Oxalato-Bridged Neutral Octanuclear Heterometallic Complexes [Ln₄K₄(L)₄(μ‑H₂O)₄(NO₃)₂(μ-Ox)] (Ln = Dy(III), Gd(III), Tb(III), Ho(III); LH₃ = N[CH₂CH₂NCH‑C₆H₃‑2-OH-3-O

Stepwise reaction of LH3 (LH3 = N­[CH2CH2NCH-C6H3-2-OH-3-OMe]3) with Ln­(NO3)3·​nH2O and potassium oxalate [K2Ox] afforded discrete heterometallic neutral octanuclear complexes [Ln4K4(L)4­(μ-H2O)4(NO3)2­(μ-Ox)] (Ln = Dy­(III), Gd­(III), Tb­(III), Ho­(III); LH3 = N­[CH2CH2NCH-C6H3-2-OH-3-OMe]3; Ox = (C2O4)2–). The molecular structures of 1–4 were confirmed by single-crystal X-ray crystallography. The asymmetric unit of these compounds contains two lanthanide­(III) ions and two potassium cations present in the opposite corners of a distorted rectangle. Such a motif is further bridged by an oxalate anion to generate the octanuclear heterometallic complex. The lanthanides are eight-coordinate in a distorted trigonal dodecahedron geometry. On the other hand, the potassium ions adopt a nine-coordinate coordination sphere in a distorted tricapped trigonal prism geometry. Magnetic studies on 1–4 reveal the absence of significant magnetic interactions between the magnetic centers present in these complexes.