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) (Fe
2+
), cobalt(II) (Co
2+
), nickel(II) (Ni
2+
), copper(II) (Cu
2+
), zinc(II)
(Zn
2+
), cadmium(II) (Cd
2+
), and manganese(II)
(Mn
2+
). Electrochemical assays revealed good detection
properties, with very low limits of detection (LOD), for Co
2+
, Cu
2+
, and Cd
2+
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 (10
5
–10
6
M
–1
) and low LOD, especially for Zn
2+
and Co
2+
(at the nanomolar concentration level).