Search results for " palladium catalyst"

showing 4 items of 4 documents

Catalytic Carbonylative Double Cyclization of 2-(3-Hydroxy-1-yn-1-yl)phenols in Ionic Liquids Leading to Furobenzofuranone Derivatives

2019

A catalytic carbonylative double cyclization method for the synthesis of furo[3,4-b]benzofuran-1(3H)-ones is reported. It is based on the reaction between readily available 2-(3-hydroxy-1-yn-1-yl)phenols, CO, and oxygen carried out in the presence of catalytic amounts of PdI2 (1 mol %) in conjunction with KI (20 mol %) and 2 equiv of diisopropylethylamine at 80 degrees C for 24 h under 30 atm of a 1:4 mixture of CO-air. Interestingly, the process was not selective when carried out in classical organic non-nucleophilic solvents (such as MeCN or DME), leading to a mixture of the benzofurofuranone derivative and the benzofuran ensuing from simple cycloisomerization, whereas it turned out chemo…

010405 organic chemistryOrganic Chemistrychemistry.chemical_elementIonic LiquidsCarbonylationSettore CHIM/06 - Chimica Organica010402 general chemistry01 natural sciencesCarbonylation; Palladium; Cyclization; Ionic Liquids0104 chemical sciencesCatalysischemistry.chemical_compoundIonic liquids palladium catalyst benzofuranchemistryCyclizationIonic liquidOrganic chemistryPhenolsCarbonylationPalladiumPalladium
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Recyclable heterogeneous palladium catalysts in pure water: sustainable developments in Suzuki, Heck, Sonogashira and Tsuji-Trost reactions

2010

This review summarizes the progress made essentially these last ten years on heterogeneous palladium catalysis in pure water. The work covers four important palladium-catalyzed transformations for carbon-carbon bond formation: Suzuki, Heck, Sonogashira and Tsuji-Trost reactions. The discussion focuses on the efficiency and reusability of the heterogeneous catalysts as well as on the experimental conditions from a sustainable chemistry point of view. The review is introduced by a discussion on mechanistic aspects inherent to heterogeneous catalysis.

Green chemistryheterogeneous palladium catalysts010405 organic chemistrywaterSonogashira couplingchemistry.chemical_elementGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryHeterogeneous catalysis01 natural sciences7. Clean energySuzuki reaction -Tsuji-Trost reaction0104 chemical sciencesCatalysisTsuji–Trost reaction[ CHIM.CATA ] Chemical Sciences/CatalysisHeck reactionchemistrySuzuki reactionHeck reactionOrganic chemistrySonogashira reactionComputingMilieux_MISCELLANEOUSPalladium
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A New Heterogeneous Catalyst Obtained via Supramolecular Decoration of Graphene with a Pd2+ Azamacrocyclic Complex

2019

A new G-(H2L)-Pd heterogeneous catalyst has been prepared via a self-assembly process consisting in the spontaneous adsorption, in water at room temperature, of a macrocyclic H2L ligand on graphene (G) (G + H2L = G-(H2L)), followed by decoration of the macrocycle with Pd2+ ions (G-(H2L) + Pd2+ = G-(H2L)-Pd) under the same mild conditions. This supramolecular approach is a sustainable (green) procedure that preserves the special characteristics of graphene and furnishes an efficient catalyst for the Cu-free Sonogashira cross coupling reaction between iodobenzene and phenylacetylene. Indeed, G-(H2L)-Pd shows an excellent conversion (90%) of reactants into diphenylacetylene under mild conditio…

Models MolecularChemical PhenomenaIodobenzeneMolecular ConformationPharmaceutical ScienceSonogashira couplingLigands010402 general chemistryHeterogeneous catalysiscross coupling01 natural sciencesArticleCoupling reactionAnalytical Chemistrylaw.inventionCatalysislcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryCoordination ComplexeslawDrug DiscoveryPolymer chemistryPhysical and Theoretical ChemistryDiphenylacetyleneMolecular Structurecatalysis010405 organic chemistryGrapheneSpectrum AnalysisOrganic ChemistrySonogashirapalladium catalystHydrogen-Ion Concentrationsupramolecular interactions0104 chemical sciencesSolutionsazamacrocycleschemistryPhenylacetyleneChemistry (miscellaneous)surface adsorptionMolecular MedicineGraphitecatalysis palladium catalyst; Sonogashira graphenePalladiumMolecules
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α-d-Glucopyranose Adsorption on a Pd30 Cluster Supported on Boron Nitride Nanotube

2016

Boron nitride nanotube (BNNT) as an innovative support for carbohydrate transformation processes was evaluated, using density functional theory. The α-d-glucopyranose adsorption on a Pd30 cluster, supported on BNNT, was used to check both the local activity of topologically different metallic sites and the effects of the proximity of the BNNT surface to the same metallic sites. Detailed geometrical and electronic analyses performed on Pd30/BNNT and α-d-glucopyranose/Pd30/BNNT systems were discussed. It was observed that the deposition of the Pd30 cluster onto the BNNT support gives rise to an electronic rearrangement, determining a charge transfer from the support to the adsorbed metal clus…

Surface site reactivityChemical substanceNanotechnologyElectron donor02 engineering and technology010402 general chemistryDFT01 natural sciencesBoron nitride nanotubeCatalysisCatalysiCatalysisMetalchemistry.chemical_compoundAdsorptionSupported palladium catalystCluster (physics)Chemistry (all)Molecular electrostatic potentialGeneral Chemistry021001 nanoscience & nanotechnologyBoron nitride nanotube; DFT; Molecular electrostatic potential; Supported palladium catalyst; Surface site reactivity; α-d-Glucopyranose adsorption; Catalysis; Chemistry (all)0104 chemical scienceschemistryChemical physicsvisual_artα-d-Glucopyranose adsorptionvisual_art.visual_art_mediumDensity functional theory0210 nano-technologyScience technology and societyTopics in Catalysis
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