Search results for "Catalysis"

showing 10 items of 5944 documents

Hydrogenation of light hydrocarbons on palladium: theoretical study of the local surface arrangements

2001

Abstract Quantum mechanical calculations at HF, MP2 and DFT levels were used to rationalise the surface effects of the hydrocarbon lateral interactions occurring on single planar metal surfaces or on different adjacent surfaces during the hydrogenation on palladium catalyst. The different values of electronic charge, found in the different atoms of palladium clusters, were suggested as a possible explanation of the non-homogeneous behaviour already inferred for catalyst surface sites having non-isotropic local arrangement.

chemistry.chemical_classificationSurface (mathematics)Chemistrychemistry.chemical_elementCondensed Matter PhysicsElementary chargeBiochemistryCatalysisMetalPlanarHydrocarbonChemical physicsvisual_artvisual_art.visual_art_mediumOrganic chemistryPhysics::Chemical PhysicsPhysical and Theoretical ChemistryQuantumPalladiumJournal of Molecular Structure: THEOCHEM
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Kinetically Controlled Sequential Growth of Surface-Grafted Chiral Supramolecular Copolymers.

2016

We report a facile strategy to grow supramolecular copolymers on Au surfaces by successively exposing a surface-anchored monomer to solutions of oppositely charged peptide comonomers. Charge regulation on the active chain end of the polymer sufficiently slows down the kinetics of the self-assembly process to produce kinetically trapped copolymers at near-neutral pH. We thereby achieve architectural control at three levels: The β-sheet sequences direct the polymerization away from the surface, the height of the supramolecular copolymer brushes is well-controlled by the stepwise nature of the alternating copolymer growth, and 2D spatial resolution is realized by using micropatterned initiatin…

chemistry.chemical_classificationSurface (mathematics)Materials science010405 organic chemistryKineticsSupramolecular chemistryNanotechnologyGeneral ChemistryPolymer010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundMonomerchemistryPolymerizationCopolymerSelf-assemblyAngewandte Chemie (International ed. in English)
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Surface-Functionalized Latex Particles as Controlling Agents for the Mineralization of Zinc Oxide in Aqueous Medium

2005

Polystyrene latex particles modified at the surface with different hydrophilic functional groups were prepared by miniemulsion polymerization and used as controlling agents in the crystallization of zinc oxide from aqueous medium. The effects of the chemical nature of the surface functionalization and the latex concentration on the crystal growth, morphology, and crystalline structure of the resulting zinc oxide were analyzed. Micro- and submicrosized crystals with a broad variety of morphologies depending on the functionalization were obtained. Among the different latexes studied, the acrylic-acid-derived particles were shown to be a convenient system for further quantitative investigation…

chemistry.chemical_classificationSurface PropertiesChemistryOrganic ChemistryWaterGeneral ChemistryPolymerMicrospheresCatalysislaw.inventionMiniemulsionAdsorptionX-Ray DiffractionChemical engineeringPolymerizationlawPolymer chemistryWettabilityPolystyrenesSurface modificationWettingParticle sizeParticle SizeZinc OxideCrystallizationChemistry - A European Journal
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ChemInform Abstract: Microwave-Assisted Tandem Organocatalytic Peptide-Coupling Intramolecular aza-Michael Reaction: α,β-Unsaturated N-Acyl Pyrazoles…

2015

Conjugated N-acyl pyrazoles are successfully employed in the organocatalytic enantioselective intramolecular aza-Michael reaction as ester surrogates.

chemistry.chemical_classificationTandemeducationEnantioselective synthesisPeptideGeneral MedicineConjugated systembehavioral disciplines and activitiesCombinatorial chemistryhumanitiesCoupling (electronics)chemistryOrganocatalysisIntramolecular forceMichael reactionlipids (amino acids peptides and proteins)ChemInform
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ChemInform Abstract: Stereoselective Synthesis of 8,12-Furanoeudesmanes from Santonin. Absolute Stereochemistry of Natural Furanoeudesma-1,3-diene an…

2010

Ketobutenolide 3, easily obtained from santonin (1), has been transformed into two natural furanoeudesmanes 4 and 5, isolated from Commiphora molmol and Tubipora musica, respectively. trans- And cis-decalin systems were obtained by stereoselective reduction of the C4−C5 double bond in 3 in the following way:  hydrogenation of 3 over Pd/C followed by acidic treatment gave the cis isomer 10 as the major product; selective hydrogenation of the C1-C2 double bond with the Wilkinson’s catalyst followed by reduction with NaTeH yielded mainly the trans isomer 9. Compounds 9 and 10 were transformed into 4 and 5 in parallel sequences. Optical rotation and CD measurements of the synthetic products rev…

chemistry.chemical_classificationTerpenechemistry.chemical_compoundDouble bondDieneChemistryStereochemistryStereoselectivityGeneral MedicineEnantiomerCis–trans isomerismSantoninCatalysisChemInform
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A New Structural Motif for an Enantiomerically Pure Metallosupramolecular Pd4L8Aggregate by Anion Templating

