Search results for " rate constant"

showing 10 items of 220 documents

Conformational and structural studies of N-methylacetohydroxamic acid and of its mono- and bis-chelated uranium(VI) complexes

2015

The thermodynamics and kinetics of the cis/trans isomerism of N-methylacetohydroxamic acid (NMAH) and its conjugated base (NMA(-)) have been reinvestigated in aqueous media by (1)H NMR spectroscopy. Hindered rotation around the central C-N bond due to electronic delocalization becomes slow enough on the NMR time scale to observe both rotamers in equilibrium in D2O at room temperature. By properly assigning the methyl group resonances, evidence for the prevalence of the E over the Z form is unambiguously provided [K300=[E]/[Z]=2.86(2) and 9.63(5) for NMAH and NMA(-), respectively], closing thereby a long-lasting dispute about the most stable conformer. To that end, calculations of the chemic…

Models MolecularMolecular ConformationX-ray crystal structuresCrystallography X-RayHydroxamic AcidsSpectrum Analysis RamanBiochemistryInorganic Chemistrychemistry.chemical_compoundDelocalized electronReaction rate constantEXSY spectroscopyCoordination ComplexesSpectroscopyConformational isomerismChelating AgentsUranium(VI) complexesChemical shiftWater[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryCrystallographyHydroxamic acidchemistry[ CHIM.THEO ] Chemical Sciences/Theoretical and/or physical chemistryRaman spectroscopyProton NMRQuantum TheoryUraniumDensity functional theoryMethyl group
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Protein isotope effects in dihydrofolate reductase from Geobacillus stearothermophilus show entropic-enthalpic compensatory effects on the rate const…

2014

Catalysis by dihydrofolate reductase from the moderately thermophilic bacterium Geobacillus stearothermophilus (BsDHFR) was investigated by isotope substitution of the enzyme. The enzyme kinetic isotope effect for hydride transfer was close to unity at physiological temperatures but increased with decreasing temperatures to a value of 1.65 at 5 °C. This behavior is opposite to that observed for DHFR from Escherichia coli (EcDHFR), where the enzyme kinetic isotope effect increased slightly with increasing temperature. These experimental results were reproduced in the framework of variational transition-state theory that includes a dynamical recrossing coefficient that varies with the mass of…

Models MolecularRate constantsStatic ElectricityDihydrofolate reductaseMolecular ConformationThermodynamicsBiochemistryCatalysisCatalysisModerately thermophilicGeobacillus stearothermophilusColloid and Surface ChemistryReaction rate constantDihydrofolate reductaseKinetic isotope effectEscherichia coliGeobacillus stearothermophilusQDTransmission coefficientIncreasing temperaturesCarbon IsotopesbiologyIsotopeNitrogen IsotopesHydrideChemistryKinetic isotope effectsGeneral ChemistryCrystallographyTetrahydrofolate Dehydrogenasebiology.proteinThermodynamicsJournal of the American Chemical Society
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Single-electron self-exchange between cage hydrocarbons and their radical cations in the gas phase.

2010

We show that the radical cations of adamantane (C(10)H(16)(*+), 1H(*+)) and perdeuteroadamantane (C(10)D(16)(*+), 1D(*+)) are stable species in the gas phase. The radical cation of adamantylideneadamantane (C(20)H(28)(*+), 2H(*+)) is also stable (as in solution). By using the natural (13)C abundances of the ions, we determine the rate constants for the reversible isergonic single-electron transfer (SET) processes involving the dyads 1H(*+)/1H, 1D(*+)/1D and 2H(*+)/2H. Rate constants for the reaction 1H(*+)+1D 1H+1D(*+) are also determined and Marcus' cross-term equation is shown to hold in this case. The rate constants for the isergonic processes are extremely high, practically collision-co…

Models MolecularReaction mechanismAdamantaneAdamantaneAtomic and Molecular Physics and OpticsGas phaseIonElectron Transportchemistry.chemical_compoundElectron transferReaction rate constantchemistryRadical ionComputational chemistryAb initio quantum chemistry methodsPhysical chemistryComputer SimulationGasesPhysical and Theoretical ChemistryChemphyschem : a European journal of chemical physics and physical chemistry
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Chemistry and Photochemistry of 2,6-Bis(2-hydroxybenzilidene)cyclohexanone. An Example of a Compound Following the Anthocyanins Network of Chemical R…

