The menshutkin reaction in the gas phase and in aqueous solution: A valence bond study

Peifeng Su, Fuming Ying, Wei Wu*, Philippe C. Hiberty, Sason Shaik

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

37 Scopus citations

Abstract

The recently developed (L. Song, W. Wu, Q. Zhang, S. Shaik, J. Phys. Chem. A 2004, 108, 6017-6024) valence bond method coupled to a polarized continuum model (VBKM) is applied to the Menshutkin reaction, NH3+CH 3Cl→CH3NH3+ +Cl-, in the gas phase and in aqueous solution. The computed barriers and reaction energies at the level of the breathing orbital VB method (P. C. Hiberty, J. P. Flament, E. Noizet, Chem. Phys. Lett. 1992, 189, 259), BOVB and VBPCM//BOVB, are comparable to CCSD(T) and CCSD(T)//PCM results and to experimental values in solution. The gas-phase reaction is endothermic and leads to an ion-pair complex via a late transition state. By contrast, the reaction in the aqueous phase is exothermic and leads to separate solvated ions as reaction products, via an early transition state. The VB calculations provide also the reactivity parameters needed to apply the valence bond state correlation diagram method, VBSCD (S. Shaik, A. Shurki, Angew. Chem. Int. Ed. 1999, 38, 586). It is shown that the reactivity parameters along with their semi-empirical derivations provide together a satisfactory qualitative and quantitative account of the barriers.

Original languageEnglish
Pages (from-to)2603-2614
Number of pages12
JournalChemPhysChem
Volume8
Issue number18
DOIs
StatePublished - 20 Dec 2007

Keywords

  • Ab initio calculations
  • Menshutkin reaction
  • Reaction mechanisms
  • Solvent effects
  • Valence bond theory

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