Romero Tomás, Caballero Antonio, Espinosa Arturo, Tárraga Alberto, Molina Pedro
Departamento de Química Orgánica, Universidad de Murcia; 30100, Murcia, Spain.
Dalton Trans. 2009 Mar 28(12):2121-9. doi: 10.1039/b819778d. Epub 2009 Jan 30.
The preparation, electrochemical, electronic, and cation sensing properties of an indole-ferrocene-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 behaves as a highly selective dual-redox and chromogenic chemosensor molecule for Hg(2+) cations: the oxidation redox peak is anodically shifted (DeltaE(1/2) = 210 mV), and the low energy band of the absorption spectrum is red-shifted (Deltalambda = 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. (1)H NMR as well as DFT calculations have been carried out to get information about the molecular sites which are involved in bonding.
本文介绍了一种吲哚-二茂铁-吲哚三联体的制备方法及其电化学、电子和阳离子传感特性。这种新结构基序的一个显著特点是,氧化还原活性有机金属片段通过不饱和氮官能团与吲哚环相连。三联体对Hg(2+)阳离子表现为一种高选择性的双氧化还原和显色化学传感器分子:与该金属阳离子络合后,氧化还原峰阳极位移(ΔE(1/2)=210 mV),吸收光谱的低能带红移(Δλ=120 nm)。吸收光谱的这种变化伴随着颜色从橙色到绿色的显著变化,这使得“肉眼”检测成为可能。已进行了(1)H NMR以及DFT计算,以获取有关参与键合的分子位点的信息。