Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.513455
Title: Kinetic and mechanistic studies of Pd-catalyzed amination of aryl halides
Author: Ferretti, Antonio
Awarding Body: Imperial College London
Current Institution: Imperial College London
Date of Award: 2009
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Abstract:
The Pd-catalyzed amination of aryl halides (Buchwald-Hartwig amination) has become a versatile and widely used technology to synthesize and produce aromatic amines relevant in pharmaceutical and agrochemical industries. The aim of the work presented in this thesis is to achieve a better mechanistic understanding of this reaction. The methodologies used were not traditional and focused on kinetic studies, carried out using in-situ tools, mainly reaction calorimetry. Reactions using different amines have been considered: the kinetic behaviour of a straight-chain primary amine (n-hexylamine) was found to be very different from the kinetics of benzophenone hydrazone. This difference was rationalised by considering the mechanism and by proposing a change in the rate-limiting step. Spectroscopic studies, aimed at determining the catalyst resting state, supported our proposals. We subsequently started studies on the competitive system of two amines and one aryl halide. We found that, surprisingly, the less reactive amine, when in competition, reacted first. This intriguing behaviour was rationalised by considering the Curtin- Hammett principle and by recognizing that in this case selectivity was controlled by relative stability of intermediates, not relative reactivity. This was termed “monopolizing” regime, in contrast to the “major-minor” regime in which the minor but more reactive intermediate produces the major product. Subsequent studies revealed that the benzophenone hydrazone product also binds to the Pd/BINAP catalyst, and, during the hexylamine reaction, inhibits the rate and induces a change in the rate limiting step and catalyst resting state. Reactions using benzophenone imine were then studied. The competitive system of benzophenone imine and benzophenone hydrazone provided an example of a system showing a change from the “monopolizing regime” to the “major-minor” regime. These concepts can be generalized and applied to explain selectivity in other competitive catalytic systems.
Supervisor: Blackmond, Donna Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.513455  DOI: Not available
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