http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104628753-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02E10-549 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F5-022 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09B57-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K85-322 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C09B57-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F5-02 |
| filingDate | 2014-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2017-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2017-04-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-104628753-B |
| titleOfInvention | A boron fluoride complexed dipyrromethene derivative modified by a meso-position triphenylamine-substituted 3,5-position aryl and its preparation method |
| abstract | The invention discloses a boron fluoride complexed dipyrromethene derivative (BODIPY) modified by meso-position triphenylamines substituting 3 and 5-position aromatic groups (BODIPY) and a preparation method thereof, which has a structure of general formula I. Compared with the ultraviolet absorption of the BODIPY parent, the boron fluoride complexed dipyrromethene derivative has an obvious red-shift phenomenon, and its fluorescence emission peak tends to the near-infrared region; and the synthesis method is simple, easy to control, and the yield is high. universality. The BODIPY dyes can be efficiently synthesized and widely used in life science, analytical chemistry, environmental energy science and other fields, especially in organic solar cells. |
| priorityDate | 2014-12-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 61.