Characterization of a Rhodium(I) σ-Methane Complex in Solution

Author:

Bernskoetter Wesley H.1,Schauer Cynthia K.1,Goldberg Karen I.2,Brookhart Maurice1

Affiliation:

1. Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599–3290, USA.

2. Department of Chemistry Box 351700, University of Washington, Seattle, WA 98195–1700, USA.

Abstract

Methane Loosely Bound For the most part, molecular bonds involve sharing of electrons between two discrete atoms. In certain cases, however, a third atom can also attract a portion of the electron density without fully cleaving the bond. Such loose complexes between C-H bonds and transition metals are often invoked as short-lived intermediates in metal-catalyzed reactions of hydrocarbons, though they are rarely observed directly. Bernskoetter et al. (p. 553 ) glimpse this coordination motif for methane (CH 4 ) and rhodium (Rh) using low-temperature nuclear magnetic resonance spectroscopy after protonation of an Rh-CH 3 precursor. Kinetics measurements revealed a half-life of just over 80 minutes at −87°C.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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