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A mechanistic investigation into the covalent chemical derivatisation of graphite and glassy carbon surfaces using aryldiazonium salts

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dc.contributor.author Abiman, P.
dc.contributor.author Wildgoos, G.G
dc.contributor.author Compton, R.G
dc.date.accessioned 2022-09-26T08:48:07Z
dc.date.available 2022-09-26T08:48:07Z
dc.date.issued 2008
dc.identifier.issn 08943230
dc.identifier.uri http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/8137
dc.description.abstract Modification of carbon materials such as graphite and glassy carbon in bulk quantities using diazonium salts is developed. We used both 4-nitrobenzenediazonium tetrafluoroborate and 1-antharaquinonediazonium chloride to modify graphite and glassy carbon surfaces. Experiments were carried out in the presence and absence of hypophosphorous acid and the mechanism involved in both cases were studied using cyclic voltammetry. The observed peak potentials for both the 4-nitrophenyl and 1-anthraquinonyl modified materials were found to differ depending on whether or not the hypophosphorous acid reducing agent was used. In the absence of hypophosphorous acid the derivatisation reaction was inferred to go through a cationic intermediate, whilst in the presence of the hypophosphorous acid the mechanism likely involves either a purely radical intermediate or a mixture of radical and cationic species. Derivatisation experiments from 5 to 70°C allowed us to determine the optimum derivatisation temperature for both cases, in the presence and absence of hypophosphorous acid. Optimum temperature was 20°C for the former and 35°C for the later. en_US
dc.language.iso en en_US
dc.publisher John Wiley & Sons, Ltd en_US
dc.subject Aryldiazonium salts en_US
dc.subject Cationic en_US
dc.subject Chemical modification en_US
dc.subject Glassy carbon en_US
dc.subject Mechanism en_US
dc.subject Radical en_US
dc.subject Graphite en_US
dc.title A mechanistic investigation into the covalent chemical derivatisation of graphite and glassy carbon surfaces using aryldiazonium salts en_US
dc.type Article en_US


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