Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.482160
Title: The design and synthesis of chiral and achiral inclusion compounds
Author: Swanson, Stephen
ISNI:       0000 0001 3493 5072
Awarding Body: University of Glasgow
Current Institution: University of Glasgow
Date of Award: 1979
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Abstract:
An overview of inclusion phenomena, both in the solid state and in solution, is given. Following this orientating survey, a study of the systematic modification of some selected hexahosts is described. The versatile hexahost hexakis(benzyl-thiomethyl)benzene was chosen for detailed study. Substitution of each of the six outer aromatic rings was found to give a series of hosts with wide-ranging inclusion behaviour and differing guest selectivities. General inclusion properties have also been established for hexakis(2-phenylethylthiomethyl)-benzene, the first hexahost possessing a four atom inter-ring chain. An X-ray analysis of the 1,4-dioxan adduct of hexakis-(benzylthiomethyl)benzene has revealed a true clathrate structure for this material.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.482160  DOI: Not available
Keywords: Organic chemistry
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