Strong spin-orbit coupling facilitates C-H activation in the reactions of Os+ with CH3F

Theoretical investigations

Joonghan Kim, Kiryong Hong, Hyun Kook Kim, Yoon Sup Lee, Tae Kyu Kim

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

The relativistic effects are essential for a complete understanding of the reactions involving heavy transition metal cations with hydrocarbons. Despite this, spin-orbit coupling (SOC) along the reaction pathway is rarely considered. In this work, we demonstrate an unusual SOC on the chemical reactivity of a reaction of Os+ with methyl fluoride (CH3F) using density functional theory (DFT), high-level ab initio, and spin-orbit multiconfigurational ab initio methods. With the inclusion of the SO effect in the relevant potential energy surfaces (PESs), C-H bond activation by an Os + cation occurs readily via almost barrierless (about 2 kcal/mol) PESs of the SO coupled ground state. In contrast, a substantial reaction barrier was observed for C-F bond activation. The calculated results are in line with recent systematic experimental findings for reactions of transition metal cations with CH3F. These results show that the SO effect can facilitate specific bond activation in chemical reactions associated with catalytic transition metal cations.

Original languageEnglish
Pages (from-to)1087-1092
Number of pages6
JournalJournal of Chemical Theory and Computation
Volume9
Issue number2
DOIs
Publication statusPublished - 2013 Feb 12

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Cations
Orbits
Positive ions
Chemical activation
activation
Transition metals
orbits
Potential energy surfaces
cations
transition metals
Chemical reactivity
potential energy
Hydrocarbons
Ground state
Heavy metals
Density functional theory
Chemical reactions
heavy metals
relativistic effects
fluorides

All Science Journal Classification (ASJC) codes

  • Physical and Theoretical Chemistry
  • Computer Science Applications

Cite this

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abstract = "The relativistic effects are essential for a complete understanding of the reactions involving heavy transition metal cations with hydrocarbons. Despite this, spin-orbit coupling (SOC) along the reaction pathway is rarely considered. In this work, we demonstrate an unusual SOC on the chemical reactivity of a reaction of Os+ with methyl fluoride (CH3F) using density functional theory (DFT), high-level ab initio, and spin-orbit multiconfigurational ab initio methods. With the inclusion of the SO effect in the relevant potential energy surfaces (PESs), C-H bond activation by an Os + cation occurs readily via almost barrierless (about 2 kcal/mol) PESs of the SO coupled ground state. In contrast, a substantial reaction barrier was observed for C-F bond activation. The calculated results are in line with recent systematic experimental findings for reactions of transition metal cations with CH3F. These results show that the SO effect can facilitate specific bond activation in chemical reactions associated with catalytic transition metal cations.",
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Strong spin-orbit coupling facilitates C-H activation in the reactions of Os+ with CH3F : Theoretical investigations. / Kim, Joonghan; Hong, Kiryong; Kim, Hyun Kook; Lee, Yoon Sup; Kim, Tae Kyu.

In: Journal of Chemical Theory and Computation, Vol. 9, No. 2, 12.02.2013, p. 1087-1092.

Research output: Contribution to journalArticle

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