Abstract Methyldiphenylphosphonium cyclopentadienylide, C5H4PMePh2 (II), has been synthesized and characterized spectroscopically and crystallographically, and has been found to exhibit properties consistent with the zwitterionic structure IIb. New group 6 complexes, (η5-C5H4PMePh2)M(CO)3, have been synthesized and fully characterized. Comparisons of ν(CO) of these complexes with those of the isoelectronic (η6-C6H6)M(CO)3 and [(η5-C5H5)M(CO)3]- suggest that the electron donating ability of the ylide is between that of the cyclopentadienyl anion (Cp-) and benzene, but closer to Cp-. The electronic structures of II and of (η5- C5H4PMePh2)Cr(CO)3 have been investigated using ab initio methodologies. Thermal and photochemical substitutions of the CO ligands of (η5-C5H4PMePh2)M(CO)3 (M = Cr, Mo) by equimolar amounts of PMe3 and PPh3 were not observed, but the ylide is displaced photochemically from (η5-C5H4PMePh2)Mo(CO)3 by excess PMe3 to form fac- Mo(CO)3(PMe3)3 while (η5-C5H4PMePh2)Mo(CO)3 reacts with I2 to form [(η5- C5H4PMePh2)Mo(CO)3I]I. One electron oxidations of (η5-C5H4PMePh2)M(CO)3 (M = Cr, Mo, W) have been performed to give the cationic radicals [(η5-C5H4PMePh2)M(CO)3]+, which undergo dimerization to give dicationic metal-metal bonded dimers ((η5-C5H4PMePh2)M(CO)3)2 2+ in the solid state. These complexes have been fully characterized spectroscopically and crystallographically. It has been determined that the chromium dimer ((η5- C5H4PMePh2)Cr(CO)3)2 2+ undergoes dissociation extensively in solution to the persistent radical cation monomer (η5-C5H4PMePh2)Cr(CO)3 +, but that the heavier metal analogues iii ((η5-C5H4PMePh2)M(CO)3)2 2+ (M = Mo, W) dissociate very little, if at all. The Cr-Cr bond distance of the chromium complex is 3.3509(7) Å, which is the longest Cr-Cr bond distance known for a compound not containing some type of ligand bridging the metalmetal bond. The hitherto unknown indenyl-derived ylide, C9H6PMePh2, has been synthesized and characterized spectroscopically and crystallographically. The chromium tricarbonyl complex of this ligand, (η5-C9H6PMePh2)Cr(CO)3, has been synthesized and characterized spectroscopically and crystallographically. This complex is a mixture of two isomers exhibiting planar chirality generated upon coordination of the ligand. This complex represents the first structurally characterized phosphorus noncyclopentadienylide coordinated in an η5 manner. The spectroscopic and crystallographic behaviour of C9H6PMePh2 demonstrates that this ylide behaves much like the related cyclopentadienylides. / Thesis (Ph.D, Chemistry) -- Queen's University, 2007-09-07 11:46:39.391

This thesis describes studies into Group 5 and Group 6 transition metal imido complexes, with particular emphasis on the development of complexes which can be applied to catalytic processes. Chapter 1 highlights the electronic and structural aspects of the imido and alkylidene ligands. The isolobal analogy between Group 4 bent metallocene. Group 5 half-sandwich imido and Group 6 bis(imido) metal fragments is outlined. In addition, Ziegler-Natta type a-olefin polymerisation and Ring Opening Metathesis Polymerisation (ROMP) are briefly reviewed. Chapter 2 describes initial screening of half-sandwich vanadium imido and chromium bis((^t)butylimido) dichloride complexes as catalyst precursors. Synthesis of the chromium bis(imido) dialkyl complex Cr(N(^t)Bu)(_2)(CH(_2)Ph)(_2) (1) is described, its conversion to a cationic alkyl species is probed and the polymerisation activity associated with the resultant compound is addressed. Finally this chapter details the synthesis and characterisation of a range of bis(adamantylimido) chromium complexes. Chapter 3 presents a synthetic entry point into the bis(arylimido) chemistry of chromium. The complex Cr(NAr)(_2)(NH(^t)Bu)Cl (12) is described (Ar = 2,6-(^i)Pr(_2)C(_6)H(_3)) and its conversion to the dichloride complex Cr(NAr)(_2)Cl(_2) (14) is examined. 14 forms the stable monoadduct with pyridine, the X-ray crystallographic study of which reveals a distorted square based pyramidal geometry about the chromium atom. The inclusion of the arylimido ligand at the metal centre allows stabilisation of the chromium bis- phosphine complexes Cr(NAr)(_2)(PMe(_3))(_2) (18) and Cr(NAr)(_2)(PMe(_2)Ph)(_2) (19). The reactivity of 18 towards unsaturated hydrocarbon substrates is briefly investigated. Chapter 4 focuses on the organometallic chemistry of the [Cr(NAr)(_2)] moiety. A range of dialkyl derivatives are isolated and the molecular structures of a selection are solved. The generation of the nascent species [Cr(NAr)(_2)(=CHCMe(_3))] is investigated and the conversion of Cr(NAr)(_2)(CH(_2)CMe(_3))(_2) (24) to Cr(NAr)(-2)(CHDCMe(_3))(C(_6)D(_5)) (25) is the subject of a kinetic study. In chapter 5, the ROMP of a series of amino acid derived norbomene monomers is studied. The resultant polymers are fully characterised and a brief molecular modelling study is carried out on representative polymers chain lengths. Chapter 6 contains experimental details to chapters 2-5.

Diploma thesis is focused on manufacturing process of waveguide filter. Thesis is divided to 8 chapters. There is summarized theory of possible execution of waveguide filter, used materials, their influence and risks during production. Then are described possible steps of realization and necessary relations for its design, simulation and also practical realization. At conclusion are summarized, compared and described reached results.