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  • Structural characterization of a non-heme iron active site in zeolites that hydroxylates methane PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA Snyder, B. R., Bottger, L. H., Bols, M. L., Yan, J. J., Rhoda, H. M., Jacobs, A. B., Hu, M. Y., Zhao, J., Alp, E., Hedman, B., Hodgson, K. O., Schoonheydt, R. A., Sels, B. F., Solomon, E. I. 2018; 115 (18): 4565–70

    Abstract

    Iron-containing zeolites exhibit unprecedented reactivity in the low-temperature hydroxylation of methane to form methanol. Reactivity occurs at a mononuclear ferrous active site, α-Fe(II), that is activated by N2O to form the reactive intermediate α-O. This has been defined as an Fe(IV)=O species. Using nuclear resonance vibrational spectroscopy coupled to X-ray absorption spectroscopy, we probe the bonding interaction between the iron center, its zeolite lattice-derived ligands, and the reactive oxygen. α-O is found to contain an unusually strong Fe(IV)=O bond resulting from a constrained coordination geometry enforced by the zeolite lattice. Density functional theory calculations clarify how the experimentally determined geometric structure of the active site leads to an electronic structure that is highly activated to perform H-atom abstraction.

    View details for DOI 10.1073/pnas.1721717115

    View details for Web of Science ID 000431119600036

    View details for PubMedID 29610304

    View details for PubMedCentralID PMC5939097