Single molecule magnet with an unpaired electron trapped between two lanthanide ions inside a fullerene

被引:218
作者
Liu, Fupin [1 ]
Krylov, Denis S. [1 ]
Spree, Lukas [1 ]
Avdoshenko, Stanislav M. [1 ]
Samoylova, Nataliya A. [1 ]
Rosenkranz, Marco [1 ]
Kostanyan, Aram [2 ]
Greber, Thomas [2 ]
Wolter, Anja U. B. [1 ]
Buechner, Bernd [1 ]
Popov, Alexey A. [1 ]
机构
[1] Leibniz Inst Solid State & Mat Res, Helmholtzstr 20, D-01069 Dresden, Germany
[2] Univ Zurich, Phys Inst, Winterthurerstr 190, CH-8057 Zurich, Switzerland
基金
欧洲研究理事会;
关键词
ENDOHEDRAL METALLOFULLERENES; METAL ATOMS; SPIN; HYSTERESIS; RELAXATION; EXTRACTION; ANISOTROPY; EXCHANGE; BLOCKING; DESIGN;
D O I
10.1038/ncomms16098
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Increasing the temperature at which molecules behave as single-molecule magnets is a serious challenge in molecular magnetism. One of the ways to address this problem is to create the molecules with strongly coupled lanthanide ions. In this work, endohedral metallofullerenes Y-2@C-80 and Dy-2@C-80 are obtained in the form of air-stable benzyl monoadducts. Both feature an unpaired electron trapped between metal ions, thus forming a single-electron metal-metal bond. Giant exchange interactions between lanthanide ions and the unpaired electron result in single-molecule magnetism of Dy-2@C-80(CH2Ph) with a record-high 100 s blocking temperature of 18 K. All magnetic moments in Dy-2@C-80(CH2Ph) are parallel and couple ferromagnetically to form a single spin unit of 21 mB with a dysprosium-electron exchange constant of 32 cm(-1). The barrier of the magnetization reversal of 613 K is assigned to the state in which the spin of one Dy centre is flipped.
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页数:9
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