Electrogenerated chemiluminescence of ruthenium (II) bipyridyl complex directly immobilized on glassy carbon electrodes
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作者:
Minghui Xiang
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机构:Peking University,Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Beijing National Laboratory for Molecular Science (BNLMS), Institute of Analytical Chemistry, College of Chemistry and Molecular Engineering
Minghui Xiang
Rong Lei
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机构:Peking University,Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Beijing National Laboratory for Molecular Science (BNLMS), Institute of Analytical Chemistry, College of Chemistry and Molecular Engineering
Rong Lei
Na Li
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机构:Peking University,Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Beijing National Laboratory for Molecular Science (BNLMS), Institute of Analytical Chemistry, College of Chemistry and Molecular Engineering
Na Li
Kean Li
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机构:Peking University,Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Beijing National Laboratory for Molecular Science (BNLMS), Institute of Analytical Chemistry, College of Chemistry and Molecular Engineering
Kean Li
机构:
[1] Peking University,Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, Beijing National Laboratory for Molecular Science (BNLMS), Institute of Analytical Chemistry, College of Chemistry and Molecular Engineering
Ru(bpy)3Cl2 was used to modify the glass carbon electrodes (GCE) by oxidation and co-deposition on the electrode surface. The modified electrodes were characterized by atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS). About 2.2 × 10−9 mol Ru(bpy)32+ was immobilized on the GCE surface (ϕ = 4 mm). The modified GC electrodes showed stable electrochemiluminescence with tripropylamine (TPrA) as the co-reactant with a linear range from 10 to 500 μM (R2 = 0.999). Among the 10 amino acids tested, the modified electrode system showed selective response to arginine and lysine, indicating that the molecular structure played an important role as co-reactant. This simple and sensitive electrode modifying method when combined with flow-injection or liquid chromatography systems has the potential for amino acid analyses.