Assembling Dysprosium Dimer Units into a Novel Chain Featuring Slow Magnetic Relaxation via Formate Linker

• Published in: Inorganic chemistry 2016-12, Vol.55 (24), p.12904-12911
• Main Authors: Chen, Qi, Ma, Fang, Meng, Yin-Shan, Sun, Hao-Ling, Zhang, Yi-Quan, Gao, Song
• Format: Article
• Language: English
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.6b02276

A dinuclear complex [DyLCl­CH3­OH)]2 (1) and a one-dimensional compound [DyL­(HCOO)­(CH3­OH)] n (2) have been synthesized using an organic ligand of N′-(2-hydroxy­benzyl­idene)­picolino­hydra­zide (H2L). Complex 1 exhibits a symmetric dinuclear structure, in which the Dy3+ centers reside in a pentagonal-bipyramidal coordination environment. In 2, the dinuclear units of 1 are strung into chains by formate anions, in which Dy3+ ions are situated in an octa-coordinated, hula-hoop-like coordination geometry. Magnetic studies reveal that ferromagnetic coupling is found between Dy3+ ions in both compounds. Complexes 1 and 2 exhibit slow magnetic relaxation under zero dc field with effective energy barriers of 88.4 and 175.8 K, respectively. Magnetic study combined with ab initio calculations indicates that the better performance of 2 is related to the unique molecular geometry and relatively stronger Dy3+–Dy3+ magnetic interaction within and/or between the dimer units.