Browsing by Subject "Catalytic"
Now showing 1 - 4 of 4
Results Per Page
Sort Options
Item Carbon-carbon bond formation via catalytic hydrogenation and transfer hydrogenation : application in the total synthesis of bryostatin 7(2012-08) Lu, Yu, active 2012; Krische, Michael J.Under the conditions of transfer hydrogenation employing ortho-cyclometallated iridium C,O-benzoate catalysts, two protocols of iterative chain elongation of 1,3-diols to furnish 1,3-polyols were developed. First, one-directional chain elongation employing mono-protected 1,3-diols as starting materials was achieved. In all cases, high levels of catalyst-directed enantioselectivity and diastereoselectivity were observed. Then, double asymmetric allylation of 1,n-glycols to deliver C₂-symmetric adducts with exceptional level of enantioselectivity was devised. Iterative two-directional elongation of 1,3-diols to furnish 1,3-polyols with high level of catalyst-directed diastereoselectivity was then achieved. Implementation of this methodology and other hydrogenative C-C bond formations proved to be effective means for the preparation of a known bryostatin A-ring fragment and the total synthesis of bryostatin 7.Item Catalytic destruction of monochloramine using granular activated carbon for point of use applications(2013-05) Cherasia, Eric Charles; Katz, Lynn Ellen; Speitel, Gerald E.Chloramines are used for disinfection in many water treatment facilities because of their ability to provide residual protection of water supplies while minimizing the formation of disinfection-by-products. However, chloramines can impart taste and odor to the water, which can lead to customer complaints. Furthermore, the removal of monochloramine from water is essential for certain industries. Previous research at the University of Texas at Austin has demonstrated the potential of several granular activated carbons (GAC) for removal of monochloramine under conditions typical of water treatment plants. The goal of this research project is to further quantify steady-state monochloramine reduction in fixed bed reactors (FBR) with three commercially available GACs, and improve the understanding of the physical and chemical properties that influence removal. The research was divided into 3 phases: 1. A laboratory scale fixed bed reactor experiment was used to quantify steady state monochloramine removal over time. City of Austin tap water viii was used for three GAC types (Jacobi CAT, Norit CAT, Nority CNS) at pH 8 and 9. 2. Physical characterization of each GAC was performed using analysis of nitrogen adsorption isotherms. Specific surface area, pore volume, and pore distribution were determined. Chemical characterization was performed quantitatively using Boehm titrations. Qualitative analysis was performed by analyzing FTIR spectra of untreated activated carbon samples. 3. The Monochloramine Catalysis (MCAT) model was calibrated using results from the Phase 1 and 2 experiments. Simulations of full scale point of use drinking water filters were run for various empty bed contact times and influent monochloramine concentrations. These results were compared against National Sanitation Foundation monochloramine reduction certification criteria. Results show that steady state removal was achieved for all of the activated carbons tested and this removal efficiency can reach nearly 90% using a 0.75-minute empty bed contact time. This steady state performance indicated that catalysis of the monochloramine was occurring, and removal could theoretically occur for very long periods of time. The second stage of the research shows correlation between chemical characteristics (acidity and basicity) and removal efficiency. Furthermore, physical characteristics, mainly micro-porosity, were shown to largely impact performance. Finally, the MCAT model provides a reasonable estimate of steady state removal, and is used to predict full scale point of use performance.Item Synthetic studies of N-heterocycles via catalytic reductive C-C bond formation and tertiary neopentyl substitution(2012-05) Grant, Christopher Donald; Krische, Michael J.; Martin, Stephen F.; Siegel, Dionicio R.; Brodbelt, Jennifer S.; Kerwin, Sean M.Whilst there are a large number of C-C bond forming reactions available for the construction of heterocycles a number of these protocols require the use of stoichiometric organometallic reagents. Since heterocycles are present in the vast majority of pharmaceutical agents the ability to forge these structures efficiently with a minimal amount of stoichiometric metallic waste is important. With this in mind we initiated a series of projects that focus on the use of [pi]-unsaturates to serve as surrogates to toxic, air and moisture sensitive nucleophilic organometallic reagents utilized in traditional C-C bond forming reactions. This has allowed us to develop catalytic couplings of vinyl azines to imines to form branched amines, to couplings of dimethylallene to isatin forming a tert-prenyl hydroxy oxindole and this neopentyl alcohol can be substituted with C-nucleophiles forming two contiguous quaternary all-carbon centers in our synthetic studies tert-prenyl indole alkaloid natural products.Item The design of new ligands and transition metal compounds for the oxidation of organic compounds(2009-06-02) Grill, Joseph MichaelA review of metal-mediated epoxidation is given. Jacobsen's catalyst and the Sharpless asymmetric epoxidation catalyst are discussed. The origins of enantioselectivity are explained using stereochemical models. Several new salen-type ligands were synthesized based on biphenol and binaphthol. The synthesis of these ligands and their subsequent coordination to transition metals were described. The transition metal complexes were structurally characterized by X-ray diffraction of single crystals. The manganese (III) complexes were evaluated for catalytic activity in epoxidation reactions. Despite the fact that these many of these complexes were optically active, little asymmetric induction was observed in any of the epoxidation reactions. The investigation of a soluble nickel salen complex for the epoxidation of olefins led to the discovery of a new heterogeneous catalyst for the epoxidation of ?,?- unsaturated carboxylic acids. Nickel salen complexes, upon reaction with commercial bleach, yield a fine black powder, which we identified as nickel oxide hydroxide-a known but poorly characterized nickel peroxide containing species. The reaction of an aqueous nickel (II) source with commercial bleach also yields nickel oxide hydroxide. This material was characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA). Extremely broad peaks in the X-ray diffraction pattern suggested that this material consisted of particles with a very small diameter and this was confirmed by TEM. This insoluble material was found to function as a heterogeneous catalyst for the epoxidation of ?,?-unsaturated carboxylic acids in the presence of sodium hypochlorite. The high activity of this catalyst in the epoxidation of certain olefins is due in part to its small particle size, which increases the overall surface area of this heterogeneous catalyst. Large particles of nickel oxide hydroxide were prepared and the catalytic activity was comparatively less. The oxidation of several other organic substrates was also explored using this catalyst. Both primary and secondary alcohols can be oxidized with our nickel-based system. Primary alcohols go through an aldehyde intermediate which is then in turn oxidized to the carboxylic acid.