Structural diversity of neutral bis-(β-iminoaldehyde) complexes of nickel(II)

Series of NiII and CuII complexes with dianionic [N2O2] ligands were synthesized and characterised applying spectroscopic and X-ray diffraction techniques. The ligands were obtained by 1:2 condensation of ethylene- and propylenediamine with malonic aldehyde derivatives (R2 = H, R1 = H or OCH3). Although the molecular formulae of the complexes are quite similar, the X-ray investigations have proved a significant structural diversity in the solid state. Among others, we found some simple nearly planar molecules stacked in the crystal lattice with electron density of six-membered rings delocalised over the chelate rings as well as some very complex polymeric or nickel acetate bridged trinuclear complexes. The coordination of the nickel ion by surrounding oxygen and nitrogen atoms is square-planar in the simplest case and octahedral in the most complex one. Small topological differences in similar molecules generate completely different crystal structures.From magnetic studies, a small, negative value of J obtained confirms the occurrence of weak antiferromagnetic interactions between the NiII ions in polymeric chain of the propylenediamine dialdehyde substituted derivative.

Series of NiII (and CuII) complexes with dianionic [N2O2] ligands exhibits significant structural diversity. In the case of the ethylene linkers, the complexes are square-planar. For the propylene linker, the central Ni atom becomes octahedrally coordinated with apparently increasing charge at the carbonyl oxygen atoms. In the most complex situation, a dimeric trinuclear complex is formed (6Ni). From magnetic studies of 4Ni, a small negative value of J obtained confirms the occurrence of weak antiferromagnetic interactions between the NiII ions in the polymeric complex.Figure optionsDownload as PowerPoint slide