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Articles 61 - 90 of 146
Full-Text Articles in Chemistry
Sulfur-Oxidation Enhances Nitrile Hydration In Bioinspired Ruthenium Complexes : Catalytic, Kinetic, And Dft Investigations., Davinder Kumar
Sulfur-Oxidation Enhances Nitrile Hydration In Bioinspired Ruthenium Complexes : Catalytic, Kinetic, And Dft Investigations., Davinder Kumar
Electronic Theses and Dissertations
The current dissertation focuses on the effects of sulfur‒oxidation on nitrile hydration activity of a series of ruthenium(II) complexes inspired by nitrile hydratase (NHase). NHase catalytically hydrates nitriles to amides at a low spin non‒heme Fe(III) or non‒corrin Co(III) metal center. The active‒site employs a N2S3X type donor set using two carboxamido nitrogens and three cofacial cysteinic sulfurs that are present in distinct oxidation states as sulfinate (RSO2¯), sulfenate (RSO¯), and thiolate (RS¯). The apical site is occupied by substrate or solvent. A lack of sulfur‒oxidation renders the enzyme inactive. Three precatalysts, LnRuPPh3 (n = 1‒3), are employed to assess …
Synthetic And Mechanistic Studies Of Catalytic Oxidations By Manganese(Iii) Porphyrin And Iodobenzene Diacetate, Kawai Kwong
Synthetic And Mechanistic Studies Of Catalytic Oxidations By Manganese(Iii) Porphyrin And Iodobenzene Diacetate, Kawai Kwong
Mahurin Honors College Capstone Experience/Thesis Projects
With iodobenzene diacetate [PhI(OAc)2] as the oxygen source, manganese(III) porphyrin complexes exhibit remarkable catalytic activity towards the selective oxidation of hydrocarbons. The readily soluble PhI(OAc)2 in the presence of small amount of water is more efficient oxygen source than the commonly used PhIO under the same conditions, leading to a potent catalytic system for the efficient oxidation of alkenes and activated hydrocarbons. When the reactions were carried out in the presence of a small amount of water at 50 oC, high selectivity for epoxides and excellent catalytic efficiency with up to 10,000 TON have been achieved in alkene epoxidations. In …
Naio4 Oxidation Of Mussel Adhesive Protein Film And Its Corrosion Protection For Mg-1.0ca Alloy, Rui-Qing Hou, Ping-Li Jiang, Shi-Gang Dong, Chang-Jian Lin
Naio4 Oxidation Of Mussel Adhesive Protein Film And Its Corrosion Protection For Mg-1.0ca Alloy, Rui-Qing Hou, Ping-Li Jiang, Shi-Gang Dong, Chang-Jian Lin
Journal of Electrochemistry
The effect of oxidation of mussel adhesive protein (Mefp-1) film on the corrosive resistance for Mg-1.0Ca alloy was investigated by scanning electron microscopy (SEM), atom force microscopy (AFM), electron probe microanalysis (EPMA), Infrared reflection absorption spectroscopy (IRAS) and electrochemical methods. The results showed that the NaIO4 induced oxidation of the pre-formed Mefp-1 film with porous morphology involved structural change of the DOPA group in the protein and resulted in a more uniform film with net-like morphology. The protein film without oxidation had an increasing resistance for the corrosion of Mg-1.0Ca alloy up to 7 days exposure. After oxidation, Epit …
The Critical Role Of Water At The Gold-Titania Interface In Catalytic Co Oxidation, Johnny Saavedra, H. Doan, Christopher J. Pursell, L. C. Grabow, Bert D. Chandler
The Critical Role Of Water At The Gold-Titania Interface In Catalytic Co Oxidation, Johnny Saavedra, H. Doan, Christopher J. Pursell, L. C. Grabow, Bert D. Chandler
Chemistry Faculty Research
We provide direct evidence of a water-mediated reaction mechanism for room-temperature CO oxidation over Au/TiO2 catalysts. A hydrogen/deuterium kinetic isotope effect of nearly 2 implicates O-H(D) bond breaking in the rate-determining step. Kinetics and in situ infrared spectroscopy experiments showed that the coverage of weakly adsorbed water on TiO2 largely determines catalyst activity by changing the number of active sites. Density functional theory calculations indicated that proton transfer at the metal-support interface facilitates O2 binding and activation; the resulting Au-OOH species readily reacts with adsorbed Au-CO, yielding Au-COOH. Au-COOH decomposition involves proton transfer to water and was suggested to be …
