- Title
- Supramolecular chemistry considerations of fluorenyl-derived host compounds
- Creator
- McFarlane, Duncan William
- Subject
- Supramolecular chemistry
- Subject
- Organic compounds
- Subject
- Chemistry, Organic
- Date Issued
- 2024-12
- Date
- 2024-12
- Type
- Master's theses
- Type
- text
- Identifier
- http://hdl.handle.net/10948/69371
- Identifier
- vital:77227
- Description
- This work examined various supramolecular aspects of 9-fluorenone-derived host compounds, namely 4,4’-(9-fluorenylidene)diphenol (H1), 9,9-(1,4-phenylene)bis(fluoren-9-ol) (H2), 9,9- (ethyne-1,2-diyl)bis(fluoren-9-ol) (H3) and 9,9-(biphenyl-4,4-diyl)bis(fluoren-9-ol) (H4). These compounds were successfully synthesized and then screened for their host ability for, and host behaviour in, various organic compounds. At the outset, molecular modelling calculations were carried out on each of the four host compounds. Various structural parameters and the geometries of the low energy conformers that were calculated were then compared with these aspects of the guest-free host molecules obtained from single crystal X-ray diffraction (SCXRD) analysis. The host behaviour of H1 was, furthermore, assessed in the presence of four alkylnitriles, namely acetonitrile (ACE), acrylonitrile (ACRY), propionitrile (PROP) and butyronitrile (BUT). All four guests complexed with H1 with 1:1 host:guest (H:G) ratios. From SCXRD analyses, each of the complexes crystallized in the monoclinic crystal system and the centrosymmetric space group P21/n, and the host packing was isostructural in each instance. The complexes were stabilized by a plethora of short inter- and intramolecular contacts. The thermal stabilities of the four complexes were also examined together with Hirshfeld surface considerations. Finally, lattice energy calculations were carried out and the results of these compared with the relative thermal stabilities of the four complexes. The compounds H2 and H3 were examined for their selectivity behaviour in mixtures of aniline, N-methylaniline and N,N’-dimethylaniline (ANI, NMA and DMA). Both host compounds were able to form complexes with ANI and DMA with various H:G ratios, while only H3 possessed enclathration ability for NMA (H:G 1:1). SCXRD analyses showed that all of the complexes were stabilized by means of classical (host)O‒H···N(guest) hydrogen bonds in addition to other short contacts. Equimolar binary guest competition experiments with H2 revealed an extremely high host selectivity for DMA (ANI/DMA and DMA/NMA experiments furnished crystals with > 91% DMA), while the experiment with all three anilines present also resulted in a complex with an
- Description
- Thesis (MSc) -- Faculty of Science, School of Biomolecular & Chemical Sciences, 2024
- Format
- computer
- Format
- online resource
- Format
- application/pdf
- Format
- 1 online resource (213 pages)
- Format
- Publisher
- Nelson Mandela University
- Publisher
- Faculty of Science
- Language
- English
- Rights
- Nelson Mandela University
- Rights
- All Rights Reserved
- Rights
- Open Access
- Hits: 3
- Visitors: 4
- Downloads: 2
Collections
NMU School of BioMolecular and Chemical Sciences
| Thumbnail | File | Description | Size | Format | |||
|---|---|---|---|---|---|---|---|
| View Details Download | SOURCE1 | McFarlane, D.pdf | 15 MB | Adobe Acrobat PDF | View Details Download |