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Electronic versatility of vanadium in tris-chelates with redox-active ligands.

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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… Click to show full 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.

Keywords: tris chelates; redox active; vanadium tris; electronic versatility; chelates redox; versatility vanadium

Journal Title: Dalton transactions
Year Published: 2022

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