Search results for " Heterogeneous Catalysis"

showing 10 items of 23 documents

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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Carbocatalytic Oxidative Dehydrogenative Couplings of (Hetero)Aryls by Oxidized Multi‐Walled Carbon Nanotubes in Liquid Phase

2019

HNO3-oxidized carbon nanotubes catalyze oxidative dehydrogenative (ODH) carbon-carbon bond formation between electron-rich (hetero)aryls with O-2 as a terminal oxidant. The recyclable carbocatalytic method provides a convenient and an operationally easy synthetic protocol for accessing various benzofused homodimers, biaryls, triphenylenes, and related benzofused heteroaryls that are highly useful frameworks for material chemistry applications. Carbonyls/quinones are the catalytically active site of the carbocatalyst as indicated by model compounds and titration experiments. Further investigations of the reaction mechanism with a combination of experimental and DFT methods support the compet…

Reaction mechanism116 Chemical sciencesoxidative dehydrogenative couplingLiquid phaseOxidative phosphorylationCarbon nanotube010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysislaw.inventionlawcarbon nanotubecarbon nanotubesbiology010405 organic chemistryChemistryOrganic ChemistryC−C couplingCationic polymerizationcarbon nanotubes; C−C coupling; heterogeneous catalysis; oxidative dehydrogenative couplingActive siteGeneral ChemistryCombinatorial chemistry0104 chemical sciencesheterogeneous catalysisbiology.proteinheterogeneous catalysiTitrationC-C couplingChemistry – A European Journal
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Toward More Efficient Organocatalysts

2011

Settore CHIM/06 - Chimica OrganicaOrganocatalysys Heterogeneous catalysis proline
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Preface

2019

Preface of the book "Heterogeneous Photocatalysis Relationships with Heterogeneous Catalysis and Perspectives"

Thermal heterogeneous catalysis heterogeneous photocatalysisSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie
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Green Oxidation of Alcohols to Carbonyl Compounds by Heterogeneous Photocatalysis

2010

TitaniumAldehydesChemistryGeneral Chemical EngineeringKetonesHeterogeneous catalysisPhotochemistryPhotochemical ProcessesSilicon DioxideCatalysisGeneral EnergyAlcohol oxidationAlcoholsAlcohols Chemoselectivity Heterogeneous Catalysis Oxidation PhotocatalysisPhotocatalysisEnvironmental ChemistryOrganic chemistryGeneral Materials ScienceChemoselectivityOxidation-ReductionEnvironmental Restoration and Remediation
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Imidazolium-Functionalized Carbon Nanohorns for the Conversion of CO2 Unprecedented Increase of Catalytic Activity after Recycling

2017

Carbon nanohorns (CNHs) were selected as a novel catalytic platform for the design of imidazolium based hybrid materials able to promote the conversion of carbon dioxide into cyclic carbonates. Several heterogeneous catalysts were prepared using a one-step procedure based on the radical polymerization of various bis-vinylimidazolium salts in the presence of pristine CNHs. The as-synthesized materials were tested for the fixation of CO2 into epoxides. The excellent catalytic performances were evaluated in terms of turnover number and productivity. The versatility of the above hybrids was proved using several epoxides as substrate. Catalysts recyclability was successfully verified for several…

carbon dioxide conversion carbon nanohorns cyclic carbonates heterogeneous catalysis imidazolium saltsSettore CHIM/06 - Chimica Organica
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Effect of Pre-Reduction on the Properties and the Catalytic Activity of Pd/Carbon Catalysts: A Comparison with Pd/Al2O3

2013

The effect of pre-reduction in solution with chemical reagents on the catalytic performance and catalyst properties of Pd/carbon catalysts was systematically investigated with a multitechnique approach. The results are critically discussed in comparison to those recently obtained on analogous Pd/alumina catalysts. It was proved that the Pd phase on the carbon surface is characterized by a high mobility, opposite to what occurs on alumina. As a result, the Pd particles on carbon aggregate together during pre-reduction, with a consequent decrease in available metal surface. Pd particles remain aggregated also in reaction conditions; the decreased Pd dispersion negatively affects the catalyst …

