Search results for " rate constant"

showing 10 items of 220 documents

Ab initioanalysis on metal ion catalysis in the enolization reactions of some acetylheterocycles: kinetics of the enolization reactions of 3-acetyl-5…

2002

Kinetic data on the enolization reaction of 3-acetyl-5-methylisoxazole, 5-acetyl-3-methylisoxazole, 3(5)-acetylpyrazole and some previously studied acetylheterocycles have been the object of a comprehensive ab initio analysis. Enolization rate constants were measured spectrophotometrically by the halogen trapping technique at 25 °C and ionic strength of 0.3 mol dm−3 in water, in acetate buffers, in dilute hydrochloric acid, in dilute sodium hydroxide and in the presence of some metal ion salts. In the spontaneous (water) and base (acetate) catalysed reactions the ketones investigated are generally more reactive than acetophenone, according to the electron-withdrawing effect of the heterocyc…

ChemistryOrganic ChemistryHeteroatomInorganic chemistryAb initioProtonationKeto–enol tautomerismCatalysischemistry.chemical_compoundReaction rate constantComputational chemistryAb initio quantum chemistry methodsPhysical and Theoretical ChemistryAcetophenoneJournal of Physical Organic Chemistry
researchProduct

Quantum dynamics of 16O + 36O2 and 18O + 32O2 exchange reactions

2015

We present quantum dynamical investigations of (16)O + (36)O2 and (18)O + (32)O2 exchange reactions using a time-independent quantum mechanical method and an accurate global potential energy surface of ozone [Dawes et al., J. Chem. Phys. 135, 081102 (2011)]. Initial state-selected integral cross sections, rate constants, and Boltzmann averaged thermal rate constants are obtained and compared with earlier experimental and theoretical results. The computed thermal rate constants for the oxygen exchange reactions exhibit a negative temperature dependence, as found experimentally. They are in better agreement with the experiments than the previous studies on the same reactions.

ChemistryQuantum dynamicsGeneral Physics and AstronomyThermodynamicsPotential energyChemical kineticssymbols.namesakeReaction rate constantPotential energy surfaceBoltzmann constantsymbolsPhysical chemistryPhysical and Theoretical ChemistryNegative temperatureQuantumThe Journal of Chemical Physics
researchProduct

Kinetic modeling of ion conduction in KcsA potassium channel.

2005

KcsA constitutes a potassium channel of known structure that shows both high conduction rates and selectivity among monovalent cations. A kinetic model for ion conduction through this channel that assumes rapid ion transport within the filter has recently been presented by Nelson. In a recent, brief communication, we used the model to provide preliminary explanations to the experimental current-voltage J-V and conductance-concentration g-S curves obtained for a series of monovalent ions (K(+),Tl(+), and Rb(+)). We did not assume rapid ion transport in the calculations, since ion transport within the selectivity filter could be rate limiting for ions other than native K(+). This previous wor…

ChemistrySodiumPositive IonsIonic ConductivityAnalytical chemistryKcsA potassium channelUNESCO::FÍSICAGeneral Physics and AstronomyConductanceIon-associationRubidiumIonReaction rate constant:FÍSICA [UNESCO]Biomembrane TransportPotassium ; Thallium ; Rubidium ; Sodium ; Positive Ions ; Ionic Conductivity ; Biomembrane TransportPotassiumIonic conductivityPhysical and Theoretical ChemistryThalliumIon transporterIon channelThe Journal of chemical physics
researchProduct

Reaction of complex ligands: Part 95. Chromium tricarbonyl complexes of polysubstituted naphthohydroquinones: regioselective synthesis via [3+2+1]-be…

