{"id":{"repo_id":"lsu-thes","oai_identifier":"oai:repository.lsu.edu:gradschool_dissertations-1365"},"canonical_url":"https://search.dev.ndltd.org/etd/lsu-thes/oai:repository.lsu.edu:gradschool_dissertations-1365","repository":{"repo_id":"lsu-thes","name":"Lousiana State University","base_url":"https://repository.lsu.edu/do/oai/"},"display":{"title":"Peroxynitrite-mediated oxidations: nitration and nitrosation","abstract":"Using a direct ultraviolet second-derivative spectroscopy method, three peroxynitrite preparative methods were investigated for the nitrite and nitrate present either as impurities or produced during peroxynitrite decomposition: (I) ozonation of azide, reaction of hydrogen peroxide with (II) isoamyl nitrite and (III) nitrous acid. The oxidation of morpholine by peroxynitrite in the presence and absence of added carbonate gives N-nitromorpholine and N-nitrosomorpholine. Nitration and nitrosation of morpholine are catalyzed by low levels of CO2; however, excess CO2 dramatically reduces the yields of nitrosation but not nitration, and the combined yields of the products are about the same under conditions of high and low concentrations of CO2. These data indicate that both nitration and nitrosation by peroxynitrite are free radical processes. The morpholine radical, formed from the reactions of carbonate and/or hydroxyl radicals with morpholine, reacts with either •NO or •NO2 and serves as a common precursor for both products. The peroxynitrite-mediated oxidation of α-tocopherol and γ-tocopherol dispersed in 1,2-dilauroyl-sn-glycero-3-phosphocholine liposomes in the presence and absence of added carbonate gives α-tocopherylquinone and 5-nitro-γ-tocopherol, respectively. The formation of the products is consistent with the current understanding of the free radical nature of oxidations of peroxynitrite and its CO2-adducts; the overall reaction involves a one-electron oxidation of α-tocopherol and γ-tocopherol by HO• or CO3•-, followed by the reaction with •NO2. When α-tocopherol and γ-tocopherol were present in the same liposome and exposed to peroxynitrite, there was preferential oxidation of α-tocopherol over γ-tocopherol. An explanation for the protection of γ-tocopherol by α-tocopherol could be that γ- and α-tocopheryl radicals, formed from the respective reactions of α-tocopherol and γ-tocopherol with HO• or CO3•-, disproportionate to give α-tocopherylquinone and regenerated γ-tocopherol. This is consistent with the lack of protection of γ-tocopherol by α-tocopherol when α-tocopherol and γ-tocopherol dispersed in different liposomes but present in the same incubation mixer are subjected to oxidation by peroxynitrite.","abstract_html":"Using a direct ultraviolet second-derivative spectroscopy method, three peroxynitrite preparative methods were investigated for the nitrite and nitrate present either as impurities or produced during peroxynitrite decomposition: (I) ozonation of azide, reaction of hydrogen peroxide with (II) isoamyl nitrite and (III) nitrous acid. The oxidation of morpholine by peroxynitrite in the presence and absence of added carbonate gives N-nitromorpholine and N-nitrosomorpholine. Nitration and nitrosation of morpholine are catalyzed by low levels of CO<sub>2</sub>; however, excess CO<sub>2</sub> dramatically reduces the yields of nitrosation but not nitration, and the combined yields of the products are about the same under conditions of high and low concentrations of CO<sub>2</sub>. These data indicate that both nitration and nitrosation by peroxynitrite are free radical processes. The morpholine radical, formed from the reactions of carbonate and/or hydroxyl radicals with morpholine, reacts with either <sup>•</sup>NO or <sup>•</sup>NO<sub>2</sub> and serves as a common precursor for both products. The peroxynitrite-mediated oxidation of α-tocopherol and γ-tocopherol dispersed in 1,2-dilauroyl-<i>sn</i>-glycero-3-phosphocholine liposomes in the presence and absence of added carbonate gives α-tocopherylquinone and 5-nitro-γ-tocopherol, respectively. The formation of the products is consistent with the current understanding of the free radical nature of