Majumdar Soumabrata, Mezari Brahim, Zhang Huiyi, van Aart Jeroen, van Benthem Rolf A T M, Heuts Johan P A, Sijbesma Rint P
Department of Chemical Engineering & Chemistry and Institute for Complex Molecular Systems, Eindhoven University of Technology, 5600 MB Eindhoven, The Netherlands.
Department of Chemical Engineering & Chemistry, Laboratory of Inorganic Materials and Catalysis, Eindhoven University of Technology, 5600 MB Eindhoven, The Netherlands.
Macromolecules. 2021 Sep 14;54(17):7955-7962. doi: 10.1021/acs.macromol.1c01504. Epub 2021 Aug 17.
Bond exchange via neighboring group-assisted reactions in dynamic covalent networks results in efficient mechanical relaxation. In Nature, the high reactivity of RNA toward nucleophilic substitution is largely attributed to the formation of a cyclic phosphate ester intermediate via neighboring group participation. We took inspiration from RNA to develop a dynamic covalent network based on β-hydroxyl-mediated transesterifications of hydroxyethyl phosphate triesters. A simple one-step synthetic strategy provided a network containing phosphate triesters with a pendant hydroxyethyl group. P solid-state NMR demonstrated that a cyclic phosphate triester is an intermediate in transesterification, leading to dissociative network rearrangement. Significant viscous flow at 60-100 °C makes the material suitable for fast processing via extrusion and compression molding.
通过动态共价网络中相邻基团辅助反应进行的键交换可实现高效的机械松弛。在自然界中,RNA对亲核取代反应的高反应活性很大程度上归因于通过相邻基团参与形成环状磷酸酯中间体。我们从RNA中获得灵感,开发了一种基于β-羟基介导的磷酸三乙酯酯交换反应的动态共价网络。一种简单的一步合成策略提供了一个包含带有侧链羟乙基的磷酸三乙酯的网络。磷固态核磁共振表明,环状磷酸三酯是酯交换反应的中间体,导致解离性网络重排。在60-100°C下显著的粘性流动使该材料适合通过挤出和压缩成型进行快速加工。