Search results for "Palladium"

showing 10 items of 956 documents

Bis[S-hexyl 3-(thiophen-2-ylmethylidene)dithiocarbazato-κ2N3,S]palladium(II)

2016

In the title complex, [Pd(C12H17N2S3)2], the PdIIatom exhibits a square-planar coordination geometry with theN,S-chelating ligands arranged in atransconfiguration. Intramolecular C—H...S hydrogen bonds are observed. In the crystal, molecules are linked by weak C—H...N hydrogen-bond interactions, forming chains parallel to thebaxis.

inorganic chemicalsQuantitative Biology::Biomoleculescrystal structureChemistryStereochemistryHydrogen bondThio-chemistry.chemical_elementGeneral MedicineCrystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesMedicinal chemistryhumanitiespalladium(II) complex0104 chemical sciencesCrystalTrans configurationlcsh:QD901-999lcsh:Crystallographydithiocarbazate ligandCoordination geometryPalladiumIUCrData
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Formation and growth of palladium nanoparticles inside porous poly(4-vinyl-pyridine) monitored by operando techniques: The role of different reducing…

2017

In this work we followed the formation of palladium nanoparticles, starting from palladium (II) acetate precursor, inside a poly(4-vinylpyridine-co-divinylbenzene) polymer in presence of different reducing agents. The formation and growth of palladium nanoparticles in presence of H-2 was followed as a function of temperature by simultaneous XANES-SAXS techniques, coupled with DRIFT spectroscopy in operando conditions. It was found that the pyridyl functional groups in the polymer plays a fundamental role in the stabilization of the palladium (II) acetate precursor, as well as in the stabilization of the palladium nanoparticles. The effect of a thermal treatment in alcohol (ethanol and 2-pro…

inorganic chemicalsReducing agentInfrared spectroscopychemistry.chemical_element02 engineering and technologyThermal treatment010402 general chemistryPhotochemistry01 natural sciencesAEROBIC ALCOHOL OXIDATIONCatalysisCatalysiCatalysisP4VPRUTHENIUM NANOPARTICLESMoleculeOrganic chemistryOperandoCATALYTIC-ACTIVITYchemistry.chemical_classificationPD NANOPARTICLESDRIFT; Operando; P4VP; Palladium nanoparticles; SAXS; XANESChemistryIN-SITUChemistry (all)SAXSGeneral ChemistryPolymerPalladium nanoparticleSELECTIVE OXIDATION021001 nanoscience & nanotechnologyPalladium nanoparticlesXANESX-RAY-SCATTERINGPARTICLE-SIZE0104 chemical sciencesDRIFTColloidal goldGOLD NANOPARTICLESVIBRATIONAL PROPERTIESDRIFT; Operando; P4VP; Palladium nanoparticles; SAXS; XANES; Catalysis; Chemistry (all)0210 nano-technologyPalladiumCatalysis Today
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A facile cleavage of allyl ethers on solid phase

2000

Abstract A simple and efficient protocol for the cleavage of allyl ethers on solid phase using a palladium(0)-catalyzed allyl transfer reaction is reported.

inorganic chemicalsSolid-phase synthesischemistryorganic chemicalsOrganic ChemistryDrug DiscoveryPolymer chemistryfood and beveragesOrganic chemistrychemistry.chemical_elementCleavage (crystal)BiochemistryPalladiumTetrahedron Letters
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Ni(II) and Pd(II) complexes of camphor-derived diazadiene ligands: steric bulk tuning and ethylene polymerization

1998

Abstract Nickel(II) and palladium(II) centers were coordinated to a series of chiral 1,4-diazadiene ligands. The ligand backbones are camphor derivatives and the imine nitrogens are attached to independently varied 2- and 2,6-substituted aryl groups. Upon activation with methyl-aluminoxane, the dibromo nickel complexes polymerize ethylene and 1-hexene. The polymerization properties are dependent on the steric features of the aryl substituents on the imine nitrogens.

inorganic chemicalsSteric effectsEthyleneChemistryLigandArylIminechemistry.chemical_elementPhotochemistryInorganic Chemistrychemistry.chemical_compoundNickelPolymerizationPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryPalladiumInorganic Chemistry Communications
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Precatalyst or dosing-device? The [Pd2{μ-(C6H4) PPh2}2{μ-O2C(C6H5)}2] complex anchored on a carboxypolystyrene polymer as an effective supplier of pa…

2020

Abstract A new catalyst has been synthesized from the precursor [Pd2{μ-(C6H4) PPh2}2 {μ-O2C(C6H5)}2] immobilized on a carboxypolystyrene polymer that exhibits an excellent dispersion of the Pd (II) centers, reusability, and catalytic activity in front of phenyl bromides. The activity of this new material was studied in detail for the Suzuki-Miyaura reaction and compared to that of Pd nanoparticles (NPs) supported on UVM-7 (a mesoporous silica), and Pd NPs stabilized with polyvinylpirrolydone. The homogeneous/heterogeneous character of the catalytic process was determined from the results of the hot-filtration, centrifugation, poisoning, three phases tests, and from differential sensitivity …

inorganic chemicalschemistry.chemical_classification010405 organic chemistryNanoparticlechemistry.chemical_elementPolymerMesoporous silica010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistryX-ray photoelectron spectroscopyChemical engineeringCatalytic cycleOxidation statePhysical and Theoretical ChemistryPalladiumJournal of Catalysis
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Versuche zur Herstellung linolsäurearmen Ölsäureesters über eine Hydrierung mit Palladium