2014

The kinetics and thermodynamics of the 2,6-bis(2-hydroxybenzilidene)cyclohexanone chemical reactions network was studied at different pH values using NMR, UV-vis, continuous irradiation, and flash photolysis. The chemical behavior of the system partially resembles anthocyanins and their analogue compounds. 2,6-Bis(2-hydroxybenzilidene)cyclohexanone exhibits a slow color change from yellow to red styrylflavylium under extreme acidic conditions. The rate constant for this process (5 × 10(-5) s(-1)) is pH independent and controlled by the cis-trans isomerization barrier. However, the interesting feature is the appearance of the colorless compound, 7,8-dihydro-6H-chromeno[3,2-d]xanthene, isolat…

Models MolecularXantheneMolecular StructureCyclohexanonesKineticsCyclohexanoneHydrogen-Ion ConcentrationPhotochemical ProcessesPhotochemistryChemical reactionAnthocyaninschemistry.chemical_compoundReaction rate constantchemistryBenzyl CompoundsProton NMRFlash photolysisPhysical and Theoretical Chemistryta116IsomerizationThe Journal of Physical Chemistry A
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Study of aromatic nucleophilic substitution with amines on nitrothiophenes in room-temperature ionic liquids: are the different effects on the behavi…

2006

The kinetics of the nucleophilic aromatic substitution of some 2-L-5-nitrothiophenes (para-like isomers) with three different amines (pyrrolidine, piperidine, and morpholine) were studied in three room-temperature ionic liquids ([bmim][BF4], [bmim][PF6], and [bm(2)im][BF4], where bmim = 1-butyl-3-methylimidazolium and bm(2)im = 1-butyl-2,3-dimethylimidazolium). To calculate thermodynamic parameters, a useful instrument to gain information concerning reagent-solvent interactions, the reaction was carried out over the temperature range 293-313 K. The reaction occurs faster in ionic liquids than in conventional solvents (methanol, benzene), a dependence of rate constants on amine concentration…

Molecular StructureChemistryOrganic ChemistryInorganic chemistrySolvationImidazolesTemperatureIonic LiquidsStereoisomerismThiophenesMedicinal chemistryPyrrolidinechemistry.chemical_compoundKineticsReaction rate constantSolubilityNucleophilic aromatic substitutionMorpholineIonic liquidBoratesNucleophilic substitutionSolventsSolvent effectsAminesThe Journal of organic chemistry
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Pillar[n]arenes-a Novel, Highly Promising Class of Macrocyclic Host Molecules

2014

Since 2008 a new field of supramolecular chemistry has developed rapidly: the chemistry of pillar[n]arenes. These “younger brothers and sisters” of calixarenes are conveniently accessible and extremely guest-friendly. Guests from many different classes of organic compounds are welcome. Nevertheless, a high selectivity for the threading of guest molecules in the macrocyclic cavities can be achieved. The complex stability is characterized by association constants Ka between 10 and 1×108 M−1. The rate constants of the threading vary over several orders of magnitude. The focus of this article lies on the preparation (sections 2 and 3) and the structures (section 4) of pillar[n]arenes (n=5–10) i…

Molecular dynamicsReaction rate constantStereochemistryChemistryOrganic ChemistryCalixarenePillarSupramolecular chemistryMoleculeThreading (protein sequence)SelectivityCombinatorial chemistryAsian Journal of Organic Chemistry
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Reversible Dioxygen Binding and Phenol Oxygenation in a Tyrosinase Model System

2000

The complex [Cu2(L-66)]2+ (L-66 = a,a'-bis¿bis[2-(1'-methyl-2'-benzimidazolyl)ethyl]amino¿-m-xylene) undergoes fully reversible oxygenation at low temperature in acetone. The optical [lambda(max) = 362 (epsilon 15000), 455 (epsilon 2000), and 550 nm (epsilon 900M(-1)cm(-1))] and resonance Raman features (760 cm(-1), shifted to 719cm(-1)(-1) with 18O2) of the dioxygen adduct [Cu2(L-66)(O2)]2+ indicate that it is a mu-eta2:eta2-peroxodicopper(II) complex. The kinetics of dioxygen binding, studied at - 78 degrees C, gave the rate constant k1 = 1.1M(-1) 5(-1) for adduct formation, and k(-1) =7.8 x 10(-5)s(-1), for dioxygen release from the Cu2O2 complex. From these values, the O2 binding consta…

