1,2,3-Tnazol-4-yl (triazolyl)-containing tetradentate ligand 1 undergoes fluorescence enhancement upon binding to zinc ion (Zn2+) in both organic (acetonitrile) and aqueous solutions. A 1.1 complex of 1 with a trigonal bipyramidal Zn2+ was characterized by X-ray crystallography. The cyclic voltammogram (CV) of 1 suggests that an intramolecular photoinduced electron transfer (PET) process is thermodynamically feasible which would quench the fluorescence of the 2-anthryltnazolyl fluorophore On the basis of the X-ray and CV data, it was initially postulated that the 11 binding between Zn2+ and ligand 1 shuts down the PET quenching pathway of the free ligand, which leads to the fluorescence enhancement of 1. However, the nuance of the interaction between 1 and Zn2+ was revealed by isothermal titration calonmetry (ITC) and H-1 NMR titration experiments. A two-step binding process was observed which proceeds through an intermediate species of 2 1 (ligand/Zn2+) stoichiometry Upon close examination of the fluorescence spectra of 1 during the Zn2+ titration experiment, the fluorescence profile is in fact consistent with a two-step binding process in which a moderate fluorescence enhancement was observed during the early stage of the titration, followed by a bathochromic shift in conjunction with a more pronounced enhancement as Zn2+ concentration increases The studies on compounds 2-5 support the amended hypothesis that upon increasing Zn2+ concentration, compound 1 first undergoes fluorescence enhancement because of the formation of a 2:1 (ligand to Zn2+) complex which slows down the PET quenching process As Zn2+ concentration increases, the 2.1 complex is converted into a 1.1 complex which facilitates an intramolecular exciplex formation between the excited 2-anthryltriazolyl fluorophore and the Zn2+ bound pyridyl moiety Finally, the potential of compound 1 as an intracellular fluorescent indicator for Zn2+ was evaluated HeLa cells loaded with compound 1 grown in Zn2+-rich media show stronger fluorescence than those grown under Zn2+-deprived conditions, confirming the promise that the tnazolyl-containing polyaza fluoroionophores can be developed into intracellular fluorescent indicators targeting biological Zn2+