstract 1
- 239000000987 azo dye Substances 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 239000012954 diazonium Substances 0.000 abstract 1
- 150000001989 diazonium salts Chemical class 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- ORTFAQDWJHRMNX-UHFFFAOYSA-N hydroxidooxidocarbon(.) Chemical compound O[C]=O ORTFAQDWJHRMNX-UHFFFAOYSA-N 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- OWFXIOWLTKNBAP-UHFFFAOYSA-N isoamyl nitrite Chemical compound CC(C)CCON=O OWFXIOWLTKNBAP-UHFFFAOYSA-N 0.000 abstract 1
- HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical compound CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 abstract 1
- CJQANEIQSNYREL-UHFFFAOYSA-N n-(5-hydroxynaphthalen-1-yl)-4-methylbenzenesulfonamide Chemical compound C1=CC(C)=CC=C1S(=O)(=O)NC1=CC=CC2=C(O)C=CC=C12 CJQANEIQSNYREL-UHFFFAOYSA-N 0.000 abstract 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 1
- 150000004672 propanoic acids Chemical class 0.000 abstract 1
- 235000019260 propionic acid Nutrition 0.000 abstract 1
- 239000000376 reactant Substances 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 159000000000 sodium salts Chemical class 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 1
- FDDDEECHVMSUSB-UHFFFAOYSA-N sulfanilamide Chemical compound NC1=CC=C(S(N)(=O)=O)C=C1 FDDDEECHVMSUSB-UHFFFAOYSA-N 0.000 abstract 1
- 229950000244 sulfanilic acid Drugs 0.000 abstract 1
- 229940124530 sulfonamide Drugs 0.000 abstract 1
- XTHPWXDJESJLNJ-UHFFFAOYSA-N sulfurochloridic acid Chemical compound OS(Cl)(=O)=O XTHPWXDJESJLNJ-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B29/00—Monoazo dyes prepared by diazotising and coupling
- C09B29/10—Monoazo dyes prepared by diazotising and coupling from coupling components containing hydroxy as the only directing group
-
- 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/02—Photosensitive materials characterised by the image-forming section
- G03C8/08—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds
- G03C8/10—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds of dyes or their precursors
-
- 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
- G03C8/00—Diffusion transfer processes or agents therefor; Photosensitive materials for such processes
- G03C8/02—Photosensitive materials characterised by the image-forming section
- G03C8/08—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds
- G03C8/10—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds of dyes or their precursors
- G03C8/12—Photosensitive materials characterised by the image-forming section the substances transferred by diffusion consisting of organic compounds of dyes or their precursors characterised by the releasing mechanism
- G03C8/14—Oxidation of the chromogenic substances
- G03C8/16—Oxidation of the chromogenic substances initially diffusible in alkaline environment
- G03C8/18—Dye developers
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US33172973A | 1973-02-12 | 1973-02-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1465184A true GB1465184A (en) | 1977-02-23 |
Family
ID=23295134
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB624974A Expired GB1465184A (en) | 1973-02-12 | 1974-02-12 | Photographic silver halide elements useful in colour diffusion transfer processes and chemical compounds useful in said elements |
Country Status (7)
| Country | Link |
|---|---|
| JP (1) | JPS49126332A (enrdf_load_stackoverflow) |
| BE (1) | BE796042A (enrdf_load_stackoverflow) |
| CH (1) | CH588096A5 (enrdf_load_stackoverflow) |
| DE (2) | DE2462184A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2217726B1 (enrdf_load_stackoverflow) |
| GB (1) | GB1465184A (enrdf_load_stackoverflow) |
| NL (1) | NL7401911A (enrdf_load_stackoverflow) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3954476A (en) * | 1974-02-05 | 1976-05-04 | Eastman Kodak Company | Diffusable dye-releasing compounds which are cleavable upon oxidation |
| US5234800A (en) * | 1990-02-22 | 1993-08-10 | Eastman Kodak Company | Photographic material and process comprising wash-out naphtholic coupler |
| TW201000568A (en) * | 2008-05-22 | 2010-01-01 | Sumitomo Chemical Co | Azo compound or salt thereof, and method of producing same |
-
1973
- 1973-02-26 FR FR7306646A patent/FR2217726B1/fr not_active Expired
- 1973-02-27 BE BE128173A patent/BE796042A/xx unknown
-
1974
- 1974-02-11 CH CH185474A patent/CH588096A5/xx not_active IP Right Cessation
- 1974-02-12 NL NL7401911A patent/NL7401911A/xx not_active Application Discontinuation
- 1974-02-12 DE DE19742462184 patent/DE2462184A1/de active Pending
- 1974-02-12 DE DE19742406626 patent/DE2406626A1/de active Pending
- 1974-02-12 GB GB624974A patent/GB1465184A/en not_active Expired
- 1974-02-12 JP JP1706374A patent/JPS49126332A/ja active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CH588096A5 (enrdf_load_stackoverflow) | 1977-05-31 |
| JPS49126332A (enrdf_load_stackoverflow) | 1974-12-03 |
| AU6549174A (en) | 1975-08-14 |
| DE2406626A1 (de) | 1974-08-29 |
| DE2462184A1 (de) | 1976-03-18 |
| FR2217726B1 (enrdf_load_stackoverflow) | 1983-01-14 |
| BE796042A (fr) | 1973-08-27 |
| FR2217726A1 (enrdf_load_stackoverflow) | 1974-09-06 |
| NL7401911A (enrdf_load_stackoverflow) | 1974-08-14 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |