Search results for " Catalyst"

showing 10 items of 292 documents

Switchable palladium-catalyst reaction of bromomethyl sulfoxides, CO, and N-nucleophiles: aminocarbonylation at Csp3 versus oxidative carbonylation o…

2012

The palladium-catalyzed reaction of α-bromomethyl sulfoxides, carbon monoxide, and N-nucleophiles follows different reaction pathways according to the catalytic system and the reaction conditions. The Pd-xantphos catalyst affords high yields of α-sulfinyl amides by an aminocarbonylation process and is the first example of this type of transformation for a nonbenzylic sp(3)-hybridized carbon. On the other hand, the oxidative carbonylation of amines occurs with α-bromomethyl sulfoxides, carbon monoxide, and catalytic Pd(PPh(3))(4) under aerobic conditions, yielding ureas and oxalamides from either primary or secondary amines. The reaction with ambident nucleophiles such as amino alcohols was …

chemistry.chemical_compoundPrimary (chemistry)NucleophileChemistryOxidative carbonylationOrganic Chemistrychemistry.chemical_elementOrganic chemistryAlcoholPalladium catalystCarbonCarbon monoxideCatalysisThe Journal of organic chemistry
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ChemInform Abstract: Water-Soluble Palladium Nanoparticles: Click Synthesis and Applications as a Recyclable Catalyst in Suzuki Cross-Couplings in Aq…

2011

Polyethylene glycol-tagged macrocycle (I) is prepared by a three-fold copper-catalyzed [3 + 2] cycloaddition reaction.

chemistry.chemical_compoundWater solubleAqueous mediumChemistryPolymer chemistryPalladium nanoparticlesGeneral MedicinePolyethyleneThiophene derivativesRecyclable catalystCycloadditionChemInform
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Die herstellung einiger gekennzeichneter, aliphatischer azoverbindungen und ihre anwendung als initiatoren der polymerisation

1970

Es wird die Herstellung von vier Azoverbindungen beschrieben, die sich zum Teil vom α.α′-Azo-(isobuttersaurenitril) ableiten. Zwei Verbindungen geben bei der Polymerisation von Methacrylsauremethylester und Styrol Endgruppen, die in den Polymeren photometrisch leicht zu bestimmen sind; fur eine wird gezeigt, das sie die Polymerisation von Styrol startet, ohne das storende Nebenreaktionen auftreten. Die beiden anderen Azoverbindungen sind wegen ihrer hohen Zersetzungspunkte geeignet, radikalische Polymerisationen bei hoheren Temperaturen auszulosen (160°C). The preparation of four derivatives of α.α′-azo-bis-isobutyronitrile is described. The polymerization of methylmethacrylate and styrene …

chemistry.chemical_compoundchemistryPolymerizationPolymer chemistryThermal stabilityPolymerization catalystsColorimetry (chemical method)StyreneDie Makromolekulare Chemie
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l-Arabinose Conformers Adsorption on Ruthenium Surfaces: A DFT Study

2012

Adsorption of 5 L-arabinose tautomers – one acyclic and four cyclic (α and β, pyranose and furanose) species – on a ruthenium surface was studied as a precursor-process of the, nowadays more and more, industrially important sugar catalytic hydrogenation on metal surfaces in water medium. The study was mostly referred to a 37-atom metal catalyst fragment, even though border-effects on the adsorption processes were also checked employing a 61-atom metal fragment. In order to figure out conformational effects on the title process the tautomer flexibility was, at first, investigated by the genetic-algorithm based code Balloon, considering the conformational spaces of the different aquo tautomer…

chemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesMetalAdsorptionComputational chemistryPhysical and Theoretical Chemistryl-Arabinose species conformational analysis ruthenium catalysts adsorption energies DFT studiesConformational isomerismchemistry.chemical_classification021001 nanoscience & nanotechnologyFuranoseTautomer0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsRutheniumGeneral EnergyPyranosechemistrySettore CHIM/03 - Chimica Generale E Inorganicavisual_artvisual_art.visual_art_mediumDensity functional theory0210 nano-technologyThe Journal of Physical Chemistry C
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Characterization of Nanostructured SilicaCat Pd0

2011

Structural investigation on nanostructured SiliaCat Pd0 palladium catalyst sheds light into the origins of the remarkable activity of these new catalytic materials.

