Search results for "Reaction"

showing 10 items of 6134 documents

Kinetics of streptolysin O self-assembly.

1995

Streptolysin O is a member of a family of membrane-damaging toxins that bind to cell membranes containing cholesterol and then polymerize to form large pores. We have examined the kinetics of toxin action using 125I-labelled streptolysin O. Binding of toxin monomers to membranes displays first-order kinetics and is reversible; the rate of desorption from red cells shows a marked dependence on temperature. To study oligomerization, toxin was bound to erythrocytes at 0 degrees C. Oligomer formation was then triggered by a sudden temperature shift and stopped by solubilization of membranes with deoxycholate. While at moderately high streptolysin O concentrations oligomerization behaves as a re…

Reaction mechanismErythrocytesToxinMacromolecular SubstancesKineticsErythrocyte MembraneDithionitrobenzoic Acidmedicine.disease_causeOligomerBiochemistrychemistry.chemical_compoundCrystallographyKineticsMembraneMonomerchemistryPolymerizationBacterial ProteinsStreptolysinsmedicineBiophysicsCentrifugation Density GradientAnimalsStreptolysinRabbitsEuropean journal of biochemistry
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Photodecomposition of adsorbed ethanoic acid over silica gel catalyst in a flow system

1986

Abstract The photodecomposition of ethanoic acid adsorbed on silica gels from various sources was studied at wavelengths greater than 300 nm. The experiments were carried out in a flow apparatus. A few photoreactivity tests using acetone or ethanol were also performed. The photodecomposition of ethanoic acid and acetone produced mainly carbon dioxide and methane, in the ratio 2:1, and traces of ethane and methanol. Adsorbed ethanol was not affected at all by the radiation. Infrared and UV-vis reflectance spectra of ethanoic acid adsorbed on silica gels as well as UV-vis reflectance spectra of acetone and ethanol adsorbed on silica gels were recorded. The spectra show the presence of a varie…

Reaction mechanismEthanolSilica gelInorganic chemistryPhotochemistryCatalysisMethaneCatalysischemistry.chemical_compoundAdsorptionchemistryAcetoneMethanolPhysical and Theoretical ChemistryJournal of Catalysis
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A Molecular Electron Density Theory Study of the Reactivity and Selectivities in [3 + 2] Cycloaddition Reactions of C,N-Dialkyl Nitrones with Ethylen…

2018

The zw-type [3 + 2] cycloaddition (32CA) reactions of C,N-dialkyl nitrones with a series of ethylenes of increased electrophilic character have been studied within the Molecular Electron Density Theory (MEDT) at the MPWB1K/6-311G(d,p) computational level. Both, reactivity and selectivities are rationalized depending on the polar character of the reaction. Due to the strong nucleophilic character of C,N-dialkyl nitrones, the corresponding zw-type 32CA reactions are accelerated with the increased electrophilic character of the ethylene, which also plays a crucial role in the reaction mechanism, thus determining the regio- and stereoselectivities experimentally observed. While, in the 32CA rea…

Reaction mechanismEthylene010405 organic chemistryOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesMedicinal chemistryCycloaddition0104 chemical scienceschemistry.chemical_compoundNucleophilechemistryElectrophileSingle bondReactivity (chemistry)The Journal of Organic Chemistry
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A theoretical study on the decomposition mechanism of β-propiolactone and β-butyrolactone

1998

Abstract The reaction mechanism associated with the decomposition of β-propiolactone and β-butyrolactone in the gas phase to form carbon dioxide and ethylene or propene, respectively, has been theoretically characterized by using analytical gradients at the B3LYP/6-31G**, B3LYP/6-31++G**, MP2/6-31G** and MP2/6-31++G** calculation levels, as well as by single point calculations at QCISD(T)/6-31++G**//MP2/6-31++G**. A detailed analysis of the results points out that the reaction pathway can be described as an asynchronous concerted process. The geometrical parameters and the components of the transition vector are weakly dependent on the computational method. By applying transition state theo…

Reaction mechanismEthyleneChemistryGeneral Physics and AstronomyThermodynamicsβ-propiolactoneDecompositionPropenechemistry.chemical_compoundTransition state theoryComputational chemistryTheoretical methodsPhysical and Theoretical ChemistrySingle pointChemical Physics Letters
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Selective hydrogenation of acetylene in ethylene feedstocks on Pd catalysts

1996

Abstract Pumice supported palladium catalysts were compared with Pd SiO 2 and Pd Al 2 O 3 in the hydrogenation of acetylene using typical industrial ethylene feedstocks: front-end and tail-end cuts. Pd/pumice catalysts exhibit good activity and excellent selectivity and stability in the title reaction. Their activity/selectivity pattern is controlled by the composition of the reaction mixture. The turnover frequency (TOF) increases, and the apparent activation energy (Ea) decreases, with the H 2 C 2 H 2 ratio, but they are not affected by the C 2 H 2 C 2 H 4 ratio. The selectivity to ethane (SE) does not change with acetylene conversion at low H 2 C 2 H 2 ratio (tail-end cut) and increases …

Reaction mechanismEthyleneHydrogenProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementActivation energyCatalysisCatalysischemistry.chemical_compoundchemistryAcetyleneOrganic chemistrySelectivityPalladiumApplied Catalysis A: General
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Hydrogenation of acetylene in ethylene rich feedstocks: Comparison between palladium catalysts supported on pumice and alumina

