An Ionic Liquid Dependent Mechanism for Base Catalyzed beta-Elimination Reactions from QM/MM Simulations

作者：Allen Caley; Sambasivarao Somisetti V; Acevedo Orlando^*

来源：Journal of the American Chemical Society, 2013, 135(3): 1065-1072.

DOI：10.1021/ja3098614

Ionic liquids have been proposed to induce a mechanistic change in the reaction pathway for the fundamentally important base-induced beta-elimination class compared to conventional solvents. The role of the reaction medium in the elimination of 1,1,1-tribromo-2,2-bis(3,4-dimethoxyphenyl)ethane via two bases, piperidine and pyrrolidine, has been computationally investigated using methanol and the ionic liquids 1-buty1-3-methylimidazolium tetrafluoroborate and hexafluorophosphate [BMIM][BF4] and [BMIM] [PF6], respectively. QM/MM Monte Carlo simulations utilizing free-energy perturbation theory found the ionic liquids did produce a reaction pathway change from an ElcB-like mechanism in methanol to a pure E2 route that is consistent with experimental observations. The origin of the ionic liquid effect has been found as: (1) a combination of favorable electrostatic interactions, for example, bromine-imidazolium ion, and (2) pi-pi interactions that enhance the coplanarity between aromatic rings maximizing the electronic effects exerted on the reaction route. Solute solvent interaction energies have been analyzed and show that liquid clathrate solvation of the transition state is primarily responsible for the observed mechanistic changes. This work provides the first theoretical evidence of an ionic liquid dependent mechanism and elucidates the interplay between sterics and electrostatics crucial to understanding the effect of these unique solvents upon chemical reactions.

• 出版日期2013-1-23