Effect of Ionic Liquid Structure on the Electrochemical Response of Dopamine at Room Temperature Ionic Liquid-Modified Carbon Paste Electrodes (IL–CPE)
Por:
Hernandez-Vargas, Salvador G., Alberto Cevallos-Morillo, Carlos, Aguilar-Cordero, Julio C.
Publicada:
1 sep 2020
Ahead of Print:
1 ene 2020
Resumen:
In this work 12 different ionic liquids (ILs) have been used added as co-binders in the preparation of modified carbon paste electrodes (IL–CPEs) used for the voltammetric analysis of dopamine in Britton-Robinson buffer. The ionic liquids studied were selected based on three main criteria: (1) increasing chain length of alkyl substituents (studying 1-ethylimidazolium and ethyl, propyl, butyl, hexyl and decylmethylimidazolium bis(trifluoromethylsulfonyl)imide ionic liquids); (2) nature of the counter ion (dicyanamide, bis(trifluoromethylsulfonyl)imide and hexafluorophosphate) in 1-butyl-3-methylimidazolium ionic liquids; and (3) cation ring structures (1-butyl-3-methylimidazolium, 1-butyl-1-methylpiperidinium, 1-butyl-1-methylpyrrolidinium and 1-butyl-3-methylpyridinium) in bis(trifluoromethylsulfonyl)imide or hexafluorophosphate (1-butyl-3-methylimidazolium or 1-butyl-3-methylpyridinium as cations) ionic liquids. The use of IL as co-binders in IL–CPE results in a general enhancement of both the sensitivity and the reversibility of dopamine oxidation. In square wave voltammetry experiments, the peak current increased up to a 400 % when 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide was used as co-binder, as compared to the response found with the unmodified CPE. Experimental data provide evidence that electrostatic and steric effects are the most important ones vis-à-vis these electrocatalytic effects on the anodic oxidation of dopamine on IL–CPE. The relative hydrophilicity of dicyanamide anions reduced the electrocatalytic effects of the corresponding ionic liquids, while the use of 1-ethyl-3-methylimidazolium hexafluorophosphate or 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (two relatively small and highly hydrophobic ionic liquids) as co-binders in IL–CPE resulted in the highest electrocatalytic activity among all of the IL–CPE studied. © 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
Filiaciones:
Hernandez-Vargas, Salvador G.:
Departamento de Química Analítica, Facultad de Química, Universidad Nacional Autónoma de México, Ciudad de México, CP 04310, Mexico
Univ Nacl Autonoma Mexico, Dept Quim Analit, Fac Quim, Mexico City 04310, DF, Mexico
Alberto Cevallos-Morillo, Carlos:
Departamento de Química Analítica, Facultad de Química, Universidad Nacional Autónoma de México, Ciudad de México, CP 04310, Mexico
Univ Nacl Autonoma Mexico, Dept Quim Analit, Fac Quim, Mexico City 04310, DF, Mexico
Aguilar-Cordero, Julio C.:
Departamento de Química Analítica, Facultad de Química, Universidad Nacional Autónoma de México, Ciudad de México, CP 04310, Mexico
Univ Nacl Autonoma Mexico, Dept Quim Analit, Fac Quim, Mexico City 04310, DF, Mexico
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