Synthesis of two tartaric acid-derived host compounds and their behaviour in mixed pyridines and mixed heterocyclic guest compounds
- Authors: Recchia, Daniella Loridana
- Date: 2024-12
- Subjects: Compounds -- guest/host , Chemistry, Organic , Chemistry
- Language: English
- Type: Master's theses , text
- Identifier: http://hdl.handle.net/10948/69441 , vital:77256
- Description: The host compounds (4R,5R)-bis(diphenylhydroxymethyl)-2-spiro-1’-cyclopentane-1,3-dioxolane (TADDOL5) and (4R,5R)-bis(diphenylhydroxymethyl)-2-spiro-1’-cyclohexane-1,3-dioxolane (TADDOL6) were successfully synthesized after initially reacting diethyl tartrate with either 1,1-dimethoxycyclopentane or 1,1-dimethoxycyclohexane to afford the intermediates diethyl 2-spiro-1’-cyclopentane-1,3-dioxolan-4,5-dicarboxylate or diethyl 2-spiro-1’-cyclohexane-1,3-dioxolan-4,5-dicarboxylate. These were then each subjected to a Grignard addition reaction with PhMgBr to furnish TADDOL5 and TADDOL6 in reasonably high yields (77 and 80%, respectively). Computational calculations were performed on TADDOL5 and TADDOL6 using the software programs Avogadro and ORCA. The optimised geometries of these host molecules were obtained using the MMFF94 force field in Avogadro, while ORCA was used to perform the computational modelling at the BLYP level using the 6-31G*, 6-31G**, 6-311G* and 6-311G** basis sets and, also, the B3LYP functional (with the same basis sets) to obtain the three lowest energy conformers. The final geometries of each conformer for both TADDOL5 and TADDOL6 at the B3LYP 6-311G* level were overlaid with the molecules obtained from their crystal structures. Significantly different geometries were thus noted for the calculated conformers compared with the guest-free TADDOL5 and TADDOL6 structures obtained from the SCXRD experiments. When TADDOL5 was crystallized independently from each of PYR, 2MP, 3MP and 4MP, 1:1 H:G inclusion complexes formed in each instance. This host compound was then investigated for its host separation ability of mixed pyridines through supramolecular chemistry protocols. These mixed guest experiments revealed that TADDOL5 possessed a notable selectivity towards 3MP and PYR (in the absence of 3MP) followed by 4MP and 2MP, and it was shown that TADDOL5 is a suitable host candidate for the separation of many of the mixed pyridines employed here. The results of the SCXRD analyses indicated that the only significant (host)π···π(guest) stacking interaction present was between TADDOL5 and the most favoured guest species PYR and 3MP. Furthermore, significantly shorter (host)O‒H···N(guest) hydrogen bonds were also observed in the complexes formed between this host compound and 3MP and PYR compared with these bonds involving disfavoured 4MP and 2MP. Hirshfeld surface considerations provided an explanation for the affinity of TADDOL5 for PYR (but not 3MP), while thermal analyses successfully explained this affinity: the 3MP-containing complex with the most preferred guest species was the most thermally stable one, followed by TADDOL5·PYR, as obtained through a consideration of the Ton values (the temperature at which the guest release event initiated) of the four complexes. As with TADDOL5, TADDOL6 formed 1:1 H:G inclusion compounds with each of the four pyridines. TADDOL6 was, furthermore, also assessed for its separation ability for mixed pyridines, and these guest competition experiments showed that the selectivity of TADDOL6 was for PYR and 3MP (in the absence of PYR), followed by 4MP and 2MP. (Interestingly, TADDOL5 preferred 3MP and then PYR, while both host compounds disfavoured 4MP and 2MP.) The results obtained in this work indicated that TADDOL6 may also serve as an efficient host candidate for the separation of many of these pyridyl solutions. SCXRD experiments demonstrated that the only significant (host)π···π(guest) stacking interactions were those between TADDOL6 and preferred PYR and 3MP, as was the case for TADDOL5. These experiments also revealed that the strongest (host)O‒H···N(guest) hydrogen bonds were between TADDOL6 and these favoured guest species. A consideration of Hirshfeld surfaces and quantification of the (guest)N···H(host) intermolecular interactions correlated with the host selectivity order, as did thermal analyses, where the Ton values confirmed that the thermal stabilities of these complexes decreased in the guest order PYR > 3MP > 4MP > 2MP. The behaviour of TADDOL5 was further investigated in guest compounds DIO, PYR, PIP and MOR. Each guest solvent formed 1:1 H:G inclusion complexes with the host species, with the exception of DIO, which formed a 2:1 H:G complex. Mixed