UNT Theses and Dissertations - 51 Matching Results

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A Study of Asymmetric Syntheses in Coordination Chemistry

Description: Since only one example of an asymmetric synthesis which involved an intermediate containing an optically active ligand has been reported, two questions immediately arise: "Is this type of asymmetric synthesis an isolated example, or is it a stepping stone toward a generalized trend for Co (III) which may be extended to include levo rotatory, as well as dextro rotatory molecules?" In addition, asymmetric synthesis affords a new avenue for synthesizing resolved neutral complexes.
Date: August 1963
Creator: Pennington, David Eugene
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Partner: UNT Libraries
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An Infrared Study of some Ω-Phenyl and Ω-Benzoyl Alkanoic Acids

Description: There is no available information in the literature on interaction between carboxyl hydrogen and ω-phenyl groups. Consequently, it was of interest to seek such interactions. Some form of interaction is evident from the study of the spectra of some phenylalkanoic acids and benzoyalkanoic acids.
Date: August 1963
Creator: Chanslor, Robert Janes
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Synthesis and Infrared Spectra of Substituted Phthalimidines

Description: A number of N-substituted-3-hydroxy-3-phenylphthal-imidines and some of the isomeric amides have been prepared in order to study changes in the infrared spectra of these compounds due to structural changes in the molecule, particularly with reference to a hydroxyl band at 3.0µ and a carbonyl band at 5.75µ.
Date: June 1962
Creator: Reeves, Linda R.
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Infrared Studies of Anions of Barbituric Acids

Description: As long ago as 1881, it was realized that a functional group of atoms in a molecule would cause an absorption band to appear at a particular frequency in the infrared spectrum of the molecule. In more recent years, the concept of characteristic group frequencies has become firmly established and has resulted in the present widespread use of infrared spectroscopy. There appear to have been relatively few studies of infrared absorption of organic acids as compared with their salts.
Date: August 1960
Creator: Barnhart, Richard Lee
Item Type: Refine your search to only Thesis or Dissertation
Partner: UNT Libraries
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Selective Lipid Absorption

Description: An experiment was designed to study in the same animal any preferential absorption of a free fatty acid in the presence of a triglyceride of the same fatty acid. Rats were administered a mixture of free fatty acid and its triglyceride labeled with carbon-13 and carbon-14 respectively. Each isotope in the fed lipid and in the lipid recovered from the gastrointestinal tract was measured. The isotope effect, if any, was studied by administering a mixture of palmitic acid-1-C13 and palmitic acid-1-… more
Date: January 1960
Creator: Marcia, John Albion
Item Type: Refine your search to only Thesis or Dissertation
Partner: UNT Libraries
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Synthesis of Ether-free Organomagnesium Compounds

Description: At the time this work was begun, there was some confusion about the technique necessary for the successful synthesis of organomagnesium compounds in hydrocarbon solvents and without solvents. It was decided to repeat the work of Bryce-Smith and Zakharkin. Thus began the study of the synthesis of organomagnesium compounds without solvents; the study of the reaction products of these organomagnesium compounds in hydrocarbons plus 2-butanone compared to the reaction products of the corresponding … more
Date: August 1967
Creator: Hanicak, John E.
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Some Studies Involving Pyridine N-oxide Reductase

Description: The study herein described involved the detection of pyridine N-oxide reductase activity in cell-free extracts of E. coli 9723, the determination of co-factors necessary for the enzymatic process, a study of the optimum conditions for enzyme catalysis, and a general characterization of the enzyme.
Date: August 1968
Creator: Waters, Samuel Wayne
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Preparation of N-Substituted Hydroxylamines from Oxaziridines

Description: In many series of compounds, intensity of biological activity and chemical reactivity are proportional. Generally whenever a alkyl group replaces a reactive hydrogen atom, as would be the case for an N-substituted hydroxylamine as compared to hydroxylamine, the over-all biological activity of the resulting compound is lower than that of its nonalkylated analogue. Since toxicity and physiological activity are not proportional, this comparison can only suggest possible types of derivatives to p… more
Date: January 1968
Creator: Truitt, Sharon G.
Item Type: Refine your search to only Thesis or Dissertation
Partner: UNT Libraries
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