GB1458471A - Compounds having a diffusible dye moiety and photosensitive silver halide elements containing said compounds - Google Patents
Compounds having a diffusible dye moiety and photosensitive silver halide elements containing said compoundsInfo
- Publication number
- GB1458471A GB1458471A GB624774A GB624774A GB1458471A GB 1458471 A GB1458471 A GB 1458471A GB 624774 A GB624774 A GB 624774A GB 624774 A GB624774 A GB 624774A GB 1458471 A GB1458471 A GB 1458471A
- Authority
- GB
- United Kingdom
- Prior art keywords
- optionally substituted
- hydroxy
- alkyl
- compounds
- car
- 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
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 150000001875 compounds Chemical class 0.000 abstract 6
- -1 phenylsulphonyloxy Chemical group 0.000 abstract 6
- 239000000047 product Substances 0.000 abstract 6
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- FYXJXUMICYGRKV-UHFFFAOYSA-N 2-[(2-amino-5-nitrophenyl)methylsulfonylmethyl]-4-nitroaniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1CS(=O)(=O)CC1=CC([N+]([O-])=O)=CC=C1N FYXJXUMICYGRKV-UHFFFAOYSA-N 0.000 abstract 2
- GDBANHJMXDZUNE-UHFFFAOYSA-N 5-hydroxynaphthalene-2-sulfonic acid Chemical compound OS(=O)(=O)C1=CC=C2C(O)=CC=CC2=C1 GDBANHJMXDZUNE-UHFFFAOYSA-N 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- 150000002790 naphthalenes Chemical class 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 abstract 1
- LHRIICYSGQGXSX-UHFFFAOYSA-N 2-chloro-4,6-dinitroaniline Chemical compound NC1=C(Cl)C=C([N+]([O-])=O)C=C1[N+]([O-])=O LHRIICYSGQGXSX-UHFFFAOYSA-N 0.000 abstract 1
- HOTZLWVITTVZGY-UHFFFAOYSA-N 4-nitro-2-(trifluoromethyl)aniline Chemical compound NC1=CC=C([N+]([O-])=O)C=C1C(F)(F)F HOTZLWVITTVZGY-UHFFFAOYSA-N 0.000 abstract 1
- LBPHSQSBTZZQFT-UHFFFAOYSA-N 5-hydroxy-4-(propanoylamino)naphthalene-1-sulfonic acid Chemical compound C1=CC(O)=C2C(NC(=O)CC)=CC=C(S(O)(=O)=O)C2=C1 LBPHSQSBTZZQFT-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 230000010933 acylation Effects 0.000 abstract 1
- 238000005917 acylation reaction Methods 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 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
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 238000010168 coupling process Methods 0.000 abstract 1
- 238000006193 diazotization reaction Methods 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- 239000012467 final product Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical class C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 abstract 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 abstract 1
- 229910052709 silver Inorganic materials 0.000 abstract 1
- 239000004332 silver Substances 0.000 abstract 1
- 239000007858 starting material Substances 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
-
- 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)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Glass Compositions (AREA)
- Holo Graphy (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US33172773A | 1973-02-12 | 1973-02-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1458471A true GB1458471A (en) | 1976-12-15 |
Family
ID=23295123
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB624774A Expired GB1458471A (en) | 1973-02-12 | 1974-02-12 | Compounds having a diffusible dye moiety and photosensitive silver halide elements containing said compounds |
Country Status (6)
| Country | Link |
|---|---|
| JP (2) | JPS5926014B2 (enrdf_load_stackoverflow) |
| BE (1) | BE796041A (enrdf_load_stackoverflow) |
| DE (2) | DE2462010A1 (enrdf_load_stackoverflow) |
| FR (1) | FR2217723B1 (enrdf_load_stackoverflow) |
| GB (1) | GB1458471A (enrdf_load_stackoverflow) |
| NL (1) | NL7401930A (enrdf_load_stackoverflow) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2217723B1 (enrdf_load_stackoverflow) * | 1973-02-12 | 1978-03-03 | Eastman Kodak Co | |
| US4013635A (en) * | 1975-02-26 | 1977-03-22 | Eastman Kodak Company | Cyan azo dye-providing compounds |
| JPS5735462Y2 (enrdf_load_stackoverflow) * | 1977-10-12 | 1982-08-05 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3288778A (en) * | 1964-10-05 | 1966-11-29 | Polaroid Corp | Azo and anthraquinone dye developers |
| US3443940A (en) * | 1967-07-24 | 1969-05-13 | Polaroid Corp | Diffusion transfer employing ringclosure to release color-providing material for transfer |
| FR2217723B1 (enrdf_load_stackoverflow) * | 1973-02-12 | 1978-03-03 | Eastman Kodak Co |
-
1973
- 1973-02-26 FR FR7306645A patent/FR2217723B1/fr not_active Expired
- 1973-02-27 BE BE128172A patent/BE796041A/xx unknown
-
1974
- 1974-02-12 DE DE19742462010 patent/DE2462010A1/de active Pending
- 1974-02-12 DE DE19742406653 patent/DE2406653C3/de not_active Expired
- 1974-02-12 JP JP1706174A patent/JPS5926014B2/ja not_active Expired
- 1974-02-12 GB GB624774A patent/GB1458471A/en not_active Expired
- 1974-02-12 NL NL7401930A patent/NL7401930A/xx not_active Application Discontinuation
-
1984
- 1984-01-06 JP JP36284A patent/JPS59131932A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6235662B2 (enrdf_load_stackoverflow) | 1987-08-03 |
| DE2406653A1 (de) | 1974-08-29 |
| FR2217723A1 (enrdf_load_stackoverflow) | 1974-09-06 |
| DE2462010A1 (de) | 1975-07-17 |
| JPS59131932A (ja) | 1984-07-28 |
| NL7401930A (enrdf_load_stackoverflow) | 1974-08-14 |
| BE796041A (fr) | 1973-08-27 |
| AU6549074A (en) | 1975-08-14 |
| DE2406653C3 (de) | 1981-03-19 |
| JPS5926014B2 (ja) | 1984-06-23 |
| JPS49126331A (enrdf_load_stackoverflow) | 1974-12-03 |
| FR2217723B1 (enrdf_load_stackoverflow) | 1978-03-03 |
| DE2406653B2 (de) | 1980-06-12 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |