http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109336776-B
Outgoing Links
| Predicate | Object |
|---|---|
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C217-86 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H10K85-631 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01L51-54 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C217-86 |
| filingDate | 2018-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2021-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 2021-09-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-109336776-B |
| titleOfInvention | A kind of large sterically hindered alkoxy substituted conjugated compound with triarylamine as end group and its application |
| abstract | A large sterically hindered alkoxy-substituted conjugated compound with triarylamine as an end group relates to the field of organic synthesis, and its structural formula I is as follows: Wherein, Ar is phenyl, naphthyl or anthracenyl, R 1 is H, CH 3 or OCH 3 , and R 2 is a large sterically hindered alkoxy chain. In the present invention, organic triarylamines with better stability are selected as redox active end groups, and conjugated ligands wrapped with dendritic alkoxy groups are used as bridge chains to synthesize compounds attached to large sterically hindered alkoxy chains. It can be seen from electrochemical experiments that the end groups of the triarylamine conjugated compound in the present invention have extremely strong electronic interaction and better charge transport capability, and are particularly suitable for use in insulated molecular wires. |
| priorityDate | 2018-11-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 45.