http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-944363-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_592ecc4fd30a3ecbc69f338002ba18b4 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/G03G5-07 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G61-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G61-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G03G5-07 |
| filingDate | 1960-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1963-12-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-944363-A |
| titleOfInvention | Photographic reproduction |
| abstract | Resinous products are obtained by Friedel-Craft reaction of (1) an aralkyl halide with itself, or (2) an aromatic carbocyclic or heterocyclic compound with a halogenated hydrocarbon containing at least 2 halogen atoms. Specified aralkyl halides are benzyl chloride, benzyl bromide and 1-chloromethyl-naphthalene. Specified aromatic compounds are benzene, diphenyl, terphenyl, naphthalene, 2-methyl-naphthalene, 2-chloro-naphthalene, 2-dimethyl-aminonaphthalene, anthracene, phenanthrene, acenaphthene, fluoranthene, dibenzofuran, benzo-naphtho-furan, 9-methyl-carbazole, 9-ethyl-carbazole, and mixtures of these. In general the nuclei may be substituted by alkyl, alkoxy, halogen or dialkylamino. Suitable halogenated hydrocarbons are methylene chloride, ethylene chloride, 1:2-dibromopropane, 1:2:3-tribromopropane, 1:3- and 1:4-dibromobutane, 1:2- and 1:4-dichlorobutane, 1-chloro-4-bromo-butane, 1:5-di-iodo-pentane, 1:10-di-bromodecane, benzylidene dichloride, p-xylylene dichloride, dibromide and di-iodide, 9:10-bis-chloromethyl-anthracene, halogenated polymers such as chlorinated polyethylene, and mixtures of these. The products usually contain halogen but some do not. The reaction takes place in an inert solvent such as tetrachlorethane, chlorobenzene or carbon disulphide. The catalyst may be aluminium chloride or bromide, ferric chloride or stannic chloride. Photoconductive compositions contain the above reaction products with dyestuffs, pigments (ZnO, TiO2), electron-accepting substances as activators, and optionally other resins, e.g. ketone resins or chlorinated polyvinyl chloride. Specified electron-accepting substances are those with strongly polarizing groups such as cyano, nitro, halogen, ketone, quinone, ester, acid or anhydride. Specified solvents for the reaction products are butanone, benzene and toluene. Compositions containing the stilbene and diarylbutadiene compounds of Specification 944,362 are disclaimed. |
| priorityDate | 1959-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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