Metal-metal bond in lanthanide single-molecule magnets

被引:64
|
作者
Zhu, Zhenhua [1 ,2 ]
Tang, Jinkui [1 ,3 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] Univ Sci & Technol China, Sch Appl Chem & Engn, Hefei 230026, Peoples R China
基金
中国国家自然科学基金;
关键词
CRYSTAL-STRUCTURE; ENERGY BARRIERS; COMPLEXES; ANISOTROPY; RELAXATION; BLOCKING; SYMMETRY; ATOM; SPIN; DESIGN;
D O I
10.1039/d2cs00516f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lanthanide (Ln) compounds represent a unique chemical platform for developing high-temperature single-molecule magnets (SMMs). The shift in research focus from increasing the magnetic anisotropy barrier (U-eff) to raising the blocking temperature (T-B) has upgraded the design criteria from considering only the static crystal field (CF) to paying attention to the effects of molecular vibrations beyond the first coordination environment on the relaxation of magnetization. Although the realization of high working temperatures for Ln SMMs remains a formidable challenge, recent remarkable advances in dimetallofullerenes (di-EMFs) with Ln ions and mixed-valence dilanthanide complexes both feature single-electron Ln-Ln bonds to afford room-temperature molecular magnets. In this review, we provide critical discussion on the achievements of metal-metal (MM) bonded lanthanide SMMs, focusing on the effects of MM bonds on the magnetization dynamics, and shedding light on the future developments of high-temperature Ln SMMs.
引用
收藏
页码:9469 / 9481
页数:13
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