Issue 12, 2009

A multiresponsive two-arm ferrocene-based chemosensor molecule for selective detection of mercury

Abstract

The preparation, electrochemical, electronic, and cation sensing properties of an indoleferrocene–indole triad, are presented. A salient feature of this new structural motif is that the redox-active organometallic fragment is linked to the indole rings by unsaturated nitrogen functionalities. Triad 4 behaves as a highly selective dual-redox and chromogenic chemosensor molecule for Hg2+ cations: the oxidation redox peak is anodically shifted (ΔE1/2 = 210 mV), and the low energy band of the absorption spectrum is red-shifted (Δλ = 120 mm), upon complexation with this metal cation. This change in the absorption spectrum is accompanied by a dramatic colour change from orange to green which allows the potential for “naked eye” detection. 1H NMR as well as DFT calculations have been carried out to get information about the molecular sites which are involved in bonding.

Graphical abstract: A multiresponsive two-arm ferrocene-based chemosensor molecule for selective detection of mercury

Supplementary files

Article information

Article type
Paper
Submitted
06 Nov 2008
Accepted
16 Dec 2008
First published
30 Jan 2009

Dalton Trans., 2009, 2121-2129

A multiresponsive two-arm ferrocene-based chemosensor molecule for selective detection of mercury

T. Romero, A. Caballero, A. Espinosa, A. Tárraga and P. Molina, Dalton Trans., 2009, 2121 DOI: 10.1039/B819778D

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