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Unprecedented 1,3-diaza[3]ferrocenophane scaffold as molecular probe for anions
Authors:Sola Antonia  Orenes Raúl A  García María Ángeles  Claramunt Rosa M  Alkorta Ibon  Elguero José  Tárraga Alberto  Molina Pedro
Institution:Departamento de Qui?mica Orga?nica, Facultad de Qui?mica, Campus de Espinardo, Universidad de Murcia, E-30100 Murcia, Spain.
Abstract:The guanidine unit in the guise of 2-aminoimidazole in the new structural motif 2-arylamino-1,3-diaza3]ferrocenophane 4 acts as a binding site for anions. The electrochemical behavior of this compound has been studied by cyclic voltammetry (CV) and differential pulse voltammetry (DPV) and was found to exhibit a quasi reversible oxidation peak, associated to the Fe(II)/Fe(III) redox couple (Ep = 440 mV), and a non-reversible oxidation wave (Ep = 817 mV), probably associated to the oxidation of the C═N unit present in the guanidine bridge. Recognition of AcO(-), PhCO(2)(-), F(-), Cl(-), and Br(-) anions by the free receptor and the less basic anions Br(-), Cl(-), and NO(3)(-) by its monoprotonated form takes place by unusual redox-ratiometric measurements and spectroscopic ((1)H NMR and UV-vis) changes.
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