Manganese–Cobalt Oxido Cubanes Relevant to Manganese-Doped Water Oxidation Catalysts
Article 2017 en
Authors
AN
Andy I. Nguyen
DS
Daniel L. M. Suess
LD
Lucy E. Darago
Abstract
1 min read
Incorporation of Mn into an established water oxidation catalyst based on a Co(III)<sub>4</sub>O<sub>4</sub> cubane was achieved by a simple and efficient assembly of permanganate, cobalt(II) acetate, and pyridine to form the cubane oxo cluster MnCo<sub>3</sub>O<sub>4</sub>(OAc)<sub>5</sub>py<sub>3</sub> (OAc = acetate, py = pyridine) (1-OAc) in good yield. This allows characterization of electronic and chemical properties for a manganese center in a cobalt oxide environment, and provides a molecular model for Mn-doped cobalt oxides. The electronic properties of the cubane are readily tuned by exchange of the OAc<sup>-</sup> ligand for Cl<sup>-</sup> (1-Cl), NO<sub>3</sub><sup>-</sup> (1-NO<sub>3</sub>), and pyridine ([1-py]<sup>+</sup>). EPR spectroscopy, SQUID magnetometry, and DFT calculations thoroughly characterized the valence assignment of the cubane as [Mn<sup>IV</sup>Co<sup>III</sup><sub>3</sub>]. These cubanes are redox-active, and calculations reveal that the Co ions behave as the reservoir for electrons, but their redox potentials are tuned by the choice of ligand at Mn. This MnCo<sub>3</sub>O<sub>4</sub> cubane system represents a new class of easily prepared, versatile, and redox-active oxido clusters that should contribute to an understanding of mixed-metal, Mn-containing oxides.
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