摘要
In an effort to reduce hazardous chemicals, a one-pot two-step process with active bases and inactive salts was developed for the synthesis of high molar mass PEO-block-PCL-block-P(L-or D, L-LA) amphiphilic triblock copolymers. A series of poly(epsilon-caprolactone) (PCL)/poly(L- or D, L-lactide) (P(L- or D, L-LA)) di- and triblock copolymers have been prepared in bulk from metal-free catalytic systems and starting from either 1-pyrenemethanol or poly(ethylene oxide) (PEO) macroinitiator. The controlled generation of such structures was obtained after screening and comparing a wide variety of organic activators. Narrower dispersity characterizing each sample prepared from the PEO macroinitiator were elucidated by theoretical modeling. Finally, the ability of those triblock copolymers to self-associate in water was studied by dynamic light scattering and compared to PEO-b-P(CL-co-LA) copolymers.
- 出版日期2014