Monophenol MonooxygenaseChemistrySpectrophotometry AtomicTyrosinaseOrganic ChemistryKineticsGeneral ChemistryResonance (chemistry)PhotochemistryMedicinal chemistryBinding constantCatalysisQuinoneAdductOxygenchemistry.chemical_compoundReaction rate constantModels ChemicalPhenolsAcetoneOxidation-ReductionChemistry - A European Journal
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Convergence of Theory and Experiment on the Role of Preorganization, Quantum Tunneling, and Enzyme Motions into Flavoenzyme-Catalyzed Hydride Transfer

2017

Hydride transfer is one of the most common reactions catalyzed by enzymatic systems, and it has become an object of study because of possible significant quantum tunneling effects. In the present work, we provide a combination of theoretical QM/MM simulations and experimental measurements of the rate constants and kinetic isotopic effects (KIEs) for the hydride transfer reaction catalyzed by morphinone reductase, MR. Quantum mechanical tunneling coefficients, computed in the framework of variational transition-state theory, play a significant role in this reaction, reaching values of 23.8 ± 5.5 for the lightest isotopologue—one of the largest values reported for enzymatic systems. This pred…

Morphinone reductase010304 chemical physicsHydrideChemistryThermodynamicsGeneral Chemistry010402 general chemistry01 natural sciencesQM/MMCatalysismolecular dynamicsArticle0104 chemical sciencesReaction coordinateQM/MMMolecular dynamicsReaction rate constantComputational chemistrykinetic isotope effectshydride transfer0103 physical sciencesmorphinone reductaseQuantumQuantum tunnelling
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Transition state theory thermal rate constants and RRKM-based branching ratios for the N((2)D) + CH(4) reaction based on multi-state and multi-refere…

2012

International audience; Multireference single and double configuration interaction (MRCI) calculations including Davidson (+Q) or Pople (+P) corrections have been conducted in this work for the reactants, products, and extrema of the doublet ground state potential energy surface involved in the N(2D) + CH4 reaction. Such highly correlated ab initio calculations are then compared with previous PMP4, CCSD(T), W1, and DFT/B3LYP studies. Large relative differences are observed in particular for the transition state in the entrance channel resolving the disagreement between previous ab initio calculations. We confirm the existence of a small but positive potential barrier (3.86 +/- 0.84 kJ mol-1…

N(D-2)ThermodynamicsUPPER-ATMOSPHERE010402 general chemistry01 natural sciencesATOMSMOLECULESTransition state theoryMETHANEReaction rate constantAb initio quantum chemistry methodsN(2(2)D)0103 physical sciencesDESCENTPOTENTIAL-ENERGY SURFACES[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]RRKM theorySIZE-EXTENSIVE MODIFICATION010304 chemical physicsElectronic correlationChemistryGeneral ChemistryConfiguration interaction0104 chemical sciencesComputational Mathematics[ PHYS.PHYS.PHYS-AO-PH ] Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]Potential energy surfaceAtomic physicsGround stateJournal of computational chemistry
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Mechanism of Reaction of Melatonin with Human Myeloperoxidase

2001

Recently, it was suggested that melatonin (N-acetyl-5-methoxytryptamine) is oxidized by activated neutrophils in a reaction most probably involving myeloperoxidase (Biochem. Biophys. Res. Commun. (2000) 279, 657-662). Myeloperoxidase (MPO) is the most abundant protein of neutrophils and is involved in killing invading pathogens. To clarify if melatonin is a substrate of MPO, we investigated the oxidation of melatonin by its redox intermediates compounds I and II using transient-state spectral and kinetic measurements at 25 degrees C. Spectral and kinetic analysis revealed that both compound I and compound II oxidize melatonin via one-electron processes. The second-order rate constant measur…

NeutrophilsStereochemistryBiophysicsElectron donorIn Vitro TechniquesBiochemistryRedoxMedicinal chemistrySubstrate SpecificityElectron TransportSuperoxide dismutaseMelatoninchemistry.chemical_compoundReaction rate constantChloridesmedicineHumansMolecular BiologySodium cyanideMelatoninPeroxidasebiologyCyclohexanonesChemistryCell BiologyHydrogen-Ion ConcentrationKineticsSpectrophotometryMyeloperoxidasebiology.proteinFerricOxidation-Reductionmedicine.drugBiochemical and Biophysical Research Communications
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