Abstract
A series of chiral block copolymers (BCPs*), poly(4-vinylpyridine)- block-poly(l-lactide) (P4VP-PLLA), are synthesized through atom transfer radical polymerization and living ring-opening polymerization. Except for typical microphase-separated phases, such as lamellae (L) and hexagonally packed cylinders (HC), a helical phase (H*) with hexagonally packed PLLA helices in a P4VP matrix can be found in the self-assembly of P4VP-PLLA BCPs*, reflecting the chirality effect on BCP self-assembly. The H* formation is strongly dependent upon the solvent evaporation rate for solution casting at which fast evaporation gives the H* phase and slow evaporation results in the HC phase. To further examine the metastability of the H* phase associated with the dynamics of BCP* chains during self-assembly, P4VP-PLLA BCPs* having different molecular weights at a constant composition are utilized for self-assembly. Under the same evaporation rate for solution casting, the H* phase can be obtained in high-molecular-weight P4VP-PLLA BCP* whereas a stable HC phase is found in low-molecular-weight P4VP-PLLA BCP*, indicating the kinetic origin of H* formation due to the long and highly entangled chains in solution for self-assembly. Consequently, the H* phase can be driven by solvent evaporation through a kinetically trapped process and is regarded as a long-lived metastable phase. © 2012 American Chemical Society.