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The Nucleophile Carbon 11C/14C Kinetic Isotope Effect for the Reactions between Cyanide Ions and Ethyl Substrates in DMSO
Uppsala University, Teknisk-naturvetenskapliga vetenskapsområdet, Faculty of Science and Technology, Biology, Department of Bioorganic Chemistry.
Manuscript (Other academic)
URN: urn:nbn:se:uu:diva-95362OAI: oai:DiVA.org:uu-95362DiVA: diva2:169543
Available from: 2007-01-05 Created: 2007-01-05 Last updated: 2010-01-13Bibliographically approved
In thesis
1. Isotopes as Mechanism Spies: Nucleophilic Bimolecular Substitution and Monoamine Oxidase B Catalysed Amine Oxidation Probed with Heavy Atom Kinetic Isotope Effects
Open this publication in new window or tab >>Isotopes as Mechanism Spies: Nucleophilic Bimolecular Substitution and Monoamine Oxidase B Catalysed Amine Oxidation Probed with Heavy Atom Kinetic Isotope Effects
2006 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

This thesis concerns the study of reaction mechanisms by means of kinetic isotope effects (KIEs). Studies of the nucleophilic bimolecular substitution (SN2) reaction had the dual purpose of improving our fundamental understanding of molecular reactivity and assessing the ability of kinetic isotope effects to serve as mechanistic tools. The transition state of the SN2 reaction between a cyanide ion and ethyl chloride in tetrahydrofuran was found to be reactant like and only slightly tighter than has been found previously for the same reaction in dimethyl sulphoxide. One conclusion was that the transition-state structure in this reaction was predicted fairly well by the theoretical calculations, even without solvent modelling. The SN2 reactions between cyanide ions and para-substituted benzyl chlorides were found to have reactant-like transition states, of which the Cα-Cl bond was most influenced by the para-substitution. Theoretical calculations indicated that the chlorine KIEs could be used as probes of the substituent effect on the Cα-Cl bond if bond fission was not too advanced in the transition state. Furthermore, the nucleophile carbon 11C/14C KIEs were determined for the reactions between cyanide ions and various ethyl substrates in dimethyl sulphoxide.

Precision conductometry was employed to estimate the aggregation status of tetrabutylammonium cyanide in tetrahydrofuran and in dimethyl sulphoxide, which is of interest as tetrabutylammonium cyanide is frequently used as the nucleophilic reagent in mechanistic investigations and synthetic reactions. The tendency for ion-pair formation was found to be very slight, significant, and very strong in dimethyl sulphoxide, water, and tetrahydrofuran, respectively.

The nitrogen kinetic isotope effect on monoamine oxidase B catalysed deamination of benzylamine was determined in an attempt to obtain conclusive evidence regarding the mechanism of the oxidation. Monoamine oxidase is an important drug target in connection with the treatment of, for example, depression and Parkinson’s disease, and knowledge on how the enzyme effects catalysis would facilitate the design of highly selective and efficient inhibitors.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2006. 93 p.
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 265
Organic chemistry, nucleophilic bimolecular substitution/SN2, kinetic isotope effects, precision conductometry, monoamine oxidase B/MAO B, reaction mechanism, carbon 11C/14C kinetic isotope effect, ion pairing/triple-ion formation, para-substituted benzyl chlorides, tetrabytylammonium cyanide, Organisk kemi
urn:nbn:se:uu:diva-7441 (URN)978-91-554-6776-8 (ISBN)
Public defence
2007-01-27, B22, BMC, Husargatan 3, Uppsala, 09:15
Available from: 2007-01-05 Created: 2007-01-05Bibliographically approved

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