Electron transfer reaction and mechanism of oxidation of Inosine
Creators
- 1. Department of Chemistry, Indian Institute of Technology Roorkee, Roorkee-247 667 (India)
Description
Electrochemical oxidation of Inosine has been studied in the phosphate buffers of pH range 3.3-10.9 at pyrolytic graphite electrode. In the entire pH range a single well-defined oxidation peak (I a) was observed, when the sweep was initiated in the positive direction. In the reverse sweep no cathodic peak was obtained. The peak potential of the oxidation peak was dependent on pH and shifted to less positive potential with increase in pH. The kinetics of the UV absorbing intermediate was followed spectrophotometrically and the decay occurred in a pseudo first order reaction having k values in the range 0.50-0.92 x 10-3 s-1 in the entire pH range studied. The value of n was found to be 2.95 ± 0.3. The products of oxidation were silylated and characterized by using GC-Mass. Two tetramers having C-C, C-N, N-N, C-O-N and C-O-O-C linkages were identified. A plausible mechanism for the electrooxidation of Inosine has been suggested
Additional details
Identifiers
- DOI
- 10.1016/j.electacta.2006.03.057;
- PII
- S0013-4686(06)00298-2;
Publishing Information
- Journal Title
- Electrochimica Acta
- Journal Volume
- 51
- Journal Issue
- 24
- Journal Page Range
- p. 5095-5102
- ISSN
- 0013-4686
- CODEN
- ELCAAV
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 38016481
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- DECAY; ELECTRODES; ELECTRON TRANSFER; GRAPHITE; INOSINE; OXIDATION; PEAKS; PH VALUE; PHOSPHATES; PURINES; SULFUR IONS
- Descriptors DEC
- AROMATICS; AZAARENES; CARBON; CHARGED PARTICLES; CHEMICAL REACTIONS; ELEMENTS; HETEROCYCLIC COMPOUNDS; IONS; MINERALS; NONMETALS; NUCLEOSIDES; NUCLEOTIDES; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; OXYGEN COMPOUNDS; PHOSPHORUS COMPOUNDS; PURINES; RIBOSIDES
Optional Information
- Copyright
- Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.