Inversion of methane on transition-metal complexes: A possible mechanism for inversion of stereochemistry

Kazunari Yoshizawa, Akiya Suzuki, Tokio Yamabe

研究成果: Contribution to journalArticle査読

36 被引用数 (Scopus)

抄録

The inversion of methane bound to first-row transition-metal ions from Sc+ to Cu+ is systematically investigated using the B3LYP method, a hybrid density-functional-theory method of Becke and Lee, Yang, and Parr. The computed transition states for the methane inversion on the M+(CH4) complexes have a C(s) structure in which one pair of C-H bonds is about 1.2 Å in length and the other pair is about 1.1 Å. The barrier height for the methane inversion is significantly decreased from 109 kcal/mol for free methane to 43-48 kcal/mol on the late transition-metal complexes, Fe+(CH4), Co+(CH4), Ni+(CH4), and Cu+(CH4). Since each activation energy involves the binding energy of the complex (16 kcal/mol on the average), the actual barrier height should be lower by this quantity if measured from the dissociation limit. The inversion of methane can therefore occur at the transition-metal active center of catalysts or enzymes under ambient conditions through a thermally accessible transition state, and it would reasonably lead to inversion of stereochemistry at a carbon atom in catalytic reactions of hydrocarbons. We propose that a radical mechanism based on a planar carbon species may not be the sole source of the observed loss of stereochemistry in transition-metal-catalyzed hydrocarbon hydroxylations and other related reactions.

本文言語英語
ページ(範囲)5266-5273
ページ数8
ジャーナルJournal of the American Chemical Society
121
22
DOI
出版ステータス出版済み - 6 9 1999
外部発表はい

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Chemistry(all)
  • Biochemistry
  • Colloid and Surface Chemistry

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