Use this URL to cite or link to this record in EThOS: | https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.482160 |
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Title: | The design and synthesis of chiral and achiral inclusion compounds | ||||||
Author: | Swanson, Stephen |
ISNI:
0000 0001 3493 5072
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Awarding Body: | University of Glasgow | ||||||
Current Institution: | University of Glasgow | ||||||
Date of Award: | 1979 | ||||||
Availability of Full Text: |
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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.
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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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