Thesis (Ph. D.)--University of Wyoming, 2006. / Title from PDF title page (viewed on Dec. 21, 2007). Includes bibliographical references.

In dieser Arbeit wurden die Molekülstrukturen und die elektronischen Eigenschaften von Vanadium(IV)- und Oxo-Rhenium(V)-Chelaten mit einem kombinierten molekülmechanisch-quantenchemischen Ansatz untersucht, um sterische und elektronische Effekte der Komplexierung mit einem theoretischen Modell zu quantifizieren. Es konnte gezeigt werden, daß auf diese Weise detaillierte Aussagen zu den Bindungsverhältnissen der Metallchelate getroffen werden können. Die Berechnung der Molekülstrukturen gelingt mit exzellenter Übereinstimmung mit den Kristallstrukturen der Komplexe. Die molekülmechanischen Berechnungen erfolgen auf der Grundlage des Extensible Systematic Force Field ESFF und des Consistent Force Field 91 (CFF91). Dabei konnte die hohe Flexibilität und Zuverlässigkeit des regelbasierten ESFF für eine Vielzahl verschiedenster Metallchelate nachgewiesen werden. Aufgrund der mangelhaften Ergebnisse für trigonal-prismatische Komplexgeometrien mit dem ESFF wurden eine Anpassung des CFF91 für derartige Vanadiumkomplexe vorgenommen. Auf Grundlage von theoretischen Ergebnissen wurden die alternativen Strukturen von isoelektronischen Vanadiumkomplexen berechnet und in Übereinstimmung mit experimentellen Daten, theoretischen Modellen der Komplexchemie und empirischen Fakten eine Hypothese für die Ursache der strukturellen Differenzen erarbeitet.<br> Der hier vorgestellte, kombinierte Algorithmus aus kraftfeldbasierter Geometrieoptimierung und single-point-Rechnung an diesen Strukturen ist ein zuverlässiger und relativ schneller Weg Molekülgeometrien von Metallkomplexen zu berechnen. Er kann somit zur Voraussagen von Komplexstrukturen und zur gezielten Modellierung definierter Koordinationsgeometrien verwendet werden. / In this work the molecular structures and the electronic properties of Vanadium(IV)- and Oxo-Rhenium(V)-chelates have been investigated to quantify steric and electronic effects of complexation. It has been shown, that in this way detailed insight can be gained into the bonding conditions of that metal complexes. Molecular mechanic calculations based on the Extensible Systematic Force Field (ESFF) and the Consistent Force Field 91 (CFF91) have been carried out. High flexibility and reliability of the rule based ESFF has been proven for a large variety of different metal chelates. Due to the poor ESFF-results for trigonal-prismatic complex geometries, a fit of the CFF91 for that species was done. Based on the theoretical results the alternative structure of isoelectronical vanadium(IV)- complexes have been calculated and a hypothesis on the reason for the structural differnces have been stated in accordance with experimental results, theoretical models of complex chemistry, and empirical facts. This combined approach of force field based geometry optimization and single point calculation at these structures has been proven to be a reliable and fast way to get molecular structures of metal complexes. It can be used to predict complex structures for modelling destinct coordination geometries.

