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Isolated Fe Sites in Metal Organic Frameworks Catalyze the Direct Conversion of Methane to Methanol

Osadchii, DY; Olivos-Suarez, AI; Szecsenyi, A; Li, G; Nasalevich, MA; Dugulan, JA; Crespo, PS; ... Gascon, J; + view all (2018) Isolated Fe Sites in Metal Organic Frameworks Catalyze the Direct Conversion of Methane to Methanol. ACS Catalysis , 8 (6) pp. 5542-5548. 10.1021/acscatal.8b00505. Green open access

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Abstract

Hybrid materials bearing organic and inorganic motifs have been extensively discussed as playgrounds for the implementation of atomically resolved inorganic sites within a confined environment, with an exciting similarity to enzymes. Here, we present the successful design of a site-isolated mixed-metal metal organic framework (MOF) that mimics the reactivity of soluble methane monooxygenase enzyme and demonstrates the potential of this strategy to overcome current challenges in selective methane oxidation. We describe the synthesis and characterization of an Fe-containing MOF that comprises the desired antiferromagnetically coupled high-spin species in a coordination environment closely resembling that of the enzyme. An electrochemical synthesis method is used to build the microporous MOF matrix while integrating the atomically dispersed Fe active sites in the crystalline scaffold. The model mimics the catalytic C–H activation behavior of the enzyme to produce methanol and shows that the key to this reactivity is the formation of isolated oxo-bridged Fe units.

Type: Article
Title: Isolated Fe Sites in Metal Organic Frameworks Catalyze the Direct Conversion of Methane to Methanol
Open access status: An open access version is available from UCL Discovery
DOI: 10.1021/acscatal.8b00505
Publisher version: https://doi.org/10.1021/acscatal.8b00505
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher’s terms and conditions.
Keywords: enzyme-mimicing catalysts; isolated metal sites; methane oxidation; MOFs
UCL classification: UCL
UCL > Provost and Vice Provost Offices > UCL BEAMS
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Maths and Physical Sciences > Dept of Chemistry
URI: https://discovery.ucl.ac.uk/id/eprint/10066223
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