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Spectroscopic Studies Of The Hydrogen-Chlorine Flame, Gonzalo Pizarro

Masters Theses

No abstract provided.

Composition And Structure Of A Stress Relieving Removable Epoxy Resin, Cecelia Victoria Krapcha Carter

Chemistry and Chemical Biology ETDs

The aqueous modification of polyol modified anhydride cured diglycidyl ether of bisphenol A exhibits properties of a brittle solid when subjected to an impulse stress, and properties of a viscous fluid when subjected to a steady state stress. This behavior is markedly different from the nonaqueous system. Early attempts to understand the nature of the change in properties and the physical mechanism involved have not been completely successful. These attempts have typically taken a physical chemistry approach and have not fully investigated the organic nature of the polymer. In order to fully understand a polymer system an important step should …

The Synthesis Of New Maleimide Addition Polymer Precursors, Richard B. Brown

Chemistry & Biochemistry Theses & Dissertations

1H-2,3-dimethylpyrrolo(1,2-a) benzimidazol-l-one (27) and 1H,9H- 2,3,7,8-tetramethyl-bispyrrolo(1,2-a:6,7-a')benzodiimidazo1-1,9-dione (32) have been synthesized from dimethylmaleic anhydride and o-phenylenediamine and 1,2,4,5-tetraaminobenzene, respectively. The presence of reactive olefinic double bonds in the synthesized compounds was of interest as a site for possible addition polymerization.

The synthetic route involved, in both cases, a simple nucleophilic substitution reaction between the diamine(or tetraamine) and the anhydride to form an intermediate amide-acid-amine which rapidly cyclized to the imide amine. The final ring closure required more rigorous conditions and occurred at melt reaction temperatures.

Calculation Of Pseudocontact Shifts For Co( Ch30h)5x2+ Complexes, Jerry Goodisman

Chemistry - All Scholarship

In this article, we calculate pseudocontact shifts for tetragonal high-spin Co(I1) complexes using a crystal field model. Calculated results for the dipolar field strength and its variation with temperature are compared with values derived from experimental measurements on complexes of the form Co(CH30H)5X2+. The calculation involves evaluation of the anisotropy of the magnetic susceptibility, and proceeds by the following steps: (a) from the crystal field parameters Dq, Ds, Dt, and B the three orbital wave functions of lowest energy are found. (b) The effect of spin-orbit coupling over the 12 states (three orbital wave functions coupled with four spin states) …

Steric Effects On The Dimerization Of Alkyl Substituted Aldoketenes, Barbara Carol Pittner

Chemistry Honors Papers

This 34 page thesis uses nmr spectral absorption to examine product yields in reactions of isovaleryl chloride and t-butyl acetyl chloride.

Studies In Transition Metal Chemistry, Steven David Brown

Dissertations and Theses

The electronic and vibrational spectra of liquid chromium pentafluoride have been investigated. They were found to be consistent with a d¹ system that is extensively fluorine-bridged at room temperature. The vibrational spectra were not consistent with C_4v or D_3h monomers.

The Reaction Of Dimethyl-And Di-N-Butylcopper Lithium With 3-Bromo-2-(2-Phenylacetamido) Acrylic Acid, Kim David Richards

All Graduate Theses and Dissertations, Spring 1920 to Summer 2023

The reaction of dimethylcopper lithium and di-n-butylcopper lithium with 3-bromo-2-(2-phenylacetamido) acrylic acid, mp 174 - 175°, produced as major products 3-methyl-2-(2-phenylacetamido) acrylic acid and 3-n-butyl-2-(2-phenylacetamido) acrylic acid, respectively. The dimethylcopper lithium reaction was stereospecific for the E geometrical isomer, mp 198 - 199°, and produced 3-methyl-2-(2-phenylacetamido) acrylic acid and 2-(2-phenylacetamido) acrylic acid in a 3:1 molar ratio, respectively. The di-n-butylcopper lithium reaction produced as the main products 3-n-butyl-2-(2-phenylacetamido) acrylic acid and 2-(2- phenylacetamido) acrylic acid in a 7:1 molar ratio, respectively, with the 3-n-butylacrylic acid comprising 83% of the product. The reaction …

