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Fluorine-Containing Triazole-Decorated Silver(I)-Based Cationic Metal–Organic Framework for Separating Organic Dyes and Removing Oxoanions from Water

Authors :
Kumar, Sandeep
Liu, Songyuan
Mohan, Brij
Zhang, Mingjian
Tao, Zhiyu
Wan, Zhijian
You, Hengzhi
Sun, Feiyun
Li, Mu
Ren, Peng
Source :
Inorganic Chemistry; May 2021, Vol. 60 Issue: 10 p7070-7081, 12p
Publication Year :
2021

Abstract

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.

Details

Language :
English
ISSN :
00201669 and 1520510X
Volume :
60
Issue :
10
Database :
Supplemental Index
Journal :
Inorganic Chemistry
Publication Type :
Periodical
Accession number :
ejs55922375
Full Text :
https://doi.org/10.1021/acs.inorgchem.0c03688