Search results for " Catalysis"

showing 10 items of 585 documents

Photodegradation of pharmaceutical drugs in aqueous TiO2 suspensions: mechanism and kinetics

2007

WOS: 000251165800003

Settore ING-IND/24 - Principi Di Ingegneria ChimicaAqueous solutionendocrine system diseasesChemistryKineticsInorganic chemistryHeterogeneous PhotocatalysisGeneral ChemistryMineralization (soil science)Heterogeneous catalysisHeterogeneous photocatalysiCatalysischemistry.chemical_compoundTamoxifenTitanium dioxidePhotocatalysisTitanium dioxidePartial oxidationGemfibrozilPhotodegradationDrug photodegradation
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Determination of Photoadsorption Capacity of Polychrystalline TiO2 Catalyst in Irradiated Slurry

2009

WOS: 000322711800002

Settore ING-IND/24 - Principi Di Ingegneria ChimicaLangmuirTIO2 photocatalysis photoadsorptionChemistryLangmuir adsorption modelHeterogeneous catalysisCatalysissymbols.namesakeAdsorptionChemical engineeringChemisorptionsymbolsPhotocatalysisOrganic chemistryFreundlich equationSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie
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Supported ionic liquids. New recyclable materials for the L-proline-catalyzed aldol reaction

2006

New materials for L-proline recycling have been developed. These materials have been applied to the L-proline-catalyzed aldol reaction between acetone and several aldehydes. The L-proline has been supported on the surface of modified silica gels with a monolayer of covalently attached ionic liquid with or without additional adsorbed ionic liquid. Good yields and ee values, comparable with those obtained under homogeneous conditions, have been obtained especially with imidazolinium-modified and 4-methylpyridinium-modified silica gels. Moreover, these materials have been easily recovered by simple filtration and studies about their reuse have been carried out. These studies showed that these …

Silica gelInorganic chemistrySilica gelSettore CHIM/06 - Chimica OrganicaGeneral Chemistryb-hydroxy ketonelaw.inventionCatalysisIonic liquidschemistry.chemical_compoundOrganic catalysisAdsorptionchemistryAldol reactionlawSupported catalystIonic liquidMonolayerAcetoneAldol reactionOrganic chemistryionicliquidorganic catalysiFiltrationβ-hydroxy ketonesAdvanced Synthesis and Catalysis
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Organic Monolayers by B(C6F5)3-Catalyzed Siloxanation of Oxidized Silicon Surfaces

2017

Inspired by the homogeneous catalyst tris(pentafluorophenyl) borane [B(C6F5)3], which acts as a promotor of Si-H bond activation, we developed and studied a method of modifying silicon oxide surfaces using hydrosilanes with B(C6F5)3 as the catalyst. This dedihydrosiloxanation reaction yields complete surface coverage within 10 min at room temperature. Organic monolayers derived from hydrosilanes with varying carbon chain lengths (C8-C18) were prepared on oxidized Si(111) surfaces, and the thermal and hydrolytic stabilities of the obtained monolayers were investigated in acidic (pH 3) medium, basic (pH 11) medium, phosphate-buffered saline (PBS), and deionized water (neutral conditions) for …

SiliconInorganic chemistrySilici Compostoschemistry.chemical_elementHomogeneous catalysis02 engineering and technologyBorane010402 general chemistry01 natural sciencesQuímica de superfíciesCatalysischemistry.chemical_compoundHydrolysisMonolayerElectrochemistryLife ScienceGeneral Materials ScienceSilicon oxideSpectroscopyVLAGOrganic ChemistrySurfaces and Interfaces021001 nanoscience & nanotechnologyCondensed Matter PhysicsOrganische ChemieSilane0104 chemical scienceschemistry0210 nano-technologyQuímica orgànicaLangmuir
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Halloysite nanotubes as nanoreactors for heterogeneous micellar catalysis

2021

Abstract Hypothesis Electrostatic attractions between the anionic head group of sodium alkylsulphates and the positively charged inner surface of halloysite nanotubes (HNTs) drive to the formation of tubular inorganic micelles, which might be employed as nanoreactors for the confinement of non polar compounds in aqueous media. On this basis, sodium alkylsulphates/halloysite hybrids could be efficient nanocatalysts for organic reactions occurring in water. Experiments Sodium decylsulphate (NaDeS) and sodium dodecylsulphate (NaDS) were selected for the functionalization of the halloysite cavity. The composition, the structure and the surface charge properties of the hybrid nanotubes were dete…

SodiumMicellar catalysischemistry.chemical_elementNanoreactorengineering.materialHalloysiteMicelleCatalysisBiomaterialsMicroviscosityColloid and Surface ChemistryPulmonary surfactantNanotechnologyMicellesNanotubesChemistryHalloysite nanotubesSodium alkylsulphatesNanomaterial-based catalystSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsInorganic micellesChemical engineeringengineeringSurface modificationClay
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A new class of heterogeneous Pd catalysts for synthetic organic chemistry

2011

A new series of leach-proof nanostructured Pd(0) catalysts able to catalyze a number of fundamental organic transformations including C–C bond formation has been developed. Reactions in general proceed with high yield and often at completion, while the catalysts can be reused in further reaction runs. This establishes a new class of relevant solid catalysts for synthetic organic chemistry trademarked SiliaCat Pd0 Hydrogel.

