镧系元素
磁铁
各向异性
单晶
离子
化学物理
材料科学
磁各向异性
单分子磁体
锕系元素
分子
化学
纳米技术
磁场
结晶学
无机化学
机械工程
磁化
物理
有机化学
工程类
量子力学
作者
Jeffrey D. Rinehart,Jeffrey R. Long
出处
期刊:Chemical Science
[Royal Society of Chemistry]
日期:2011-01-01
卷期号:2 (11): 2078-2078
被引量:2116
摘要
Scientists have long employed lanthanide elements in the design of materials with extraordinary magnetic properties, including the strongest magnets known, SmCo5 and Nd2Fe14B. The properties of these materials are largely a product of fine-tuning the interaction between the lanthanide ion and the crystal lattice. Recently, synthetic chemists have begun to utilize f-elements—both lanthanides and actinides—for the construction of single-molecule magnets, resulting in a rapid expansion of the field. The desirable magnetic characteristics of the f-elements are contingent upon the interaction between the single-ion electron density and the crystal field environment in which it is placed. This interaction leads to the single-ion anisotropies requisite for strong single-molecule magnets. Therefore, it is of vital importance to understand the particular crystal field environments that could lead to maximization of the anisotropy for individual f-elements. Here, we summarize a qualitative method for predicting the ligand architectures that will generate magnetic anisotropy for a variety of f-element ions. It is hoped that this simple model will serve to guide the design of stronger single-molecule magnets incorporating the f-elements.
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