[Mn4O4{O2P(OtBu)2}6] (1), an Mn4O4 cubane complex combining the structural inspiration of the photosystem II oxygen-evolving complex with thermolytic precursor ligands, was synthesized and fully characterized. Core oxygen atoms within complex 1 are transferred upon reaction with an oxygen-atom acceptor (PEt3), to give the butterfly complex [Mn4O2{O2P(OtBu)2}6(OPEt3)2]. The cubane structure is restored by reaction of the latter complex with the O-atom donor PhIO. Complex 1 was investigated as a precursor to inorganic Mn metaphosphate/pyrophosphate materials, which were studied by X-ray absorption spectroscopy to determine the fate of the Mn4O4 unit. Under the conditions employed, thermolyses of 1 result in reduction of the manganese to Mn(II) species. Finally, the related butterfly complex [Mn4O2{O2P(pin)}6(bpy)2] (pin = pinacolate) is described.
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http://dx.doi.org/10.1002/chem.201406114 | DOI Listing |
J Chem Phys
February 2024
Institute of Theoretical Chemistry, Faculty of Chemistry, University of Vienna, Währinger Str. 17, 1090 Vienna, Austria.
Understanding the protonation behavior of metal-oxo water oxidation catalysts is essential to improve catalyst efficiency and long-term performance, as well as to tune their properties for specific applications. In this work, we explore the basicity and protonation effects of the highly active water oxidation catalyst [(Mn4O4) (V4O13) (OAc)3]3- using density functional theory. We computed the relative free energies of protonation in a systematic fashion for all symmetry-inequivalent O atoms, where the presence of multiple oxidation states from Mn4IV to Mn4III and a rich Jahn-Teller isomerism adds a significant amount of complexity.
View Article and Find Full Text PDFACS Catal
November 2021
Institute of Theoretical Chemistry, Faculty of Chemistry, University of Vienna, Währinger Straße 17, 1090 Vienna, Austria.
Understanding how water oxidation to molecular oxygen proceeds in molecular metal-oxo catalysts is a challenging endeavor due to their structural complexity. In this report, we unravel the water oxidation mechanism of the highly active water oxidation catalyst [MnVO(OAc)], a polyoxometalate catalyst with a [MnO] cubane core reminiscent of the natural oxygen-evolving complex. Starting from the activated species [Mn VO(OAc)(HO)(OH)], we scrutinized multiple pathways to find that water oxidation proceeds via a sequential proton-coupled electron transfer (PCET), O-O bond formation, another PCET, an intramolecular electron transfer, and another PCET resulting in O evolution, with a predicted thermodynamic overpotential of 0.
View Article and Find Full Text PDFChem Commun (Camb)
April 2020
College of Materials Science and Technology, Jiangsu Key Laboratory of Electrochemical Energy Storage Technologies, Nanjing University of Aeronautics and Astronautics, 211106, Nanjing, P. R. China.
A BiVO4 photoanode was combined with bioinspired Mn4O4-cubane, which has a structure and composite similar to those of the oxygen-evolving complex (Mn4CaO5) in photosystem II. The hybrid photoanode exhibited a lower onset potential and higher photocurrent than the pristine photoanode because of the faster kinetics of the reaction and reduced rate of recombination of the carriers.
View Article and Find Full Text PDFInorg Chem
November 2019
Department of Chemistry and Chemical Engineering , California Institute of Technology, 1200 E. California Blvd MC 127-72 , Pasadena , California 91125 , United States.
The function of proteins involved in electron transfer is dependent on cofactors attaining the necessary reduction potentials. We establish a mode of cluster redox tuning through steric pressure on a synthetic model related to Photosystem II. Resembling the cuboidal [CaMnO] subsite of the biological oxygen evolving complex (OEC), [MnO] and [YMnO] complexes featuring ligands of different basicity and chelating properties were characterized by cyclic voltammetry.
View Article and Find Full Text PDFInorg Chem
September 2016
Department of Chemistry, University of Florida, Gainesville, Florida 32611-7200, United States.
Three complexes are reported from the initial use of dimethylarsinic acid (Me2AsO2H) in Mn(III/IV) cluster chemistry, [Mn4O4(O2AsMe2)6] (3; 2Mn(III), 2Mn(IV)), and [Mn16X4O8(O2CPh)16(Me2AsO2)24] (X = Ca(2+) (4) or Sr(2+) (5); 16Mn(III)). They were obtained from reactions with [Mn12O12(O2CR)16(H2O)4] (R = Me, Ph) either without (3) or with (4 and 5) the addition of X(2+) salts. Complex 3 contains a [Mn4O4](6+) cubane, whereas isostructural 4 and 5 contain a planar loop structure comprising four Mn4 asymmetric "butterfly" units linked by alternating anti,anti μ-O2AsMe2 and {X2(O2AsMe2)(O2CPh)2} units.
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