The Dual-Stereocontrol Mechanism: Heteroselective Polymerization of rac-Lactide and Syndioselective Polymerization of meso-Lactide by Chiral Aluminum Salan Catalysts

摘要

We describe alkoxo-aluminum catalysts of chiral bipyrrolidine-based salan ligands that follow the dual-stereocontrol mechanism wherein a given combination of stereogeneities at the metal site and the proximal center of the last inserted lactidyl ("match") is active towards lactide having a proximal stereogenic center of the opposite configuration, while the diastereomeric combination of stereogeneities ("mismatch") is inactive towards any lactide. Polymerization of rac-LA by the enantiomerically pure catalysts was sluggish and gave stereoirregular poly(lactic acid) (PLA) because selective insertion to a match diastereomer gives a mismatch diastereomer. The racemic catalysts showed higher activity and led to highly heterotactic PLA following polymeryl exchange between two mismatched catalyst enantiomers. A succession of match diastereomers in selective meso-LA insertions led to syndiotactic PLAs reaching a syndiotacticity degree of alpha=0.96. This polymer featured a T-m of 153 degrees C matching the highest reported value, and the highest crystallinity (Delta H-m=56 J g(-1)) ever reported for syndiotactic PLA.