Abstract

Two coordination polymers, {[Cd(L1)2(L2)] · 0.25H2O} n (I) and {[Cd(L1)(L3)H2O] · 2H2O} n (II) (L1 = 2-pyrimidineamidoxime, L2 = 4-sulfobenzoate dianion and L3 = 5-sulfosalicylate dianion), has been synthesized and structurally characterized by single-crystal X-ray diffraction (CIF files CCDC nos. 1565646 (I) and 1565728 (II)). Complex I crystallizes in monoclinic space group P21/n with a = 10.1462(3), b = 16.0152(5), c = 14.0349(5) A, β = 93.267(3)°, V = 2276.87(13) A3, C68H66N32O29S4Cd4, M = 2373.36, ρcalcd = 1.731 g/cm3, μ(MoKα) = 1.109 mm−1, F(000) = 1186, GOOF = 0.806, Z = 1, the final R1 = 0.0287 and wR2 = 0.0733 for I > 2σ(I). Complex II crystallizes in monoclinic space group P21 with a = 6.882(2), b = 17.138(2), c = 7.883(2) A, β = 103.83(3)°, V = 902.8(4) A3, C12H16N4O10SCd, M = 520.75, ρcalcd = 1.916 g/cm3, μ(MoKα) = 1.388 mm−1, F(000) = 520, GOOF = 1.047, Z = 2, the final R1 = 0.0739 and wR2 = 0.2041 for I > 2σ(I). Crystal structural analysis reveals that complex I possesses the corrugated 1D chain structure extending along the $$[\bar 101]$$ direction. However, complex II displays a 2D coordination network lying on the ab crystal plane, which can be simplified as a binodal 3-connected 63 topological network by considering Cd2+ ions and L3 ligands as 3-connected nodes. Their photoluminescent and thermal properties were also investigated.

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