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Substitution Chemistry of Ruthenium Clusters with the Diphosphine Ligands: 4,5-Bis(Diphenylphosphino)-4-Cyclo-Penten-1,3-Dione (bpcd), (Z)-Ph₂PCH=CHPP₂ and 3,4-Bis(Diphenylphosphino)-5-Methoxy-2(5H)-Furanone (bmf) (open access)

Substitution Chemistry of Ruthenium Clusters with the Diphosphine Ligands: 4,5-Bis(Diphenylphosphino)-4-Cyclo-Penten-1,3-Dione (bpcd), (Z)-Ph₂PCH=CHPP₂ and 3,4-Bis(Diphenylphosphino)-5-Methoxy-2(5H)-Furanone (bmf)

The chemistry of transition metal clusters has been a fast developing area of organometallic research in recent years. Compared to mononuclear metal complexes, polynuclear clusters offer more opportunities to study cooperative effects and electron reservoir properties between contiguous metal centers, in addition to functioning as storehouses for the release of catalytically active small fragments capable of exhibiting heterosite subtrate activation. Theoretically, metal clusters are intermediates between mononuclear complexes and metal surfaces, i.e., they serve as a bridge between molecular and solid-state chemistry. Transition metal clusters are ideal candidates to study M-M interactions stretching from the single bond to the collective metallic behavior found in a three-dimensional network of metal atoms. The reaction between the redox-active diphoshpine ligand bpcd and RU(CO) has been examined under a variety of conditions. The disubstituted cluster Ru3(CO)10(bpcd)(2) has been synthesized and shown to contain a chealating bpcd ligand, on the basis of IR and 31P NMR data. The cluster 2 (chelating isomer) undergoes cluster fragmentation at ambient temperatures in the dark to give the binuclear compound 3 and Ru3(CO)12, with no evidence for the formation of 4. Both 3 and 4 have been isolated and fully characterized in solution by IR and NMR spectroscopy, and …
Date: May 1997
Creator: Shen, Huafeng
System: The UNT Digital Library
Solution Studies of ⁶Li Enriched Organolithium Compounds Using New NMR Techniques (open access)

Solution Studies of ⁶Li Enriched Organolithium Compounds Using New NMR Techniques

With the values of 6Li T1 measured and the literature values of J(13C-6Li) for these compounds, three new 13C NMR techniques are developed for the analysis of organolithium compounds. Modifications to the spectrometer are discussed, as well as calibrations of the 6Li decoupler channel needed to set up these new experiments. The theoretical development of each technique is presented, as well as data from their verification, using organolithium compounds of known structure. Once qualified, the new experimental techniques are used to analyze a series of alkyllithium / lithium alkoxide mixed aggregates in solution, where structures and values of J(13C-6Li) may not be known. The combination of Ti relaxation measurements and 13C{1H, 6Li} triple resonance techniques serves as a means of determining the structure of organolithium aggregates in solution.
Date: May 1990
Creator: Ellington, Donald H. (Donald Howard)
System: The UNT Digital Library
Kinetic Study of the Reactions of Oxygen Atoms with Nitric Oxide and Silane (open access)

Kinetic Study of the Reactions of Oxygen Atoms with Nitric Oxide and Silane

The rate constant for the reactions of oxygen atoms with nitric oxide and silane were determined using a discharge flow apparatus. A microwave discharge through O2N2 and Ar was used to produce oxygen atoms. The rate constant for the reaction O + NO + Ar was determined to be (7.0+0.4) x 10^32 cm^6 s^-1 and is in good agreement with previous measurements. Modeling of the O +SiH₄ reaction was performed to determine the correction to the rate constant due to secondary reactions. The rate constant for the reaction O + SiH₄ was determined to be (3.3 +/- 0.3) x 10⁻¹³ cm³ s⁻¹ and is in good agreement with previous measurements. Previous literature, thermochemistry, and spin conservation were used to determine a probable mechanism for the O + SiH₄ reaction.
Date: August 1992
Creator: Taylor, Craig A. (Craig Allan)
System: The UNT Digital Library
Synthesis and 2-D NMR Analysis of a New Phenyl-Substituted Polycyclic Compound (open access)

