Hydrocarbon reactivity in the superacid SbF5/HF: An ab initio molecular dynamics study

Simone Raugei, Michael L. Klein

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)


The free energy profiles for the protonation of simple alkanes in SbF5/HF superacid solution have been studied by ab initio molecular dynamics simulations. It is shown that the presence of extremely reactive protons at high SbF5 concentrations open reaction channels for the C-H protonation with a considerably decreased barrier with respect to dilute solutions and the gas phase. It is proposed that this, along with the progressive presence of neutral SbF5, is responsible for the experimentally observed increased reactivity of these solutions as the concentration of SbF5 is increased. It has also been found that in solution an electrostatic stabilization of the transition state contributes to the lowering of the reaction barrier. In the case of ethane C-H protonation is in competition with C-C protonation. In fact, nearby, the transition state of C-C protonation, alternative reaction pathways that lead to the C-H protonation are accessible.

Original languageEnglish
Pages (from-to)11596-11605
Number of pages10
JournalJournal of Physical Chemistry B
Issue number44
Publication statusPublished - Nov 7 2002

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Surfaces, Coatings and Films
  • Materials Chemistry

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