Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.695504
Title: Immobilised N-heterocyclic carbene metal complexes in catalysis
Author: Collinson, John Michael
ISNI:       0000 0004 5989 4926
Awarding Body: Imperial College London
Current Institution: Imperial College London
Date of Award: 2014
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Abstract:
Transition metal-based catalysts are one of the most powerful tools available to chemists and the development of ligand systems with which to modify their activity is a constant area of research. In the last twenty years N-Heterocyclic carbenes (NHCs) have established themselves at the forefront of organometallic chemistry. To increase the lifetime of the catalyst these ligands are increasingly being immobilised on supports as, this allows recovery and reuse while attempting to retain the activity. Cleaner, greener and safer processes are increasingly important and the recovery of the catalyst by simple separation also removes contamination and enables the possibility of re-use. This thesis describes the development of a new concept to immobilise transition metal complexes through an N-heterocyclic carbene ligand. The introductory Chapter provides an overview of transition metal catalysis, introducing the use of supported catalysis including the use of magnetic nanoparticles to aid the recovery of the catalyst systems. A discussion is included of N-heterocyclic carbene ligands, including their synthesis, activity in catalysis as ligands for metal complexes as well as attempts to support the systems and their use in various reactions. Chapter 2 provides an in-depth introduction to palladium catalysis, focusing on cross-coupling and dehalogenation reactions. The design of palladium catalysts, concentrating on palladium-NHC complexes and covers the use of supported catalysts. The synthesis and immobilisation of a novel palladium carbene complex is also described. The supported and unsupported complexes were screened in the Suzuki-Miyaura reaction and dehalogenation reaction. The activity and recycling properties of the supported catalyst system are discussed. The next Chapter outlines the use of copper-NHC complexes in the 1,3-dipolar cycloaddition reaction of azides and alkynes to form 1,2,3-triazoles. The preparation and characterisation of a novel N-heterocyclic carbene ligand is described, along with the construction of the supported copper systems. These catalysts were then investigated in the cycloaddition reaction and assessed for their activity and recovery. The scope of the reaction is also explored, investigating functional group tolerance. The final Chapter contains experimental procedures and characterisation data for all compounds synthesised during this project.
Supervisor: Díez-González, Silvia ; Wilton-Ely, James ; Long, Nicholas Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.695504  DOI: Not available
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