“… [25–30] . Our investigations in this area are aimed to disclose the structure‐properties relationship in the coordination chemistry of heterometallic carboxylates [31–36] including polynuclear heterometallic lanthanide derivatives of the types {M 2 Ln} (e. g., M=Zn, Ln=Tb, Eu; M=Co, Ln=La, Gd; M=Cd, Ln=Sm, Eu, Tb, Dy, Ho, Er, Yb) [37–41] and {M 2 Ln 2 } (e. g., M=Zn, Cd, Ln=La; Eu, Nd, Gd, Tb, Dy; M=Cu, Ln=Gd, Tb, Dy, Ho, Yb) [42–45] supported mainly by different donor ligands: pyridine, [37,40,42] 2,2′‐bipyridine, 1,10‐phenanthroline, [37,40,42–44] triphenylphosphine, [39] N‐heterocyclic carbene [38] . Trinuclear {Co 2 Gd} complexes based on pivalic acid and supported by substituted pyridine ligands were found to demonstrate a ferromagnetic exchange Co II −Gd III ( J Co−Gd =0.15–0.18 cm −1 ) which is only weakly affected by the structural changes depending on the type of pyridine ligand [40] .…”