| Full text | |
| Author(s): |
Arantes, Guilherme M.
;
Ribeiro, Mauro C. C.
Total Authors: 2
|
| Document type: | Journal article |
| Source: | Journal of Chemical Physics; v. 128, n. 11 MAR 21 2008. |
| Web of Science Citations: | 14 |
| Abstract | |
The solvation effect of the ionic liquid 1-N-butyl-3-methylimidazolium hexafluorophosphate on nucleophilic substitution reactions of halides toward the aliphatic carbon of methyl p-nitrobenzenesulfonate (pNBS) was investigated by computer simulations. The calculations were performed by using a hybrid quantum-mechanical/molecular-mechanical (QM/MM) methodology. A semiempirical Hamiltonian was first parametrized on the basis of comparison with ab initio calculations for Cl- and Br- reaction with pNBS at gas phase. In condensed phase, free energy profiles were obtained for both reactions. The calculated reaction barriers are in agreement with experiment. The structure of species solvated by the ionic liquid was followed along the reaction progress from the reagents, through the transition state, to the final products. The simulations indicate that this substitution reaction in the ionic liquid is slower than in nonpolar molecular solvents proper to significant stabilization of the halide anion by the ionic liquid in comparison with the transition state with delocalized charge. Solute-solvent interactions in the first solvation shell contain several hydrogen bonds that are formed or broken in response to charge density variation along the reaction coordinate. The detailed structural analysis can be used to rationalize the design of new ionic liquids with tailored solvation properties. (c) 2008 American Institute of Physics. (AU) | |
| FAPESP's process: | 07/02371-5 - Computer simulations of nucleophilic reactions solvated by ionic liquids |
| Grantee: | Guilherme Menegon Arantes |
| Support Opportunities: | Research Grants - Meeting - Abroad |