Activation of the C-H bond of alkanes by surface metal hydrides: From alkanes metathesis to non oxidative methane coupling

Jean Marie Basset*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

Transformation of alkanes remains a difficult challenge because of the relative inertness of the C?H and C-C bonds. The rewards for asserting synthetic control over unfunctionalized, saturated hydrocarbons are considerable, however, because converting short alkanes into longer chain analogues is usually a value-adding process. Alkane metathesis is a novel catalytic and direct transformation of two molecules of a given alkane into its lower and higher homologues; moreover, the process proceeds at relatively low temperature (ambient conditions or higher). It was discovered through the use of a silica-supported tantalum hydride, (≡SiO) 2TaH, a multifunctional catalyst with a single site of action. This reaction completes the story of the metathesis reactions discovered over the past 40 years: olefin metathesis, alkyne metathesis, and ene?yne cyclizations. In this lecture we examine the fundamental mechanistic aspects of alkane metathesis as well as the novel reactions that have been derived from its study.The silica-supported tantalum hydride was developed as the result of systematic and meticulous studies of the interaction between oxide supports and organometallic complexes, a field of study denoted surface organometallic chemistry (SOMC). A careful examination of this surface-supported tantalum hydride led to the later discovery of alumina-supported tungsten hydride, W(H) 3/Al 2O 3, which proved to be an even better catalyst for alkane metathesis. Supported tantalum and tungsten hydrides are highly unsaturated, electron-deficient species that are very reactive toward the C?H and C?C bonds of alkanes. They show a great versatility in various other reactions, such as cross-metathesis between methane and alkanes, cross-metathesis between toluene and ethane, or even methane nonoxidative coupling. Moreover, tungsten hydride exhibits a specific ability in the transformation of isobutane into 2,3-dimethylbutane.

Original languageEnglish (US)
JournalACS National Meeting Book of Abstracts
StatePublished - 2011

ASJC Scopus subject areas

  • Chemistry(all)
  • Chemical Engineering(all)

Fingerprint

Dive into the research topics of 'Activation of the C-H bond of alkanes by surface metal hydrides: From alkanes metathesis to non oxidative methane coupling'. Together they form a unique fingerprint.

Cite this