Deaggregation properties and transmetalation studies of a zinc() salen-type Schiff-base complex

This paper reports the synthesis and the deaggregation properties of a Lewis acidic Zn( ii ) salen-type Schiff-base complex derivative from diaminomaleonitrile and a systematic detailed study of its transmetalation with other metal ions in solution. In a solution of non-coordinating solvents, the complex is in a dimeric form, while in coordinating solvents or upon addition of a Lewis base it is stabilized as monomeric adducts. Experiments done in two solvents with different Lewis basicities indicate a major role of the stability of the starting adduct in transmetalation. Thus, using nitrate or perchlorate salts, acetonitrile solutions of the complex give an immediate and complete transmetalation with Cu 2+ , while with Co 2+ and Ni 2+ a much slower transmetalation rate is observed. Instead, using chloride salts a fast and complete transmetalation is observed for divalent ions of the first transition series (Mn 2+ , Fe 2+ , Co 2+ , Ni 2+ , Cu 2+ ), indicating the role of the chloride in stabilizing the transition state of the transmetalation. On the other hand, DMF solutions of the complex are less prone to transmetalation, according with the greater basicity of the solvent and, hence, the greater stability of the related adducts with the complex. Therefore, the nature of the solvent and the counteranion allow controlling the transmetalation process of this Zn( ii ) Schiff-base complex. A Lewis acidic zinc( ii ) Schiff-base complex exhibits deaggregation properties. The monomeric adducts undergo transmetalation with divalent ions of the first transition series depending on the nature of the solvent and the counteranion.