No description available.

A series of new 1,5-dimethyl-6-0x0-verdazyl radicals were prepared bearing either a hydroquinone or the 3,5-di-tertiary-butyl phenol substituent in the 3 position of the verdazyl ring as precursors to verdazyl 1 semiquinone diradical anions or verdazyl 1 phenoxyl diradicals. All radical precursor tetrazanes were characterized by 'H / 13c NMR and FTIR spectroscopies, MS, and elemental analysis. Oxidation of the tetrazane precursors with NaI04 or A ~ + gave verdazyl radicals as microcrystalline solids. All verdazyl radicals were characterized by EPR, UV-visible, and FTIR spectroscopies, and high-resolution MS or elemental analysis. All attempts to oxidize the hydroquinone or phenol moieties were unsuccessful as was coordination chemistry with those verdazyls bearing a chelating ortho-hydroquinone. Several molecules were synthesized as building blocks towards tris(2,6- disubstituted-4-pyridy1)methyl radicals where the substituents were ether chloro- or methoxy- groups. All of these building blocks (aldehydes, ester, alcohol, and ketone) were characterized by 'H / 13c NMR and FTIR spectroscopies, MS, and elemental analysis. All attempts to insert a third ring onto bis(2,6-dichloro-4-pyridy1)ketone to give the radical precursor triarylmethanol have been unsuccessful. Supervisor: Dr. R. G. Hicks (Department of Chemistry)

No description available.

Includes bibliographical references. / 381 p. ; / Title page, contents and abstract only. The complete thesis in print form is available from the University Library. / A comprehensive study into the design, understanding and utilisation of free-radical homolytic substitution chemistry / Thesis (D.Sc.)--University of Adelaide, Dept. of Chemistry, 2000?

Several experiments were undertaken to investigate the mechanism of photodechlorination of pentachlorobenzene. The thermal methoxydechlorination reaction of pentachlorobenzene was studied. In DMSO at 50 °C sodium methoxide reacts smoothly with pentachlorobenzene to give three tetrachloroanisole isomers. A second-order kinetic plot for this reaction is linear to high precision, indicating that the reaction is second order overall. The rate of the reaction and the product regioisomer distribution are not affected by the presence of radical traps such as galvinoxyl, by reaction in the absence of oxygen or by benzyne intermediate traps such as 1,3-diphenylisobenzofuran. The rate of the reaction is reduced linearly as the starting mixture is diluted with methanol. These facts suggest that the reaction follows the classical S[subscript N]Ar mechanism. The proposed structure of the pentachlorobenzene radical anion formed by photolysis in the presence of triethylamine is analogous to the σ-complex intermediate in the S[subscript N]Ar reaction. The regiochemistry of these two types of dechlorination was compared and showed a fair correlation. The differences in regiochemistry were attributed to steric effects between the nucleophile and the aromatic ortho chlorine atoms in the S[subscript N]Ar reaction. Tetrachlorophenyl radicals were generated by thermal decomposition of 1 ,2,4,5-tetrachlorobenzeneazotriphenylmethane in the presence of CCl₄ and a hydrogen atom donor. The selectivies of chlorine versus hydrogen or deuterium atom abstraction were determined in several systems and applied to selectivity of atom abstraction observed in photochemical experiments. The results support the hypothesis that, in the photolysis of pentachlorobenzene in the presence of triethylamine, the intermediate tetrachlorophenyl radical exists as an unencumbered free radical rather than in a solvent caged pair with triethylamine. It was anticipated that the rate of photodechlorination would increase in micellar solutions if triethylamine was added. Experiments showed no such expected increase in rate, and showed regiochemistry similar to that of the same reaction in the absence of triethylamine. / Graduation date: 1992

Graduation date: 1992

Thesis (M.A. in Security Studies (Middle East, South Asia, Sub-Saharan Africa))--Naval Postgraduate School, December 2009. / Thesis Advisor(s): Hafez, Mohammad ; Russell, James. "December 2009." Description based on title screen as viewed on January 27, 2010. Author(s) subject terms: Deradicalization, Indonesia, Rehabilitation, Saudi Arabia, Singapore, Yemen. Includes bibliographical references (p. 65-68). Also available in print.

Thesis (Ph. D.)--University of Texas at Austin, 2002. / Vita. Includes bibliographical references. Available also from UMI Company.

Thesis (Ph. D.)--Ohio State University, 2003. / Title from first page of PDF file. Document formatted into pages; contains xxiv, 173 p.: ill. (some co.). Includes abstract and vita. Advisor: Terry A. Miller, Dept. of Chemistry. Includes bibliographical references (p. 171-173).

Thesis (M.S.)--Central Connecticut State University, 2002. / Thesis advisor: Michael A. La Fontaine. " ... in partial fulfillment of the requirements for the degree of Master in Natural Science-Chemistry." Includes bibliographical references (leaves 61-66). Also available via the World Wide Web.