Search results for "Palladium"

showing 10 items of 956 documents

Palladium-Catalyzed Carbon–Carbon Cross-Coupling Reactions in Thermomorphous Double Emulsions

2015

The method of combining the concept of fluorous biphasic catalysis (FCB) with micro multiple emulsions benefits from the advantages of homogeneous as well as from heterogeneous catalysis in continuous micro flow. In this particular case, three immiscible fluid phases in continuous micro segmented flow were used to perform palladium-catalyzed Heck crosscoupling reactions of styrene with aryl halides. A capillary tube-in-tube coaxial flow setup in combination with a glass micro reactor was used to produce monodisperse aqueous phase/organic phase/perfluorinated phase double emulsions. The resulting emulsions had a core-shell droplet structure composed of a perfluorcarbon fluid in which a palla…

Fluid Flow and Transfer ProcessesOrganic ChemistryInorganic chemistryAqueous two-phase systemchemistry.chemical_elementHeterogeneous catalysisCoupling reactionCatalysischemistryChemistry (miscellaneous)Heck reactionPhase (matter)MicroreactorPalladiumJournal of Flow Chemistry
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Ammonium formate-Pd/C as a new reducing system for 1,2,4-oxadiazoles. Synthesis of guanidine derivatives and reductive rearrangement to quinazolin-4-…

2021

1,2,4-Oxadiazole is a heterocycle with wide reactivity and many useful applications. The reactive O-N bond is usually reduced using molecular hydrogen to obtain amidine derivatives. NH4CO2H-Pd/C is here demonstrated as a new system for the O-N reduction, allowing us to obtain differently substituted acylamidine, acylguanidine and diacylguanidine derivatives. The proposed system is also effective for the achievement of a reductive rearrangement of 5-(2′-aminophenyl)-1,2,4-oxadiazoles into 1-alkylquinazolin-4(1H)-ones. The alkaloid glycosine was also obtained with this method. The obtained compounds were preliminarily tested for their biological activity in terms of their cytotoxicity, induce…

Formatesquinazolin-4-onemedicine.disease_causeGuanidineschemistry.chemical_compoundBiology (General)CytotoxicityAmmonium formateSpectroscopyOxadiazolesMolecular StructureChemistryAlkaloidBiological activityGeneral MedicineComputer Science ApplicationsChemistryOxidation-ReductionPalladiumCell SurvivalQH301-705.5Dipeptidyl Peptidase 4chemistry.chemical_elementAntineoplastic AgentsreductionArticleCatalysisInorganic ChemistryAmidine4-oxadiazolereduction;Cell Line TumorDiabetes MellitusAmmonium formatemedicineHumansHypoglycemic AgentsReactivity (chemistry)Physical and Theoretical ChemistryMolecular BiologyQD1-999QuinazolinonesSettore MED/04 - Patologia GeneralediacylguanidineOrganic Chemistry124-oxadiazolealpha-GlucosidasesacylguanidineSettore CHIM/06 - Chimica OrganicapalladiumCombinatorial chemistryModels ChemicalA549 CellsOxidative stress
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Inside Back Cover: Boron Nitride‐supported Sub‐nanometer Pd 6 Clusters for Formic Acid Decomposition: A DFT Study (ChemCatChem 9/2017)

2017

Formic acidOrganic ChemistryInorganic chemistrychemistry.chemical_elementDecompositionCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryBoron nitrideCover (algebra)NanometrePhysical and Theoretical ChemistryPalladiumChemCatChem
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Fonctionnalisation et métallisation des diamantoïdes

2015

The thesis deals with development of synthetic methods for preparation of novel carbon-metal organohybrid based on diamondoid and palladium. The vapor pressure of various diamondoids was measured from a new measurement protocol at solid-vapor thermodynamic equilibrium state. Their volatile tendency opened a possibility to do deposition from gas phase and at various pressure (ambient, primary vacuum, and high vacuum) of diamondoids on silicon or mica substrates. SEM observations have shown that depending on the type of functional groups on the diamondoid, different crystal shapes can be produced (rods, needles, triangles, truncated octahedral form).OMCVD of palladium on functionalized diaman…

Functionalized diamondoidfunctionalized diamondoidsOMCVD de palladiumChemistry & allied sciencesPd OMCVDhybrid materialair-stable phosphineAir-stable phosphineorganic self-assemblyOrganic self-assembly[CHIM.OTHE] Chemical Sciences/Other[ CHIM.OTHE ] Chemical Sciences/Otherddc:540[CHIM.OTHE]Chemical Sciences/OtherHybrid material
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1989

Synthese a partir du dibromo-1,5 di t-butyl-3,7 naphtalene via un monomere bifonctionnel (action du butyllithium et du triisopropoxyborane)

Gel permeation chromatographyTert butylchemistry.chemical_compoundChemistryStereochemistryMoleculechemistry.chemical_elementSolubilityMedicinal chemistryOligomerCatalysisPalladiumDie Makromolekulare Chemie, Rapid Communications
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Size-activity relationship of iridium particles supported on silica for the total oxidation of volatile organic compounds (VOCs)

