A Non-sandwiched Macrocyclic Monolanthanide Single-Molecule Magnet: The Key Role of Axiality

被引:219
作者
Feltham, Humphrey L. C. [1 ,2 ]
Lan, Yanhua [3 ]
Kloewer, Frederik [1 ,2 ,3 ]
Ungur, Liviu [4 ,5 ]
Chibotaru, Liviu F. [4 ]
Powell, Annie K. [3 ]
Brooker, Sally [1 ,2 ]
机构
[1] Univ Otago, Dept Chem, Dunedin 9054, New Zealand
[2] Univ Otago, MacDiarmid Inst Adv Mat & Nanotechnol, Dunedin 9054, New Zealand
[3] Karlsruhe Inst Technol, Inst Inorgan Chem, D-76131 Karlsruhe, Germany
[4] Katholieke Univ Leuven, Div Quantum & Phys Chem, B-3001 Louvain, Belgium
[5] Katholieke Univ Leuven, INPAC Inst Nanoscale Phys & Chem, B-3001 Louvain, Belgium
关键词
dysprosium; imine relaxation; macrocycle; magnetism; single-molecule magnet; SCHIFF-BASE MACROCYCLES; ANISOTROPIC BARRIER; CHAIN MAGNET; RELAXATION; COMPLEXES; BEHAVIOR; MAGNETIZATION; LIGANDS; ANALOGS; UNITS;
D O I
10.1002/chem.201100438
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Macrocyclic single-molecule magnet: The dynamic behavior of the tetranuclear zinc(II)-dysprosium(III) complex of the hexaimine [3+3] macrocycle (LPr)6- under an external DC field (1500 Oe) indicates that it is a single-molecule magnet (SMM). It is the first to contain a single lanthanide ion (in orange, see graphic) coordinated inside the cavity of a single macrocyclic ligand and thus represents a new class of SMM. © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
引用
收藏
页码:4362 / 4365
页数:4
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