2014

An enantiomerically pure BINOL-based bis(3-pyridyl) ligand 1 assembles into a homochiral [Pd4(1)8] complex upon coordination to tetravalent PdII ions. The formation of this aggregate is templated by two tetrafluoroborate counterions that are encapsulated in two peripheral cavities. The resulting structure is a new structural motif for this kind of metallosupramolecular assemblies that arranges the palladium ions in a distorted tetrahedral fashion and forces ligand 1 to adopt two different conformations. Both phenomena are unique and cause an overall three-dimensional structure that has another confined, chiral, and hydrophilic central cavity.

chemistry.chemical_classificationTetrafluoroborateLigandStereochemistryAggregate (data warehouse)chemistry.chemical_elementGeneral ChemistryCatalysisIonCrystallographychemistry.chemical_compoundchemistrySelf-assemblyCounterionStructural motifta116PalladiumAngewandte Chemie International Edition
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Enantioselective self-assembly of antiferromagnetic hexacopper(ii) wheels with chiral amino acid oxamates

2013

The Cu(2+)-mediated self-assembly of oxamato-based ligands derived from either the (S)- or (R)-enantiomers of the amino acid valine leads to the formation of two antiferromagnetically coupled homochiral anionic hexacopper(II) wheels in the presence of templating tetramethylammonium countercations.

chemistry.chemical_classificationTetramethylammoniumStereochemistryMagnetic PhenomenaMetals and AlloysEnantioselective synthesisStereoisomerismValineGeneral ChemistryLigandsCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAmino acidchemistry.chemical_compoundchemistryCoordination ComplexesValineMaterials ChemistryCeramics and CompositesAntiferromagnetismSelf-assemblyCopperChemical Communications
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Eco-friendly functionalization of natural halloysite clay nanotube with ionic liquids by microwave irradiation for Suzuki coupling reaction

2014

Abstract Microwave assisted halloysite (HNT) external surface functionalization with ionic liquids is described. HNTs modification was achieved in two steps: a) grafting of 3-mercaptopropyl trimethoxysilane on the external surface of HNT by a microwave irradiation; b) anchorage of vinylimidazolium ionic liquids by a thiol-ene reaction. MW irradiation allowed us to obtain high loading onto the HNT surface compared to those obtained through conventional synthesis. Fourier transform infrared spectroscopy and thermogravimetric analysis confirmed that the grafting has occurred only on the external surface of HNT. Turbidimetric and dynamic light scattering analyses showed that the introduction of…

chemistry.chemical_classificationThermogravimetric analysisAryl halideOrganic Chemistrychemistry.chemical_elementSettore CHIM/06 - Chimica Organicaengineering.materialBiochemistryHalloysiteInorganic Chemistrychemistry.chemical_compoundSuzuki reactionchemistryChemical engineeringIonic liquidMaterials ChemistryengineeringSurface modificationSynthesis solvent-free Halloysite Catalysis ILPhysical and Theoretical ChemistryFourier transform infrared spectroscopyPalladiumSettore CHIM/02 - Chimica Fisica
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Photocatalytic Selective Oxidation of 4-Methoxybenzyl Alcohol to Aldehyde in Aqueous Suspension of Home-Prepared Titanium Dioxide Catalyst

2007

WOS: 000246040000026

chemistry.chemical_classificationTitanium DioxideAqueous solutionInorganic chemistryAlcoholGeneral ChemistrySelective OxidationAldehydeCatalysischemistry.chemical_compoundchemistryAlcohol oxidationTitanium dioxideTitanium tetrachloridePhotocatalysisPhotocatalysisP-Anisaldehyde ProductionAdvanced Synthesis & Catalysis
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Heterogeneous oxidation of pyrimidine and alkyl thioethers in ionic liquids over mesoporous Ti or Ti/Ge catalysts.

2004

Heterogeneous catalytic oxidation of a series of thioethers (2-thiomethylpyrimidine, 2-thiomethyl-4,6-dimethyl-pyrimidine, 2-thiobenzylpyrimidine, 2-thiobenzyl-4,6-dimethylpyrimidine, thioanisole, and n-heptyl methyl sulfide) was performed in ionic liquids by using MCM-41 and UVM-type mesoporous catalysts containing Ti, or Ti and Ge. A range of triflate, tetrafluoroborate, trifluoroacetate, lactate and bis(trifluoromethanesulfonyl)-imide-based ionic liquids were used. The oxidations were carried out by using anhydrous hydrogen peroxide or the urea-hydrogen peroxide adduct and showed that ionic liquids are very effective solvents, achieving greater reactivity and selectivity than reactions p…

chemistry.chemical_classificationTitaniumMolecular StructureChemistryGermaniumOrganic ChemistryThioanisoleInorganic chemistryGeneral ChemistrySulfidesHeterogeneous catalysisSilicon DioxidePeroxideCatalysisCatalysischemistry.chemical_compoundPyrimidinesCatalytic oxidationIonic liquidSolventsParticle SizeTrifluoromethanesulfonateOxidation-ReductionPorosityAlkylChemistry (Weinheim an der Bergstrasse, Germany)
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