http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113292528-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08F2-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-86 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F2-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D335-16 |
| filingDate | 2021-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2022-06-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2022-06-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-113292528-B |
| titleOfInvention | Thioxanthone photoinitiator with high migration stability, preparation method and application |
| abstract | The invention provides a thioxanthone photoinitiator with high migration stability, a preparation method and application thereof. The structure of the thioxanthone photoinitiator with high migration stability is shown as a formula (I), wherein R is allyl, benzyl, 4-dimethylaminobenzyl, 4-methylbenzyl, 3-methylbenzyl, 2-methylbenzyl, 4-benzyloxy benzyl, 4-tert-butylbenzyl, 4-methoxybenzyl, 3- (trifluoromethyl) benzyl, 4-bromobenzyl, 3-cyanobenzyl, 3-nitrobenzyl, 2- (trifluoromethyl) benzyl, 3, 5-bis (trifluoromethyl) benzyl, 4-iodobenzyl, 4-bromobenzyl or 4-cyanobenzyl. The thioxanthone photoinitiator provided by the invention has good compatibility with acrylic ester, has high migration stability, does not need to add a solvent to dissolve the photoinitiator, and can effectively initiate monomer polymerization without an auxiliary agent. The thioxanthone photoinitiator provided by the invention has the advantages of simple structure and simple and convenient synthesis, and is suitable for large-scale production. |
| priorityDate | 2021-06-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 93.