Ring-expansion polymerization (REP) of L-lactide with cyclic tin(II) bisphenoxides

Five new cyclic catalysts were prepared by a new synthetic method from tin(II)-2-ethyhexanoate and silylated catechols, silylated 2,2'dihydroxybiphenyl or silylated 1,1'-bisnaphthol. These catalysts were compared with regard to their usefulness as catalysts for the ring expansion polymerization (REP) of L-lactide in bulk at 160 degrees C, and with two different tin(IV) derivatives of 1,1'bisnaphthol. Best results were obtained using seven-membered cyclic tin(II)bisphenoxides, which yielded colorless cyclic poly(L-lactide)s free of racemization with weight average molecular weights (M-w) up to 305,000 g mol(-1). Furthermore, these catalysts were active even at a lactide/catalyst ratio of 20,000/1. Our new results were superior to those obtained from all other previously published catalysts yielding cyclic poly(L-lactide). The seven-membered cycles also proved to be more active than tin(II) 2-ethylhexanoate with and without the addition of alcohol.