http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107629151-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D335-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-76 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F2-48 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09D11-101 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-28 |
| filingDate | 2017-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2020-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2020-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-107629151-B |
| titleOfInvention | Polymerizable free radical type II photoinitiator and preparation method thereof |
| abstract | The invention discloses a polymerizable free radical II type photoinitiator shown in the following formulas I and II, which is prepared by taking a carboxylic acid compound containing II type photoinitiation functional groups as a raw material, carrying out substitution reaction with methyl chloroacetate under an alkaline condition, and then carrying out ester exchange reaction with a hydroxyl compound containing polymerizable groups to generate the polymerizable photoinitiator. The photoinitiator structurally contains polymerizable groups, so that the compatibility of the photoinitiator with a photopolymerization system is improved, the surface mobility is greatly reduced in the photocuring process, and the photoinitiator can be used as a monomer for synthesizing a macromolecular photoinitiator, and therefore, the photoinitiator has a wide application prospect in the photocuring field. (I) or （Ⅱ）。 |
| priorityDate | 2017-10-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 67.