Electrochemical Fabrication Of Two-Dimensional Flower-Like Pt Nanostructures For Methanol Electrocatalytic Oxidation, Xia Wang, Jun Hu, Yong-Jun Li
Electrochemical Fabrication Of Two-Dimensional Flower-Like Pt Nanostructures For Methanol Electrocatalytic Oxidation, Xia Wang, Jun Hu, Yong-Jun Li
Journal of Electrochemistry
Two-dimensional flower-like Pt nanostructures (2D FPNs) were fabricated on glassy carbon substrates by galvanostatical electrochemical technique. The electrolyte was the HAuCl4 + HClO4 aqueous solution without addition of any structure-directing organic reagent, which made as-prepared Pt nanostructures cleaner, exhibiting much higher reactivity. Scanning electron microscopic images revealed that 2D FPNs were spherical Pt nano-flowers constructed by the smallest building blocks, nano-leaves. The number density of spherical Pt nano-flowers can be tuned by controlling the electrodeposition time. High resolution transmission electron microscopic images indicated that each nano-leaf was formed by growing along Pt(111) direction. Electrocatalytic activities of as-prepared 2D …
Characterization Of Organic Carbon In Sediments From Old Rifle, Co, A Former Uranium Mill, Francis Michael Tee, Morris Jones, Sharon Bone, Michael Schaefer, Scott Fendorf, John Bargar
Characterization Of Organic Carbon In Sediments From Old Rifle, Co, A Former Uranium Mill, Francis Michael Tee, Morris Jones, Sharon Bone, Michael Schaefer, Scott Fendorf, John Bargar
STAR Program Research Presentations
Characterization of sediments from Old Rifle, CO, a former uranium mill
More than 34 million gallons (~129 million liters) of groundwater are contaminated with uranium at Old Rifle, Colorado – a former uranium-processing site that operated until 1958. The original Department of Energy strategy for remediation, involving natural flushing of U from the groundwater through mixing with surface water, has not been as successful as predicted. The uranium plume is replenished when insoluble U(IV) is oxidized to the more mobile U(VI). Relatively thin pockets of silt-, clay-, and organic-rich sediments contain reduced uranium, iron and sulfur and are referred to …
Selective Oxidations By Iron(Iii) Porphyrins And Iron(Iii) Corroles, Aaron Dalnamath Carver
Selective Oxidations By Iron(Iii) Porphyrins And Iron(Iii) Corroles, Aaron Dalnamath Carver
Masters Theses & Specialist Projects
The selective oxidation of organic compounds represents a leading technology for chemical industries. They are used in chemical synthesis in the pharmaceutical and petrochemicals industries, and possible the decontamination of harmful substances. However, oxidations reaction are among the most challenging processes to control. Many stoichiometric oxidants with heavy metals are expensive, or toxic maybe both, and therefore unfeasible to be utilized. The ideal processes for catalytic oxidation would use molecular oxygen or hydrogen peroxide as the primary oxygen source, with transition metal catalysts to mimic the predominant oxidation catalysts in Nature, the cytochrome P450 enzymes. This study focuses on the …
Speciation Behavior Of Americium Higher Oxidation States For The Separation Of Americium From Curium, Catherine Lynn Riddle
Speciation Behavior Of Americium Higher Oxidation States For The Separation Of Americium From Curium, Catherine Lynn Riddle
UNLV Theses, Dissertations, Professional Papers, and Capstones
