化学
阳离子聚合
三氟甲基
金属有机骨架
吸附
吡啶
氟
无机化学
金属
水溶液
高分子化学
有机化学
烷基
作者
Sandeep Kumar,Songyuan Liu,Brij Mohan,Dongke Zhang,Zhiyu Tao,Zhijian Wan,Hengzhi You,Feiyun Sun,Mu Li,Peng Ren
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2021-04-22
卷期号:60 (10): 7070-7081
被引量:23
标识
DOI:10.1021/acs.inorgchem.0c03688
摘要
Four new triazole-decorated silver(I)-based cationic metal–organic frameworks (MOFs), {[Ag(L1)](BF4)}n (1), {[Ag(L1)](NO3)}n (2), {[Ag(L2)](BF4)}n (3), and {[Ag(L2)](NO3)}n (4), have been synthesized using two newly designed ligands, 3-fluoro-5-(4H-1,2,4-triazol-4-yl)pyridine (L1) and 3-(4H-1,2,4-triazol-4-yl)-5-(trifluoromethyl)pyridine (L2). When the fluorine atom was changed to a trifluoromethyl group at the same position, tremendous enhancement in the MOF dimensionality was achieved [two-dimensional to three-dimensional (3D)]. However, changing the metal salt (used for the synthesis) had no effect. The higher electron-withdrawing tendency of the trifluoromethyl group in L2 aided in the formation of higher-dimensional MOFs with different properties compared with those of the fluoro derivatives. The fluoride group was introduced in the ligand to make highly electron-deficient pores inside the MOFs that can accelerate the anion-exchange process. The concept was proved by density functional theory calculation of the MOFs. Both 3D cationic MOFs were used for dye adsorption, and a remarkable amount of dye was adsorbed in the MOFs. In addition, owing to their cationic nature, the MOFs selectively removed anionic dyes from a mixture of anionic, cationic, and neutral dyes in the aqueous phase. Interestingly, the present MOFs were also highly effective for the removal of oxoanions (MnO4– and Cr2O72–) from water.
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