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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/6832
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dc.contributor.advisorSmith, D.R.en_US
dc.contributor.authorBrown, Edgar Carlen_US
dc.date.accessioned2014-06-18T16:37:05Z-
dc.date.available2014-06-18T16:37:05Z-
dc.date.created2010-05-28en_US
dc.date.issued1987-10en_US
dc.identifier.otheropendissertations/2136en_US
dc.identifier.other2763en_US
dc.identifier.other1335470en_US
dc.identifier.urihttp://hdl.handle.net/11375/6832-
dc.description.abstract<p>The infrared multiphoton dissociation (IRMPD) of "neat" hexafluoroethane has been investigated for the first time. The stable products of photolysis are CF₄, C₂F₄, C₃F₈ and C₄F₁₀. Product analysis involved tunable diode laser (TDL) and fourier transform infrared spectroscopy, as well as gas chromatography where applicable. The high sensitivity and resolution of the TDL allows for the measurement of the stable products CF₄ and C₂F₄ after irradiation by a single infrared laser pulse.</p> <p>A high frequency modulation TDL technique has been developed to monitor the transient infrared absorptions produced by the IRMPD of various fluorocarbons. The technique was applied to the detection of CF₂ and CF₃ radicals produced by the IRMPD of known precursors. In the case of hexafluoroethane the TDL modulation technique was used to confirm that the primary dissociation pathway involves c-c bond session.</p> <p>The role of added H₂, leading to elimination of CF₄ and increase of C₂F₄ as products, is clarified. Evidence for a second dissociation pathway producing C₂F₅ and a F atom is also presented. The understanding of the overall chemical mechanism of IRMPD of C₂F₆ and reaction of the intermediates formed has been considerably extended.</p>en_US
dc.subjectChemistryen_US
dc.subjectChemistryen_US
dc.titleThe Infrared Multiphoton Dissociation of Hexafluoroethaneen_US
dc.typethesisen_US
dc.contributor.departmentChemistryen_US
dc.description.degreeDoctor of Philosophy (PhD)en_US
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