A robust porous quinoline cage: transformation of a [4+6] salicylimine cage by povarov cyclization

Porous shape-persistent organic cages have become the object of interest in recent years because they are soluble and thus processable from solution. A variety of cages can be achieved by applying dynamic covalent chemistry (DCC), but they are less chemically stable. Here the transformation of a sal...

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Hauptverfasser: Alexandre, Pierre-Emmanuel (VerfasserIn) , Zhang, Wen-Shan (VerfasserIn) , Rominger, Frank (VerfasserIn) , Elbert, Sven (VerfasserIn) , Schröder, Rasmus R. (VerfasserIn) , Mastalerz, Michael (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 2020
In: Angewandte Chemie
Year: 2020, Jahrgang: 132, Heft: 44, Pages: 19843-19847
ISSN:1521-3757
DOI:10.1002/ange.2020070488
Online-Zugang:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/ange.2020070488
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/10.1002/ange.202007048
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Verfasserangaben:Pierre-Emmanuel Alexandre, Wen-Shan Zhang, Frank Rominger, Sven M. Elbert, Rasmus R. Schröder, and Michael Mastalerz
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Zusammenfassung:Porous shape-persistent organic cages have become the object of interest in recent years because they are soluble and thus processable from solution. A variety of cages can be achieved by applying dynamic covalent chemistry (DCC), but they are less chemically stable. Here the transformation of a salicylimine cage into a quinoline cage by a twelve-fold Povarov reaction as the key step is described. Besides the chemical stability of the cage over a broad pH regime, it shows a unique absorption and emission depending on acid concentration. Furthermore, thin films for the vapor detection of acids were investigated, showing color switches from pale-yellow to red, and characteristic emission profiles.
Beschreibung:First published: 10 June 2020
Gesehen am 02.11.2021
Beschreibung:Online Resource
ISSN:1521-3757
DOI:10.1002/ange.2020070488