Deng, B. X.; Lai, H. Z.; Jiang, L.; Yu, L.; Cheng, L.; Chen, D. Y. Topology-regulated co-assembly of single chain polymer nanoparticles and block copolymers into hierarchical micelle@vesicle composite structures. Chinese J. Polym. Sci. 2026, 44, 2982–2989
Bai-Xue Deng, Hong-Zhu Lai, Li Jiang, et al. Topology-regulated Co-assembly of Single Chain Polymer Nanoparticles and Block Copolymers into Hierarchical Micelle@Vesicle Composite Structures[J]. Chinese Journal of Polymer Science, 2026, 44(9): 2982-2989.
Deng, B. X.; Lai, H. Z.; Jiang, L.; Yu, L.; Cheng, L.; Chen, D. Y. Topology-regulated co-assembly of single chain polymer nanoparticles and block copolymers into hierarchical micelle@vesicle composite structures. Chinese J. Polym. Sci. 2026, 44, 2982–2989DOI: 10.1007/s10118-026-3713-7.
Bai-Xue Deng, Hong-Zhu Lai, Li Jiang, et al. Topology-regulated Co-assembly of Single Chain Polymer Nanoparticles and Block Copolymers into Hierarchical Micelle@Vesicle Composite Structures[J]. Chinese Journal of Polymer Science, 2026, 44(9): 2982-2989.DOI: 10.1007/s10118-026-3713-7.
Topology-regulated Co-assembly of Single Chain Polymer Nanoparticles and Block Copolymers into Hierarchical Micelle@Vesicle Composite Structures
Topology-regulated co-assembly of single-chain polymer nanoparticles and block copolymers proceeds through a stepwise pathway
forming hierarchical micelle@vesicle composite structures and offering a new strategy for constructing complex polymer assemblies.
Abstract
Polymer co-assembly provides a versatile route to hierarchical nanostructures
yet achieving precise structural control remains a significant challenge. In particular
understanding how topological differences in polymer building blocks influence co-assembly behavior is important for expanding the design of complex polymer materials. In this work
a co-assembly system of amphiphilic block copolymers (BCPs) and single chain polymer nanoparticles (SCPs) was designed to investigate the effect of topological variations. At certain SCP/BCP mass ratios
BCPs and SCPs co-assembled to form a hierarchical composite structure with vesicles growing on the surface of micelles
following a path-dependent stepwise co-assembly mechanism
where SCPs co-assembled with BCP to form core micelles and self-assembled into vesicles from the micelle surface into hierarchical micelle@vesicle (M@V) composite structure. The SCP/BCP mass ratio significantly influences the morphology and size of the M@V composite structure
and the strategy is applicable to copolymer systems with wide range of hydrophobic/hydrophilic volume ratios. This work provides new insights into topology-regulated polymer co-assembly and offers a useful strategy for the design of hierarchical and multifunctional polymer materials.
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