. Can. J. Chem. 68, 1598 (1990).The electrochemical oxidation of a metallic sacrificial anode (M = Zn, Cd, Sn, In, Cu) in a non-aqueous solution of 3-hydroxy-2-methyl-4-pyrone (= HL) yields the ML, complexes (M = Zn, Cd, Sn, Cu, n = 2; M = In, n = 3). Adducts of the type ML2.B (M = Zn, Cd, B = N,N,N1,N'-tetramethylethylenediamine (tmen); M = Cu, B = triphenylphosphine) were obtained by the reaction between the appropriate ligand (B) and the previously synthesized complexes (M = Zn, Cd), or by arranging for the initial electrolytic phase to include the base (M = Cu). The tin(I1) compound shows the typical reactions of such low oxidation state species by reacting with iodine and ortho-quinones by oxidative addition. All compounds were characterized by elemental analysis and by IR, 'H and I3C n1111. spectroscopy. The structure of CdL2.tmen was determined by X-ray crystallography, which identified the Cd04N2 kernel, and partial electron delocalization within the pyronate ring. Key words: electrochemical synthesis, cadmium complexes, zinc complexes, tin(I1) oxidation, 3-hydroxy-2-methy 1-4-pyrone. Mots cle's: synthkse tlectrochimique, complexes du cadmium, complexes du zinc, oxydation du Zn(II), 3-hydroxy-2-mtthyl-4-pyrone.[Traduit par la revue]