Search results for "Reaction rate"

showing 10 items of 346 documents

Efficiency range of the Belousov-Zhabotinsky reaction to induce the self-organization of transient bonds in metallo-supramolecular polymeric systems.

2020

The periodic change of the oxidation state of the metal catalyst in the oscillating Belousov-Zhabotinsky (BZ) reaction has been reported to establish a periodic organization of metallo-supramolecular bonds in polymeric systems, which results in autonomous viscosity oscillations. To appraise the possible extent of quantitative control on the viscosity oscillation features, we assess how the kinetics of the BZ reaction affects the periodic self-organization of the metal-ligand coordination, and vice versa. Our model system includes mono-, bis-, and tetra-functional polyethyleneglycol (PEG) precursors end grafted with terpyridine ligands that are complexed with ruthenium ions, which oscillate …

DiffusionKineticsGeneral Physics and Astronomy02 engineering and technologyReaction intermediate010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesReaction rateViscositychemistry.chemical_compoundBelousov–Zhabotinsky reactionchemistryChemical physicsOxidation statePhysical and Theoretical ChemistryTerpyridine0210 nano-technologyPhysical chemistry chemical physics : PCCP
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The reduction mechanism of the CO group.

2001

A detailed study of the electrochemical reduction of benzil in aqueous medium between H0=−5 and pH 11 is presented. A global 2e−, 3H+ or 2e−, 2H+ surface reaction leads to cis and trans endiols. Analysis, using the theory of the square schemes with protonations at equilibrium, shows that in all the pH range the reaction is controlled by the second electron uptake, the paths being successively H+, e− and e−, H+. The electrochemical reaction is followed by surface isomerizations whose rate constants vary from 7 to 200 s−1 for the trans/cis and from 1 to 2000 s−1 for the cis/trans transformations.

DiketoneReaction mechanismAqueous solution010405 organic chemistryStereochemistryGeneral Chemical Engineering010402 general chemistryElectrochemistry01 natural sciencesCis trans isomerization0104 chemical scienceschemistry.chemical_compoundReaction rate constantchemistryElectrochemistryPhysical chemistryBenzilCis–trans isomerismElectrochimica Acta
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Zur kinetik der anionischen polymerisation von methyl-methyacrylat in tetrahydrofuran bei −75°C

1973

Die anionische Polymerisation von Methylmethacrylat (MMA) in Tetrahydrofuran (THF) verlauft bei −75°C mit Cumylcasium bzw. oligomerem α-Methylstyrylcasium als Initiatoren ohne erkennbare Nebenreaktionen analog der anionischen Polymerisation von unpolaren Monomeren in atherischen Losungsmitteln. Als Beweis wird hauptsachlich die enge Molekulargewichtsverteilung der unter diesen Bedingungen hergestellten Polymethylmethacrylate angefuhrt. Bei −75°C betragen die Geschwindigkeitskonstanten fur die Monomeranlagerung an das Ionenpaar kw(±) = 80 dm3 mol−1 s−1 und an das freie Anion etwa kw(−) ≈ 6 · 104 dm3 mol−1 s−1. Leitfahigkeitsmessungen ergeben, das die Dissoziationskonstante des Polymethylmeth…

Dissociation constantchemistry.chemical_compoundMonomerAnionic addition polymerizationReaction rate constantchemistryPolymerizationPolymer chemistryMolar mass distributionTetrahydrofuranDie Makromolekulare Chemie
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The reaction of 2-methoxy-3-nitrothiophene with N-benzylmethylamine in methanol

1990

The kinetics of the title reaction has been studied in methanol as a function of amine and methoxide ion concentrations. The kinetic coefficients obtained point out that the reaction is catalysed by methoxide through a SB catalysis mechanism.

