http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109134830-B
Outgoing Links
Predicate | Object |
---|---|
classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-3246 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-71 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-3221 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-124 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-18 |
classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G61-126 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G61-124 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G61-12 |
filingDate | 2018-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
grantDate | 2021-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationDate | 2021-01-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | CN-109134830-B |
titleOfInvention | Porphyrin-benzothiadiazole bifunctional covalent organic framework material and preparation method and application thereof |
abstract | The invention relates to the technical field of porous materials, in particular to a porphyrin-diazosulfide bifunctional covalent organic framework material and a preparation method and application thereof. The porphyrin-benzothiadiazole bifunctional covalent organic framework material provided by the invention has better ultraviolet light absorption performance. The preparation method of the porphyrin-benzothiadiazole bifunctional covalent organic framework material provided by the invention comprises the following steps: carrying out polymerization reaction on 4, 7-di (p-formylphenyl) -2,1, 3-benzothiadiazole and pyrrole in the presence of organic acid to obtain a covalent organic framework material; the temperature of the polymerization reaction is 130-150 ℃. |
priorityDate | 2018-09-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 49.