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Articles 181 - 210 of 224

Full-Text Articles in Chemistry

Gram Scale Synthesis Of The C(18)-C(34) Fragment Of Amphidinolide C., Nicholas A Morra, Brian L Pagenkopf Feb 2011

Gram Scale Synthesis Of The C(18)-C(34) Fragment Of Amphidinolide C., Nicholas A Morra, Brian L Pagenkopf

Chemistry Publications

The synthesis of the C(18)-C(34) fragment of amphidinolide C has been achieved via two routes, culminating in both the shortest (11 steps) and highest yielding (26% overall yield) approaches to this segment. The highly convergent approach will facilitate the synthesis of analogues, including the C(18)-C(29) fragment of amphidinolide F. Synthetic highlights include the selective methylation of a diyne, and the highly efficient use of a second generation cobalt catalyst in the Mukaiyama oxidative cyclization to form the trans-THF ring.

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Investigation Of Nanoceria-Modified Platinum-Gold Composite Electrodes For The Electrochemical Reduction Of Oxygen In Alkaline Media, Rahul Hegishte Jan 2011

Investigation Of Nanoceria-Modified Platinum-Gold Composite Electrodes For The Electrochemical Reduction Of Oxygen In Alkaline Media, Rahul Hegishte

Electronic Theses and Dissertations

Platinum-gold and nanoceria-modified platinum-gold electrodes were prepared on a platinum surface via electrochemical reduction of solutions of platinum and gold salts in the dispersion of nanoceria. The molar ratios of Pt and Au were varied in both PtAu and PtAu/CeO₂ electrodes while the total concentration of the metals was maintained at 2 x 10⁻³M and the concentration of nanoceria was maintained constant at 5 x 10⁻³M. The electrodes were characterized by their cyclic voltammetry curves in 0.5M sulfuric acid solution. The electrochemically active area of the electrodes was determined using the copper underpotential deposition method. The linear sweep voltammograms of …

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Microwave-Induced Indium-Catalyzed Synthesis Of Pyrrole Fused With Indoline In Water, Dina Abrego, Debasish Bandyopadhyay, Bimal K. Banik Jan 2011

Microwave-Induced Indium-Catalyzed Synthesis Of Pyrrole Fused With Indoline In Water, Dina Abrego, Debasish Bandyopadhyay, Bimal K. Banik

School of Integrative Biological & Chemical Sciences (Formerly Dept. of Chemistry)

An expeditious microwave-induced indium metal-catalyzed synthesis of pyrrole fused with indoline in water is developed by reacting isatin and 4-hydroxyproline.

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Microwave-Induced Bismuth Nitrate-Catalyzed Expeditious Enamination Of Β-Dicarbonyl Compounds Under Solvent-Free Conditions, Debasish Bandyopadhyay, Bimal K. Banik Jan 2011

Microwave-Induced Bismuth Nitrate-Catalyzed Expeditious Enamination Of Β-Dicarbonyl Compounds Under Solvent-Free Conditions, Debasish Bandyopadhyay, Bimal K. Banik

School of Integrative Biological & Chemical Sciences (Formerly Dept. of Chemistry)

Bismuth nitrate-catalyzed, automated microwave-assisted expeditious synthesis of β- enaminones and β-enaminoesters has been carried out in an efficient manner under solvent-free condition. The reaction is general for primary, secondary (cyclic, heterocyclic and acyclic), benzylic as well as aromatic amines.

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Phosphoric Acid Catalyzed Aza-Michael Reaction In Water: An Ecofriendly Procedure, Debasish Bandyopadhyay, Stephanie Maldonado, Bimal K. Banik Jan 2011

Phosphoric Acid Catalyzed Aza-Michael Reaction In Water: An Ecofriendly Procedure, Debasish Bandyopadhyay, Stephanie Maldonado, Bimal K. Banik

School of Integrative Biological & Chemical Sciences (Formerly Dept. of Chemistry)

Phosphoric acid catalyzed aza-Michael reaction in water has been carried out in an efficient manner at room temperature. The reaction is general for primary, secondary (cyclic, heterocyclic and acyclic), benzylic as well as aromatic amines. No bis-addition was observed for primary amines.

