GB1336295A - Photographic compositions - Google Patents
Photographic compositionsInfo
- Publication number
- GB1336295A GB1336295A GB5679570A GB5679570A GB1336295A GB 1336295 A GB1336295 A GB 1336295A GB 5679570 A GB5679570 A GB 5679570A GB 5679570 A GB5679570 A GB 5679570A GB 1336295 A GB1336295 A GB 1336295A
- Authority
- GB
- United Kingdom
- Prior art keywords
- heptene
- bis
- reacting
- formula
- bicyclo
- 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
- 239000000203 mixture Substances 0.000 title 1
- 229920000642 polymer Polymers 0.000 abstract 6
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexamethylene diamine Natural products NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 abstract 3
- -1 2 - mercaptoethyl Chemical group 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 150000008064 anhydrides Chemical class 0.000 abstract 2
- JDRPUJZWZDQJMD-UHFFFAOYSA-N 2-(2-bicyclo[2.2.1]hept-1-enylmethyl)-6,6-dimethylbicyclo[2.2.1]hept-2-ene Chemical compound CC1(CC2C=C(C1C2)CC1=C2CCC(C1)C2)C JDRPUJZWZDQJMD-UHFFFAOYSA-N 0.000 abstract 1
- KSJBMDCFYZKAFH-UHFFFAOYSA-N 2-(2-sulfanylethylsulfanyl)ethanethiol Chemical compound SCCSCCS KSJBMDCFYZKAFH-UHFFFAOYSA-N 0.000 abstract 1
- YIOOXGOQSWEQEX-UHFFFAOYSA-N 2-ethylhex-4-ene-1,1-diol Chemical compound OC(C(CC)CC=CC)O YIOOXGOQSWEQEX-UHFFFAOYSA-N 0.000 abstract 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 abstract 1
- ATTZFSUZZUNHBP-UHFFFAOYSA-N Piperonyl sulfoxide Chemical group CCCCCCCCS(=O)C(C)CC1=CC=C2OCOC2=C1 ATTZFSUZZUNHBP-UHFFFAOYSA-N 0.000 abstract 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 abstract 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 abstract 1
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 230000032050 esterification Effects 0.000 abstract 1
- 238000005886 esterification reaction Methods 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 125000001174 sulfone group Chemical group 0.000 abstract 1
- 125000000101 thioether group Chemical group 0.000 abstract 1
- NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 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
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
- G03C1/34—Fog-inhibitors; Stabilisers; Agents inhibiting latent image regression
- G03C1/346—Organic derivatives of bivalent sulfur, selenium or tellurium
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/68—Polyesters containing atoms other than carbon, hydrogen and oxygen
- C08G63/688—Polyesters containing atoms other than carbon, hydrogen and oxygen containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C08G73/06—Polycondensates having nitrogen-containing heterocyclic rings in the main chain of the macromolecule
- C08G73/10—Polyimides; Polyester-imides; Polyamide-imides; Polyamide acids or similar polyimide precursors
- C08G73/1057—Polyimides containing other atoms than carbon, hydrogen, nitrogen or oxygen in the main chain
- C08G73/1064—Polyimides containing other atoms than carbon, hydrogen, nitrogen or oxygen in the main chain containing sulfur
-
- 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
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/04—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Polyesters Or Polycarbonates (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
1336295 Polymers containing sulphur atoms and bicyclic rings EASTMAN KODAK CO 30 Nov 1970 [28 Nov 1969] 56795/70 Heading C3R [Also in Divisions G2 and C2] Condensation polymers are described containing a [2.2.1]-bicyclic ring directly attached to a sulphur atom which may form a thio ether group, a sulphoxide group or a sulphone group. Specific polymers are listed (nos. 1-12, 14, 34-37, 39-52 and 54) and include those of the formulae Copoly - [bicycio - [2.2.1] - 5 - heptene - 2:3- dicarboxylic anhydride - bis - (2 - mercaptoethyl)sulphide - hexamethylene diamine] (Formula 9) is prepared by reacting bicyclo- [2.2.1] - 3 - heptene - 2:3 - dicarboxylic anhydride with bis-(2-mercaptoethyl)sulphide and then with hexamethylene diamine. Copoly- [1 : 2 - bis - (2 - mercaptoethoxy)ethanedodecahydro - 1 : 4 : 5 : 8 - dimethanoanthraquinonylene-2 : 6(or 7)] (Formula 14) is made by reacting 1 : 4 : 4a : 5 : 8 : 8a : 9a : 10aoctahydro - 1 : 4 : 5 : 8 - dimethano - 9 : 10- anthraquinone with 1 : 2 - bis - (2 - mercaptoethoxy)ethene. Polymer of Formula 41 is made by reacting bicyclo-[2.2.1]-2-methyl-3 : 3-dihydroxymethyl - 5 - heptene with mercaptosuccinic acid following by heating with an esterification catalyst. Polymer of Formula 45 is made by reacting 3-methyl bicyclo-[2.2.1]- 5 - heptene - 2 - ylmethyl 3 - methyl bicyclo- [2.2.1] - 5 - heptene - 2 - carboxylate and hydrogen sulphide with irradiation. Polymer of Formula 51 is made by reacting 5 : 5<SP>1</SP> (or 5 : 6<SP>1</SP>) - thio bis - (bicyclo - [2.2.1] heptane- 2 : 3-dicarboxylic acid anhydride) or its dimethyl half-ester with 4 : 4<SP>1</SP>-methylene dianiline.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US88089569A | 1969-11-28 | 1969-11-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1336295A true GB1336295A (en) | 1973-11-07 |
Family
ID=25377348
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB5679570A Expired GB1336295A (en) | 1969-11-28 | 1970-11-30 | Photographic compositions |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US3666476A (en) |
| AU (1) | AU2275170A (en) |
| BE (1) | BE759675A (en) |
| BR (1) | BR7024122D0 (en) |
| CA (1) | CA941221A (en) |
| DE (1) | DE2058472A1 (en) |
| FR (1) | FR2072600A5 (en) |
| GB (1) | GB1336295A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2818678A1 (en) * | 1978-04-27 | 1979-10-31 | Agfa Gevaert Ag | PHOTOGRAPHIC SILVER HALOGENIDE EMULSIONS |
| US4420471A (en) * | 1983-01-10 | 1983-12-13 | Lever Brothers Company | Citrus flavored mouthwash formulation method |
| US4808638A (en) * | 1986-10-14 | 1989-02-28 | Loctite Corporation | Thiolene compositions on based bicyclic 'ene compounds |
-
0
- BE BE759675D patent/BE759675A/en unknown
-
1969
- 1969-11-28 US US880895A patent/US3666476A/en not_active Expired - Lifetime
-
1970
- 1970-10-06 CA CA094,887A patent/CA941221A/en not_active Expired
- 1970-11-25 BR BR224122/70A patent/BR7024122D0/en unknown
- 1970-11-27 DE DE19702058472 patent/DE2058472A1/en active Pending
- 1970-11-27 AU AU22751/70A patent/AU2275170A/en not_active Expired
- 1970-11-30 GB GB5679570A patent/GB1336295A/en not_active Expired
- 1970-11-30 FR FR7042885A patent/FR2072600A5/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| CA941221A (en) | 1974-02-05 |
| DE2058472A1 (en) | 1971-06-09 |
| FR2072600A5 (en) | 1971-09-24 |
| BE759675A (en) | 1971-04-30 |
| US3666476A (en) | 1972-05-30 |
| BR7024122D0 (en) | 1973-05-17 |
| AU2275170A (en) | 1972-06-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |