准分子
苝
二亚胺
分子内力
部分
光化学
聚合物
分子间力
荧光
材料科学
丙烯酸酯
超分子化学
超分子聚合物
高分子化学
化学
分子
立体化学
共聚物
有机化学
光学
复合材料
物理
作者
Hanna Traeger,Yoshimitsu Sagara,Derek J. Kiebala,Stephen Schrettl,Christoph Weder
标识
DOI:10.1002/ange.202105219
摘要
Abstract A supramolecular mechanophore that can be integrated into polymers and indicates deformation by a fluorescence color change is reported. Two perylene diimides (PDIs) were connected by a short spacer and equipped with peripheral atom transfer polymerization initiators. In the idle state, the motif folds into a loop and its emission is excimer dominated. Poly(methyl acrylate) (PMA) chains were grown from the motif and the mechanophore‐containing polymer was blended with unmodified PMA to afford materials that display a visually discernible fluorescence color change upon deformation, which causes the loops to unfold. The response is instant, and correlates linearly with the applied strain. Experiments with a reference polymer containing only one PDI moiety show that looped mechanophores that display intramolecular excimer formation offer considerable advantages over intermolecular dye aggregates, including a concentration‐independent response, direct signaling of mechanical processes, and a more pronounced optical change.
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