guest experiments revealed a clear preference for PIP and MOR, while PYR and DIO were less favoured. The host selectivity was demonstrated to be in the order PIP > MOR > PYR > DIO. SCXRD experiments showed that TADDOL5 formed a much shorter (and more linear) (host)O‒H···N(guest) hydrogen bond with the most favoured guest, PIP, compared to those involving MOR and PYR. A (host)O‒H···O(guest) hydrogen bond was also observed in the DIO-containing inclusion complex. A consideration of the Hirshfeld surface interactions was not useful in explaining the host selectivity order for these heterocyclic guests, but thermal analyses confirmed that the most stable complex was the one with favoured PIP, followed by those with PYR, MOR and DIO. TADDOL6, on the other hand, formed 1:1 H:G inclusion compounds with all four of the heterocyclic guest solvents. Experiments in mixed guests showed that the selectivity of this host compound for these guests was in the order PYR > PIP > MOR > DIO, which differed from the TADDOL5 (which favoured PIP and then MOR). Interestingly, the strongest classical hydrogen bond was not formed with the most favoured guest PYR, but with PIP instead (this bond with TADDOL5 was also strongest with PIP, but PIP was favoured in that work). Hirshfeld surface investigations again were not useful in understanding the host selectivity behaviour. However, thermal analyses agreed with the observations made in the mixed guest experiments: the most stable complex was with PYR (favoured) and the least stable one was with DIO (least preferred). , Thesis (MSc) -- Faculty of Science, School of Biomolecular & Chemical Sciences, 2024
- Full Text:
- Date Issued: 2024-12
- Authors: Recchia, Daniella Loridana
- Date: 2024-12
- Subjects: Compounds -- guest/host , Chemistry, Organic , Chemistry
- Language: English
- Type: Master's theses , text
- Identifier: http://hdl.handle.net/10948/69441 , vital:77256
- Description: The host compounds (4R,5R)-bis(diphenylhydroxymethyl)-2-spiro-1’-cyclopentane-1,3-dioxolane (TADDOL5) and (4R,5R)-bis(diphenylhydroxymethyl)-2-spiro-1’-cyclohexane-1,3-dioxolane (TADDOL6) were successfully synthesized after initially reacting diethyl tartrate with either 1,1-dimethoxycyclopentane or 1,1-dimethoxycyclohexane to afford the intermediates diethyl 2-spiro-1’-cyclopentane-1,3-dioxolan-4,5-dicarboxylate or diethyl 2-spiro-1’-cyclohexane-1,3-dioxolan-4,5-dicarboxylate. These were then each subjected to a Grignard addition reaction with PhMgBr to furnish TADDOL5 and TADDOL6 in reasonably high yields (77 and 80%, respectively). Computational calculations were performed on TADDOL5 and TADDOL6 using the software programs Avogadro and ORCA. The optimised geometries of these host molecules were obtained using the MMFF94 force field in Avogadro, while ORCA was used to perform the computational modelling at the BLYP level using the 6-31G*, 6-31G**, 6-311G* and 6-311G** basis sets and, also, the B3LYP functional (with the same basis sets) to obtain the three lowest energy conformers. The final geometries of each conformer for both TADDOL5 and TADDOL6 at the B3LYP 6-311G* level were overlaid with the molecules obtained from their crystal structures. Significantly different geometries were thus noted for the calculated conformers compared with the guest-free TADDOL5 and TADDOL6 structures obtained from the SCXRD experiments. When TADDOL5 was crystallized independently from each of PYR, 2MP, 3MP and 4MP, 1:1 H:G inclusion complexes formed in each instance. This host compound was then investigated for its host separation ability of mixed pyridines through supramolecular chemistry protocols. These mixed guest experiments revealed that TADDOL5 possessed a notable selectivity towards 3MP and PYR (in the absence of 3MP) followed by 4MP and 2MP, and it was shown that TADDOL5 is a suitable host candidate for the separation of many of the mixed pyridines employed here. The results of the SCXRD analyses indicated that the only significant (host)π···π(guest) stacking interaction present was between TADDOL5 and the most favoured guest species PYR and 3MP. Furthermore, significantly shorter (host)O‒H···N(guest) hydrogen bonds were also observed in the complexes formed between this host compound and 3MP and PYR compared with these bonds involving disfavoured 4MP and 2MP. Hirshfeld surface considerations provided an explanation for the affinity of TADDOL5 for PYR (but not 3MP), while thermal analyses successfully explained this affinity: the 3MP-containing complex with the most preferred guest species was the most thermally stable one, followed by TADDOL5·PYR, as obtained through a