Zhu Zhenhua, Zhao Chen, Feng Tingting, Liu Xiaodong, Ying Xu, Li Xiao-Lei, Zhang Yi-Quan, Tang Jinkui
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, P. R. China.
University of Chinese Academy of Sciences, Beijing 100049, P. R. China.
J Am Chem Soc. 2021 Jul 14;143(27):10077-10082. doi: 10.1021/jacs.1c05279. Epub 2021 Jun 28.
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, -Dy-F () and -Dy-F (), 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.
设计并合成空气稳定且易于定制的高性能单分子磁体(SMM)对于在分子基磁电子器件中实现SMM具有重要意义。在此,通过在赤道配体上引入吸电子的氟化取代基,获得了两种手性Dy(III)大环配合物,即-Dy-F()和-Dy-F(),对于所有已知的空气稳定SMM,其各向异性势垒超过1800 K,在2.0 K时最长弛豫时间接近2500 s。基态克莱默斯二重态(KD)近乎完美的轴向性使得在磁稀释样品中能够实现高达20 K的开放磁滞回线。值得注意的是,它们结构刚性高、热稳定性好,并且顶端配体可以定制以携带合适的表面结合基团。这一发现不仅改善了空气稳定SMM的磁性能,还为在表面沉积SMM提供了一条新途径。