Abstract
A new sodium/potassium crown ether complex system with a series of bichelating sulfonamides as ligands was developed for the ring-opening polymerization (ROP) of rac-lactide. In this system, the side reaction of cyclic polymerization can be suppressed very well because of very different ROP rates initiated by BnOH and sulfonamide anion. The synthesis of high molecular weight linear polylactide with molecular weight high up to 107 kg/mol was successful. The best isoselectivity also can reach to a high value of Pm = 0.84. The NMR analysis of the reaction mixture of rac-lactide and complex 3 together with kinetic studies suggests the mechanism of ROP in the absence of alcohol is a coordination–insertion mechanism. After addition of BnOH, the ROP rate can increase remarkably due to the cooperation interaction of alcohol and complex 3.
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