Polymer Mechanochemistry in Confined Spaces

被引:0
|
作者
Hu, Hui [1 ]
Zhou, Yang [2 ]
Xi, Bin [1 ]
Li, Yuanchao [1 ]
机构
[1] Sun Yat Sen Univ, Sch Mat Sci & Engn, Key Lab Polymer Composite & Funct Mat, Minist Educ, Guangzhou 510006, Peoples R China
[2] Wuhan Text Univ, Sch Text Sci & Engn, State Key Lab New Text Mat & Adv Proc Technol, Wuhan 430200, Peoples R China
关键词
polymer mechanochemistry; confined spaces; activation; mechanophores; confinement effects; ANTI-ARRHENIUS CLEAVAGE; MECHANOPHORE ACTIVATION; MECHANICAL ACTIVATION; INTERFACE STRENGTH; CHEMICAL-REACTIONS; COVALENT BONDS; BRUSHES; MACROMOLECULES; WEAK; ANNOUNCEMENT;
D O I
10.1002/anie.202417357
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
With the development of mechanophores, polymer mechanochemistry has emerged as a powerful tool for creating force-responsive materials with a variety of desired functions, ranging from color change to molecular release. However, it remains challenging to improve the efficiency of mechanochemical activation, especially for mechanophores embedded within polymer networks, which has profound implications for translating mechanochemical responses into materials-centered applications. The physical and chemical conditions under spatial confinement differ significantly from those in the surrounding bulk environment, offering opportunities to facilitate mechanochemical activation. In this Minireview, we discuss and summarize recent progress in polymer mechanochemistry within confined spaces including surfaces/interfaces, polymer assemblies, and other nanostructures, specifically focusing on the effects of spatial confinement on the enhancement of mechanophore activation. We envision that combining confinement effects with advances in molecular and materials engineering will further improve the activation efficiency, capitalizing more fully on the potential of mechanophores toward practical applications.
引用
收藏
页数:14
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