Search results for " solution"

showing 10 items of 3084 documents

Visible-light-induced oxidation of trans-ferulic acid by TiO2 photocatalysis

2012

Abstract The oxidation of trans-ferulic acid (C10H10O4) in aqueous TiO2 dispersion occurs via the formation of a charge-transfer complex on the TiO2 surface that is able to absorb visible light (λ ⩾ 400 nm). The main product is CO2, whereas secondary oxidation products are organic species such as vanillin, caffeic acid, homovanillic acid, and vanillylmandelic acid. Oxidation through the formation of a charge-transfer complex occurs only in the presence of specific TiO2 samples. Experiments in the absence of oxygen, in the presence of bromate ions and by using a phosphate-modified TiO2, have been carried out for investigating the reaction mechanism. In order to study the interaction between …

Reaction mechanismAqueous solutiontrans-Ferulic acid photo-oxidationChemistryVanillinInorganic chemistryCharge-transfer complexPhotochemistryBromateCatalysisCatalysisFerulic acidchemistry.chemical_compoundtrans-Ferulic acid photo-oxidation Visible-light photocatalysis TiO2 Charge-transfer complexVisible-light photocatalysiPhotocatalysisCaffeic acidTitanium dioxideSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical ChemistryJournal of Catalysis
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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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New sulfonamide complexes with essential metal ions [Cu (II), Co (II), Ni (II) and Zn (II)]. Effect of the geometry and the metal ion on DNA binding …

2019

Abstract Mixed divalent Cu, Co, Ni and Zn complexes containing the new sulfonamide ligand N–(2–(pyridin–2–yl)ethyl)quinoline–8–sulfonamide (HQSEP) were prepared and characterized by physico-chemical techniques. The tetracoordinate [Cu(QSEP)X] [X = Br (1), Cl (2)] compounds present a seesaw geometry (τ4 = 0.56 (1) and 0.50 (2)). The Cu(II) in the [Cu(QSEP)(NO3)(MeOH)] (3) complex is five coordinate with a slightly distorted SP geometry (τ = 0.11). The [M(QSEP)(benz)] [M = Cu(II) (4), Ni(II) (5), Co(II) (6) and Zn(II) (7); benz = benzoate] compounds are configurationally isotypic. The coordination geometries of the M(II) ions can be best described as distorted SP (τ = 0.29, 0.15, 0.34 and 0.1…

Reaction mechanismMetal ions in aqueous solutionGeometry010402 general chemistry01 natural sciencesBiochemistryDivalentInorganic ChemistryMetalBovine serum albuminDNA Cleavagechemistry.chemical_classificationSulfonamidesDeoxyribonucleasesTetracoordinatebiology010405 organic chemistryChemistryLigandSerum Albumin BovineDNA0104 chemical sciencesSulfonamideMetalsvisual_artvisual_art.visual_art_mediumbiology.proteinJournal of inorganic biochemistry
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Molecular dynamics simulation in aqueous solution of N -methylazetidinone as a model of β -lactam antibiotics

1999

In this article, we analyze the results of a molecular dynamics simulation in aqueous solution of the N-methylazetidinone molecule, often used to model β-lactam antibiotics. The radial distribution functions (RDFs) corresponding to the most interesting atoms, in terms of reactivity, are presented. We focus our study on the effect of a polar environment on the molecule. The solvent structure around the system is compared to the structure of β-lactam-water complexes, as obtained in a previous study of reaction mechanisms for the neutral and alkaline hydrolyses of N-methylazetidinone. Two types of complexes have been considered which are related to different hydrolysis mechanisms having simila…

Reaction mechanismMolecular dynamicsAqueous solutionChemistryComputational chemistryInorganic chemistryAb initioCluster (physics)MoleculeReactivity (chemistry)Physical and Theoretical ChemistrySolvent effectsTheoretical Chemistry Accounts: Theory, Computation, and Modeling (Theoretica Chimica Acta)
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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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Catalytic Reaction Mechanism in Native and Mutant Catechol- O-methyltransferase from the Adaptive String Method and Mean Reaction Force Analysis.

2018

Catechol- O-methyltransferase is an enzyme that catalyzes the methylation reaction of dopamine by S-adenosylmethionine, increasing the reaction rate by almost 16 orders of magnitude compared to the reaction in aqueous solution. Here, we combine the recently introduced adaptive string method and the mean reaction force method, in combination with the structural and electronic descriptors to characterize the reaction mechanism. The catalytic effect of the enzyme is addressed by the comparison of the reaction in the human wild-type enzyme, in the less effective Y68A mutant, and in aqueous solution. The influence of these different environments at different stages of the chemical process and th…

