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Please use this identifier to cite or link to this item: http://hdl.handle.net/11375/8506
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dc.contributor.advisorKing, G.W.en_US
dc.contributor.authorMeatherall, Charles Roberten_US
dc.date.accessioned2014-06-18T16:43:06Z-
dc.date.available2014-06-18T16:43:06Z-
dc.date.created2010-12-20en_US
dc.date.issued1974-05en_US
dc.identifier.otheropendissertations/3707en_US
dc.identifier.other4724en_US
dc.identifier.other1703367en_US
dc.identifier.urihttp://hdl.handle.net/11375/8506-
dc.description.abstract<p>The 4190 Å absorption (C-) system of selenium dioxide has been studied in the gas phase and has been assigned to the ³B₂ ← X ¹A₁ electronic transition. The three ground state and the three excited state fundamental frequencies for Se⁷⁸O₂¹⁶, Se⁷⁸O₂¹⁸ and Se⁸⁰O₂¹⁶ isotopes are determined from the vibrational analysis. The intensity of the singlet-triplet transition is borrowed via the spin-orbit and the spin-vibronic coupling mechanism. The geometry of selenium dioxide in the excited state has been determined from the rotational analysis of the 2³₀3⁰₁ vibronic band. The intensities of the rotational transitions for this band are borrowed from singlet-singlet transitions between the ¹A₁ ground state and the ¹B₁ and ¹B₂ excited states. Coupling of the electronic and the orbital angular moments in the ³B₂ excited state is closely approximated by that in the Case (b) coupling limit.</p>en_US
dc.subjectChemistryen_US
dc.subjectPhysical Sciences and Mathematicsen_US
dc.subjectChemistryen_US
dc.titleThe 4190 Å Absorptipn System of Selenium Dioxideen_US
dc.typethesisen_US
dc.contributor.departmentChemistryen_US
dc.description.degreeDoctor of Philosophy (PhD)en_US
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