Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.388506
Title: Chemistry of some model compounds related to fluorinated polymers
Author: Odello, Paolo
ISNI:       0000 0001 3455 0172
Awarding Body: Durham University
Current Institution: Durham University
Date of Award: 1993
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Abstract:
The work described in this thesis is concerned with three areas which are the generation of stable carbocations from saturated model compounds related to poly- vinylidenefluoride, the development of synthetic routes to fluoro-organo-phosphazenes with intention of obtaining some potential additives for perfluoropolyether fluids operating at elevated temperatures, and pericyclic reactions involving fluorinated olefins.1. We reported that some remarkable conjugated cations, and di-cations (4a) are obtained by reaction of hydrofluorocarbon precursors (4) with an excess of antimony pentafluoride. Cations (4a) bear the fluorine atoms at the charged sites, which of course, leads to stabilisation of the systems We investigated the effect of both re-hybridisation and charge on (^13)C, (^19)F, (^1)H n.m.r. chemical shifts and we applied the empirical criterion of (^13)C chemical shifts additivity to these systems to confirm the structure of some carbo-mono-cations and.-di- cations.2. The mechanism of displacement reactions in halophosphazenes was rationalised by reacting the systems in study with selected nucleophiles in competition reactions. Some fluoro-organo-phosphazenes were synthesised using halophosphazenes as starting materials. Different methodologies were used and their effectiveness was limited by the reactivity of the halophosphazenes towards the fluoroalkylating agents. The methodologies used include nucleophilic displacement of the halogen with fluorinated alcohols (R(_F)CH(_2)OH), and perfluoroalkylating agents (eg.: CF(_3)SiMe(_3)); perfluoroalkylation of organo-phosphazene using hexafluoropropene under gamma ray irradiation. Potential stabilising agents for perfluoropolyether fluids were synthesised and their effectiveness was tested.3. Some pericyclic reactions of heptafluorobut-2-ene and hexafluorobut-2-ene with dienes have been studied in an attempt to synthesise a series of benzenoid and heteroaromatic compounds containing two trifluoromethyl groups in high yields.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.388506  DOI: Not available
Keywords: Carbocations; Phosphazene chemistry Chemistry, Organic
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