Covalent Modification of Carbon Surfaces by Direct and Redox Catalysed Oxidation of Carboxylates in Acetonitrile – Concepts and Mechanisms

Author:

Morales‐Martínez Daniel12,Ramírez‐Chan Daniel E.1,Palacios‐Ramírez Jesús I.1,Galicia Mónica3,González Felipe J.1

Affiliation:

1. Departamento de Química Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional Av. Instituto Politécnico Nacional 2508 07360 Mexico City Mexico

2. Department of Chemistry University of Padova Via Marzolo 1 35131 Padova Italy

3. Departamento de Ciencias Químico Biológicas Universidad Autónoma de Ciudad Juárez Av. Benjamín Franklin No. 4650 Zona PRONAF 32315, Cd. Juárez Chihuahua Mexico

Abstract

AbstractElectrografting is a relevant process that allows getting modified electrodes where organic molecules are covalently bonded to the electrode surface. The modification is typically performed using electrochemical reactions, where the transient passage by free radicals allows the formation of covalent bonds with the electrode surface. These intermediaries are generated over a wide potential window, and they are commonly prone to a second electron transfer (oxidation or reduction). Thus, this reaction competes with the surface reactions, slowing down the formation of films on the electrode. In the case of carboxylate oxidation, these competitive processes have been minimized by using a redox‐catalysed process which occurs at low oxidation potentials. The rate at which modifications procedures occur is relevant in the sense that they determine the properties of the polymeric films covalently attached to the electrode surfaces. Therefore, this review focuses on the main aspects of the direct and redox‐catalysed oxidation of carboxylates as a tool for the covalent modification of the surface of different carbon electrodes.

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

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