Gao Rui Han, Hua Zi-Yi, Chen Kai, Xu Jing, Zhu Qian-Jiang, Tao Zhu, Zhao Jiang-Lin
Key Laboratory of Macrocyclic and Supramolecular Chemistry of Guizhou Province, Guizhou University, Guiyang 550025, P. R. China.
Dalton Trans. 2018 Feb 6;47(6):1942-1947. doi: 10.1039/c7dt03361c.
Coordination supramolecular assemblies of monohydroxycucurbit[7]uril ((HO)Q[7]) with alkaline earth metal ions (AE) have been formed in aqueous HCl solution in the presence of tetrachloride cadmium anions ([CdCl]) as a structure directing agent. The driving force for the assembly could be attributed to the interaction of the positive electro-potential outer-surface of (HO)Q[7] molecules with [CdCl] anions and ionic dipole interaction of the hydroxyl of (HO)Q[7] molecules with [CdCl] anions. Moreover, the porous structure of the (HO)Q[7]/AE-based coordination supramolecular assemblies could result in potential applications in the selective sorption of polar volatile organic molecules, which may be useful in molecular sieves, sensors, absorption and separation.
在作为结构导向剂的四氯化镉阴离子([CdCl])存在下,单羟基葫芦[7]脲((HO)Q[7])与碱土金属离子(AE)在盐酸水溶液中形成了配位超分子组装体。组装的驱动力可归因于(HO)Q[7]分子带正电的外表面与[CdCl]阴离子之间的相互作用以及(HO)Q[7]分子的羟基与[CdCl]阴离子之间的离子偶极相互作用。此外,基于(HO)Q[7]/AE的配位超分子组装体的多孔结构可能在极性挥发性有机分子的选择性吸附方面有潜在应用,这在分子筛、传感器、吸收和分离中可能是有用的。