Institut für Anorganische Chemie | Universität Würzburg | D-97074 Würzburg



The Braunschweig Group

 

Research in the Braunschweig group covers a wide range of organometallic and main group element chemistry. Motivation for our work arises from the fundamental interest in novel molecular species, and much emphasis lies with the elucidation of their detailed electronic structure and reactivity patterns, thus disclosing potential applications in organic synthesis, catalysis, or materials science. Commonly, sophisticated synthetic protocols, as well as state-of-the-art analytical and computational methods are applied to meet these goals. Significant achievements over the past decades were made in various independent, highly topical and competitive sub-areas of (i) organometallic chemistry such as metal boron complexes (borane, boryl, borylene, boride, oxoboryl), metallo-arenophanes, or metal-only Lewis pairs, and (ii) main group element chemistry such as novel boron heterocycles (boroles, azaborinines, etc.) and boron boron multiple bonded species (diborenes, diborynes).




Selected Recent Publications

 

 

C. Saalfrank, F. Fantuzzi, T. Kupfer, B. Ritschel, K. Hammond, I. Krummenacher, R. Bertermann, R. Wirthensohn, M. Finze, P. Schmid, V. Engel, B. Engels, H. Braunschweig

cAAC-Stabilized 9,10-diboraanthracenes – Acenes with Open-Shell Singlet Biradical Ground States (VIP)

Angew. Chem. Int. Ed. 2020, 59, 19338–19343. [pdf]

 

 

 

S. Nees, T. Kupfer, A. Hofmann, H. Braunschweig

Planar Cyclopenten-4-yl Cations – Highly Delocalized π Aromatics Stabilized by Hyperconjugation

Angew. Chem. Int. Ed. 2020, 59, 18809–18815. [pdf]

 

 

 

T. Thiess, G. Bélanger-Chabot, F. Fantuzzi, M. Michel, M. Ernst, B. Engels, H. Braunschweig

Diborane(4) Azides: Surprisingly Stable Sources of Transient Iminoboranes

Angew. Chem. Int. Ed. 2020, 59, 15480–15486. [pdf]

 

 

Y.-M. Tian, X.-N. Guo, Z. Wu, A. Friedrich, S. A. Westcott, H. Braunschweig, U. Radius, T. B. Marder

Ni-Catalyzed Traceless, Directed C3-Selective C-H Borylation of Indoles
J. Am. Chem. Soc. 2020142, 13136–13144. [pdf]

 

 

 

F. Rauch, S. Fuchs, A. Friedrich, D. Sieh, I. Krummenacher, H. Braunschweig, M. Finze, T. B. Marder

Highly Stable, Readily Reducible, Fluorescent, Trifluoromethylated 9-Borafluorenes (VIP)
Chem. Eur. J. 202026, 12794–12808. [pdf]

 



The homepage for our newly-established research institute - the Institute for Sustainable Chemistry & Catalysis with Boron (ICB) is now online. 

Visit the ICB homepage.