Search results for "Turnover number"

showing 10 items of 11 documents

Rate of photon absorption and turnover number: two parameters for the comparison of heterogeneous photocatalytic systems in a quantitative way

1993

Abstract In order to correctly compare the performance of different photocatalytic systems using polycrystalline semiconductor oxides, two parameters are proposed: the rate of photon absorption (rpa) and the turnover number (tn). From these quantities the quantum yield (qy), which indicates the efficiency of the absorbed photons for promoting a reaction event, can be determined. The phenol photodegradation reaction, carried out in aqueous dispersions of polycrystalline TiO2 (anatase) of different preparation methods and sources, has been used as “test reaction” in order to determine the tn, rpa and qy values.

AnatasePhotonAqueous solutionChemistryInorganic chemistryAnalytical chemistryQuantum yieldTurnover numberInorganic ChemistryMaterials ChemistryPhotocatalysisPhysical and Theoretical ChemistryPhotodegradationAbsorption (electromagnetic radiation)Coordination Chemistry Reviews
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ChemInform Abstract: Rate of Photon Absorption and Turnover Number: Two Parameters for the Comparison of Heterogeneous Photocatalytic Systems in a Qu…

2010

Abstract In order to correctly compare the performance of different photocatalytic systems using polycrystalline semiconductor oxides, two parameters are proposed: the rate of photon absorption (rpa) and the turnover number (tn). From these quantities the quantum yield (qy), which indicates the efficiency of the absorbed photons for promoting a reaction event, can be determined. The phenol photodegradation reaction, carried out in aqueous dispersions of polycrystalline TiO2 (anatase) of different preparation methods and sources, has been used as “test reaction” in order to determine the tn, rpa and qy values.

AnatasePhotonChemistryAnalytical chemistryPhotocatalysisQuantum yieldGeneral MedicineCrystallitePhotodegradationAbsorption (electromagnetic radiation)Turnover numberChemInform
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Sequestration of biological reactive intermediates by trapping as covalent enzyme-intermediate complex

2001

One important class of biological reactive intermediates arising in the course of human xenobiotic metabolism are arene and alkene oxides. The major safeguard against the potential genotoxic effects of these compounds is the microsomal epoxide hydrolase (mEH). This enzyme has a broad substrate specificity but--on the first sight--seems to be inadequately suited for this protection task due to its low turnover number with most of its substrates. The recent progress in the understanding of the mechanism of enzymatic epoxide hydrolysis has shed new light on this apparent dilemma: Epoxide hydrolases convert their substrates via the intermediate formation of a covalent enzyme-substrate complex, …

Epoxide hydrolase 2Reactive intermediateSubstrate (chemistry)10050 Institute of Pharmacology and Toxicology610 Medicine & health10079 Institute of Veterinary Pharmacology and ToxicologyTurnover numberchemistry.chemical_compoundchemistry1300 General Biochemistry Genetics and Molecular BiologyMicrosomal epoxide hydrolaseStyrene oxideEpoxide HydrolasesBiophysics570 Life sciences; biologyEpoxide hydrolase
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Imidazolium-Functionalized Carbon Nanohorns for the Conversion of Carbon Dioxide

2016

Six new hybrid materials composed of carbon nanohorns (CNHs) and highly cross-linked imidazolium salts were easily synthesized using a one-step procedure based on the radical oligomerization of bis-vinylimidazolium salts (bVImiX) in the presence of pristine CNHs. The hybrid materials were characterized and employed as the sole catalysts for the conversion of carbon dioxide into cyclic carbonate by reaction with epoxides. The solids displayed excellent turnover number and productivity. Moreover, four catalysts were investigated in recycling experiments. Two catalysts containing an octyl linker between the imidazolium units and a bromide or an iodide anion showed no loss in activity after thr…

Epoxy Compounds/chemistryGeneral Chemical EngineeringIodidechemistry.chemical_elementcyclic carbonatesimidazolium salts010402 general chemistryHeterogeneous catalysis01 natural sciencesSettore CHIM/04 - Chimica IndustrialeCatalysisCatalysischemistry.chemical_compoundcarbon nanohornBromideImidazoles/chemistryOrganic chemistryEnvironmental ChemistryGeneral Materials ScienceChemical Engineering (all)Recyclingchemistry.chemical_classificationNanotubes010405 organic chemistryNanotubes CarbonImidazolesSettore CHIM/06 - Chimica OrganicaCarbon Dioxide0104 chemical sciencesTurnover numbercarbon dioxide conversionGeneral Energycyclic carbonateEnergy (all)heterogeneous catalysischemistrycarbon nanohornsCarbon/chemistryCarbon dioxideEpoxy Compoundsheterogeneous catalysiMaterials Science (all)Hybrid materialCarbonCarbon Dioxide/chemistryimidazolium saltChemSusChem
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High Turnover Catalase Activity of a Mixed‐Valence Mn II Mn III Complex with Terminal Carboxylate Donors

