Search results for " rate constant"

showing 10 items of 220 documents

In situ spectroelectrochemical study of the reductive coupling of benzaldehyde catalyzed by Ti(III) complexes in the presence of Mg(II)

2003

Abstract The UV–vis spectroelectrochemical technique has been used to visualize for the first time, the formation of a trimetallic intermediate Ti(III)Mg(II)Ti(III) during the reductive coupling of benzaldehyde in the presence of electrogenerated Ti(III) and MgCl 2 . This intermediate is supposed to induce the high diastereoselectivity of the reaction. We have built a special thin layer cell adapted from the scheme proposed by A. Neudeck and L. Dunsch [‘J. Electroanal. Chem. 370 (1994) 17; J. Electroanal. Chem. 386 (1995) 135’] which allows the simultaneous recording of the cyclic voltammogram and of a great quantity of UV–vis spectra at a frequency of 1 spectrum per second by means of a …

Reaction mechanismChemistryMagnesiumGeneral Chemical Engineeringchemistry.chemical_elementElectrochemistryPhotochemistryAnalytical ChemistryCatalysisReaction rateBenzaldehydechemistry.chemical_compoundReaction rate constantElectrochemistryPhysical chemistryCyclic voltammetryJournal of Electroanalytical Chemistry
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Kinetic evidence for the solubilization of pyridine-2-azo-p-dimethylaniline in alkanediyl-α,ω-bis(dimethylcetylammonium nitrate) surfactants. Role of…

2004

The incorporation of the bidentate ligand pyridine-2-azo-p-dimethylaniline (PADA) into micellar aggregates of the dimeric cationic surfactants propanediyl-, hexanediyl- and dodecanediyl-alpha,omega-bis(dimethylcetylammonium nitrate) (16-3-16,2NO(3)(-), 16-6-16,2NO(3)(-) and 16-12-16,2NO(3)(-), respectively) has been studied at 25 degreesC by examining the kinetics of the complexation reaction of the Ni(II) ion with this ligand. For comparison, cetyltrimethylammonium nitrate ( CTAN), which can be considered as the "monomeric'' surfactant of 16-3-16,2NO(3)(-), has also been used. The kinetic data have shown that, for 16-3-16,2NO(3)(-) and CTAN, at a surfactant concentration below the critical…

Reaction mechanismInorganic chemistryMicelleCATIONIC GEMINI SURFACTANTSCatalysisHydrophobic effectReaction rate constantPulmonary surfactantDIMERIC SURFACTANTSPolymer chemistryMaterials ChemistryWATERELECTRON TRANSFERANGLE NEUTRON SCATTERINGInterfaces (materials) Optical waveguides metal ionsAqueous solutionAGGREGATION PROPERTIESChemistryAQUEOUS SOLUTIONCationic polymerizationGeneral ChemistryANIONIC MICELLESSUBSTITUTED FERROCENESCritical micelle concentrationBROMIDE SURFACTANTSANGLE NEUTRON SCATTERING; CATIONIC GEMINI SURFACTANTS; AQUEOUS SOLUTION; BROMIDE SURFACTANTS; DIMERIC SURFACTANTS; SUBSTITUTED FERROCENES; AGGREGATION PROPERTIES; ELECTRON TRANSFER; ANIONIC MICELLES; WATERNew J. Chem.
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The electrochemical reduction of thioisonicotinamide in an aqueous medium

1998

Abstract The electrochemical reduction of thioisonicotinamide NRCSNH 2 has been examined in an aqueous medium between H 0 =−1 and pH=13.7. As shown by cyclic voltammetry and polarography, a global 2e − reversible transfer is followed by two successive first-order chemical reactions and a 2e − , 2H + reduction (EC 1 C 2 E process). A mechanism is proposed, beginning with the 2e − reduction of NRCSNH 2 to the formal diionized form NRC − (SH)(NH 3 + ), the first chemical reaction, C 1 , being a formal proton transfer which yields the 4- gem aminosulfanylmethylpyridine; the rate constant of this reaction is 2×10 4  s −1 in acidic medium and diminishes in neutral medium. The second process, C 2 …

Reaction mechanismPolarographyAqueous solutionStereochemistryGeneral Chemical EngineeringInorganic chemistryIsonicotinic acidChemical reactionchemistry.chemical_compoundReaction rate constantchemistryElectrochemistryIsonicotinamideCyclic voltammetryElectrochimica Acta
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Dynamics and reactivity in Thermus aquaticus N6-adenine methyltransferase.

