• Kim, Yongtae
• Joo, Sang Hoon
• Park, Kang Hyun
• Jang, Hyun-Sook
• Ahn, Suk-Kyun
• Son, Jinha
• Kim, Inhye
• Cho, Seungwan
• Ahn, Hyungju

Abstract

Control of polymer architecture can be a powerful strategy to refine the structure and properties without changing the chemical structure of the monomers. Here, we exploit a highly branched bottlebrush architecture to access tailored self-assembled morphologies and nanoporous structures. To this end, a series of well-defined bottlebrush random copolymers are synthesized by macromonomer approach, where polystyrene (PS) and poly(D,L-lactide) (PLA) side chains of non-equal molecular weights are grafted to the polynorbornene backbone. These bottlebrush copolymers exhibit microphase-separated structures including lamellar, hexagonal cylinders and disordered structures with the domain sizes of 13–20 nm depending on the relative volume fraction (f) of PS and PLA side chain. Due to highly asymmetric nature, these bottlebrush copolymers exhibit cylinders at f PS = 41–50% and lamellar at f PS = 67–70%, unlike the case of linear diblock copolymers. The selective degradation of PLA from these bottlebrushes allows for nanoporous structures to be created of which size, distribution and connectivity of pores are dictated by the composition of bottlebrush precursors. The ability to exploit the bottlebrush architecture to manipulate self-assembled morphologies and nanoporous structures may be a useful way to design materials for adsorptions, separations, catalysis and gas storages. © 2019 Elsevier Ltd

Topics

• pore
• random
• molecular weight
• copolymer
• bottlebrush
• self-assembly
• random copolymer