Search results for "Catalysis"

showing 10 items of 5944 documents

Ethylene polymerization catalysts based on nickel(II) 1,4-diazadiene complexes: the influence of the 1,4-diazadiene backbone substituents on structur…

1998

Abstract Thermally sensitive dialkyl nickel complexes {DAD(H,H)}Ni(CH2SiMe3)2 and {DAD(Me,Me)}Ni(CH2SiMe3)2 [DAD(X,X)=2,6-iPr2C6H4–NC(X)–C(X)N–C6H4iPr2-2,6] were synthesized and were characterized by X-ray diffraction studies on single crystals. The substituents X on the backbone of the α-diimine ligand significantly influence the conformation of the 2,6-diisopropylphenyl substituents. This effect is thought to be of crucial importance for the polymerization of ethylene when {DAD(X,X)}NiBr2/MAO is used as catalyst. The influence of the catalyst structure, pressure, and temperature on the polymerization activity, molar mass, glass transition temperature, melting temperature and branching o…

EthyleneTrimethylsilylOrganic Chemistrychemistry.chemical_elementPhotochemistryBranching (polymer chemistry)BiochemistryMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundNickelchemistryPolymerizationX-ray crystallographyMaterials ChemistryPhysical and Theoretical ChemistryCarbonylationJournal of Organometallic Chemistry
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Isolated Fe(III)-O Sites Catalyze the Hydrogenation of Acetylene in Ethylene Flows under Front-End Industrial Conditions

2018

[EN] The search for simple, earth-abundant, cheap, and nontoxic metal catalysts able to perform industrial hydrogenations is a topic of interest, transversal to many catalytic processes. Here, we show that isolated FeIII¿O sites on solids are able to dissociate and chemoselectively transfer H2 to acetylene in an industrial process. For that, a novel, robust, and highly crystalline metal¿organic framework (MOF), embedding FeIII¿OH2 single sites within its pores, was prepared in multigram scale and used as an efficient catalyst for the hydrogenation of 1% acetylene in ethylene streams under front-end conditions. Cutting-edge X-ray crystallography allowed the resolution of the crystal structur…

EthylenebiologyChemistryActive site02 engineering and technologyGeneral ChemistryCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundColloid and Surface ChemistryQUIMICA ORGANICAAcetyleneChemical engineeringbiology.proteinCubic zirconiaMetal catalyst0210 nano-technologyEfficient catalyst
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Dichlorovanadium(IV) diamine-bis(phenolate) complexes for ethylene (co)polymerization and 1-olefin isospecific polymerization

2018

Abstract Two vanadium complexes bearing amine-bis(phenolate) ligands with the amino side-arm donor, [V{Me2NCH2CH2N(CH2-2-O-3,5-tBu2-C6H2)2}Cl2] (1) and [V{Me2NCH2CH2N(CH2-2-O-3,5-tBu2-C6H2)(CH2-2-O-C6H4)}Cl2] (2), were synthesised and characterized by FTIR and 1H NMR spectroscopy. Upon activation with Al(iBu)3/Ph3CB(C6F5)4, these complexes became active catalysts for 1-octene polymerization giving highly stereoregular polymers (mmmm ∼ 90%) having regioirregularly arranged units. The catalytic activity of the catalysts in ethylene homo- and copolymerization, and their ability to incorporate a comonomer were highly dependent on both the activator type and the complex structure. 1/EtAlCl2 exhi…

EthylenemicrostructureDispersityZiegler-Natta polymerization010402 general chemistry01 natural sciencesCatalysisTREFchemistry.chemical_compoundDiaminediamine-bis(phenolate) ligandPolymer chemistryethyleneCopolymerPhysical and Theoretical Chemistrychemistry.chemical_classificationOlefin fiber010405 organic chemistryChemistryComonomerPolymer0104 chemical sciencescopolymerizationVanadium catalystPolymerization1-octeneJournal of Catalysis
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The Influence of Microbiome Dysbiosis and Bacterial Biofilms on Epidermal Barrier Function in Atopic Dermatitis—An Update

2021

Atopic dermatitis (AD) is a common inflammatory dermatosis affecting up to 30% of children and 10% of adults worldwide. AD is primarily driven by an epidermal barrier defect which triggers immune dysregulation within the skin. According to recent research such phenomena are closely related to the microbial dysbiosis of the skin. There is growing evidence that cutaneous microbiota and bacterial biofilms negatively affect skin barrier function, contributing to the onset and exacerbation of AD. This review summarizes the latest data on the mechanisms leading to microbiome dysbiosis and biofilm formation in AD, and the influence of these phenomena on skin barrier function.