2014

M.TaqI is a DNA methyltransferase from Thermus aquaticus that catalyzes the transfer of a methyl group from S-adenosyl-l-methionine to the N6 position of an adenine, a process described only in prokaryotes. We have used full atomistic classical molecular dynamics simulations to explore the protein–SAM–DNA ternary complex where the target adenine is flipped out into the active site. Key protein–DNA interactions established by the target adenine in the active site are described in detail. The relaxed structure was used for a combined quantum mechanics/molecular mechanics exploration of the reaction mechanism using the string method. According to our free energy calculations the reaction takes…

Reaction mechanismSite-Specific DNA-Methyltransferase (Adenine-Specific)BioinformaticsStereochemistryProtein ConformationMolecular Dynamics SimulationBiochemistryCatalysisMolecular dynamicschemistry.chemical_compoundColloid and Surface ChemistryReaction rate constantAbstractingA-DNAThermusTernary complexThermus aquaticusbiologyActive siteGeneral ChemistryDNAbiology.organism_classificationchemistryFunctional groupsbiology.proteinAmino acidsNucleic Acid ConformationQuantum TheoryThermodynamicsMethyl groupJournal of the American Chemical Society
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Magnetoelectrochemical modulation of pre-organization processes in a 4,4′-dinitrobiphenyl azacrown macrocyclic lactam

2004

A magnetoelectrochemical effect consisting on the modulation of the reaction rate of pre-organization reactions in a 4,4′-dinitrobiphenyl azacrown lactam is described. The electrochemical response of that compound in DMSO solution at microelectrodes consists in two successive dinitrobiphenyl-centred one-electron transfer processes at −0.9 and −1.6 V vs. AgCl/Ag involving the transition from the dihedral geometry of the neutral starting compound to the planar geometry of the final dianion, resulting in an overall ECE mechanism. In the presence of moderate (0.05–0.2 T) static magnetic fields, the second electron transfer process decreases significantly, the apparent rate constant of the dihed…

Reaction mechanismStereochemistryDihedral angleElectrochemistryReaction ratelcsh:ChemistryCrystallographychemistry.chemical_compoundElectron transferReaction rate constantchemistrylcsh:Industrial electrochemistrylcsh:QD1-999ElectrochemistryLactamCyclic voltammetrylcsh:TP250-261Electrochemistry Communications
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Mechanism of four-electron reduction of dioxygen to water by ferrocene derivatives in the presence of perchloric acid in benzonitrile, catalyzed by c…

2004

The selective two-electron reduction of dioxygen occurs in the case of a monocobalt porphyrin [Co(OEP)], whereas the selective four-electron reduction of dioxygen occurs in the case of a cofacial dicobalt porphyrin [Co(2)(DPX)]. The other cofacial dicobalt porphyrins [Co(2)(DPA), Co(2)(DPB), and Co(2)(DPD)] also catalyze the two-electron reduction of dioxygen, but the four-electron reduction is not as efficient as in the case of Co(2)(DPX). The micro-superoxo species of cofacial dicobalt porphyrins were produced by the reactions of cofacial dicobalt(II) porphyrins with dioxygen in the presence of a bulky base and the subsequent one-electron oxidation of the resulting micro-peroxo species by…

Reaction mechanismchemistry.chemical_elementGeneral ChemistryPhotochemistryBiochemistryPorphyrinCatalysisCatalysischemistry.chemical_compoundBenzonitrileElectron transferColloid and Surface ChemistryReaction rate constantchemistryPerchloric acidCobaltJournal of the American Chemical Society
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Calculation of the rate constants for hydrogen abstraction reactions by Hydroperoxyl radical from Methanol, and the investigation of stability of CH3…

