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Preparation, Purification, and Characterization of Lanthanide Complexes for Use as Contrast Agents for Magnetic Resonance Imaging
Published on: July 21, 2011
Pentanuclear lanthanide pyramids based on thiacalix[4]arene ligand exhibiting slow magnetic relaxation
Jing-Yuan Ge1, Jing Ru, Feng Gao
1State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Collaborative Innovation Center of Advanced Microstructures, Nanjing University, Nanjing 210093, P. R. China. zuojl@nju.edu.cn.
Abstract:
A series of pentanuclear Ln(III) clusters, [Ln5(μ4-OH)(μ3-OH)4(L1)(acac)6] (H4L1 = p-tert-butylthiacalix[4]arene; acac = acetylacetonate; Ln = Dy, Ho, Er) and [Ln5(μ5-OH)(μ3-OH)4(L1)(L2)2(acac)2(CH3OH)2] (H3L2 = 5,11,17,23-tetrakis(1,1-dimethylethyl)-25,26,27-trihydroxy-28-methoxy thiacalix[4]arene; Ln = Dy, Ho, Er), have been synthesized based on the thiacalix[4]arene ligand. All of these complexes feature a square-based pyramid with four triangular Ln3 structural motifs. One μ4-OH group bridges four Ln(III) ions in the basal plane of , while the OH group in complexes adopts the μ5-coordination mode. Our results illuminate the coordination modes of the versatile thiacalix[4]arene ligands and their application to new cluster compounds. The structural and magnetic studies confirm that the molecular symmetries and coordination geometries for lanthanide metal cores have a significant effect on some parameters as single-molecule magnets. Among them, two Dy5 pyramids exhibit distinct slow magnetic relaxation.
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