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Sythesis Of Glucose Peracetate Via Bismuth Nitrate-Induced Reaction, Jose Lerma, Bimal K. Banik Jan 2011

Sythesis Of Glucose Peracetate Via Bismuth Nitrate-Induced Reaction, Jose Lerma, Bimal K. Banik

School of Integrative Biological & Chemical Sciences (Formerly Dept. of Chemistry)

Simple synthesis peracetylated glucose has been achieved starting from glucose and acetic anhydride in the absence of solvent via bismuth nitrate-catalyzed reaction. This method does not need large excess of acetic anhydride.

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Synthesis And Catalytic Activity Of Nanostructured Cerium Oxide, Neil J. Lawrence Dec 2010

Synthesis And Catalytic Activity Of Nanostructured Cerium Oxide, Neil J. Lawrence

Department of Chemistry: Dissertations, Theses, and Student Research

Cerium oxide (ceria, CeO2-x where x is 0 to 0.5) has been one of the most widely used heterogeneous catalysts particularly in three way catalytic converters. Most of the catalytic traits can be attributed to two properties of ceria: first, the high mobility and storage capacity of oxygen within the lattice; second, the ease with which cerium changes between Ce3+ and Ce4+ states. These properties, combined with the abundance of cerium on earth, make ceria a low-cost highly effective alternative to noble metal catalysts. Recent research has been focused on the nanoscale properties of ceria.

The effect …

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A Highly Efficient Bismuth Salts-Catalyzed Route For The Synthesis Of Alpha-Aminophosphonates, Antara Banik, Sahil Batta, Debasish Bandyopadhyay, Bimal K. Banik Nov 2010

A Highly Efficient Bismuth Salts-Catalyzed Route For The Synthesis Of Alpha-Aminophosphonates, Antara Banik, Sahil Batta, Debasish Bandyopadhyay, Bimal K. Banik

School of Integrative Biological & Chemical Sciences (Formerly Dept. of Chemistry)

A convenient synthesis of different types of α-amino phosphonates via one-pot solvent-free three component reactions of aldehydes, amines and phosphites catalyzed by bismuth salts has been investigated. Bismuth triflate is found to be the most effective catalyst for this reaction.

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Ytterbium Triflate Catalyzed Synthesis Of Alkoxy-Substituted Donor-Acceptor Cyclobutanes And Their Formal [4 + 2] Cycloaddition With Imines: Stereoselective Synthesis Of Piperidines., Mahmoud M Abd Rabo Moustafa, Brian L Pagenkopf Oct 2010

Ytterbium Triflate Catalyzed Synthesis Of Alkoxy-Substituted Donor-Acceptor Cyclobutanes And Their Formal [4 + 2] Cycloaddition With Imines: Stereoselective Synthesis Of Piperidines., Mahmoud M Abd Rabo Moustafa, Brian L Pagenkopf

Chemistry Publications

A new synthesis of 2-alkoxy-1,1-cyclobutane diesters and their first use in dipolar cycloadditions is reported. Both the formation of the donor-acceptor cyclobutanes and their subsequent annulation with in situ formed imines are catalyzed by Yb(OTf)(3). Cyclobutanes with carbon donor groups give piperidines with high trans stereoselectivity.

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Formal [4 + 2] Cycloaddition Of Alkoxy-Substituted Donor-Acceptor Cyclobutanes And Aldehydes Catalyzed By Yb(Otf)3., Mahmoud M Abd Rabo Moustafa, Andrew C Stevens, Ben P Machin, Brian L Pagenkopf Oct 2010

Formal [4 + 2] Cycloaddition Of Alkoxy-Substituted Donor-Acceptor Cyclobutanes And Aldehydes Catalyzed By Yb(Otf)3., Mahmoud M Abd Rabo Moustafa, Andrew C Stevens, Ben P Machin, Brian L Pagenkopf

Chemistry Publications

The cycloaddition between 2-alkoxy-1,1-cyclobutane diesters and aromatic, heteroaromatic, or aliphatic aldehydes under Yb(OTf)(3) catalysis generates tetrahydropyrans in high yields with exclusive cis-stereochemistry.

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Synthesis, Kinetic And Photocatalytic Studies Of Porphyrin-Ruthenium-Oxo Complexes, Yan Huang Aug 2010

Synthesis, Kinetic And Photocatalytic Studies Of Porphyrin-Ruthenium-Oxo Complexes, Yan Huang

Masters Theses & Specialist Projects

Macrocyclic ligand-complexed transition metal-oxo intermediates are the active oxidizing species in a variety of important biological and catalytic oxidation reactions. Many transition metal catalysts have been designed to mimic the predominant oxidation catalysts in Nature, namely the cytochrome P450 enzymes. Ruthenium porphyrin complexes have been the center of the research and have successfully been utilized, as catalysts, in major oxidation reactions such as the hydroxylation of alkanes. This study focuses on kinetic and photocatalytic studies of oxidation reactions with wellcharacterized high-valent ruthenium-oxo porphyrin complexes.
The trans-dioxoruthenium(VI) porphyrins have been among the best characterized metal-oxo intermediates and their involvement as …

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Diels-Alder Chemistry Of Siloles And Their Transformation Into Cyclohex-2-Ene-1,4-Cis-Diols., Andrew C Stevens, Brian L Pagenkopf Jul 2010

Diels-Alder Chemistry Of Siloles And Their Transformation Into Cyclohex-2-Ene-1,4-Cis-Diols., Andrew C Stevens, Brian L Pagenkopf

Chemistry Publications

The synthesis of siloles with substitution patterns that are continuative toward natural product synthesis are described. Their reactivity in Diels-Alder chemistry was explored through thermal, Lewis acid, and high-pressure reactions. Furthermore, bicyclic adducts were oxidatively cleaved to reveal a highly functionalized cyclohexene core.

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Synthesis Of Meta-Terphenyl Scaffolded Molecules For Catalysis And Sensor Applications, Brad Morgan May 2010

Synthesis Of Meta-Terphenyl Scaffolded Molecules For Catalysis And Sensor Applications, Brad Morgan

All Dissertations

The utility of the m-terphenyl has been observed in a wide variety of applications since its first discovery. The tunable conformational flexibility contributes to the unique properties and resulting applications thereof. Chapter 1 goes into detail about the concepts used throughout and defines the tools needed to understand the chemistry in the
resulting chapters.
The primary use of the m-terphenyl herein is as a canopy that shields a pocket created underneath the central ring. Functionalization within this pocket allows metal binding in defined coordination environments. with the use of donor ligands attached to the flanking rings. The applications of these …

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Metal-Organic Materials: From Design Principles To Practical Applications, Mohamed H. Alkordi Mar 2010

Metal-Organic Materials: From Design Principles To Practical Applications, Mohamed H. Alkordi

USF Tampa Graduate Theses and Dissertations

The works presented herein outline rational design approaches towards construction of solid state materials with great potentials to answer some of current demanding applications. Specifically, the materials targeted are metal−organic materials with desirable structural features and functional properties. Metal−organic materials are constructed from organic linker molecules and metal ions under relatively mild solvothermal reaction conditions that preserve the structural features of the relatively simple building blocks. Therefore, it is feasible to conceive a retrospective pathway of the reaction and thus deconstruct the desirable structures into simple, chemicallyrelevant, building blocks in an approach known as the molecular building block approach. Due …

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Remarkable Iodine-Catalyzed Synthesis Of Novel Pyrrole- Bearing N-Polyaromatic B-Lactams, Debasish Bandyopadhyay, Gildardo Rivera, Isabel Salinas, Hector Aguilar, Bimal K. Banik Feb 2010

Remarkable Iodine-Catalyzed Synthesis Of Novel Pyrrole- Bearing N-Polyaromatic B-Lactams, Debasish Bandyopadhyay, Gildardo Rivera, Isabel Salinas, Hector Aguilar, Bimal K. Banik

School of Integrative Biological & Chemical Sciences (Formerly Dept. of Chemistry)

Because of their interesting biological properties various methods for the synthesis of substituted pyrroles are described in the literature. However, synthesis of pyrroles fused with a β-lactam ring has not been reported. Our group has demonstrated synthesis and biological evaluation of various β-lactams as anticancer agents. The anticancer activities of these compounds have prompted us to study the synthesis of pyrroles bound to the β-lactams. We have identified an expeditious synthetic method for the preparation of pyrroles fused with β-lactams by reacting 3-amino β-lactams with acetonylacetone in the presence of catalytic amounts (5 mol%) of molecular iodine at room temperature. …

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Increased Yields And Simplified Purification With A Second-Generation Cobalt Catalyst For The Oxidative Formation Of Trans-Thf Rings., Cory Palmer, Nicholas A Morra, Andrew C Stevens, Barbora Bajtos, Ben P Machin, Brian L Pagenkopf Nov 2009

Increased Yields And Simplified Purification With A Second-Generation Cobalt Catalyst For The Oxidative Formation Of Trans-Thf Rings., Cory Palmer, Nicholas A Morra, Andrew C Stevens, Barbora Bajtos, Ben P Machin, Brian L Pagenkopf

Chemistry Publications

The synthesis of a second-generation cobalt catalyst for the formation of trans-THF products via the Mukaiyama aerobic oxidative cyclization is reported. Two procedures have been developed with the new water-soluble catalyst that give superior yields and greatly simplify purification compared to the previous catalysts.

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A General Asymmetric Aldol Reaction Of Silyl Ketene Acetals Derived From Simple Esters To Aryl Alpha-Ketoesters, Brian Pagenkopf, Julie Le Engers Oct 2009

A General Asymmetric Aldol Reaction Of Silyl Ketene Acetals Derived From Simple Esters To Aryl Alpha-Ketoesters, Brian Pagenkopf, Julie Le Engers

Chemistry Publications

No abstract provided.

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Adsorption Of Co On Supported Gold Nanoparticle Catalysts: A Comparative Study, Heather Hartshorn, Christopher J. Pursell, Bert D. Chandler Apr 2009

Adsorption Of Co On Supported Gold Nanoparticle Catalysts: A Comparative Study, Heather Hartshorn, Christopher J. Pursell, Bert D. Chandler

Chemistry Faculty Research

The adsorption of CO on three different gold nanoparticle catalysts supported on high surface area TiO2 was studied using infrared transmission spectroscopy at room temperature and CO pressures typically used in CO oxidation reactions. The three, real-world catalysts were Au catalysts synthesized in our laboratory from thiol monolayer protected clusters (MPCs) and two commercial catalysts from the World Gold Council (WGC and AuTEK). Within experimental reproducibility, the adsorption data for the three catalysts are indistinguishable. While showing approximately Langmuir behavior, the adsorption data also show coverage dependence, as others have observed for many catalyst systems. Two approaches were used …

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New Generation Of Electrochemical Sensors For Nitric Oxide;Ruthenium/Carbon-Based Nanostructures And Colloids As Electrocatalytic Platforms, W. Pubudu M. Peiris Jan 2009

New Generation Of Electrochemical Sensors For Nitric Oxide;Ruthenium/Carbon-Based Nanostructures And Colloids As Electrocatalytic Platforms, W. Pubudu M. Peiris

ETD Archive

Nitric oxide (NO) is an important intercellular messenger that acts in many tissues to regulate a diverse range of physiological and pathological processes. The physiologically implications of NO function are far from being completely understood. The multifaceted reactivity of NO prompted the need for accurate determination of the concentration of this molecule. However, it is difficult to detect nitric oxide, particularly in biological media and near live cells due to its short half-life, a result of its reactivity and the low levels of NO produced in vivo. As a result, the accurate and reliable detection of NO under varying experimental …

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H_2{So}_4-Silica As An Efficient And Chemoselective Catalyst For The Synthesis Of Acylal From Aldehydes Under Solvent-Free Conditions, Seied Ali Pourmousavi, Zahra Zinati Jan 2009

H_2{So}_4-Silica As An Efficient And Chemoselective Catalyst For The Synthesis Of Acylal From Aldehydes Under Solvent-Free Conditions, Seied Ali Pourmousavi, Zahra Zinati

Turkish Journal of Chemistry

A variety of aldehydes react with acetic anhydride in the presence of a catalytic amount of H_2SO_4-silica to afford the corresponding 1,1-diacetates (acylals) in excellent yields. Ketones are not affected under the reaction conditions. The advantages are the simplicity of the acylation procedure, and the relatively non-toxic nature of the catalyst as well as its easy availability and low cost.

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Preparations Of Composite Electrodes Of Pt With HXWo3 And Catalytic Activity Toward Oxygen Reduction Reaction, Pan-Pan Guo, You-Ju Huang, Hong-Yan Yang, Wei Li, Qing-Long Zhang, Wei-Shan Li Nov 2008

Preparations Of Composite Electrodes Of Pt With HXWo3 And Catalytic Activity Toward Oxygen Reduction Reaction, Pan-Pan Guo, You-Ju Huang, Hong-Yan Yang, Wei Li, Qing-Long Zhang, Wei-Shan Li

Journal of Electrochemistry

Three composite electrodes of platinum with hydrogen tungsten bronze(HxWO3)were prepared by voltammetry: hydrogen tungsten bronze deposited on platinum(HxWO3/Pt);platinum deposited on hydrogen tungsten bronze(Pt/HxWO3) and codeposited platinum and hydrogen tungsten bronze(Pt-HxWO3).The eletro-catalytic activities of three electrodes toward oxygen reduction reaction were studied.It is found that the catalytic activity of platinum can be improved by introducing with hydrogen tungsten bronze.Among these composite electrodes Pt/HxWO3,and the electrode shows the best eletro-catalytic activity toward oxygen reduction reaction,hence,provides a new way for reducing loading of …

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Tetrahymena Thermophila And Candida Albicans Group I Intron-Derived Ribozymes Can Catalyze The Trans-Excision-Splicing Reaction, P. Patrick Dotson Ii, Ashley K. Johnson, Stephen M. Testa Sep 2008

Tetrahymena Thermophila And Candida Albicans Group I Intron-Derived Ribozymes Can Catalyze The Trans-Excision-Splicing Reaction, P. Patrick Dotson Ii, Ashley K. Johnson, Stephen M. Testa

Chemistry Faculty Publications

Group I intron-derived ribozymes can catalyze a variety of non-native reactions. For the trans-excision-splicing (TES) reaction, an intron-derived ribozyme from the opportunistic pathogen Pneumocystis carinii catalyzes the excision of a predefined region from within an RNA substrate with subsequent ligation of the flanking regions. To establish TES as a general ribozyme-mediated reaction, intron-derived ribozymes from Tetrahymena thermophila and Candida albicans, which are similar to but not the same as that from Pneumocystis, were investigated for their propensity to catalyze the TES reaction. We now report that the Tetrahymena and Candida ribozymes can catalyze the excision of a …

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Hydrogenase Inhibition By O2: Density Functional Theory/Molecular Mechanics Investigation, Daniela Dogaru Jan 2008

Hydrogenase Inhibition By O2: Density Functional Theory/Molecular Mechanics Investigation, Daniela Dogaru

ETD Archive

[Fe-Fe]-hydrogenases are enzymes that reversibly catalyze the reduction of protons to molecular hydrogen, which occurs in anaerobic media. In living systems, [Fe-Fe]-hydrogenases shift the reversible reaction towards H2 formation. The [Fe-Fe]-hydrogenase H-cluster is the active site, which contains two iron atoms (Fep-Fed, i.e., proximal and distal iron). Because most experimental and theoretical investigations confirm that the structure of di-iron air inhibited species is FepII-FedII-O-O-H-, O2 has to be prevented from binding to Fed in all di-iron subcluster oxidation states in order to retain a catalytically active enzyme. By understanding the catalytic processes of metalloenzymes, researches are enabled to produce an …

