Abstract

AbstractUnder hydrothermal conditions, three new AgI coordination polymers, [Ag(L1)(Hmip)]n (1), [Ag(L2)0.5(ndc)0.5]n (2), and {[Ag(L3)0.5(Htbi)]·0.25H2O}n (3) [H2mip = 5‐methylisophthalic acid, L1 = 1,4‐bis(2‐methylbenzimidazol‐1‐ylmethyl)benzene, H2ndc = 2,6‐naphthalenedicarboxylic acid, L2 = 1,3‐bis(2‐methylbenzimidazol‐1‐ylmethyl)benzene, H2tbi = 5‐tert‐butyl isophthalic acid, L3 = 1,4‐bis(5,6‐dimethylbenzimidazole)butane] were synthesized by employing flexible bis(benzimidazole) and dicarboxylic acid ligands. Polymer 1 displays a 2D 4‐connected 4L2 underlying net topology with the point symbol of (65.8) in standard representation. Compound 2 possesses a 2D uninodal 4‐connected Shubnikov tetragonal plane net (sql) based on a dinuclear AgI clusters with the point symbol (44.62), which is further extended into a 3D supramolecular framework by π–π interactions. Compound 3 possesses dinuclear molecular complex groups, which form chains by weak Ag–O (2.6 Å) coordination bonds, and further assembled into a 2D supramolecular layer by hydrogen bonds and π–π stacking interactions. These complexes exhibit intense fluorescent emissions in solid state. UV/Vis diffuse reflection spectra and the excellent catalytic activity for the degradation of the congo red azo dye in a Fenton‐like process are discussed.

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