Browsing by Subject "epoxides"
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Item Conversion of CO2 to Polycarbonates and Other Materials: Insights through Computational Chemistry(2014-09-25) Yeung, Andrew DThe use of carbon dioxide as a chemical feedstock for the copolymerization with epoxides to give polycarbonates, and for coupling with hydrocarbons to give carboxylic acids, was probed using computational chemistry. Metal-free systems were modeled at high levels using composite methods that give ?chemical accuracy?, whereas metal-bound systems were studied using density functional theory, benchmarked to these high-accuracy results for confidence. The thermodynamics of polymer vs. cyclic carbonate formation was calculated, and polymer is the exothermic product, whereas cyclic carbonate is the entropic product. The barriers for the metal-free carbonate and alkoxide backbiting reactions were also determined, carbonate backbiting having a higher barrier than alkoxide backbiting. The base degradation of polymers to epoxide co-monomers, and the acid- and base-catalyzed degradation of glycerol carbonate to glycidol were investigated too. Poly(cyclopentene carbonate) preferentially degrades to epoxide co-monomer instead of cyclic carbonate due to angle strain for alkoxide backbiting. Conversely, glycerol carbonate only yields glycidol instead of the isomeric 3-hydroxyoxetane because formation of the latter has a higher barrier. The (salen)Cr(III)- and (salen)Co(III)-catalyzed copolymerization reactions were studied for a variety of epoxides, and the overall displacement of a polymeric carbonate by an epoxide, followed by ring-opening, was found to be rate limiting. Chromium(III)-catalyzed systems have higher free energy barriers than cobalt(III) systems due to enthalpy, which explains why such polymerization reactions have to be run at higher temperatures. The metal-bound polymer carbonate and alkoxide backbiting reactions generally have higher barriers than when unbound, due to the terminal oxygen atoms? reduced nucleophilicity. The carboxylation of metal-hydride and metal-carbon bonds was studied for a series of trans-ML2XY complexes, and thermodynamics of carboxylation of the M-X bond are influenced by M, L, and Y, in decreasing order. Similar cis-complexes did not exhibit as clear trends. Examination of these complexes indicated that the three steps for the overall conversion of hydrocarbons to carboxylic acids (oxidative addition of hydrocarbon, carboxylation, and reductive elimination of the carboxylic acid) must be optimized in parallel for the successful direct synthesis of carboxylic acids.Item Coupling of CO_(2) and CS_(2) with Novel Oxiranes: Polycarbonate vs. Cyclic Carbonate Production(2013-07-09) Wilson, Stephanie JoPolycarbonates are a type of engineering thermoplastic that have countless uses in modern society. Currently, the major industrial production of polycarbonates involves the polycondensation of a diol and phosgene or phosgene derivative. Though there are many advantages to this process, it creates large amounts of waste and requires dangerous chemicals in order to proceed. Over the past four decades, the coupling of CO_(2) and epoxides has grown into a viable, greener alternative for the production of select polycarbonates. The byproduct of this reaction, cyclic carbonates, also have use as polar, high boiling solvents. This dissertation will be divided into three parts. First, the coupling of indene oxide and CO_(2) to form poly(indene carbonate) and cis-indene carbonate will be discussed. Poly(indene carbonate) has the highest Tg yet reported for polymers derived CO_(2) /epoxides coupling, up to 138degreeC. Polycarbonate production requires the use of (salen)Co(III) catalysts and low temperatures, though some cyclic carbonate production is still observed. Selective production of poly(indene carbonate) has been achieved through the use of bifunctional cobalt(III) complexes. The effects of temperature and cosolvent choices on polymer production will be thoroughly discussed. Though polycarbonate is the kinetic product from the coupling of CO_(2) and epoxides, the thermodynamic product is cyclic carbonate. There are six potential mechanisms that yield this undesired byproduct, though there is limited research into which pathways are the most active during polymerization reactions. Temperature-dependent kinetic studies were performed to obtain the activation parameters for the direct, polymer-free coupling of cyclopentene oxide, indene oxide, 1,2-butylene oxide, and styrene oxide with CO_(2) utilizing (salen)CrCl/nBu_(4)NCl to yield their corresponding cyclic carbonates. Additionally, the metal-free backbiting of the singly-coupled styrene oxide/CO_(2) intermediate was simulated utilizing the halohydrin 2-chloro-1-phenylethanol. Finally, the coupling of cyclopentene oxide with carbon disulfide to yield poly[thio]carbonates and cyclic [thio]carbonates utilizing (salen)CrCl/PPNX will be discussed. In each reaction, scrambling of the oxygen and sulfur atoms in both the polymeric and cyclic product is observed. Long reaction times lead to increased amounts of [thio]ether linkages and therefore polymers with lower glass transition temperatures. Insights into both the coupling and scrambling mechanisms will be presented.