1980

Uber eine Hydrierung mit Palladium auf Aktivkohle konnen geringe Gehalte an Linolsaure in Gegenwart eines hohen Olsaureuberschusses recht selektiv reduziert werden. Der Linolsauregehalt eines Fettsauremethylestergemisches wurde von 10% auf 2% gesenkt, dabei entstanden 3% cis-, 4% trans-Monoenfettsauren sowie 1% Stearinsaure. The Preparation of Oleic Ester with Reduced Linoleic Acid Content by Hydrogenation with Palladium By hydrogenation with palladium on charcoal low contents of linoleic acid can be reduced quite selectively in the presence of an excess of oleic acid ester. In a mixture of fatty acid methylesters the content of linoleic acid was reduced from 10% to 2% with the formation of…

inorganic chemicalschemistry.chemical_classificationOleic acidchemistry.chemical_compoundchemistryLinoleic acidvisual_artvisual_art.visual_art_mediumFatty acidchemistry.chemical_elementCharcoalNuclear chemistryPalladiumFette, Seifen, Anstrichmittel
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Synthesis, characterization and antimicrobial activity of palladium(II) complexes with some alkyl derivates of thiosalicylic acids: Crystal structure…

2012

Abstract S-Alkyl (R = benzyl, methyl, ethyl, propyl and butyl) derivatives of thiosalicylic acid and the corresponding palladium(II) complexes were prepared and their structures were proposed on the basis of infrared, 1H and 13C NMR spectroscopy. The cis geometrical configurations of the isolated complexes were proposed on the basis of an X-ray structural study of the bis(S-benzyl-thiosalicylate)–palladium(II), [Pd(S-bz-thiosal)2] complex. Antimicrobial activity of the tested compounds was evaluated by determining the minimum inhibitory concentration (MIC) and minimum microbicidal concentration (MMC) in relation to 26 species of microorganisms. The tested ligands, with a few exceptions, sho…

inorganic chemicalschemistry.chemical_classificationThiosalicylic acidbiologyStereochemistrychemistry.chemical_elementCrystal structurebiology.organism_classificationAntimicrobialMedicinal chemistryAspergillus fumigatusInorganic Chemistrychemistry.chemical_compoundMinimum inhibitory concentrationchemistryMaterials ChemistryPhysical and Theoretical ChemistryAntibacterial activityta116AlkylPalladiumPolyhedron
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Soluble/MOF-Supported Palladium Single Atoms Catalyze the Ligand-, Additive-, and Solvent-Free Aerobic Oxidation of Benzyl Alcohols to Benzoic Acids.

2021

Metal single-atom catalysts (SACs) promise great rewards in terms of metal atom efficiency. However, the requirement of particular conditions and supports for their synthesis, together with the need of solvents and additives for catalytic implementation, often precludes their use under industrially viable conditions. Here, we show that palladium single atoms are spontaneously formed after dissolving tiny amounts of palladium salts in neat benzyl alcohols, to catalyze their direct aerobic oxidation to benzoic acids without ligands, additives, or solvents. With this result in hand, the gram-scale preparation and stabilization of Pd SACs within the functional channels of a novel methyl-cystein…

inorganic chemicalschemistry.chemical_element010402 general chemistry01 natural sciencesBiochemistryCatalysisCatalysisMetalColloid and Surface ChemistryAtom economyMetal·lúrgiaDissolutionSolvent freeChemistryLigandQuímicaGeneral ChemistryCombinatorial chemistry0104 chemical sciencesSoluble/MOFOrganic reactionAlcoholsvisual_artvisual_art.visual_art_mediumPalladiumJournal of the American Chemical Society
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Direct arylation of heteroaromatic compounds with congested, functionalised aryl bromides at low palladium/triphosphane catalyst loading.

2011

International audience; A new ferrocenyl triphosphane ligand associated to palladium was found to be an efficient catalyst for the direct coupling of highly congested, functionalised aryl bromides with a variety of heteroarenes. These coupling reactions can generally be performed by using a low-loading (0.1-0.5 mol%) of the catalyst. The present protocol tolerates important and useful functional groups, which allows for further elaboration into more sophisticated heterocyclic molecules. The straightforward arylation of heteroaromatic compounds with congested ortho-substituted aryl bromides may permit further convergent syntheses of diverse ligands, biologically active molecules and molecula…

inorganic chemicalschemistry.chemical_element010402 general chemistry01 natural sciencesCatalysisCoupling reactionCatalysis[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundMoleculeOrganic chemistryEfficient catalystaryl bromidesheterocycles010405 organic chemistryChemistryLigandArylOrganic Chemistryferrocenyl polyphosphaneGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysispalladium0104 chemical sciencesC[BOND]H activationTriphosphanePalladium
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Linear Triphosphines as Ligands for Metal Complexes Immobilization in Ionic Liquids: Palladium-Catalyzed Methoxylation of Alkynes

2012

Several novel palladium triphosphine complexes have been synthesized and tested as recyclable catalysts for the methoxylation of alkynes into acetals in ionic liquids. A complete conversion of phenylacetylene was achieved with only 0.2% of (Pd(Triphos)NCMe)((PF6)2) in a methanol/(BMIM)(BF4) mixture. We discovered that the addition of an ionic liquid to methanol allowed not only to increase the activity of the palladium catalyst but also to provide a recyclable catalyst which can be reused several times with a weaker drop of activity. To complete these catalytic studies, we describe the synthesis of the first poor -electron-donating/strong -electron-acceptor linear Triphosphine which, afte…

inorganic chemicalschemistry.chemical_elementCombinatorial chemistryTriphosCatalysisMetalchemistry.chemical_compoundchemistryPhenylacetylenevisual_artIonic liquidvisual_art.visual_art_mediumOrganic chemistryMethanolSelectivityPalladiumThe Open Organic Chemistry Journal
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