2003

Abstract A series of polysubstituted naphthohydroquinoid tricarbonyl chromium complexes were prepared by chromium mediated [3+2+1]-benzannulation of Fischer-type carbene complexes with alkynes. The kinetics and the thermodynamic data of the η6-η6-haptotropic rearrangements were investigated by in-situ NMR spectroscopy. The free activation energies ΔG# range from 23 to 26 kcal mol−1 and only slightly depend on the bulk and the donor/acceptor properties of the substituents. Equilibrium of metal migration was observed for naphthohydroquinone complexes bearing methoxy substituents at the non-hyroquinoid ring (ring A). In complexes bearing methyl groups or only hydrogen substituents at ring A th…

ChemistryStereochemistryOrganic ChemistryDiastereomerRegioselectivityHexafluorobenzenechemistry.chemical_elementNuclear magnetic resonance spectroscopyRing (chemistry)BiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundChromiumReaction rate constantMaterials ChemistryPhysical and Theoretical ChemistryCarbeneJournal of Organometallic Chemistry
researchProduct

Organometallic nucleophiles. Mechanism of halide displacement at saturated carbon by 2-pyridyl and 4-Pyridyl complexes [M(dmtc)(C5H4N-Cn)(L)] (M  Pd…

1992

Abstract A mechanistic study is reported of nucleophilic halide substitution by pyridyl complexes [M(dmtc)C 5 H 4 N- C 2 )(L)] (M  Pd or Pt; L  PMe 3 , PEt 3 or PPh 3 ) and [Pd(dmtc)C 5 H 4 N- C 4 )(L)] (L  PMe 3 or PPh 3 ) on organic halides XCH 2 R (X  Cl or Br; R  CHCH 2 , COMe, Ph, or CN) in various solvents, yielding the pyridylium derivatives [M(dmtc)1-CH 2 R)C 5 H 4 N- C 2 (L)] + and [Pd(dmtc)(1-CH 2 R)(C 5 H 4 N- C 4 (L)] + , respectively. The kinetics obey a second-order rate law: rate  k 2 [XCH 2 R][Complex]. A similar rate law is observed for the analogous reactions involving 4-dimethyl-aminopyridine (4-dmapy) as the nucleophile. The effects of solvent and leaving group, a…

ChemistryStereochemistryOrganic ChemistrySubstituentLeaving groupHalideBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundReaction rate constantNucleophilePyridineMaterials ChemistryNucleophilic substitutionPhysical and Theoretical ChemistrySolvent effectsJournal of Organometallic Chemistry
researchProduct

Nonenzymatic glycation reaction of folate with reducing sugars: A case study on [6S]-5-methyltetrahydrofolate and fructose

2006

In the Maillard reaction, free amino groups react with reducing sugars to form nonenzymatic glycation products. It has recently been shown that in the presence of reducing sugars (i.e. fructose) folic acid is subjected to a non-enzymatic glycation reaction, which may represent an important pathway of folate degradation besides the established oxidative degradation pathways. In the current study, the thermal stability of [6S]-5-methyltetrahydrofolic acid ([6S]-5-CH3H4PteGlu, 0.4µM), the predominant naturally occuring folate derivate, was investigated on a qualitative and kinetic basis in the presence of different fructose concentrations (0-3M) in milliQ water (8.11ppm O2). Samples were isoth…

ChromatographyChemistryFirst-order reactionKineticsFructoseMaillard reactionsymbols.namesakechemistry.chemical_compoundReaction rate constantGlycationsymbolsOrganic chemistryThermal stabilityDestabilisation13th World Congress of Food Science & Technology
researchProduct

Study of the effect of the membrane composition on ion transfer across a supported liquid membrane

2003

Abstract The rate of ion transfer across the supported liquid membrane (SLM) is studied in the rotating diffusion cell (RDC), varying the chemical composition of the SLM from net-cloth supported gel membranes to radiation-grafted polymer membranes. Steady-state current–voltage curves are measured as a function of the rotation rate, and values for the standard rate constant, k 0 , are determined for a series of tetraalkylammonium cations from the analysis of the initial slopes and the diffusion limiting currents. The analysis gives values for k 0 of the order of 10 −2 –10 −4 cm s −1 , which is in rather good agreement with the values found in the literature for this type of the system. As co…

