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Boron radical cations from the facile oxidation of electron-rich diborenes
Philipp Bissinger1, Holger Braunschweig, Alexander Damme
1Institut für Anorganische Chemie, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074 Würzburg (Germany).
Abstract:
The realization of a phosphine-stabilized diborene, Et3P⋅(Mes)B=B(Mes)⋅PEt3 (4), by KC8 reduction of Et3P⋅B2Mes2Br2 in benzene enabled the evaluation and comparison of its electronic structure to the previously described NHC-stabilized diborene IMe⋅(Dur)B=B(Dur)⋅IMe (1). Importantly, both species feature unusual electron-rich boron centers. However, cyclic voltammetry, UV/Vis spectroscopy, and DFT calculations revealed a significant influence of the Lewis base on the reduction potential and absorption behavior of the BB double bond system. Thus, the stronger σ-donor strength and larger electronegativity of the NHC ligand results in an energetically higher-lying HOMO, making 1 a stronger neutral reductant as 4 (1: E(1/2)=-1.55 V; 4: -1.05 V), and a smaller HOMO-LUMO gap of 1 accompanied by a noticeable red-shift of its lowest-energy absorption band with respect to 4. Owing to the highly negative reduction potentials, 1 and 4 were easily oxidized to afford rare boron-centered radical cations (5 and 6).
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