Abstract
Synthesis, characterization, and crystal engineering of a tris chelate compound, [NiIIL3](N3)Cl (1), (L = diequatorial trans-1,2-diaminocyclohexane) have been described. The compound crystallizes in the cubic P4332 space group with a = 13.859(12) Å and Z = 4. In this structure, the azide anion is highly disordered. Each chloride in 1 interacts with six amine hydrogens and is surrounded by three mononuclear cations, each of which, in turn, are linked with three chlorides to form a three-dimensional channel network. This is the first report of hexafurcated (acceptor) N–H ⋅s Cl− hydrogen bonds in metalloorganic systems and the first report of the three-dimensional framework resulted basically due to the multifurcated acceptor nature of the halide anion.
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Nayak, M., Kundu, P., Drew, M.G.B. et al. Synthesis, Characterization, and Crystal Engineering of [NiII(1,2-Diaminocyclohexane)3](N3)Cl: Three-Dimensional Framework by Hexafurcated N–H ⋅s Cl− Hydrogen Bonds. Struct Chem 16, 629–633 (2005). https://doi.org/10.1007/s11224-005-8251-2
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DOI: https://doi.org/10.1007/s11224-005-8251-2