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Kinetic Evaluation Of Highly Active Supported Gold Catalysts Prepared From Monolayer-Protected Clusters: An Experimental Michaelis-Menten Approach For Determining The Oxygen Binding Constant During Co Oxidation Catalysis, Cormac G. Long, John D. Gilbertson, G. Vijayaraghavan, K. J. Stevenson, Christopher J. Pursell, Bert D. Chandler Jan 2008

Kinetic Evaluation Of Highly Active Supported Gold Catalysts Prepared From Monolayer-Protected Clusters: An Experimental Michaelis-Menten Approach For Determining The Oxygen Binding Constant During Co Oxidation Catalysis, Cormac G. Long, John D. Gilbertson, G. Vijayaraghavan, K. J. Stevenson, Christopher J. Pursell, Bert D. Chandler

Chemistry Faculty Research

Thiol monolayer-protected Au clusters (MPCs) were prepared using dendrimer templates, deposited onto a high-surface-area titania, and then the thiol stabilizers were removed under H2/N2. The resulting Au catalysts were characterized with transmission electron microscopy, X-ray photoelectron spectroscopy, and infrared spectroscopy of adsorbed CO. The Au catalysts prepared via this route displayed minimal particle agglomeration during the deposition and activation steps. Structural data obtained from the physical characterization of the Au catalysts were comparable to features exhibited from a traditionally prepared standard Au catalyst obtained from the World Gold Council (WGC). A differential kinetic study of CO oxidation catalysis by the …

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Dielectric Behavior Of The Catalyst Zeolite Nay, Ertuğrul İzci̇, Ali̇me İzci̇ Jan 2007

Dielectric Behavior Of The Catalyst Zeolite Nay, Ertuğrul İzci̇, Ali̇me İzci̇

Turkish Journal of Chemistry

Zeolites are crystalline hydrated aluminosilicates of alkaline and alkaline earth metals. The basic zeolite structure is an anionic frame of Si and Al T-atoms, which are tetrahedral and coordinated with oxygen atoms. The electrical properties of zeolites are of enormous technical importance due to their manifold applications as solid catalysts. Zeolite NaY was used in this investigation. Zeolite NaY is a synthetic zeolite and it has a faujasite structure. The electrical conductivity, dielectric permittivity, and loss factor of Na ion exchanged zeolite NaY was carried out in the 10^4-10^6 Hz frequency region at room temperature and different water contents using …

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Tuning Supported Catalyst Reactivity With Dendrimer-Templated Pt-Cu Nanoparticles, Natalie N. Hoover, Bethany J. Auten, Bert D. Chandler Mar 2006

Tuning Supported Catalyst Reactivity With Dendrimer-Templated Pt-Cu Nanoparticles, Natalie N. Hoover, Bethany J. Auten, Bert D. Chandler

Chemistry Faculty Research

The effects of particle composition on heterogeneous catalysis were studied using dendrimer-encapsulated nanoparticles (DENs) as precursors to supported Pt-Cu catalysts. Bimetallic Pt-Cu DENs with varying Pt/Cu ratios were prepared in an anaerobic aqueous solution and deposited onto a high-purity commercial alumina support. The dendrimer template was then thermally removed to yield supported nanoparticle catalysts, which were studied with toluene hydrogenation and CO oxidation catalysis as well as infrared spectroscopy of adsorbed CO. Incorporating Cu into Pt nanoparticles had opposite effects on the two test reactions. Cu acted as a mild promoter for CO oxidation catalysis, and the promoting effect was …

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Low-Temperature Activation Conditions For Pamam Dendrimer Templated Pt Nanoparticles, Anil Singh, Bert D. Chandler Aug 2005

Low-Temperature Activation Conditions For Pamam Dendrimer Templated Pt Nanoparticles, Anil Singh, Bert D. Chandler