ChromatographyChemistryGeneral Chemical EngineeringCapacitive sensingSynthetic membraneAnalytical chemistryIonic bondingAnalytical ChemistryReaction rate constantMembraneElectrochemistryElectric currentDiffusion (business)Drug carrierJournal of Electroanalytical Chemistry
researchProduct

Determination of rate constants of ion transfer kinetics across immiscible electrolyte solutions

1998

Abstract The rotating diffusion cell was used to study ion transfer across the interface between two immiscible electrolyte solutions. Tetrabutylammonium was chosen as the transferring cation and lithium chloride as the supporting electrolyte in aqueous phase. Tetrabutylammonium tetrakis-(4-fluorophenyl)-borate in 2-nitrophenyl-octylether was used as the organic electrolyte solution supported in the porous membrane. The quasi-steady state current–voltage curves were measured both by applying potential steps and by imposing a slow potential sweep. The analysis of experimental results was based on the comparison with the theoretical current–voltage curves and on the Koutecky–Levich plots. The…

ChromatographySupporting electrolyteGeneral Chemical EngineeringAqueous two-phase systemThermodynamicsConcentration effectElectrolytechemistry.chemical_compoundReaction rate constantElectrical resistance and conductancechemistryElectrochemistryLithium chlorideITIESElectrochimica Acta
researchProduct

Determination of kinetic parameters of redox reactions using CE‐ICP‐MS: A case study for the reduction of Np(V) by hydroxylamine hydrochloride

2018

The rate constants k of the reduction of 5 × 10-5  M Np(V) to Np(IV) by hydroxylamine hydrochloride (HAHCl) in 1 M HCl have been determined by CE-ICP-MS in the temperature range of ϑ = 30-70°C and with varying concentrations of HAHCl from 1 to 7.2 M. The reaction was found to have (pseudo)first order kinetics with respect to HAHCl. The experimental results for k ranged from 0.0029(1) min-1 (ϑ = 40°C, c(HAHCl) = 3 M) to 0.039(7) min-1 (ϑ = 60°C, c(HAHCl) = 7.2 M). The activation energy of the reaction was determined as EA  = (72 ± 10) kJ/mol. These results and a comparison with literature data show that the coupling of CE to ICP-MS provides a powerful analytical tool for the investigation of…

Clinical BiochemistryInorganic chemistrychemistry.chemical_elementHydroxylamine02 engineering and technologyActivation energy01 natural sciencesBiochemistryRedoxMass SpectrometryAnalytical ChemistryNeptuniumReaction rate constantTransition metalChemistryNeptunium010401 analytical chemistryTemperatureElectrophoresis CapillaryActinideRate equationAtmospheric temperature range021001 nanoscience & nanotechnology0104 chemical sciencesKineticsReducing Agents0210 nano-technologyOxidation-ReductionELECTROPHORESIS
researchProduct

OPKINE, a multipurpose program for kinetics

1991

The program OPKINE is presented for the study of reaction mechanisms and multicomponent analysis in dynamic conditions. This program is written in FORTRAN-77 for IBM 30/90 and VAX 8300 computers, and permits the simultaneous evaluation of both rate constants and initial reagent concentrations or, alternatively, rate constants and sensitivities. Up to 20 kinetic curves, with up to 400 points each, can be treated to evaluate up to 40 parameters. Integration of the system of differential equations is performed by means of the Runge–Kutta–Fehlberg method. OPKINE is provided with the Simplex, and modified versions of the Davidon–Fletcher–Powell and Gauss–Newton–Marquardt optimization methods. A …

Computational MathematicsReaction rate constantSimplexSystem of differential equationsComputer scienceReagentMonte Carlo methodKineticsOptimization methodsApplied mathematicsGeneral ChemistryKinetic energyAlgorithmJournal of Computational Chemistry
researchProduct