Molecular nanomagnets

被引:18
作者
Hendrickson, DN [1 ]
Christou, G
Ishimoto, H
Yoo, J
Brechin, EK
Yamaguchi, A
Rumberger, EM
Aubin, SMJ
Sun, ZM
Aromi, G
机构
[1] Univ Calif San Diego, Dept Chem & Biochem 0358, La Jolla, CA 92093 USA
[2] Indiana Univ, Dept Chem, Bloomington, IN 47405 USA
[3] Univ Tokyo, Inst Solid State Phys, Minato Ku, Tokyo 1068666, Japan
关键词
nanomagnet; single-molecule magnet; magnetization tunneling; superparamagnet;
D O I
10.1080/10587250210781
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Quantum mechanical tunneling of the direction of magnetization is discussed for several examples of single-molecule magnets (SMM's). Magnetization tunneling is described for two crystallographically different forms of [Mn12O12(O2CC6H4-p-Me)(16)(H2O)(4)] . solvate. The two Mn-12 complexes are isomers. The magnetization versus magnetic field hysteresis loops are quite different for the two isomeric Mn-12 complexes. One Mn-12 Complex exhibits a magnetization hysteresis loop that is characteristic of considerably faster magnetization tunneling than in the other Mn-12 isomer. The unusual orientation of Jahn-Teller elongation axes in one isomer leads to greater rhombic zero-field splitting that is the origin of the faster magnetization tunneling. In addition to data for Mn-12 complexes, magnetization relaxation rate versus temperature responses of three mixed-valence Mn-4 complexes are also reported. In all three cases the Arrhenius plot of the logarithm of the magnetization relaxation rate versus the inverse absolute temperature shows a temperature-independent region as well as a temperature-dependent region. The temperature-independent relaxation rate is definitive evidence of magnetization tunneling in the lowest-energy zero-field component of the ground state.
引用
收藏
页码:301 / 313
页数:13
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