Incorporation of Mn into an established water oxidation catalyst based on a Co(III) 4 O 4 cubane was achieved by a simple and efficient assembly of permanganate, cobalt(II) acetate, and pyridine to form the cubane oxo cluster MnCo 3 O 4 (OAc) 5 py 3 (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 – ligand for Cl – ( 1-Cl ), NO 3 – ( 1-NO 3 ), and pyridine ( [1-py] + ). EPR spectroscopy, SQUID magnetometry, and DFT calculations thoroughly characterized the valence assignment of the cubane as [Mn IV Co III 3 ]. 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 3 O 4 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.
No takes yet. Share an insight, caveat, or question.
Nguyen et al. (2017) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: