Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/44564
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dc.contributor.authorYao, Wei Weien
dc.date.accessioned2011-06-02T06:31:10Zen
dc.date.available2011-06-02T06:31:10Zen
dc.date.copyright2011en
dc.date.issued2011en
dc.identifier.citationYao, W. W. (2011). Voltammetric studies on vitamin E in organic solvents and within lipid bilayer membranes. Doctoral thesis, Nanyang Technological University, Singapore.en
dc.identifier.urihttps://hdl.handle.net/10356/44564en
dc.description.abstractA series of model tocopherol compounds with differing degrees of methyl substitution around the aromatic ring were studied by variable scan rate (0.1- 500 V s-1) cyclic voltammetry experiments in CH3CN and CH2Cl2. On short voltammetric timescales α-TOH is oxidised in a chemically reversible –2e–/–H+ process to form a phenoxonium cation (α-TO+). The equilibrium and rate constants associated with the chemical steps were estimated by digital simulations of the variable scan rate data over a range of temperatures (T = 253-313K). α-Tocopherol films were deposited on the surface of gold, glassy carbon and platinum electrodes and their voltammetric behavior examined in aqueous solutions between pH 3 and 13. The voltammetric mechanism involved α-tocopherol being oxidised in a –2e–/–H+ process to form a phenoxonium cation (similar to the experiments in non-aqueous solvents), which underwent rapid reaction with water (or –OH¯ at pH > 7) and rearrangement to form α-tocopherol quinone in a chemically irreversible process. Electrochemical experiments were also performed by incorporating α-tocopherol into lecithin multilayers deposited onto the electrode surfaces. The results were very similar to those obtained for pure α-tocopherol films. α-tocopherol was oxidised to α-tocopherol quinone within the lecithin multilayers. However, the reduction process of α-tocopherol quinone appeared to be less chemically reversible as the pH was increased above pH 7. Two methods were used to incorporate α-tocopherol within the lecithin multilayers and both methods yielded similar electrochemical results.en
dc.format.extent185 p.en
dc.language.isoenen
dc.subjectDRNTU::Science::Chemistry::Physical chemistry::Electrochemistryen
dc.titleVoltammetric studies on vitamin E in organic solvents and within lipid bilayer membranesen
dc.typeThesisen
dc.contributor.supervisorRichard David Websteren
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.description.degreeDOCTOR OF PHILOSOPHY (SPMS)en
dc.identifier.doi10.32657/10356/44564en
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