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Covalent Modification of Glassy Carbon Surfaces by Using Electrochemical and Solid-Phase Synthetic Methodologies: Application to Bi- and Trifunctionalisation with Different Redox Centres
- Source :
- Chemistry - A European Journal. 15:11928-11936
- Publication Year :
- 2009
- Publisher :
- Wiley, 2009.
-
Abstract
- Glassy carbon electrodes functionalised with two redox centres have been prepared by using electrochemical and solid-phase synthetic methodologies. Initially the individual coupling of anthraquinone, nitrobenzene and dihydroxybenzene to a glassy carbon electrode bearing an ethylenediamine linker was optimised by using different coupling agents and conditions. Bifunctionalisation was then carried out, either simultaneously, with a mixture of nitrobenzene and dihydroxybenzene, or sequentially, with anthraquinone then nitrobenzene and with anthraquinone then dihydroxybenzene. Characterisation of these electrodes by cyclic voltammetry and differential pulse voltammetry clearly proved the attachment of the pairs of redox centres to the glassy carbon electrode. Their partial surface coverages can be controlled by varying the coupling agent or by controlling the substrate concentration during the solid-phase coupling process. Trifunctionalisation was also realised according to this methodology.
- Subjects :
- Surface Properties
Inorganic chemistry
chemistry.chemical_element
Anthraquinones
02 engineering and technology
Glassy carbon
010402 general chemistry
Electrochemistry
01 natural sciences
Anthraquinone
Redox
Catalysis
Nitrobenzene
chemistry.chemical_compound
Electrodes
Nitrobenzenes
Phenol
Organic Chemistry
General Chemistry
021001 nanoscience & nanotechnology
Carbon
0104 chemical sciences
chemistry
Glass
Differential pulse voltammetry
Cyclic voltammetry
0210 nano-technology
Oxidation-Reduction
Subjects
Details
- ISSN :
- 15213765 and 09476539
- Volume :
- 15
- Database :
- OpenAIRE
- Journal :
- Chemistry - A European Journal
- Accession number :
- edsair.doi.dedup.....59d353cee13532b28dea51d26c46feae
- Full Text :
- https://doi.org/10.1002/chem.200901135