Several countries are currently expanding the use of nuclear energy as a method for the safe generation of carbon free energy and a number are evaluating starting up a nuclear power program. Closed fuel cycle technologies may be key to waste reduction and a sustainable nuclear energy future and to support the development of more efficient fuel cycles, the investigation of the chemical properties of key actinides is at the forefront of separations research. In this work the characterization of higher oxidation states of americium (Am) has been performed using spectroscopic methods. Americium in the formal oxidation state of Am(V) …
Selective Oxidations By Metalloporphyrins And Metallocorroles, Tse-Hong Chen
Selective Oxidations By Metalloporphyrins And Metallocorroles, Tse-Hong Chen
Masters Theses & Specialist Projects
Highly reactive transition metal-oxo intermediates are important active oxidant involved in numerous enzymes such as cytochrome P450 monooxygenases as well as in many useful metal-catalyzed oxidations. Many transition metal catalysts are designed for biomimetic studies of the predominant oxidation catalysts in Nature, the cytochrome P450 enzymes. In this work, a series of metalloporphyrin and metallocorrole complexes have been successfully synthesized and spectroscopically characterized by UV-vis, GCMS and 1H-NMR. The utilization of these complexes as catalysts for selective oxidation of sulfides and photocatalytic aerobic oxidations of activated hydrocarbons were investigated. Ruthenium(II) porphyrin complexes (2) and iron(III) corrole complexes (4) with …
Big Horned, Juniper Harrower
Big Horned, Juniper Harrower
The Transdisciplinary STEAM+ Journal
Tinta y tinto (Spanish for black ink and red wine)
Through a process of oxidation, reduction, and light manipulation, Juniper stains and colors paper with red wine and a rich black pigment made of the wild harvested mushroom Coprinopsis atramentaria.
Pulse Electrodeposition Of Pd-Ni Alloy Nanoparticles For Electrocatalytic Oxidation Of Formic Acid, Fang-Zu Yang, Jun-Pei Yue, Zhong-Qun Tian, Shao-Min Zhou
Pulse Electrodeposition Of Pd-Ni Alloy Nanoparticles For Electrocatalytic Oxidation Of Formic Acid, Fang-Zu Yang, Jun-Pei Yue, Zhong-Qun Tian, Shao-Min Zhou
Journal of Electrochemistry
The Pd-Ni alloy nanoparticles with nickel atomic contents of 12.0%, 16.4% and 22.6% were successfully electrodeposited from a Pd-Ni alloy electrolyte by square wave pulse plating. The alloy nanoparticles were in the spherical shape with a diameter of 50 ~ 80 nm. As the growth potential of the alloy was negatively shifted, the nickel content of the alloy was increased, and the size of the nanoparticles was almost the same, whereas the number, the degree of crosslinking and the real active area of the nanoparticles were increased. As the nickel content of the alloy nanoparticles increased, the peak current for …
Selective Oxidation Of Sulfides And Hydrocarbons With H_2o_2 Over Manganese Catalyst Supported On Nanoparticles, Massomeh Ghorbanloo, Roghayeh Tarasi, Jun Tao, Hidenori Yahiro
Selective Oxidation Of Sulfides And Hydrocarbons With H_2o_2 Over Manganese Catalyst Supported On Nanoparticles, Massomeh Ghorbanloo, Roghayeh Tarasi, Jun Tao, Hidenori Yahiro
Turkish Journal of Chemistry
A new magnetically separable catalyst consisting of binuclear Mn(II) complex [Mn_2(HL)_2(H_2O)_4], HL = 2-[(2-hydroxy-benzylidene)-amino]-3-(4-hydroxyphenyl)-propionic acid, supported on (3-chloropropyl)-trimethoxysilane (CPTMS) functionalized silica-coated magnetic nanoparticles (MNPs) was prepared. The synthesized catalyst was characterized by several physico-chemical and spectroscopic methods. This immobilized complex was found to be an efficient heterogeneous catalyst for the oxidation of different sulfides and hydrocarbons using hydrogen peroxide (H_2O_2) as an oxidant. The catalyst is readily recovered by simple magnetic decantation and can be recycled several times with no considerable loss of catalytic activity.
