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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
21

... The structure of biphenyl, o-terphenyl and tetraphenylene,

Karle, Isabella Helen Lugoski, Brockway, L. O. January 1900 (has links)
Taken from Thesis (Ph. D.)--University of Michigan, 1944. / "Contribution from the Chemistry laboratory of the University of Michigan." "Reprinted from the Journal of the American chemical society, 66 ... (1944)."
22

The isomerization of cis-trans ethylene isomers by halogen acids ...

Mansfield, Joseph Victor, January 1945 (has links)
Thesis (Ph. D.)--University of Chicago, 1942. / Reproduced from type-written copy. Description based on print version record. Bibliographical foot-notes.
23

The non-isomerization of free radicals in solution ...

Dannley, Ralph L. January 1943 (has links)
Thesis (Ph. D.)--University of Chicago, 1943. / Lithoprinted. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.
24

Studies on the synthesis and stereochemistry of the 16 keto isomers of estrone

Stoutamire, Donald Wesley, January 1957 (has links)
Thesis (Ph. D.)--University of Wisconsin--Madison, 1957. / Typescript. Abstracted in Dissertation abstracts, v. 17 (1957) no. 8, p. 1669-1670. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.
25

Studies in the thermal decomposition of the isomeric hexanes

Chrysochoos, John January 1964 (has links)
An investigation has been made of the pyrolysis of n-hexane, S-methyl-pentane, 3-methyl-pentane, 2, 8-dimethyl-butane and 2,3-dimethyl-butane in a static system at temperatures between 490° and 530°C. The normal pyrolysis and also the pyrolysis inhibited by nitric oxide have been studied. The effect of variation of initial hydrocarbon pressure on the distribution of products and on energies of activation and frequency factors was determined for the uninhibited reactions. The effect of variation in surface-to-volume ratio on rates and on product distribution has also been investigated. A study of factors governing overall reaction rates has provided information on the kinetics of chain termination processes. All pyrolyses at low pressures are significantly inhibited by reactions occurring on the surface of the quartz vessel. Mechanisms have been proposed to account qualitatively for observed decomposition products and the kinetics of pyrolysis of each of the isomers. In the reactions inhibited by nitric oxide, the effect of the pressure of nitric oxide on the rates and product distributions has been examined. The effect of an increase in surface-to-volume ratio on reaction rates and on product distributions has been investigated. The pressure of NO required for maximum inhibition appears to be independent of the partial pressure of the hydrocarbon and also of the nature of the latter. The kinetic and analytical evidence indicates that nitric oxide acts "both homogeneously and heterogeneously as an inhibitor. Significant consumption of nitric oxide was found for all branched isomers. The reduction in inhibition observed as the branching of the isomers increases is attributed in part to increased heterogeneous initiation reactions, from an increase in the extent of adsorption of the more branched isomers relative to the less-branched isomers. A mechanism is proposed for the inhibited pyrolysis of each of the isomers, which accounts qualitatively for the experimental results. A major conclusion drawn from the present study is that nitric oxide acts as an inhibitor through reactions occurring on the surface of the reaction vessel as well as through reactions occurring in the gas phase. / Science, Faculty of / Chemistry, Department of / Graduate
26

Separation of the isotopes and spin isomers of the molecular hydrogens by preferential adsorption at low temperatures /

Haubach, Walter Jennings January 1963 (has links)
No description available.
27

Stereospecific synthesis of Geometric isomers of acyclic C₆₋ conjugated dienes and their reactions /

Roy, Bhairab Nath January 1964 (has links)
No description available.
28

Pharmacological and biochemical studies on disposition of optical isomers of catecholamines /

Garg, Bhagwan Dass January 1972 (has links)
No description available.
29

RCHDCHDX compounds as stereochemical probes : INDO and UMINDO investigations of a test to distinguish erythro and threo diastereomers

Bloss, Richard E. January 1979 (has links)
This research has investigated the validity of a recently proposed test for distinguishing erythro and threo diastereomers of RCHDCHDX compounds on the basis of temperature dependent nmr spectra. INDO and UMINDO semiempirical molecular orbital calculations were used to calculate all nmr vicinal proton-proton coupling constants of a series of CH3CH2CH2X compounds (X = BH2, CH3, NH2, OH, F, PH2, SH, Cl). These data were used to predict the relative temperature dependence of the time-averaged vicinal proton-proton coupling constants of the corresponding CH3CHDCHDX` compounds.Standard bond lengths and angles were used for the input of trial geometries. Coupling constant data were obtained for molecules with no geometry optimization, optimization of the CH3CCX dihedral angle and total geometry optimization. All results suggest that the proposed test for distinguishing erythro and threo diastereomers of RCHDCHDX compounds is valid.
30

Nuclear structure of 86Zr and 20O and beam pulsing techniques

Wiedeking, Mathis. Tabor, Samuel L. Wiedenhoever, Ingo L. January 2004 (has links)
Thesis (Ph. D.)--Florida State University, 2004. / Advisor: Dr. Samuel L. Tabor and Dr. Ingo L. Wiedenhoever, Florida State University, College of Arts and Sciences, Dept. of Physics. Title and description from dissertation home page (viewed June 6, 2005). Document formatted into pages; contains xv, 143 pages. Includes bibliographical references (p. 138-142).

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