oxidations of peroxynitrite and its CO<sub>2</sub>-adducts; the overall reaction involves a one-electron oxidation of α-tocopherol and γ-tocopherol by HO<sup>•</sup> or CO<sub>3</sub><sup>•-</sup>, followed by the reaction with <sup>•</sup>NO<sub>2</sub>. When α-tocopherol and γ-tocopherol were present in the same liposome and exposed to peroxynitrite, there was preferential oxidation of α-tocopherol over γ-tocopherol. An explanation for the protection of γ-tocopherol by α-tocopherol could be that γ- and α-tocopheryl radicals, formed from the respective reactions of α-tocopherol and γ-tocopherol with HO<sup>•</sup> or CO<sub>3</sub><sup>•-</sup>, disproportionate to give α-tocopherylquinone and regenerated γ-tocopherol. This is consistent with the lack of protection of γ-tocopherol by α-tocopherol when α-tocopherol and γ-tocopherol dispersed in different liposomes but present in the same incubation mixer are subjected to oxidation by peroxynitrite.","abstract_has_math":false,"creators":["Bolzan, Rachel"],"institution":"Chemistry","degree_name":"Doctor of Philosophy (PhD)","degree_level":"Dissertation","degree_discipline":"Chemistry","degree_department":null,"school":null,"contributors":[],"advisors":[],"committee_chairs":[],"committee_members":[],"year":2002,"date_issued":"2002-01-01T08:00:00Z","date_published":"2002-01-01T08:00:00Z","updated_at":"2026-07-24T02:57:30Z","subjects":["mechanism"],"languages":[],"rights":["unrestricted","Release the entire work immediately for access worldwide."],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["etd-0612102-234815","https://repository.lsu.edu/gradschool_dissertations/366"],"render_values":[{"text":"etd-0612102-234815","href":null,"code":true},{"text":"https://repository.lsu.edu/gradschool_dissertations/366","href":"https://repository.lsu.edu/gradschool_dissertations/366","code":true}]}]},"links":{"outbound_url":"https://doi.org/10.31390/gradschool_dissertations.366","outbound_label":"DOI","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:creator","label":"Author","values":["Bolzan, Rachel"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2002-05-22"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2022-05-12T23:08:35Z"]},{"key":"thesis:degree_discipline","label":"Discipline","values":["Chemistry"]},{"key":"thesis:degree_level","label":"Degree Level","values":["Dissertation"]},{"key":"thesis:degree_name","label":"Degree Name","values":["Doctor of Philosophy (PhD)"]},{"key":"thesis:institution_name","label":"Thesis Institution Name","values":["Chemistry"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["mechanism"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:rights","label":"Dc Rights","values":["unrestricted","Release the entire work immediately for access worldwide."]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["etd-0612102-234815","10.31390/gradschool_dissertations.366","https://repository.lsu.edu/gradschool_dissertations/366"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Using a direct ultraviolet second-derivative spectroscopy method, three peroxynitrite preparative methods were investigated for the nitrite and nitrate present either as impurities or produced during peroxynitrite decomposition: (I) ozonation of azide, reaction of hydrogen peroxide with (II) isoamyl nitrite and (III) nitrous acid. The oxidation of morpholine by peroxynitrite in the presence and absence of added carbonate gives N-nitromorpholine and N-nitrosomorpholine. Nitration and nitrosation of morpholine are catalyzed by low levels of CO2; however, excess CO2 dramatically reduces the yields of nitrosation but not nitration, and the combined yields of the products are about the same under conditions of high and low concentrations of CO2. These data indicate that both nitration and nitrosation by peroxynitrite are free radical processes. The morpholine radical, formed from the reactions of carbonate and/or hydroxyl radicals with morpholine, reacts with either •NO or •NO2 and serves as a common precursor for both products. The peroxynitrite-mediated oxidation of α-tocopherol and γ-tocopherol dispersed in 1,2-dilauroyl-sn-glycero-3-phosphocholine