Synthesis and 2-D NMR Analysis of a New Phenyl-Substituted Polycyclic Compound

Diels-Alder [4+2] cycloaddition of a mixture of 1- and 2 methylcyclopentadiene to 2-phenyl-g.-benzoquinone affords a mixture of four nd cycloadducts. A single, isomerically pure cycloadduct was isolated by careful column chromatography. Stereospecific reduction of this material with sodium borohydride and cerium(III) chloride 'affords a single, isomerically pure tricyclic diol. The structures of the cycloadduct and this tricyclic diol, established via analysis of their one- and two-dimensionial NMR spectra, were shown to be (1-methyl-5-phenyltricyclo[6.2.1.02,7]undec a-4,9 diene-3,6-dione and 1-methyl-5-phenyltricyclo[6.2.1.0 2 ,7 ]undeca-4,9-diene t.&A-3-=.a-6-diol), respectively. Intramolecular [2+2] photocyclization of this tricyclic diol afforded the corresponding cage diol, 3-methyl-7phenylpentacyclo[5.4.0.0 2 ,6 .03 , 1 0 .05, 9 ]undecane-.exogxa-8,11-diol. Oxidation of this cage diol with pyridinium chlorochromate in dry dichloromethane afforded a single, isomerically pure cage hydroxyketone, 3-methyl-7 phenylpentacyclo[5.4.02,6.03,l .1519]undecane-xA-8-ol-II-one, whose structure was established by single crystal X-ray crystallographic methods.
Date: May 1991
Creator: Tsay, Fuh-Rong
System: The UNT Digital Library
A Kinetic Study of the Recombination Reacton Na + SO₂ + Ar (open access)

A Kinetic Study of the Recombination Reacton Na + SO₂ + Ar

The recombination reaction Na + S02 + Ar was investigated at 787 16 K and at pressures from 1.7 to 80 kPa. NaI vapor was photolyzed by an excimer laser at 308 nm to create Na atoms, whose concentration was monitored by time-resolved resonance absorption at 589 nm. The rate constant at the low pressure limit is ko = (2.7 0.2) x 10-21 cm6 molecule-2 s~1. The Na-SO 2 dissociation energy E0 = 170 35 kJ mol1 was calculated with RRKM theory. The equilibrium constant gave a lower limit E0 > 172 kJ mol~ 1. By combination of these two results, E0 = 190 15 kJ mol~ 1 is obtained. The high pressure limit is k, = (1 - 3) x 10-10 cm3 molecule 1 s~1, depending on the extrapolation method used. Two versions of collision theory were employed to estimate k,.. The 'harpoon' model shows the best agreement with experiment.
Date: December 1990
Creator: Shi, Youchun
System: The UNT Digital Library
Aqueous Solubilities and Transformation of Chlorinated Benzenes (open access)

Aqueous Solubilities and Transformation of Chlorinated Benzenes

Aqueous solubilities of twelve chlorinated benzenes were determined by two methods. In one method, the solutions in water were prepared by a vigorous stirring method followed by n-hexane extraction and GC-ECD analysis. In the second method, HPLC was used to prepare the saturated solutions. Experimental results were compared with the predictive values, the relative standard deviations are around 10%. Most of the chlorinated benzenes exhibit water induced transformations. The transformation products were either isomeric or with higher and lower numbers of chlorine substituents. The transformation phenomena can be explained by polarity, symmetry, reactivity of the chlorine atoms, and hydrophobic interactions. The mechanism of the transformation is governed by the radical mechanism.
Date: August 1990
Creator: Wang, Hui-Wen
System: The UNT Digital Library
Synthesis, Structure, and Solution Dynamics of Co₄(CO)₈(dmpe)(mu₄-PPh)₂ (open access)