2015

The neutral dimanganese(II,III) complex [Mn-2(BCPMP)-(OAc)(2)] [1; BCPMP3- = 2,6-bis({(carboxymethyl)[(1-pyridyl)-methyl] amino} methyl)-4-methylphenolato] has been synthesized and characterized. The complex contains two terminal carboxylate donors. Complex 1 was found to be an effective catalyst for the disproportionation of H2O2 with high catalytic rate and a turnover number of 7500, the highest turnover reported to date for a catalase mimic. The rates and TON were significantly higher than recorded for a dicationic dimanganese( II,III) counterpart ([Mn-2(BPBP)(OAc)(2)]center dot(ClO4)(2), 2; BPBP- = 2,6-bis{[bis(2-pyridylmethyl)amino]methyl}-4-butylphen-olato), which lacks the terminal c…

ManganeseReaction mechanismbiologyChemistryEnzyme modelsReaction mechanismschemistry.chemical_elementDisproportionationManganeseCatalaseHydrogen peroxidePhotochemistryMedicinal chemistryCatalysisTurnover numberInorganic Chemistrychemistry.chemical_compoundDinucleating ligandsCatalytic cycleCatalasebiology.proteinCarboxylateta116European Journal of Inorganic Chemistry
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Activation of Anthranilate Phosphoribosyltransferase from Sulfolobus solfataricus by Removal of Magnesium Inhibition and Acceleration of Product Rele…

2009

Anthranilate phosphoribosyltransferase from the hyperthermophilic archaeon Sulfolobus solfataricus (ssAnPRT) is encoded by the sstrpD gene and catalyzes the reaction of anthranilate (AA) with a complex of Mg(2+) and 5'-phosphoribosyl-alpha1-pyrophosphate (Mg.PRPP) to N-(5'-phosphoribosyl)-anthranilate (PRA) and pyrophosphate (PP(i)) within tryptophan biosynthesis. The ssAnPRT enzyme is highly thermostable (half-life at 85 degrees C = 35 min) but only marginally active at ambient temperatures (turnover number at 37 degrees C = 0.33 s(-1)). To understand the reason for the poor catalytic proficiency of ssAnPRT, we have isolated from an sstrpD library the activated ssAnPRT-D83G + F149S double …

Models MolecularProtein ConformationStereochemistryMutantved/biology.organism_classification_rank.speciesAnthranilate PhosphoribosyltransferaseAnthranilate phosphoribosyltransferaseCrystallography X-RayBiochemistryCatalysisEscherichia coliMagnesiumchemistry.chemical_classificationbiologyved/biologySulfolobus solfataricusSubstrate (chemistry)Active siteRecombinant ProteinsTurnover numberComplementationKineticsEnzymechemistryBiochemistrySulfolobus solfataricusbiology.proteinBiochemistry
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Single-Walled Carbon Nanotube–Polyamidoamine Dendrimer Hybrids for Heterogeneous Catalysis

2016

We report the synthesis and catalytic properties of single-walled carbon nanotube-polyamidoamine dendrimers hybrids (SWCNT-PAMAM), prepared via a convergent strategy. The direct reaction of cystamine-based PAMAM dendrimers (generations 2.5 and 3.0) with pristine SWCNTs in refluxing toluene, followed by immobilization and reduction of [PdCl4](2-), led to the formation of highly dispersed small palladium nanoparticles homogeneously confined throughout the nanotube length. One of these functional materials proved to be an efficient catalyst in Suzuki and Heck reactions, able to promote the above processes down to 0.002 mol % showing a turnover number (TON) of 48 000 and a turnover frequency (T…

