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The kinetics and associated equilibria of high oxidation state osmium complexesMcFadzean, Belinda Julie January 2007 (has links)
The reduction of osmium tetroxide by a series of alcohols was studied spectrophotometrically. The reaction was observed to occur in two steps, unlike previously reported studies on this reaction. The identities of both reactants and products were established via a range of techniques. Equilibrium and kinetic data were gathered and reaction models were evaluated using equilibrium and kinetic modelling software. The following complexation reaction model emerged that simulates both the equilibrium and kinetic data. Os(VIII) + RCH2OHOs(VI) + RCHO2 Os(VIII) + Os(VI)k+2k1Complexk-2 Conditional rate constants and equilibrium constants were generated. Rate constants for the alcohol reactions were correlated with the Taft σ* constant. The ρ* value obtained (-1.4) is consistent with a hydride transfer mechanism coupled with synchronous removal of the hydroxyl proton. The identity of the osmium(VIII)-osmium(VI) complex has been suggested. Thermodynamic parameters were also reported. The rate constants for benzyl alcohol and 2-chloroethanol deviated from those predicted by the Taft plot. An explanation of enhanced resonance effects is offered for benzyl alcohol and an alternative reaction mechanism, involving proton abstraction, is offered for 2-chloroethanol. The reaction of the oxidation products of alcohols, namely ketones, with osmium tetroxide produced rate constants that were, perhaps surprisingly, far larger than those of the alcohols. A reaction mechanism for the oxidation of the ketones is suggested, which involves the enolate ion as the reactive starting reagent.
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The Revival of Electrochemistry: Electrochemical Deposition of Metals in Semiconductor Related ResearchWang, Chen 08 1900 (has links)
Adherent Cu films were electrodeposited onto polycrystalline W foils from purged solutions of 0.05 M CuSO4 in H2SO4 supporting electrolyte and 0.025 M CuCO3∙Cu(OH)2 in 0.32 M H3BO3 and corresponding HBF4 supporting electrolyte, both at pH = 1. Films were deposited under constant potential conditions at voltages between -0.6 V and -0.2 V versus Ag/AgCl. All films produced by pulses of 10 s duration were visible to the eye, copper colored, and survived a crude test called "the Scotch tape test", which involves sticking the scotch tape on the sample, then peeling off the tape and observing if the copper film peels off or not. Characterization by scanning electron microscopy (SEM)/energy dispersive X-ray (EDX) and X-ray photon spectroscopy (XPS) confirmed the presence of metallic Cu, with apparent dendritic growth. No sulfur impurity was observable by XPS or EDX. Kinetics measurements indicated that the Cu nucleation process in the sulfuric bath is slower than in the borate bath. In both baths, nucleation kinetics does not correspond to either instantaneous or progressive nucleation. Films deposited from 0.05 M CuSO4/H2SO4 solution at pH > 1 at -0.2 V exhibited poor adhesion and decreased Cu reduction current. In both borate and sulfate baths, small Cu nuclei are observable by SEM upon deposition at higher negative overpotentials, while only large nuclei (~ 1 micron or larger) are observed upon deposition at less negative potentials. Osmium metal has been successfully electrodeposited directly onto p-Si (100) from both Os3+ and Os4+ in both sulfuric and perchloric baths. This electrochemical deposition of osmium metal can provide sufficient amount of osmium which overcome ion beam implantation limitations. The deposited metal can undergo further processing to form osmium silicides, such as Os2Si3, which can be used as optical active materials. The higher osmium concentration results in large deposition currents and more negative peak potential due to larger transfer coefficient. No matter which supporting electrolyte is used, no stripping peak exists in this study. The oxidation ability of anion plays an important role in osmium electrodeposition because it will change the silicon substrate conductivity. In our case, perchloric acid oxidized silicon surface severely. Os4+ seems more favorable for reduction but has a stronger oxidization ability to lower the conductivity. The microscopic images verified osmium is deposited on silicon and forms cluster sizes of < 1 µm to > 10 µm. The Rutherford backscattering spectroscopy (RBS) data indicate osmium can diffuse into the silicon as far as 500 nm and the Si crystal structure is unchanged by the process. This means that the Si does not disassociate and migrate into deposited Os. Osmium is distributed randomly throughout the lattice interstitially. It appears field assisted diffusion can significantly drive the Os into Si (100). This finding is very valuable but needs further study.
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Analysis of Ruthenium and Osmium Abundances in Sulfide Minerals from the Sudbury Ores, OntarioHsieh, Shuang-shii 10 1900 (has links)
Page 20 missing from the thesis. / <p> This work was undertaken to evaluate neutron activation analysis as a technique for simultaneous determination of Ru and Os in sulfide minerals by counting the γ radiation of 97Ru and 103Ru, and the β^-radiation of 191Os and 193Os. The samples studied were collected from the Strathcona and Frood-Stobie Cu-Ni sulfide deposits of Sudbury. Sulfide minerals, including pyrrhotite, chalcopyrite, pentlandite and cubanite were separated from samples including representatives of both ore grade and non-commercial material. The minerals were analysed for Ru and Os to determine their concentration ranges in these sulfides, the degree of geochemical coherence of the metals in sulfides from both high grade ore zones and weakly mineralized rocks and their distribution between coexisting sulfides.</p> / Thesis / Master of Science (MSc)
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Os-Sr-Nd-Pb ISOTOPIC AND TRACE ELEMENT STUDY OF MAGMATIC PROCESSES WITHIN THE SIERRA DEL CHICHINAUTZIN VOLCANIC FIELD, TRANS-MEXICAN VOLCANIC BELTCosky, Brian Wright 10 December 2010 (has links)
No description available.
