http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106749154-B

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D219-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D335-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D311-84
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D219-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D311-84
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D335-14
filingDate 2016-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2019-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2019-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106749154-B
titleOfInvention Sulfide compound and its synthetic method
abstract The invention discloses a kind of sulfide compound and its synthetic method, structure such as Formulas I.Wherein X, R 1‑10 As defined in invention.Its synthesis path finally synthesizes product by adding hydrogen, thioetherification, pulling out hydrogen and four reaction steps of alkylation from the miscellaneous anthracene -9- ketone of 9H-X.Such sulfide compound can play certain initiation in free radical polymerization, and reversible coupling-cleavage reaction can be carried out with propagating radical, so that propagating radical be made to form suspend mode kind, polymerization be made to show certain controllability.Simultaneously, compared with the reagent used in traditional " activity "/controllable free-radical polymerisation system, such compound have many advantages, such as nontoxic, tasteless, colourless, non-metallic ion and without in addition use ligand there is preferable dissolubility, free radical polymerization field with good application prospect.
priorityDate 2016-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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