“…Schiff bases can coordinate transition metals; therefore, they are used to manufacture palladium catalysts for the Suzuki-Miyaura cross-coupling [16] and Mizoroki-Heck reaction [17] and heteronuclear complexes with lanthanides [18], octahedral nickel(II) complexes [19], copper(II) [20][21][22][23], scandium(III) [24], and cobalt(II) [25] complexes, as well as redox-active complexes with germanium(IV) [26]. Palladium(II) and chromium(III) complexes formed by azomethines containing heterocycles inhibit the growth of S. marcescent, E. coli, and M. luteus bacteria and possess a pronounced antitumor activity against MCF-7, HepG-2, and HCT-116 cancer cells [27].…”