聚乙炔
聚合物
材料科学
化学工程
化学
复合材料
工程类
作者
Zhixing Chen,Jaron A. M. Mercer,Xiaolei Zhu,Joseph A. H. Romaniuk,Raphael Pfattner,Lynette Cegelski,Todd J. Martı́nez,Noah Z. Burns,Yan Xia
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2017-08-03
卷期号:357 (6350): 475-479
被引量:332
标识
DOI:10.1126/science.aan2797
摘要
Biological systems sense and respond to mechanical stimuli in a complex manner. In an effort to develop synthetic materials that transduce mechanical force into multifold changes in their intrinsic properties, we report on a mechanochemically responsive nonconjugated polymer that converts to a conjugated polymer via an extensive rearrangement of the macromolecular structure in response to force. Our design is based on the facile mechanochemical unzipping of polyladderene, a polymer inspired by a lipid natural product structure and prepared via direct metathesis polymerization. The resultant polyacetylene block copolymers exhibit long conjugation length and uniform trans-configuration and self-assemble into semiconducting nanowires. Calculations support a tandem unzipping mechanism of the ladderene units.
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