Topochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis

Stabilization of covalent organic frameworks (COFs) by post-synthetic locking is a powerful tool to push the limits of COF utilization. Here the authors demonstrate a sulfur-assisted conversion of an imine-linked COF into a thiazole-linked COF, with retention of crystallinity and porosity, allowing...

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Autores principales:	Frederik Haase, Erik Troschke, Gökcen Savasci, Tanmay Banerjee, Viola Duppel, Susanne Dörfler, Martin M. J. Grundei, Asbjörn M. Burow, Christian Ochsenfeld, Stefan Kaskel, Bettina V. Lotsch
Formato:	article
Lenguaje:	EN
Publicado:	Nature Portfolio 2018
Materias:	Science Q
Acceso en línea:	https://doaj.org/article/84db9441b03b489aa5f82d3b804c4278
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spelling	oai:doaj.org-article:84db9441b03b489aa5f82d3b804c42782021-12-02T17:33:17ZTopochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis10.1038/s41467-018-04979-y2041-1723https://doaj.org/article/84db9441b03b489aa5f82d3b804c42782018-07-01T00:00:00Zhttps://doi.org/10.1038/s41467-018-04979-yhttps://doaj.org/toc/2041-1723Stabilization of covalent organic frameworks (COFs) by post-synthetic locking is a powerful tool to push the limits of COF utilization. Here the authors demonstrate a sulfur-assisted conversion of an imine-linked COF into a thiazole-linked COF, with retention of crystallinity and porosity, allowing for direct imaging of defects in COFs.Frederik HaaseErik TroschkeGökcen SavasciTanmay BanerjeeViola DuppelSusanne DörflerMartin M. J. GrundeiAsbjörn M. BurowChristian OchsenfeldStefan KaskelBettina V. LotschNature PortfolioarticleScienceQENNature Communications, Vol 9, Iss 1, Pp 1-10 (2018)
institution	DOAJ
collection	DOAJ
language	EN
topic	Science Q
spellingShingle	Science Q Frederik Haase Erik Troschke Gökcen Savasci Tanmay Banerjee Viola Duppel Susanne Dörfler Martin M. J. Grundei Asbjörn M. Burow Christian Ochsenfeld Stefan Kaskel Bettina V. Lotsch Topochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis
description	Stabilization of covalent organic frameworks (COFs) by post-synthetic locking is a powerful tool to push the limits of COF utilization. Here the authors demonstrate a sulfur-assisted conversion of an imine-linked COF into a thiazole-linked COF, with retention of crystallinity and porosity, allowing for direct imaging of defects in COFs.
format	article
author	Frederik Haase Erik Troschke Gökcen Savasci Tanmay Banerjee Viola Duppel Susanne Dörfler Martin M. J. Grundei Asbjörn M. Burow Christian Ochsenfeld Stefan Kaskel Bettina V. Lotsch
author_facet	Frederik Haase Erik Troschke Gökcen Savasci Tanmay Banerjee Viola Duppel Susanne Dörfler Martin M. J. Grundei Asbjörn M. Burow Christian Ochsenfeld Stefan Kaskel Bettina V. Lotsch
author_sort	Frederik Haase
title	Topochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis
title_short	Topochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis
title_full	Topochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis
title_fullStr	Topochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis
title_full_unstemmed	Topochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis
title_sort	topochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis
publisher	Nature Portfolio
publishDate	2018
url	https://doaj.org/article/84db9441b03b489aa5f82d3b804c4278
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Topochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis

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