Search results for " Catalysis"

showing 10 items of 585 documents

How a Second Mg2+ Ion Affects the Phosphoryl Transfer Mechanism in a Protein Kinase: A Computational Study

2020

<div>In this contribution, the phosphoryl transfer reaction in CDK2 has been studied in detail considering the presence of an additional Mg2+ ion in the active site. For this purpose, QM/MM (quantum mechanics/molecular mechanics) free energy calculations with the adaptive string method were performed, which showed that indeed the system containing two Mg2+ ions exhibits a lower activation free energy, corroborating the experimental observations.</div>

biologyKinaseChemistryChemical physicsCyclin-dependent kinase 2Transfer mechanismbiology.proteinC++ string handlingActive siteMolecular mechanicsIonEnzyme catalysis
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Organocatalytic Enantioselective Friedel-Crafts Alkylation of 1-Naphthol Derivatives and Activated Phenols with Ethyl Trifluoropyruvate

2015

An organocatalytic enantioselective Friedel–Crafts alkylation of a series of substituted 1- naphthol derivatives and activated phenols with ethyl trifluoropyruvate, catalyzed by a quinine-derived squaramide, is presented. Good yields and high to excellent enantioselectivities of the Friedel– Crafts alkylation products were obtained.

biologyOrganocatalysis1-NaphtholEnantioselective synthesisGeneral ChemistryNaphtholsbiology.organism_classificationTrifluoropyruvatesReaccions químiqueschemistry.chemical_compoundEthyl trifluoropyruvatechemistryCatàlisiOrganocatalysisFISICA APLICADAAsymmetric catalysisOrganic chemistryPhenolsValenciaFriedel–Crafts reactionQuímica orgànicaFriedel–Crafts reaction
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Computational Modeling of Biological Systems: The LDH Story

2010

Lactate dehydrogenases, LDH, catalyzed reaction has been used in this chapter as a conductor wire to present the evolution and difficulties on computing methods to model chemical reactions in enzymes, since the early calculations based at semiempirical level carried out in gas phase to the recent sophisticated simulations based on hybrid Quantum Mechanical/Molecular Mechanics Dynamics (QM/MM MD) schemes. LDH catalyzes the reversible transformation of pyruvate into lactate. The chemical step consists in a hydride and a proton transfer from the cofactor (NADH) and a protonated histidine (His195), respectively. This fact has generated a lot of controversy about the timing of both transfers in …

biologyProtonChemistryHydridebiology.proteinActive siteThermodynamicsProtonationPotential of mean forceChemical reactionQuantumEnzyme catalysis
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Cu/P(4-PVP) stereochemistry in tetralin liquid-phase oxidation

2007

Abstract Cu/P(4-PVP) catalyst was used as catalyst for oxidation of tetralin in liquid phase. The catalyst was prepared by reaction of a Cu(II) salt with a 4-vinylpyridine-co-divinylbenzene polymer receptor and characterized by solid 1 H and 13 C NMR, XPS, FTIR, ESR spectroscopies, and by chemical reaction with pure tetralin. That information was used to gain insight into the stereochemistry of the active site needed to orient the reaction toward tetralone production. It was found that the Cu coordination with the pyridine was critical in influencing the peroxy-radical catalytic reaction, and that polyvinylpyridine was able to limit the autothermal oxidation. The active center is postulated…

biologyStereochemistryActive siteHeterogeneous catalysisChemical reactionCatalysisCatalysisActive centerchemistry.chemical_compoundchemistryPyridinebiology.proteinTetraloneTetralinPhysical and Theoretical ChemistryJournal of Catalysis
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2015

Chemical ligation has been used to alter motions in specific regions of dihydrofolate reductase from E. coli and to investigate the effects of localized motional changes on enzyme catalysis. Two isotopic hybrids were prepared; one with the mobile N-terminal segment containing heavy isotopes (2H, 13C, 15N) and the remainder of the protein with natural isotopic abundance, and the other one with only the C-terminal segment isotopically labeled. Kinetic investigations indicated that isotopic substitution of the N-terminal segment affected only a physical step of catalysis, whereas the enzyme chemistry was affected by protein motions from the C-terminal segment. QM/MM studies support the idea th…

biologyStereochemistryChemistryProtein dynamicsNatural abundanceGeneral ChemistryCatalysisEnzyme catalysisCatalysisIntramolecular forceKinetic isotope effectDihydrofolate reductasebiology.proteinChemical ligationAngewandte Chemie International Edition
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Exploiting the Chiral Ligands of Bis(imidazolinyl)- and Bis(oxazolinyl)thiophenes : Synthesis and Application in Cu-Catalyzed Friedel–Crafts Asymmetr…