This work was initially launched to study the synthesis of low-valent group 13 compounds bearing the bis(imino)pyridine ligand framework. Since its inception, this project has grown beyond the boundaries of group 13 to include low valent tin, silver, and rhenium. Alongside the reports of novel coordination compounds, we utilized computational chemistry to uncover unprecedented interactions which challenge conventional concepts of bonding. Synthesis, characterization, and complimentary computational studies are presented herein. Chapter 1 presents a historical overview of the bis(imino)pyridine ligand as well as our synthetic methodology and characterization of new ligand variants we have contributed to the literature. Chapter 2 presents the synthesis of a series of In(I) and In(III) bis(imino)pyridine complexes with varied sterics. Ligand-metal interaction and effect of ligand steric bulk on complex stability, as well as computational studies highlighting weak covalent interactions will be discussed. Chapter 3 presents the synthesis of Ga(III) bis(imino)pyridine complexes. Reactivity with “GaI” synthon as well as varied-stoichiometry one-pot synthesis attempts to generate low valent Ga-bis(imino)pyridine complexes will be discussed. Chapter 4 presents the synthesis of a series of Tl(I) bis(imino)pyridine complexes with varied sterics analogous to the approach taken with indium(I). Unprecedented weak ligand-metal as well as Tl-arene interactions will be discussed. Chapter 5 presents the synthesis of a series of Sn(II) bis(imino)pyridine complexes with varied sterics and halide substituents. Preferential cation-anion pair formation and attempted reactivity will be discussed. Chapter 6 presents the synthesis of a series of Ag(I) bis(imino)pyridine complexes with varied sterics. Resulting ligand-metal interactions as well as reactivity towards Lewis basic donor ligands will be discussed. Chapter 7 presents the synthesis of first crystallographically authenticated examples of rhenium(I) pincer complexes utilizing the bis(imino)pyridine ligand. Chapter 8 presents a general conclusion to the work.

Heterocyclic organic and organometallic compounds (e.g. polypyrrole), and their derivatives, have been of great interest for conductive polymers due to their novel properties and environmental stability as compared to non-aromatic analogs (e.g. polyacetylene). Our current interests focus upon the potential role of pyridazines in next generation electronic devices that utilize organics as the semiconducting material. Pyridazines, 6-membered aromatic rings with two adjacent nitrogens, are promising candidates for a variety of materials and commercial applications. These molecular electronic materials posses several advantages over traditional inorganic semiconducting materials including lower cost of production, higher processibility, and the ability to function on flexible substrates (so called “plastic electronics”). These compounds offer new materials suitable for a variety of real world applications such as Organic Light Emitting Diodes (OLEDs) and Organic Photovoltaic Cell (OPVs). Our recent efforts has been focused on the synthesis of a variety of 5,6-fused ring pyridazines. These fused heterocycles will serve as synthetic models and building blocks for potential organic or organometallic conducting polymers. Our work is focused on the synthesis of pyridazines and their organometallic rhenium complexes and polymer research. Several aryl-substituted 5,6-fused ring pyridazines have been synthesized and characterized. A pyridazyl complexe of rhenium was synthesized in three steps beginning with a 5,6-fused pyridazine. Off-metal synthesis and characterization of [Re(CO)3{1,2-C5H3(CC6H5N)(CC6H5N)}] and some aryl-substituted pyridazines (1,2-C5H3(CRNH)(CRN); R = C6H5, C4H3S, C8H5S) are reported herein.

The cyanide ligand has frequently been used to prepare clusters with novel magnetic properties due to its ability to provide an efficient pathway for superexchange between metal centers that are bound in an end-to-end fashion. One of the common synthetic approaches in this chemistry is to design suitable cyanide containing precursors and then to react such building blocks with metal complexes consisting of accessible sites. The triphos ligand (triphos: 1,1,1-tris(diphenylphosphinomethyl)ethane) has been employed in this vein to prepare metal complexes, one of which is a five coordinate paramagnetic complex (S = 1/2) with a square pyramidal metal center, [CoII(triphos)(CN)2]. A family of molecular squares, [{MIICl2}2{CoII(triphos)(CN)2}2] (M= Mn (2), Fe (3), Co (4), Ni (5), and Zn (6)), has been synthesized by the reaction of CoII(triphos)(CN)2 and MCl2 (M= Mn, Co, Ni, Zn) or Fe4Cl8(THF)6 in CH2Cl2/EtOH mixture. A series of cyanide-bridged trinuclear complexes, {[Co(triphos)(CN)2]2 [M(MeOH)4]}(ClO4)2 ( M = Mn (7), Fe (8), Co (9), and Ni (10)) and tetranuclear complexes, {[Co(triphos)(CN)2]2[M(MeOH)4]2}(ClO4)4 ([Co2M2] M = Mn (11) and Ni (12)) have been synthesized in a similar fashion by the reaction of CoII(triphos)(CN)2 and M(ClO4)2.6H2O (M= Mn, Fe, Co, Ni) in methanol. The trinuclear compounds (7-9), and tetranuclear complexes (2-6, 11, 12), are characterized by antiferromagnetic coupling between metal centers while magnetic behavior of 10 indicates the presence of ferromagnetic interactions between the paramagnetic metal centers. Interactions between magnetic orbitals of Co(II) and M(II) ions were also investigated by means of the density functional theoretical (DFT) calculations. Another triphos containing building block, [(triphos)Re(CN)3] anion (13), has been employed to prepare derivatives of a cubic SMM cluster with four octahedral Re(II) ions and four tetrahedral Mn(II) sites bridging through cyanide ligand. The reactions of Re(II) precursor with MnI2 and solvated Mn(II) ions resulting in derivatives of Re4Mn4 cube with different ligands attached to the Mn center other than the chloride atom were reported. Our efforts on linking these cubes using organo cyanide ligands such as dicyanamide (dca) and 7,7,8,8-tetracyanoquinodimethane (TCNQ) to form extended networks were also discussed.

