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Updated: Jan 4, 2026
Preparation, Purification, and Characterization of Lanthanide Complexes for Use as Contrast Agents for Magnetic Resonance Imaging
Published on: July 21, 2011
Two mononuclear dysprosium(iii) complexes with their slow magnetic relaxation behaviors tuned by coordination
Shui Yu1, Zilu Chen, Huancheng Hu
1State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin 541004, P. R. China. zlchen@mailbox.gxnu.edu.cn fliangoffice@yahoo.com.
Abstract:
Two mononuclear dysprosium(iii) complexes [Dy(H3NAP)2Cl2]Cl·EtOH (1) and [Dy(H3NAP)2(H2O)Cl2]Cl·-2CH3CN·MeOH·0.5H2O (2) were obtained by coordinating an in situ formed Schiff base ligand of 1,3-bis(2-hydroxynaphthalenemethyleneamino)-propan-2-ol (H3NAP) to the dysprosium(iii) ion. Their Dy(iii) centers are six and seven-coordinated in octahedral and pentagonal-bipyramidal coordination geometries, respectively. Their structural difference is caused by the additional coordinated water molecule in the equatorial positions of complex 2 in comparison with that of complex 1. The well designed semi-rigid ligand contributes significantly to the low coordination numbers of Dy(iii) ions in the two title complexes, as well as to their structural difference. Magnetic investigations revealed that complexes 1 and 2 are both field-induced single-ion magnets (SIMs) with their effective energy barriers being 22.9(6) and 153.9(5) K, respectively. They are typical SIM examples with their performances tuned by the coordination geometries of metal ions.
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