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Structure and reactivity of selected inclusion compounds

Includes bibliographical references.

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Bibliographic Details
Main Author: Coetzee, Anita
Other Authors: Nassimbeni, Luigi R
Format: Thesis
Language:English
Published: Department of Chemistry 2016
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access_status_str Open Access
author Coetzee, Anita
author2 Nassimbeni, Luigi R
author_browse Coetzee, Anita
Nassimbeni, Luigi R
author_facet Nassimbeni, Luigi R
Coetzee, Anita
author_sort Coetzee, Anita
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/18110
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:07.214Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2016
publishDateRange 2016
publishDateSort 2016
publisher Department of Chemistry
publisherStr Department of Chemistry
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/18110 Structure and reactivity of selected inclusion compounds Coetzee, Anita Nassimbeni, Luigi R Caira, Mino R Chemistry Includes bibliographical references. Selected inclusion compounds of hydroxy hosts from three different classes were investigated. The host compounds in class A are 2,7-substituted 2,2'-bis(9-hydroxy-9-fluorenyl)biphenyls, with the substituents being Cl, Br or tert-butyl. They readily form inclusion compounds with a wide variety of solvents. Their inclusion compounds with 1 ,4-dioxane, 1 ,3-dioxane, 1 ,3-dioxolane and acetone were investigated. The crystal structure of an unsolvated, α-phase, of the host compound 2,2'-bis(2,7-dichloro-9-hydroxy-9-fluorenyl)biphenyl was elucidated. The host compounds in class B are modified dihydroanthracenes. The inclusion compounds of trans-9, 1 0-dihydroxy-9, 1 0-diphenyl-9, 1 0-dihydroanthracene with 1,3-dioxolane, trans-9, 1 0-dihydroxy-9, 1 0-di-a-naphtyl-9, 1 0-dihydroanthracene with 1 ,3-dioxolane and with benzene, as well as trans-9, 1 0-dihydroxy-9, 1 0-di-p-tertbutylphenyl-9,10-dihydroanthracene with methanol and with benzene, were studied. The host in class C, 2,2'-bis(diphenylhydroxymethyl)-1, 1 '-biphenyl (H), is similar to the host compounds in class A, but is rendered conformationally more flexible. It forms two structurally similar inclusion compounds, H·H₂0·1/6 C₆H₆ and H-21/₆H2₂.The crystal structure of a p-xylene inclusion compound was also elucidated. The crystal structures of all these inclusion compounds were elucidated. All the compounds were characterised using thermal analysis and X-ray powder diffraction. The kinetics of desolvation of all the inclusion compounds in class A and B were studied, using isothermal or programmed temperature thermogravimetry. Attempts were made to describe the kinetic behaviour in terms of the crystal structures of these compounds. The Arrhenius parameters for the desolvation of all the inclusion compounds under investigation were found to show the compensation effect. The kinetics of solvation of trans-9, 1 0-dihydroxy-9, 1 0-diphenyl-9, 1 0-dihydroanthraceneand 1, 3-dioxolane was studied, using a quartz microbalance designed especially forth is purpose. 2016-03-21T19:24:52Z 2016-03-21T19:24:52Z 1996 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/18110 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Coetzee, Anita
Structure and reactivity of selected inclusion compounds
thesis_degree_str Doctoral
title Structure and reactivity of selected inclusion compounds
title_full Structure and reactivity of selected inclusion compounds
title_fullStr Structure and reactivity of selected inclusion compounds
title_full_unstemmed Structure and reactivity of selected inclusion compounds
title_short Structure and reactivity of selected inclusion compounds
title_sort structure and reactivity of selected inclusion compounds
topic Chemistry
url http://hdl.handle.net/11427/18110
work_keys_str_mv AT coetzeeanita structureandreactivityofselectedinclusioncompounds