N-Bridged Dimers Of Tetrapyrroles Complexed By Transition Metals: Syntheses, Characterization Methods, And Uses As Oxidation Catalysts, Ümi̇t İşci̇, Fabienne Dumoulin, Alexander B. Soroki̇n, Vefa Ahsen
N-Bridged Dimers Of Tetrapyrroles Complexed By Transition Metals: Syntheses, Characterization Methods, And Uses As Oxidation Catalysts, Ümi̇t İşci̇, Fabienne Dumoulin, Alexander B. Soroki̇n, Vefa Ahsen
Turkish Journal of Chemistry
N-bridged dimers of tetrapyrroles complexed by transition metals have been known for nearly four decades, and gained renewed attention when their powerful oxidation properties were recently evidenced. This article is a state of the art review of the reported complexes and of their synthetic methods. Beyond classical chemistry characterization tools, specific methods appropriate to their structure are used and are presented in detail. Finally, their uses and importance of oxidation catalysts are reviewed.
Oxidation Of Hydrocarbons With Tetra-N-Butylammonium Peroxy Monosulfate Catalyzed By \Beta-Tetrabromo-Meso-Tetrakis(4-Methoxyphenyl)- And \Beta-Tetrabromo-Meso-Tetraphenylporphyrinatomanganese(Iii), Saeed Rayati, Saeed Zakavi, Hossein Valinejad
Oxidation Of Hydrocarbons With Tetra-N-Butylammonium Peroxy Monosulfate Catalyzed By \Beta-Tetrabromo-Meso-Tetrakis(4-Methoxyphenyl)- And \Beta-Tetrabromo-Meso-Tetraphenylporphyrinatomanganese(Iii), Saeed Rayati, Saeed Zakavi, Hossein Valinejad
Turkish Journal of Chemistry
\beta-Tetrabromo-meso-tetrakis(4-methoxyphenyl)porphyrin, H_2T(4-OCH_3P)PBr_4, was synthesized and characterized by UV-Vis and ^1H NMR spectroscopy. Oxidation of alkanes and olefins with tetra-n-butylammonium peroxymonosulfate (n-Bu_4NHSO_5) was studied in the presence of MnT(4-OCH_3P)PBr_4(OAc) and MnTPPPBr_4(OAc) (TPP = meso-tetraphenylporphyrin). While significance differences were observed between the catalytic activities of the title complexes in the oxidation of alkanes, the 2 manganese porphyrins showed comparable activities in oxidation of most of the olefins used. However, the latter showed greater catalytic performance in the oxidation of the hydrocarbons. Moreover, the oxidative degradation of the former (60 %) was greater than that of the latter (45 %) in the oxidation …
Electronic Effects In Oxidation Reactions Utilizing Dinuclear Copper Complexes With The Bis[3-(2-Hydroxybenzylideneamino)Phenyl] Sulfone Ligand, Armando M. Guidote Jr, Ronald L. Reyes, Riyo Kashihara, Yasuhiko Kurusu, Yoshihiro Masuyama
Electronic Effects In Oxidation Reactions Utilizing Dinuclear Copper Complexes With The Bis[3-(2-Hydroxybenzylideneamino)Phenyl] Sulfone Ligand, Armando M. Guidote Jr, Ronald L. Reyes, Riyo Kashihara, Yasuhiko Kurusu, Yoshihiro Masuyama
Chemistry Faculty Publications
Copper acetate and the ligands bis[3-(3-tert-butyl-2-hydroxy-5-methoxybenzylideneamino)phenyl] sulfone and bis[3-(3,5-di-tert-butyl-2-hydroxybenzylideneamino)phenyl] sulfone were reacted to form the complexes with 2:1 copper:ligand ratio, Cu2[B(t-Bu) (OMe)BAPS](µ-OCH3)2 (4) and with 2:2 copper:ligand ratio, Cu2[B(t-Bu)2BAPS]2 (5), respectively. Structures of 4 and 5 were determined based on IR, UV-Vis, and FAB-MS data in comparison with previously characterized related copper complexes. The two complexes 4 and 5 were utilized in the oxidation of the substrates 2,4- and 2,6-di-tertbutylphenol (dtbp) at -50C with H2O2 in CH2Cl2. The coupling products are preferred in both cases. For 2,4-dtbp, yields of 4,600% and 7,200% of 3,3’,5,5’-tetra-tert-butyl-2,2’- biphenol were achieved with the use …