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An Anomalous Breccia in the Mesoproterozoic (~1.1 Ga) Atar Group, Mauritania: Endogenic vs. Exogenic GenesisAden, Douglas J. 22 September 2010 (has links)
No description available.
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Reaction of nucleic acid components with oxo-osmium compounds /Daniel, Francis Bernard January 1974 (has links)
No description available.
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A multinuclear 1H, 13C and 11B solid-state MAS NMR study of 16- and 18-electron organometallic ruthenium and osmium carborane complexesBarry, Nicolas P.E., Kemp, T.F., Sadler, P.J., Hanna, J.V. 20 February 2014 (has links)
Yes / The first 1H, 13C, 31P and 11B solid state MAS NMR studies of electron-
deficient carborane-containing ruthenium and osmium
complexes [Ru/Os(p-cym)(1,2-dicarba-closo-dodecaborane-1,2-
dithiolate)] are reported. The MAS NMR data from these 16-electron
complexes are compared to those of free carborane-ligand
and an 18-electron triphenylphosphine ruthenium adduct, and
reveal clear spectral differences between 16- and 18-electron
organometallic carborane systems in the solid state. / We thank the Swiss National Science Foundation (grant no. PA00P2-145308 to NPEB), the ERC (grant no. 247450 to PJS), EPSRC (grant no. EP/F034210/1) and EC COST Action CM1105 for support. JVH thanks EPSRC and the University of Warwick for partial funding of the solid state NMR infrastructure at Warwick, and acknowledges additional support obtained through Birmingham Science City: Innovative Uses for Advanced Materials in the Modern World (West Midlands Centre for Advanced Materials Project 2), with support from Advantage West Midlands (AWM) and partial funding by the European Regional Development Fund (ERDF).
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The synthesis and unexpected solution chemistry of thermochromic carborane-containing osmium half-sandwich complexesPitto-Barry, Anaïs, South, A., Rodger, A., Barry, Nicolas P.E. 24 December 2015 (has links)
Yes / The functionalisation of the 16-electron complex [Os(η6-p-cymene)(1,2-dicarba-closo-dodecarborane-
1,2-dithiolato)] (1) with a series of Lewis bases to give the 18-electron complexes of general formula
[Os(η6-p-cymene)(1,2-dicarba-closo-dodecarborane-1,2-dithiolato)(L)] (L = pyridine (2), 4-dimethylaminopyridine
(3), 4-cyanopyridine (4), 4-methoxypyridine (5), pyrazine (6), pyridazine (7), 4,4’-bipyridine
(8) and triphenylphosphine (9)) is reported. All 18-electron complexes are in equilibrium in solution with
the 16-electron precursor, and thermochromic properties are observed in some cases (2, 3, 5, 8, and 9).
The binding constants and Gibbs free energies of the equilibria are determined using UV-visible titrations
and their stabilities investigated. Synthetic routes for forcing the formation of the 18-electron species are
proposed, and analytical methods to characterise the equilibria are described. / We thank the Leverhulme Trust (Early Career Fellowship No. ECF-2013-414 to NPEB), and the University of Warwick (Grant No. RD14102 to NPEB).
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Effect of temperature on the nucleation and growth of precious metal nanocrystalsPitto-Barry, Anaïs, Barry, Nicolas P.E. 23 October 2019 (has links)
Yes / Understanding the effect of physical parameters (e.g., temperature) on crystallisation dynamics is of paramount importance for the synthesis of nanocrystals of well‐defined sizes and geometries. However, imaging nucleation and growth is an experimental challenge owing to the resolution required and the kinetics involved. Here, by using an aberration‐corrected transmission electron microscope, we report the fabrication of precious metal nanocrystals from nuclei and the identification of the dynamics of their nucleation at three different temperatures (20, 50, and 100 °C). A fast, and apparently linear, acceleration of the growth rate is observed against increasing temperature (78.8, 117.7, and 176.5 pm min−1, respectively). This work appears to be the first direct observation of the effect of temperature on the nucleation and growth of metal nanocrystals. / The Royal Society. Grant Number: UF150295 Leverhulme Trust. Grant Number: ECF-2013-414 The Academy of Medical Sciences. Grant Number: SBF003\1170
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Géochimie isotopique Re-Os et Pb-Pb : approches environnementale et météoritique /Poirier, André, January 2005 (has links)
Thèse (D.R.Min.) -- Université du Québec à Chicoutimi, programme en association avec l'Université du Québec à Montréal, 2006. / Bibliogr.: f. 95-101. Document électronique également accessible en format PDF. CaQCU
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