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Isostructural Three-Dimensional Covalent Organic Frameworks
Stockholm University, Faculty of Science, Department of Materials and Environmental Chemistry (MMK). Peking University, China.
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Number of Authors: 82019 (English)In: Angewandte Chemie International Edition, ISSN 1433-7851, E-ISSN 1521-3773, Vol. 58, no 29, p. 9770-9775Article in journal (Refereed) Published
Abstract [en]

Herein, we reported the designed synthesis of three isostructural three-dimensional covalent organic frameworks (3D COFs) with -H, -Me, or -F substituents, which have similar crystallinity and topology. Their crystal structures were determined by continuous rotation electron diffraction (cRED), and all three 3D COFs were found to adopt a fivefold interpenetrated pts topology. More importantly, the resolution of these cRED datasets reached up to 0.9-1.0 angstrom, enabling the localization of all non-hydrogen atomic positions in a COF framework directly by 3D ED techniques for the first time. In addition, the precise control of the pore environments through the use of different functional groups led to different selectivities for CO2 over N-2. We have thus confirmed that polycrystalline COFs can be definitely studied to the atomic level as other materials, and this study should also inspire the design and synthesis of 3D COFs with tailored pore environments for interesting applications.

Place, publisher, year, edition, pages
2019. Vol. 58, no 29, p. 9770-9775
Keywords [en]
covalent organic 3D frameworks, continuous rotation electron diffraction, gas separation, structure elucidation
National Category
Chemical Sciences
Identifiers
URN: urn:nbn:se:su:diva-171731DOI: 10.1002/anie.201905591ISI: 000476615900008PubMedID: 31106938OAI: oai:DiVA.org:su-171731DiVA, id: diva2:1349971
Available from: 2019-09-10 Created: 2019-09-10 Last updated: 2019-09-10Bibliographically approved

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