Oxidation Of Gold Clusters By Thiols, Brian M. Barngrover, Christine M. Aikens
Oxidation Of Gold Clusters By Thiols, Brian M. Barngrover, Christine M. Aikens
Faculty Publications
The formation of gold–thiolate nanoparticles via oxidation of gold clusters by thiols is examined in this work. Using the BP86 density functional with a triple ζ basis set, the adsorption of methylthiol onto various gold clusters AunZ (n = 1–8, 12, 13, 20; Z = 0, −1, +1) and Au384+ is investigated. The rate-limiting step for the reaction of one thiol with the gold cluster is the dissociation of the thiol proton; the resulting hydrogen atom can move around the gold cluster relatively freely. The addition of a second thiol can lead to H2 …
Mass Spectrometric Analysis Of Oxidized Eicosapentaenoic Acid Sodium Salt, Kelsey D. Jordan, Rita K. Upmacis
Mass Spectrometric Analysis Of Oxidized Eicosapentaenoic Acid Sodium Salt, Kelsey D. Jordan, Rita K. Upmacis
Faculty Papers and Publications
Eicosapentaenoic acid (EPA) is an omega-3 polyunsaturated fatty acid (PUFA) with 20 carbon atoms and 5 carbon-carbon double bonds. Mammalian cells cannot synthesize long chain PUFAs such as EPA de novo, and, thus, the most effective way to enrich cells in EPA is by dietary intake of fish oils. EPA supplementation causes an increase in its concentration in plasma lipids and in cell membrane phospholipids. Many beneficial effects of EPA supplementation have been noted, including (1) the potential to sensitize cancerous tumors towards chemotherapy, (2) the promotion of cardiovascular health, and (3) the alleviation of some mental disorders, but results …
Co Adsorption On Supported Gold Nanoparticle Catalysts: Application Of The Temkin Model, Christopher J. Pursell, Bert D. Chandler, M. Manzoli, F. Boccuzzi
Co Adsorption On Supported Gold Nanoparticle Catalysts: Application Of The Temkin Model, Christopher J. Pursell, Bert D. Chandler, M. Manzoli, F. Boccuzzi
Chemistry Faculty Research
The adsorption of CO on the supported gold nanoparticle catalysts Au/TiO2, Au/Fe2O3, and Au/ZrO2 was examined using infrared transmission spectroscopy to quantify the isobaric CO coverage as a function of temperature. The Temkin adsorbate interaction model was then applied to account for the adsorption behavior. To test the general applicability of the Temkin model, this treatment was also applied to three data sets from the literature. This included another real-world catalyst and two model catalysts. All data sets were accurately represented by the Temkin adsorbate interaction model. The resulting thermodynamic metrics are consistent with previous determinations and reflect a particle …
Chemoselective Oxidation Of 6,13-Bis(Decylthio) Pentacene, Claire Eunhye Cho
Chemoselective Oxidation Of 6,13-Bis(Decylthio) Pentacene, Claire Eunhye Cho
Theses and Dissertations
