Department of Chemistry, University of California, Irvine, California 92697, United States.
J Am Chem Soc. 2015 May 27;137(20):6492-5. doi: 10.1021/jacs.5b03551. Epub 2015 May 15.
Despite numerous strategies involving dynamic covalent bond exchange for dynamic and self-healing materials, it remains a challenge to be able to tune the malleability and self-healing properties of bulk materials through simple small molecule perturbations. Here we describe the use of tunable rates of boronic ester transesterification to tune the malleability and self-healing efficiencies of bulk materials. Specifically, we used two telechelic diboronic ester small molecules with variable transesterification kinetics to dynamically cross-link 1,2-diol-containing polymer backbones. The sample cross-linked with fast-exchanging diboronic ester showed enhanced malleability and accelerated healing compared to the slow-exchanging variant under the same conditions. Our report demonstrates the possibility of transferring small molecule kinetics to dynamic properties of bulk solid material and may serve as a guide for the rational design of tunable dynamic materials.
尽管涉及动态共价键交换的众多策略可用于制备动态和自修复材料,但通过简单的小分子扰动来调节块状材料的延展性和自修复性能仍然是一个挑战。在这里,我们描述了利用硼酸酯酯交换的可调速率来调节块状材料的延展性和自修复效率。具体来说,我们使用了两种具有不同酯交换动力学的末端双硼酸酯小分子,以动态交联含有 1,2-二醇的聚合物主链。在相同条件下,与缓慢交换的变体相比,用快速交换的硼酸酯交联的样品表现出增强的延展性和加速的愈合。我们的报告证明了将小分子动力学转移到块状固体材料的动态特性的可能性,并可能为可调动态材料的合理设计提供指导。