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通过机械化学揭示的内酯化增强聚合物的机械降解。

Enhanced polymer mechanical degradation through mechanochemically unveiled lactonization.

机构信息

Department of Chemistry, Duke University, Durham, NC, 27708, USA.

出版信息

Nat Commun. 2020 Oct 5;11(1):4987. doi: 10.1038/s41467-020-18809-7.

Abstract

The mechanical degradation of polymers is typically limited to a single chain scission per triggering chain stretching event, and the loss of stress transfer that results from the scission limits the extent of degradation that can be achieved. Here, we report that the mechanically triggered ring-opening of a [4.2.0]bicyclooctene (BCOE) mechanophore sets up a delayed, force-free cascade lactonization that results in chain scission. Delayed chain scission allows many eventual scission events to be initiated within a single polymer chain. Ultrasonication of a 120 kDa BCOE copolymer mechanically remodels the polymer backbone, and subsequent lactonization slowly (~days) degrades the molecular weight to 4.4 kDa, > 10× smaller than control polymers in which lactonization is blocked. The force-coupled kinetics of ring-opening are probed by single molecule force spectroscopy, and mechanical degradation in the bulk is demonstrated. Delayed scission offers a strategy to enhanced mechanical degradation and programmed obsolescence in structural polymeric materials.

摘要

聚合物的机械降解通常仅限于每个引发链拉伸事件的单个链断裂,而断裂导致的应力传递损失限制了可以实现的降解程度。在这里,我们报告说,[4.2.0]双环辛烯(BCOE)机械触发的开环引发了延迟的、无外力的级联内酯化,导致链断裂。延迟的链断裂允许在单个聚合物链内引发许多最终的链断裂事件。对 120 kDa BCOE 共聚物进行超声处理会使聚合物主链发生机械重塑,随后内酯化会缓慢(~数天)将分子量降低至 4.4 kDa,比阻止内酯化的对照聚合物小 10 倍以上。通过单分子力谱探测到开环的力耦合动力学,并在本体中证明了机械降解。延迟的断裂为增强结构聚合物材料的机械降解和程序化损耗提供了一种策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3d7e/7536186/0644c66a22b9/41467_2020_18809_Fig1_HTML.jpg

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