Formation of High-Oxidation-State Metal–Carbon Double Bonds
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6b00825.docx
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722.43 KB
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Author(s)
Schrock, Richard Royce
Copéret, Christophe
Date Issued
May 2017
Journal
Organometallics
Publisher
American Chemical Society (ACS)
Citation
Schrock, Richard R. and Christophe Copéret. “Formation of High-Oxidation-State Metal–Carbon Double Bonds.” Organometallics 36, 10 (March 2017): 1884–1892 © 2017 American Chemical Society
Version
Author's final manuscript
Abstract
This tutorial explores the major pathways of forming metal–carbon double bonds in high-oxidation-state alkylidene complexes that began with the alkylidene chemistry of tantalum complexes in the 1970s and continued with the organometallic chemistry of Mo, W, and Re and the development of homogeneous catalysts for the metathesis of olefins. It also explores recent findings in surface organometallic chemistry and discusses the link between molecularly defined and heterogeneous catalysts. Recent results suggest that heterogeneous olefin metathesis catalysts that are activated toward metathesis upon exposure to olefins produce a d[superscript 0] alkylidene through formation of a metallacyclopentane ring at d[superscript 2] metal sites followed by “a ring contraction” to a metallacyclobutane, a reaction that was first observed in tantalum chemistry.
MIT Department
Massachusetts Institute of Technology. Department of Chemistry
Terms of Use
Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.
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DOI of Published Version
https://doi.org/10.1021/acs.organomet.6b00825