The focus of this thesis is to improve upon the existing neutron cross section data for rhenium (Re) in the energy range 0.01 eV to 1 keV. Neutron transmission and capture yield measurements were performed using natural rhenium samples at the Rensselaer Polytechnic Institute Gaerttner Linear Accelerator Center. Measurements were performed using the time of flight method, in which neutron energies are differentiated using the elapsed times between neutron emission from a pulsed neutron source and the subsequent detector interactions. Transmission measurements were performed using ⁶Li glass scintillation detectors. Capture measurements were performed utilizing a 16-segment NaI(Tl) multiplicity detector. Most measurements were performed at a flight path length of 25 meters, with one set of experiments (thermal transmission) performed at 15 meters. The experiments used several metallic, elemental rhenium samples of various thicknesses, ranging from 1 mil to 100 mils. (1 mil = 0.001 inch = 0.0254 mm) Following the reduction of the experimental data, SAMMY was used to perform the data analysis. SAMMY is a shape-fitting Bayesian analysis code that determines resonance parameters by fitting neutron time of flight data using the Reich-Moore approximation of R-matrix theory. The combined transmission and capture yield data analysis determined resonance parameters for rhenium resonances in the energy range of 0.01 eV to 1 keV. The updated rhenium resonance parameters are compared to previously published parameters and ENDF/B-VII.1. / text

published_or_final_version / Chemistry / Doctoral / Doctor of Philosophy

Dans les dispositifs électronique, il est prochainement attendu que la réduction de la taille des composant atteingne prochainement la limite quantique. De ce fait, manipuler l'information quantique apparait comme un nouveau challenge. Les Qubits supraconducteurs basé sur la physique du solide et les Jonctions Josephson sont des systèmes prometteurs qui profitent des avantage des technologies de la micro-électronique. Toutefois, le temps de décohérence des états quantique est encore un facteur limitant. Cette limitation est généralement attribuée à la faible qualité cristalline des matériaux utilisés (défauts cristallins, impuretés). La technique d'épitaxie par jets moléculaires a été utilisé pour la croissance de couches minces de rhénium de haute qualité cristalline sur des substrat de saphir dans un environnement Ultra Haut Vide. Le misfit existant entre les réseaux cristallins du rhénium et du saphir est suffisamment bas pour permettre une croissance épitaxiale du rhénium sur le saphir, mais également une croissance d'une barrière tunnel en oxyde d'aluminium monocristallin sur la couche de rhénium elle-même. Afin d'améliorer la qualité cristallographique de la couche de rhénium, des simulations et de nombreuses techniques de caractérisation ont été utilisées. Puis les propriétés supraconductrices des films de rhénium ont été étudié à des températures ultra basses afin de comparer ces propriétés à la qualité cristallographique de nos films. / In electronic devices, it is expected that the quantum limit will soon be reached with decreasing system size. Therefore, manipulating quantum information appears as a new challenge. Solid state Qubits based on superconducting Josephson junction are promising systems which take advantage of microelectronics technology. However, decoherence time of the quantum states is still a limiting factor. This has been generally ascribed to the poor crystallographic quality of the materials used so far (crystallographic defects, impurities). The Molecular Beam Epitaxy (MBE) technique may be used to grow rhenium (Re) films of high quality on sapphire substrates in an Ultra High Vacuum (UHV) environment. So far, the misfit between Re and sapphire is low enough to permit the growth of a single crystal aluminium oxide thin film on top of the Re layer. In order to improve the crystallographic quality of the Re film, some simulations and several characterizations techniques have been used. Then, the superconducting properties of rhenium films have been studied at Ultra Low Temperature in order to compare with their crystallographic qualities.

