Search results for "ATAL"

showing 10 items of 10591 documents

Highly Active Co3O4-Based Catalysts for Total Oxidation of Light C1–C3 Alkanes Prepared by a Simple Soft Chemistry Method: Effect of the Heat-T…

2021

9 figures, 2 tables.

inorganic chemicalsTechnologyInorganic chemistryTotal oxidationcobalt oxidechemistry.chemical_elementalkane oxidationpropaneHeterogeneous catalysissurface oxygen vacanciesMethaneArticleCatalysischemistry.chemical_compoundPropaneAlkane oxidationSurface oxygen vacanciesPropanetotal oxidationvolatile organic compoundsGeneral Materials ScienceReactivity (chemistry)Volatile organic compoundsCobalt oxideAlkanechemistry.chemical_classificationHeterogeneous catalysisEthaneMicroscopyQC120-168.85methaneTQH201-278.5ethaneEngineering (General). Civil engineering (General)TK1-9971heterogeneous catalysischemistryDescriptive and experimental mechanicsMixed oxideElectrical engineering. Electronics. Nuclear engineeringTA1-2040cobalt oxide; total oxidation; alkane oxidation; heterogeneous catalysis; volatile organic compounds; propane; ethane; methane; surface oxygen vacanciesCobaltMethaneMaterials; Volume 14; Issue 23; Pages: 7120
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Predicting the activity of single isolated Lewis acid sites in solid catalysts.

2006

An experimental study of the activity of Ti-, Zr- and Sn-beta catalysts in different types of oxidation reactions is combined with a quantum-chemical analysis of the electronic properties of the active sites and the adsorbed reactants. The differences observed in the catalytic behaviour of the three materials are explained in terms of the molecular orbital distribution of each system. The intrinsic Lewis acid strength of the isolated active site, the degree of back-donation from the catalyst to the empty orbitals of the organic reactant and the net atomic charges on selected atoms are proposed as predictors of reactivity.

inorganic chemicalsbiologyChemistryOrganic ChemistryInorganic chemistryActive siteGeneral ChemistryRedoxCatalysisCatalysisAdsorptionAtomic orbitalbiology.proteinMolecular orbitalReactivity (chemistry)Lewis acids and basesChemistry (Weinheim an der Bergstrasse, Germany)
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Impact of α,β-dehydroamino acid residues on the binding abilities of di-, tri- and tetra-peptides

2000

Insertion of a dehydroamino acid residue into a sequence of di-, tri- or tetra-peptide changed considerably the binding abilities of peptide ligands towards copper(II) ions. Potentiometric and spectroscopic (EPR, UV-VIS and CD) data have shown that the amide nitrogen of the dehydroamino acid residue is more effective in co-ordination than its parent analogue. In the case of the bulky ΔPhe residue also the (Z–E) isomerisation has a critical impact on the co-ordination equilibria in the system studied.

inorganic chemicalsbiologyStereochemistryPotentiometric titrationchemistry.chemical_elementGeneral Chemistrybiology.organism_classificationCopperCatalysislaw.inventionchemistry.chemical_compoundResidue (chemistry)chemistrylawAmideMaterials ChemistryTetraElectron paramagnetic resonanceIsomerizationPeptide ligandNew Journal of Chemistry
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ChemInform Abstract: Gold(I)-Catalyzed Intermolecular Oxyarylation of Alkynes: Unexpected Regiochemistry in the Alkylation of Arenes.

2010

The reaction between acetylenes and sulfoxides, studied as a test case for gold-catalyzed intermolecular addition, provides the oxyarylation compounds 3 in good yields. Unpredictably, in all cases a single regioisomer arising from the electrophilic aromatic alkylation at the position adjacent to the sulfur atom is obtained instead of the expected Friedel−Crafts regioisomer. A new concerted mechanism based on DFT calculations is proposed to account for the products in this intermolecular gold(I)-catalyzed reaction.

inorganic chemicalschemistryConcerted reactionIntermolecular forceElectrophileStructural isomerchemistry.chemical_elementRegioselectivityGeneral MedicineAlkylationSulfurMedicinal chemistryCatalysisChemInform
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Efficient ethylene polymerisation catalysis by a cationic benzyl hafnium complex containing pyrrolide-imine ligandsElectronic supplementary informati…

