Efficient Exchange in a Bioinspired Dynamic Covalent Polymer Network via a Cyclic Phosphate Triester Intermediate

Soumabrata Majumdar, Brahim Mezari, Huiyi Zhang, Jeroen van Aart, Rolf A.T.M. van Benthem, Johan P.A. Heuts, Rint P. Sijbesma (Corresponding author)

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23 Citations (Scopus)
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Abstract

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. 31P 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.

Original languageEnglish
Pages (from-to)7955–7962
Number of pages8
JournalMacromolecules
Volume54
Issue number17
DOIs
Publication statusPublished - 14 Sept 2021

Funding

This work was funded by the Dutch Research Council (NWO), project no. 731.016.202.

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