SUMMARY: Structurally characterized, chiral heterobimetallic yttrocene derivatives Li[Y(g 5 : g 1 -C 5 R 4 SiMe 2 NCH 2 CH 2 OMe) 2 ] (R = Me, H) have been shown to be active in the controlled ring-opening polymerization of L-lactide to give poly(L-lactide)s with high molecular weights and moderately narrow molecular weight distributions (M -w /M -n a 1.50). Both transesterification and racemization appear to be less prominent. 1 H NMR spectroscopic tetrad analysis of copolymers prepared using a mixture of L-and D-lactide demonstrates the absence of any preference for one enantiomer during the polymerization.