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Interpenetration of a 3D Icosahedral M@Ni12 (M=Al,Ga) Framework with Porphyrin‐Reminiscent Boron Layers in MNi9B8
Authors:Dr. Qiang Zheng  Dr. Frank R. Wagner  Dr. Alim Ormeci  Dr. Yurii Prots  Dr. Ulrich Burkhardt  Dr. Marcus Schmidt  Dr. Walter Schnelle  Prof. Yuri Grin  Dr. Andreas Leithe‐Jasper
Affiliation:Max‐Planck‐Institut für Chemische Physik fester Stoffe, N?thnitzer Str. 40, 01187 Dresden (Germany)
Abstract:Two ternary borides MNi9B8 (M=Al, Ga) were synthesized by thermal treatment of mixtures of the elements. Single‐crystal X‐ray diffraction data reveal AlNi9B8 and GaNi9B8 crystallizing in a new type of structure within the space group Cmcm and the lattice parameters a=7.0896(3) Å, b=8.1181(3) Å, c=10.6497(4) Å and a=7.0897(5) Å, b=8.1579(4) Å, c=10.6648(7) Å, respectively. The boron atoms build up two‐dimensional layers, which consist of puckered [B16] rings with two tailing B atoms, whereas the M atoms reside in distorted vertices‐condensed [Ni12] icosahedra, which form a three‐dimensional framework interpenetrated by boron porphyrin‐reminiscent layers. An unusual local arrangement resembling a giant metallo‐porphyrin entity is formed by the [B16] rings, which, due to their large annular size of approximately 8 Å, chelate four of the twelve icosahedral Ni atoms. An analysis of the chemical bonding by means of the electron localizability approach reveals strong covalent B?B interactions and weak Ni?Ni interactions. Multi‐center dative B?Ni interaction occurs between the Al–Ni framework and the boron layers. In agreement with the chemical bonding analysis and band structure calculations, AlNi9B8 is a Pauli‐paramagnetic metal.
Keywords:borides  chemical bonding  crystal structures  electronic structure  X‐ray diffraction
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