Issue 16, 2004
From the journal:

Chemical Communications

Mesoionic bora-tetraazapentalenes – fully reversible two step redox systems†

Tillmann Gebauer,a   Rainer Beckert,*a   Dieter Weiß,a   Katrin Knop,a   Christian Käpplingera  and  Helmar Görlsb  

* Corresponding authors

a Institute of Organic and Macromolecular Chemistry, Friedrich Schiller University, Lessingstr. 8, D-07743 Jena, Germany
E-mail: c6bera@uni-jena.de
Fax: +49 3641 948212
Tel: +49 3641 948230

b Institute of Inorganic and Analytical Chemistry, Friedrich Schiller University, August-Bebelstr. 2, D-07743 Jena, Germany

Abstract

Bora-tetraazapentalenes have been synthesised and characterized; the radical anion shows an unusual thermodynamic stability (semiquinone formation constants KSEM of ca. 1014).

Graphical abstract: Mesoionic bora-tetraazapentalenes – fully reversible two step redox systems

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Article information

DOI
https://doi.org/10.1039/B403480E
Article type
Communication
Submitted
08 Mar 2004
Accepted
20 May 2004
First published
30 Jun 2004

Chem. Commun., 2004, 1860-1861

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Mesoionic bora-tetraazapentalenes – fully reversible two step redox systems

T. Gebauer, R. Beckert, D. Weiß, K. Knop, C. Käpplinger and H. Görls, Chem. Commun., 2004, 1860 DOI: 10.1039/B403480E

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