首页> 外文期刊>Collection of Czechoslovak Chemical Communications >ELECTROOXIDATION AND DETERMINATION OF SULFITE IN ETHANOL-WATER SOLUTIONS USING POLY-Cu(II)-TETRAKIS(x-AMINOPHENYL)PORPHYRIN/GLASSY CARBON MODIFIED ELECTRODES
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ELECTROOXIDATION AND DETERMINATION OF SULFITE IN ETHANOL-WATER SOLUTIONS USING POLY-Cu(II)-TETRAKIS(x-AMINOPHENYL)PORPHYRIN/GLASSY CARBON MODIFIED ELECTRODES

机译:聚铜(II)-四(x-氨基苯基)卟啉/玻璃碳修饰电极在乙醇-水溶液中的氧化和亚硫酸根的测定

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A comparison is made of the behavior of three Cu(II)-porphyrins (with the amino substituents in different positions on the periphery of the ligand) electropolymerized on glassy carbon electrodes in HCl as solvent. The electropolymerized films show a certain degree of demetallation but the Cu amount of porphyrin in each case is sufficient to catalyze the oxidation of sulfite and hydrogensulfite in ethanol-water solutions. The ligands of the porphyrins are almost inactive in the electrocatalysis of the sulfite. The oxidation processes are favored at low scan rates. The foot of the oxidation waves depends on the positions. The most active porphyrin bears the substituents with the amino groups in para position, the oxidation occurring at low positive potentials. All the modified electrodes can be used as amperometric sensors for sulfite; they show linear relationships between the current and sulfite concentration in the range in which sulfites are present in red wines. The modified electrodes are stable and all of them promote the oxidation of sulfite to sulfate. [PUBLICATION ABSTRACT]
机译:比较了在HCl溶剂中在玻碳电极上电聚合的三种Cu(II)-卟啉(在配体外围的不同位置具有氨基取代基)的行为。电聚合膜显示出一定程度的脱金属,但是在每种情况下,卟啉的铜含量足以催化乙​​醇-水溶液中亚硫酸盐和亚硫酸氢盐的氧化。卟啉的配体在亚硫酸盐的电催化中几乎没有活性。低扫描速率有利于氧化过程。氧化波的底脚取决于位置。最具活性的卟啉带有氨基在对位的取代基,氧化发生在低正电位下。所有的修饰电极都可以用作亚硫酸盐的安培传感器。它们显示了红酒中亚硫酸盐含量范围内电流与亚硫酸盐浓度之间的线性关系。修饰的电极是稳定的,它们都促进亚硫酸盐氧化成硫酸盐。 [出版物摘要]

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    Paz BRAVO(a1), Yo-Ying CHEN(a2), Galo RAMIREZ(b), Maria J. CANALES(c),Betty MATSUHIRO(a3), Leonora MENDOZA(a4), Mauricio ISAACS(d1),Macarena GARCÍA(d), Maria C. AREVALO(c) and Maria J. AGUIRRE(u5)*a Facultad de Química y Biología, Universidad de Santiago de Chile,Av. B. O'Higgins 3363, Estación Central, 9170022 Santiago, Chile,e-mail: 1 bravo.paz@gmail.com, 2 ychen@usach.cl, 3 bmatsuhi@usach.cl,4 lmendoza@usach.cl, s maguirre@usach.clb Departamento de Ciencias Químicas, facultad de Ecología y Recursos Naturales,Universidad Andrés Bello, República 275, 8370146 Santiago, Chile, e-mail: gramirez@unab.cic Departamento de Ciencias Químicas, Facultad de Ingeniería, Ciencias y Administración,Universidad de La Frontera, Av. Francisco Salazar 01145, 4780000 Temuco, Chile,e-mail: jcanales@ufro.cid Departamento de Química, Facultad de Ciencias, Universidad de Chile,Las Palmeras 3425, Casilla 653, 7800024 Santiago, Chile, e-mail: 1 misaacs@uchile.cle Departamento de Química Física, Facultad de Química, Universidad de La Laguna,38071-La Laguna, S/C de Tenerife, Spain, e-mail: carevalo@ull.esReceived August 13, 2008Accepted December 17, 2008Published online March 22, 2009,;

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