Search results for " Catalysis"

showing 10 items of 585 documents

Inside a Shell—Organometallic Catalysis Inside Encapsulin Nanoreactors

2021

Abstract Compartmentalization of chemical reactions inside cells are a fundamental requirement for life. Encapsulins are self‐assembling protein‐based nanocompartments from the prokaryotic repertoire that present a highly attractive platform for intracellular compartmentalization of chemical reactions by design. Using single‐molecule Förster resonance energy transfer and 3D‐MINFLUX analysis, we analyze fluorescently labeled encapsulins on a single‐molecule basis. Furthermore, by equipping these capsules with a synthetic ruthenium catalyst via covalent attachment to a non‐native host protein, we are able to perform in vitro catalysis and go on to show that engineered encapsulins can be used …

Mycobacterium smegmatisHomogeneous catalysisNanotechnologyNanoreactor010402 general chemistrysingle-molecule FRET01 natural sciences7. Clean energyCatalysisCatalysis03 medical and health sciencesBacterial ProteinsFluorescence Resonance Energy TransferOrganometallic CompoundsParticle SizeResearch Articles030304 developmental biology0303 health sciencesChemistryencapsulinsGeneral Medicineself-assemblyGeneral ChemistrySingle-molecule FRETCompartmentalization (psychology)Bioorthogonal Chemistryhomogeneous catalysisNanostructures0104 chemical sciencesFörster resonance energy transferMicroscopy FluorescenceCovalent bondSelf-assemblyMINFLUXResearch ArticleAngewandte Chemie International Edition
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Using synchrotrons and XFELs for time-resolved X-ray crystallography and solution scattering experiments on biomolecules

2015

International audience; Time-resolved structural information is key to understand the mechanism of biological processes, such as catalysis and signalling. Recent developments in X-ray sources as well as data collection and analysis methods are making routine time-resolved X-ray crystallography and solution scattering experiments a real possibility for structural biologists. Here we review the information that can be obtained from these techniques and discuss the considerations that must be taken into account when designing a time-resolved experiment.

NanotechnologyElectrons010402 general chemistryCrystallography X-Ray01 natural sciencesCatalysi03 medical and health sciencesStructural BiologyScattering radiationHumansScattering RadiationStructural DynamicMolecular BiologyAnalysis method030304 developmental biologychemistry.chemical_classificationPhysics[PHYS]Physics [physics]0303 health sciencesScatteringBiomoleculeLasersReaction TriggeringSettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)0104 chemical sciencesSolutionschemistryX-ray crystallographyAtomic physicsStructural Biology; Structural Dynamics; Catalysis; Reaction TriggeringSynchrotronsCurrent Opinion in Structural Biology
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A study on the stability of carbon nanoforms–polyimidazolium network hybrids in the conversion of co2 into cyclic carbonates

2021

Three different carbon nanoforms (CNFs), single-walled and multi-walled carbon nanotubes (SWCNTs, MWCNTs) and carbon nanohorns (CNHs), have been used as supports for the direct polymerization of variable amounts of a bis-vinylimidazolium salt. Transmission electron microscopy confirmed that all CNFs act as templates on the growth of the polymeric network, which perfectly covers the nanocarbons forming a cylindrical (SWCNTs, MWCNTs) or spherical (CNHs) coating. The stability of these hybrid materials was investigated in the conversion of CO2 into cyclic carbonate under high temperature and CO2 pressure. Compared with the homopolymerized monomer, nanotube-based materials display an improved c…

NanotubeHeterogeneous catalysisMaterials scienceCarbon dioxide fixationGeneral Chemical EngineeringCarbon nanotubesCyclic carbonateschemistry.chemical_elementCarbon nanotubeSettore CHIM/06 - Chimica Organicaengineering.materiallaw.inventionCatalysisChemistryCoatingPolymerizationchemistryChemical engineeringTransmission electron microscopylawengineeringGeneral Materials ScienceHybrid materialCarbonQD1-999Nanomaterials
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Single-Walled Carbon Nanotube–Polyamidoamine Dendrimer Hybrids for Heterogeneous Catalysis

2016

We report the synthesis and catalytic properties of single-walled carbon nanotube-polyamidoamine dendrimers hybrids (SWCNT-PAMAM), prepared via a convergent strategy. The direct reaction of cystamine-based PAMAM dendrimers (generations 2.5 and 3.0) with pristine SWCNTs in refluxing toluene, followed by immobilization and reduction of [PdCl4](2-), led to the formation of highly dispersed small palladium nanoparticles homogeneously confined throughout the nanotube length. One of these functional materials proved to be an efficient catalyst in Suzuki and Heck reactions, able to promote the above processes down to 0.002 mol % showing a turnover number (TON) of 48 000 and a turnover frequency (T…

Nanotubepalladium nanoparticleMaterials scienceGeneral Physics and AstronomyC-C cross coupling; carbon nanotubes; heterogeneous catalysis; palladium nanoparticles; PAMAM dendrimers; TEM; Materials Science (all); Engineering (all); Physics and Astronomy (all)02 engineering and technologyCarbon nanotubePAMAM dendrimers010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysislaw.inventionPhysics and Astronomy (all)Engineering (all)Suzuki reactionlawDendrimerOrganic chemistrypalladium nanoparticlesGeneral Materials ScienceC-C cross couplingcarbon nanotubePAMAM dendrimercarbon nanotubesGeneral EngineeringSettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesTurnover numberheterogeneous catalysisChemical engineeringTEMheterogeneous catalysiMaterials Science (all)0210 nano-technologyHybrid materialACS Nano
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ChemInform Abstract: Merging Visible-Light-Photoredox and Nickel Catalysis

2015

Review: [scope and limitations of the combination of nickel and photoredox catalysis for Csp3—Csp2 cross-coupling reactions; 18 refs.

