Search results for " Catalyst"

showing 10 items of 292 documents

Modification of Nanocrystalline WO3 with a Dicationic Perylene Bisimide: Applications to Molecular Level Solar Water Splitting

2015

[(N,N?-Bis(2-(trimethylammonium)ethylene) perylene 3,4,9,10-tetracarboxylic acid bisimide)(PF6)2] (1) was observed to spontaneously adsorb on nanocrystalline WO3 surfaces via aggregation/hydrophobic forces. Under visible irradiation (? > 435 nm), the excited state of 1 underwent oxidative quenching by electron injection (kinj > 108 s-1) to WO3, leaving a strongly positive hole (Eox ? 1.7 V vs SCE), which allows to drive demanding photo-oxidation reactions in photoelectrochemical cells (PECs). The casting of IrO2 nanoparticles (NPs), acting as water oxidation catalysts (WOCs) on the sensitized electrodes, led to a 4-fold enhancement in photoanodic current, consistent with hole transfer from …

Models MolecularMolecular ConformationNanoparticleImidesPhotochemistryBiochemistryTungstenCatalysisNOCatalysiElectron Transportchemistry.chemical_compoundColloid and Surface ChemistryTheoryofComputation_ANALYSISOFALGORITHMSANDPROBLEMCOMPLEXITYWO3ComputingMethodologies_SYMBOLICANDALGEBRAICMANIPULATIONperylenePhotoelectrochemical cellIrO2Quenching (fluorescence)Chemistry (all)charge transferWaterOxidesGeneral ChemistryPhotoelectrochemical cellPhotochemical ProcessesSolar fuelChemistry (all); Catalysis; Biochemistry; Colloid and Surface ChemistryNanocrystalline materialperylene WO3 charge transfer IrO2MicrosecondchemistryWater SplittingSunlightVISIBLE-LIGHT; ARTIFICIAL PHOTOSYNTHESIS; PHOTOELECTROCHEMICAL CELL; OXIDATION CATALYSTS; ELECTRON-TRANSFER; FABRICATIONNanoparticlesPerylene bisimideWater splittingPeryleneMathematicsofComputing_DISCRETEMATHEMATICS
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Enantioselective Mannich reaction of β-keto esters with aromatic and aliphatic imines using a cooperatively assisted bifunctional catalyst

2014

An efficient urea-enhanced thiourea catalyst enables the enantioselective Mannich reaction between β-keto esters and N-Boc-protected imines under mild conditions and minimal catalyst loading (1–3 mol %). Aliphatic and aromatic substituents are tolerated on both reaction partners, affording the products in good enantiomeric purity. The corresponding β-amino ketones can readily be accessed via decarboxylation without loss of enantiomeric purity.

Molecular StructureChemistryDecarboxylationOrganic ChemistryEnantioselective synthesisThioureaEstersStereoisomerismKetonesBiochemistryDecarboxylationCatalysisCatalysisBifunctional catalystchemistry.chemical_compoundThioureaOrganic chemistryUreaIminesPhysical and Theoretical ChemistryEnantiomerMannich reactionta116Organic Letters
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The role of water in the photocatalytic degradation of acetonitrile and toluene in gas-solid and liquid-solid regimes

2006

Photocatalytic degradation of acetonitrile and toluene was carried out both in gas-solid and in liquid-solid regimes by using commercialTiO2samples (Merck and Degussa P25). The investigation was mainly aimed to study the influence of water present in the reaction environment on the mechanism and degradation rate of two probe molecules. In gas-solid regime, the reacting mixture consisted of toluene or acetonitrile, oxygen, nitrogen, and water vapour. The main degradation product of toluene wasCO2with small amounts of benzaldehyde. In the presence of water vapour, the activity ofTiO2Merck remained stable but greatly decreased if water was absent.TiO2Degussa P25 continuously deactivated, even …

Muconic acidADSORPTIONBENZENEInorganic chemistrylcsh:TJ807-830lcsh:Renewable energy sourcesHUMIDIFIED AIRANATASE TIO2 CATALYSTOXIDATIONCH3CNBenzaldehydechemistry.chemical_compoundGeneral Materials ScienceFORMALDEHYDEBenzenePhotodegradationAcetonitrileBenzoic acidTITANIUM-DIOXIDERenewable Energy Sustainability and the EnvironmentGeneral ChemistryVAPOR-PHASETolueneAtomic and Molecular Physics and OpticsANATASE TIO2 CATALYST; TITANIUM-DIOXIDE; HUMIDIFIED AIR; VAPOR-PHASE; OXIDATION; ADSORPTION; BENZENE; CH3CN; FORMALDEHYDE; BEHAVIORchemistryBenzyl alcoholBEHAVIORInternational Journal of Photoenergy
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Silver-Catalyzed C-C Bond Formation between Methane and Ethyl Diazoacetate in Supercritical CO2

2011

Even in the context of hydrocarbons’ general resistance to selective functionalization, methane’s volatility and strong bonds pose a particular challenge. We report here that silver complexes bearing perfluorinated indazolylborate ligands catalyze the reaction of methane (CH4) with ethyl diazoacetate (N2CHCO2Et) to yield ethyl propionate (CH3CH2CO2Et). The use of supercritical carbon dioxide (scCO2) as the solvent is key to the reaction’s success. Although the catalyst is only sparingly soluble in CH4/CO2 mixtures, optimized conditions presently result in a 19% yield of ethyl propionate (based on starting quantity of the diazoester) at 40°C over 14 hours.

