The study of counterion effect on the reactivity of nucleophiles in some SN2 reactions in gas phase and solvent media

The effect of counterion on the reactivity of ion pairs along the backside and frontside identity exchange reactions Nuc + CH3X -> XCH3 + Nuc (Nuc = X-, Li+X-, Na+X-, K+X-; X = F, Cl, Br) was investigated at -311+++. G(d,p) level of theory in the gas phase and solvent media. Single point QCISD(T) calculations were performed on all MP2 optimized structures in order to decrease the differences between theoretical and experimental values of energy in the gas phase. By intrinsic reaction coordinates (IRC) calculations, CH3X... M+X- complexes were confirmed along two paths. The complexation enthalpies Delta H-comp decrease with increasing the diameter of counterion in the gas phase. The energy barriers (Delta H-ovr(double dagger) and Delta H-cent(double dagger)) decrease with increasing the size of counterion in the backside attack whereas they increase in the frontside path. Solvent effect on the reaction profile has also been studied using isodensity surface polarized continuum model (IPCM). The values of Delta H-comp in solvent media are smaller than gas phase and are negative for some nucleophiles in the presence of solvents with high dielectric constants. The values of Delta H-ovr(double dagger) and Delta H-cent(double dagger) are higher in solution C tion and grow by the increase in dielectric constant of solvent. The calculated energy values of reactants, complexes, and transition state (TS) structures in the presence of solvent are more negative than the gas phase and reduce with increasing the dielectric constant. Energy decreases in a higher rate for reactants in comparison with complexes and TS structures. (C) 2007 Elsevier B.V. All rights reserved.