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Articles 1 - 5 of 5
Full-Text Articles in Physical Sciences and Mathematics
Greening Of Catalytic Processes Using First-Row Transition Metals For Atom Transfer Radical Addition And Transfer Hydrogenation, Gabrielle Pros
Greening Of Catalytic Processes Using First-Row Transition Metals For Atom Transfer Radical Addition And Transfer Hydrogenation, Gabrielle Pros
Electronic Theses and Dissertations
This work focused on “greening” catalytic processes, atom transfer radical addition (ATRA), which adds an alkyl halide across and alkene, and transfer hydrogenation/dehydrogenation, which reduces a carbonyl without needing direct H2 gas. Part of “greening” of these processes is through using abundant first row metals, Cu and Ni for catalysis. One aim was to design new ligands which would be more active in these systems; the second was investigation of additives for catalyst regeneration to reduce the catalyst loading necessary for high yields.
The TPMA* family was investigated in ATRA. Rate constants followed the expected trend, which increased …
Engineering Of Escherichia Coli 2-Oxoglutarate Dehydrogenase Complex With Mechanistic And Synthetic Goals, Joydeep Chakraborty
Engineering Of Escherichia Coli 2-Oxoglutarate Dehydrogenase Complex With Mechanistic And Synthetic Goals, Joydeep Chakraborty
Dissertations
The Escherichia coli 2-oxoglutarate dehydrogenase complex (OGDHc) compromises multiple copies of three enzymes - 2-oxoglutarate dehydrogenase (E1o), dihydrolipoyl succinyltransferase (E2o), and dihydrolipoyl dehydrogenase (E3). OGDHc is found in the Krebs cycle and catalyzes the formation of the all-important succinyl-Coenzyme A (succinyl-CoA). OGDHc was engineered to understand the catalytic mechanism and optimized for chemical synthetic goals.
Succinyl-CoA formation takes place within the catalytic domain of E2o via a transesterification reaction. The succinyl group from the thiol ester of S8-succinyldihydrolipoyl-E2o is transferred to the thiol group of CoA. Mechanistic studies were designed to investigate enzymatic transthioesterification. His375 and Asp374 was shown to …
Past, Present, And Future Of Waste Cooking Oil (Beyond Biofuel), Jihyun Kim
Past, Present, And Future Of Waste Cooking Oil (Beyond Biofuel), Jihyun Kim
Open Educational Resources
In this project, students in “General Chemistry” will explore the development of a facile, eco-friendly, and simple preparation method of fluorescent carbon dots (CDs) from a mixture of waste cooking oil and orange waste peels. Orange waste peels are one of the most underutilized bio-waste residues on earth, therefore, it would make better sense to utilize a mixture of the two wastes.
Hydrogen Storage In Formic Acid As A Renewable Energy Source Using Heterogeneous Catalysis, Obaid Aldosari
Hydrogen Storage In Formic Acid As A Renewable Energy Source Using Heterogeneous Catalysis, Obaid Aldosari
Turkish Journal of Chemistry
One of the most vital chemicals, which is not only found naturally but can also be synthesized in the laboratory, is formic acid (FA). FA is a key byproduct of several second-generation biorefinery processes as well, and it is used in several pharmaceutical and industrial applications. Recently, another significant use of FA that is taking the lead is as a form of fuel. This could either involve reformation, as a possible form of chemical hydrogen storage, or be done without reformation in the form of FA fuel cells, in particular because FA fuel cells are much more effective than other …
Sustainable Process For The Production Of Symmetrical Dibasic Acid Ester-Based Thermal Energy Storage Materials From Lipids, Ayhan Yildirim, Kaan Kiraylar
Sustainable Process For The Production Of Symmetrical Dibasic Acid Ester-Based Thermal Energy Storage Materials From Lipids, Ayhan Yildirim, Kaan Kiraylar
Turkish Journal of Chemistry
Oleochemical-based long-chain diesters are potential organic phase change materials convenient for thermal energy storage. The development of efficient and green methods is an important requirement for the preparation of these environmentally friendly compounds, which also are finding wide industrial application. Thus, in the present work, a series of dibasic acid esters were synthesized through ionic liquid catalyzed scalable chemical esterification or transesterification reactions in a solvent-free medium. The starting compounds, dicarboxylic acids or their methyl esters and fatty alcohols or cholesterol, were reacted in the ratio of 1:2 respectively and the synthesized esters were characterized by FT-IR, $^{1}$H NMR, and …