Synthesis of symmetrically and unsymmetrically substituted cationic diborane(4) compounds with distinct structural motifs and properties

The introduction of electron-donating, bridging guanidinate substituents in diborane(4) compounds allows the synthesis of a variety of new cationic diborane(4) compounds. In this work, strategies for the directed synthesis of cationic di- and tetraboron compounds are presented, leading to the synthe...

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Main Authors: Filbeck, Erik (Author) , Kistner, Lucas (Author) , Vogler, Daniel (Author) , Bučak Gasser, David (Author) , Flórido Martins, Lilliana (Author) , Schöner, Maximilian (Author) , Kaifer, Elisabeth (Author) , Himmel, Hans-Jörg (Author)
Format: Article (Journal)
Language:English
Published: 14 November 2022
In: European journal of organic chemistry
Year: 2022, Issue: 43, Pages: 1-12
ISSN:1099-0690
DOI:10.1002/ejoc.202201105
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1002/ejoc.202201105
Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.202201105
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Author Notes:Erik Filbeck, Lucas Kistner, Daniel Vogler, David Bučak Gasser, Lilliana Flórido Martins, Maximilian Schöner, Elisabeth Kaifer, and Hans-Jörg Himmel
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Summary:The introduction of electron-donating, bridging guanidinate substituents in diborane(4) compounds allows the synthesis of a variety of new cationic diborane(4) compounds. In this work, strategies for the directed synthesis of cationic di- and tetraboron compounds are presented, leading to the synthesis and complete characterization of several new compounds with distinct structural motifs, all exhibiting BII atoms directly bound to each other. Hence, we report on tetracationic donor-acceptor cyclophanes with diboron donor linkers and organic π-acceptor units, on paddlewheel-type cationic diboranes, and on unsymmetrically-substituted monocationic diboranes.
Item Description:Gesehen am 19.12.2022
Physical Description:Online Resource
ISSN:1099-0690
DOI:10.1002/ejoc.202201105