- Title
- Investigation of four roof-shaped host compounds for their separation potential of mixtures of guest Isomers and related compounds
- Creator
- Senekal, Ulrich
- Subject
- Grignard reagents
- Subject
- Optical isomers -- Analysis
- Subject
- Supramolecular chemistry
- Date Issued
- 2024-04
- Date
- 2024-04
- Type
- Doctoral theses
- Type
- text
- Identifier
- http://hdl.handle.net/10948/64368
- Identifier
- vital:73684
- Description
- The inclusion ability of four roof-shaped host compounds, namely trans-9,10-dihydro-9,10- ethanoanthracene-11,12-dicarboxylic acid (H1), dimethyl trans-9,10-dihydro-9,10- ethanoanthracene-11,12-dicarboxylate (H2), trans-α,α,α’,α’-tetraphenyl-9,10-dihydro-9,10- ethanoanthracene-11,12-dimethanol (H3) and trans-α,α,α’,α’-tetrakis(4-chlorophenyl)-9,10- dihydro-9,10-ethanoanthracene-11,12-dimethanol (H4), were investigated when presented with numerous guest series (eight in number), including the xylene isomers and ethylbenzene, pyridine and the methylpyridine isomers, structurally related toluene, ethylbenzene and cumene, the dichlorobenzenes, six-membered heterocyclic ring compounds (dioxane, morpholine, piperidine and pyridine), anisole and the methylanisole isomers, anisole and the bromoanisole guests, and phenol and the methoxyphenol isomers. The four host compounds were synthesized via Diels-Alder (H1), esterification (H2) and Grignard addition (H3 and H4) reactions, producing yields of product of up to 93%. The yields for the Grignard reactions were lower, 54 and 37%, for the corresponding procedures using phenylmagnesium bromide or 4-chlorophenylmagnesium bromide. Computational molecular modelling studies were conducted on all four host compounds, and the resultant molecular geometries compared with the apohost (guest-free) crystal structures, when available. The geometries of the lowest energy conformers were in close correlation with the observed host structures as obtained from the apohost crystal structures (unfortunately, H3 and H4 were not able to form adequate quality crystals for SCXRD analyses). Interestingly, H1–H4 displayed intramolecular non-classical C–H∙∙∙O hydrogen bonds, while only H1 and H2 demonstrated intermolecular interactions of this type. H3 and H4 assumed one of two forms depending on the guest that was employed: the “active” form presented a strong intramolecular O–H∙∙∙O hydrogen bond, while the “inactive” form possessed weak π∙∙∙π and O–H∙∙∙π interactions. All of the host compounds were subjected to crystallization experiments from each of the guest species, as well as from mixtures of guests from each series (the guest competition experiments), where 1H-, 13C-NMR spectroscopy, GC-MS and/or GC-FID were used to analyse any resultant solids formed, as applicable. Single crystal X-ray diffraction (SCXRD) experiments were carried out on each single solvent complex produced in this work, where the crystal quality was suitable, while thermal analyses were also employed on these to determine their relative thermal stabilities. During the single-guest crystallization experiments, H4 was found to be remarkable in its inclusion ability, forming complexes with all but p-dichlorobenzene, typically with a 1:1 host:guest (H:G) ratio. H1 was more selective in its inclusion behaviour, not enclathrating cumene, 3-bromoanisole, phenol or the three methoxyphenol isomers (favouring 1:1 or 2:1 H:G ratios where complexation was successful). Interestingly, H1 formed salts when presented with 2- and 3-methylpyridine, and morpholine and piperidine. H2 and H3 were less remarkable in their inclusion ability, furnishing apohost crystals or gels in some experiments (typically a 3:1 H:G ratio was favoured for both when complexation occurred). Of the four roof-shaped host compounds, H1 and H4 displayed enhanced selectivities for certain guest species, showing near-complete affinity for a specific guest compound when presented with a guest mixture. H1 was able to include 100.0 and 98.8% p-dichlorobenzene (p-DCB) (from m-DCB/p-DCB and o-DCB/p-DCB mixtures), 96.6 and 93.6% p-xylene (p-Xy) (from m-Xy/p-Xy and o-Xy/p-Xy), 99.3% 4-methylanisole (4-MA) (from 2-MA/4-MA) and 97.1% 4-bromoanisole (4-BA) (from ANI/2-BA/3-BA/4-BA, where ANI is anisole). Host compound H4 was able to include ≈ 90% of selected meta-substituted guests, while H2 and H3 demonstrated moderate preferences for the guest compounds employed in this work (< 60%). It was concluded that some xylene guest mixtures may be purified using all but H2, whereas only H1 and H2 showed potential in separating the pyridines. All but H2 may also be employed in the separation of selected dichlorobenzene mixtures, while H2 showed potential for the separation of the six-membered heterocyclic guest compounds (dioxane, morpholine, piperidine and pyridine), were these ever required to be separated. Both H1 and H4 exhibited an overwhelming affinity for the methyl- and bromoanisole guest compounds, and this work has shown that these are likely host candidates for the purification of a variety of these guest mixtures through supramolecular strategies. SCXRD analyses showed that H1 experienced intermolecular host···host hydrogen bonding interactions between the carboxylic acid functional groups, while H2 typically demonstrated intermolecular non-classical hydrogen bonds in its complexes, forming sheets of host molecules along the c-axis. H4 preferred the “inactive” form whereas H3 assumed either an “active” or “inactive“ form. Various host···guest interactions such as π∙∙∙π, C–H∙∙∙π, C–O∙∙∙π, hydrogen bonding and other short contacts were responsible for guest retention in the crystal structures. Thermal analyses were conducted on all of the successfully formed complexes. Ton (the guest release onset temperature) and Tp (the temperature at which the guest release was most rapid) were recorded, when possible, while the mass losses associated with the guest release event were compared with those mass losses expected, in most cases.
- Description
- Thesis (PhD) -- Faculty of Science, School of Biomolecular & Chemical Sciences, 2024
- Format
- computer
- Format
- online resource
- Format
- application/pdf
- Format
- 1 online resource (xii, 364 pages)
- Format
- Publisher
- Nelson Mandela University
- Publisher
- Faculty of Science
- Language
- English
- Rights
- Nelson Mandela University
- Rights
- All Rights Reserved
- Rights
- Open Access
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