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Redox-State-Driven Site Selectivity and Kinetic Gating in Polyoxovanadate Methylation
Journal article   Open access   Peer reviewed

Redox-State-Driven Site Selectivity and Kinetic Gating in Polyoxovanadate Methylation

Nghia Le and Pere Miró
Inorganic chemistry, Vol.65(32), pp.18563-18571
08/06/2026
DOI: 10.1021/acs.inorgchem.6c01638
PMID: 42606270
url
https://doi.org/10.1021/acs.inorgchem.6c01638View
Published (Version of record) Open Access

Abstract

Polyoxovanadate clusters offer atomically defined platforms for studying how electronic structure influences reactivity at molecular metal-oxide surfaces. In this computational study, we investigated the coupling between reduction state and alkylation reactivity in the hexavanadate cluster [V6O13(TRIOLX)2]2– (TRIOL = tris(hydroxymethyl)methane; X = −CH3, −NO2) through a systematic analysis of successive methylation and reduction pathways using density functional theory and microkinetic modeling. The calculations show that changes in electron count redistribute the nucleophilicity of bridging μ2-oxo ligands, leading to redox-dependent regioselectivity during sequential methylation. Microkinetic simulations further indicate that several thermodynamically accessible intermediates do not accumulate because they are rapidly consumed in subsequent transformations, consistent with the need for stepwise synthetic strategies to isolate certain dimethylated species. In addition, substituent effects on the TRIOL ligands follow Hammett-type correlations, allowing rapid estimation of electronic trends without additional quantum chemical calculations. Overall, the results provide a detailed picture of how reduction state influences accessibility and selectivity during polyoxovanadate methylation.

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