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We have reported the synthesis and structural characterization of a unique Zn(II) metallacycle ( 1 ) and its utilization as a fluorescent probe for the shape-specific selective recognition (turn-off) of Fe 3+ and IO 4 – ions. The relevant Stern–Volmer graphs indicate that the recognitions of Fe 3+ and IO 4 – ions are examples of diphasic and monophasic quenchings, respectively. The title metallacycle has been prepared by the reaction of a novel N-heterocyclic carbene precursor, 1,3-bis(2,6-diisopropyl-4-(pyridin-4-yl)phenyl)-1 H -imidazol-3-ium chloride/bromide ( L ), and zinc(II) chloride salt. Notably, the ligand itself did not show any type of recognition for any ions. DFT calculations were performed on L and metallacycle 1 using the geometric parameters, obtained from their single-crystal X-ray diffraction data, to understand the electronic structures of the ligand and macrocycle. The detection limit for the recognition of the Fe 3+ ion was determined to be 2.5 × 10 –6 mol/L, and that for IO 4 – ion was found to be 6.3 × 10 –5 mol/L.
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Kumar et al. (2017) studied this question.
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