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Updated: Sep 21, 2025

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions
Published on: October 10, 2016
Orthogonal Folding of Amphiphilic/Fluorous Random Block Copolymers for Double and Multicompartment Micelles in Water
Mayuko Matsumoto1, Mitsuo Sawamoto1,2, Takaya Terashima1
1Department of Polymer Chemistry, Graduate School of Engineering, Kyoto University, Katsura, Nishikyo-ku, Kyoto 615-8510, Japan.
Abstract:
Here, we report orthogonal folding and self-assembly systems of amphiphilic/fluorous random block copolymers for double core and multicompartment micelles in water. For this, we developed the precision folding techniques of polymer chains via the selective self-assembly of the pendant groups. Typically, A/C-B/C random block copolymers were designed: Hydrophobic dodecyl groups (A) and fluorous fluorinated octyl groups (B) were introduced into the respective blocks, while hydrophilic poly(ethylene glycol) chains (C) were randomly incorporated into all the segments. By controlling the chain length and composition of the respective blocks, the copolymers induce orthogonal single-chain folding in water to form double-compartment micelles comprising hydrophobic and fluorous cores. The copolymers were site-selectively folded in a fluoroalcohol to result in tadpole unimer micelles comprising a hydrophobic A/C unimer micelle and an unfolded fluorous B/C chain. Additionally, asymmetric A/C-B/C random block copolymers with short and highly hydrophobic or fluorous segments were effective for multicompartment micelles in water.
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