Abstract
AbstractThe synthesis, crystal structures and magnetic properties of linear heptanuclear nickel(II) complexes [Ni7(μ7‐teptra)4X2], (teptra = tetrapyridyltriamido), with the axial ligand X = Cl− (1), NCS− (2), are reported. The hepta‐nuclear metal chain is helically wrapped by four syn‐syn‐syn‐syn‐syn‐syn teptra3− ligands. Both of the [Ni7(μ7‐teptra)4]2+ moiety are isostructural involving a Ni7 linear chain unit with all of the ∠Ni‐Ni‐Ni being 180°, terminated by two axial ligands. Three types of NiNi distances are found in these complexes. The longest ones bonded with the axial ligands are 2.383(1), 2.374(2) and 2.375(2), 2.354(2), and the intermediate ones are 2.310(1), 2.304(1) and 2.300(2), 2.303(2) Å for (1) and (2), respectively. The innermost NiNi distances are the shortest ones with the distances of 2.226(2), 2.214(2) and 2.194(2), 2.206(2) Å for (1) and (2), respectively. Two terminal Ni(II) ions bonded with the axial ligands are in a square‐pyramidal (NiN4X) environment and exhibit long NiN bonds (−2.10 Å) which are consistent with a high‐spin Ni(II) configuration. The inner five Ni(II) ions displayed short NiN (∼1.90 Å) bond distances which are consistent with a square‐planar (NiN4), diamagnetic arrangement of a low‐spin Ni(II) configuration. The magnetic measurement of (1) shows an antiferromagnetic interaction of two terminal high‐spin Ni(II) ions with the coupling constant J = −3.8 cm−1. The NiNi, NiN distances and magnetic behavior among tri‐, penta‐, and hepta‐nickel(II) complexes are compared and discussed.
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