Two complexes {[GdCu5(GlyHA)5(H2O)7Cr(C2O4)3]·11.02H2O}n (1) and {{[GdCu5(GlyHA)5(H2O)6]μ2-[Cu(C2O4)2(H2O)]}2μ4-[Cu(C2O4)2]·15.8H2O}n (2), were obtained as outcomes of the reactions between the cationic hexanuclear {GdCu5(GlyHA)5}3+ 15-metallacrown-5 complex (where GlyHA2- = glycinehydroxamate) and the anionic oxalate complexes K3[Cr(C2O4)3] or K2[Cu(C2O4)2]. Both 1 and 2 possess polymeric 1D-chain structures according to X-ray structural analysis. As a consequence of the geometric orientations of the donor atoms in the oxalates from [Cr(C2O4)3]3-, the Cu5 mean planes of neighboring 15-metallacrown-5 units {GdCu5(GlyHA)5}3+ are angled at 75.5° to each other, which leads to formation of a zig-zag motif in the 1D-chains of complex 1. The centrosymmetric complex 2 contains two structurally different bis(oxalato)cuprate anions μ2-[Cu(C2O4)2(H2O)]2-, for one of which, coordination to two adjacent {GdCu5(GlyHA)5}3+ units leads to formation of linear 1D-chains in 2, while the second type, μ4-[Cu(C2O4)2]2-, is coordinated to four {GdCu5(GlyHA)5}3+ units, causing the cross-linking of single 1D-chains into a double-chain 1D coordination polymer. Studies of χMT vs. T data for 1 and 2 in a 2-300 K temperature range revealed the presence of both ferromagnetic and antiferromagnetic interactions amongst paramagnetic centres. The experimental χMT vs. T data for 1 were fitted using a model which takes into account exchange interactions between adjacent copper(II) ions, the Gd-Cu exchange interactions within {GdCu5(GlyHA)5}3+ units and additionally Gd-Cr exchange interactions. Fitting of the χMT vs. T data for 2 was not possible, since coordination of μ4-[Cu(C2O4)2]2- to {GdCu5(GlyHA)5}3+ led to the non-equivalence of several Cu-Cu exchange interactions within the metallacrown units and hence a superfluity of fittable parameters. Complexes 1 and 2 are the first examples of 15-metallacrown-5 complexes demonstrating a magnetocaloric effect (-ΔSM at 13 T reaches 24.26 J K-1 kg-1 at 5 K and 19.14 J K-1 kg-1 at 4 K for 1 and 2, respectively).
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