Multiblock and di-/tri-block copolymers are successfully synthesized for the first time via the metal-free terpolymerization of propylene oxide (PO), ʟ-lactide (LA) and CO2 in one-pot/one-step and one-pot/two-step protocols respectively. Firstly, triethyl borane (TEB) and bis(triphenylphosphine)iminium chloride (PPNCl) Lewis pair is employed in the ring-opening polymerization of LA, wherein the catalytic efficiency is significantly correlated to the TEB/PPNCl feed ratio. Next, a series of TEB/base pairs are selected to synthesize the PO/LA/CO2 terpolymer (PPCLA) in one-pot/one-step strategy. In PPCLA synthesis, LA exhibits the fastest reaction rate but severe transesterification is almost unavoidable, resulting in low molecular weight products. In order to prepare high-molecular-weight terpolymers, a one-pot/two-step methodology has to be applied. By this method, the copolymerization of PO/CO2 proceeds first to form poly(propylene carbonate) (PPC) macroinitiators, which triggers the polymerization of LA to polylactide (PLA), leading to PLA-PPC or PLA-PPC-PLA block copolymers. The synthesized PLA-PPC-PLA block copolymers display improved thermal stability compared with PPC.