ExacerbationQH301-705.5microbiomeReviewmedicine.disease_causeCatalysisDermatitis AtopicInorganic ChemistryAnimalsHumansMedicineskin barrierMicrobiomeBiology (General)Physical and Theoretical ChemistryQD1-999Molecular BiologySpectroscopySkinstaphylococciEpidermal barrierBacteriaatopic dermatitisintegumentary systembusiness.industryMicrobiotaOrganic ChemistryBiofilmGeneral MedicineAtopic dermatitisImmune dysregulationmedicine.diseaseComputer Science ApplicationsChemistryImmunologyDysbiosisEpidermisbiofilmsbusinessDysbiosisFunction (biology)International Journal of Molecular Sciences
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First principles investigations of Pd-on-Au nanostructures for trichloroethene catalytic removal from groundwater

2010

Catalytic groundwater remediation from chlorinated organic solvents like trichloroethene (TCE) has been found to be more effective and sustainable than traditional non-destructive methods. Among the experimentally studied catalyst materials, Pd-decorated Au nanoparticles show the highest activity and selectivity combined with the best resistance towards poisoning by chemicals present in groundwater. In this study the thermochemistry and adsorption geometries of TCE and its hydrodechlorination products are investigated via density functional theory calculations. Various model systems for Pd-supported Au nanoparticles are addressed. The adsorption of TCE is endothermic on bare Au(111), almost…

Exothermic reactionModels MolecularHalogenationSurface PropertiesInorganic chemistryGroundwater remediationMolecular ConformationGeneral Physics and AstronomyMetal NanoparticlesEndothermic processCatalysisOverlayerCatalysisWater PurificationAdsorptionThermochemistryPhysical and Theoretical Chemistryta116ChemistryWaterTrichloroethyleneKineticsChemisorptionQuantum TheoryThermodynamicsAdsorptionGoldPalladiumPhysical Chemistry Chemical Physics
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Mechanisms of covalent dimerization on a bulk insulating surface

2017

Combining density functional theory and high resolution NC-AFM experiments, we have studied the on surface reaction mechanisms' responsible for the covalent dimerization of 4-iodobenzoic acid (IBA) organic molecules on the calcite (10.4), insulating surface. When annealed at 580 K, the Molecules assemble in one-dimensional chains of covalently bound dimers: The chains have a unique orientation and result from a complex set of processes, including a nominally rather. costly double dehalogenation reaction followed by dimerization. First, focusing on the latter two processes and using the nudged elastic band method, we analyze a number of possible mechanisms involving one and two molecules, an…

Exothermic reactionReaction mechanismStereochemistryChemistryHalogenation02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology53001 natural sciences0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysisGeneral EnergyF170 Physical ChemistryCovalent bondChemical physicsIntermediate stateMoleculeDensity functional theoryF200 Materials ScienceF343 Computational PhysicsPhysical and Theoretical Chemistry0210 nano-technology
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Extrapolation of water and formaldehyde harmonic and anharmonic frequencies to the B3LYP/CBS limit using polarization consistent basis sets

2010

The harmonic and anharmonic frequencies of fundamental vibrations in formaldehyde and water were successfully estimated using the B3LYP Kohn-Sham limit. The results obtained with polarization- and correlation-consistent basis sets were fitted with a two-parameter formula. Anharmonic corrections were obtained by a second order perturbation treatment (PT2). We compared the performance of the PT2 scheme on the two title molecules using SCF, MP2 and DFT (BLYP, B3LYP, PBE and B3PW91 functionals) methods combined with polarization consistent pc-n (n = 0, 1, 2, 3, 4) basis sets, Dunning’s basis sets (aug)-cc-pVXZ where X = D, T, Q, 5, 6 and Pople’s basis sets up to 6-311++G(3df,2pd). The influence…

