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dc.contributor.advisorGarner, Charles M. (Charles Manley), 1957-
dc.contributor.authorFisher, Henry C.
dc.contributor.otherBaylor University. Dept. of Chemistry and Biochemistry.
dc.date.accessioned2006-02-16T17:04:30Z
dc.date.available2006-02-16T17:04:30Z
dc.date.copyright2005.
dc.date.issued2006-02-16T17:04:30Z
dc.identifier.urihttp://hdl.handle.net/2104/1571
dc.descriptionIncludes bibliographical references (p. 148-149).en
dc.description.abstractAn unprecedented reaction, the base-catalyzed fragmentation of pentafluorobenzylic alcohols, was investigated. Studies on a variety of C6F5-derived alcohols show that a dual reaction pathway occurs in mixed solvent systems such as DMSO and methanol. 19F NMR and GC-MS analyses have been used to examine the mechanism of the fragmenation. Other reaction variables, which involved changing the base and/or solvent conditions, have been studied to determine their effect on fragmentation. The relative rates of reactivity of a variety of pentafluorobenzylic alcohols were determined. A new technique to screen metal catalysts rapidly via GC-MS using modified injection port liners has been developed. A variety of interesting reactions of organic molecules catalyzed by metal salts in the gas phase have been discovered. This technique has also been applied to the fragmentation reactions above.en
dc.description.statementofresponsibilityby Henry C. Fisher.en
dc.format.extentxiv, 149 p. : ill.en
dc.format.extent4783137 bytes
dc.format.mimetypeapplication/pdf
dc.language.isoen_USen
dc.rightsBaylor University theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. Contact librarywebmaster@baylor.edu for inquiries about permission.en
dc.subjectChemistry, Organic.en
dc.titleUnique fragmentation of pentafluorobenzylic alcohols and the use of modified injection port liners in the gas chromatographic-based screening for catalytic activity.en
dc.typeThesisen
dc.description.degreeM.S.en
dc.rights.accessrightsWorldwide accessen
dc.contributor.departmentChemistry and Biochemistry.en


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