Reaction mechanismS-AdenosylmethionineDopamine010402 general chemistryCatechol O-Methyltransferase01 natural sciencesMethylationCatalysisCatalysisReaction ratechemistry.chemical_compoundCatalytic Domain0103 physical sciencesMaterials ChemistryMoleculeHumansPhysical and Theoretical ChemistryCatecholAqueous solution010304 chemical physicsbiologyChemistryActive siteWaterCombinatorial chemistry0104 chemical sciencesSurfaces Coatings and FilmsMutationbiology.proteinSN2 reactionThermodynamicsThe journal of physical chemistry. B
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Electroreduction of aliphatic chlorides at silver cathodes in water

2010

The effect of water on the reduction of aliphatic chlorides at silver cathodes was investigated by cyclovoltammetric experiments in acetonitrile, water and their mixture and focused electrolyses in water solutions. The addition of water to acetonitrile gives rise to the formation of new peaks and/or the displacement of pre-existent peaks at dramatically less negative potentials. In a water medium, silver shows a very large electrocatalytic effect towards the reduction of chlorinated aliphatic compounds belonging to the classes of chloromethanes, chloroethanes and chloroethenes, dramatically higher than that observed in aprotic solvents such as dimethylformamide (DMF) or acetonitrile (ACN). …

Reaction mechanismSilverAqueous solutionChemistryGeneral Chemical EngineeringElectrocatalysiInorganic chemistryDe-halogenationSettore ING-IND/27 - Chimica Industriale E TecnologicaElectrochemistryElectrocatalystAnalytical Chemistrychemistry.chemical_compoundElectrochemistryDimethylformamideWater treatmentElectrochemical remediationAliphatic compoundAcetonitrileAliphatic chlorideJournal of Electroanalytical Chemistry
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Theoretical study of phosphodiester hydrolysis in nucleotide pyrophosphatase/phosphodiesterase. Environmental effects on the reaction mechanism.

2010

We here present a theoretical study of the alkaline hydrolysis of methyl p-nitrophenyl phosphate (MpNPP(-)) in aqueous solution and in the active site of nucleotide pyrophosphatase/phosphodiesterase (NPP). The analysis of our simulations, carried out by means of hybrid quantum mechanics/molecular mechanics (QM/MM) methods, shows that the reaction takes place through different reaction mechanisms depending on the environment. Thus, while in aqueous solution the reaction occurs by means of an A(N)D(N) mechanism, the enzymatic process takes place through a D(N)A(N) mechanism. In the first case, we found associative transition-state (TS) structures, while in the enzyme TS structures have dissoc…

Reaction mechanismStereochemistrydnaNAlkaline hydrolysis (body disposal)Molecular Dynamics SimulationBiochemistryCatalysisHydrolysisColloid and Surface ChemistryCatalytic DomainPyrophosphatasesAqueous solutionbiologyChemistryNucleotidesPhosphoric Diester HydrolasesHydrolysisActive sitePhosphodiesteraseWaterGeneral ChemistryAlkaline PhosphataseSolutionsZincPhosphodiester bondbiology.proteinXanthomonas axonopodisThermodynamicsJournal of the American Chemical Society
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ChemInform Abstract: Oxidative Transformation of Aryls Using Molybdenum Pentachloride

2012

Molybdenum pentachloride combines a strong Lewis acid character with an unusually high oxidation potential creating a powerful reagent for oxidative transformations. Since the oxidative coupling reaction of aryls is induced at an extraordinarily high reaction rate, a variety of labile groups, e.g. iodo, tert-alkyl, etc., are tolerated on the aromatic core. Furthermore, the co-formed molybdenum salts can either be exploited for template effects to obtain uncommon geometries in a preferred manner, or redox-play starts after aqueous workup. Therefore MoCl5 represents a unique and easily available reagent.

Reaction rateAqueous solutionchemistryMolybdenumReagentchemistry.chemical_elementOxidative coupling of methaneGeneral MedicineOxidative phosphorylationLewis acids and basesMolybdenum pentachlorideCombinatorial chemistryChemInform
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LINKING TEACHER PROFESSIONAL DEVELOPMENT NEEDS WITH APPROPRIATE SOLUTIONS: INSIGHTS FROM AN INIATIVE IN LATVIA

2021

International surveys have stated that each year teachers spend, on average, more than 10 days engaged in different professional development activities. The purpose for this investment in teacher professional development (TPD) is clear: teachers’ competence must develop according to changes in curriculum and 21st century requirements. In previous research we have developed a theoretical teacher competence framework, implemented it to identify teacher (N=263) groups competence gaps and professional development needs. The goal of this research is to link identified professional development needs related to the instruction of 21st century skills (criteria - instructional design, learning goals…

Reading comprehensionInstructional designProfessional developmentMathematics educationevidence-based professional development solutions teacher collaborative professional learning teacher professional development needsPsychologyCurriculumCompetence (human resources)SOCIETY. INTEGRATION. EDUCATION. Proceedings of the International Scientific Conference
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