NickelScope (project management)chemistryPhotoredox catalysischemistry.chemical_elementGeneral MedicinePhotochemistryCatalysisVisible spectrumChemInform
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Metal-Organic Frameworks as Versatile Heterogeneous Solid Catalysts for Henry Reactions

2021

Metal–organic frameworks (MOFs) have become one of the versatile solid materials used for a wide range of applications, such as gas storage, gas separation, proton conductivity, sensors and catalysis. Among these fields, one of the more well-studied areas is the use of MOFs as heterogeneous catalysts for a broad range of organic reactions. In the present review, the employment of MOFs as solid catalysts for the Henry reaction is discussed, and the available literature data from the last decade are grouped. The review is organized with a brief introduction of the importance of Henry reactions and structural properties of MOFs that are suitable for catalysis. The second part of the review dis…

Nitroaldol reactionMaterials sciencePharmaceutical ScienceReviewHeterogeneous catalysisCatalysisAnalytical ChemistryCatalysislcsh:QD241-441metal–organic frameworkslcsh:Organic chemistryCatalytic DomainDrug DiscoveryUreaGas separationAminesPhysical and Theoretical ChemistryMetal-Organic FrameworksHeterogeneous catalysisPrimary (chemistry)Organic ChemistryAmidesOrganic reactionChemical engineeringChemistry (miscellaneous)Molecular MedicineMetal-organic frameworkAmine gas treatingHenry reactionCopperMolecules
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Cyclodextrines confinantes : synthèse, propriétés complexantes et utilisation en catalyse asymétrique

2014

This manuscript is concerned with the design of novel catalytic systems derived from metallocyclodextrins. The first part describes new ways of functionalising the cyclodextrin primary face regioselectively for accessing inherently chiral P,P’ chelators. These heterodentate ligands gavequantitatively cis-chelate complexes with various d8 cations. Their rhodium(I) complexes were assessed in the asymmetric hydrogenation and hydroformylation of prochiral olefins. Thecoordination and catalytic properties of two phosphines derived from a- and b-cyclodextrin are also reported. With their phosphorus lone pair pointing toward the CD core, these confining ligands force the coordinated metal centre t…

NitrogenAzotePhosphorus (III)Confining ligandHomogeneous catalysisHydrogénation asymétriqueCyclodextrineAsymmetric hydrogenationCatalyse homogène[CHIM.OTHE] Chemical Sciences/OtherPhosphore (III)RhodiumLigand confinantHydroformylation asymétrique[CHIM.OTHE]Chemical Sciences/OtherAsymmetric hydroformylation
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Understanding the role of the Lewis acid catalyst on the 1,3-dipolar cycloaddition of N-benzylideneaniline N-oxide with acrolein: a DFT study

2007

Abstract The Lewis acid (LA) catalyzed 1,3-dipolar cycloaddition of N -benzylideneaniline N -oxide with acrolein has been studied using DFT calculations. Coordination of AlCl 3 to the acrolein oxygen atom produces a drastic change in the mechanism along the more favorable meta reactive channel. The process is characterized by a strong nucleophile/electrophile interaction allowing the formation of a zwitterionic intermediate, a Michael-type addition. The subsequent ring closure constitutes the rate-determining step. The energies obtained with the inclusion of solvent effect by means of the polarizable continuum model are in good agreement with experimental findings. Analysis of the global an…

NucleophileChemistryComputational chemistryOrganic ChemistryDrug DiscoveryElectrophile13-Dipolar cycloadditionLewis acids and basesSolvent effectsBiochemistryPolarizable continuum modelCycloadditionLewis acid catalysisTetrahedron
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Enantioselective Synthesis of 4-Substituted Dihydrocoumarins through a Zinc Bis(hydroxyamide)-Catalyzed Conjugate Addition of Terminal Alkynes

2013

A new enantioselective catalyst for the conjugate addition of terminal alkynes has been developed. Terminal alkynes react with 3-alkoxycarbonylcoumarins in the presence of diethylzinc and bis(hydroxyamide) ligands to give chiral non-racemic dihydrocoumarins substituted with an alkynyl group on the C-4 position with good yields and enantiomeric excesses up to 95%.

Nucleophilic additionChemistryStereochemistryN O ligandsEnantioselective synthesischemistry.chemical_elementAlkynylationGeneral ChemistryZincCatalysisOxygen heterocyclesAlkynylationFISICA APLICADAAsymmetric catalysismedia_common.cataloged_instanceEuropean unionNucleophilic additionmedia_commonConjugateAdvanced Synthesis & Catalysis
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DFT Study of Ethylene and Propylene Copolymerization over a Heterogeneous Catalyst with a Coordinating Lewis Base

2005

The copolymerization of ethylene and propylene over a heterogeneous Ti(III) catalyst containing tetrahydrofuran (THF) as a Lewis base and MgCl2 as a support has been studied by means of DFT. Two feasible models of active sites have been examined thoroughly, and one of them turned out to be favorable in terms of both catalytic activity and the microstructure of the resulting polymer. The external barriers of olefin insertion for this model range from 3.1 to 16.0 kcal/mol and are influenced by a variety of factors, such as the structure of the growing polymer chain and the nature of the incoming olefin as well as the orientation of the ligands around the titanium atom. Stochastic simulations …

Olefin fiberEthylenePolymers and PlasticsComonomerOrganic ChemistryHeterogeneous catalysisCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryCopolymerLewis acids and basesTetrahydrofuranMacromolecules
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