Single-Chain Magnetic Behavior in a Hetero-Tri-Spin Complex Mediated by Supramolecular Interactions with TCNQF•- Radicals

被引:82
作者
Wang, Zhao-Xi [1 ,2 ]
Zhang, Xuan [1 ]
Zhang, Yuan-Zhu [1 ]
Li, Ming-Xing [2 ]
Zhao, Hanhua [1 ]
Andruh, Marius [3 ]
Dunbar, Kim R. [1 ]
机构
[1] Texas A&M Univ, Dept Chem, College Stn, TX 77842 USA
[2] Shanghai Univ, Dept Chem, Coll Sci, Shanghai 200444, Peoples R China
[3] Univ Bucharest, Inorgan Chem Lab, Fac Chem, Bucharest 020464, Romania
基金
中国国家自然科学基金;
关键词
radical ions; single-chain magnets; TCNQ radicals; X-ray diffraction; - stacking interactions; TCNQ; MN; NI; RELAXATION; TECTONS; SYSTEMS; CU2+; FE; CO;
D O I
10.1002/anie.201407628
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The self-assembly of organic TCNQF(.-) radicals (2-fluoro-7,7,8,8-tetracyano-p-quinodimethane) and the anisotropic [Tb(valpn)Cu](3+) dinuclear cations produced a single-chain magnet (SCM) involving stacking interactions of TCNQF(.-) radicals (H(2)valpn is the Schiff base from the condensation of o-vanillin with 1,3-diaminopropane). Static and dynamic magnetic characterizations reveal that the effective energy barrier for the reversal of the magnetization in this hetero-tri-spin SCM is significantly larger than the barrier of the isolated single-molecule magnet based on the {TbCu} dinuclear core.
引用
收藏
页码:11567 / 11570
页数:4
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