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Dioxygen dissociation over man-made system at room temperature to form the active α-oxygen for methane oxidation
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SYSNO ASEP 0524418 Document Type J - Journal Article R&D Document Type Journal Article Subsidiary J Článek ve WOS Title Dioxygen dissociation over man-made system at room temperature to form the active α-oxygen for methane oxidation Author(s) Tabor, Edyta (UFCH-W) RID, ORCID
Dědeček, Jiří (UFCH-W) RID, ORCID
Mlekodaj, Kinga (UFCH-W) RID, ORCID
Sobalík, Zdeněk (UFCH-W) RID
Andrikopoulos, Prokopis C. (UFCH-W) RID, ORCID
Sklenák, Štěpán (UFCH-W) RID, ORCID, SAIArticle number eaa9776 Source Title Science Advances. - : American Association for the Advancement of Science - ISSN 2375-2548
Roč. 6, č. 20 (2020)Number of pages 8 s. Language eng - English Country US - United States Keywords INITIO MOLECULAR-DYNAMICS ; N2O DECOMPOSITION ; SELECTIVE OXIDATION Subject RIV CF - Physical ; Theoretical Chemistry OECD category Physical chemistry R&D Projects GA17-00742S GA ČR - Czech Science Foundation (CSF) Method of publishing Open access Institutional support UFCH-W - RVO:61388955 UT WOS 000533573300033 EID SCOPUS 85084786355 DOI 10.1126/sciadv.aaz9776 Annotation Activation of dioxygen attracts enormous attention due to its potential for utilization of methane and applications
in other selective oxidation reactions. We report a cleavage of dioxygen at room temperature over distant binuclear
Fe(II) species stabilized in an aluminosilicate matrix. A pair of formed distant -oxygen species [i.e., (Fe(IV)═O)2+]
exhibits unique oxidation properties reflected in an outstanding activity in the oxidation of methane to methanol
at room temperature. Designing a man-made system that mimicks the enzyme functionality in the dioxygen activation
using both a different mechanism and structure of the active site represents a breakthrough in catalysis.
Our system has an enormous practical importance as a potential industrial catalyst for methane utilization because
(i) the Fe(II)/Fe(IV) cycle is reversible, (ii) the active Fe centers are stable under the reaction conditions, and (iii)
methanol can be released to gas phase without the necessity of water or water-organic medium extraction.Workplace J. Heyrovsky Institute of Physical Chemistry Contact Michaela Knapová, michaela.knapova@jh-inst.cas.cz, Tel.: 266 053 196 Year of Publishing 2021 Electronic address http://hdl.handle.net/11104/0308778
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