Pei Shaomin, Hu Zhaobo, Chen Zilu, Yu Shui, Li Bo, Liang Yuning, Liu Dongcheng, Yao Di, Liang Fupei
State Key Laboratory for Chemistry and Molecular Engineering of Medicinal Resources, School of Chemistry and Pharmaceutical Sciences, Guangxi Normal University, Guilin 541004, P. R. China.
Dalton Trans. 2018 Feb 6;47(6):1801-1807. doi: 10.1039/c7dt04003b.
To achieve a heterometallic single-molecule magnet with novel topologies, two isostructural hexanuclear clusters [NiLn(μ-OH)L(OAc)]·HO [Ln = Dy, 1; Y, 2] were prepared from the reactions of 1,3-diamine-2-propanol (HL) with MCl·6HO (M = Dy, Y) and Ni(OAc)·4HO in acetonitrile, in which the studies for 2 with the diamagnetic metal ion of Y(iii) are just for further understanding of the magnetic properties of 1. Single-crystal X-ray diffraction measurements indicate that both heterometallic hexanuclear complexes possess an S-shaped double-pocket skeleton with the two M(iii) ions separated by a chair-like NiO moiety. The temperature- and frequency-dependent alternating-current (ac) susceptibility measurements under zero dc fields revealed a single-molecule magnet for 1. Its magnetic properties can be further understood based on the magnetic analysis of 2.
为了获得具有新颖拓扑结构的异金属单分子磁体,通过1,3 - 二氨基 - 2 - 丙醇(HL)与MCl₃·6H₂O(M = Dy,Y)和Ni(OAc)₂·4H₂O在乙腈中的反应制备了两个同构的六核簇合物[NiLn(μ - OH)L(OAc)]·H₂O [Ln = Dy,1;Y,2],其中对具有Y(iii)抗磁性金属离子的2的研究只是为了进一步理解1的磁性。单晶X射线衍射测量表明,这两个异金属六核配合物都具有S形双口袋骨架,两个M(iii)离子被一个椅状的NiO部分隔开。在零直流场下的温度和频率依赖的交流(ac)磁化率测量揭示了1是一个单分子磁体。基于对2的磁性分析可以进一步理解其磁性。