Organic semiconductors present much potential for industrial use because of their possible low cost production, Pentacene and pentacene derivatives are promising candidates for organic semiconductor research since their ^-conjugated electronic structures possess small HOMO- LUMO gaps and high field effect mobility. Whereas there is much potential in devices made from pentacenes they do however undergo short lifetimes and poor processability due to photodegradation and poor solubility of pentacene. Previous research has shown that the pentacene lifetime and solubility can be enhanced by arylthio and alkylthio substituents placed on the pentacene backbone. For example 6,13-i?/s(decylthio)pentacene was one of the longest lived …
Synthesis Of Novel Ionic Liquid Tagged Porphryin Media Designed For The Oxidation Of Lignin, Joseph Hugh Franklin Baker
Synthesis Of Novel Ionic Liquid Tagged Porphryin Media Designed For The Oxidation Of Lignin, Joseph Hugh Franklin Baker
Online Theses and Dissertations
The ever growing need for a viable renewable fuel source has led to this thesis project; the biomimetic lignin degradation by means of a homogeneous oxidative catalyst in corresponding ionic liquids. Lignin comprises nearly a third of lignocellulosic biomass and is cross-linked to both cellulose and hemicellulose. Current utilization methods of lignin do not generate the full value of the polymer, because they do not yield many of the valuable feed stock chemicals it is comprised of. To improve the value of the biomass as a whole and create a viable economy for the US's transition to biofuels, better utilization …
Synthesis, Structural Characterization, And Benzyl Alcohol Oxidation Activity Of Mononuclear Manganese(Ii) Complex With 2,2'-Bipyridine: [Mn(Bipy)_2(Clo_4)_2], İbrahi̇m Kani̇, Mehmet Kurtça
Synthesis, Structural Characterization, And Benzyl Alcohol Oxidation Activity Of Mononuclear Manganese(Ii) Complex With 2,2'-Bipyridine: [Mn(Bipy)_2(Clo_4)_2], İbrahi̇m Kani̇, Mehmet Kurtça
Turkish Journal of Chemistry
A manganese(II) complex of 2,2'-bipyridine (bipy) was synthesized and characterized by X-ray diffraction, IR, and UV-vis spectroscopy. The activity of the complex was tested for oxidation of benzyl alcohols using t-BuOOH as an oxidant in organic solvents and in an organic/water biphasic system (hexane/H_2O, toluene/H_2O). The effect of solvent, temperature, oxidant, and some additives (KBr, N(C_4H_9)Br, and N-bromosuccinimide) on the oxidation of benzyl alcohol is reported. The results show that benzyl alcohol was selectively converted to benzaldehyde in 71.9% yield within 4 h in acetonitrile. Control experiments performed without catalyst and the corresponding metal salt as catalyst produced no benzaldehyde …
Recent Applications Of The Simple Hydrocarbon Cyclooctatetrene As A Starting Material For Complex Molecule Synthesis, Kevin W. Glaeske, William A. Donaldson
Recent Applications Of The Simple Hydrocarbon Cyclooctatetrene As A Starting Material For Complex Molecule Synthesis, Kevin W. Glaeske, William A. Donaldson
Chemistry Faculty Research and Publications
Cyclooctatetraene [COT], a simple non-aromatic cyclic polyene, is capable of undergoing a variety of oxidation and cycloaddition reactions to afford polycyclic structures. In addition, complexation of COT or the cycloaddition products with transition metals facilitates bond formation. Recent developments in the reactivity of COT and application to the synthesis of naturally occurring and non-naturally occurring compounds is reviewed.