1998

Abstract The activity–selectivity patterns of Pd/pumice catalysts are compared with industrial and home prepared Pd/Al2O3 catalysts in the hydrogenation of acetylene in ethylene rich feedstocks (front-end and tail-end cuts). The iso-kinetic relationship (IKR) approach and a new mathematical model, surface site evolution model (SSEM), are employed in this comparison. Pumice and alumina supported Pd catalysts show different metal redox properties. A similar reaction mechanism is adequate to describe the reaction pathway independently by the catalysts and the gas mixtures considered. This mechanism involves the formation of surface polymers during the catalytic reactions and different catalyti…

Reaction mechanismEthyleneProcess Chemistry and Technologychemistry.chemical_elementHeterogeneous catalysisCatalysisCatalysischemistry.chemical_compoundTransition metalchemistryAcetyleneChemical engineeringReagentOrganic chemistryPalladium
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Kinetic Study of the Oxidation of n-Butane on Vanadium Oxide Supported on Al/Mg Mixed Oxide

1997

The reaction kinetics of the oxidative dehydrogenation (ODH) of n-butane over vanadia supported on a heat-treated Mg/Al hydrotalcite (37.3 wt % of V2O5) was investigated by both linear and nonlinear regression techniques. A reaction network including the formation of butenes (1-, 2-cis-, and 2-trans-butene), butadiene, and carbon oxides by parallel and consecutive reactions, at low and high n-butane conversions, has been proposed. Langmuir−Hinshelwood (LH) models can be used as suitable models which allows reproduction of the global kinetic behavior, although differences between oxydehydrogenation and deep oxidation reactions have been observed. Thus, the formation of oxydehydrogenation pro…

Reaction mechanismGeneral Chemical EngineeringInorganic chemistryButaneGeneral ChemistryRedoxIndustrial and Manufacturing EngineeringVanadium oxideCatalysisChemical kineticschemistry.chemical_compoundchemistryMixed oxideDehydrogenation
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Mechanism of the palladium-catalysed electrosynthesis of diethyl carbonate from carbon monoxide and ethanol

2004

Abstract A mechanism is proposed for the PdBr2(PPh3)2-catalysed electrosynthesis of diethyl carbonate from carbon monoxide and ethanol, proceeding at room temperature and atmospheric CO pressure. The mechanism is investigated by cyclic voltammetry and 31P NMR spectroscopy. The active Pd0 complex able to coordinate CO is generated by the chemical reduction of PdBr2(PPh3)2 by EtO– ions generated from EtOH at the cathode. After reaction of EtO– ions with Pd0(PPh3)2(CO), the ensuing anionic complex [(PPh3)2Pd0–COOEt]– is oxidized at the anode in a key step leading to BrPdII–COOEt(PPh3)2. A nucleophilic attack of ethoxide on the latter generates diethyl carbonate and the Pd0 complex active in th…

Reaction mechanismGeneral Chemical EngineeringInorganic chemistryDiethyl carbonatechemistry.chemical_elementGeneral ChemistryElectrosynthesisCatalysischemistry.chemical_compoundchemistryCyclic voltammetryCarbonylationCarbon monoxidePalladiumComptes Rendus Chimie
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A DFT study of IRMOF-3 catalysed Knoevenagel condensation

2011

It has been recently reported that IRMOF-3 [Gascon et al., J. Catal, 2009, 261, 75] may behave as a basic catalyst, active in the Knoevenagel condensation. In particular, it has been shown that the basicity of aniline-like amino moieties is enhanced, along with the catalytic activity, when incorporated into MOF structures. The computational study here was aimed at finding possible atomistic explanations of the increased basicity and catalytic activity of the IRMOF-3 embedded aniline groups, experimentally claimed. It was, moreover, aimed at guessing a reaction mechanism for the IRMOF-3 catalysed Knoevenagel condensation of benzaldehyde and ethyl-cyanoacetate. Within the DFT framework we hav…

Reaction mechanismGeneral Physics and AstronomyProtonationCatalysisBenzaldehydechemistry.chemical_compoundAnilinechemistryCatalytic cycleComputational chemistryOrganic chemistryMoleculeKnoevenagel condensationPhysical and Theoretical ChemistryIRMOF knoevenagel condensation computational chemistryPhysical Chemistry Chemical Physics
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Enantioselective Palladium-Catalyzed Oxidative β,β-Fluoroarylation of α,β-Unsaturated Carbonyl Derivatives

2016

© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim The site-selective palladium-catalyzed three-component coupling of deactivated alkenes, arylboronic acids, and N-fluorobenzenesulfonimide is disclosed herein. The developed methodology establishes a general, modular, and step-economical approach to the stereoselective β-fluorination of α,β-unsaturated systems.

Reaction mechanismHydrocarbons FluorinatedHalogenationStereochemistrychemistry.chemical_elementStereoisomerismAlkenes010402 general chemistry01 natural sciencesArticleCatalysisCatalysisFluorinatedfluorineOrganic chemistrychemistry.chemical_classificationSulfonamidesMolecular StructurealkenesAlkene010405 organic chemistryOrganic ChemistryEnantioselective synthesisHalogenationStereoisomerismGeneral ChemistryGeneral MedicinepalladiumBoronic AcidsHydrocarbons0104 chemical sciencesreaction mechanismschemistryChemical Sciencessynthetic methodsStereoselectivityOxidation-ReductionPalladiumPalladium
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