Synthesis, Reactions, and Molecular and Electronic Structure of the Radical Cation [Mo2(μ-C8Me8)(η-C5H5)2]+: An Intermediate in the Redox Activation of an Alkyl C−H Bond
Author:
Affiliation:
1. School of Chemistry, University of Bristol, Bristol BS8 1TS, U.K., and Department of Chemistry, Brown University, Providence, Rhode Island 02912
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/om950529i
Reference20 articles.
1. Electron-transfer mechanism for a hydride-transfer reaction: evidence for selective .alpha.-hydride abstraction from a transition metal alkyl
2. New mechanistic probes of hydride abstraction from rhenium-alkyl complexes (.eta.5-C5H5)Re(NO)(PPh3)(R) by Ph3C+ PF6-. Evidence for initial electron transfer
3. Reactions of (CO)2(η5-C5H5)Fe Alkyls and Ph3C+ BF4
4. Activation of µ-alkylidene ligands through oxidation–deprotonation: a new synthesis of µ-methyne, and is hydrogenation to µ-methyl
5. Activation of a µ3-ethylidyne ligand through oxidation–deprotonation: X-ray structure of [Ru3(µ3-CMe)(µ-CO)3(η-C5Me5)3][BF4]
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