MultidisciplinarySupercritical carbon dioxideHomogeneous catalysisMethaneSupercritical fluidCatalysisC-H functionalizationSolventDiazocompoundchemistry.chemical_compoundEthyl propionatechemistryEthyl diazoacetateOrganic chemistrySurface modificationMethane activationSilver catalyst
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Structural and Thermal Properties of Ethylene-Norbornene Copolymers Obtained Using Vanadium Homogeneous and SIL Catalysts

2020

The series of ethylene-norbornene (E-NB) copolymers was obtained using different vanadium homogeneous and supported ionic liquid (SIL) catalyst systems. The 13C and 1H NMR (carbon and proton nuclear magnetic resonance spectroscopy) together with differential scanning calorimetry (DSC) were applied to determine the composition of copolymers such as comonomer incorporation (CNB), monomer dispersity (MD), monomer reactivity ratio (re), sequence length of ethylene (le) and tetrad microblock distributions. The relation between the type of catalyst, reaction conditions and on the other hand, the copolymer microstructure, chain termination reaction analyzed by the type of unsaturation are discusse…

NMR investigationMaterials sciencePolymers and PlasticsComonomerDispersityVanadiumchemistry.chemical_elementnorborneneGeneral ChemistryPost-metallocene catalystArticlelcsh:QD241-441chemistry.chemical_compoundcopolymerizationMonomerDifferential scanning calorimetrychemistryChemical engineeringlcsh:Organic chemistryIonic liquidpost-metallocene catalystethyleneDSC and SSA investigationNorbornenePolymers
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From Single Molecules to Nanostructured Functional Materials: Formation of a Magnetic Foam Catalyzed by Pd@FexO Heterodimers

2017

Multicomponent nanostructures containing purely organic or inorganic as well as hybrid organic–inorganic components connected through a solid interface are, unlike conventional spherical particles, able to combine different or even incompatible properties within a single entity. They are multifunctional and resemble molecular amphiphiles, like surfactants or block copolymers, which makes them attractive for the self-assembly of complex structures, drug delivery, bioimaging, or catalysis. We have synthesized Pd@FexO heterodimer nanoparticles (NPs) to fabricate a macroporous, hydrophobic, magnetically active, three-dimensional (3D), and template-free hybrid foam capable of repeatedly separati…

NanostructureMaterials scienceHydrosilylationNucleationNanoparticleNanochemistry02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesNanomaterial-based catalyst0104 chemical scienceschemistry.chemical_compoundChemical engineeringchemistryAmphiphileGeneral Materials Science0210 nano-technologyHybrid materialACS Applied Nano Materials
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Carbon nanotube bags: catalytic formation, physical properties, two-dimensional alignment and geometric structuring of densely filled carbon tubes.

2001

The catalytic CVD synthesis, using propyne as carbon precursor and Fe(NO3)3 as catalyst precursor inside porous alumina, gives carbon nanotube (CNT) bags in a well-arranged two-dimensional order. The tubes have the morphology of bags or fibers, since they are completely filled with smaller helicoidal CNTs. This morphology has so far not been reported for CNTs. Owing to the dense filling of the outer mother CNTs with small helicoidal CNTs, the resulting CNT fibers appear to be stiff and show no sign of inflation, as sometimes observed with hollow CNTs. The fiber morphology was observed by raster electron microscopy (REM), transmission electron microscopy (TEM), and atomic force microscopy (A…

NanotubeNanostructureChemistryOrganic ChemistryChemiechemistry.chemical_elementNanotechnologyGeneral ChemistryCarbon nanotubeCatalysislaw.inventionsymbols.namesakeField electron emissionChemical engineeringTransmission electron microscopylawsymbolsCarbon nanotube supported catalystRaman spectroscopyCarbonChemistry (Weinheim an der Bergstrasse, Germany)
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Microstructure of ethylene-1-hexene and ethylene-1-octene copolymers obtained over Ziegler–Natta catalysts supported on MgCl 2 (THF) 2

2001

Abstract The ethylene copolymerizations with 1-hexene or 1-octene in the presence of hydrogen using three catalysts, MgCl 2 (THF) 2 /VOCl 3 /Et 2 AlCl, MgCl 2 (THF) 2 /VCl 4 /Et 2 AlCl, MgCl 2 (THF) 2 /TiCl 4 /Et 2 AlCl, were investigated. It was found that the addition of hydrogen into the copolymerization feed reduces the molecular weight of the copolymers produced and decreases the activity of all the studied catalysts. The microstructure of the copolymers obtained was determined on the basis of 13 C NMR investigations and the reactivity ratios of the comonomers were calculated. The lack of tendency of the olefin comonomers to the creation of the polymer block was confirmed. It was found…

Olefin fiberEthyleneCopolymerization of ethylene with α-olefinPolymers and PlasticsComonomerOrganic ChemistryPolyethyleneMicrostructure of copolymers1-Hexenechemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryZiegler–Natta catalystsReactivity (chemistry)Ziegler–Natta catalyst1-OctenePolymer
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Organocatalysts and metal-based catalysts: a journey toward the development of new catalytic materials

2015

Organocatalysis and metal-based catalysis represent two of the main pillars of catalytic reactions and have witnessed a huge interest in the last decade. Immobilization, recovery and reuse of these catalysts is of primary importance because of the large amount used especially in the case of organocatalysts. On the other hand, metal-based catalysts must be recovered even if used in low amount, in order to avoid contamination of the product. In this context, we started several years ago investigations on the use of supported ionic liquid phases for the asymmetric organocatalysis mediated by proline.1 This approach is an example of a “release and catch” catalytic system.2 Starting from this ex…

Organocatalysirecyclable catalystscatalysiSettore CHIM/06 - Chimica Organica
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Recyclable Organocatalysts in Asymmetric Reactions

2011

Organocatalysis Supported catalystChemistryOrganocatalysisOrganic chemistrySettore CHIM/06 - Chimica Organica
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