2021

Five new C2-symmetric chiral ligands of 2,5-bis(imidazolinyl)thiophene (L1–L3) and 2,5-bis(oxazolinyl)thiophene (L4 and L5) were synthesized from thiophene-2,5-dicarboxylic acid (1) with enantiopure amino alcohols (4a–c) in excellent optical purity and chemical yield. The utility of these new chiral ligands for Friedel–Crafts asymmetric alkylation was explored. Subsequently, the optimized tridentate ligand L5 and Cu(OTf)2 catalyst (15 mol%) in toluene for 48 h promoted Friedel–Crafts asymmetric alkylation in moderate to good yields (up to 76%) and with good enantioselectivity (up to 81% ee). The bis(oxazolinyl)thiophene ligands were more potent than bis(imidazolinyl)thiophene analogues for …

bis-imidazolinekemiallinen synteesithiophenekatalyytitFriedel−Crafts alkylationasymmetric catalysisliganditkompleksiyhdisteetbis-oxazolineindolesβ-nitroolefins
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Imidazolium-Functionalized Carbon Nanohorns for the Conversion of CO2 Unprecedented Increase of Catalytic Activity after Recycling

2017

Carbon nanohorns (CNHs) were selected as a novel catalytic platform for the design of imidazolium based hybrid materials able to promote the conversion of carbon dioxide into cyclic carbonates. Several heterogeneous catalysts were prepared using a one-step procedure based on the radical polymerization of various bis-vinylimidazolium salts in the presence of pristine CNHs. The as-synthesized materials were tested for the fixation of CO2 into epoxides. The excellent catalytic performances were evaluated in terms of turnover number and productivity. The versatility of the above hybrids was proved using several epoxides as substrate. Catalysts recyclability was successfully verified for several…

carbon dioxide conversion carbon nanohorns cyclic carbonates heterogeneous catalysis imidazolium saltsSettore CHIM/06 - Chimica Organica
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Effect of Pre-Reduction on the Properties and the Catalytic Activity of Pd/Carbon Catalysts: A Comparison with Pd/Al2O3

2013

The effect of pre-reduction in solution with chemical reagents on the catalytic performance and catalyst properties of Pd/carbon catalysts was systematically investigated with a multitechnique approach. The results are critically discussed in comparison to those recently obtained on analogous Pd/alumina catalysts. It was proved that the Pd phase on the carbon surface is characterized by a high mobility, opposite to what occurs on alumina. As a result, the Pd particles on carbon aggregate together during pre-reduction, with a consequent decrease in available metal surface. Pd particles remain aggregated also in reaction conditions; the decreased Pd dispersion negatively affects the catalyst …

characterization techniqueCO chemisorptionInorganic chemistryPd-based catalystchemistry.chemical_elementTPRHeterogeneous catalysisPd/CarbonCatalysisCatalysisMetalCharacterization techniquesCatalyst pre-reductionTemperature-programmed reductionX-ray absorption spectroscopymetal nanoparticlein situPd-based catalystsPd/aluminaSAXSGeneral ChemistryXANESSmall Angle X-ray ScatteringX-ray Absorption SpectroscopyPd/Carbon; Pd/alumina; metal nanoparticle; catalysis; Catalyst pre-reduction; in situ; SAXS; XANES; Pd-based catalysts; heterogeneous catalysis; Characterization techniques; Temperature-programmed reduction; TPR; CO chemisorption; TEM; X-ray absorption spectroscopy; Small Angle X-ray Scatteringheterogeneous catalysischemistryReagentvisual_arttemperature-programmed reductionvisual_art.visual_art_mediumTEMheterogeneous catalysiSmall Angle X-ray SpectroscopyDispersion (chemistry)Carbon
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Influence of Sodium on the Structure and HDS Activity of Co–Mo Catalysts Supported ON Silica and Aluminosilicate

2000

Abstract Structural changes and catalytic performances of hydrodesulfurization (HDS) Co–Mo catalysts, supported on amorphous aluminosilicate (ASA) and amorphous SiO 2 were investigated as a function of the amount of sodium ions added to the supports. The catalysts were prepared according to the incipient wet impregnation method using (NH 4 ) 6 Mo 7 O 24 as molybdenum precursor and CoCl 2 or Co(NO 3 ) 2 as cobalt precursor. Structural and morphological characterisations of the materials were performed with X-ray diffraction (XRD) and surface area measurements (BET). In the case of the ASA-supported catalysts, increasing the amount of sodium resulted in a gradual decrease of the catalyst surf…

chemistryAluminosilicateSodiumInorganic chemistrychemistry.chemical_elementPhysical and Theoretical ChemistryHeterogeneous catalysisCristobaliteHydrodesulfurizationCobaltCatalysisCatalysisAmorphous solidJournal of Catalysis
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Visible Light-Induced Sulfonylation/Arylation of Styrenes in a Double Radical Three-Component Photoredox Reaction

2019

Simultaneous sulfonylation/arylation of styrene derivatives is achieved in a photoredox-catalyzed three-component reaction using visible light. A broad variety of difunctionalized products is accessible in mostly excellent yields and high diastereoselectivity. The developed reaction is scalable and suitable for the modification of styrene-functionalized biomolecules. Mechanistic investigations suggest the transformation to be operating through a designed sequence of radical formation and radical combination.

chemistry.chemical_classification010405 organic chemistryChemistryBiomoleculeOrganic ChemistryPhotoredox catalysisGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysis0104 chemical sciencesStyrenechemistry.chemical_compoundRadical formationVisible spectrum
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