Metallogrid Single-Molecule Magnet: Solvent-Induced Nuclearity Transformation and Magnetic Hysteresis at 16 K

被引:83
|
作者
Huang, Wei [1 ]
Shen, Fu-Xing [1 ]
Wu, Shu-Qi [2 ]
Liu, Li [1 ]
Wu, Dayu [1 ]
Zheng, Zhe [1 ]
Xu, Jun [1 ]
Zhang, Ming [1 ]
Huang, Xing-Cai [1 ]
Jiang, Jun [1 ]
Pan, Feifei [1 ]
Li, Yao [1 ]
Zhu, Kun [1 ]
Sato, Osamu [2 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Collaborat Innovat Ctr Adv Catalysis & Green Mfg, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Jiangsu, Peoples R China
[2] Kyushu Univ, Inst Mat Chem & Engn, Nishi Ku, 744 Motooka, Fukuoka 8190395, Japan
基金
中国国家自然科学基金;
关键词
LANTHANIDE CLUSTER; SQUARE GRIDS; DY-4; ANALOG; ION MAGNET; RELAXATION; BEHAVIOR; COMPLEXES; TETRANUCLEAR; ANISOTROPY; DYNAMICS;
D O I
10.1021/acs.inorgchem.6b00500
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Structural assembly and reversible transformation between a metallogrid Dy-4 SMM (2) and its fragment Dy-2 (1) were established in the different solvent media. The zero-field magnetization relaxation was slowed for dysprosium metallogrid (2) with relaxation barrier of U-eff = 61.3 K when compared to Dy-2 (1). Both magnetic dilution and application of a moderate magnetic field suppress ground-state quantum tunneling of magnetization and result in an enhanced U-eff of 119.9 and 96.7 K for 2, respectively. Interestingly, the lanthanide metallogrid complex (2) exhibits magnetic hysteresis loop even up to 16 K at a given field sweep rate of 500 Oe/s.
引用
收藏
页码:5476 / 5484
页数:9
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