2002

A dibenzyl hafnium(IV) complex containing pyrrolide-imine chelate ligands was synthesized and investigated as an ethylene polymerisation catalyst.

inorganic chemicalschemistryEthylene polymerizationPolymer chemistryCationic polymerizationchemistry.chemical_elementOrganic chemistryChelationGeneral ChemistryImine ligandsHafniumCatalysisJournal of the Chemical Society, Dalton Transactions
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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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CO2 Fixation by Copper(II) Complexes of a Terpyridinophane Aza Receptor

2004

CO2 is fixed by a Cu2+ complex of a macrocyclic terpyridinophane ligand forming a carbamate group. Several features of the structure mimic the enzyme rubisco.

inorganic chemicalschemistry.chemical_classificationCarbamateReaction mechanismbiologyChemistryStereochemistrymedicine.medical_treatmentfungiCarbon fixationRuBisCOfood and beverageschemistry.chemical_elementmacromolecular substancesGeneral ChemistryLigand (biochemistry)BiochemistryCopperCatalysisColloid and Surface ChemistryEnzymemedicinebiology.proteinReceptorJournal of the American Chemical Society
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Promoting the activity and selectivity of high surface area Ni–Ce–O mixed oxides by gold deposition for VOC catalytic combustion

2011

Gold supported on nickel cerium oxide catalysts (Ni–Ce–O) have been studied for the total oxidation of propane, as a model for hydrocarbon volatile organic compound emission control. High surface area Ni–Ce–O catalysts were synthesized using a very simple evaporation method, where cerium and nickel salts were evaporated in the presence of a mixture of methanol and oxalic acid. Gold catalysts were prepared following a deposition–precipitation method. A very efficient catalyst for the oxidation of propane, in terms of both activity and selectivity, was obtained. This high activity has been related to the high surface area of the catalyst (and therefore to the presence of more active sites ava…

inorganic chemicalschemistry.chemical_classificationCerium oxideorganic chemicalsGeneral Chemical EngineeringInorganic chemistryOxalic acidchemistry.chemical_elementCatalytic combustionGeneral ChemistryIndustrial and Manufacturing EngineeringCatalysisCeriumchemistry.chemical_compoundNickelHydrocarbonCatalytic oxidationchemistryEnvironmental Chemistryheterocyclic compoundsChemical Engineering Journal
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Magnetic Core–Shell Nanoparticles as Carriers for Olefin Dimerization Catalysts

2013

We report the covalent support of functionalized nickel complexes on magnetic core–shell hybrid particles γ-Fe2O3/SiO2. Two completely different ways of connecting the particle with these nickel complexes were carried out. The first approach used the hydrosilylation method between the alkene-substituted nickel complex and a silane. In a second approach, the particles were connected with the complexes by means of click chemistry (copper-catalyzed Huisgen 1,3-dipolar cycloaddition). For this purpose, the nickel complexes were substituted with an alkyne moiety. Transmission and scanning electron microscopies, energy-dispersive X-ray diffraction, and FTIR spectroscopy were the methods employed …

inorganic chemicalschemistry.chemical_classificationHydrosilylationNanoparticleAlkynechemistry.chemical_elementPhotochemistryCycloadditionCatalysisInorganic Chemistrychemistry.chemical_compoundNickelchemistryotorhinolaryngologic diseasesClick chemistryMoietyEuropean Journal of Inorganic Chemistry
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Pressure- and temperature-induced valence tautomeric interconversion in a o-dioxolene adduct of a cobalt-tetraazamacrocycle complex

2001

An electronic switch at the molecular level has been realized by using a class of ionic compounds of the formula [Co(L)(diox)]Y (L = tetraazamacrocyclic ligand, Y = mononegative anion). Such compounds undergo temperature- and pressure-induced intramolecular one-electron transfer equilibria. The transition temperature of interconversion varies with the nature of the counterions Y (Y = PF6, BPh4, I). Surprisingly the effect of the anion on the transition temperature is not only governed by its volume but also by its coulombic interaction.

inorganic chemicalschemistry.chemical_classificationQuantitative Biology::BiomoleculesValence (chemistry)Transition temperatureOrganic ChemistryIonic bondingGeneral ChemistryPhotochemistryTautomerCatalysisAdductElectron transferCrystallographychemistryIntramolecular forceCondensed Matter::Strongly Correlated ElectronsPhysics::Chemical PhysicsCounterion
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