Effects Of Activated Carbon Surface Chemistry Modification On The Adsorption Of Mercury From Aqueous Solution, Emily K. Faulconer
Effects Of Activated Carbon Surface Chemistry Modification On The Adsorption Of Mercury From Aqueous Solution, Emily K. Faulconer
Publications
Mercury (Hg), a naturally occurring element, is toxic and can lead to negative health impacts for humans and ecosystems. Activated carbon adsorption is effective in treating Hg-laden aqueous effluent for safe discharge. Two modifications of commercially available activated carbon were investigated: iron impregnation to allow for magnetic sorbent recapture and wet chemical oxidation to enhance aqueous Hg capture. The modified carbons were characterized by nitrogen adsorption-desorption, XRD, pHpzc, vibrating sample magnetometry, elemental analysis, and total acidity titration. The 3:1 C:Fe magnetic powdered activated carbon (MPAC) retained a high surface area of 790 m2 /g and was 95% magnetically recoverable, with …
Reactivity Of Acyclic (Pentadienyl)Iron(1+) Cations: Synthetic Studies Directed Toward The Frondosins, Do W. Lee, Rajesh K. Pandey, Sergey V. Lindeman, William A. Donaldson
Reactivity Of Acyclic (Pentadienyl)Iron(1+) Cations: Synthetic Studies Directed Toward The Frondosins, Do W. Lee, Rajesh K. Pandey, Sergey V. Lindeman, William A. Donaldson
Chemistry Faculty Research and Publications
A short, 4-step route to the scaffold of frondosin A and B is reported. The [1-methoxycarbonyl-5-(2′,5′-dimethoxyphenyl)pentadienyl]Fe(CO)3+ cation was prepared in two steps from (methyl 6-oxo-2,4-hexadienoate)Fe(CO)3. Reaction of this cation with isopropenyl Grignard or cyclohexenyllithium reagents affords (2-alkenyl-5-aryl-1-methoxycarbonyl-3-pentene-1,5-diyl)Fe(CO)3 along with other addition products. Oxidative decomplexation of these (pentenediyl)iron complexes, utilizing CuCl2, affords 6-aryl-3-methoxycarbonyl-1,4-cycloheptadienes via the presumed intermediacy of a cis-divinylcyclopropane.
Physico-Chemical And Microbiological Parameters In The Deterioration Of Virgin Coconut Oil, Ian Ken D. Dimzon, Melodina F. Valde, Jaclyn Elizabeth R. Santos, Mark Joseph Garrovillas, Henson M. Dejarme, Jo Margarette W. Remollo, Fabian M. Dayrit
Physico-Chemical And Microbiological Parameters In The Deterioration Of Virgin Coconut Oil, Ian Ken D. Dimzon, Melodina F. Valde, Jaclyn Elizabeth R. Santos, Mark Joseph Garrovillas, Henson M. Dejarme, Jo Margarette W. Remollo, Fabian M. Dayrit
Chemistry Faculty Publications
The deterioration of virgin coconut oil (VCO) due to physico-chemical oxidation and hydrolysis and microbiological processes was studied. The physico-chemical oxidation of VCO in the air at room temperature was negligible. Oxidation of VCO was observed only in the presence of air, UV radiation, ferric ion (Fe3+), and high free fatty acid (FFA) content. Chemical hydrolysis was performed at varying moisture levels and temperatures. The rate of hydrolysis to produce FFAs was measured using 31P NMR under conditions of saturated water (0.22%) and 80°C was found to be 0.066 µmol/g-hr (expressed as lauric acid). At 0.084% moisture and 80°C, the …
Ligand Fluorination To Optimize Preferential Oxidation Of Carbon Monoxide By Water-Soluble Rhodium Porphyrins, Justin C. Biffinger, Shriharsha Uppaluri, Haoran Sun, Stephen G. Dimagno
Ligand Fluorination To Optimize Preferential Oxidation Of Carbon Monoxide By Water-Soluble Rhodium Porphyrins, Justin C. Biffinger, Shriharsha Uppaluri, Haoran Sun, Stephen G. Dimagno
Stephen DiMagno Papers