Synthesis, Structure, and Solution Dynamics of Co₄(CO)₈(dmpe)(mu₄-PPh)₂

Reaction of the tetracobalt cluster Co4(CO)10(t 4-PPh)2 with 1,2-bis(dimethylphosphino)ethane (dmpe) affords the bis-substituted cluster Co4(CO)8(dmpe)(t 4-PPh)2. The bidentate dmpe ligand is shown to bind to the cluster in a chelating fashion by IR, NMR, and X-ray diffractions analyses. The fluxional nature of the ancillary carbonyl groups has been studied by variable temperature 13C NMR measurements which reveal two distinct carbonyl scrambling pathways. The stability of the phosphine-ligated cluster has been examined using in situ Cylindrical Internal Reflection (CIR) Spectroscopy. The effect of the dmpe ligand on the cluster polyhedron will be discussed with respect to the observed crystallographic and spectroscopic results
Date: May 1990
Creator: Schulman, Cheryl Lutins
System: The UNT Digital Library
Static and Flow Properties of Dilute Polymer Solutions (open access)

Static and Flow Properties of Dilute Polymer Solutions

Small weight percentages of certain high-molecular weight polymers added to liquids in turbulent flow through conduits can result in dramatic friction reduction. Although many current and potential uses of the drag reduction phenomenon exist, there is a fundamental problem: drag reduction efficacy decreases rapidly with flow time due to the mechanical degradation in flow of the added polymer. In this thesis study, dilute aqueous solutions of polyacrylamide were tested under turbulent flow conditions in an attempt to determine where mechanical degradation in flow occurs.
Date: August 1991
Creator: Whang, Kyu-ho
System: The UNT Digital Library
The Precipitation of Strontium Sulfate in Gels (open access)

The Precipitation of Strontium Sulfate in Gels

The growth of strontium sulfate precipitate by diffusion in various gels was studied by using optical transmission and confocal microscopies, scanning and transmission electron microscopies, and energy dispersive X ray fluorescence. Pure silica gel, pure agarose gel and the silica/agarose mixed gel at pH 7 - 10 were used throughout the present study. Precipitate morphology is sensitive to pH and to the nature of the growth medium. The morphology was observed as a function of time. The lack of change is presumably because of rapid depletion of the limiting reagent after the very beginning of precipitation. The problem of separating strontium sulfate precipitate from the gel medium is discussed.
Date: December 1991
Creator: Lee, Ya
System: The UNT Digital Library
The Metal-Organic Chemical Vapor Deposition of Cu(II)-bishexafluoroacetylacetonate on a Tungsten Substrate (open access)

The Metal-Organic Chemical Vapor Deposition of Cu(II)-bishexafluoroacetylacetonate on a Tungsten Substrate

Evidence is reported for the formation of carbon-containing contamination products at the copper-tungsten (Cu-W) interface during the metal organic chemical vapor deposition (MOCVD) of copper on tungsten. Cu(II)bishexafluoroacetylacetonate [Cu(hfac)_2] was physisorbed onto lightly oxidized tungsten (WO_x) at 115K, under ultra-high vacuum conditions, and then annealed sequentially to higher temperatures. Copper reduction was observed by 320K. Carbonaceous and carbidic contamination of the WO_x surface was observed, even after sample warming to 625K in UHV. The results indicate that low temperature MOCVD of Cu may be possible, but interfacial contamination from the organic ligand fragmentation is a major concern.
Date: May 1992
Creator: Welton, Theresa E. (Theresa Eilene)
System: The UNT Digital Library
Thermochemical Investigation of Ternary Nonelectrolyte Mixtures (open access)

