Reaction of 2, 5-bis(pyridin-2-yl)-1, 3, 4-thiadiazole and sodium azide with nickel(II) triflate yielded the mononuclear title complex, [Ni(N3)2(C12H8N4S)2]. The NiII ion is located on a centre of symmetry and is octahedrally coordinated by four N atoms of the two bidentate heterocyclic ligands in the equatorial plane. The axial positions are occupied by the N atoms of two almost linear azide ions [N - N - N = 178.8 (2)°]. The thiadiazole and pyridine rings of the heterocyclic ligand are almost coplanar, with a maximum deviation from the mean plane of 0.0802 (9) Å. The cohesion of the crystal structure is ensured by π-π interactions between parallel pyridine rings of neighbouring molecules [centroid-to-centroid distance = 3.6413 (14) Å], leading to a layered arrangement of the molecules parallel to (001).
CITATION STYLE
Laachir, A., Bentiss, F., Guesmi, S., Saadi, M., El Ammari, L., & Weil, M. (2015). Crystal structure of bis(azido-κN)bis[2, 5-bis(pyridin-2-yl)-1, 3, 4-thiadiazole-κ2N2,N3]nickel(II). Acta Crystallographica Section E: Structure Reports Online, 71(2), m24–m25. https://doi.org/10.1107/S2056989015000201
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