- Title
- Synthesis, X-Ray characterization, spectroscopic and Hirshfeld surface analysis of dimeric metal centers featuring phenacyl-esters
- Creator
- Qomfo, Vuyiseka
- Subject
- Spectrum analysis
- Subject
- Spectroscopic imaging
- Subject
- Diagnostic imaging -- Digital techniques
- Date Issued
- 2024-12
- Date
- 2024-12
- Type
- Master's theses
- Type
- text
- Identifier
- http://hdl.handle.net/10948/69426
- Identifier
- vital:77254
- Description
- In this study, the synthesis and characterization of carboxylate paddlewheel copper complexes were investigated and reported. The complexes consist of O-, and N- donor ligands which coordinated in the apical positions of the copper (II) paddlewheel complexes. The primary focus was the investigation of the influence of the incoming substituents on the structure; more especially with regards to the spectral properties and thermal properties of the synthesized compounds. Synthesized complexes ranged from simple mononuclear complexes and dinuclear dimers to supramolecular 1D networks and a tetranuclear copper (II) compound. Characterization of complexes was done using analytical, and spectroscopic techniques such as single crystal diffraction studies, FT-IR spectroscopy, thermal analysis and Hirshfeld surface analysis. Structural analysis of the mononuclear complex obtained in the reaction of the Cu2(o-CH3-PhCO2)4(THF)2 with the ligand ,2-oxo-phenylethylnicotinate, revealed a square-planar geometry. The series of dinuclear paddlewheel complexes obtained with ligands (L = THF (1), C4H8O (2), C14H11NO3 (3)) revealed a square pyramidal geometry with the methyl-substituted phenyl carboxylate groups bridging the two copper atoms in the syn-syn coordination mode. Extended supramolecular complexes were synthesized via the reaction of three synthesized structurally bifunctional organic ligands and the tetrakis(μ-carboxylato-O,O)dicopper(II) core. Two of the six reactions synthesized successfully to form paddlewheel cage type structures; resulting in dinuclear paddlewheel complexes with four carboxylate ligands occupying the equatorial positions and the bifunctional ligands coordinating in the apical positions. Four of the nine reactions produced mononuclear copper complexes. Due to the inconsistent power supply because of load-shedding, the other three crystals synthesized could not be confirmed by single-crystal diffraction before the submission of this thesis.
- Description
- Thesis (MSc) -- Faculty of Science, School of Biomolecular & Chemical Sciences, 2024
- Format
- computer
- Format
- online resource
- Format
- application/pdf
- Format
- 1 online resource (220 pages)
- Format
- Publisher
- Nelson Mandela University
- Publisher
- Faculty of Science
- Language
- English
- Rights
- Nelson Mandela University
- Rights
- All Rights Reserved
- Rights
- Open Access
- Hits: 13
- Visitors: 15
- Downloads: 5
Collections
NMU School of BioMolecular and Chemical Sciences
| Thumbnail | File | Description | Size | Format | |||
|---|---|---|---|---|---|---|---|
| View Details Download | SOURCE1 | QOMFO, V.pdf | 8 MB | Adobe Acrobat PDF | View Details Download |