Helical Phase Driven by Solvent Evaporation in Self-Assembly of Poly(4-vinylpyridine)-block-poly(l‑lactide) Chiral Block Copolymers

• Published in: Macromolecules 2012-12, Vol.45 (24), p.9727-9733
• Main Authors: Chung, Tsai-Ming, Wang, Hsiao-Fang, Lin, Tao, Chiang, Yeo-Wan, Chen, Yi-Chun, Ko, Bao-Tsan, Ho, Rong-Ming
• Format: Article
• Language: English
• Subjects: Applied sciences; Exact sciences and technology; Organic polymers; Physicochemistry of polymers; Properties and characterization; Solution and gel properties
• ISSN: 0024-9297; 1520-5835
• DOI: 10.1021/ma302159p

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.