Close Coupling Test Of Classical And Semiclassical Cross Sections For Rotationally Inelastic Ar-N2 Collisions, Russell T. Pack

Faculty Publications

Accurate quantum mechanical close coupling (CC) integral cross sections are reported for rotationally inelastic Ar-N2 collisions at room temperature using an empirical intermolecular potential. These cross sections are used to test the infinite order sudden (IOS) approximation and the results of several methods [classical trajectories (CT), full sudden (SA), generalized phase shift (GPS), and classical limit generalized phase shift (CGPS)] as reported in the preceding paper by Pattengill. The IOS approximation works very well for cross sections involving low rotational states. The CT method works well for all the cross sections examined, justifying the popular belief that the rotational motion …

A Comparative Investigation Of Mammalian Serine Transhydroxymethylases, Sanha Panichajakul

Theses and Dissertations

Serine transhydroxymethylase was purified one thousand-fold from bovine brain and one hundred and twenty-fold from bovine liver. Both enzymes were yellow due to the presence of the coenzyme pyridoxal 5'-phosphate. Polyacrylamide gel electrophoresis of the liver enzyme showed one major band containing 95% of the protein, while in the case of the brain enzyme two major bands of nearly equal intensity were observable. The specific activity of the crude liver enzyme was about sixty times higher than that of brain. The liver enzyme was also more heat stable than the brain enzyme. The purified enzymes exhibited L-allothreonine and L-threonine aldolase …

The Kinetics And Mechanism Of A Free Radical Decay In Aqueous Solution, Denzel Lee Fillmore

Theses and Dissertations

The decomposition of nitrosyl disulfonate ion was studied in strongly alkaline solution of 10-2 to 5 m sodium hydroxide. The decomposition was found to be first-order in both hydroxide and nitrosyl disulfonate ions. A multi-step mechanism involving sulfite ion, sulfite ion radical and nitrosyl monosulfonate ion radical as intermediates was proposed, with the initiating step being the SN2 replacement of a sulfite ion by a hydroxide ion. The rate constant for the initiating step ranged from 1.2 x 10-7 to 2.25 x 10-5 M-1s-1 for the solution concentration range of the study. The products of the decomposition were identified as …

Composition, Time, And Size Distributions Of Airborne Particulate Material In Utah Valley, Douglas R. Lawson

Theses and Dissertations

The Lundgren impactor is used to determine the variations in time and size distributions of particulate matter in Utah Valley. Charged particle X-ray fluorescence is employed in this study to determine elemental concentrations. Air samples are taken during two 24-hour periods in downtown Provo, 24 hours near U.S. Steel Corporation, Geneva Works, and 12 hours at Lindon Elementary School, and diurnal particulate variations are compared. The amounts of lead and bromine are four times greater on a weekday than on a Sunday in downtown Provo, suggesting the effect of the automobile on atmospheric particulate concentrations. Paraffin coated impaction surfaces are …

Development Of Proton-Induced X-Ray Emission Techniques With Application To Multielement Analyses Of Human Autopsy Tissues And Obsidian Artifacts, Kirk Kay Nielson

Theses and Dissertations

A method of trace element analysis using proton-induced X-ray emission (PIXE) techniques with energy dispersive X-ray detection methods is described. Data were processed using the computer program ANALEX. PIXE analysis methods were applied to the analysis of liver, spleen, aorta, kidney medulla, kidney cortex, abdominal fat, pancreas and hair from autopsies of Pima Indians. Tissues were freeze dried and low temperature ashed before analysis. Concentrations were tabulated for K, Ca, Ti, Mn, Fe, Co, Ni, Cu, Zn, Pb, Se, Br, Rb, Sr, Cd and Cs and examined for significant differences related to diabetes. Concentrations of Ca and Sr in aorta, …

Double Beta Decay Of ¹²⁸Te, Edward W. Hennecke, Oliver Manuel, Dwarka D. Sabu

Chemistry Faculty Research & Creative Works

The half-life of ¹²⁸Te relative to the half-life of ¹³⁰Te has been found to be t12128t12130=(1.59±0.05)×10³ by measurement of the ββ-decay products, ¹²⁸Xe and ¹³⁰Xe, in a geologically old (2.4×10⁹ yr) telluride ore. These results yield an upper limit on the lepton nonconservation parameter, η≤0.8×10^-4. RADIOACTIVITY ββ-decay ¹²⁸Te; measured T_1/2=1.5×1024 yr; deduced η≤0.8×10^-4. Detected excess ¹²⁸Xe in old Te ore.

