Guo Mingming, Liu Sixu, Guo Huadong, Sun Yingying, Guo Xianmin, Deng Ruiping
Department of Chemistry, Changchun Normal University, Changchun, 130032, P. R. China.
Dalton Trans. 2017 Nov 7;46(43):14988-14994. doi: 10.1039/c7dt02506h.
A unique microporous anionic metal-organic framework, namely Zn(btb)(bbis)·6DMF (1), has been synthesized and structurally characterized [bbis = bis(4-benzylimidazol-ylphenyl)sulfone and Hbtb = 4,4',4''-benzene-1,3,5-triyltribenzoic acid]. This compound exhibits a 4-fold interpenetrated anionic framework with ins topology. The post-synthetic cation exchange of 1 with Eu, Tb, Dy and Sm afforded lanthanide(iii)-loaded materials. Eu@1 and Tb@1 can be used as the potential luminescent probes in nitrobenzene. The adsorption behavior of 1 towards organic dyes was investigated, revealing rapid and selective separation of methylene blue.
一种独特的微孔阴离子金属有机框架,即Zn(btb)(bbis)·6DMF (1),已被合成并进行了结构表征[bbis = 双(4-苄基咪唑基苯基)砜,Hbtb = 4,4',4''-苯-1,3,5-三基三苯甲酸]。该化合物呈现出具有ins拓扑结构的4重互穿阴离子框架。1与Eu、Tb、Dy和Sm进行的后合成阳离子交换得到了负载镧系(iii)的材料。Eu@1和Tb@1可作为硝基苯中的潜在发光探针。研究了1对有机染料的吸附行为,结果表明其对亚甲基蓝具有快速且选择性的分离效果。