consideration of the Ton values (the temperature at which the guest release event initiated) of the four complexes. As with TADDOL5, TADDOL6 formed 1:1 H:G inclusion compounds with each of the four pyridines. TADDOL6 was, furthermore, also assessed for its separation ability for mixed pyridines, and these guest competition experiments showed that the selectivity of TADDOL6 was for PYR and 3MP (in the absence of PYR), followed by 4MP and 2MP. (Interestingly, TADDOL5 preferred 3MP and then PYR, while both host compounds disfavoured 4MP and 2MP.) The results obtained in this work indicated that TADDOL6 may also serve as an efficient host candidate for the separation of many of these pyridyl solutions. SCXRD experiments demonstrated that the only significant (host)π···π(guest) stacking interactions were those between TADDOL6 and preferred PYR and 3MP, as was the case for TADDOL5. These experiments also revealed that the strongest (host)O‒H···N(guest) hydrogen bonds were between TADDOL6 and these favoured guest species. A consideration of Hirshfeld surfaces and quantification of the (guest)N···H(host) intermolecular interactions correlated with the host selectivity order, as did thermal analyses, where the Ton values confirmed that the thermal stabilities of these complexes decreased in the guest order PYR > 3MP > 4MP > 2MP. The behaviour of TADDOL5 was further investigated in guest compounds DIO, PYR, PIP and MOR. Each guest solvent formed 1:1 H:G inclusion complexes with the host species, with the exception of DIO, which formed a 2:1 H:G complex. Mixed guest experiments revealed a clear preference for PIP and MOR, while PYR and DIO were less favoured. The host selectivity was demonstrated to be in the order PIP > MOR > PYR > DIO. SCXRD experiments showed that TADDOL5 formed a much shorter (and more linear) (host)O‒H···N(guest) hydrogen bond with the most favoured guest, PIP, compared to those involving MOR and PYR. A (host)O‒H···O(guest) hydrogen bond was also observed in the DIO-containing inclusion complex. A consideration of the Hirshfeld surface interactions was not useful in explaining the host selectivity order for these heterocyclic guests, but thermal analyses confirmed that the most stable complex was the one with favoured PIP, followed by those with PYR, MOR and DIO. TADDOL6, on the other hand, formed 1:1 H:G inclusion compounds with all four of the heterocyclic guest solvents. Experiments in mixed guests showed that the selectivity of this host compound for these guests was in the order PYR > PIP > MOR > DIO, which differed from the TADDOL5 (which favoured PIP and then MOR). Interestingly, the strongest classical hydrogen bond was not formed with the most favoured guest PYR, but with PIP instead (this bond with TADDOL5 was also strongest with PIP, but PIP was favoured in that work). Hirshfeld surface investigations again were not useful in understanding the host selectivity behaviour. However, thermal analyses agreed with the observations made in the mixed guest experiments: the most stable complex was with PYR (favoured) and the least stable one was with DIO (least preferred). , Thesis (MSc) -- Faculty of Science, School of Biomolecular & Chemical Sciences, 2024
- Full Text:
- Date Issued: 2024-12
The on-demand continuous flow generation, separation, and utilization of monosilane gas, a feedstock for solar-grade silicon
- Authors: Mathe, Francis Matota
- Date: 2024-04
- Subjects: Chemistry, Organic , Chemistry , Silicon -- Synthesis
- Language: English
- Type: Doctoral theses , text
- Identifier: http://hdl.handle.net/10948/64179 , vital:73660
- Description: This research is dedicated to the development of a continuous flow process for the production and utilization of monosilane gas. The utilization of continuous flow techniques was instrumental in addressing the challenges and conditions associated with the handling of monosilane gas. Furthermore, the integration of Process Analytical Technologies (PAT) facilitated in-process monitoring and analysis. Chapter one of this research provides an extensive background and literature review encompassing the purification methods of silicon, the latest advancements in the direct synthesis of alkoxysilanes, current synthesis methods for monosilane, the various applications of monosilane, as well as the utilization of continuous flow technology and process analytical technologies. In chapter two, a detailed account of the experimental procedures employed in this research is presented. Chapter three delves into the results derived from each section of the research. The first section discusses an attempt to upscale the continuous flow synthesis