chemistry.chemical_elementNanoparticleGeneral ChemistryOrmosilCatalysisCharacterization (materials science)Catalysischemistry.chemical_compoundchemistryChemical engineeringPalladium ORMOSIL SiliaCat Cross-coupling NanoparticlePalladium catalystOrganometallic chemistryPalladium
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Proximity Effect using a Nanocage Structure: Polyhedral Oligomeric Silsesquioxane-Imidazolium Tetrachloro- palladate Salt as a Precatalyst for the Su…

2016

A polyhedral oligomeric silsesquioxane-imidazolium tetrachloropalladate salt (POSS-Imi-PdCl4) was prepared by the reaction of a polyhedral oligomeric silsesquioxane-imidazolium chloride salt (POSS-Imi-Cl) with PdCl2 and used as a pre-catalyst for the Suzuki-Miyaura reaction in water at 100 °C at a low loading (0.08-0.16 mol %). Biphenyl compounds were isolated in high to excellent yields. A comparison of the POSS-based catalyst with the corresponding catalyst without the nanocage structure (i.e., 1-butyl-3-methylimidazolium tetrachloropalladate) highlighted the role of the POSS structure to reach higher yields in the Suzuki-Miyaura reaction. This result is ascribed to a proximity effect of …

chemistry.chemical_elementSalt (chemistry)supported catalyst010402 general chemistry01 natural sciencesCatalysisCatalysisInorganic Chemistrychemistry.chemical_compoundNanocagesX-ray photoelectron spectroscopyPolymer chemistryOrganic chemistrysupported catalystsPhysical and Theoretical Chemistrychemistry.chemical_classification010405 organic chemistryChemistryOrganic Chemistrypalladiumcage compoundSilsesquioxane0104 chemical sciencesBiphenyl compoundphase-transfer catalysiphase-transfer catalysisC-C couplingcage compoundsProximity effect (atomic physics)Palladium
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Applications and stereoselective syntheses of P-chirogenic phosphorus compounds.

2016

International audience; Phosphorus compounds bearing chirality on the P-center are usually qualified as P-chirogenic or P-stereogenic. This chemical class concerns natural products, agrochemistry, molecular materials, biology and pharmacy, although it is certainly in coordination chemistry and in asymmetric catalysis using chiral transition metal complexes that P-chirogenic phosphorus compounds are the most used. The chiral phosphine ligands and their uses in asymmetric metal-catalyzed reactions have been widely reviewed in literature. However, an overview covering the applications as well as the stereoselective syntheses of all classes of phosphorus compounds has not yet been provided. Thi…

chemistry.chemical_elementring-closing metathesis010402 general chemistryenantioselective transfer hydrogenation[ CHIM ] Chemical Sciences01 natural sciencesCoordination complexcatalyzed asymmetric hydrogenationchemistry.chemical_compoundactive phosphine oxides[CHIM]Chemical Scienceschiral diphosphine ligandsOrganic chemistryMolecular materialstransition-metal catalysischemistry.chemical_classificationacyl-transfer catalysts010405 organic chemistryPhosphorusEnantioselective synthesisc migration rearrangementGeneral Chemistry0104 chemical scienceschemistrytert-butylphenylphosphine oxideStereoselectivityray crystal-structureChirality (chemistry)PhosphineChemical Society reviews
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Studies of structural composition distribution heterogeneity in ethylene/1-hexene copolymers using thermal fractionation technique (SSA): Effect of c…

2005

Investigations into the compositional heterogeneity of ethylene/1-hexene copolymers obtained with various zirconocene/MAO catalysts, either homogeneous or supported on inorganic carriers such as a complex of magnesium chloride with tetrahydrofuran or methyl alcohol, were conducted. The dependence between metallocene structure, as well as catalyst immobilization, and the compositional heterogeneity of the related products was investigated. It was found that the heterogeneity of copolymers is determined by the metallocene catalyst structure. The amount of peaks on the DSC thermograms of copolymers and their division increase with the increase of bulkiness of the ligand in the catalytic system…

compositional heterogeneitysupportcopolymersstructuremetallocene catalystThermochimica Acta
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Increased conformational rigidity of humic substances by oxidative biomimetic catalysis

