Issue 2, 2015

Orthoester exchange: a tripodal tool for dynamic covalent and systems chemistry

Abstract

Reversible covalent reactions have become an important tool in supramolecular chemistry and materials science. Here we introduce the acid-catalyzed exchange of O,O,O-orthoesters to the toolbox of dynamic covalent chemistry. We demonstrate that orthoesters readily exchange with a wide range of alcohols under mild conditions and we disclose the first report of an orthoester metathesis reaction. We also show that dynamic orthoester systems give rise to pronounced metal template effects, which can best be understood by agonistic relationships in a three-dimensional network analysis. Due to the tripodal architecture of orthoesters, the exchange process described herein could find unique applications in dynamic polymers, porous materials and host–guest architectures.

Graphical abstract: Orthoester exchange: a tripodal tool for dynamic covalent and systems chemistry

Supplementary files

Article information

Article type
Edge Article
Submitted
14 Nov 2014
Accepted
03 Dec 2014
First published
03 Dec 2014
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2015,6, 1399-1403

Orthoester exchange: a tripodal tool for dynamic covalent and systems chemistry

R. Brachvogel and M. von Delius, Chem. Sci., 2015, 6, 1399 DOI: 10.1039/C4SC03528C

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