Aromaticity and sterics control whether a cationic olefin radical is resistant to disproportionation.
Journal
Chemical science
ISSN: 2041-6520
Titre abrégé: Chem Sci
Pays: England
ID NLM: 101545951
Informations de publication
Date de publication:
28 Apr 2020
28 Apr 2020
Historique:
received:
06
02
2020
accepted:
28
03
2020
entrez:
11
11
2021
pubmed:
30
3
2020
medline:
30
3
2020
Statut:
epublish
Résumé
We elucidate why some electron rich-olefins such as tetrathiafulvalene (TTF) or paraquat (1,1'-dimethyl-4,4'-bipyridinylidene) form persistent radical cations, whereas others such as the dimer of
Identifiants
pubmed: 34760147
doi: 10.1039/d0sc00699h
pii: d0sc00699h
pmc: PMC8562513
doi:
Types de publication
Journal Article
Langues
eng
Pagination
4138-4149Commentaires et corrections
Type : ErratumIn
Informations de copyright
This journal is © The Royal Society of Chemistry.
Déclaration de conflit d'intérêts
There are no conflicts to declare.
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