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

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 alcoho...

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Detalles Bibliográficos
Autores principales: Brachvogel, René-Chris, von Delius, Max
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811105/
https://www.ncbi.nlm.nih.gov/pubmed/29560228
http://dx.doi.org/10.1039/c4sc03528c
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author Brachvogel, René-Chris
von Delius, Max
author_facet Brachvogel, René-Chris
von Delius, Max
author_sort Brachvogel, René-Chris
collection PubMed
description 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.
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spelling pubmed-58111052018-03-20 Orthoester exchange: a tripodal tool for dynamic covalent and systems chemistry Brachvogel, René-Chris von Delius, Max Chem Sci Chemistry 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. Royal Society of Chemistry 2015-02-01 2014-12-03 /pmc/articles/PMC5811105/ /pubmed/29560228 http://dx.doi.org/10.1039/c4sc03528c Text en This journal is © The Royal Society of Chemistry 2015 http://creativecommons.org/licenses/by-nc/3.0/ This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
spellingShingle Chemistry
Brachvogel, René-Chris
von Delius, Max
Orthoester exchange: a tripodal tool for dynamic covalent and systems chemistry
title Orthoester exchange: a tripodal tool for dynamic covalent and systems chemistry
title_full Orthoester exchange: a tripodal tool for dynamic covalent and systems chemistry
title_fullStr Orthoester exchange: a tripodal tool for dynamic covalent and systems chemistry
title_full_unstemmed Orthoester exchange: a tripodal tool for dynamic covalent and systems chemistry
title_short Orthoester exchange: a tripodal tool for dynamic covalent and systems chemistry
title_sort orthoester exchange: a tripodal tool for dynamic covalent and systems chemistry
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811105/
https://www.ncbi.nlm.nih.gov/pubmed/29560228
http://dx.doi.org/10.1039/c4sc03528c
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AT vondeliusmax orthoesterexchangeatripodaltoolfordynamiccovalentandsystemschemistry