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在异质界面处的机械载子激活。

Mechanophore activation at heterointerfaces.

机构信息

Beckman Institute for Advanced Science and Technology, Department of Materials Science and Engineering, Department of Chemistry, University of Illinois at Urbana-Champaign , Urbana, Illinois 61801, United States.

出版信息

J Am Chem Soc. 2014 Nov 12;136(45):15925-8. doi: 10.1021/ja509949d. Epub 2014 Oct 31.

Abstract

Silica nanoparticles grafted with poly(methyl acrylate) (PMA) chains anchored by a maleimide-anthracene cycloadduct were synthesized to demonstrate mechanochemically selective activation of mechanophores at heterogeneous interfaces. By quantifying the anthracene-containing cleaved PMA polymers, which are generated via retro-[4 + 2] cycloaddition reactions, the first-order kinetic coefficient was determined. Activation characteristics of mechanophores anchored to a nanoparticle exhibit behavior similar to mechanophore-linked polymers, e.g., threshold molecular weight and linear increase in rate coefficient with molecular weight above the threshold. This model system is thus valuable as a probe to test stress activation of interfacially bonded mechanophores relevant to the design of fiber-reinforced polymer composites.

摘要

用马来酰亚胺-蒽环加成物锚定的聚甲基丙烯酸甲酯(PMA)链接枝的二氧化硅纳米粒子被合成,以证明在非均相界面上机械化学选择性地激活机械力敏剂。通过定量含有蒽的 PMA 聚合物,这些聚合物是通过反-[4 + 2]环加成反应生成的,确定了一级反应系数。锚定在纳米粒子上的机械力敏剂的激活特性表现出与机械力敏剂连接聚合物相似的行为,例如,阈值分子量和速率系数随分子量线性增加超过阈值。因此,这个模型系统作为一种探针,可以测试与纤维增强聚合物复合材料设计相关的界面键合机械力敏剂的应力激活。

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