Pendant la première année le microscope à microSQUID était mis en fonctionnement. On a avancé sur le plan cryogenique (dilution) et électronique (programmation de boucles de régulation et d'une détection synchrone). Les composants étaient testés à température ambiante et on est en train de tout tester à basse température. Une méthode était conçu pour déterminer la longueur de pénétration du champ magnétique dans un supraconducteur avec les données qui pourront être fait avec notre microscope. Ceci va être utilisé pour l'échantillon PrOs4Sb12. Il s'agit de trancher le débat sur la nature multibande de la supraconductivité dans ce composé. En deuxième année le developpement a continué, en particulière le microscope était mis à froid. Des différents problèmes due aux basses températures (mouvement de moteur, thermalisation, câblage) ont été resolues. Ensuite on a avancé sur le plan informatique, notamment le contrôle de differents composants. Pendant le deuxième année quelques images magnétique ont été faites, validant le concept. En troisième année on a commence a mésurer des domaines magnetiques d'un supraconducteur ferromagnetique (UCoGe) en Avril - Aout. On a obtenu des resultats tres interessants. Le même dispositif sera ainsi opérationnel pour l'imagerie de domaines dans des bolomètres supraconducteurs.

Understanding Earth&rsquo;s accretion and primary differentiation is a long-standing goal of geology. The segregation of FeNi metal from molten silicate to form Earth&rsquo;s core is expected to deplete and fractionate the highly siderophile elements (HSEs). Estimates of the primitive upper mantle (PUM) composition however, reveal only modest HSE depletions and chondritic element ratios. Past experiments to determine if the mantle composition is set by high-temperature metal-silicate equilibrium have involved measuring the solubility of HSEs in silicate melt at conditions more reducing than the iron-wustite (IW) buffer. Accurate determination of solubilities at such conditions has been hindered by the formation of dispersed metal inclusions; this work describes methods to circumvent the problem. Results of three separate studies are presented which document the solubility of Re, Pt and Au in molten silicate which is demonstrably nugget-free. Data obtained from experiments done at 0.1 MPa&ndash;2 GPa, 1573&ndash;2573 K and ~ IW -1.5 to +3 reveal: 1) Re, Pt and Au solubility increases with increasing temperature, 2) Re solubility increases with increasing oxygen fugacity (fO2), consistent with dissolution as oxide species, 3) Below ~ IW +3, Pt and Au solubility increases with decreasing fO2, consistent with dissolution as neutral or silicide species, and 4) that Au is amongst the most soluble HSE in molten silicate, with values increasing with temperature, but insensitive to changes in P, fO2 and melt composition, making it well suited as a geothermometer for core formation. Partition coefficients calculated from these and previous solubility measurements indicate that metal-silicate equilibrium is unable to reproduce the Re/Os and Pt/Os ratios required by PUM Os isotope systematics if simultaneously accounting for the observed absolute element abundances. Instead, results support late accretion of material following core formation, elevating element abundances and endowing chondritic inter-element ratios. Experimental results are incorporated into a terrestrial accretion model, which differs from the standard approach by explicitly accounting for the distribution of oxygen. Model results show siderophile element abundances in PUM are best reproduced if the mantle undergoes oxidation during accretion and metal-silicate equilibrium occurs near the peridotite solidus.