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Coordination and Electrochemical Switching on Paddle-Wheel Complexes Containing an As−Ru or a Sb−Ru Axis

Gericke, R.; Wagler, J.

Inspired by the known complex [PhP(μ-PyO)₄Ru(CO)] (PyO = 2-pyridyloxy), the family of group 15 paddle-wheel complexes has been expanded to [PhPn(μ-PyO)₄Ru(L)] (Pn = P, As, Sb; L = NCMe, CO). Solvent-dependent reversible switching between [PhAs(μ-PyO)₄Ru(NCMe)] and [PhAs(μ-PyO)₃Ru(κ²-PyO)] was detected. Electrochemical investigations of the [PhPn(μ-PyO)₄Ru(L)] complexes showed reversible oxidation of the complexes with L = NCMe and back-formation of the complexes with L = NCMe upon oxidation of the complexes with L = CO in NCMe. In the series of [PhPn(μ-PyO)₄RuL)] complexes, the Pn→Ru bonding mode is shifted from L-type Pn to X-type upon going from Pn = P and As to Pn = Sb, resulting in a pronounced electron-rich Ru site in the latter case. The easily accessible complex [PhSb(μ-PyO)₄RuCl] exhibits reversible electrochemical and coordinative exchange with its reduced analogue [PhSb(μ-PyO)₄Ru(NCMe)] under retention of the paddle-wheel motif and Sb−Ru bond properties.

Keywords: ambidentate ligands; ruthenium; pnictogen; hetero bimetallic; electrochemical switching

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  • Secondary publication expected from 23.11.2022

Permalink: https://www.hzdr.de/publications/Publ-33447
Publ.-Id: 33447