In the course of attempting to prepare 3,6-bis(hydroxy-methyl)-s-tetrazine via the reduction of 3,6-bis(carboxy)-s-tetrazine with lithium aluminum hydride, it became apparent that the tetrazine ring was cleaved.

A series of compounds were prepared by condensing 2,3-dimethyl-4,9-dioxo-1-(2-propyl)-naphth[2,3-d] imidazolium iodide with various aromatic aldehydes.

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.

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.

The present work is a part of a systematic investigation of the frequency shifts in infrared absorption produced by changing to the anions carbonyl containing acidic compounds.

It is proposed in this thesis that the imperfect systems of Cram and of Schubert be combined with some modifications.

Since 1955 research has been conducted at North Texas State College on diffusion in molten salts. The object of this work was a continuation of the diffusion studies, specifically the diffusion of Pb210 and Cl36 in molten PbCl2-NaCl mixtures.

The turbidimetric method for the determination of lead ion developed in this work is not intended as a replacement for standard analytical procedures, but is presented solely as a laboratory exercise for courses in elementary instructional analysis.

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.

The experiment in this thesis involves a study of some 1-alkyl-1,2-dihydro-3-hydroxybenzo[g]quinoxaline-5,10-diones.

This thesis examines the optical properties of Christiansen filter systems.

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-C14.

The preparation of 3B-(2-mercaptoethylamino)-cholestane was set as the goal of this thesis project.

This paper studies the the synthesis of certain alkoxy compounds of 2,3-dichloro-1,4-naphthoquinone that can be considered chemotherapeutic agents.

Part one of this thesis concerns the polymerizability of some α,β-unsaturated monaldehydes and also relates the synthesis of some new polyaldehydes which have not been reported in the literature. Part two concerns the polymerization of glyoxal, the simplest dialdehyde, and the structure elucidation of this new polymer.

The purpose of this investigation is two-fold. Some new complex compounds, where one of the bidentate molecules is an optically active amino acid, were prepared, and attempts to separate those complex isomers by different methods were made. The replacement of the amino acids by optically inactive ligands was studied.

This paper is an attempt to appraise the usefulness of the dropping gallium electrode (DGE) in fused LiNO3-KNO3, to compare it with the dropping mercury electrode (DME), and to study the DGE in fused LiCl-KCl.

The study of some acylurea derivatives of 2-amino-3-alkylamino- and -3-arylamino-1,4-naphthoquinones was undertaken to determine the course of reaction under conditions similar to those used by J. R. Hoover and A. R. Day to prepare 2-alkyl-1H-naphth[2,3-d] imidazole-4.9-diones from 2-acylamino-3-amino-1,4-naphthoquinones.

The original purpose of this investigation was to attempt to apply the coulostatic method directly to a molten salt system. The inability to duplicate the reported capacity data for this system resulted in an investigation of the probable cause of this discrepancy between the data obtained by these different methods (14, 15).

Transition metal complexes derived from Schiff bases have rendered an important contribution to the development of modern coordination chemistry. Various stable compounds have been prepared having synthetic, biological, and physicochemical interest. In particular, complexes of salicylaldimines, B-ketoamines, and closely related ligand systems have been investigated.

That Lactobacillus arabinosus 17-5, ATCC 8014, can supply its own requirement for the amino acid, lysine, is demonstrated by the fact that the organism is capable of growth in media devoid of lysine. Since the final biosynthetic step in lysine formation in all bacteria studied to date involves the decarboxylation of meso-dlaminopimelic acid (DAP) to produce lysine, it was of interest to determine whether an enzyme catalyzing such a reaction (DAP decarboxylase) is present in L. arabinosus.

In the work undertaken here, NMR has been used to ascertain the structure of some 1,2,4-triazoles. The investigation provides information concerning the structure of potentially tautomeric triazoles such as hydroxy- and aminotriazole. Connected with this aspect of triazole chemistry is the larger problem of mesohydric tautomerism. The present study also yields information for a comparison of substituent effects in triazoles, N-heteroaromatic substances and benzene.

From a review of the published work in the field of cycloadditions, it is evident that further research is needed to establish the mechanism of ketene cycloadditions. This work was initiated with the intent of obtaining kinetic data which will contribute to the elucidation of the mechanism of ketene cycloadditions.

Organolitnium compounds have been employed in synthetic worK for many years. However only during the last decade has much progress been made in establishing the mechanistic pathways for the reactions of these compounds.