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Updated: Sep 28, 2025

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Electronic versatility of vanadium in tris-chelates with redox-active ligands
1WestCHEM, School of Chemistry, University of Glasgow, Glasgow G12 8QQ, UK. stephen.sproules@glasgow.ac.uk.
Abstract:
Spectroscopic and computational examination of the neutral tris-dioxolene complex [V(dbcat)3] (dbcat2- = 3,6-di-tert-butylcatecholate) reveals a Class III mixed-valent ground state. The radical is stabilised by delocalisation across the ligands mediated by the energy matched d orbital manifold of the V(V) centre. This electronic structure is compared to the tris-dithiolene and tris-diimine analogues that possess V(IV) and V(II) ions, respectively.
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