Catalytic, low temperature preferential oxidation (PROX) of carbon monoxide by aqueous [5,10,15,20-tetrakis- (4-sulfonatophenyl)-2,3,7,8,12,13,17,18-octafluoroporphyrinato]- rhodium(III) tetrasodium salt, (1[Rh(III)]) and [5,10,15, 20-tetrakis(3-sulfonato-2,6-difluorophenyl)-2,3,7,8,12,13, 17,18-octafluoroporphyrinato]rhodium(III) tetrasodium salt, (2[Rh(III)]) is reported. The PROX reaction occurs at ambient temperature in buffered (4 ≤ pH ≤ 13) aqueous solutions. Fluorination on the porphyrin periphery is shown to increase the CO PROX reaction rate, shift the metal centered redox potentials, and acidify ligated water molecules. Most importantly, β-fluorination increases the acidity of the rhodium hydride complex (pKa = 2.2 ± 0.2 for 2[Rh-D]); the dramatically increased acidity of the Rh(III) hydride complex precludes proton reduction …
Dications Of Benzylidenefluorene And Diphenylmethylidene Fluorene: The Relationship Between Magnetic And Energetic Measures Of Antiaromaticity, Catherine Do, Julianne Hatfield, Shirali Patel, D Vasudevan, Cornelia Tirla, Nancy S. Mills
Dications Of Benzylidenefluorene And Diphenylmethylidene Fluorene: The Relationship Between Magnetic And Energetic Measures Of Antiaromaticity, Catherine Do, Julianne Hatfield, Shirali Patel, D Vasudevan, Cornelia Tirla, Nancy S. Mills
Chemistry Faculty Research
Oxidation of m- and p-substituted benzylidene fluorenes to antiaromatic dications was attempted by electrochemical and chemical means. Electrochemical oxidation to dications was successful for benzylidene fluorenes with p-methoxy, p-methyl, p-fluoro, and unsubstituted phenyl rings in the 3-position; attempts to oxidize the m-substituted derivatives via electrochemistry were unsuccessful. Chemical oxidation with SbF5/SO2ClF gave the dication of 9-[(4-methoxyphenyl)methylene]-9H-fluorene cleanly; oxidation of all other substituted benzylidene fluorenes resulted in mixtures of products. The excellent linear relationship between the chemical shifts calculated by the GIAO method and the experimental shifts for the p-methoxy-substituted benzylidene fluorene dication …
Chromium Salen, Gráinne Hargaden, Pier Giorgio Cozzi
Antiaromatic Dianions: Dianions Of Dixanthylidene By Reduction And Attempted Excited-State Deprotonation, Mary Black, Clifford Woodford, Nancy S. Mills
Antiaromatic Dianions: Dianions Of Dixanthylidene By Reduction And Attempted Excited-State Deprotonation, Mary Black, Clifford Woodford, Nancy S. Mills
Chemistry Faculty Research
Reduction of dixanthylidene with potassium or lithium resulted in formation of the antiaromatic dianion in high yield. Attempts to form the dianion by excited-state deprotonation of dixanthene with n-butyllithium/TMEDA resulted in formation of the tetraanion from deprotonation ortho to the oxygen. Orientation of the sp3 hydrogens presumably allows preferential deprotonation of the xanthene rings.
Characteristics And Stability Of Oxide Films On Plutonium Surfaces, Harry Guillermo García Flores
Characteristics And Stability Of Oxide Films On Plutonium Surfaces, Harry Guillermo García Flores
Department of Chemistry: Dissertations, Theses, and Student Research
The oxidation of plutonium (Pu) metal continues to be an area of considerable activity. The reaction characteristics have significant implications for production use, storage, and disposition of this radiological material. Developing an accurate physical model of the structures, oxidation states, and oxygen concentration gradients present during oxidation are essential to understanding this process. Traditionally, the stable oxides of Pu have been thought to be plutonium sesquioxide (Pu2O3, O/Pu = 1.5, Pu3+) and plutonium dioxide (PuO2, O/Pu = 2.0, Pu4+), existing in a layered structure on Pu metal. Many of the …