http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103755588-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D217-14 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G12-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C241-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C243-38 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-02 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/B01J31-06 |
| filingDate | 2014-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2015-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2015-09-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-103755588-B |
| titleOfInvention | A kind of synthetic method of covalent organic frame material and application |
| abstract | The present invention discloses a kind of synthetic method of covalent organic frame material.The method comprises the steps: equal benzene trioxin and 2,5-bis-(N, N-dimethyl) amino-1, after 4-benzene two hydrazides mixes in organic solvent, covalent organic frame material is obtained by reacting, described equal benzene trioxin and 2,5-bis-(N under the catalysis of acetic acid, N-dimethyl) mol ratio 1:(0.5 ~ 3 of amino-Isosorbide-5-Nitrae-benzene two hydrazides).The covalent organic frame material that employing method obtains has larger specific surface area and regular, that aperture is adjustable pore passage structure, thus is conducive to the mass transfer of reactant and product in photoabsorption and catalytic process, can be used as photocatalyst.The productive rate of this material to the dehydrogenation linked reaction of 2-phenyl-1,2,3,4-tetrahydroisoquinoline and Nitromethane 99Min. can bring up to 89% by 39% during catalyst-free. |
| priorityDate | 2014-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 40.