Photochemical Behavior Of Some Nitrogen Heterocyclics, James Wesley Harris

Master's Theses

The compounds, 3,6-dimethoxypyridazine, l,2-dimethyl- 3,6(1H,2H)-pyridazinedione, and 6-methoxy-2-methyl-3(2H)­ pyridazinone, were prepared by using reported preparations. Their photochemistry was investigated and compared to the thermal chemistry and photochemistry of maleic hydrazide.

Electrochemical Machining (Ecm) With Alternating Current, S. J. Shine

Tanzania Journal of Science

Electrochemistry has had several practical uses in industry for a long time; but one of the more recent applications is the machining of metals. Direct current ECM has been applied in industry for the last two decades. However, ECM with alternating current is still in the early stage of research and development. This paper shows that ECM with normal a.c supply is feasible and practicable if special tools are used. ECM with d.c. is first introduced to provide a better insight for the machining with a.c.

Piericiden A Sensitivity, Site 1 Phosphorylation, And Reduced Nicotinamide Adenine Dinucleotide Dehydrogenase During Iron-Limited Growth Of Candida Utilis, John G. Cobley, T. P. Singer, H. Beinert, S. Grossman

Chemistry Faculty Publications

It has been reported that cells of Candida utilis, grown in continuous culture under iron-limited conditions, develop site 1 phosphorylation, without the appearance of piericidin sensitivity and without changes in the iron-sulfur centers of NADH dehydrogenase, on aeration in the presence of cycloheximide, as well as on increasing the supply of iron during growth. These findings were reinvestigated in the present study. The parameters and properties followed during these transitions were sensitivity of NADH oxidation to piericidin, presence or absence of coupling site 1, EPR signals appearing on reduction with NADH or dithionite, the specific activities of NADH oxidase, NADH-ferricyanide …

Properties Of Intercalated 2h-Nbse2, 4hb-Tas2 And 1t-Tas2, S. F. Meyer, R. E. Howard, G. R. Stewart, Juana Vivó Acrivos, T. H. Geballe

Faculty Publications, Chemistry

The layered compounds 2H-NbSe, 24Hb-TaS, 2and 1T-TaS2 have been intercalated with organic molecules; and the resulting crystal structure, heat capacity, conductivity, and superconductivity have been studied. The coordination in the disulfide layers was found to be unchanged in the product phase. Resistance minima appear and the superconducting transition temperature is reduced in the NbSe2 complex. Conversely, superconductivity is induced in the 4Hb-TaS2 complex. Corresponding evidence of a large change of the density of states, negative for 2H-NbSe2 and positive for 4Hb-TaS2, was also observed upon intercalation. The transport properties of all the intercalation complexes show a pronounced dependence upon the …

Properties Of Hxtas2, D. W. Murphy, F. J. Disalvo, G. W. Hull, J. V. Waszczak, S. F. Meyers, G. R. Stewart, S. Early, Juana Vivó Acrivos, T. H. Geballe

Faculty Publications, Chemistry

The preparation of Hx TaS2 (0 < x < 0.87) is described. The compounds are only marginally stable at room temperature, slowly evolving H2S and H2 (and possibly Hp in air). Magnetic susceptibility data show that a low temperature transformation in 2H ... TaS2 (at so•K) is suppressed with the addition of hydrogen, and· at the same time the superconducting transition temperature T c rises from 0.8 to ~4.2•K at x = 0.11. Heat capacity measurements near this concentration show the superconductivity to be a bulk effect. Finally, by correlation of this data with susceptibility and T c measurements in other intercalation compounds, we suggest that the rise of T c (at low electron transfer) is due to suppression of the low temperature transformation and not due to an excitonic mechanism of superconductivity.

