Mechanistic insights into the rhenium-catalyzed alcohol-to-olefin dehydration reaction

Chemistry. 2013 Sep 23;19(39):13224-34. doi: 10.1002/chem.201300209. Epub 2013 Aug 14.

Abstract

Rhenium-based complexes are powerful catalysts for the dehydration of various alcohols to the corresponding olefins. Here, we report on both experimental and theoretical (DFT) studies into the mechanism of the rhenium-catalyzed dehydration of alcohols to olefins in general, and the methyltrioxorhenium-catalyzed dehydration of 1-phenylethanol to styrene in particular. The experimental and theoretical studies are in good agreement, both showing the involvement of several proton transfers, and of a carbenium ion intermediate in the catalytic cycle.

Keywords: alcohols; dehydration reaction; density functional calculations; reaction mechanisms; rhenium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohols / chemistry
  • Alkenes / chemistry*
  • Catalysis
  • Coordination Complexes / chemistry*
  • Dehydration
  • Organometallic Compounds / chemistry*
  • Protons
  • Quantum Theory
  • Rhenium / chemistry*

Substances

  • Alcohols
  • Alkenes
  • Coordination Complexes
  • Organometallic Compounds
  • Protons
  • Rhenium
  • methyltrioxorhenium VII