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dc.contributor.authorMcDonald, Aidan
dc.date.accessioned2020-10-19T20:47:59Z
dc.date.available2020-10-19T20:47:59Z
dc.date.issued2020
dc.date.submitted2020en
dc.identifier.citationMondal, P., Lovisari, M., Twamley, B., McDonald, A.R., Fast Hydrocarbon Oxidation by a High-Valent Nickel-Fluoride Complex, Angewandte Chemie International Edition, 2020en
dc.identifier.otherY
dc.descriptionPUBLISHEDen
dc.description.abstractIn the search for highly reactive oxidants we have identified high‐valent metal–fluorides as a potential potent oxidant. The high‐valent Ni–F complex [NiIII(F)(L)] (2, L=N,N′‐(2,6‐dimethylphenyl)‐2,6‐pyridinedicarboxamidate) was prepared from [NiII(F)(L)]− (1) by oxidation with selectfluor. Complexes 1 and 2 were characterized by using 1H/19F NMR, UV‐vis, and EPR spectroscopies, mass spectrometry, and X‐ray crystallography. Complex 2 was found to be a highly reactive oxidant in the oxidation of hydrocarbons. Kinetic data and products analysis demonstrate a hydrogen atom transfer mechanism of oxidation. The rate constant determined for the oxidation of 9,10‐dihydroanthracene (k2=29 m−1 s−1) compared favorably with the most reactive high‐valent metallo‐oxidants. Complex 2 displayed reaction rates 2000–4500‐fold enhanced with respect to [NiIII(Cl)(L)] and also displayed high kinetic isotope effect values. Oxidative hydrocarbon and phosphine fluorination was achieved. Our results provide an interesting direction in designing catalysts for hydrocarbon oxidation and fluorinationen
dc.language.isoenen
dc.relation.ispartofseriesAngewandte Chemie International Edition;
dc.rightsYen
dc.titleFast Hydrocarbon Oxidation by a High¿Valent Nickel¿Fluoride Complexen
dc.typeJournal Articleen
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/aimcdona
dc.identifier.rssinternalid220860
dc.rights.ecaccessrightsopenAccess
dc.identifier.orcid_id0000-0002-8930-3256
dc.identifier.urihttps://doi.org/10.1002/anie.202004639
dc.identifier.urihttp://hdl.handle.net/2262/93855


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