Institute of Chemistry, Chair of Macromolecular Chemistry, Faculty of Natural Sciences II, Martin-Luther-Universität Halle-Wittenberg von Danckelmann-Platz 4, 06120 Halle (Saale) (Germany).
Institute of Physics, Faculty of Natural Sciences II, Martin-Luther-Universität Halle-Wittenberg, Kurth-Mothes-Strasse 2, 06120 Halle (Saale) (Germany).
Angew Chem Int Ed Engl. 2015 Aug 24;54(35):10188-92. doi: 10.1002/anie.201504136. Epub 2015 Jul 1.
Integrating self-healing capability into supramolecular architectures is an interesting strategy, and can considerably enhance the performance and broaden the scope of applications for this important class of polymers. Herein we report the rational design of novel V-shaped barbiturate (Ba) functionalized soft-hard-soft triblock copolymers with a reversible supramolecular healing motif (Ba) in the central part of the hard block, which undergoes autonomic repair at 30 °C. The designed synthesis also offers a suitable macromolecular building block to further self-assemble with heterocomplementary α,ω-Hamilton wedge (HW) functionalized polyisoprene (PI; HW-PI-HW), resulting in an H-shaped supramolecular architecture with efficient self-healing capabilities that can recover up to around 95 % of the original mechanical performance at 30 °C within 24 h.
将自修复能力整合到超分子结构中是一种有趣的策略,可以显著提高这类重要聚合物的性能和拓宽其应用范围。在此,我们报告了一种新型 V 形巴比妥酸(Ba)功能化软-硬-软三嵌段共聚物的合理设计,其中在硬段的中心部分具有一个可自动修复的超分子修复基序(Ba),在 30°C 下可自动修复。该设计的合成还提供了合适的大分子构建块,可进一步与杂互补的α,ω-汉密尔顿楔形(HW)功能化聚异戊二烯(PI;HW-PI-HW)自组装,形成具有高效自修复能力的 H 形超分子结构,在 30°C 下 24 小时内可恢复原始机械性能的约 95%。