Thermochemical Investigation of Ternary Nonelectrolyte Mixtures

Excess molar volumes have been determined for four ternary chlorobenzene + dibutyl ether + alkane mixtures at 25°C. Results of these measurements are used to test the applications and limitations of BAB, Redlich-Kister, Kohler and Hwang et al. cubic models. For the systems studied, Redlich- Kister, Kohler and Cubic models were found to provide reasonable predictions. Differences between experimental and predicted ΔV^ex_123 values were about ±0.020 cm^3mol^-1 or less at most ternary compositions. Solubilities are reported for anthracene in binary mixtures containing propanol and butanol with alkanes at 25°C. Results of these measurements are used to test the NIBS/Redlich-Kister expression. The three-parameter form of this expression is found to provide reasonable mathematical representation with deviations between experimental and back-calculated values being less than ±1%.
Date: December 1992
Creator: Teng, I-Lih
System: The UNT Digital Library
Syntheses and Structures of Substituted Polycyclic Molecules and Analysis of the Two-Dimensional NMR Spectrum of Thiele's Ester (open access)

Syntheses and Structures of Substituted Polycyclic Molecules and Analysis of the Two-Dimensional NMR Spectrum of Thiele's Ester

Diels-Alder cycloaddition of methylcyclopentadienes to 2,5-dibromo-p-benzoquinone was performed. A single, isomerically pure cycloadduct was isolated, whose structure was assigned via analysis of its 1-D and 2-D NMR spectra. Diels-Alder cycloaddition of methylcyclopentadienes to 2 -methoxy-p-benzoquinone was performed. A single, isomerically pure cycloadduct was isolated, whose structure was assigned via analysis of the 1-D and 2-D NMR spectra of this cycloadduct and its reduction product obtained via stereo-specific reduction with sodium borohydride in the presence of cerous chloride. The structure of Thiele's ester was assigned via analysis of its 1-D and 2-D NMR spectra.
Date: May 1990
Creator: Lu, Shao-Po
System: The UNT Digital Library
Synthesis and Characterization of Methylated PCU Dimers (open access)

Synthesis and Characterization of Methylated PCU Dimers

Conversion of 1-Methylpentacyclo[5.4.0.0²⋅⁶.0³⋅¹⁰.0⁵⋅⁹]undecane- 8,11-dione into the corresponding mono(ethylene ketal) followed by Wolff-Kishner reduction resulted in a mixture of two isomers (i.e., 1- and 7-methyl-8-[2',-(1',3',dioxolano)]pentacyclo[5.4.0.0²⋅⁶.0³⋅¹⁰.0⁵⋅⁹] undecane. Hydrolysis of each isomer in turn resulted in 1- and 7- methyl pentacyclo[5.4.0.0²⋅⁶.0³⋅¹⁰.0⁵⋅⁹ ]undecan-8-ones (i.e.,"methylated PCU-8-ones"), respectively. "Titanium-promoted reductive dimerization of each of the methylated pentacycloundecane (PCU)-8-ones afforded mixtures of "methylated PCU alkene dimers". Individual isomers have been isolated from these mixtures via column chromatography by using silver nitrate impregnated silica gel as adsorbent followed by fractional recrystallizations of individual chromatography fractions. Structures of three isomerically pure methylated PCU alkene dimers (C₂₄H₂₈) have been established unequivocally by application of single crystal X-ray crystallographic methods.
Date: August 1993
Creator: Zope, Anjali U. (Anjali Umesh)
System: The UNT Digital Library
Photochemical Silaylide, Silylene and Silene Syntheses (open access)

Photochemical Silaylide, Silylene and Silene Syntheses

The synthesis of o-(N,N-dimethylamino)methylphenyl tris (trimethylsilyl) silane (II), a photochemical precursor of o- (N,N-dimethylamino) methylphenyl (trimethylsilyl) sila ammonium ylide (intramolecular silylene complex) and otolyl(trimethylsilyl)silylene is reported. Photolysis of II at room temperature in a cyclohexane solution of triethyl silane produced the silylene ylide and the presumably uncomplexed isomer, a silylene, which is trapped to afford the 2-(o-(N,N-dimethylamino)methylphenyl) -1,1,1-triethyl 3,3,3-trimethyltrisilane, 33% yield. A second decomposition pathway, a photodeamination, produced o-tris(trimethyl silyl) silyltoluene. UV spectra of the silaammonium ylide formed in the photochemical reaction of II was observed at 77k in hard or soft matrices.
Date: August 1990
Creator: Tan, Changqing
System: The UNT Digital Library
Structure, Energetics and Reactions of Bisketenes: An Ab Initio and Density Functional Theory Study (open access)

