- Title
- The characterization and application of novel xanthenyland thioxanthenyl-derived compounds as hosts in the presence of various applicable guest mixtures
- Creator
- Jooste, Daniel Victor
- Subject
- Organic compounds -- Synthesis
- Date Issued
- 2020
- Date
- 2020
- Type
- Thesis
- Type
- Doctoral
- Type
- PhD
- Identifier
- http://hdl.handle.net/10948/49104
- Identifier
- vital:41601
- Description
- In this work, the host potential of four novel, structurally-related compounds, trans- N,N’-bis(9-phenyl-9-xanthenyl)cyclohexane-1,2-diamine (1,2-DAX), trans-N,N’-bis(9- phenyl-9-thioxanthenyl)cyclohexane-1,2-diamine (1,2-DAT), trans-N,N’-bis(9-phenyl- 9-xanthenyl)cyclohexane-1,4-diamine (1,4-DAX), and trans-N,N’-bis(9-phenyl-9- thioxanthenyl)cyclohexane-1,4-diamine (1,4-DAT), were investigated for their possible employment in the separation of isomers and other related compounds using host– guest chemistry. These hosts were synthesized following a Grignard reaction with phenylmagnesium bromide on either xanthone or thioxanthone. The resultant alcohol was treated with perchloric acid, before finally being linked with either trans-1,2- or trans-1,4-diaminocyclohexane to afford the four title host compounds. Initially, the feasibility of these hosts for separating isomers and related compounds was investigated by recrystallizing each one independently from various guest compounds including the methylpyridines and pyridine, xylenes and ethylbenzene, heterocyclic six-membered ring compounds, aniline, N-methylaniline and N,Ndimethylaniline, and also the alkylbenzenes toluene, cumene and ethylbenzene. 1HNMR spectroscopy was used to ascertain if inclusion of the guest species had occurred in this manner and, if so, the host:guest ratio of the complex. Guest–guest competitions were subsequently conducted in order to establish the selectivity of the hosts when presented with a mixture of guests, and if the host would be able to discriminate between them. Gas chromatography-mass spectrometry (GC-MS) was the analytical method of choice here if 1H-NMR spectroscopy was not suitable owing to guest–guest signal overlap. Here, the host was recrystallized from binary, ternary and quaternary mixed guests, where each was present in equimolar amounts. Additionally, binary competition experiments were conducted in mixed guest solvents where the molar ratios of the guests were varied, and host selectivity for these guests evaluated visually by means of selectivity profiles. Single crystal X-ray diffraction (SC-XRD) and thermal analysis were performed on any complexes that afforded crystals of suitable quality in order to relate inherent host–guest interactions and thermal stability to the observed host selectivity from the competition experiments. The more prevalent interactions that were evident in these inclusion complexes between host and guest species were, more usually, and interactions, as well as other short contacts. Hydrogen bonding interactions were observed in only a few of the complexes. Guest accommodation type was also investigated, and these species resided in either discrete cavities or channels within the host crystal, depending on the guest. For the most part, traces obtained from thermal analyses were highly convoluted and difficult to interpret. As a result, guest release onset temperatures could not be determined for all of the inclusion complexes. In some cases, however, this temperature was successfully measured and correlated directly with the observed selectivity order of the host suggested by the competition experiments. Both enhanced and contrasting results were obtained for the four host compounds. In all cases, 1,2-DAX and 1,2-DAT successfully formed complexes with each of the guest species from each series. Interestingly, the 1,4-derived hosts, however, were more selective in that 1,4-DAX did not complex with only one of the guest solvents, while 1,4-DAT did not enclathrate as many as ten of these solvents. The competition investigations showed that, in most of these experiments, the host compounds displayed selectivity for one of the guests present in the mixture, and in some cases, this selectivity was pronounced, alluding to the feasibility of separating related guests from one another through host–guest chemistry principles. Computational calculations were, additionally, conducted on each of the host molecules in order to gain a better understanding of their geometries, and to compare these with the apohost crystal structures. Significant geometry differences were noted between the calculated and crystal structures.
- Format
- xiv,304 leaves
- Format
- Publisher
- Nelson Mandela University
- Publisher
- Faculty of Science
- Language
- English
- Rights
- Nelson Mandela University
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