Abstract

A triazole tethered triferrocene receptor, C40H40O2N6Fe33, has been synthesized from the reaction of mono-alkynyl substituted ferrocene, 1 and 1,1′-bis-(azidomethyl)ferrocene, 2. Consequently the cation and anion sensing properties of 3 have been examined. The receptor 3 was found to be highly selective electrochemical (ΔE1/21=145mV,ΔE1/22=92mV), optical and chromogenic chemosensor for Hg2+ ion in aqueous environment. The substantial changes in its absorption spectra are accompanied by the appearance of a new low-energy peak at 631 nm (ɛ = 3400 M−1 cm−1). This is also accompanied by a strong color change from yellow to purple, that allows a prospective for the “naked eye” detection of Hg2+ ion over other competitor cations such as Pb2+, Cd2+, Zn2+, etc. In addition, among various anions, 3 shows a distinct electrochemical recognition of dihydrogen phosphate anion by its multiple H-bonding (C–H⋯O), which is supported by electrochemical (large cathodic shift ΔE1/2 = −175 mV) and 1H NMR titration results.

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