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Issue 4, 2012
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Quantum chemical characterization of the mechanism of an iron-based water oxidation catalyst

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Abstract

Theoretical models are used to demonstrate a catalytic cycle for the generation of O2 from an iron(III)-centered tetraamido macrocycle in water that is consistent with experimentally observed energetics in the presence of a sacrificial oxidant. Application of density functional theory and multireference second-order perturbation theory indicates that two proton-coupled electron transfer steps followed by an electron-transfer step first generate a reactive species that is well described as an iron(V)-oxo supported by a macrocycle that has also suffered a one-electron oxidation. Subsequent O–O bond formation occurs through water nucleophilic attack on the iron-oxo with the local solvent shell serving to relay a proton away from the reacting partners. Subsequent steps of proton-coupled electron transfer and low-energy water displacement of O2 complete the catalytic cycle. Modification of the TAML ligand to reduce the likely instability of the non-innocent aromatic radical may prove useful in future catalyst design.

Graphical abstract: Quantum chemical characterization of the mechanism of an iron-based water oxidation catalyst

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Publication details

The article was received on 08 Dec 2011, accepted on 05 Jan 2012 and first published on 12 Jan 2012


Article type: Edge Article
DOI: 10.1039/C2SC01030E
Citation: Chem. Sci., 2012,3, 1293-1299
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    Quantum chemical characterization of the mechanism of an iron-based water oxidation catalyst

    M. Z. Ertem, L. Gagliardi and C. J. Cramer, Chem. Sci., 2012, 3, 1293
    DOI: 10.1039/C2SC01030E

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