Structure and reactivity of selected organic inclusion compounds
type: CreativeWork
description: The inclusion behaviour of the two host compounds 1,1 ,6,6-tetraphenylhexa-2,4- diyne-l,6-diol and cyclotriveratrylene (2,3,7,8,12,13-hexamethoxy-5,lO-dihydro- 15H-tribenzo[ a,d,g]cyclononene) was studied. Small organic guests were complexed with these hosts and their crystal structures determined. The stability and reactivity of these inclusion compounds were investigated. Kinetics of desolvation were determined for some of the inclusion compounds using both isothermal and non-isothermal methods. Rate laws were proposed and activation energies established. The selectivity of the host 1,1 ,6,6-tetraphenylhexa-2,4-diyne- 1,6-diol for certain guests was determined by competition experiments. Lattice energies were calculated in some cases. Solid state reactions were performed with the host 1,1 ,6,6-tetraphenylhexa-2,4-diyne-1 ,6-diol and selected solid guests. The resultant complexes were analysed using X-ray powder diffraction. Guest exchange reactions were also performed and the reactions were monitored either by differential scanning calorimetry or thermogravimetry. The structures of the inclusion compounds were reconciled with their physico-chemical properties.
abstract: The inclusion behaviour of the two host compounds 1,1 ,6,6-tetraphenylhexa-2,4- diyne-l,6-diol and cyclotriveratrylene (2,3,7,8,12,13-hexamethoxy-5,lO-dihydro- 15H-tribenzo[ a,d,g]cyclononene) was studied. Small organic guests were complexed with these hosts and their crystal structures determined. The stability and reactivity of these inclusion compounds were investigated. Kinetics of desolvation were determined for some of the inclusion compounds using both isothermal and non-isothermal methods. Rate laws were proposed and activation energies established. The selectivity of the host 1,1 ,6,6-tetraphenylhexa-2,4-diyne- 1,6-diol for certain guests was determined by competition experiments. Lattice energies were calculated in some cases. Solid state reactions were performed with the host 1,1 ,6,6-tetraphenylhexa-2,4-diyne-1 ,6-diol and selected solid guests. The resultant complexes were analysed using X-ray powder diffraction. Guest exchange reactions were also performed and the reactions were monitored either by differential scanning calorimetry or thermogravimetry. The structures of the inclusion compounds were reconciled with their physico-chemical properties.
author: Jacobs, Ayesha
language: eng
date published: 2002
date modified: 2026-07-22T22:23:16Z
provider: University of Cape Town
publisher: Networked Digital Library of Theses and Dissertations
type: WebPage
source organization: Department of Chemistry

PropertyValue
property ID: Handle
value: http://hdl.handle.net/11427/6313