Search results for "Reaction mechanisms"

showing 10 items of 21 documents

Ring Expansion versus Cyclization in 4-Oxoazetidine-2- carbaldehydes Catalyzed by Molecular Iodine: Experimental and Theoretical Study in Concert

2010

13 páginas, 3 figuras, 12 esquemas, 2 tablas.-- El documento en word es el articulo post-print.

Reaction mechanismAldehydesLactamsReaction mechanismschemistry.chemical_elementGeneral ChemistryRing (chemistry)IodineMedicinal chemistryCatalysisCatalysischemistryOrganic chemistryIodine
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Palladium‐Catalyzed Electrophilic C–H‐Bond Fluorination: Mechanistic Overview and Supporting Evidence

2018

International audience; Palladium-catalyzed electrophilic fluorination is a particularly attractive and challenging synthetic issue. Because of the rapid evolution of this topic, a critical point on the mechanistic and experimental advances is provided herein. In the present review, we focused on current mechanistic understanding in electrophilic fluorination (and related halogenations) catalyzed by palladium, mainly with N-directing group. Our discussion is based on the well-characterized or calculated pertinent metal species and intermediates used for analyzing the plausible catalytic cycles. A particular effort has been devoted to gathering supporting data for the putative species involv…

Reaction mechanismC h bond[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryChemistryReaction mechanismsOrganic Chemistrychemistry.chemical_element[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistry01 natural sciencesMedicinal chemistryCatalysis Fluorination0104 chemical sciencesCatalysisC–H halogenationElectrophilePhysical and Theoretical ChemistryFluorinated compoundsPalladiumPalladiumEuropean Journal of Organic Chemistry
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Benzyl alcohol to benzaldehyde oxidation on MnOx clusters: Unraveling atomistic features

2021

Abstract The catalytic oxidation of benzyl alcohol with O 2 is a promising option for the production of benzaldehyde, from both environmental and economical viewpoints. In particular, highly dispersed MnO x systems feature good activity and selectivity in a wide range of temperatures, although deactivation phenomena by over-oxidation and/or poisoning of active sites are generally recorded. On this account, a density functional theory study was performed on cluster-sized catalyst models, namely Mn 4 O 8 and over-oxygenated Mn 4 O 9 fragments, to predict the reactivity pattern of MnO x catalysts in the selective aerobic oxidation of benzyl alcohol. Several pathways concur to determine the who…

Reaction mechanismCatalyst deactivationReaction mechanismsProcess Chemistry and TechnologyMnOx based catalystsPhotochemistryDFTCatalysisCatalysisBenzaldehydechemistry.chemical_compoundchemistryCatalytic oxidationBenzyl alcoholAlcohol oxidationCatalyst deactivation; DFT; MnO; x; based catalysts; Oxidative dehydrogenation; Reaction mechanismsReactivity (chemistry)Physical and Theoretical ChemistryOxidative dehydrogenationSettore CHIM/02 - Chimica FisicaBenzoic acidMolecular Catalysis
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Enantioselective Palladium-Catalyzed Oxidative β,β-Fluoroarylation of α,β-Unsaturated Carbonyl Derivatives

2016

© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim The site-selective palladium-catalyzed three-component coupling of deactivated alkenes, arylboronic acids, and N-fluorobenzenesulfonimide is disclosed herein. The developed methodology establishes a general, modular, and step-economical approach to the stereoselective β-fluorination of α,β-unsaturated systems.

Reaction mechanismHydrocarbons FluorinatedHalogenationStereochemistrychemistry.chemical_elementStereoisomerismAlkenes010402 general chemistry01 natural sciencesArticleCatalysisCatalysisFluorinatedfluorineOrganic chemistrychemistry.chemical_classificationSulfonamidesMolecular StructurealkenesAlkene010405 organic chemistryOrganic ChemistryEnantioselective synthesisHalogenationStereoisomerismGeneral ChemistryGeneral MedicinepalladiumBoronic AcidsHydrocarbons0104 chemical sciencesreaction mechanismschemistryChemical Sciencessynthetic methodsStereoselectivityOxidation-ReductionPalladiumPalladium
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Nanoscale etching of III-V semiconductors in acidic hydrogen peroxide solution: GaAs and InP, a striking contrast in surface chemistry

2019

In this study of nanoscale etching for state-of-the-art device technology, the importance of surface chemistry, in particular the nature of the surface oxide, is demonstrated for two III-V materials. Striking differences in etching kinetics were found for GaAs and InP in sulphuric and hydrochloric acidic solutions containing hydrogen peroxide. Under similar conditions, etching of GaAs was much faster, while the dependence of the etch rate on pH, and on H2O2 and acid concentrations also differed markedly for the two semiconductors. Surface analysis techniques provided information on the product layer present after etching: strongly non-stoichiometric porous (hydr)oxides on GaAs and a thin st…

Reaction mechanismta221OxideGeneral Physics and Astronomysurface chemistry02 engineering and technologyreaktiomekanismit010402 general chemistry01 natural scienceschemistry.chemical_compoundpuolijohteetEtching (microfabrication)Hydrogen peroxideDissolutionta114nanoelektroniikkabusiness.industryGaAsInPfungitechnology industry and agricultureSurfaces and InterfacesGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physicspintakemia0104 chemical sciencesSurfaces Coatings and Filmsreaction mechanismsSemiconductorchemistryChemical engineeringIII-V oxideHydroxidenanoscale etching0210 nano-technologybusinessStoichiometryApplied Surface Science
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Hydrolysis of Phosphotriesters: A Theoretical Analysis of the Enzymatic and Solution Mechanisms

