Transition-metal σ-alkynyl complexes are valuable functional materials that have found application as sructural units in the assembly of polymetallic arrays and large molecular structures, reagents for the transfer, oligomerisation or functionalisation of alkynes, magnetic or optical materials and putative components for use in a future molecular-based electronics platform. Many σ-alkynyl complexes are redox-active, undergoing facile oxidation (reduction) at moderate potentials to generate radical cations (anions) in which the charge and spin density can be tuned from being largely metal-centred to alkynyl ligand-centred by variation of the nature of the metal, supporting ligands and alkynyl substituents. This review summarises the diverse ...
The ethynyl-phenylene substituted 2,2′:6′,2′′-terpyridine (tpy) derivatives, 4-(phenyl-ethynyl)-2,2′...
The work described in this dissertation is subdivided into two main parts. Part 1 addresses how new...
The theme of this study is reactivity at the ligand and how remote, relative to the metal, activatio...
Reaction of RuHCl(CO)(PPh3)3 with aryl alkynes HCCC6H4R-4 [1: R = N(C6H4Me-4)2 (a), OMe (b), Me (c),...
This article surveys the current knowledge in metal alkyl complexes with homolytically weak metal–ca...
This thesis sets out to explore the electronic structures and redox properties of organometallic com...
The work described herein focuses on the ability of redox-active ligands to enable multi-electron re...
A series of ruthenium(II) complexes with face-capping [9]ane-S3 ligands are described. The compounds...
My thesis combined a wide variety of research interests and allowed me to gain expertise in a divers...
Many homogeneous and heterogeneous catalyst systems contain one or more transition metals. The wides...
Reactions of the 16-electron ruthenium complex [Ru(dppe)2Cl][PF6] with metal-free and zinc ethynylph...
The structures and optoelectronic properties of tricarbonylrhenium(I) complexes of di(2-pyrazolyl-p-...
A pair of diastereomeric dinuclear complexes, [Tp′(CO)BrW{μ-η2-C,C′-κ2-S,P-C2(PPh2)S}Ru(η5-C5H5)(PPh...
η6-Coordination of arenes to transition metals results in a significant alteration of arene properti...
α-Diimine ligands, in particular 1,4-diazabutadiene (dad) and bis(iminoacenaphthene) (bian) derivati...
The ethynyl-phenylene substituted 2,2′:6′,2′′-terpyridine (tpy) derivatives, 4-(phenyl-ethynyl)-2,2′...
The work described in this dissertation is subdivided into two main parts. Part 1 addresses how new...
The theme of this study is reactivity at the ligand and how remote, relative to the metal, activatio...
Reaction of RuHCl(CO)(PPh3)3 with aryl alkynes HCCC6H4R-4 [1: R = N(C6H4Me-4)2 (a), OMe (b), Me (c),...
This article surveys the current knowledge in metal alkyl complexes with homolytically weak metal–ca...
This thesis sets out to explore the electronic structures and redox properties of organometallic com...
The work described herein focuses on the ability of redox-active ligands to enable multi-electron re...
A series of ruthenium(II) complexes with face-capping [9]ane-S3 ligands are described. The compounds...
My thesis combined a wide variety of research interests and allowed me to gain expertise in a divers...
Many homogeneous and heterogeneous catalyst systems contain one or more transition metals. The wides...
Reactions of the 16-electron ruthenium complex [Ru(dppe)2Cl][PF6] with metal-free and zinc ethynylph...
The structures and optoelectronic properties of tricarbonylrhenium(I) complexes of di(2-pyrazolyl-p-...
A pair of diastereomeric dinuclear complexes, [Tp′(CO)BrW{μ-η2-C,C′-κ2-S,P-C2(PPh2)S}Ru(η5-C5H5)(PPh...
η6-Coordination of arenes to transition metals results in a significant alteration of arene properti...
α-Diimine ligands, in particular 1,4-diazabutadiene (dad) and bis(iminoacenaphthene) (bian) derivati...
The ethynyl-phenylene substituted 2,2′:6′,2′′-terpyridine (tpy) derivatives, 4-(phenyl-ethynyl)-2,2′...
The work described in this dissertation is subdivided into two main parts. Part 1 addresses how new...
The theme of this study is reactivity at the ligand and how remote, relative to the metal, activatio...