化学
配体(生物化学)
磁铁
各向异性
分子
放松(心理学)
磁滞
结晶学
热稳定性
化学物理
凝聚态物理
有机化学
受体
物理
生物化学
量子力学
心理学
社会心理学
作者
Zhenhua Zhu,Chen Zhao,Tingting Feng,Xiaodong Liu,Ying Xu,Xiaolei Li,Yi‐Quan Zhang,Jinkui Tang
摘要
Design and synthesis of air-stable and easily tailored high-performance single-molecule magnets (SMMs) are of great significance toward the implementation of SMMs in molecular-based magneto-electronic devices. Here, by introducing electron-withdrawing fluorinated substituents on equatorial ligand, two chiral Dy(III) macrocyclic complexes, RRRR-Dy-D6hF12 (1) and SSSS-Dy-D6hF12 (2), with a record anisotropy barrier exceeding 1800 K and the longest relaxation time approaching 2500 s at 2.0 K for all known air-stable SMMs, were obtained. The nearly perfect axiality of the ground Kramers doublet (KD) enables the open hysteresis loops up to 20 K in the magnetically diluted sample. It is notable that they are structurally rigid with high thermal stability and the apical ligand can be tailored to carry proper surface-binding groups. This finding not only improves the magnetic properties for air-stable SMMs but also provides a new avenue for deposition of SMMs on surfaces.
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