characterization techniqueCO chemisorptionInorganic chemistryPd-based catalystchemistry.chemical_elementTPRHeterogeneous catalysisPd/CarbonCatalysisCatalysisMetalCharacterization techniquesCatalyst pre-reductionTemperature-programmed reductionX-ray absorption spectroscopymetal nanoparticlein situPd-based catalystsPd/aluminaSAXSGeneral ChemistryXANESSmall Angle X-ray ScatteringX-ray Absorption SpectroscopyPd/Carbon; Pd/alumina; metal nanoparticle; catalysis; Catalyst pre-reduction; in situ; SAXS; XANES; Pd-based catalysts; heterogeneous catalysis; Characterization techniques; Temperature-programmed reduction; TPR; CO chemisorption; TEM; X-ray absorption spectroscopy; Small Angle X-ray Scatteringheterogeneous catalysischemistryReagentvisual_arttemperature-programmed reductionvisual_art.visual_art_mediumTEMheterogeneous catalysiSmall Angle X-ray SpectroscopyDispersion (chemistry)Carbon
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Hemicellulose hydrolysis catalysed by solid acids

2013

Depolymerising hemicellulose into platform sugar molecules is a key step in developing the concept of an integrated biorefinery. This reaction is traditionally catalysed by either enzymes or homogeneous mineral acids. We compared various solid catalysts for hemicellulose hydrolysis, running reactions in water, under neutral pH and relatively mild temperature and pressure (120°C and 10 bar) conditions. Sulphonated resins are highly active, but they leach out sulphonic groups. Sulphonated silicas are less active, but more stable. They have weakly and strongly bound sites and the strongly bound ones do not leach. Zeolites are moderately active and stable. Among them, H-ferrierite especially, d…

chemistry.chemical_classificationChemistryBiorefineryCatalysisCatalysischemistry.chemical_compoundHydrolysisEnzymeHemicellulose heterogeneous catalysis solid acids xylose arabinose zeolitesHomogeneousOrganic chemistryMoleculeQDHemicelluloseSugar
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Heterogeneously catalyzed Suzuki-Miyaura conversion of broad scope

2012

The reaction tolerates a broad range of functional groups in the coupling partners and is usually performed in solution under homogeneous conditions at T ¢ 60 uC using 2–3 mol% catalytic amounts. The catalyst is often a Pd(0) complex with triarylphosphane ligands. 2 The catalytic cycle (Scheme 2) begins with the oxidative addition of an aryl halide to a Pd(0) species formed in situ to form an arylpalladium(II) halide intermediate. 3 Chloroarenes, especially nonactivated aryl chlorides, are notoriously less reactive due to the stability of the C–Cl bond (the relative reactivity of Ar–X is correlated to the respective bond dissociation energy: Ph–Cl: 96 kcal mol 21 ,P h–Br: 81 kcal mol 21 ,P …

chemistry.chemical_classificationGeneral Chemical EngineeringAryl halideArylchemistry.chemical_elementHomogeneous catalysisGeneral ChemistryOxidative additionCatalysiscross-coupling heterogeneous catalysis palladium Suzuki–Miyaurachemistry.chemical_compoundchemistryCatalytic cycleOrganic chemistryReactivity (chemistry)Palladium
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Polystyrene-supported proline as recyclable catalyst in the Baylis–Hillman reaction of arylaldehydes and methyl or ethyl vinyl ketone

2008

Abstract Polystyrene-supported proline has been used as co-organocatalyst (10 mol%) with imidazole (10 mol%) in the Baylis–Hillman reaction between methyl or ethyl vinyl ketone and arylaldehydes. Recycling studies showed that the proline resin can be used up to five cycles with high isolated yields. This study represents the first example of supported proline as heterogeneous catalyst in the above reaction and broaden the scope of this catalytic material.

chemistry.chemical_classificationKetoneProcess Chemistry and TechnologySettore CHIM/06 - Chimica OrganicaGeneral ChemistryHeterogeneous catalysisorganocatalysis heterogeneous catalysis Baylis-Hilmann reactionCatalysisCatalysischemistry.chemical_compoundchemistryOrganocatalysisImidazoleOrganic chemistryBaylis–Hillman reactionPolystyreneProlineCatalysis Communications
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