Structure, Energetics and Reactions of Bisketenes: An Ab Initio and Density Functional Theory Study

The effect of varying substituents on structure and energies of bisketenes was studied using ab initio methods. Effect of substituents on ring closing reaction of bisketenes to the corresponding cyclobutenediones was also studied using ab initio methods. One or two of the following substituents were used to study the effect of varying substituents: BH2, CH3, NH2, OH, F, AlH2, SiH3, PH2, SH, Cl. Studies were done at the Hartree-Fock (HF), Møller-Plesset (MP2), and Density Functional Theory (B3LYP) levels of theory using the 6-31G* basis set.
Date: December 1997
Creator: Palmer, Prem
System: The UNT Digital Library
Kinetic Studies of the Reactions of Cl and Br with Silane and Trimethylsilane (open access)

Kinetic Studies of the Reactions of Cl and Br with Silane and Trimethylsilane

The temperature dependence of the reactions of halogen atoms Cl and Br with SiH4 and (CH3)3SiH have been investigated with the flash photolysis-resonance fluorescence technique. CCI4 and CH2Br2 were used as precursors to produce Cl and Br atoms, respectively. Experiments gave {k(Cl + SiH4) (295 - 472 K)} = (1.56 +0.11) x 10-1 exp[(2.0 + 0.2) kJ mol'/RT] cm3 s4, {k(Br + SiH4)(295 - 575 K)} = (9.0 + 1.5) x 10-" exp[-(17.0 + 0.6) Id mol'/RT] cm3 s', {k(Cl + (CH3)3SiH)(295 - 468 K)} = (1.24 0.35) x 104 exp[(1.3 + 0.8) Id mol4/RT] cm3 s', and {k(Br + (CH3)3SiH)(295 - 456 K)} = (7.6 + 3.3) x 1010 exp[-(28.4 + 1.3) Id mol'/RT] cm3 s'. The results were compared with values from earlier work.
Date: May 1992
Creator: Ding, Luying
System: The UNT Digital Library
Comparison of 43Sn/43Pb/14Bi Solder and Standard 60Sn/40Pb Solder by Thermocyclic Fatigue Analysis (open access)

Comparison of 43Sn/43Pb/14Bi Solder and Standard 60Sn/40Pb Solder by Thermocyclic Fatigue Analysis

The thermocyclic fatigue behavior of the low-melting solder 43Sn/43Pb/14Bi has been investigated and compared to that of standard 60Sn/4OPb solder via metallographic analysis (using scanning electron microscopy) and evaluation of the degree of fatigue development (using a fatigue scale as a function of thermocycles). Specimens were subjected to shearing strains imposed by several hundred fatigue thermocycles. Both solder types fatigue by the same microstructural failure mechanism as described by other workers. The mechanism is characterized by a preferential coarsening of the solder joint microstructure at the region of maximum stress concentration where cracks originate.
Date: August 1991
Creator: Calderon, Jose Guadalupe
System: The UNT Digital Library
Solderability Study of Tin/Lead Alloy Under Steam-Aging Treatment by Electrochemical Reduction Analysis and Wetting Balance Tests (open access)

Solderability Study of Tin/Lead Alloy Under Steam-Aging Treatment by Electrochemical Reduction Analysis and Wetting Balance Tests

