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dc.contributor.authorWu, Chia-Hua
dc.date.accessioned2014-11-25T05:30:16Z
dc.date.available2014-11-25T05:30:16Z
dc.date.issued2014-05
dc.identifier.otherwu_chia-hua_201405_phd
dc.identifier.urihttp://purl.galileo.usg.edu/uga_etd/wu_chia-hua_201405_phd
dc.identifier.urihttp://hdl.handle.net/10724/30810
dc.description.abstractThe mechanisms and properties of SN2 halide identity exchange, radical-radical abstraction reactions and hydroxycarbene tunneling reactions are investigated via high accuracy quantum mechanical computations. The origin of the SN2 intrinsic reaction rate enhancement has been addressed in this study. A detailed analysis is performed of R–CH2X + X– (RCH2 = propyl, ethyl, methyl, allyl, benzyl, acetonitrile; X = F, Cl) SN2 identity exchange reactions. In the traditional view, fast SN2 rates for substrates with a multiple bond at Cβ (carbon
adjacent to the reacting Cα center) are primarily due to π-conjugative stabilization in the SN2 transition state. However, our results give a definite answer that electrostatic interactions among Cα, Cβ and the attacking halide anion are the main driving force of the SN2 rate acceleration. The quantum tunneling computations demonstrate that several members of the hydroxycarbene family (R–COH, R = H, methyl, phenyl) are able to penetrate through ~30 kcal mol–1 activation barriers to isomerize to aldehyde derivatives (R–CHO) with half-lives of 1–2 hrs. The intrinsic reaction path is mapped out and the Wentzel–Kramers–Brillouin approximation is used to compute tunneling probabilities. In addition, semi-classical transition state theory shows that multidimensional vibrational coupling increases the half-life by a factor of 3-5 relative to the one-dimensional reaction coordinate analysis. Finally, rigorous one-dimensional reaction profiles are constructed for several radical-radical abstraction reactions using Mukherjee state-specific multireference coupled cluster theory (Mk-MRCC). We demonstrate that the performance of Mk-MRCCSD(T) is superior to other popular multireference methods and its root-mean-square deviation from full CI is only 0.24 kcal mol–1 for binding energies. The energy profile for each level of theory is extrapolated to the complete basis set limit to facilitate future kinetic studies.
dc.languageeng
dc.publisheruga
dc.rightspublic
dc.subjectcomputational chemistry
dc.subjectbasis set extrapolation
dc.subjectfocal point analysis
dc.subjectphysical organic chemistry
dc.subjectSN2 reaction
dc.subjectelectrostatic interactions
dc.subjectπ-conjugative effect
dc.subjectcombustion chemistry
dc.subjectradical-radical interactions
dc.subjectmultireference coupled cluster theory (Mk-MRCC)
dc.subjectquantum tunneling effect
dc.subjecthydroxycarbenes
dc.titleExploring chemical reaction mechanisms via high accuracy ab initio quantum chemistry
dc.typeDissertation
dc.description.degreePhD
dc.description.departmentChemistry
dc.description.majorChemistry
dc.description.advisorWesley D. Allen
dc.description.committeeWesley D. Allen
dc.description.committeeHenry F. Schaefer, III
dc.description.committeeMichael Duncan


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