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Electrochemical and spectral studies of auto-assembled arrays of calix4arenequinhydrone charge-transfer complex on indium–tin oxide (ITO) glass

机译:杯氧化铟锡(ITO)玻璃上杯4亚芳基苯醌电荷转移配合物自动组装的电化学和光谱研究

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摘要

A sensing materiel based on calix[4]arene molecules is electrochemically deposited on ITO electrode coated. A brown film was electrodeposited at a potential Eimp = –1.00 V versus SCE in acetonitrile solvent, however in dichloromethane solvent, a bluish film auto-assembled on the ITO electrode coated at a potential Eimp = −0.65 V versus SCE. Both films are subsequently analyzed by cyclic voltammetry and UV–Vis spectroscopy. This investigation shows that in acetonitrile solvent, the charge-transfer complex, calix[4]arenequinhydrone was formed in electrolytic solution and it was not self-assembled on the ITO electrode. The related UV–Vis spectrum shows a single absorption band towards a wavelength about 350 nm. The optical behaviour of the blue film shows two absorption bands: the first one appears on the first absorption band of the acceptor at 305 nm and the second one in the visible range at 502 nm. The band situated in the visible range correspond to a well-defined charge-transfer band indicating the presence of the charge-transfer complex, the calix[4]arenequinhydrone.
机译:基于杯[4]芳烃分子的传感材料被电化学沉积在涂覆的ITO电极上。在乙腈溶剂中,相对于SCE的电势为Eimp = 1.00 V的棕色膜被电沉积,但是在二氯甲烷溶剂中,相对于SCE的电势Eimp等于-0.65 V的ITO电极上自动组装了一层蓝色膜。随后通过循环伏安法和UV-Vis光谱仪分析了这两种膜。该研究表明,在乙腈溶剂中,电荷转移络合物杯[4]芳基苯醌在电解液中形成,并且未在ITO电极上自组装。相关的UV-Vis光谱显示在约350 nm波长处有一个吸收带。蓝色薄膜的光学行为显示出两个吸收带:第一个出现在305 nm受体的第一个吸收带上,第二个出现在502 nm的可见光范围内。位于可见光范围内的谱带对应于明确定义的电荷转移谱带,表明存在电荷转移络合物杯[4]亚芳基醌氢醌。

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