Mechanisms and Energetics of Alkane Activation by Transition Metal Ions in the Gas Phase

<p>The mechanisms and energetics of alkane activation by transition metal ions in the gas phase are studied using an ion beam apparatus. These investigations concentrate on the reactivity of several early first row transition metal ions (Sc<sup>+</sup>, Ti<sup>+</sup>,...

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Main Author: Tolbert, Margaret A.
Format: Others
Language:en
Published: 1986
Online Access:https://thesis.library.caltech.edu/11868/1/Tolbert_MA_1986.pdf
Tolbert, Margaret A. (1986) Mechanisms and Energetics of Alkane Activation by Transition Metal Ions in the Gas Phase. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/3047-z490. https://resolver.caltech.edu/CaltechTHESIS:10282019-140307646 <https://resolver.caltech.edu/CaltechTHESIS:10282019-140307646>
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spelling ndltd-CALTECH-oai-thesis.library.caltech.edu-118682021-04-17T05:02:14Z https://thesis.library.caltech.edu/11868/ Mechanisms and Energetics of Alkane Activation by Transition Metal Ions in the Gas Phase Tolbert, Margaret A. <p>The mechanisms and energetics of alkane activation by transition metal ions in the gas phase are studied using an ion beam apparatus. These investigations concentrate on the reactivity of several early first row transition metal ions (Sc<sup>+</sup>, Ti<sup>+</sup>, V<sup>+</sup>) and the second row group 8-10 metal ions (Ru<sup>+</sup>, Rh<sup>+</sup>, Pd<sup>+</sup>). The reaction mechanisms are probed using deuterium labelled alkanes. Experimental and theoretical metal-ligand bond dissociation energies are used to help interpret the observed metal ion reactivities.</p> <p>Chapter II provides a detailed study of the reactions of Ru<sup>+</sup>, Rh<sup>+</sup> and Pd<sup>+</sup> with alkanes. The reactivity observed is contrasted to that of their first row congeners Fe<sup>+</sup>, Co<sup>+</sup> and Ni<sup>+</sup>.</p> <p>Chapter III presents a determination of the heterolytic, M<sup>+</sup>-H<sup>-</sup>, and homolytic, M-H, bond dissociation energies for the first and second row group 8-10 metals. A correlation is found between the homolytic bond energies and the metal atom promotion energy to a state derived from an s<sup>1</sup>d<sup>n</sup> electronic configuration.</p> <p>Chapter IV examines the reactions of Ti<sup>+</sup> and V<sup>+</sup> with alkanes and deuterium labelled alkanes. Dehydrogenation mechanisms and deuterium isotope effects are explored.</p> <p>Chapter V reports the unusual reactivity of Sc<sup>+</sup> with alkanes. The ability of Sc<sup>+</sup> to form two strong metal-ligand sigma bonds results in alkane activation processes which are not observed for most other transition metal ions.</p> 1986 Thesis NonPeerReviewed application/pdf en other https://thesis.library.caltech.edu/11868/1/Tolbert_MA_1986.pdf Tolbert, Margaret A. (1986) Mechanisms and Energetics of Alkane Activation by Transition Metal Ions in the Gas Phase. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/3047-z490. https://resolver.caltech.edu/CaltechTHESIS:10282019-140307646 <https://resolver.caltech.edu/CaltechTHESIS:10282019-140307646> https://resolver.caltech.edu/CaltechTHESIS:10282019-140307646 CaltechTHESIS:10282019-140307646 10.7907/3047-z490
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language en
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description <p>The mechanisms and energetics of alkane activation by transition metal ions in the gas phase are studied using an ion beam apparatus. These investigations concentrate on the reactivity of several early first row transition metal ions (Sc<sup>+</sup>, Ti<sup>+</sup>, V<sup>+</sup>) and the second row group 8-10 metal ions (Ru<sup>+</sup>, Rh<sup>+</sup>, Pd<sup>+</sup>). The reaction mechanisms are probed using deuterium labelled alkanes. Experimental and theoretical metal-ligand bond dissociation energies are used to help interpret the observed metal ion reactivities.</p> <p>Chapter II provides a detailed study of the reactions of Ru<sup>+</sup>, Rh<sup>+</sup> and Pd<sup>+</sup> with alkanes. The reactivity observed is contrasted to that of their first row congeners Fe<sup>+</sup>, Co<sup>+</sup> and Ni<sup>+</sup>.</p> <p>Chapter III presents a determination of the heterolytic, M<sup>+</sup>-H<sup>-</sup>, and homolytic, M-H, bond dissociation energies for the first and second row group 8-10 metals. A correlation is found between the homolytic bond energies and the metal atom promotion energy to a state derived from an s<sup>1</sup>d<sup>n</sup> electronic configuration.</p> <p>Chapter IV examines the reactions of Ti<sup>+</sup> and V<sup>+</sup> with alkanes and deuterium labelled alkanes. Dehydrogenation mechanisms and deuterium isotope effects are explored.</p> <p>Chapter V reports the unusual reactivity of Sc<sup>+</sup> with alkanes. The ability of Sc<sup>+</sup> to form two strong metal-ligand sigma bonds results in alkane activation processes which are not observed for most other transition metal ions.</p>
author Tolbert, Margaret A.
spellingShingle Tolbert, Margaret A.
Mechanisms and Energetics of Alkane Activation by Transition Metal Ions in the Gas Phase
author_facet Tolbert, Margaret A.
author_sort Tolbert, Margaret A.
title Mechanisms and Energetics of Alkane Activation by Transition Metal Ions in the Gas Phase
title_short Mechanisms and Energetics of Alkane Activation by Transition Metal Ions in the Gas Phase
title_full Mechanisms and Energetics of Alkane Activation by Transition Metal Ions in the Gas Phase
title_fullStr Mechanisms and Energetics of Alkane Activation by Transition Metal Ions in the Gas Phase
title_full_unstemmed Mechanisms and Energetics of Alkane Activation by Transition Metal Ions in the Gas Phase
title_sort mechanisms and energetics of alkane activation by transition metal ions in the gas phase
publishDate 1986
url https://thesis.library.caltech.edu/11868/1/Tolbert_MA_1986.pdf
Tolbert, Margaret A. (1986) Mechanisms and Energetics of Alkane Activation by Transition Metal Ions in the Gas Phase. Dissertation (Ph.D.), California Institute of Technology. doi:10.7907/3047-z490. https://resolver.caltech.edu/CaltechTHESIS:10282019-140307646 <https://resolver.caltech.edu/CaltechTHESIS:10282019-140307646>
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