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A dianionic allene bound to vanadium(iii) enables interconversion between vanadatetrahedranes, vanadacyclobutadienes and deprotiovanadacyclobutadienes

Russell JB, Grigas DP, Körber E, Bacon AM, Gau MR, Meyer K, Reiß F, Beweries T, Mindiola DJ (2026)

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Publication Type: Journal article

Publication year: 2026

Journal

DOI: 10.1039/d6sc05321a

Abstract

Herein we disclose a novel route to redox-active vanadacyclobutadiene (VCBD) and vanadatetrahedrane (VTd) complexes, which circumvents a vanadium alkylidyne precursor ([V^V]CR). [V^V] VCBD salts and VTd's are prepared through an unusual, non-classical oxidative addition reaction via the addition of electrophiles to a low-spin [V^III] deprotiovanadacyclobutadiene (dVCBD). The microscopic reverse reaction, a reductive elimination, reverts the [V^V] VCBD and VTd scaffolds back to the low-spin [V^III] dVCBD species via the addition of a Brønsted base. The interconversion of the [V^V] VCBD salts and VTd's is mediated through anion exchange, which promotes a change in the spin-state and geometry of the organometallic species, highlighting the redox active nature of the allene ligand (C3) bound to vanadium (V). Single electron reduction of the [V^V] VCBD or VTd with cobaltocene (CoCp2) led to the formation of neutral and radical-based [V^IV] VCBDs. Oxidation of the [V^IV] VCBDs with ferrocenium based salts ([FeCp2][X], X = BArF20⁻, BArF24⁻, OTf⁻) or chloride-delivering oxidants (i.e. triphenylmethyl chloride (Ph3CCl) or lead(ii) chloride (PbCl2)) regenerates the discrete [V^V] VCBD salts or VTd's, respectively. Cyclic voltammetry studies reveal quasi-reversible one electron redox couples, while X-band electron paramagnetic resonance (EPR) spectroscopic studies confirms the presence of a paramagnetic [V^IV], d¹ system in the VCBD. Computational analysis of the dVCBD, VTd, and VCBD complexes affords detailed insight into the structure and bonding of this unusual class of molecules and delineates the role of the anion in their interconversion. Further examination of the reaction of dVCBD with electrophiles corroborates the nonclassical character of the oxidative addition sequence involving metal–ligand cooperation, with ligand-centered redox activity, rather than a formal two-electron oxidation at the metal center. The present work demonstrates how these rare dVCBD, VCBD, and VTd scaffolds can all be interconverted via reversible C–C bond formation and splitting pathways using the right combination of anion exchange, redox, and Brønsted acid–base chemistry.

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How to cite

APA:

Russell, J.B., Grigas, D.P., Körber, E., Bacon, A.M., Gau, M.R., Meyer, K.,... Mindiola, D.J. (2026). A dianionic allene bound to vanadium(iii) enables interconversion between vanadatetrahedranes, vanadacyclobutadienes and deprotiovanadacyclobutadienes. Chemical Science. https://doi.org/10.1039/d6sc05321a

MLA:

Russell, John B., et al. "A dianionic allene bound to vanadium(iii) enables interconversion between vanadatetrahedranes, vanadacyclobutadienes and deprotiovanadacyclobutadienes." Chemical Science (2026).

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