Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.395805
Title: Perfluoroalkylation of aromatic systems
Author: Magron, Corinne
ISNI:       0000 0001 3616 4355
Awarding Body: Durham University
Current Institution: Durham University
Date of Award: 1997
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Abstract:
I. We have concentrated on the synthesis of aromatic systems containing CH(_2)R(_F) groups, where R(_F) is a bulky group derived from hexafluoropropene dimer, using fluoride ion induced methodology. A variety of procedures have been explored and methods of synthesis are described. We have made a major advance in this area by the simple expedient of extracting the polyfluoroalkylated products directly into commercially available perfluorinated fluids: FC-84 (bp 8O C), enabling simple purification. II. This new class of perfluoroalkylated derivatives has allowed us to explore some further chemistry. Synthesis and reactions are presented and the results are discussed in terms of electronic effects of the perfluoroalkyl group on the benzene ring. The unusual miscibility properties of fluorocarbon solvents have also prompted us to investigate the potential utility of these systems for dyes and catalysis. III. Synthetically useful perfluoroalkylated-s-triazines have been synthesised from 2,4,6-trifluoro-s-triazine, by fluoride ion induced reaction with hexafluoropropene. These systems so produced were extensively studied, and particular attention was paid to reactions with oxygen-centered nucleophiles. Model chemistry to demonstrate that attachment of perfluorocarbon groups to surfaces could be a useful form of treatment by using this methodology and was explored.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.395805  DOI: Not available
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