Please use this identifier to cite or link to this item: https://etd.cput.ac.za/handle/20.500.11838/2442
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dc.contributor.advisorJacobs, Ayesha, Profen_US
dc.contributor.authorTangouna Liambo Bissa, Marie-Louiseen_US
dc.date.accessioned2017-05-26T08:48:14Z-
dc.date.available2017-05-26T08:48:14Z-
dc.date.issued2016-
dc.identifier.urihttp://hdl.handle.net/20.500.11838/2442-
dc.descriptionThesis (MTech (Chemistry))--Cape Peninsula University of Technology, 2016en_US
dc.description.abstractInclusion compounds of two hydroxyl hosts with a variety of guests have been investigated. These host compounds are bulky molecules and have the ability to interact with smaller organic guests to form new compounds. The host 9-(1-naphthyl)-9H-xanthen-9-ol (H1), forms inclusion compounds with pyridine (PYR), N,N-dimethylacetamide (DMA), morpholine (MORP) and N-methyl-2-pyrrolidinone (NMP). The crystal structures of H1•NMP, H1•DMA and H1•MORP1 were successfully solved in the triclinic space group PĪ, whereas the inclusion compound H1•PYR crystallised in the monoclinic space group P21/c. A different inclusion compound involving morpholine, H1•MORP2 resulted from dissolution of H1 in a 1:1 molar ratio of MORP: DMA. H1•MORP2 crystallised in the space group PĪ. All of the abovementioned inclusion compounds demonstrated a host: guest ratio of 1:1 except for H1•MORP1 (host: guest ratio = 1: ). H1 interacts with pyridine and morpholine guests via (Host)O-H•••N(Guest) hydrogen bonds and via (Host)OH•••O(Guest) hydrogen bonds with N-methyl-2-pyrrolidinone and N,N-dimethylacetamide.en_US
dc.language.isoenen_US
dc.publisherCape Peninsula University of Technologyen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/3.0/za/-
dc.subjectHydroxyl groupen_US
dc.subjectX-ray crystallographyen_US
dc.subjectX-rays -- Diffractionen_US
dc.subjectSupramolecular chemistryen_US
dc.titleHost-guest compounds: structure and thermal behaviouren_US
dc.typeThesisen_US
Appears in Collections:Chemistry - Masters Degrees
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