| Literature DB >> 27647692 |
Jilai Li1,2, Shaodong Zhou1, Maria Schlangen1, Thomas Weiske1, Helmut Schwarz3.
Abstract
The reactivity of the cationic gold carbide [AuC]+ (bearing an electrophilic carbon atom) towards methane has been studied using Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR-MS). The product pairs generated, that is, Au+ /C2 H4 , [Au(C2 H2 )]+ /H2 , and [C2 H3 ]+ /AuH, point to the breaking and making of C-H, C-C, and H-H bonds under single-collision conditions. The mechanisms of these rather efficient reactions have been elucidated by high-level quantum-chemical calculations. As a major result, based on molecular orbital and NBO-based charge analysis, an unprecedented hydride transfer from methane to the carbon atom of [AuC]+ has been identified as a key step. Also, the origin of this novel mechanistic scenario has been addressed. The mechanistic insights derived from this study may provide guidance for the rational design of carbon-based catalysts.Entities:
Keywords: C−H bond activation; carbide; gas-phase reactions; hydride transfer
Year: 2016 PMID: 27647692 DOI: 10.1002/anie.201606707
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336