Electroanalysis of ascorbate and dopamine at a gold electrode modified with a positively charged self-assembled monolayer

被引:168
作者
Raj, CR [1 ]
Ohsaka, T [1 ]
机构
[1] Tokyo Inst Technol, Interdisciplinary Grad Sch Sci & Engn, Dept Elect Chem, Midori Ku, Yokohama, Kanagawa 2268502, Japan
关键词
self-assembled monolayer; electroanalysis; di-positive nicker macrocycle; ascorbate; dopamine;
D O I
10.1016/S0022-0728(00)00335-1
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The self-assembled monolayer (SAM) of a di-positive nickel macrocycle (1) (dinickel(II) (2,2'-bis(1,3,5,8,12-pentaazacyclotetradec-3-yl)-diethyl disulfide) perchlorate) has been utilized for the electroanalysis of ascorbate (AA) and dopamine (DA). A very large decrease (similar to 450 mV) in the overpotential for the oxidation of AA has been observed at the SAM-1 modified gold electrode. The electrostatic interaction of negatively charged AA with the di-positive SAM-1 facilitates the oxidation of AA at the monolayer-modified electrode. The electrostatic interaction of AA with the SAM-1 has been verified with the mixed monolayers of 1 and diethyl disulfide (DEDS). The peak potential for the oxidation of AA shifts towards more positive potential and the oxidation peak current decreases as the fraction of DEDS increases. The oxidation of DA at the monolayer-modified electrode is less favorable owing to the electrostatic repulsion between DA and the di-positive monolayer. The SAM-1 modified gold electrode resolves well the voltammetric peaks of these analytes, which are indistinguishable at the bare electrode. The catalytic oxidation of AA by oxidized DA has been successfully eliminated at the monolayer-modified electrode. The SAM-1 electrode has been used for the simultaneous determination of AA and DA. The results obtained at the SAM-1 electrode are compared with those at the gold electrode modified with a mono-positive monolayer of cystamine (CYST). (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:44 / 49
页数:6
相关论文
共 33 条
[1]   PROBING BRAIN CHEMISTRY WITH ELECTROANALYTICAL TECHNIQUES [J].
ADAMS, RN .
ANALYTICAL CHEMISTRY, 1976, 48 (14) :1126-&
[2]   Nickel (II) tetraaza macrocycle modified electrodes for the electrocatalytic determination of L-ascorbic acid by the flow injection method [J].
Bae, ZU ;
Park, JH ;
Lee, SH ;
Chang, HY .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 468 (01) :85-90
[3]  
BOULTON AA, 1995, VOLTAMMETRIC METHODS
[4]   Detection of dopamine in the presence of a large excess of ascorbic acid by using the powder microelectrode technique [J].
Chen, J ;
Cha, CS .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 463 (01) :93-99
[5]   Permselectivity sensitivity, and amperometric pH sensing at thioctic acid monolayer microelectrodes [J].
Cheng, Q ;
BrajterToth, A .
ANALYTICAL CHEMISTRY, 1996, 68 (23) :4180-4185
[6]   FREE-ENERGY AND TEMPERATURE-DEPENDENCE OF ELECTRON-TRANSFER AT THE METAL-ELECTROLYTE INTERFACE [J].
CHIDSEY, CED .
SCIENCE, 1991, 251 (4996) :919-922
[7]   Polyeugenol-modified platinum electrode for selective detection of dopamine in the presence of ascorbic acid [J].
Ciszewski, A ;
Milczarek, G .
ANALYTICAL CHEMISTRY, 1999, 71 (05) :1055-1061
[8]   Electrochemical behavior of gold electrodes modified with self-assembled monolayers with an acidic end group for selective detection of dopamine [J].
Dalmia, A ;
Liu, CC ;
Savinell, RF .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1997, 430 (1-2) :205-214
[9]   RESPONSE OF MICROVOLTAMMETRIC ELECTRODES TO HOMOGENEOUS CATALYTIC AND SLOW HETEROGENEOUS CHARGE-TRANSFER REACTIONS [J].
DAYTON, MA ;
EWING, AG ;
WIGHTMAN, RM .
ANALYTICAL CHEMISTRY, 1980, 52 (14) :2392-2396
[10]  
Finklea HO, 1996, ELECTROANAL CHEM, V19, P109