V. Simic et al., Synthesis and characterization of some block copolymers of lactides with cyclic monomers using yttrium alkolxide as initiator, MACRO SYMP, 153, 2000, pp. 109-121
Block copolymers were prepared by sequential addition oft or D-lactide to a
living epsilon-caprolactone prepared with Y(OC(2)H(4)OiPr)(3) initiator. I
n contrast, epsilon-caprolactone (CL) was not polymerized when added to a l
iving polyL-lactide (LA) prepared with the same initiator in the same condi
tions. The polymerization of an equimolecular mixture of LA and CL using th
e yttrium alkoxide initiator produces only the pure lactide homopolymer. Th
e copolymerization of LA with trimethylene carbonate (TMC) exhibits a diffe
rent type of behaviour. The synthesis of pure block copolymers by sequentia
l addition of monomers is obtained if starting from a living polylactide se
quence. When starting with TMC sequence, mixture of products leading to a b
imodal MWD is obtained. The polymerization of an equimolecular mixture of L
A and RMC leads to a copolymer with a block structure. The PLA sequence is
formed first, followed by the subsequent addition of TMC monomer up to comp
lete conversion All the prepared copolymers were characterized by SEC,H-1 a
nd C-13 NMR techniques. No transesterification reactions were detected.