http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104004008-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F7-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P27-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K41-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K49-00 |
| filingDate | 2014-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2016-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-05-18-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-104004008-B |
| titleOfInvention | Fluorinated aryl benzyl oxide dendritic phthalocyanine silicon complex and its preparation method and application |
| abstract | The present invention discloses a kind of fluorinated aryl benzyl oxide dendritic phthalocyanine silicon complex and its preparation method and application, first synthetic phthalocyanine silicon dichloride; Then under potash exists, to (nitro or cyano group, ester group, benzophenone) benzyl bromine and the synthetic 2-(4-hydroxy benzenes of 2,2-bis-(4-hydroxyphenyl) HFC-236fa reaction)-2 ˊ-(4-(4-nitro or cyano group or ester group or benzophenone-benzyloxy) HFC-236fa. Last phthalocyanine silicon dichloride, respectively with 2-(4-hydroxy benzenes)-2 ˊ-(4-(4-nitro or cyano group or ester group or benzophenone-benzyloxy) HFC-236fa reacts synthetic two-(2-(4-phenoxy group)-2 ˊ-(4-(4-nitro or cyano group or ester group or benzophenone-benzyloxy) HFC-236fa) in reflux in toluene and axially replaces silicon (IV) phthalocyanine complex. Make the ligand modified phthalocyanine complex of fluoro branch become a class to have the sensitising agent of good optical dynamic therapy potentiality. |
| priorityDate | 2014-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 70.