• Hodgson, Keith O.
• Hedman, Britt
• Schoonheydt, Robert A.
• Solomon, Edward I.
• Zhao, Jiyong
• Alp, E. Ercan
• Jacobs, Ariel B.
• Hu, Michael Y.
• Sels, Bert F.
• Yan, James J.
• Rhoda, Hannah M.
• Bottger, Lars H.
• Bols, Max L.
• Snyder, Benjamin E. R.

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.

Topics

• density
• impedance spectroscopy
• theory
• Oxygen
• reactive
• density functional theory
• iron
• x-ray absorption spectroscopy
• vibrational spectroscopy