2012

A theoretical study on the alkaline hydrolysis of paraoxon, one of the most popular organophosphorus pesticides, in aqueous solution and in the active site of Pseudomonas diminuta phosphotriesterase (PTE) is presented. Simulations by means of hybrid quantum mechanics/molecular mechanics (QM/MM) potentials show that the hydrolysis of paraoxon takes place through an A(N)D(N) or associative mechanism both in solution and in the active site of PTE. The results correctly reproduce the magnitude of the activation free energies and can be used to rationalize the observed kinetic isotope effects (KIEs) for the hydrolysis of paraoxon in both media. Enzymatic hydrolysis of O,O-diethyl p-chlorophenyl …

StereochemistryReaction mechanismsMolecular dynamicsParaoxonCatalysisEnzyme catalysisHydrolysisComputational chemistryCatalytic DomainPseudomonasEnzymatic hydrolysismedicinebiologyParaoxonLigandChemistryHydrolysisOrganic ChemistryLeaving groupActive siteEnzyme catalysisGeneral ChemistryAssociative substitutionModels TheoreticalSolutionsZincPhosphoric Triester Hydrolasesbiology.proteinQuantum chemistrymedicine.drugChemistry - A European Journal
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A DFT study of the molecular mechanisms of the nucleophilic addition of ester-derived lithium enolates and silyl ketene acetals to nitrones: Effects …

2006

9 pages, 6 schemes, 3 figures, 2 tables.

chemistry.chemical_classificationNucleophilic additionSilylationReaction mechanismsOrganic ChemistryKeteneEnolatesMedicinal chemistryCycloadditionNitroneLewis acid catalysischemistry.chemical_compoundDensity functional calculationsAcetalsNucleophilechemistryOrganic chemistryLewis acids and basesPhysical and Theoretical ChemistryNucleophilic addition
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Electrosynthesis as a powerful method for the generation of catalytic intermediates: efficient isolation of a palladium aryl halide oxidative additio…

2011

International audience; Polyphosphane ligands of controlled conformation promote highly efficient palladium-catalyzed cross-coupling reactions. Electrosynthesis has been used as a new straightforward method to obtain important intermediates in the search for a better mechanistic understanding. As a proof of concept, the facile synthesis of a phenyl iodopalladium(II) complex (2) was conducted at the electrolysis scale from a readily electrogenerated unstable Pd0 precursor.

chemistry.chemical_classificationReaction mechanism010405 organic chemistryoxidative additionAryl halideOrganic Chemistrychemistry.chemical_elementGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryElectrosynthesispalladium01 natural sciencesOxidative additionCatalysis0104 chemical sciencesCatalysis[ CHIM.CATA ] Chemical Sciences/Catalysisreaction mechanismselectrosynthesischemistryOrganic chemistryaryl halidePalladium
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Overview on oxidation mechanisms of organic compounds by TiO2 in heterogeneous photocatalysis

2012

This review provides the reader with a general overview on heterogeneous photocatalytic oxidation mechanisms in the presence of TiO2, with a special address to conversion of aliphatic and aromatic organic species. The aim was to clarify the steps of the photo-oxidation of the various classes of compounds and to relate them with the properties of the catalysts and the experimental conditions used. Reactions carried out to perform complete degradation and photocatalytic partial oxidations have been deeply discussed. Recent isotopic studies highlighted new reaction pathways concerning partial oxidation of alcohols to aldehyde and oxidation of benzene while EPR investigations confirmed that not…

chemistry.chemical_classificationReaction mechanismRadicalOrganic ChemistryPhotochemistryAldehydeCatalysisCatalysischemistry.chemical_compoundchemistryOrganic reactionPhotocatalysisPartial oxidationSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical ChemistryPhotocatalysis Reaction mechanisms Organic reactions TiO2Benzene
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Best Practices in Constant pH MD Simulations: Accuracy and Sampling

2022

Various approaches have been proposed to include the effect of pH in molecular dynamics (MD) simulations. Among these, the λ-dynamics approach proposed by Brooks and co-workers [Kong, X.; Brooks III, C. L. J. Chem. Phys.1996, 105, 2414−2423] can be performed with little computational overhead and hfor each typeence be used to routinely perform MD simulations at microsecond time scales, as shown in the accompanying paper [Aho, N. et al. J. Chem. Theory Comput.2022, DOI: 10.1021/acs.jctc.2c00516]. At such time scales, however, the accuracy of the molecular mechanics force field and the parametrization becomes critical. Here, we address these issues and provide the community with guidelines on…

mallintaminenEntropyProteinsmolekyylitHydrogen-Ion ConcentrationMolecular Dynamics Simulationmonomerspeptides and proteinsreaktiomekanismitmolecular mechanicsComputer Science Applicationsreaction mechanismspeptiditHumanscomputer simulationssimulointimolekyylidynamiikkaproteiinitPhysical and Theoretical ChemistryAlgorithmsJournal of Chemical Theory and Computation
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