Haase F, Troschke E, Savasci G, Banerjee T, Duppel V, Doerfler S, Grundei MMJ, Burow AM, Ochsenfeld C, Kaskel S, Lotsch BV (2018)
Publication Type: Journal article
Publication year: 2018
Book Volume: 9
Article Number: 2600
Journal Issue: 1
DOI: 10.1038/s41467-018-04979-y
Stabilization of covalent organic frameworks (COFs) by post-synthetic locking strategies is a powerful tool to push the limits of COF utilization, which are imposed by the reversible COF linkage. Here we introduce a sulfur-assisted chemical conversion of a two-dimensional imine-linked COF into a thiazole-linked COF, with full retention of crystallinity and porosity. This post-synthetic modification entails significantly enhanced chemical and electron beam stability, enabling investigation of the real framework structure at a high level of detail. An in-depth study by electron diffraction and transmission electron microscopy reveals a myriad of previously unknown or unverified structural features such as grain boundaries and edge dislocations, which are likely generic to the in-plane structure of 2D COFs. The visualization of such real structural features is key to understand, design and control structure-property relationships in COFs, which can have major implications for adsorption, catalytic, and transport properties of such crystalline porous polymers.
APA:
Haase, F., Troschke, E., Savasci, G., Banerjee, T., Duppel, V., Doerfler, S.,... Lotsch, B.V. (2018). Topochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis. Nature Communications, 9(1). https://doi.org/10.1038/s41467-018-04979-y
MLA:
Haase, Frederik, et al. "Topochemical conversion of an imine- into a thiazole-linked covalent organic framework enabling real structure analysis." Nature Communications 9.1 (2018).
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