Dry media reactionchemistry.chemical_compoundReaction rate constantchemistryOrganic chemistryGeneral ChemistryMethanolCollection of Czechoslovak Chemical Communications
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Photophysical Properties of Charged Cyclometalated Ir(III) Complexes: A Joint Theoretical and Experimental Study

2011

The photophysical properties of a series of charged biscyclometalated [Ir(ppy)(2)(N boolean AND N)](1+) complexes, where ppyH is 2-phenylpyridine and N boolean AND N is 2,2'-bipyridine (bpy), 6-phenyl-2,2'-bipyridine (pbpy), and 6,6'-dipheny1-2,2'-bipyridine (dpbpy) for complexes 1, 2, and 3, respectively, have been investigated in detail. The photoluminescence performance in solution decreases from 1 to 3 upon attachment of phenyl groups to the ancillary ligand. The absorption spectra recorded over time suggest that complex 3 is less stable compared to complexes 1 and 2 likely due to a nucleophilic-assisted ancillary ligand-exchange reaction. To clarify this behavior, the temperature depen…

ELECTROLUMINESCENT DEVICESPhotoluminescenceAbsorption spectroscopyEMITTING ELECTROCHEMICAL-CELLSLigandChemistryCATIONIC IRIDIUM COMPLEXESAnalytical chemistryLARGE MOLECULESTURN-ON TIMESTRANSITION-METAL-COMPLEXESInorganic ChemistryCONCENTRATION GRADIENTSReaction rate constantTEMPERATURE-DEPENDENCEQUANTUM YIELDSPhysical chemistryPhysical and Theoretical ChemistryENERGY-GAP LAWInorganic Chemistry
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Electrochemical reduction and carboxylation of halobenzophenones

2002

Abstract The electrochemical reduction of a series of halogenated benzophenones XC6H4COC6H4Y (1) was studied in aprotic solvents, in the absence and presence of CO2, by cyclic voltammetry (CV) and controlled-potential electrolysis. The mechanism of electroreduction in dimethylformamide (DMF) has been investigated in some detail. Most of the compounds undergo reductive carbonhalogen bond cleavage in the time window of CV. The radical anions derived from difluorobenzophenones (X=Y=4-F; X=2-F, Y=4-F) as well as from the 3-chloro derivative are quite stable with a cleavage rate constant (kc) of the order of 10−2 s−1 or less. With 4-chloro-, 2-chloro-, 4,4′-dichloro- and 2,4′-dichorobenzophen…

ElectrolysishydroxyacidChemistryGeneral Chemical EngineeringInorganic chemistryElectrochemicalreductionReaction intermediateElectrochemistryAnalytical Chemistrylaw.inventioncarboxylationchemistry.chemical_compoundhalobenzophenoneReaction rate constantCarboxylationlawElectrochemistryDimethylformamideCyclic voltammetryBond cleavage
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EFFICIENT DEGRADATION OF CLOFIBRIC ACID BY HETEROGENEOUS PHOTOCATALYTIC OXIDATION PROCESS

2019

International audience; Emerging pollutants such as pharmaceutical active compounds were detected worldwide in different environmental compartments. Nowadays, multiple studies are focused on the investigation of their environmental fate, as well as to find new, efficient and sustainable removal technologies. Several studies demonstrated that heterogeneous photocatalysis is one of the most promising techniques used for water purification. Thus, the aim of our work was to evaluate the photodegradation efficiency of a refractory emergent compound, named clofibric acid, under UV light in aqueous solution. We report that photodegradation and mineralization efficiency are strongly dependent of th…

Environmental Engineering02 engineering and technology010501 environmental sciencesManagement Monitoring Policy and LawPhotochemistry01 natural sciencesCatalysispersistent micropollutantchemistry.chemical_compoundReaction rate constant[CHIM] Chemical Sciences[CHIM]Chemical Sciencesmineralizationnanosized catalystsPhotodegradation0105 earth and related environmental sciencesdegradationPollutantClofibric acidMineralization (soil science)021001 nanoscience & nanotechnologyPollution6. Clean waterLight intensitychemistry13. Climate actionkineticsPhotocatalysis0210 nano-technologyphotocatalysis
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Reactions at Interfaces: Oxygenation of n-Butyl Ligands Anchored on Silica Surfaces with Methyl(trifluoromethyl)dioxirane

