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Heteronuclear Complexes of Macrocyclic Oxamide with Co-ligands:  Syntheses, Crystal Structures, and Magnetic Properties

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posted on 19.02.2007, 00:00 by Li-Na Zhu, Na Xu, Wei Zhang, Dai-Zheng Liao, Kazuyoshi Yoshimura, Ko Mibu, Zong-Hui Jiang, Shi-Ping Yan, Peng Cheng
Four heteronuclear complexes Mn(CuL)2(SCN)2 (1), {[Mn(CuL)2(μ-dca)2]·2H2O}n (2), Zn(CuL)2(SCN)2 (3), and [Fe(CuL)(N3)2]2 (4) incorporating macrocyclic oxamide ligands have been synthesized and structurally characterized. L is the dianion of diethyl 5,6,7,8,15,16-hexahydro-6,7-dioxodibenzo[1,4,8,11]-tetraazacyclotetradecine-13,18-dicarboxylate, and dca is the dicyanamide. The structure of 1 or 3 consists of oxamido-bridged trinuclear [MIICuII2] molecules (for 1, M is the manganese(II) ion, and for 3, M is the zinc(II) ion). Both of them consist of 1D supramolecuar chains via π−π interactions. The structure of 2 also has the oxamido-bridged trinuclear [MnIICuII2] structure units and consists of 2D layers formed by the linkage of copper(II) and manganese(II) atoms via the oxamido and μ1, 5-dca bridges. Complex 4 consists of oxamido-bridged tetranuclear [FeII2CuII2] molecules and arranges in 1D chains. Different co-ligands may result in different structures in this macrocyclic oxamide system. The variable-temperature magnetic susceptibility measurements (2−300 K) of 1 and 2 both show the pronounced antiferromagnetic interactions between the copper(II) and manganese(II) ions.