http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-111018895-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-183 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C29-143 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/B01J31-2404 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F3-003 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07F15-0053 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-22 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F19-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F3-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C29-143 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F15-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C33-46 |
| filingDate | 2018-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2022-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2022-05-31-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-111018895-B |
| titleOfInvention | Tetrapyridyl porphyrin zinc-dimyristyl ruthenium complex as well as preparation and application thereof |
| abstract | The invention discloses a synthesis method and application of a tetrapyridyl porphyrin zinc-tetracoselenum ruthenium complex. Under the condition of room temperature, coordination reaction is carried out between coordination unsaturated porphyrin zinc-ruthenium complex serving as a raw material and a nitrogen-containing hexadentate ligand in an organic solvent, and the tetrapyridyl porphyrin zinc-icosyl ruthenium complex with higher catalytic activity is obtained through simple post-treatment after the reaction is finished. The zinc tetrapyridylporphyrin-twenty-four-core ruthenium complex can be applied to hydrogen transfer reaction and is a simple, convenient and green method for preparing secondary alcohol. |
| priorityDate | 2018-10-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 52.