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Polymerization-Induced Sulfone-Bond-Driven Self-Assembly

delete2025-01-31
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PRE
AI
J
Junrui Zhang
Q
Qili Li
T
Tanrong Yu
Y
Yi-Jian Ma
Z
Zizhuo Zhao
沈
沈程硕 (Chengshuo Shen)
刘勋山 封面图
刘勋山 (Xunshan Liu)
M
Meng Huo *
DOI:10.1021/acs.macromol.4c02860delete
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摘要

摘要

En 中文
Sulfone bonding refers to dipole-dipole interactions between sulfone groups, which have been long overlooked. Herein, sulfone bonding was employed for the first time as the driving force for the self-assembly of block copolymers via a polymerization-induced sulfone-bond-driven self-assembly (PI-SDSA) strategy. The presence of sulfone bonding in a sulfone-functionalized monomer was first confirmed by scanning tunneling microscopy break junction measurements at the single-molecule level. Successful PI-SDSA was achieved in toluene, and the polymerization kinetics confirmed the polymerization-enhanced sulfone bonding as the driving force. The PI-SDSA was demonstrated to possess a peculiar monomer/solvent library by the successful PI-SDSA of a series of sulfone-containing monomers in solvents with varying dipole moments. The as-prepared sulfone-functionalized polymer assemblies manifested unique salt-responsiveness because of the competitive ion-dipole interactions between the ions and sulfone groups, enabling the salt-responsive payload release. The use of sulfone bonding as the driving force for self-assembly has provided a new perspective for both the polymerization-induced self-assembly and the self-assembly of block copolymers and will inspire the design of stimuli-responsive supramolecular materials.
Keyword:
DISPERSION POLYMERIZATION
SULFOXIDE

期刊

Macromolecules 封面图
Macromolecules
IF:
5.2
论文数:
3.7W
被引数:
9.4W

机构

Z
Zhejiang Sci-Tech University
学者数:
1.7W
论文数: 1.0W
被引数: 1.3W
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