2020

Abstract Master equation (ME) with Lennard-Jones potential utilized to simulate the collision between CH3OH and HO2 radical in the presence of bath gas. The reaction mechanism explored through the lowest doublet potential energy surface at CCSD(T)/aug-cc-pVTZ//B3LYP/aug-cc-pVTZ level of theory that is barrierless and forms shallow energized intermediate at the entrance channel. The investigation of the fractional population showed that lifetime of CH3OH.HO2 intermediate (INT*) is fairly short due to its shallow depth, and at the low temperature, most reaction takes place by re-dissociation back to reactants and also when the pressure is high enough, the INT* is thermalized and comes into eq…

Reaction mechanismeducation.field_of_study010304 chemical physicsChemistryPopulationThermodynamics010402 general chemistryCondensed Matter PhysicsHydrogen atom abstraction01 natural sciencesBiochemistry0104 chemical scienceschemistry.chemical_compoundReaction rate constantHydroperoxyl0103 physical sciencesPotential energy surfaceMaster equationPhysical and Theoretical ChemistryeducationEquilibrium constantComputational and Theoretical Chemistry
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The nucleophilicity n index in organic chemistry

2011

The nucleophilicity N index (J. Org. Chem. 2008, 73, 4615), the inverse of the electrophilicity, 1/ω, and the recently proposed inverse of the electrodonating power, 1/ω⁻, (J. Org. Chem. 2010, 75, 4957) have been checked toward (i) a series of single 5-substituted indoles for which rate constants are available, (ii) a series of para-substituted phenols, and for (iii) a series of 2,5-disubstituted bicyclic[2.2.1]hepta-2,5-dienes which display concurrently electrophilic and nucleophilic behaviors. While all considered indices account well for the nucleophilic behavior of organic molecules having a single substitution, the nucleophilicity N index works better for more complex molecules. Unlike…

Reaction rate constantBicyclic moleculeNucleophileChemistryOrganic ChemistryElectrophileMoleculeOrganic chemistryPhysical and Theoretical ChemistryBiochemistryOrganic molecules
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The influence of aluminium cations on electrocarboxylation processes in undivided cells with Al sacrificial anodes

2005

Abstract The influence of Al cations on the electrochemical carboxylation of acenaphthylene ( 1 ), benzophenone ( 2 ), 6-methoxy-2-acetonaphthone ( 3 ), and benzyl chloride ( 4 ) has been investigated in dimethylformamide at a glassy carbon cathode. The Al 3+ ions were either added at the beginning of the experiment or were released from the anode during electrocarboxylation. It has been found that when Al cations are added to the reaction medium, they strongly influence the reduction process, in most cases leading to a complete change of the mechanism. For example, in the case of 1 , the radical anion ( 1 − ) formed upon 1e − reduction rapidly reacts with Al 3+ to give an Al(III) adduct, w…

Reaction rate constantCarboxylationChemistryGalvanic anodeGeneral Chemical EngineeringInorganic chemistryElectrochemistryDisproportionationReaction intermediateGlassy carbonElectrochemistryAnalytical ChemistryAnode
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Huge Quantum Symmetry Effect in the O + O2 Exchange Reaction.

2015

We report extensive, full quantum-mechanical calculations for the (16)O + (16)O(16)O → (16)O(16)O + (16)O collisions, for both inelastic and atom exchange processes, using a time-independent method based on hyperspherical coordinates. The rates obtained in the present study are much larger than the previously reported ones for this system. The discrepancy is attributed to a huge symmetry effect that was missing in the studies so far. This effect differs from the well-known isotope effect. Importance of this quantum effect is further confirmed by comparison with results for the (16)O + (18)O(18)O → (16)O(18)O + (18)O, exchange reaction.

Reaction rate constantChemistryAtomKinetic isotope effectPhysical chemistryGeneral Materials ScienceNanotechnologyPhysical and Theoretical ChemistryQuantum Hall effectQuantumSymmetry (physics)The journal of physical chemistry letters
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