http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103059168-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8ec6134c9f4e4bae3a27342222c4ae99
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D295-155
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-62
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08F2-48
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filingDate 2013-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8c4f92b2441039a91bb7b811fc7d0cea
publicationDate 2014-09-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103059168-B
titleOfInvention Benzophenone-type light initiator and preparation method thereof
abstract The invention discloses a benzophenone-type light initiator shown in the formula (1). As the benzophenone-type light initiator is used, the mobility of benzophenone is lowered greatly during the using process while the triggering activity of the benzophenone is not lowered, i.e. the yellow-stain phenomenon is lightened. Particularly, a tertiary amine structure is contained in the self molecular structure of the benzophenone-type light initiator, i.e. the tertiary amine structure can be effectively used as an H donor of an active functional group, so that the benzophenone-type light initiator can be triggered without additionally adding an active amine additive during the using process. Therefore, the benzophenone-type light initiator belongs to a hydrogen-seizing type light initiator which is triggered automatically. In addition, the benzophenone-type light initiator has good solubility in various resins and resin oligomers, thereby being a good BP (benzophenone) substitute.
priorityDate 2013-01-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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