Nucleophilic addition of methanol and methanethiol to acetylene in the superbasic system KOH-DMSO: a quantum chemical model

Abstract

Cluster-continuum models (KOH·nDMSO, n = 1, 5) were used to model the superbasic system “alkali metal hydroxide-dimethyl sulfoxide” within the framework of MP2/6-311++G**/ and B3LYP/6-31G* methods. The KOH molecule surrounded by five DMSO molecules exists as “solvate-loosened” ion pair with elongated K-O distance. It is proposed to consider the “solvate-loosened” ion pair of potassium cation with hydroxide anion in the surroundings of five solvent molecules as the catalytic coordination sphere of the superbasic system KOH-DMSO. Methanol and methanethiol molecules can be incorporated with ease into the first coordination sphere of potassium cation to form methoxide and methanethiolate ions. The possibility of nucleophilic attack of methoxide and methanethiolate ions on acetylene molecule in the first coordination sphere of potassium cation was studied. The model reaction system C2H2-CH3OK-H2O with one DMSO molecule included explicitly to maintain the “solvate-loosened” [CH3O]−...K+ ion pair and additional inclusion of solvent effects within the framework of the IEFPCM continuum model is the most preferable for serial calculations.