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Inclusion compounds : structure, reactivity and selectivity

Includes bibliographical references.

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Bibliographic Details
Main Author: Su, Hong
Other Authors: Nassimbeni, Luigi R
Format: Thesis
Language:English
Published: Department of Chemistry 2014
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access_status_str Open Access
author Su, Hong
author2 Nassimbeni, Luigi R
author_browse Nassimbeni, Luigi R
Su, Hong
author_facet Nassimbeni, Luigi R
Su, Hong
author_sort Su, Hong
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/9783
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:53:05.182Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2014
publishDateRange 2014
publishDateSort 2014
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:11427/9783 Inclusion compounds : structure, reactivity and selectivity Su, Hong Nassimbeni, Luigi R Chemistry Includes bibliographical references. This thesis is concerned with structure, thermodynamic and kinetic aspects of a variety of inclusion compounds which contain small organic guests. The host compounds studied are alkaline-earth metal salts of O,O’-dibenzoyl-(2R, 3R)-tartraric acid (magnesium, calcium and strontium), 1,1’-bis-(4-hydroxyphenyl)cyclohexane (DHPC) and 2,2’-dihydroxy-1,1’-binaphthyl (BINAP). The alkaline-earth metal salts form coordination complexes with 2-methoxyethanol, water or ethanol and the guests act as a part of the coordination sphere of the metal ions. The diol host DHPC preferably forms layer type inclusion compounds with the isomers of picoline, lutidine and xylidine, as well as a number of selected solvents including 1,4-dioxane, DMSO, morpholine, THF and acetone, preferably in channel type inclusion modes. In the latter two classes of inclusion compounds the inclusion is facilitated by the formation of hydrogen bonds from the host hydroxyl moieties to the guests. 2014-11-22T05:52:53Z 2014-11-22T05:52:53Z 2002 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/9783 eng application/pdf Department of Chemistry Faculty of Science University of Cape Town
spellingShingle Chemistry
Su, Hong
Inclusion compounds : structure, reactivity and selectivity
thesis_degree_str Doctoral
title Inclusion compounds : structure, reactivity and selectivity
title_full Inclusion compounds : structure, reactivity and selectivity
title_fullStr Inclusion compounds : structure, reactivity and selectivity
title_full_unstemmed Inclusion compounds : structure, reactivity and selectivity
title_short Inclusion compounds : structure, reactivity and selectivity
title_sort inclusion compounds structure reactivity and selectivity
topic Chemistry
url http://hdl.handle.net/11427/9783
work_keys_str_mv AT suhong inclusioncompoundsstructurereactivityandselectivity