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Poly(thioether)s from Closed-System One-Pot Reaction of Carbonyl Sulfide and Epoxides by Organic Bases
- Zhang, Cheng-Jian, Zhu, Tian-Cheng, Cao, Xiao-Han, Hong, Xin, Zhang, Xing-Hong
- Journal of the American Chemical Society 2019 v.141 no.13 pp. 5490-5496
- carbon dioxide, carbonyl sulfide, catalysts, epoxides, oxygen, polymerization, polymers, regioselectivity, sulfur
- The synthesis of poly(thioether), a highly desired sulfur-containing polymer, is still a key challenge. Herein, we report a simple and facile approach to poly(thioether)s by closed-system one-pot reaction of carbonyl sulfide (COS) and epoxides. This route underwent the coupling reaction of COS with epoxides, followed by decarboxylative ring-opening polymerization (ROP) of the generated mixed cyclic thiocarbonates with releasing of CO₂ and a little bit of COS. Organic base was used as catalyst and initiator in the two steps, respectively. The oxygen/sulfur exchange reaction was driven by successive regioselective elementary reactions and spontaneous releasing of CO₂ (COS), leading to the sulfur atom of COS transferring to poly(thioether)s, which was well demonstrated by DFT studies. This work provides an easy-to-handle, metal-free route to poly(thioether)s bearing diverse structures by using readily available chemicals.