Two types of solder samples, pins and through-holes were tested by SERA™ (Sequential Electrochemical Reduction Analysis) and Wetting Balance after various length of steamaging treatment. It was shown that after steam-aging, both types of specimen gave a similar electrochemical reduction curve, and solderabilty predictions made from SERA™ test agree with results obtained from Wetting Balance test on a qualitative base. Wetting balance test of pin samples after SERA™ test confirmed that SERA™ is a non-destructive testing method -- it even restored solderability. Comparison of electrochemical reduction behavior of samples under different treatment indicates that steam-aging can not reproduce exactly the effect of naturally atmospheric aging, and may not be the best artificial accelerating environment adopted.
Date: May 1993
Creator: Gao, Yang, 1966-
System: The UNT Digital Library
Anion Exchange and Competition in Layered Double Hydroxides (open access)

Anion Exchange and Competition in Layered Double Hydroxides

Exchange reactions of anions, especially ferrocyanide and carbonate, with layered double hydroxides (LDHs) were investigated in relation to the origin of life on the early Earth. The effect on ferrocyanide exchange of concentration, pH, reaction time and cations are discussed. It was found that there were two different kinds of ferrocyanide species: one was that intercalated into the layered structure, occupying a site of D symmetry within the LDHs, while in the other, the ferrocyanide group retains full O symmetry. In addition, very low concentration, ferrocyanide associated with LDH will change its FTIR absorption shape. Carbonate was much more strongly intercalated than ferrocyanide into the LDHs, probably because of the strong hydrogen bonding.
Date: August 1997
Creator: Wang, Zhiming, 1958-
System: The UNT Digital Library
Some Physical Characteristics and Heavy Metal Analyses of Cotton Gin Waste for Potential use as an Alternative Fuel (open access)

Some Physical Characteristics and Heavy Metal Analyses of Cotton Gin Waste for Potential use as an Alternative Fuel

This study examines the waste of cotton gins as a potential alternative energy source, on account of its heat content, availability, and low emission rates. To confirm that this potential energy source meets minimum industrial fuel standards, this research has carried out an investigation of some important physical characteristics and toxic element analysis of cotton gin waste. Using cotton gin waste as fuel is an attractive solution to the problems of disposing of a surplus agricultural waste as well as supplementing fuel must meet both environmental emission standards and industrial fuel standards, the physical and chemical characteristics of cotton gin waste and its toxic element concentrations are important for its objective evaluation as a fuel. Constituent components, moisture contents, and ash contents of four separate parts of cotton gin waste were determined and evaluated closely following the American Society for Testing and Materials (ASTM) test methods. The three most toxic heavy metals, Arsenic (As), Chromium (Cr), and Lead (Pb), chosen for quantitative analysis were determined by using an inductively coupled plasma atomic emission spectrometry and a microwave oven sample digestion method.
Date: August 1996
Creator: Kim, Sungsoo
System: The UNT Digital Library
Studies of Layered Double Hydroxides (open access)

Studies of Layered Double Hydroxides

This work concerns some synthetic processes and basic properties of layered double hydroxides (LDHs). A series of LDHs, a family of newly developed materials found to have many potential uses in industry, were investigated in relating to the origin of life on early Earth. In this work, I successfully intercalated some inorganic as well as organic species. Ammonium, accompanied with ferrocyanide ion, can enter the layered space. It was found there were two kin go f intercalated ferrocyanide species: one is that exchanged with anions and became a part of layered double hydroxide, while the other is suggested to be related to ammonium ferrocyanide neutral species. Formaldehyde, ethanolamine and formate can also be involved into LDHs. To improve the crystallinity, homogeneous precipitation method, which used Urea and Hexamine, was employed. The results reveal the success in the case by Urea but not in that by Hexamine. Annealing could also be used for this purpose. However, it needs to be preocessed in its mother liquor; no improvement on the crystallinity if the material has been washed before annealing.
Date: August 1995
Creator: Zhao, Jingxian
System: The UNT Digital Library
Studies of Solvent Displacement from Solvated Metal Carbonyl Complexes of Chromium, Molybdenum, and Tungsten (open access)

Studies of Solvent Displacement from Solvated Metal Carbonyl Complexes of Chromium, Molybdenum, and Tungsten