Chemistry Faculty Research

Surface immobilized polyamidoamine (PAMAM) dendrimer templated Pt nanoparticles were employed as precursors to heterogeneous catalysts. CO oxidation catalysis and in situ infrared spectroscopy were used to evaluate conditions for dendrimer removal. Infrared spectroscopy showed thatPAMAMdendrimer amide bonds begin decomposing at temperatures as low as 75 °C. Although the amide stretches are completely removed after 3 h of oxidation at 300 °C, 16 h were required to reach maximum catalytic activity. Further treatment under oxidizing or reducing atmospheres did not cause substantial changes in activity. Infrared spectroscopy of the activated materials indicated that organic residues, probably surface carboxylates, are formed during …

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Hydroxy Double Salt Anion Exchange Kinetics: Effects Of Precursor Structure And Anion Size, Everson Kandare, Jeanne Hossenlopp Feb 2005

Hydroxy Double Salt Anion Exchange Kinetics: Effects Of Precursor Structure And Anion Size, Everson Kandare, Jeanne Hossenlopp

Chemistry Faculty Research and Publications

H NMR spectroscopy and powder X-ray diffraction have been used to explore the details of anion exchange reactions of two layered hydroxy double salts (HDSs), zinc copper hydroxy acetate (ZCA), nickel zinc hydroxy acetate (NZA), and a related layered material, zinc hydroxy acetate (ZHA), at room temperature (21−22 °C). Reactions that followed Avrami−Erofe'ev kinetics with respect to temporal profiles for acetate release, ZCA with butyrate (k = 1.7 × 10-3 s-1), and octanoate (k = 0.79 × 10-3 s-1) anions, as well as ZHA with octanoate (k = 2.6 × 10 …

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The Effect Of Metal Loading On Structural Characteristics And Low Temperature Co Oxidation Activity Of Coprecipitated Co/Al_2o_3, Şeyma Özkara, Ayşe Ni̇lgün Akin, Zülal Misirli, Ahmet Erhan Aksoylu Jan 2005

The Effect Of Metal Loading On Structural Characteristics And Low Temperature Co Oxidation Activity Of Coprecipitated Co/Al_2o_3, Şeyma Özkara, Ayşe Ni̇lgün Akin, Zülal Misirli, Ahmet Erhan Aksoylu

Turkish Journal of Chemistry

The effect of metal loading on structural properties and CO oxidation activity of coprecipitated Co/Al_2O_3 catalysts was investigated. The results indicated the participation of cobalt in the Co-Al skeleton for all coprecipitated samples. Environmental-SEM-EDXS studies showed that at loadings higher than ca. 15 wt.-%, cobalt formed layer-by-layer clusters on the surface; 16.8 wt.-% Co/Al_2O_3 displayed the highest activity and stability in CO oxidation.

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Crystal Structure Of The Gtpase Domain Of Rat Dynamin 1, Thomas F. Reubold, Susanne Eschenburg, Andreas Becker, Marilyn Leonard, Sandra L. Schmid, Richard B. Vallee, F. Jon Kull, Dietmar J. Manstein Jan 2005

Crystal Structure Of The Gtpase Domain Of Rat Dynamin 1, Thomas F. Reubold, Susanne Eschenburg, Andreas Becker, Marilyn Leonard, Sandra L. Schmid, Richard B. Vallee, F. Jon Kull, Dietmar J. Manstein

Dartmouth Scholarship

Here, we present the 1.9-A crystal structure of the nucleotide-free GTPase domain of dynamin 1 from Rattus norvegicus. The structure corresponds to an extended form of the canonical GTPase fold observed in Ras proteins. Both nucleotide-binding switch motifs are well resolved, adopting conformations that closely resemble a GTP-bound state not previously observed for nucleotide-free GTPases. Two highly conserved arginines, Arg-66 and Arg-67, greatly restrict the mobility of switch I and are ideally positioned to relay information about the nucleotide state to other parts of the protein. Our results support a model in which switch I residue Arg-59 gates GTP binding …

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