The Lippmann Equation And The Ideally Polarizable Electrode, Jean- Pierre Badiali, Jerry Goodisman

Chemistry - All Scholarship

The Lippmann equation for the ideally polarizable interface is normally derived by thermodynamics, using the Gibbs dividing surface. Therefore, the quantities appearing in the Lippmann equation can have no reference to the actual charge distribution in the interfacial region. For example, the quantity referred to as surface charge is actually a sum of surface excesses, rather than the integral of a true charge density. In this article we derive, by statistical mechanical methods, the Lippmann equation for a model at the molecular level, thus giving a precise physical definition to all quantities which appear. First, we derive the conditions for …

Nitrogenous Fertilisers For Cereal Production, M G. Mason

Journal of the Department of Agriculture, Western Australia, Series 4

Among the many factors influencing crop response to nitrogen applications, the most important are the season, soil type, paddock history, time of application and source of nitrogen. Before deciding whether to use nitrogen on a cereal crop, which source to use and at what rate, the farmer needs some understanding of how these factors work.

Tetrazoline Chemistry, Norman Wallace Rokke

Electronic Theses and Dissertations

It was of interest to investigate the chemistry of some tetrazolines since they might be sources of heteroatomic analogues of trimethylenemethane. In addition, they might provide alternate means of synthesis of small ring compounds such as diaziridinones and diaziridineimines. New compounds which were prepared are 1-(2,6-dimethylphenyl)­ tetrazoline-5-one, 1-(2,6-dimethylphenyl)-4-methyltetrazoline-5-one, l-phenyl-4-methyl-5-iminotetrazoline, l-phenyl-4-methyl-5- methyliminotetrazoline, and l-phenyl-4-methyl-5-methyliminotetrazoline methiodide. The mass spectra of the tetrazolines investigated are characterized by ring fragmentations which are helpful in determining their structure. In addition, fragmentation represents one of the few examples of a retro-1,3-dipolar cycloaddition reaction initiated by electron impact. The monosubstituted tetrazolines are thermally unstable. The course of …

Interactions Of Rhenium(V) Chloride And Oxotrichlorobis(Triphenlyphosphine)Rhenium(V) With Selected Solvents, Paul Luther Holm

Electronic Theses and Dissertations

The purpose of this study was to examine the solution interactions of rhenium(V) chloride and oxotrichlorobis(triphenylphosphine)rhenium(V) in a continuation of studies of rhenium(V) chemistry. These goals were accomplished using vacuum line and Schlenk tube techniques. As a result of this work, rhenium(V) chloride was found to dissolve with reaction in 1, 4-dioxane, diethyl ether and acetone. There was only a very small amount of rhenium(V) chloride which dissolved in carbon tetrachloride, chloroform and cyclohexane. Part of what did dissolve was shown by electronic and infrared spectroscopy to be oxotetrachlororhenium(VI) which was present as an impurity in small amounts. Oxotetrachlororhenium(VI) reacts …

Process Control Of Activated Sludge Treatment, Phase Ii, Richard I. Kermode, Robert W. J. Brett, Joseph D. Pault Jr.

KWRRI Research Reports

Material balances on substrate and microorganisms were derived in conjunction with various mixing configurations thought to accurately describe the activated sludge process. These models include the completely mixed with bypass, plug flow, and plug flow with bypass. Two sets of kinetic mechanisms for substrate utilization and bacterial growth were employed.

A feed forward controller was designed from linear approximations of the material balances derived in the completely mixed with bypass mixing model. Utilizing frequency response methods, the controller was found essentially identical to a completely mixed modeled controller developed in a prior investigation.

Through computer simulation the controller's effectiveness was …

Reactions Of Tungsten Carbonyl Complexes Containing Diphenylvinylphosphine, George S. Leotsakos

Masters Theses

A new synthetic route for the production of the tungsten carbonyl complex (OC)₅WPPh₂CH₂CH₂PPh₂ has been discovered. It has been found that lithiumdiphenylphosphide reacts with diphenylvinylphosphinepentacarbonyltungsten(0) in tetrahydrofuran to produce upon hydrolysis a good yield of the pentacarbonyl product […]. No evidence for the formation of secondary products was noted nor was there evidence for preferential attack of the carbonyl group by LiPPh₂ to form a carbene complex.

