Guo Peng-Hu, Liu Jiang, Wu Zi-Hao, Yan Hua, Chen Yan-Cong, Jia Jian-Hua, Tong Ming-Liang
Inorg Chem. 2015 Aug 17;54(16):8087-92. doi: 10.1021/acs.inorgchem.5b01322. Epub 2015 Aug 6.
Thanks to the MeCN hydrolysis in situ reaction, a [2 × 2] square grid Dy(III)4 cluster based on a polypyridyl triazolate ligand, [Dy4(OH)2(bpt)4(NO3)4(OAc)2] (1), was separated successfully and characterized through single-crystal X-ray diffraction and SQUID magnetometry. The frequency-dependent signals in the out-of-phase component of the susceptibility associated with slow relaxation of the magnetization confirmed that complex 1 displays single-molecule magnet (SMM) behavior. Two distinct slow magnetic relaxation processes, with effective energy barriers Ueff1 = 93 cm(-1) for fast relaxation and Ueff2 = 143 cm(-1) for slow relaxation observed under a zero direct-current field, are mainly attributed to the origin of single-ion behavior, which can be further acknowledged by the magnetic investigation of a dysprosium-doped yttrium cluster. Besides, it should be noted that complex 1 represents so far the highest energy barrier among the pure Dy(III)4 SMMs.
由于MeCN原位水解反应,基于多吡啶三唑配体的[2×2]方形网格Dy(III)4簇合物[Dy4(OH)2(bpt)4(NO3)4(OAc)2](1)被成功分离,并通过单晶X射线衍射和超导量子干涉仪磁力测量进行了表征。与磁化强度缓慢弛豫相关的磁化率异相分量中的频率相关信号证实配合物1表现出单分子磁体(SMM)行为。在零直流场下观察到两个不同的缓慢磁弛豫过程,快速弛豫的有效能垒Ueff1 = 93 cm(-1),缓慢弛豫的有效能垒Ueff2 = 143 cm(-1),这主要归因于单离子行为的起源,这可以通过对掺镝钇簇合物的磁性研究进一步得到证实。此外,应该注意的是,配合物1是迄今为止纯Dy(III)4 SMMs中具有最高能垒的。