ExtrapolationPerturbation (astronomy)Sensitivity and SpecificityVibrationMolecular physicsCatalysisInorganic ChemistryRoot mean squareFormaldehydeQuantum mechanicsWavenumberIR and Raman theoretical spectraPhysics::Chemical PhysicsPhysical and Theoretical ChemistryBasis setOriginal PaperChemistrySpectrum AnalysisOrganic ChemistryAnharmonicityHarmonicReproducibility of ResultsWaterComplete basis set limitModels TheoreticalPolarization (waves)Computer Science ApplicationsVibrationComputational Theory and MathematicsAnharmonicJournal of Molecular Modeling
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Self-Assembly of Supramolecular Polymers of N-Centered Triarylamine Trisamides in the Light of Circular Dichroism: Reaching Consensus between Electro…

2020

The self-assembly of chiral supramolecular polymers is an intricate process that spans a wide range of length scales. Circular dichroism techniques are ideal to study this process as they provide information on the molecular scale but are at the same time also sensitive probes of the long-range interactions that control the growth and morphology of these polymers. As yet, Electronic Circular Dichroism that uses electronic transitions as a probe has by far been the method of choice while Vibrational Circular Dichroism, which uses vibrational transitions to probe structure, is much less employed. Here, we report experimental and theoretical studies of the self-assembly of helical supramolecul…

FELIX Condensed Matter Physicschemistry.chemical_classificationCircular dichroismQuantitative Biology::BiomoleculesExtrapolationGeneral ChemistryPolymerElectron010402 general chemistry01 natural sciencesBiochemistryArticleCatalysis0104 chemical sciencesSupramolecular polymersColloid and Surface ChemistrychemistryChemical physicsAtomic electron transitionVibrational circular dichroismSelf-assembly
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Counter anion binding in the phenoxyimine, salan and metallocene olefin polymerization catalysts activated with perfluorophenylborate

2012

Abstract Ion pair separation is a process that may influence the activity of homogeneous catalysts of olefin polymerization. We have studied the energy of separation for selected titanium and zirconium metallocene and post-metallocene catalytic ion pairs by means of DFT, dispersion-corrected DFT and Paired Interacting Orbitals method (PIO). Unusually weak cation–anion interactions in the bis(phenoxyimine) systems were attributed to strong electron-donating properties of the phenoxyimine ligands. Energy decomposition analysis (EDA) revealed that almost 70% of the counter ion binding energy results from electrostatic interactions. The PIO method made it possible to analyze the nature of the c…

FI catalystBinding energyPopulationchemistry.chemical_elementPhotochemistryDFTBiochemistryCatalysisInorganic Chemistrychemistry.chemical_compoundPolymer chemistryMaterials ChemistryPhysical and Theoretical ChemistryAnion bindingeducationchemistry.chemical_classificationZirconiumeducation.field_of_studyOrganic Chemistryphenoxyiminechemistrypaired interacting orbitals (PIO)Counterionolefin polymerizationMetalloceneTitaniumJournal of Organometallic Chemistry
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Surface processes in selective photocatalytic oxidation of hydroxybenzyl alcohols by TiO2 P25

2023

Aryl aldehydes and acids are important industrial intermediates, but their synthesis from the corresponding alcohols often requires the use of high temperatures and harmful solvents and oxidant agents. Heterogeneous photocatalysis represents an interesting option for the partial oxidation of alcohols to aldehydes at room temperature using water as solvent. In this work, the partial photocatalytic oxidation of 2-hydroxybenzyl alcohol (salicyl alcohol) and 4-hydroxybenzyl alcohol to the corresponding aldehydes and acids has been compared, under environmental-friendly conditions, employing TiO2 P25 as photocatalyst in water. The selectivity to the corresponding aldehydes and acids, under the s…

FT-IR spectroscopy; Salicyl alcohol; Salicylaldehyde; Salicylic acid; Environment-friendly oxidation; AdsorptionFT-IR spectroscopyEnvironment-friendly oxidationSettore CHIM/07 - Fondamenti Chimici Delle TecnologieGeneral ChemistrySalicylic acidAdsorptionSalicyl alcoholCatalysisSalicylaldehyde
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