Three Zn(II)-coordination polymers, namely, {[Zn 2 (µ 4 -L)(µ-obix) 2 ]·4DMF} n ( 1 ), {[Zn 2 (µ 4 -L)(µ-mbix) 2 ]·6H 2 O} n ( 2 ) and {[Zn 2 (µ 4 -L)(µ-pbix) 2 ]·5H 2 O} n ( 3 ), (L 4− : 5,5’-(terephthaloylbis(azanediyl))diisophthalate and obix (y = 2), mbix (y = 3), pbix (y = 4): 1,y-bis((1 H -imidazol-1-yl)methyl)benzene) were prepared with a tetracarboxylic acid and flexible isomeric bis(imidazole) linkers and characterized. The compounds displayed structural diversity depending on the rotation of imidazole rings around the –CH 2 - groups on bis(imidazole) ligands. Compounds 1–3 showed 2-fold interpenetrated 3D framework, 2D structure and 3D framework, respectively. The compounds showed high emissions in solid-state and solutions. Luminescence experiments showed that compounds 1–3 displayed sensitive detection towards Fe 3+ ions with detection limits of 2.31 ppm, 5.17 ppm and 2.61 ppm, respectively. Moreover, the compounds could selectively detect Fe 3+ ions over the other interfering metal ions via luminescence quenching. The detection mechanism could be ascribed to the competitive light absorption between Fe 3+ ions and the compounds.
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Kavak et al. (2024) studied this question.
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