Simultaneous assembly of mononuclear and dinuclear dysprosium(III) complexes behaving as single-molecule magnets in a one-pot hydrothermal synthesis

被引:17
作者
Liu, Cai-Ming [1 ]
Zhang, De-Qing [1 ]
Hao, Xiang [1 ]
Zhu, Dao-Ben [1 ]
机构
[1] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, Ctr Mol Sci,Key Lab Organ Solids, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
single-molecule magnet; single-ion magnet; dysprosium (III) complexes; slow magnetic relaxation; water aggregations; METAL-ORGANIC FRAMEWORK; SCHIFF-BASE LIGANDS; ION MAGNETS; RELAXATION; MAGNETIZATION; ANISOTROPY; CLUSTER; ACID; DYNAMICS; SOLVENT;
D O I
10.1007/s11426-016-0359-x
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two dysprosium(III) complexes derived from 2,2'-bipyridine-6,6'-dicarboxylic acid (H(2)bpdc), [Dy(bpdc)(Hbpdc)]center dot 3H(2)O (1) and [Dy-2(bpdc)(3)(H2O)(3)]center dot 2.125H(2)O (2), were isolated from the same hydrothermal reaction container as different phases. Compound 1 is a mononuclear complex with a DyN4O4 coordination polyhedron; whereas compound 2 is a dinuclear complex with two types of eight coordinated dysprosium(III) ions, showing DyN4O4 and DyN2O6 coordination polyhedra, respectively. Remarkably, a new type of (H2O)(6) supramolecular aggregate exists in the crystal structure of 2. Magnetic investigations revealed that 1 is a field-induced single-ion magnet with an effective energy barrier of 45.6 K, exhibiting two-step magnetic relaxation; while an intramolecular ferromagnetic interaction exists in 2, which is a field-induced single-molecule magnet, displaying two-step magnetic relaxation too, with effective energy barriers of 53.4 and 92.1 K, respectively.
引用
收藏
页码:358 / 365
页数:8
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