Please use this identifier to cite or link to this item: http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/8137
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dc.contributor.authorAbiman, P.
dc.contributor.authorWildgoos, G.G
dc.contributor.authorCompton, R.G
dc.date.accessioned2022-09-26T08:48:07Z-
dc.date.available2022-09-26T08:48:07Z-
dc.date.issued2008
dc.identifier.issn08943230
dc.identifier.urihttp://repo.lib.jfn.ac.lk/ujrr/handle/123456789/8137-
dc.description.abstractModification 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.isoenen_US
dc.publisherJohn Wiley & Sons, Ltden_US
dc.subjectAryldiazonium saltsen_US
dc.subjectCationicen_US
dc.subjectChemical modificationen_US
dc.subjectGlassy carbonen_US
dc.subjectMechanismen_US
dc.subjectRadicalen_US
dc.subjectGraphiteen_US
dc.titleA mechanistic investigation into the covalent chemical derivatisation of graphite and glassy carbon surfaces using aryldiazonium saltsen_US
dc.typeArticleen_US
Appears in Collections:Chemistry



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