Abstract
Twofold deprotonation of the “boronium” cation H2B(tBuImH)2+ I– provides access to the bulky bis(carbene)borate ligand H2B(tBuIm)2–. Transfer of the ligand to NiII sources affords the square‐planar, diamagnetic complex Ni[H2B(tBuIm)2]2. The properties of this complex are contrasted with the related bis(pyrazolyl)borate complex Ni[H2B(tBupyr)2]2, which is octahedral and paramagnetic. Density functional theory has been used to evaluate the reasons for the structural differences. Stabilization of the square‐planar geometry by the bis(carbene)borate ligand can be ascribed to its greater donor ability.(© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

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