Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.796508
Title: Unprecedented reactivity of fluorocarbons and the synthesis of new inclusion compounds
Author: Robertson, Colin Dick
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 1990
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Abstract:
A new and unprecedented reactivity of saturated fluorocarbons has been discovered. Application of this reaction to perfluorodecalin at ambient temperature and above is used to synthesis members of the 'octa-host' series. The mechanism of the reaction and its extension to analogous reactions, including different substrates (unsaturated fluorocarbons or other saturated fluorocarbons, particularly those with a tertiary carbon centre) and different nucleophiles is investigated. A Single Electron Transfer (SET) pathway is favoured. The 'octa-host' series itself, an extension of the 'hexa-host' series, is further investigated and new host inclusion discovered. A new class of host materials, octakis(aryloxy)naphthalenes, is synthesised. Structural investigation of six octa-hosts by X-ray single-crystal diffraction is used to elucidate their inclusion properties; uniquely one of the octa-hosts, octakis(m-tolylthio)-naphthalene has a 'clathrate' open-packed structure as a non-solvate, with no stabilisation other than by van der Waals forces . Another, octakis(cyclohexylthio)naphthalene, contains an axial C-S cyclohexyl bond conformation. These two solid-structures are also investigated by magic angle spinning solid state n.m.r. Other 'octa-host'-like variants were investigated, including routes to 'deca-hosts', anthracene based systems, both through classical synthesis routes and using the newly discovered reactivity of saturated fluorocarbons. More structural tuning of the 'hexa-'host' concept was investigated by the synthesis and solid-state structure elucidation of hexakis -(p-hydroxyphenyloxy) benzene, a potential beta-Hydroquinone analogue. Chiral legs for 'hexa-' and 'octa-hosts' were briefly investigated. The role of symmetry in partnership with molecular conformation and shape is analysed for the 'octa-hosts', C2 equivalents of the C3 'hexa-hosts', and general principles discussed. Fluorocarbon chemistry is summarised and recent progress in the directed design of inclusion compounds reviewed.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.796508  DOI: Not available
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