Dinuclear Tb and Dy complexes supported by hybrid Schiff-base/calixarene ligands: synthesis, structures and magnetic properties

Abstract

The synthesis of the new lanthanide complexes [HNEt3_{3}][Dy2_{2}(HL1^{1})(L1^{1})] (5), and [Ln2_{2}(L2_{2})2_{2}] (Ln = TbIII^{III} (7), DyIII^{III} (8)) supported by the hybrid Schiff-base/calix[4]arene ligands H4_{4}L1^{1} (25-[2-((2-methylphenol)imino)ethoxy]-26,27,28-trihydroxy-calix[4]arene) and H3_{3}L2^{2} (25-[2-((2-methylpyridine)imino)ethoxy]-26,27,28-trihydroxy-calix[4]arene) are reported. Spectroscopic data (for 5) and X-ray crystallographic analysis (for 7·4MeCN, 8·4MeCN) reveal the presence of dimeric structures, featuring doubly-bridged NO4_{4}Ln(μ-O)2_{2}LnO4_{4}N (5) or N2_{2}O3_{3}Ln(μ-O)2_{2}LnO3_{3}N2_{2} cores (7, 8) with seven-coordinated Ln3+^{3+} ions. The magnetic properties of polycrystalline samples of 5, 7 and 8 were studied by variable temperature dc and ac magnetic susceptibility measurements. The χ′′(T) vs. T plots show no maxima in zero field, but the maxima can be detected under a 3 kOe dc field. The relaxation times τ obey the Arrhenius law above 5 K. Anisotropy barriers of ∼18 cm1^{-1} (26 K) for 5 and ∼23 cm1^{-1} (33 K) for 8 were determined

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