Flash photolysis techniques were applied to studies of solvent displacement by Lewis bases (L) from solvated metal carbonyl complexes of Cr, Mo, and W. On the basis of extensive studies of the reaction rate laws, activation parameters , and linear-free-energy-relationships, it was concluded that the mechanisms of solvent displacement reactions depend on the electronic and steric properties of the solvents and L, as well as the identities of the metal atoms. The strengths of solvent-metal bonding interactions, varying from ca. 7 to 16 kcal/mol, and the bonding "modes" of solvents to metals are sensitive to the structures of the solvent molecules and the identities of the metal centers. The results indicate dissociative desolvation pathways for many arene solvents in (solvent)Cr(CO)_5 (solvent = benzene, fluorobenzene, toluene, etc.) complexes, and are consistent with competitive interchange and dissociative pathways for (n-heptane)M(CO)_5. Different types of (arene)-Cr(CO)_5 interactions were suggested for chlorobenzene (CB) vs. fluorobenzene and other non-halogenated arenes, i.e. via σ-halogen-Cr bond formation in the CB solvate vs. π-arene-Cr bond formation through "isolated" double bonds in solvates of the other arenes. The data also indicate the increasing importance of interchange pathways for solvent displacement from the solvates of Mo and W vs. that of …
Date: August 1990
Creator: Zhang, Shulin
System: The UNT Digital Library
The Analysis of PCDD and PCDF Emissions from the Cofiring of Densified Refuse Derived Fuel and Coal (open access)

The Analysis of PCDD and PCDF Emissions from the Cofiring of Densified Refuse Derived Fuel and Coal

The United States leads the world in per capita production of Municipal Solid Waste (MSW), generating approximately 200 million tons per year. By 2000 A.D. the US EPA predicts a 20% rise in these numbers. Currently the major strategies of MSW disposal are (i) landfill and (ii) incineration. The amount of landfill space in the US is on a rapid decline. There are -10,000 landfill sites in the country, of which only 65-70% are still in use. The Office of Technology Assessment (OTA) predicts an 80% landfill closure rate in the next 20 years. The development of a viable energy resource from MSW, in the form of densified Refuse Derived Fuel (dRDF), provides solutions to the problems of MSW generation and fossil fuel depletions. Every 2 tons of MSW yields approximately 1 ton of dRDF. Each ton of dRDF has an energy equivalent of more than two barrels of oil. At current production rates the US is "throwing away" over 200,000,000 barrels of oil a year. In order to be considered a truly viable product dRDF must be extensively studied; in terms of it's cost of production, it's combustion properties, and it's potential for environmental pollution. In 1987 a research …
Date: August 1990
Creator: Moore, Paul, 1962-
System: The UNT Digital Library
Synthesis, structure and redox reactivity of Co₃(CO)₆(μ₂-η²,η¹-C(Ph)C=C(PPH₂)C(O)SC(O)) (μ₂-PPh₂) (open access)

Synthesis, structure and redox reactivity of Co₃(CO)₆(μ₂-η²,η¹-C(Ph)C=C(PPH₂)C(O)SC(O)) (μ₂-PPh₂)

The tricobalt cluster PhCCo₃(CO)₉ (1) reacts with the bidentate phosphine ligand 2,3-bis(diphenylphosphino)maleic thioanhydride (bta) with added Me₃NO to yield PhCCo₃(CO)₇(bta) (2), which upon heating overnight yields Co₃(CO)₆(μ₂-η²,η¹-C(Ph)C=C(PPH₂)C(O)SC(O)) (μ₂-PPh₂) (3). Cluster (3) has been isolated and characterized by FT-IR and ³¹P NMR spectroscopy. Structural determination of the cluster has been demonstrated by X-ray diffraction analysis. Cluster (3) is analogous to the cluster synthesized by Richmond and coworkers. The redox properties of (3) have been examined by cyclic voltammetry and the data are reported within.
Date: May 1994
Creator: Muñoz, Trinidad
System: The UNT Digital Library