Mononuclear versus dinuclear complex formation in nickel(II) sulfate/phenyl(2-pyridyl)ketone oxime chemistry depending on the ligand to metal reaction ratio: synthetic, spectral and structural studies.

The reactions of phenyl(2-pyridyl)ketone oxime (py)C(ph)NOH, with nickel(II) sulfate hexahydrate under reflux, in the absence of an external base, have been investigated. The reaction of NiSO4 x 6H2O with two equivalents of (py)C(ph)NOH in H2O/MeOH leads to the dinuclear complex [Ni2(SO4)2[(py)C(ph)NOH]4] (1), while an excess of the organic ligand affords the 1:3 cationic complex Ni[(py)C(ph)NOH]3 (2). Compound 1 is transformed into 2 by a reaction with an excess of ligand in refluxing H(2)O/MeOH. Reactions of 1 and 2 with a limited amount of LiOH give the known cluster [Ni6(SO4)4(OH)[(py)C(ph)NO]3[(py)C(ph)NOH]3(H2O)3]. The structures of 1 and 2 have been determined by single-crystal X-ray crystallography. In both complexes the organic ligand chelates through its 2-pyridyl and oxime nitrogen atoms. The metal centers of 1 are bridged by two eta1:eta1:micro sulfato ligands; each metal ion has the cis-cis-trans deposition of the coordinated sulfato oxygen, pyridyl nitrogen and oxime nitrogen atoms, respectively. The cation of 2 is the fac isomer considering the positions of the coordinated pyridyl and oxime nitrogen atoms. The crystal structures of both complexes are stabilized by hydrogen bonds. Compounds 1 and 2 join a small family of structurally characterized metal complexes containing the neutral or anionic forms of phenyl(2-pyridyl)ketone oxime as ligands. The IR spectra of the two complexes are discussed in terms of the nature of bonding and their structures. From the vibrational spectroscopy viewpoint, the SO4(2-) groups in 1 and 2 appear to have lower symmetries compared with those deduced from X-ray crystallography; this is attributed to the participation of sulfates in hydrogen bonding interactions.