Synthesis and reactivity of cyclometallated complexes containing nitrogen donor ligands

This thesis describes the synthesis and reactivity of cyclometallated complexes containing nitrogen donor ligands.;Chapter One introduces the general chemistry of cyclometallated complexes containing C,N-bidentate ligands, then describes the mechanism of cyclometallated complexes. This is followed b...

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Main Author: Al-Duaij, Omar Khalid
Published: University of Leicester 2005
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Online Access:http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.423931
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spelling ndltd-bl.uk-oai-ethos.bl.uk-4239312016-12-08T03:22:14ZSynthesis and reactivity of cyclometallated complexes containing nitrogen donor ligandsAl-Duaij, Omar Khalid2005This thesis describes the synthesis and reactivity of cyclometallated complexes containing nitrogen donor ligands.;Chapter One introduces the general chemistry of cyclometallated complexes containing C,N-bidentate ligands, then describes the mechanism of cyclometallated complexes. This is followed by an overview of the applications of cyclometallated complexes.;Chapter Two provides an introduction to hemilability and reviews the synthesis of cyclopalladated complexes containing C,N,X tridentate ligands (X= N, S, O). The synthesis of new cyclopalladated imines containing oxygen-functionalised tethers is described. Coordination of the oxygen is shown to depend on i) the nature of the oxygen donor, ether, alcohol or phenol. ii) the length of the linker. iii) whether the complexes are neutral or cationic.;Chapter Three establishes the scope of acetate-assisted C-H activation for the synthesis of arene ruthenium and Cp*M (M = Ir, Rh) half-sandwich cyclometallated complexes with nitrogen-donor ligands viz. imine, amine, oxadoline and pyridine and with P(OPh)3. The method can activate sp2 C-H bonds of phenyl, pyrrole and thiophene, and one example of an sp3 C-H bond. The method also allows N-H activation of a pyrrole-imine. Preliminary investigations of the mechanism are also described.;Chapter Four reports the reactivity of the cyclometallated half-sandwich complexes (synthesised in chapter three). Alkenes and CO provide simple substitution products. Alkynes are shown to insert regioselectivity into the M-C bond. In some cases subsequent C-C or C-N bond formation occurs to form carbocyclic or heterocyclic products. With PhC-CH, insertion of two molecules can occur to give novel products. Throughout the thesis X-ray crystallography has been used to verify or identify some of the products (>40 structures).546.3University of Leicesterhttp://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.423931http://hdl.handle.net/2381/30095Electronic Thesis or Dissertation
collection NDLTD
sources NDLTD
topic 546.3
spellingShingle 546.3
Al-Duaij, Omar Khalid
Synthesis and reactivity of cyclometallated complexes containing nitrogen donor ligands
description This thesis describes the synthesis and reactivity of cyclometallated complexes containing nitrogen donor ligands.;Chapter One introduces the general chemistry of cyclometallated complexes containing C,N-bidentate ligands, then describes the mechanism of cyclometallated complexes. This is followed by an overview of the applications of cyclometallated complexes.;Chapter Two provides an introduction to hemilability and reviews the synthesis of cyclopalladated complexes containing C,N,X tridentate ligands (X= N, S, O). The synthesis of new cyclopalladated imines containing oxygen-functionalised tethers is described. Coordination of the oxygen is shown to depend on i) the nature of the oxygen donor, ether, alcohol or phenol. ii) the length of the linker. iii) whether the complexes are neutral or cationic.;Chapter Three establishes the scope of acetate-assisted C-H activation for the synthesis of arene ruthenium and Cp*M (M = Ir, Rh) half-sandwich cyclometallated complexes with nitrogen-donor ligands viz. imine, amine, oxadoline and pyridine and with P(OPh)3. The method can activate sp2 C-H bonds of phenyl, pyrrole and thiophene, and one example of an sp3 C-H bond. The method also allows N-H activation of a pyrrole-imine. Preliminary investigations of the mechanism are also described.;Chapter Four reports the reactivity of the cyclometallated half-sandwich complexes (synthesised in chapter three). Alkenes and CO provide simple substitution products. Alkynes are shown to insert regioselectivity into the M-C bond. In some cases subsequent C-C or C-N bond formation occurs to form carbocyclic or heterocyclic products. With PhC-CH, insertion of two molecules can occur to give novel products. Throughout the thesis X-ray crystallography has been used to verify or identify some of the products (>40 structures).
author Al-Duaij, Omar Khalid
author_facet Al-Duaij, Omar Khalid
author_sort Al-Duaij, Omar Khalid
title Synthesis and reactivity of cyclometallated complexes containing nitrogen donor ligands
title_short Synthesis and reactivity of cyclometallated complexes containing nitrogen donor ligands
title_full Synthesis and reactivity of cyclometallated complexes containing nitrogen donor ligands
title_fullStr Synthesis and reactivity of cyclometallated complexes containing nitrogen donor ligands
title_full_unstemmed Synthesis and reactivity of cyclometallated complexes containing nitrogen donor ligands
title_sort synthesis and reactivity of cyclometallated complexes containing nitrogen donor ligands
publisher University of Leicester
publishDate 2005
url http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.423931
work_keys_str_mv AT alduaijomarkhalid synthesisandreactivityofcyclometallatedcomplexescontainingnitrogendonorligands
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