2011

The oxygenation of n-butyl and n-butoxy chains bonded to silica with methyl(trifluoromethyl)dioxirane (1) revealed the ability of the silica matrix to release electron density toward the reacting C(2)-H σ-bond through the Si-C(1) and Si-O(1) σ-bonds connecting the alkyl chain to the surface (silicon β-effect). The silica surface impedes neither the alkyl chain adopting the conformation required for the silicon β-effect nor dioxirane 1 approaching the reactive C(2) methylene group. Reaction regioselectivity is insensitive to changes in the solvation of the reacting system, the location of organic ligands on the silica surface, and the H-bonding character of the silica surface. Reaction rates…

Ethylene OxideTrimethylsilylSiliconSurface PropertiesMolecular Conformationchemistry.chemical_elementChemistry Techniques SyntheticPhotochemistryReaction ratechemistry.chemical_compoundDioxiraneMethyleneAlkylchemistry.chemical_classificationTrifluoromethylOrganic ChemistryRegioselectivityEstersHydrogen BondingStereoisomerismSilicon DioxideOxygenSolutionsKineticschemistryButanesOxidation-ReductionThe Journal of Organic Chemistry
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Über die Stabilität Von Copolymeren aus 1,3,5-Trioxan mit verschiedenen Lactonen

1976

Der thermische Abbau von Copolymeren aus 1,3,5-Trioxan und den Lactonen β-Propiolacton (3-Propanolid), Pivalolacton (2,2-Dimethyl-3-propanolid) und e-Caprolacton (6-Hexanolid) wurde untersucht. Der langsame und vollstandige Abbau der Copolymeren wird zuruckgefuhrt auf 1 eine statistische acidolytische Kettenspaltung durch Carboxyl-Endgruppen, 2 die Abspaltung von Acrylsaure an den sauren Endgruppen, 3 die statistische Kettenspaltung durch Pyrolyse von Esterbindungen vor allem in Sequenzen aus mehreren β-Propiolactonbausteinen. Die Teilreaktionen (1) und (2) konnen durch Zusatz von Butandiol-Diglycidylather-(1,4-Bis(2,3-epoxypropoxy)butan) oder N-(2-Naphthyl)anilin oder von Epoxiden stark ve…

Ethylene oxideChain scissionPolymers and PlasticsChemistrychemistry.chemical_compoundReaction rate constantAnilineColloid and Surface ChemistryButanediolPolymer chemistryCopolymerMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryAcrylic acidColloid and Polymer Science
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Sol–gel material as a support of organometallic catalyst for ethylene polymerization

2008

Abstract The sol–gel procedure was applied to obtain powdery materials with different structures and morphology. It was possible to produce almost non-porous silica powder, with an extremely low surface area (ca. 4 m 2 /g) and very high uniformity of spherical particles as well as materials with various uniformity of particles and different porosity, most likely associated with increasing pore volume. Dependent on the properties of the carrier, the resulting supported vanadium catalysts (VOCl 3 /AlEt 2 Cl) showed significant differences concerning activity and stability. It was confirmed that improved hydrophobicity of the carrier’s surface may be useful and improve the activity of the syst…

Ethylene polymerizationPolymers and PlasticsOrganic ChemistrySupported catalystsGeneral Physics and AstronomyVanadiumchemistry.chemical_elementSilicaPolyethyleneSol–gelChlorideCatalysischemistry.chemical_compoundReaction rate constantchemistryPolymerizationChemical engineeringPolymer chemistryMaterials ChemistrymedicinePorosityPolymerization kineticmedicine.drugSol-gelEuropean Polymer Journal
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