http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102675324-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_896b11ed232c0d8e29f572d158bbd22f
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-22
filingDate 2012-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2014-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a622a927902c2ec795b6005ac4a5690d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_62017be0d124e14714db5d557e0f129f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f48ba88bc86f8aa426d3c470e0d3259
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publicationDate 2014-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102675324-B
titleOfInvention Symmetrical beta-enaminone group porphyrin and preparation method thereof
abstract The invention provides symmetrical beta-enaminone group substituted porphyrin, wherein the compound is provided with a strong emission peak at about 668nm, the compound not only remains the characteristic of porphyrin in coordination with metal, but also can take tertiary amine group, carbon-carbon double bond and carbonyl group on the newly introduced beta-enaminone group as active groups, to further react with the other matters, so as to obtain corresponding ramification, so that the type of the porphyrin compounds can be enriched; and therefore, the porphyrin can be taken as an important organic synthesis intermediate to be used in the fields such as medicine and pesticide, and can be further used for the electron transfer, the molecular recognition, the photoinduced molecular switch and the luminescent materials.
priorityDate 2012-05-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 43.