http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104151174-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C217-20 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K41-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P31-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C213-08 |
| filingDate | 2014-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2016-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2016-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-104151174-B |
| titleOfInvention | A kind of oligomerization phenylacetylene compound and preparation method and application |
| abstract | Present invention oligomerization phenylacetylene compound that a kind of formula (I) and formula (II) are provided and preparation method thereof and they during photoinduction is antibacterial as the application of photosensitizer.The preparation method using the present invention has synthesized the oligomerization phenylacetylene molecule that a kind of length is about 3.2nm the method introducing amino by end, increases the water solublity of oligomerization phenylacetylene compound.This oligomerization phenylacetylene compou nd synthesis route is simple, mild condition, and reagent is general, and productivity is high, is suitable for amplifying production and having good photoinduction antibacterial effect.Antibacterial experiment shows: formula (I) and formula (II) oligomerization phenylacetylene compound have good photolytic activity antibacterial effect, uses ultraviolet light and white light all can play antibacterial activity when shining as light source light, and antibacterial effect during not illumination is the most weak. |
| priorityDate | 2014-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 74.