The 1,3-dipolar cycloaddition reaction (click chemistry approach) was employed to create a hexa-ferrocenylated 1,3,5-triphenylbenzene derivative. Leveraging the presence of metal-chelating sites associated with 1,2,3-triazole moieties and 1,4-dinitrogen systems (ethylenediamine-like), as well as tridentate chelating sites (1,4,7-trinitrogen, diethylene triamine-like) systems, the application of this molecule as a chemosensor for divalent transition metal cations was investigated. The interactions were probed voltammetrically and spectrofluorimetrically against seven selected cations: iron(II) (Fe2+), cobalt(II) (Co2+), nickel(II) (Ni2+), copper(II) (Cu2+), zinc(II) (Zn2+), cadmium(II) (Cd2+), and manganese(II) (Mn2+). Electrochemical assays revealed good detection properties, with very low limits of detection (LOD), for Co2+, Cu2+, and Cd2+ in aqueous solution (0.03-0.09 μM). Emission spectroscopy experiments demonstrated that the title compound exhibited versatile detection properties in solution, specifically turn-off fluorescence behavior upon the addition of each tested transition metal cation. The systems were characterized by satisfactory Stern-Volmer constant values (105-106 M-1) and low LOD, especially for Zn2+ and Co2+ (at the nanomolar concentration level).