Diphenylvinylphosphinepentacarbonyltungsten(0) (mp 62-64°C), was prepared for the first time by two different methods.

I. Displacement of aniline from anilinepentacarbonyltungsten(0) complex with diphenylvinylphosphine.

II. …

Nucleophilic Substitution At Phosphorus: Phosphate Thioesters, Ronnie L. Wilde

Electronic Theses and Dissertations

It was my objective to try to determine the mechanism of nucleophilic substitution at phosphorus in monothiophosphate triesters and to apply what I learn to the other phosphate systems. I also tried to obtain more data to show that the Lewis acid-base type complex through the phosphoryl oxygen is existent and does influence the reaction.

3,3-Diphenyl-2-Morpholinone Derivatives Of 2-Amino-2-Deoxy-D-Allose., Ram Babu

University of the Pacific Theses and Dissertations

A new cyclic protective group has been fused to the cis amino alcohol group of benzyl 2-amino-3,5-o-benzylidene-2-deoxyβ-D-Allopyranoside, by way of a unique rearrangements mechanism. To establish the 2-morpholinone structure, chemical studies, such as reduction and acetylation were conducted.

Comparative spectroscopic studies using ir, pmr, and C-13 nmr confirmed the assigned structures.

The 2-morpholinone ring was cleaved by mild alkaline hydrolysis and could be closed again with acetic anhydride in pyridine. An oxazolidinone derivation of benzyl 2-amino-4,6-o-benzylidene-2-deoxyβ-D-allopyranoside was prepared in a quantitative yield by a modification of a known method.

Protective group properties of the oxazolidinone were studied prior to the …

Cyclic 4,6-Oxygen-Acetal Derivatives Of D-Glucopyrano-(2,3: 4',5')-2'-Oxazolidinones., Daniel Vernie Robinson

University of the Pacific Theses and Dissertations

No abstract provided.

Studies On The Characterization And Activiation By Soluble Factor Of A Sodium-Activated, Magnesium-Dependent, Adenosinetriphosphatase In Rat Cerebral Cortex, Alan B. Forrest

University of the Pacific Theses and Dissertations

This study presented evidence for the existence of a membrane-bound, sodium-activated ATPase which does not require potassium ions for its activity. Furthermore, the data suggest the presence of a soluble factor which activates this enzyme and may play a regulatory role in sodium transport.

The Noble Gas Record Of Terrestrial And Meteoritic Samples, Edward W. Hennecke

Doctoral Dissertations

"Analyses of tellurium and xenon in a telluride ore from Kalgoorlie, Australia resulted in the following conclusions:

1. The ratio of the double beta-decay half-life of ¹²⁸Te relative to that of ¹³⁰Te is 1.6 x 10³
2. The double beta-decay half-life of ¹³⁰Te is 1.0 x 10²¹ years.
3. The measured half-lives are consistent with values predicted for a second order process of ordinary beta-decay that occurs with the emission of two neutrinos.

A study of noble gases in Thailand tektites provided the following information on the history of these objects:

1. The isotopic compositions of nonradiogenic Ne, Ar, …

Mechanistic Studies Of Alkylation Of Cobalt(I) By Cyclobutyl Derivatives, Hao Ku

Masters Theses

A study was initiated on the hypothesis, by Ugi and co-workers, that cyclopropyl, cyclobutyl, and cyclopentyl electrophiles might under go nucleophilic substitution reactions with retention of configuration.

The synthesis of benzocyclobutenol and 2-phenylcyclobutyl tosylate is described. The reactions of these tosylates with cobalt(I) "supernucleophiles" gave low yields of products which have not been purified sufficiently for assignment of stereochemistry.

Reaction of cyclopentyl tosylate and phenylethyl tosylate with the "supernucleophiles" cobaloxime(I) and cobalt(salen)(I) is discussed for the advance of future work.