2019

12 Figures, 2 Tables.-- Datos suplementarios disponibles en línea en la página web del editor.-- © 2019. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/

General Chemical EngineeringTotal oxidationInorganic chemistryShort chain alkaneschemistry.chemical_element02 engineering and technologyIridium010402 general chemistry01 natural sciencesRedoxIndustrial and Manufacturing Engineeringlaw.inventionCatalysisMetalSize-activity relationshiplawEnvironmental ChemistryCalcinationIridiumVOCSilicaGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistryvisual_artvisual_art.visual_art_mediumParticle size0210 nano-technologyPlatinumPalladiumChemical Engineering Journal
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A Bipyridine‐Palladium Derivative as General Pre‐Catalyst for Cross‐Coupling Reactions in Deep Eutectic Solvents

2019

A versatile and DES‐compatible bipyridine palladium complex has been developed as a general pre‐catalyst for different cross‐coupling reactions (Hiyama, Suzuki‐Miyaura, Heck‐Mizoroki and Sonogashira) in deep eutectic solvents. Hydrogen bond capacity of the ligand allows to keep the excellent level of results previously obtained in classical organic solvents. Palladium pre‐catalyst showed a high catalytic activity for many cross‐coupling reactions, demonstrating a great versatility and applicability. Also, this methodology employs sustainable solvents as a reaction medium and highlights the potential of DES as alternative solvents in organometallic catalysis. The catalyst and DES were easily…

Green chemistry010405 organic chemistryHydrogen bondchemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCoupling reaction0104 chemical sciencesCatalysisHydrogen bondsLigand designchemistry.chemical_compoundBipyridineQuímica OrgánicachemistryGreen chemistryPolymer chemistryCross-couplingDerivative (chemistry)PalladiumEutectic systemPalladium
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Sustainable Approach to Waste-Minimized Sonogashira Cross-Coupling Reaction Based on Recoverable/Reusable Heterogeneous Catalytic/Base System and Ace…

2016

In this contribution, we present a chemically efficient and sustainable protocol for the palladium-catalyzed copper-free Sonogashira cross-coupling reaction, based on the use of a heterogeneous catalytic system. This consists in the combination of a palladium catalyst on highly cross-linked thiazolidine network on silica and a polystyrene-supported base. The solid catalyst/base system acts as a palladium scavenger avoiding leaching of the metal and consequent product contamination. The reaction can be conducted in safe and easily recoverable acetonitrile/water azeotrope as reaction medium. This proved to be an efficient greener alternative to the classic toxic aprotic media commonly used in…

Green chemistryAzeotrope media; Green chemistry; Heterogeneous catalysis; Sonogashira reaction; Waste minimization; Chemistry (all); Environmental Chemistry; Chemical Engineering (all); Renewable Energy Sustainability and the EnvironmentGeneral Chemical EngineeringWaste minimizationchemistry.chemical_elementSonogashira coupling010402 general chemistryHeterogeneous catalysis01 natural sciencesCoupling reactionCatalysisHeterogeneous catalysichemistry.chemical_compoundEnvironmental ChemistryOrganic chemistryChemical Engineering (all)Renewable EnergyAcetonitrileHeterogeneous catalysisSustainability and the Environment010405 organic chemistryRenewable Energy Sustainability and the EnvironmentChemistry (all)Settore CHIM/06 - Chimica OrganicaGeneral ChemistryAzeotrope mediaCombinatorial chemistry0104 chemical scienceschemistryGreen chemistryLeaching (metallurgy)Sonogashira reactionPalladiumACS Sustainable Chemistry and Engineering
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ChemInform Abstract: Recyclable Heterogeneous Palladium Catalysts in Pure Water: Sustainable Developments in Suzuki, Heck, Sonogashira and Tsuji-Tros…

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 chemistryChemistrySonogashira couplingOrganic chemistrychemistry.chemical_elementGeneral MedicineBond formationHeterogeneous catalysisPalladiumReusabilityCatalysisChemInform
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Progress in palladium-based catalytic systems for the sustainable synthesis of annulated heterocycles: a focus on indole backbones

2012

BIOVERT+LDJ; A survey highlighting the most recent palladium catalytic systems produced and their performances for progress in direct synthesis of indole backbones by heterocarbocyclization of reactive substrates is provided. The discussion is developed in relation with the principles of sustainable chemistry concerning atom and mass economy. In this respect, the general convergent character of the syntheses is of particular interest (one-pot, domino, cascade or tandem reactions), and the substrates accessibility and reactivity, together with the final waste production, are also important. This critical review clearly indicates that the development of ligand chemistry, mainly phosphines and…

Green chemistryIndole testIndolesPhosphines010405 organic chemistryLigandchemistry.chemical_elementChemistry Techniques Synthetic[CHIM.CATA]Chemical Sciences/CatalysisGeneral ChemistryLigands010402 general chemistry[SDE.ES]Environmental Sciences/Environmental and Society01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistryWaste productionAlkynesOrganic chemistryReactivity (chemistry)MethanePalladiumPalladiumChemical Society Reviews
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