Ultrafast, Robust, and Reversible Self-Assembled Nanofibers via Thiolactone Chemistry Strategy

被引:0
|
作者
Li, Haonan [1 ]
Li, Chunmei [1 ]
Ren, Hua [1 ]
Cai, Yingchao [1 ]
Tan, Jiaojun [2 ]
Huang, Xinyi [1 ]
Yin, Dezhong [1 ]
Zhang, Qiuyu [1 ]
机构
[1] Northwestern Polytech Univ, Sch Chem & Chem Engn, Minist Ind & Informat Technol, Key Lab Special Funct & Smart Polymer Mat,Xian Key, Xian 710129, Peoples R China
[2] Shaanxi Univ Sci & Technol, Coll Bioresources Chem & Mat Engn, Natl Demonstrat Ctr Expt Light Chem Engn Educ, Xian 710021, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
hydrogen bonds; hydrophobic interactions; nanofibers; thiolactone; ultrafast self-assembly; INFRARED TEMPERATURE; BLOCK-COPOLYMER; THIOL-ENE; POLYMERS; SELECTIVITY;
D O I
10.1002/smll.202411982
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Self-assembly in supramolecular chemistry is crucial for nanostructure creation but faces challenges like slow speeds and lack of reversibility. In this study, a novel comb-like polymer poly(amide sulfide) (PAS) based on thiolactone chemistry is reported, which rapidly self-assemble into stable nanofibers, offering excellent robustness and reversibility in the self-assembled structure. The PAS backbone contains pairs of amide bonds, each linked to an alkyl side chain in a controlled 2:1 ratio. The polymer rapidly forms fibrillar micelles driven by the hydrophobic side chains and then undergoes hydrogen-bonded cross-linking between the main-chain amide bonds to form stable nanofibers. N, N-dimethylacetamide/LiCl solution allows for reversible regulation of nanofiber self-assembly, without altering the fiber properties. It is anticipated that this line of research will enrich the field of macromolecular self-assembly with important advances toward the realization of ultrafast, robust, and reversible self-assembly systems.
引用
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页数:13
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