Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.256659
Title: Aspects of the denitrosation of nitroso compounds in acidic solution
Author: Hallett, Geoffrey
Awarding Body: Durham University
Current Institution: Durham University
Date of Award: 1981
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Abstract:
The thesis seeks to provide a rationale for the behaviour of a wide range of N-nitroso compounds in acidic solution. The work is introduced by a review of the various mechanisms proposed to date. It is shown that the behaviour of the system towards certain catalytic agents is dictated by the relative rates of the protonation and denitrosation reactions. The effect of changing nitroso compound structure, changing nucleophile concentrations and changing solvents has been investigated and the results used to provide a common rationale for the denitrosation and N-nitrosation reactions.Supporting data is provided in the form of investigations of the denitrosations of N-methyl-N-nitrosoaniline, N-nitrosodiphenylamine, N-methyl-N-nitrosourea and a series of p-substituted N-methyl-N- nitrosoanilines. The N-nitrosation of N-methylurea is also examined. A comprehensive study of the action of sulphur containing nucleophiles such as the thioureas has led to the proposal of a reaction between N-methyl-N-nitrosoaniline and the naturally occurring nucleophiles, cysteine, S-methylcysteine, glutathione and methionine. The results maybe important in the elucidation of cancer mechanisms. Evidence is also provided for an interaction between N-methyl-N- nitrosoaniline and the ferrous ion.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.256659  DOI: Not available
Keywords: Chemistry, general Chemistry
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