摘要
Although the design and synthesis of high-nuclear lanthanide clusters with specific shapes and functions have been an active area of research, effective experience and rules to guide further systematic expansion of lanthanide clusters with different connections are lacking. Herein, we adjusted the steric hindrance effects on the substituents of diacylhydrazone ligands (H4L1, N '(2),N '(9)-bis((E)-2-hydroxybenzylidene)-1,10-phenanthroline-2,9-dicarbohydrazide; H4L2, N '(2),N '(9)-bis((E)-2-hydroxy-3-methylbenzylidene)-1,10-phenanthroline-2,9-dicarbohydrazide; H4L3, N '(2),N '(9)-bis((E)-3-(tert-butyl)-2-hydroxybenzylidene)-1,10-phenanthroline-2,9-dicarbohydrazide) and reacted them with Dy(NO3)(3)center dot 6H(2)O under solvothermal conditions to obtain three dysprosium clusters (1-3) with different shapes. The molecular formulas of the abovementioned clusters are [Dy-16(L-1)(3)(mu(3)-OH)(25)(NO3)(11)(H2O)(10)]center dot 4CH(3)CN center dot 8CH(3)OH, [Dy-10(L-2)(4)(mu(2)-OH)(2)(mu(3)-O)(4)(NO3)(4)(CH3CN)(2)(CH3OH)(4)(H2O)(8)]center dot CH3OH center dot 8H(2)O, and [Dy-5(L-3)(2)(mu(2)-CH3O)(mu(2)-OH)(2)(mu(4)-O)(NO3)(2)(CH3OH)(2)]center dot 6CH(3)OH center dot 2CH(3)CN. Cluster 1 with a brucite-like planar structure crystallizes in the P2(1)/n space group of the monoclinic system. The Dy(iii) ions in the cluster 1 structure are bridged by mu(3)-OH- to form a plane triangle shape. In addition, the structure of cluster 1 contains three layers of Dy(iii) ions (1 + 6 + 9) with different coordination environments. Cluster 2 crystallizes in the P1 space group of the triclinic system. The cluster core in cluster 2 is composed of two molecules of missing cubane Dy4O6 and two Dy(iii) ions. The ligand (L-2)(4-) adopts two coordination modes (mu(3)-eta(1):eta(1):eta(2):eta(1):eta(1):eta(2):eta(1):eta(1) and mu(5)-eta(2):eta(1):eta(1):eta(1):eta(1):eta(1):eta(1):eta(1):eta(1):eta(2)) to chelate Dy(iii) ions. In addition, Dy(iii) ions in Dy4O6 are connected by mu(2)-OH- and mu(3)-OH-. Two molecules of planar Dy3L3 intersect to form cluster 3, and it crystallizes in the I2/a space group of the monoclinic system. The analysis of the structure of clusters 1-3 shows that they are formed by a stepwise assembly process from outside to inside. To the best of our knowledge, a very small number of examples have reported that a series of differently connected dysprosium clusters were obtained through the regulation of substitution effects. Notably, we are the first to propose the out-to-in growth mechanism of planar high-nucleus dysprosium clusters. @@@ The results of the variable temperature AC susceptibility test show that clusters 1, 2, and 3 exhibit single-molecule magnet-like behavior under zero-field conditions.
-
单位桂林理工大学