Honghua Xu, Weiya Zhang, Yiwen Shen, Lu Yu, Qiang Wang
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引用次数: 0
Abstract
Using SO2 as a sulfinic-acid building block to synthesize valuable sulfur-based electrolyte additives is an important issue in the field of green and sustainable chemistry. Glycerol sulfite, as a key intermediate for the design and synthesis of sulfite-based electrolyte additives, clarifying its synthesis mechanism is of great significance for the design and synthesis of sulfite-based additives. Herein, the reaction mechanisms of synthesizing glycerol sulfite were explored by density functional theory (DFT) calculations, based on an analysis of glycerol sulfite's structures and properties. The results show that the reaction of SOCl2 with glycerol proceeds through two steps and removes two molecules of HCl, generating glycerol sulfite. The first step of removing HCl is the rate-determining step, with an activation energy barrier of 36.97 kcal/mol. Based on this, we proposed an innovative green synthetic strategy for the atom-economical synthesis of glycerol sulfite by the direct reaction of SO2 with glycerol. The reaction of the SO2 with glycerol involves three steps and removes one molecule of H2O to form glycerol sulfite. The formation of the S-O bond in the second step is the rate-determining step. The activation energy barrier was reduced to 29.75 kcal/mol, which is better than the reaction of SOCl2 with glycerol to form glycerol sulfite. Further exploration of the three-molecule synergistic reaction of 2-cyanopyridine, SO2, and glycerol revealed that glycerol sulfite was generated through four steps. The second step, where the cyano group of 2-cyanopyridine was transformed into an imide group, was identified as the rate-determining step, with an activation energy barrier as low as 25.51 kcal/mol, which was better than the reactions of SOCl2 with glycerol and SO2 with glycerol to form glycerol sulfite. These results provide a new avenue for the design and synthesis of sulfur-based electrolyte additives.
期刊介绍:
The Journal of Physical Chemistry A is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.