Nanotubepalladium nanoparticleMaterials scienceGeneral Physics and AstronomyC-C cross coupling; carbon nanotubes; heterogeneous catalysis; palladium nanoparticles; PAMAM dendrimers; TEM; Materials Science (all); Engineering (all); Physics and Astronomy (all)02 engineering and technologyCarbon nanotubePAMAM dendrimers010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysislaw.inventionPhysics and Astronomy (all)Engineering (all)Suzuki reactionlawDendrimerOrganic chemistrypalladium nanoparticlesGeneral Materials ScienceC-C cross couplingcarbon nanotubePAMAM dendrimercarbon nanotubesGeneral EngineeringSettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesTurnover numberheterogeneous catalysisChemical engineeringTEMheterogeneous catalysiMaterials Science (all)0210 nano-technologyHybrid materialACS Nano
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Palladium nanoparticles immobilized on halloysite nanotubes covered by a multilayer network for catalytic applications

2018

The synthesis of pure fine chemicals for industrial purposes is one of the most attractive challenges of chemical research. The use of catalytic pathways mediated by palladium nanoparticles (PdNPs) for C-C bond formation is a useful way to obtain these kinds of compounds. To achieve this objective, the PdNPs can be efficiently loaded on a functionalized natural nanostructured support such as halloysite nanotubes (HNTs). Hybrid materials based on thiol functionalized halloysite nanotubes and highly cross-linked imidazolium salts were successfully developed and used for the stabilization of PdNPs. The HNT/Pd hybrids were thoroughly characterized from a physico-chemical point of view and teste…

Palladium nanoparticles immobilized on halloysite nanotubes02 engineering and technologyengineering.material010402 general chemistry01 natural sciencesHalloysiteCatalysisCoupling reactionCatalysisSuzuki reactionMaterials ChemistrySettore CHIM/02 - Chimica FisicaChemistryPalladium nanoparticlesSettore CHIM/06 - Chimica OrganicaGeneral ChemistryPalladium nanoparticles halloysite nanotubes catalyst021001 nanoscience & nanotechnology0104 chemical sciencesTurnover numberChemical engineeringMicrowave irradiationengineering0210 nano-technologyHybrid materialHalloysite nanotubes cross-coupling reactionsNew Journal of Chemistry
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α-Chymotrypsin-Catalyzed Reaction Confined in Block-Copolymer Vesicles

2010

Herein the reactivity of the enzyme α-chymotrypsin in the confinement of polystyrene-block-poly(acrylic acid) (PS-b-PAA) vesicles was investigated. Enzyme and substrate molecules were encapsulated in PS-b-PAA vesicles with internal diameters ranging from 26 nm to 165 nm during the formation of the vesicles. While the loading efficiencies of enzyme and substrate molecules were practically identical for vesicles of identical size, they were found to increase with decreasing vesicle size. The kinetics of the α-chymotrypsin catalyzed hydrolysis of N-succinyl-Ala-Ala-Phe-7-amido-4-methylcoumarin (AMC) was evaluated following the increase of the absorption of the product 7-amino-4-methylcoumarin …

PolymersKineticsAcrylic ResinsPhotochemistryMETIS-269964Ultraviolet visible spectroscopyCoumarinsChymotrypsinNanotechnologyOrganic chemistryReactivity (chemistry)Physical and Theoretical ChemistryChymotrypsinbiologyChemistryHydrolysisVesicleSubstrate (chemistry)Atomic and Molecular Physics and OpticsTurnover numberKineticsBiocatalysisbiology.proteinPolystyrenesSpectrophotometry UltravioletAbsorption (chemistry)ChemPhysChem
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Relationships between kinetic constants and the amino acid composition of enzymes from the yeast Saccharomyces cerevisiae glycolysis pathway

2012

The kinetic models of metabolic pathways represent a system of biochemical reactions in terms of metabolic fluxes and enzyme kinetics. Therefore, the apparent differences of metabolic fluxes might reflect distinctive kinetic characteristics, as well as sequence-dependent properties of the employed enzymes. This study aims to examine possible linkages between kinetic constants and the amino acid (AA) composition (AAC) for enzymes from the yeast Saccharomyces cerevisiae glycolytic pathway. The values of Michaelis-Menten constant (K M), turnover number (k cat), and specificity constant (k sp = k cat/K M) were taken from BRENDA (15, 17, and 16 values, respectively) and protein sequences of nine…

chemistry.chemical_classificationSpecificity constantbiologyResearchSaccharomyces cerevisiaeMichaelis-Menten constantTurnover numberbiology.organism_classificationMichaelis–Menten kineticsGeneral Biochemistry Genetics and Molecular BiologyYeastComputer Science ApplicationsAmino acidSequence-dependent propertiesComputational MathematicsMetabolic pathwayEnzymechemistryBiochemistryGlycolytic enzymesMultivariate relationshipsEnzyme kineticsSpecificity constantEURASIP Journal on Bioinformatics and Systems Biology
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