Synthesis, characterization and host-guest complexes of supramolecular assemblies based on calixarenes and cucurbiturils
- Authors: Baa, Ebenezer
- Date: 2022-10-14
- Subjects: Supramolecular chemistry , Calixarenes , Cucurbiturils , Metal-organic frameworks , Macrocyclic compounds , Drug delivery systems
- Language: English
- Type: Academic theses , Doctoral theses , text
- Identifier: http://hdl.handle.net/10962/365621 , vital:65765 , DOI https://doi.org/10.21504/10962/365621
- Description: The field of supramolecular chemistry has grown large and wide in both deepness of understanding, range of topics covered and scope and applications. Supramolecular self-assemblies are facilitated by a wide range of non-covalent intra and inter molecular interactions that range from hydrogen bonding to π-interaction and van der Waals. Macrocyclic compounds such as cucurbiturils and calixarenes have emerged as important classes of compounds with excellent potential of forming supramolecular assemblies. The porous nature of these compounds enables them to form host-guest supramolecular complexes stabilized by diverse range of non-covalent interactions. Furthermore, these compounds contain donor atoms capable of forming bonds with metal ions to yield metal complexes with interesting porous characteristics that deviate from their traditional hydrophobic cavity. The versatile nature of the resulting pores imply that they can accommodate diverse types of guests. This work explores the synthesis and characterization of a host of calixarenes and cucurbiturils. Self-assembly of these macrocycles with various metal ions results to the formation of porous metal organic framework (MOF) complexes. Four new calixarene typed compounds obtained from aromatic aldehydes and twenty-six cucurbituril metal complexes are reported. These macrocylces and their metal complexes also form supramolecular complexes with DMSO, methanol, isoniazid hydrochloride and ciprofloxacin hydrochlorides through either self-assembly, mechanochemistry and exposure to solvent vapors. The bulk materials have been characterized using nuclear magnetic resonance spectroscopy (NMR), Fourier transformed infrared spectroscopy (FTIR), powder and single crystal diffraction techniques and thermal studies thermogravimetric analysis (TGA) and differential thermal calorimetry (DSC). Data obtained from this study reveals that calixarenes can form supramolecular complexes with a frequently used laboratory solvents with BN22 showing appreciable selectivity for DMSO sorption from a solvent mixture. These compounds also form supramolecular complexes with drug molecules such as isoniazid and ciprofloxacin. Furthermore, the data reveals that choice of synthetic route of supramolecular ensembles dictates if the guest drug molecule will occupy the intrinsic or extrinsic pores of cucurbituril complexes. Biological studies on the obtained complexes reveal that the cucurbituril complexes are non-cytotoxic while the calixarenes show antibacterial activity against Escherichia coli and Staphylococcus aureus. Additionally, the study showed that ciprofloxacin can be successfully released from a calixarene host in a simulated body fluid although the host was also found to cross the dialysis membrane. The results of this study are important in that; - they can be exploited and developed in the selective sorption of certain guests and - that they can be used in the development of drug delivery systems that play a dual role of delivery and therapeutic activity. , Thesis (PhD) -- Faculty of Science, Chemistry, 2022
- Full Text:
- Date Issued: 2022-10-14
- Authors: Baa, Ebenezer
- Date: 2022-10-14
- Subjects: Supramolecular chemistry , Calixarenes , Cucurbiturils , Metal-organic frameworks , Macrocyclic compounds , Drug delivery systems
- Language: English
- Type: Academic theses , Doctoral theses , text
- Identifier: http://hdl.handle.net/10962/365621 , vital:65765 , DOI https://doi.org/10.21504/10962/365621
- Description: The field of supramolecular chemistry has grown large and wide in both deepness of understanding, range of topics covered and scope and applications. Supramolecular self-assemblies are facilitated by a wide range of non-covalent intra and inter molecular interactions that range from hydrogen bonding to π-interaction and van der Waals. Macrocyclic compounds such as cucurbiturils and calixarenes have emerged as important classes of compounds with excellent potential of forming supramolecular assemblies. The porous nature of these compounds enables them to form host-guest supramolecular complexes stabilized by diverse range of non-covalent interactions. Furthermore, these compounds contain donor atoms capable of forming bonds with metal ions to yield metal complexes with interesting porous characteristics that deviate from their traditional hydrophobic cavity. The versatile nature of the resulting pores imply that they can accommodate diverse types of guests. This work explores the synthesis and characterization of a host of calixarenes and cucurbiturils. Self-assembly of these macrocycles with various metal ions results to the formation of porous metal organic framework (MOF) complexes. Four new calixarene typed compounds obtained from aromatic aldehydes and twenty-six cucurbituril metal complexes are reported. These macrocylces and their metal complexes also form supramolecular