http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2752762-C1

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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02E60-10
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C211-54
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/H01M6-16
filingDate 2020-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2021-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1d9a2bc07ac1517b4c952a9bebbadd05
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f629cc928fd51994e10880a88286f392
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dfdda7afe343d3a42be75bcaee958451
publicationDate 2021-08-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2752762-C1
titleOfInvention Highly soluble triphenylamine-based catholyte and electrochemical current source based on it
abstract FIELD: electrochemistry.SUBSTANCE: invention relates to the use of a triphenylamine derivative of the general formula F1 as a soluble cathode material in the composition of a catholite for an electrochemical current source. In formula F1, the substituent R is selected independently and is a halogen atom -F,- Cl or -Br; a nitrile group -CN; a hydrocarbon radical -CnH2n+1, where n=1-20; an ether residue -O-СпН2п+1, where n=1-20; an ether substituent based on oligoethylene glycol -O(CH2CH2O)nH, where n=1-10; an ether substituent based on oligoethylene glycol -O(CH2CH2O)nCH3, where n=1-10; or an ether substituent based on oligoethylene glycol -O(CH2CH2O)nCmH2m+1, where n=1-10, m=1-12; the substituent R1 is selected independently and is a) a fragment of substituted diphenylamine,in which the substituents R3 and R4 are selected independently and represent a halogen atom -F, -Cl or -Br; a hydrocarbon radical -CnH2n+1, where n=1-20; an ether residue -О-CnH2n+1, where n=1-20; an ether substituent based on oligoethylene glycol -O(CH2CH2O)nH, where n=1-10; an ether substituent based on oligoethylene glycol -O(CH2CH2O)nCH3, where n=1-10; an ether substituent based on oligoethylene glycol-O(CH2CH2O)nCmH2m+1, where n=1-10, m=1-12; b) one of the following substituents: a halogen atom -F, -Cl or -Br; a nitrile group -CN; a hydrocarbon radical -CnH2n+1, where n=1-20; the ether residue is -О-CnH2n+1, where n=1-20; the ether substituent based on oligoethylene glycol is O(CH2CH2O)nH, where n=1-10; the ether substituent based on oligoethylene glycol is O(CH2CH2O)nCH3, where n=1-10; the ether substituent based on oligoethylene glycol is O(CH2CH2O)nCmH2m+1, where n=1-10, m=1-12; the R2 substituent is selected independently and is: a) a fragment of substituted diphenylamine,in which the substituents R5 and R6 are selected independently and represent a halogen atom -F, -Cl or-Br; a hydrocarbon radical -CnH2n+1, where n=1-20; an ether residue -О-CnH2n+1, where n=1-20; an ether substituent based on oligoethylene glycol -O(CH2CH2O)nH, where n=1-10; an ether substituent based on oligoethylene glycol -O(CH2CH2O)nCH3, where n=1-10; ether substituent based on oligoethylene glycol -O(CH2CH2O)nCmH2m+1, where n=1-10, m=1-12; b) one of the following substituents: hydrocarbon radical -CnH2n+1, where n=1-20; ether residue -O-CnH2n+1, where n=1-20; the ether substituent based on oligoethylene glycol is -O(CH2CH2O)nH, where n=1-10; the ether substituent based on oligoethylene glycol is -O(CH2CH2O)nCH3, where n=1-10; the ether substituent based on oligoethylene glycol is -O(CH2CH2O)nCmH2m+1, where n=1-10, m=1-12.EFFECT: improvement of the properties of electrochemical current sources and their stability during charge-discharge cycling.8 cl, 38 dwg, 7 ex
priorityDate 2020-10-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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