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Multinuclear beryllium amide and imide complexes: structure, properties and bonding
Deniz F Bekiş1, Lewis R Thomas-Hargreaves1, Sergei I Ivlev1
1Anorganische Chemie, Nachwuchsgruppe Hauptgruppenmetallchemie, Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Straße 4, 35032 Marburg, Germany. magnus.buchner@chemie.uni-marburg.de.
Abstract:
The beryllium amide and imide complexes [Be(HNMes)2]3, [(py)2Be(HNMes)2], [Be(HNDipp)2]2, [Be(NPh2)(μ2-HNDipp)]2 and [Be(NCPh2)2]3 have been prepared and characterised with NMR and IR spectroscopy as well as single crystal X-ray diffraction. Analysis of the localised molecular orbitals (LMOs) and intrinsic atomic orbital (IAO) atomic charges in the framework of the intrinsic bond orbital (IBO) localization method revealed a covalent bonding network consisting of 2-electron-2-centre and 2-electron-3-centre σ bonds, in which one electron pair of the anionic N-donor ligands is involved. The electron deficiency at the beryllium atoms is partially compensated through additional electron donation from the lone pair at the nitrogen atoms.
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