Ionothermal Synthesis of Imide-Linked Covalent Organic Frameworks.
covalent organic frameworks
eutectic salt mixtures
ionothermal synthesis
polyimides
Journal
Angewandte Chemie (International ed. in English)
ISSN: 1521-3773
Titre abrégé: Angew Chem Int Ed Engl
Pays: Germany
ID NLM: 0370543
Informations de publication
Date de publication:
01 Sep 2020
01 Sep 2020
Historique:
received:
21
05
2020
pubmed:
24
6
2020
medline:
24
6
2020
entrez:
24
6
2020
Statut:
ppublish
Résumé
Covalent organic frameworks (COFs) are an extensively studied class of porous materials, which distinguish themselves from other porous polymers in their crystallinity and high degree of modularity, enabling a wide range of applications. COFs are most commonly synthesized solvothermally, which is often a time-consuming process and restricted to well-soluble precursor molecules. Synthesis of polyimide-linked COFs (PI-COFs) is further complicated by the poor reversibility of the ring-closing reaction under solvothermal conditions. Herein, we report the ionothermal synthesis of crystalline and porous PI-COFs in zinc chloride and eutectic salt mixtures. This synthesis does not require soluble precursors and the reaction time is significantly reduced as compared to standard solvothermal synthesis methods. In addition to applying the synthesis to previously reported imide COFs, a new perylene-based COF was also synthesized, which could not be obtained by the classical solvothermal route. In situ high-temperature XRPD analysis hints to the formation of precursor-salt adducts as crystalline intermediates, which then react with each other to form the COF.
Identifiants
pubmed: 32573890
doi: 10.1002/anie.202007372
pmc: PMC7497034
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
15750-15758Subventions
Organisme : Bundesministerium für Bildung und Forschung
ID : 03XP0030C
Organisme : Deutsche Forschungsgemeinschaft
ID : 358283783
Organisme : Deutsche Forschungsgemeinschaft
ID : SFB1333,ProjectA03
Organisme : H2020 European Research Council
ID : 639233
Organisme : Cluster of Excellence e-conversion
ID : EXC 2089/1-390776260
Organisme : Center for Nanoscience
Organisme : Max-Planck-Gesellschaft
Informations de copyright
© 2020 The Authors. Published by Wiley-VCH GmbH.
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