Clark, Ewan R, Saines, Paul J. (2021) A Short, Versatile Route Towards Benzothiadiazinyl Radicals. Chemical Science, . ISSN 2041-6520. (doi:10.1039/D1SC04248C) (KAR id:91710)
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Official URL: https://pubs.rsc.org/en/content/articlelanding/202... |
Abstract
A family of substituted 1,2,4-benzothiadiazine 1-chlorides have been prepared by treatment of N-arylamidines in neat
thionyl chloride at reflux. The S(IV) 1-chlorides are readily reduced under mild conditions to persistent 1,2,4-
benzothiadiazinyl radicals which have been characterised by EPR spectroscopy and cyclic voltammetry. Crystallographic
studies on isolated radicals indicate that the radicals dimerise via pancake bonding in the solid-state, resulting in
spin-pairing and net diamagnetism.
Item Type: | Article |
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DOI/Identification number: | 10.1039/D1SC04248C |
Subjects: | Q Science > QD Chemistry > QD156 Inorganic synthesis |
Divisions: | Divisions > Division of Natural Sciences > Chemistry and Forensics |
Depositing User: | Ewan Clark |
Date Deposited: | 24 Nov 2021 09:28 UTC |
Last Modified: | 09 Dec 2021 08:53 UTC |
Resource URI: | https://kar.kent.ac.uk/id/eprint/91710 (The current URI for this page, for reference purposes) |
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