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The Synthesis and Characterization of Some N-Hydroxyaminopyrenes

dc.contributor.advisorMcCarry, B. E.
dc.contributor.authorMills, William James
dc.contributor.departmentChemistryen_US
dc.date.accessioned2022-06-27T15:49:18Z
dc.date.available2022-06-27T15:49:18Z
dc.date.issued1990-10
dc.description.abstractNitrated polycyclic aromatic hydrocarbons (nitro-PAH) are environmental contaminants that have been identified in extracts of particulates obtained from automobile exhaust, diesel exhaust, and power plant emissions. One of the most abundant nitro-PAH, 1-nitropyrene, has been found to be a powerful bacterial mutagen and a carcinogen in animal tests. In a bacterial strain (Salmonella tvphimurium TA98) 1- nitropyrene undergoes reduction and concomitant covalent binding to DNA, presumably via the N-hydroxy-l-aminopyrene. This labile compound was prepared by the ascorbic acid reduction of 1-nitrosopyrene and was characterized by high performance liquid chromatography (HPLC), combined liquid chromatography-mass spectrometry (LC-MS), ultraviolet-visible (UV-VIS), fluorescence and nuclear magnetic resonance (NMR) spectroscopy (1H and 15N) . In addition the pH stability and some reactions of this compound were studied. The 1,6- and 1,8-hydroxylaminonitropyrenes derived from the very potent mutagens 1,6- and 1,8 dinitropyrene were also synthesized and characterized by high performance liquid chromatography, ultraviolet-visible and nuclear magnetic resonance spectroscopy (1H and 15N) .en_US
dc.description.degreeMaster of Science (MSc)en_US
dc.description.degreetypeThesisen_US
dc.identifier.urihttp://hdl.handle.net/11375/27672
dc.language.isoenen_US
dc.subjectN-Hydroxyaminopyrenes, synthesis, nitropyrene, nitro-PAH, dinitropyrenesen_US
dc.titleThe Synthesis and Characterization of Some N-Hydroxyaminopyrenesen_US
dc.title.alternativeN-Hydroxyaminopyrenesen_US
dc.typeThesisen_US

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