of triethoxysilane, based on previous group research. Process Analytical Technologies (PAT), specifically thermocouples, were utilized in this endeavor. The study revealed temperature inconsistencies along the packed bed reactor, which had a notable impact on the reaction capabilities. The subsequent section explores the continuous flow synthesis of monosilane from triethoxysilane. A Design of Experiment (DoE) approach was employed to identify the optimal reaction conditions and compare the effectiveness of two catalysts. The study determined that Amberlyst-A26 emerged as the superior catalyst, offering stability and reasonable conversions over a 24-hour period. In a residence time of 6 minutes and at a temperature of 55 °C, the maximum triethoxysilane conversion of 100% was achieved. PAT, particularly inline FT-IR, was instrumental in monitoring catalyst activity, while continuous flow gas separation techniques facilitated the separation of monosilane. The research also demonstrated further applications of continuous flow techniques in the synthesis of monosilane from tetraethoxysilane and magnesium silicide. The former aimed to , Thesis (PhD) -- Faculty of Science, School of Biomolecular & Chemical Sciences, 2024
- Full Text:
- Date Issued: 2024-04
- Authors: Mathe, Francis Matota
- Date: 2024-04
- Subjects: Chemistry, Organic , Chemistry , Silicon -- Synthesis
- Language: English
- Type: Doctoral theses , text
- Identifier: http://hdl.handle.net/10948/64179 , vital:73660
- Description: This research is dedicated to the development of a continuous flow process for the production and utilization of monosilane gas. The utilization of continuous flow techniques was instrumental in addressing the challenges and conditions associated with the handling of monosilane gas. Furthermore, the integration of Process Analytical Technologies (PAT) facilitated in-process monitoring and analysis. Chapter one of this research provides an extensive background and literature review encompassing the purification methods of silicon, the latest advancements in the direct synthesis of alkoxysilanes, current synthesis methods for monosilane, the various applications of monosilane, as well as the utilization of continuous flow technology and process analytical technologies. In chapter two, a detailed account of the experimental procedures employed in this research is presented. Chapter three delves into the results derived from each section of the research. The first section discusses an attempt to upscale the continuous flow synthesis of triethoxysilane, based on previous group research. Process Analytical Technologies (PAT), specifically thermocouples, were utilized in this endeavor. The study revealed temperature inconsistencies along the packed bed reactor, which had a notable impact on the reaction capabilities. The subsequent section explores the continuous flow synthesis of monosilane from triethoxysilane. A Design of Experiment (DoE) approach was employed to identify the optimal reaction conditions and compare the effectiveness of two catalysts. The study determined that Amberlyst-A26 emerged as the superior catalyst, offering stability and reasonable conversions over a 24-hour period. In a residence time of 6 minutes and at a temperature of 55 °C, the maximum triethoxysilane conversion of 100% was achieved. PAT, particularly inline FT-IR, was instrumental in monitoring catalyst activity, while continuous flow gas separation techniques facilitated the separation of monosilane. The research also demonstrated further applications of continuous flow techniques in the synthesis of monosilane from tetraethoxysilane and magnesium silicide. The former aimed to , Thesis (PhD) -- Faculty of Science, School of Biomolecular & Chemical Sciences, 2024
- Full Text:
- Date Issued: 2024-04
""Of molecules and men"" : inaugural lecture delivered at Rhodes University
- Authors: Kaye, Perry T
- Date: 1989
- Subjects: Biochemistry , Chemistry, Organic , Chemistry
- Language: English
- Type: Text
- Identifier: vital:643 , http://hdl.handle.net/10962/d1020712 , ISBN 0868101842
- Description: Inaugural lecture delivered at Rhodes University , Rhodes University Libraries (Digitisation)
- Full Text:
- Date Issued: 1989
- Authors: Kaye, Perry T
- Date: 1989
- Subjects: Biochemistry , Chemistry, Organic , Chemistry
- Language: English
- Type: Text
- Identifier: vital:643 , http://hdl.handle.net/10962/d1020712 , ISBN 0868101842
- Description: Inaugural lecture delivered at Rhodes University , Rhodes University Libraries (Digitisation)
- Full Text:
- Date Issued: 1989
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