Abstract
Several phenols with structures similar to vitamin E were oxidised and the intermediate species produced were characterised by in situ infrared and UV-vis spectroscopies. The Fourier transform infrared (FTIR) measurements were performed by chemically oxidising the phenols with 2 mol equiv. of NO +SbF6- in CH3CN and recording the spectra between 1900 and 1300 cm-1 with an attenuated total reflectance (ATR) probe utilising a fiber conduit and a diamond composite sensor. The compounds that formed long-lived phenoxonium cations displayed two IR absorbances at 1665 (±15) cm-1 and one at 1600 (±10) cm-1 associated with the carbonyl, symmetric ring stretch and asymmetric ring stretch modes. The para-quinones are one of the long-term products of oxidation of the phenols, and displayed solution phase IR absorbances at 1650 (±10) cm-1. In situ electrochemical UV-vis experiments performed during the oxidation of the phenols led to the detection of bands due to the phenoxonium cations at 295 (±5) and 440 (±15) nm and due to the para-quinones at 260 (±10) nm. The concentration of the substrate and the water content of the solvent had a major effect on the yields of the intermediates and products that were produced during the oxidation reactions.
Original language | English |
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Pages (from-to) | 8863-8869 |
Number of pages | 7 |
Journal | Electrochimica Acta |
Volume | 55 |
Issue number | 28 |
DOIs | |
Publication status | Published - Dec 1 2010 |
Externally published | Yes |
ASJC Scopus Subject Areas
- General Chemical Engineering
- Electrochemistry
Keywords
- Electrochemical oxidation
- FTIR
- Nitrosonium cation
- Phenoxonium
- Reactive intermediate