Polycationic redox-active cyclophanes with integrated electron-rich diboron units

Cationic cyclophanes are widely used in a variety of applications in supramolecular chemistry and materials science. In this work the authors systematically study the integration of electron-rich diboron units with BII atoms into polycationic cyclophanes with viologen-like electron-acceptor units. T...

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Main Authors: Filbeck, Erik (Author) , Widera, Anna (Author) , Kaifer, Elisabeth (Author) , Himmel, Hans-Jörg (Author)
Format: Article (Journal)
Language:English
Published: October 8, 2021
In: Chemistry - a European journal
Year: 2021, Volume: 27, Issue: 63, Pages: 15737-15750
ISSN:1521-3765
DOI:10.1002/chem.202102656
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/chem.202102656
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.202102656
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Author Notes:Erik Filbeck, Anna Widera, Elisabeth Kaifer, and Hans-Jörg Himmel
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Summary:Cationic cyclophanes are widely used in a variety of applications in supramolecular chemistry and materials science. In this work the authors systematically study the integration of electron-rich diboron units with BII atoms into polycationic cyclophanes with viologen-like electron-acceptor units. They also report a first hexacationic cage-compound in which three diboron units connect two tris(4-pyridyl)triazine acceptor units. Moreover, di- and tetracationic open-structure compounds, in which one diboron unit connects two bispyridyl groups, were synthesized and the properties compared to those of the corresponding closed structures (cyclophanes). The combination of diboron electron-donor units and bi- or oligopyridyl electron-acceptor units leads to intriguing optical and redox properties.
Item Description:Gesehen am 27.03.2023
Physical Description:Online Resource
ISSN:1521-3765
DOI:10.1002/chem.202102656