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 NiNi 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 NiNi 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 NiN bonds (−2.10 Å) which are consistent with a high‐spin Ni(II) configuration. The inner five Ni(II) ions displayed short NiN (∼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 NiNi, NiN distances and magnetic behavior among tri‐, penta‐, and hepta‐nickel(II) complexes are compared and discussed.

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