liposomes in the presence and absence of added carbonate gives α-tocopherylquinone and 5-nitro-γ-tocopherol, respectively. The formation of the products is consistent with the current understanding of the free radical nature of oxidations of peroxynitrite and its CO2-adducts; the overall reaction involves a one-electron oxidation of α-tocopherol and γ-tocopherol by HO• or CO3•-, followed by the reaction with •NO2. When α-tocopherol and γ-tocopherol were present in the same liposome and exposed to peroxynitrite, there was preferential oxidation of α-tocopherol over γ-tocopherol. An explanation for the protection of γ-tocopherol by α-tocopherol could be that γ- and α-tocopheryl radicals, formed from the respective reactions of α-tocopherol and γ-tocopherol with HO• or CO3•-, disproportionate to give α-tocopherylquinone and regenerated γ-tocopherol. This is consistent with the lack of protection of γ-tocopherol by α-tocopherol when α-tocopherol and γ-tocopherol dispersed in different liposomes but present in the same incubation mixer are subjected to oxidation by peroxynitrite."]},{"key":"dc:title","label":"Title","values":["Peroxynitrite-mediated oxidations: nitration and nitrosation"]}]}],"canonical_facts":{"dc:creator":["Bolzan, Rachel"],"dc:date":["2002-05-22"],"dc:date.available":["2022-05-12T23:08:35Z"],"dc:description.abstract":["Using a direct ultraviolet second-derivative spectroscopy method, three peroxynitrite preparative methods were investigated for the nitrite and nitrate present either as impurities or produced during peroxynitrite decomposition: (I) ozonation of azide, reaction of hydrogen peroxide with (II) isoamyl nitrite and (III) nitrous acid. The oxidation of morpholine by peroxynitrite in the presence and absence of added carbonate gives N-nitromorpholine and N-nitrosomorpholine. Nitration and nitrosation of morpholine are catalyzed by low levels of CO2; however, excess CO2 dramatically reduces the yields of nitrosation but not nitration, and the combined yields of the products are about the same under conditions of high and low concentrations of CO2. These data indicate that both nitration and nitrosation by peroxynitrite are free radical processes. The morpholine radical, formed from the reactions of carbonate and/or hydroxyl radicals with morpholine, reacts with either •NO or •NO2 and serves as a common precursor for both products. The peroxynitrite-mediated oxidation of α-tocopherol and γ-tocopherol dispersed in 1,2-dilauroyl-sn-glycero-3-phosphocholine liposomes in the presence and absence of added carbonate gives α-tocopherylquinone and 5-nitro-γ-tocopherol, respectively. The formation of the products is consistent with the current understanding of the free radical nature of oxidations of peroxynitrite and its CO2-adducts; the overall reaction involves a one-electron oxidation of α-tocopherol and γ-tocopherol by HO• or CO3•-, followed by the reaction with •NO2. When α-tocopherol and γ-tocopherol were present in the same liposome and exposed to peroxynitrite, there was preferential oxidation of α-tocopherol over γ-tocopherol. An explanation for the protection of γ-tocopherol by α-tocopherol could be that γ- and α-tocopheryl radicals, formed from the respective reactions of α-tocopherol and γ-tocopherol with HO• or CO3•-, disproportionate to give α-tocopherylquinone and regenerated γ-tocopherol. This is consistent with the lack of protection of γ-tocopherol by α-tocopherol when α-tocopherol and γ-tocopherol dispersed in different liposomes but present in the same incubation mixer are subjected to oxidation by peroxynitrite."],"dc:identifier":["etd-0612102-234815","10.31390/gradschool_dissertations.366","https://repository.lsu.edu/gradschool_dissertations/366"],"dc:rights":["unrestricted","Release the entire work immediately for access worldwide."],"dc:subject":["mechanism"],"dc:title":["Peroxynitrite-mediated oxidations: nitration and nitrosation"],"thesis:degree_discipline":["Chemistry"],"thesis:degree_level":["Dissertation"],"thesis:degree_name":["Doctor of Philosophy (PhD)"],"thesis:institution_name":["Chemistry"]},"updated_at":"2026-07-24T02:57:30Z"}