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Photolytic Studies of Aryl and Heteroaryl Nitrenium Ions: Laser Flash Photolysis Studies

dc.contributor.advisorFalvey, Daniel Een_US
dc.contributor.authorThomas, Selina Ivanen_US
dc.description.abstractThe objective of the thesis was to understand the chemical and kinetic behavior of arylnitrenium ions and a heteroaromatic nitrenium ion through photolytic studies. <em>N</em>-(4,4'-dichlorodiphenyl) nitrenium ion and <em>N</em>-(4,4'-dibromodiphenyl) nitrenium ion are the halogenated counterparts of diphenylnitrenium ions and are generated photochemically from their respective <em>N</em>-(4,4'-dihalogenated diphenylamino)-2,4,6-trimethylpyridinium tetrafluoroborate salts. The halogenated diarylnitrenium ions are ground state singlets that live for more than 1 x 10<sup>5</sup> ns in acetonitrile. In the absence of nucleophiles, these ions decay to form a dimerized hydrazine. These ions react with nucleophiles such as water and alcohol at a rate constant of 10<sup>4</sup> - 10<sup>5</sup>M<sup>-1</sup>s<sup>-1</sup> and at diffusion limit with chlorides. With arenes, these ions react via electron transfer mechanism and nucleophilic addition process. The rate constants for the electron transfer mechanisms are between 10<sup>5</sup> - 10<sup>9</sup> M<sup>-1</sup> s<sup>-1</sup> and depend on the Eox of the arenes. Arenes with Eox above 1.78 V showed no reactivity towards the ion. Unlike other diarylnitrenium ions, the halogenated diarylnitrenium ions react with hydrogen atom donors via a hydrogen atom transfer mechanism. The triplet behavior of these ions is attributed to singlet-triplet intersystem crossing facilitated by the lower singlet-triplet energy gap. Therefore, it has been concluded that substituting halogens in diphenylnitrenium ion lowers the singlet-triplet energy gap and increases the lifetime of these ions. (<em>N</em>-Methyl-<em>N</em>-4-biphenylyl) nitrenium ion generated by photolysis was reacted with amino acids and proteins to determine their reactivity with these ions. Eight amino acids were observed to react with the ion at a rate constant of 10<sup>7</sup> - 10<sup>9</sup> M<sup>-1</sup> s<sup>-1</sup>. The rate constants depend on the nucleophilicity of the side chains of the amino acids. In addition, this ion also reacts rapidly with proteins with a rate constant of 10<sup>8</sup> M<sup>-1</sup> s<sup>-1</sup>, comparable to their reactions with ss-DNA. Investigations on generating the quinoline <em>N</em>-oxide nitrenium ions showed that the transient species from the photolysis of 4-azidoquinoline <em>N</em>-oxide (4-AzQO) shows more characteristics of a nitrenium ion. The formation of 4-aminoquinoline <em>N</em>-oxide upon photolysis of 4-AzQO in acetonitrile with 10% sulphuric acid and the electron transfer reactions observed with arenes, indicate that the transient species generated could be a heteroaromatic nitrenium ion. However, more experiments are needed to confirm the assignment.en_US
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dc.titlePhotolytic Studies of Aryl and Heteroaryl Nitrenium Ions: Laser Flash Photolysis Studiesen_US
dc.contributor.publisherDigital Repository at the University of Marylanden_US
dc.contributor.publisherUniversity of Maryland (College Park, Md.)en_US
dc.subject.pqcontrolledChemistry, Organicen_US
dc.subject.pquncontrolledNitrenium ionen_US
dc.subject.pquncontrolledArylnitrenium ionen_US
dc.subject.pquncontrolledAmino Acidsen_US
dc.subject.pquncontrolledQuinoline N-oxide nitrenium ionen_US

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