http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-11168178-B2
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_8f1cbff5070cfc09ac227ec24021214a |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-414 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-514 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-91 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-3223 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-3246 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-3243 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-122 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-1412 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-18 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-149 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-146 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C09D165-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G2261-12 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G61-126 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C08G61-122 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/H01B1-12 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C08G61-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01L51-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01L51-42 |
| filingDate | 2020-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2021-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_97ff4750e2562ea7d590392b42b6cf37 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d9d234a53900dfd73dc003bc3fcd42e5 |
| publicationDate | 2021-11-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | US-11168178-B2 |
| titleOfInvention | Method of synthesis for organic semiconducting polymers |
| abstract | A method of forming a polymer, the method comprising combining 4,7-bis(5-bromo-4-alkyl thiophen-2-yl)-5-chloro-6-fluorobenzo[c][1,2,5]thiadiazole, (3,3′-difluoro-[2,2′-bithiophene]-5,5′-diyl)bis(trimethylstannane), and benzo[1,2-b:4,5-b′]dithiophene-2,6-diyl)bis(trimethylstannane), Pd2dba3 and P(o-tol)3 to form the polymer:In this polymer, W is selected from the group consisting of: S, Se, O, and N-Q. Additionally, in this polymer Q is selected from the group consisting of: a straight-chain or branched carbyl, silyl, or hydrocarbyl, a branched or cyclic alkyl with 1 to 30 atoms, a fused substituted aromatic ring, and a fused unsubstituted aromatic ring. R1, R2, R3, R4, and R5 are independently selected from the group consisting of: F, Cl, I, Br, CN, —NCO, —NCS, —OCN, —SCN, —OX, —SX, —NH2, —C(═O)X, —C(═O)—OX, —OX, —NHX, —NXX′, —C(═O)NHX, —C(═O)NXX′, —SO3X, —SO2X, —OH, —NO2, CF3, —SF5, a straight-chain or branched carbyl, silyl, or hydrocarbyl, a branched or cyclic alkyl with 1 to 30 atoms, a fused substituted aromatic ring, and a fused unsubstituted aromatic ring, and heteroaromatic rings. Additionally, in this polymer wherein the fused aromatic rings can be independently fused with groups consisting of: a straight-chain or branched carbyl, silyl, or hydrocarbyl, a branched or cyclic alkyl with 1 to 30 atoms, a fused substituted aromatic ring, and a fused unsubstituted aromatic ring; and the ratio of x is between 0.6 to 0.8 and y is between 0.2 and 0.4. |
| priorityDate | 2019-08-27-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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