2005

A synthetic water-soluble meso-tetra(2,6-dichloro-3-sulfonatophenyl)porphyrinate of iron(III) chloride, Fe(TDCPPS)Cl, was employed as a biomimetic catalyst in the oxidative coupling of terrestrial humic materials. High-performance size-exclusion chromatography (HPSEC), solid-state nuclear magnetic resonance (CPMAS-(13)C NMR), electron paramagnetic resonance (EPR), and diffuse reflectance infrared spectroscopy (DRIFT) were used to follow conformational and structural changes brought about in different humic materials by the oxidative coupling. Increase in apparent weight-average molecular weight (Mw(a)) occurred invariably for all humic substances with the oxidative polymerization catalyzed …

conformationMagnetic Resonance SpectroscopySpectrophotometry InfraredPolymers and PlasticsDiffuse reflectance infrared spectroscopy (DRIFT)Biomimetic materialsaromatic compoundgel permeation chromatographyMolecular ConformationPhotochemistryIron compoundslaw.inventionPolymerizationenvironmental managementcovalent bondlawSize exclusion chromatographyBiomimetic catalysisBiomimeticsMaterials ChemistryOrganic chemistryHumic acidElectron paramagnetic resonanceInfrared spectroscopyChromatography High Pressure Liquidchemistry.chemical_classificationSettore CHIM/03 - Chimica Generale e InorganicaCarbon IsotopesChromatographyindustryCatalystsChemistrytetra(2articleelectrophoretic mobilitybiomimetic materialNuclear magnetic resonance spectroscopyunclassified drugConformationsacetic acidpriority journalCovalent bondSpectrophotometrySynthesis (chemical)High Pressure Liquidtechnology6 dichloro 3 sulfonatophenyl)porphyrinic acid derivativeInfraredOxidation-Reductionmolecular stabilityHumic materialsoxidationSettore AGR/13 - Chimica AgrariaSupramolecular chemistryBioengineeringcomplex mixturesCatalysisCatalysisdiffuse reflectance spectroscopyhumic substanceBiomaterialsalkyl etherElectron spin resonance spectroscopycomplex formationParticle SizeNuclear magnetic resonance spectroscopyHumic Substancesfree radicalbiomimetic oxidative humicelectron spin resonanceHigh performance size exclusion chromatography (HPSEC)ferrous chloridemolecular weightsolid statecarbon nuclear magnetic resonancePolymerizationSolubilitychemical structureOxidative coupling of methaneCatalysts; Conformations; Electron spin resonance spectroscopy; Infrared spectroscopy; Iron compounds; Nuclear magnetic resonance spectroscopy; Oxidation; Polymerization; Size exclusion chromatography; Solubility; Synthesis (chemical); Biomimetic catalysis; Diffuse reflectance infrared spectroscopy (DRIFT); High performance size exclusion chromatography (HPSEC); Humic materials; Biomimetic materials; acetic acid; alkyl ether; aromatic compound; biomimetic material; ferrous chloride; free radical; tetra(26 dichloro 3 sulfonatophenyl)porphyrinic acid derivative; unclassified drug; article; carbon nuclear magnetic resonance; catalysis; catalyst; chemical structure; complex formation; conformation; covalent bond; diffuse reflectance spectroscopy; electron spin resonance; electrophoretic mobility; environmental management; gel permeation chromatography; humic substance; industry; molecular stability; molecular weight; oxidation; polymerization; priority journal; solid state; technology; Biomimetics; Carbon Isotopes; Catalysis; Chromatography High Pressure Liquid; Electron Spin Resonance Spectroscopy; Humic Substances; Magnetic Resonance Spectroscopy; Molecular Conformation; Oxidation-Reduction; Particle Size; Spectrophotometry Infraredcatalyst
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Struktura i właściwości kopolimerów etylenu z norbornenem otrzymanych wobec katalizatora wanadocenowego

2018

Kopolimery etylenu z norbornenem ze względu na swoje wyjątkowe właściwości pozwalają na ich potencjalnie szerokie zastosowanie. Jednak w zależności od warunków prowadzenia syntezy, a przede wszystkim od zastosowanego katalizatora, właściwości takiego kopolimeru mogą się zmieniać w szerokim zakresie. W prezentowanej pracy zbadano właściwości wybranych kopolimerów etylenu (E) z norbornenem (NB) otrzymanych przy wykorzystaniu homogenicznego katalizatora wanadocenowego Cp2VCl2 aktywowanego tradycyjnym związkiem glinoorganicznym AlEt2Cl. Określono zależność pomiędzy stopniem wbudowania komonomeru w łańcuch kopolimeru a mikrostrukturą, masą molową, rozkładem mas molowych, temperaturą zeszklenia i…

copolymerkopolimerkatalizator wanadowyethylenevanadium catalystetylennorbornenenorbornen
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