Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
221144 | Journal of Electroanalytical Chemistry | 2006 | 9 Pages |
Abstract
The effect of the molecular structure of monosaccharides on their electrochemical behavior at a gold electrode in alkaline medium was investigated in order to elucidate the relation between the structure and electro-reactivity. The oxidation of the aldehyde hydrate (or hemiacetal) at C1 carbon atom is the easiest occurring at E < 0.7 V vs. RHE. The oxidation of the primary alcohol group, assisted by the adsorption of the molecule, takes place at potentials from 0.8 to 1.1 V vs. RHE. Vicinal diols oxidation which leads to the C–C bond cleavage occurs between 1.1 and 1.3 V vs. RHE. The spatial orientation of OH groups has important effect on the oxidation of vicinal diols.
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Chemical Engineering (General)
Authors
P. Parpot, N. Nunes, A.P. Bettencourt,