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Oxy-Functionalization of Nucleophilic Rhenium(I) Metal Carbon Bonds Catalyzed by Selenium(IV)
Division of Chemistry and Chemical Engineering, California Institute of Technology.ORCID iD: 0000-0002-1553-4027
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2009 (English)In: Journal of the American Chemical Society, ISSN 0002-7863, E-ISSN 1520-5126, Vol. 131, no 7, 2466-2468 p.Article in journal (Refereed) Published
Abstract [en]

We report that SeO(2) catalyzes the facile oxy-functionalization of (CO)(5)Re(I)-Me(delta-) with IO(4)(-) to generate methanol. Mechanistic studies and DFT calculations reveal that catalysis involves methyl group transfer from Re to the electrophilic Se center followed by oxidation and subsequent reductive functionalization of the resulting CH(3)Se(VI) species. Furthermore, (CO)(3)Re(I)(Bpy)-R (R = ethyl, n-propyl, and aryl) complexes show analogous transfer to SeO(2) to generate the primary alcohols. This represents a new strategy for the oxy-functionalization of M-R(delta-) polarized bonds.

Place, publisher, year, edition, pages
2009. Vol. 131, no 7, 2466-2468 p.
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Inorganic Chemistry
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URN: urn:nbn:se:kth:diva-48873DOI: 10.1021/ja806814cISI: 000263576100024OAI: oai:DiVA.org:kth-48873DiVA: diva2:488426
Note
QC 20120202Available from: 2012-02-01 Created: 2011-11-23 Last updated: 2017-12-08Bibliographically approved

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Ahlquist, Mårten

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