Structure and thermal stability of selected organic inclusion compounds

Thesis (MTech (Chemistry))--Cape Peninsula University of Technology, 2012. === Crystal engineering is the synthesis of new crystalline materials with specific chemical and physical properties which allows the comprehensive understanding of the non covalent interactions that occur between molecules...

Full description

Bibliographic Details
Main Author: Silwana, Nothemba
Other Authors: Jacobs, Ayesha
Language:en
Published: Cape Peninsula University of Technology 2018
Subjects:
Online Access:http://hdl.handle.net/20.500.11838/2618
id ndltd-netd.ac.za-oai-union.ndltd.org-cput-oai-localhost-20.500.11838-2618
record_format oai_dc
spelling ndltd-netd.ac.za-oai-union.ndltd.org-cput-oai-localhost-20.500.11838-26182018-05-28T05:09:52Z Structure and thermal stability of selected organic inclusion compounds Silwana, Nothemba Jacobs, Ayesha Organic compounds Thermal analysis Thesis (MTech (Chemistry))--Cape Peninsula University of Technology, 2012. Crystal engineering is the synthesis of new crystalline materials with specific chemical and physical properties which allows the comprehensive understanding of the non covalent interactions that occur between molecules in the crystalline state. This has lead to extensive work being done in terms of host design. The study of non-covalent interactions formed by - these materials is crucial to understanding many biological processes. This study focuses on the inclusion compounds of 1, 4-bis (diphenylhydroxymethyl) benzene H, a host compound engineered by EWeber, that conforms to Weber's rules for host design as it is bulky, rigid, and has hydroxyl moieties that act as hydrogen-bonding donors. A Cambridge Structural Database (CSDversion 5.33) search has revealed that no research has been conducted on this host compound. Characterization of the compounds were conducted using thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), hot stage microscopy (HS), gas chromatography (GC), powder X-ray diffraction(PXRD) and single X -ray diffraction. Host: guest ratios determined from TG analysis were correlated with structural analysis results. We have successfully prepared inclusion compounds with N, N- dimethylformamide(DMF) N, N- dimethylacetamide (DMA), N-methylformamide (NMF) and N-methylacetamide (NMA), 2-picoline, 3-picoline, 4-picoline, pyridine and morpholine. Following which a series of competition experiments were conducted to establish the selectivity profile of the host by dissolving the host in an excess of two guests pairs, between DMF: DMA, DMF: NMF, DMF: NMA, DMA: NMF, DMA: NMA and NMF: NMA. The results of the competition experiment showed that the host had high selectivity for DMF and the selectivity profile follows a trend as follows DMF>NMA>NMF>DMA. The results for the competition experiments between the picolines, pyridine and morpholine were inconclusive. 2018-03-23T10:16:42Z 2018-03-23T10:16:42Z 2012 Thesis http://hdl.handle.net/20.500.11838/2618 en http://creativecommons.org/licenses/by-nc-sa/3.0/za/ Cape Peninsula University of Technology
collection NDLTD
language en
sources NDLTD
topic Organic compounds
Thermal analysis
spellingShingle Organic compounds
Thermal analysis
Silwana, Nothemba
Structure and thermal stability of selected organic inclusion compounds
description Thesis (MTech (Chemistry))--Cape Peninsula University of Technology, 2012. === Crystal engineering is the synthesis of new crystalline materials with specific chemical and physical properties which allows the comprehensive understanding of the non covalent interactions that occur between molecules in the crystalline state. This has lead to extensive work being done in terms of host design. The study of non-covalent interactions formed by - these materials is crucial to understanding many biological processes. This study focuses on the inclusion compounds of 1, 4-bis (diphenylhydroxymethyl) benzene H, a host compound engineered by EWeber, that conforms to Weber's rules for host design as it is bulky, rigid, and has hydroxyl moieties that act as hydrogen-bonding donors. A Cambridge Structural Database (CSDversion 5.33) search has revealed that no research has been conducted on this host compound. Characterization of the compounds were conducted using thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), hot stage microscopy (HS), gas chromatography (GC), powder X-ray diffraction(PXRD) and single X -ray diffraction. Host: guest ratios determined from TG analysis were correlated with structural analysis results. We have successfully prepared inclusion compounds with N, N- dimethylformamide(DMF) N, N- dimethylacetamide (DMA), N-methylformamide (NMF) and N-methylacetamide (NMA), 2-picoline, 3-picoline, 4-picoline, pyridine and morpholine. Following which a series of competition experiments were conducted to establish the selectivity profile of the host by dissolving the host in an excess of two guests pairs, between DMF: DMA, DMF: NMF, DMF: NMA, DMA: NMF, DMA: NMA and NMF: NMA. The results of the competition experiment showed that the host had high selectivity for DMF and the selectivity profile follows a trend as follows DMF>NMA>NMF>DMA. The results for the competition experiments between the picolines, pyridine and morpholine were inconclusive.
author2 Jacobs, Ayesha
author_facet Jacobs, Ayesha
Silwana, Nothemba
author Silwana, Nothemba
author_sort Silwana, Nothemba
title Structure and thermal stability of selected organic inclusion compounds
title_short Structure and thermal stability of selected organic inclusion compounds
title_full Structure and thermal stability of selected organic inclusion compounds
title_fullStr Structure and thermal stability of selected organic inclusion compounds
title_full_unstemmed Structure and thermal stability of selected organic inclusion compounds
title_sort structure and thermal stability of selected organic inclusion compounds
publisher Cape Peninsula University of Technology
publishDate 2018
url http://hdl.handle.net/20.500.11838/2618
work_keys_str_mv AT silwananothemba structureandthermalstabilityofselectedorganicinclusioncompounds
_version_ 1718681938730942464