Sol gel chemistryChemistryYield (chemistry)fine chemistryOrganic chemistryheterogeneous catalysiorganically modified silica (ORMOSIL)sol-gel chemistryBond formationHeterogeneous catalysisCatalysisCatalysis
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Thiazolium-based catalysts for the etherification reaction of benzylic alcohols under solvent-free condition

2015

Thiazolium and imidazolium hybrid materials were prepared by radical reactions between a mercaptopropyl-modified SBA-15 mesoporous silica and bis-vinylthiazolium or bis-vinylimidazolium dibromide salts. These hybrid materials were characterized by several techniques and were employed in the etherification reaction of 1-phenylethanol. Solvent-free conditions at 160C under different gas phases (oxygen, air, nitrogen and argon) were used. The thiazolium-based material displayed excellent performances. Further studies were carried out using unsupported thiazolium salts, with or without a methyl group at the C-2 position of the thiazolium moiety. These studies allowed us to propose a reaction me…

Solvent freecatalysisChemistryHomogeneous catalysissupported catalystGeneral ChemistrycatalysiSettore CHIM/06 - Chimica OrganicaorganocatalysiHeterogeneous catalysisCatalysisheterogeneous catalysisOrganocatalysissynthetic methodsOrganic chemistryheterogeneous catalysiorganocatalysisSynergistic catalysissupported catalysts
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Heterogeneous Gold Catalyst: Synthesis, Characterization, and Application in 1,4-Addition of Boronic Acids to Enones

2015

The new 1 wt % Au/TiO2–UVM-7 catalyst was prepared and fully characterized. This heterogeneous catalyst proved to be active, selective and recyclable for the unprecedented gold-catalyzed 1,4-addition of various functionalized arylboronic acids to 2-cyclohexen-1-one and other selected enones using toluene as a solvent. The gold-based catalyst was recycled two times and played an active role in this reaction, and the nature of the solvent determined a remarkable change in the products’ selectivities.

Solventchemistry.chemical_compoundChemistryOrganic chemistryGeneral ChemistrySolvent effectsHeterogeneous catalysisSelectivityTolueneCatalysisCatalysisCharacterization (materials science)ACS Catalysis
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Chemoenzymatic Synthesis of Functional Sialyl LewisX Mimetics with a Heteroaromatic Core

2014

Functional mimetics of the sialyl Lewis(X) tetrasaccharide were prepared by the enzymatic sialylation of a 1,3-diglycosylated indole and a glycosyl azide, which was subsequently transformed into a 1,4-diglycosylated 1,2,3-triazole, by using the trans-sialidase of Trypanosoma cruzi. These compounds inhibited the binding of E-, L-, and P-selectin-coated nanoparticles to polyacrylamide-bound sialyl-Lewis(X) -containing neighboring sulfated tyrosine residues (sTyr/sLe(X) -PAA) at low or sub-millimolar concentrations. Except for E-selectin, the mimetics showed higher activities than the natural tetrasaccharide.

Spectrometry Mass Electrospray IonizationStereochemistryProton Magnetic Resonance SpectroscopyTrypanosoma cruziMolecular Sequence DataNeuraminidaseOligosaccharidessaccharide mimeticsBiochemistryenzyme catalysisEnzyme catalysischemistry.chemical_compoundSulfationTetrasaccharideAnimalsGlycosylTyrosineCarbon-13 Magnetic Resonance SpectroscopySialyl Lewis X AntigenGlycoproteinsIndole testheterocyclesOrganic ChemistryMolecular Mimicrycell adhesionGeneral ChemistryFull Paperscarbohydrates (lipids)Sialyl-Lewis XchemistryCarbohydrate SequenceSelectinsAzideChemistry, an Asian Journal
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Increased dynamic effects in a catalytically compromised variant of Escherichia coli dihydrofolate reductase

2013

Isotopic substitution (15N, 13C, 2H) of a catalytically compromised variant of Escherichia coli dihydrofolate reductase, EcDHFR-N23PP/S148A, has been used to investigate the effect of these mutations on catalysis. The reduction of the rate constant of the chemical step in the EcDHFR-N23PP/S148A catalyzed reaction is essentially a consequence of an increase of the quasi-classical free energy barrier and to a minor extent of an increased number of recrossing trajectories on the transition state dividing surface. Since the variant enzyme is less well set up to catalyze the reaction, a higher degree of active site reorganization is needed to reach the TS. Although millisecond active site motion…

StereochemistryCoupled motionsKnockoutHydride transferProtein dynamicsChemical stepmedicine.disease_causeTemperature-dependenceBiochemistryCatalysisArticleCatalysisEnzyme catalysisColloid and Surface ChemistryReaction rate constantDihydrofolate reductasemedicineEscherichia coliQDEscherichia colichemistry.chemical_classificationbiologyChemistryProtein dynamicsActive siteEnzyme catalysisGeneral ChemistryTetrahydrofolate DehydrogenaseEnzymeDehydrogenasebiology.proteinBiocatalysisConformational motions
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