complexes with DMSO, methanol, isoniazid hydrochloride and ciprofloxacin hydrochlorides through either self-assembly, mechanochemistry and exposure to solvent vapors. The bulk materials have been characterized using nuclear magnetic resonance spectroscopy (NMR), Fourier transformed infrared spectroscopy (FTIR), powder and single crystal diffraction techniques and thermal studies thermogravimetric analysis (TGA) and differential thermal calorimetry (DSC). Data obtained from this study reveals that calixarenes can form supramolecular complexes with a frequently used laboratory solvents with BN22 showing appreciable selectivity for DMSO sorption from a solvent mixture. These compounds also form supramolecular complexes with drug molecules such as isoniazid and ciprofloxacin. Furthermore, the data reveals that choice of synthetic route of supramolecular ensembles dictates if the guest drug molecule will occupy the intrinsic or extrinsic pores of cucurbituril complexes. Biological studies on the obtained complexes reveal that the cucurbituril complexes are non-cytotoxic while the calixarenes show antibacterial activity against Escherichia coli and Staphylococcus aureus. Additionally, the study showed that ciprofloxacin can be successfully released from a calixarene host in a simulated body fluid although the host was also found to cross the dialysis membrane. The results of this study are important in that; - they can be exploited and developed in the selective sorption of certain guests and - that they can be used in the development of drug delivery systems that play a dual role of delivery and therapeutic activity. , Thesis (PhD) -- Faculty of Science, Chemistry, 2022
- Full Text:
- Date Issued: 2022-10-14
Synthesis, crystal structures and characterization of metal–organic framework architectures involving dinuclear copper(ii) benzoic acid derivative complexes
- Authors: Ndima, Lubabalo
- Date: 2020
- Subjects: Supramolecular chemistry
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: http://hdl.handle.net/10948/46783 , vital:39657
- Description: Structural copper(II) complexes with aromatic carboxylic acids show a wide spectrum of coordination schemes. Studies of dicopper(II) carboxylates have been associated with a variety of interests for their catalytic, biological and magnetic applications [1]. Various novel dinuclear copper(II) complexes [Cu2(X-benzoate)4L2] with varying substituents (X = CH3, F, Cl, Br, I, NO2 & OCH3) with a desired octahedral geometry have been synthesized. The various complexes were characterized by single crystal X-ray diffraction studies, spectroscopic and thermal methods (UV/Vis, FTIR and TGA, DSC). In most cases, the structures consists of centrosymmetric dimers in which the Cu atoms show a square pyramidal CuO5 coordination. In all cases, dimeric paddle wheel complexes where two copper(II) ions are held together by four benzoates (forming syn– syn bridges between the copper atoms) and the apical coordination site occupied by a solvent ligand (L) or supramolecular linker were obtained. The dimers are extended into 1D chains that result from hydrogen bonding between the coordinated methanol (solvent ligand) on one Cu(II) and the carboxylate group on an adjacent Cu(II) dimer, including interactions arising from various substituents. π–π Stacking interactions are found to be present in the various crystal structures forming 3D supramolecular array. FTIR and UV/Vis spectra of each complex have shown how the resonance and inductive effect of each substituent affects spectral data of each complex.
- Full Text:
- Date Issued: 2020
- Authors: Ndima, Lubabalo
- Date: 2020
- Subjects: Supramolecular chemistry
- Language: English
- Type: Thesis , Masters , MSc
- Identifier: http://hdl.handle.net/10948/46783 , vital:39657
- Description: Structural copper(II) complexes with aromatic carboxylic acids show a wide spectrum of coordination schemes. Studies of dicopper(II) carboxylates have been associated with a variety of interests for their catalytic, biological and magnetic applications [1]. Various novel dinuclear copper(II) complexes [Cu2(X-benzoate)4L2] with varying substituents (X = CH3, F, Cl, Br, I, NO2 & OCH3) with a desired octahedral geometry have been synthesized. The various complexes were characterized by single crystal X-ray diffraction studies, spectroscopic and thermal methods (UV/Vis, FTIR and TGA, DSC). In most cases, the structures consists of centrosymmetric dimers in which the Cu atoms show a square pyramidal CuO5 coordination. In all cases, dimeric paddle wheel complexes where two copper(II) ions are held together by four benzoates (forming syn– syn bridges between the copper atoms) and the apical coordination site occupied by a solvent ligand (L) or supramolecular linker were obtained. The dimers are extended into 1D chains that result from hydrogen bonding between the coordinated methanol (solvent ligand) on one Cu(II) and the carboxylate group on an adjacent Cu(II) dimer, including interactions arising from various substituents. π–π Stacking interactions are found to be present in the various crystal structures forming 3D supramolecular array. FTIR and UV/Vis spectra of each complex have shown how the resonance and inductive effect of each substituent affects spectral data of each complex.
- Full Text:
- Date Issued: 2020
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