Search results for "Catalysis"

showing 10 items of 5944 documents

Nanoscopic hybrid systems with a polarity-controlled gate-like scaffolding for the colorimetric signalling of long-chain carboxylates

2007

Hybrid mesoporous systems containing a gate-like ensemble functionalised with imidazolium groups and a dye are used for the selective colorimetric sensing of long-chain carboxylates. Amoros del Toro, Pedro Jose, Pedro.Amoros@uv.es

Hybrid mesoporus systems ; Gate-like ; Imidazolium ; CarboxlatesScaffoldChemistryPolarity (physics)UNESCO::QUÍMICAUNESCO::QUÍMICA::Química analíticaMetals and AlloysCarboxlatesNanotechnologyGate-likeGeneral Chemistry:QUÍMICA [UNESCO]CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsHybrid mesoporus systemsHybrid systemMaterials ChemistryCeramics and CompositesImidazolium:QUÍMICA::Química analítica [UNESCO]Mesoporous materialLong chainNanoscopic scale
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Combinatorial Identification of Hydrides in a Ligated Ag40 Nanocluster with Noncompact Metal Core

2019

No formation of bulk silver hydride has been reported. Until very recently, only a few silver nanoclusters containing hydrides have been successfully prepared. However, due to the lack of effective techniques and also poor stability of hydride-containing Ag nanoclusters, the identification of hydrides' location within Ag nanoclusters is challenging and not yet achieved, although some successes have been reported on clusters of several Ag atoms. In this work, we report a detailed structural and spectroscopic characterization of the [Ag40(DMBT)24(PPh3)8H12]2+ (Ag40H12) cluster (DMBT = 2,4-dimethylbenzenethiol). The metal framework consists of three concentric shells of Ag8@Ag24@Ag8, which can…

HydrideChemistryGeneral ChemistryElectron010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesCharacterization (materials science)NanomaterialsNanoclustersNMR spectra databaseMetalCrystallographyColloid and Surface Chemistryvisual_artvisual_art.visual_art_mediumCluster (physics)Journal of the American Chemical Society
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C,N-chelated dicyclopentadienylzirconium complexes and their possible use as hydrogenation catalysts

2010

Abstract In situ generated Cp2Zr(n-Bu)Cl (6) reacts with {2-[(CH3)2NCH2]C6H4}2Pb to form exclusively {2-[(CH3)2NCH2]C6H4}Cp2ZrCl (7), [(CH3)2NCH2]C6H5, butene and elemental lead. The further derivatization of chloride (7) to fluoride (8), hydride (9), methyl derivative (10), and a reduction of 7 are also described. The crystal structures of 7–10 were determined. The catalytic activity of 9 and 10 in hydrogenation of styrene was also preliminarily tested.

HydrideInorganic chemistryCrystal structureMedicinal chemistryChlorideButeneCatalysisStyreneInorganic Chemistrychemistry.chemical_compoundTransmetalationchemistryMaterials ChemistrymedicinePhysical and Theoretical ChemistryDerivatizationmedicine.drugInorganic Chemistry Communications
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Chemistry of ?-hydridobis[pentacarbonylchromium(0)] species. Part III. Redox reactions with mercury(II) compounds and iodine

1981

[Cr2(CO)10(μ-H)]− undergoes ready hydride substitution on reaction with HgX2 (X = Cl, Br, I or SCN) or with iodine in acetone, yielding [Cr2(CO)10(μ-X)]− complex species which can be converted quantitatively into [Cr(CO)5X]− anions by reactions conducted in the presence of an excess of X−.

HydrideInorganic chemistryMetals and Alloyschemistry.chemical_elementIodineMedicinal chemistryRedoxMercury (element)CatalysisInorganic ChemistryPart iiichemistry.chemical_compoundchemistryMaterials ChemistryAcetoneOrganometallic chemistryTransition Metal Chemistry
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Gold-Catalyzed Intramolecular Hydroamination of o-Alkynylbenzyl Carbamates: A Route to Chiral Fluorinated Isoindoline and Isoquinoline Derivatives

2013

Enantiomerically pure fluorinated isoindoline and dihydroisoquinoline scaffolds have been prepared through a diastereoselective addition of fluorinated nucleophiles to Ellman’s N-(tert-butanesulfinyl)imines followed by a sequence of Sonogashira cross-coupling/gold(I)-catalyzed cycloisomerization of the corresponding carbamate. A more favored 5-exo-dig mechanism was observed mainly due to an electronic effect of the fluorinated group.

Hydrocarbons FluorinatedMolecular StructureChemistryOrganic ChemistrySonogashira couplingStereoisomerismIsoindolineIsoindolesIsoquinolinesBiochemistryMedicinal chemistryCatalysischemistry.chemical_compoundCycloisomerizationNucleophileIntramolecular forceElectronic effectOrganic chemistryHydroaminationCarbamatesGoldPhysical and Theoretical ChemistryIsoquinolineAmines
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A Versatile Approach to CF3-Containing 2-Pyrrolidones by Tandem Michael Addition-Cyclization: Exemplification in the Synthesis of Amidine Class BACE1…

2015

The synthesis of new fluorinated pyrrolidones starting from unprotected amino esters and amino nitriles through a Michael addition-lactamization sequence is described. The resulting CF3 -containing building blocks, bearing a quaternary stereogenic center adjacent to the fluorinated group, have been converted into amino pyrrolidines that display potent β-secretase 1 (BACE1) inhibitory activity. This work constitutes an example of selective fluorination as a valid strategy for the modulation of physicochemical and biological properties of lead compounds in drug discovery.

Hydrocarbons FluorinatedMolecular StructureTandemAmino estersDrug discoveryStereochemistryOrganic ChemistryAmidinesStereoisomerismSequence (biology)General ChemistryCombinatorial chemistryPyrrolidinonesCatalysisStereocenterAmidinechemistry.chemical_compoundchemistryCyclizationBiological propertyDrug DiscoveryMichael reactionAspartic Acid EndopeptidasesAmyloid Precursor Protein SecretasesChemistry - A European Journal
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Highly enantioselective synthesis of fluorinated gamma-amino alcohols through proline-catalyzed cross-Mannich reaction.

2005

A new, simple route for the synthesis of fluorinated beta-alkyl gamma-amino alcohols in optically pure form in only two steps and featuring proline catalysis from inexpensive and readily available starting materials is described. The applied strategy allows for the introduction of diversity into both the beta-fluoroalkyl and alpha-alkyl groups of these compounds. [reaction: see text]

Hydrocarbons FluorinatedProlineStereochemistryChemistryOrganic ChemistryEnantioselective synthesisStereoisomerismGeneral MedicineBiochemistryCombinatorial chemistryAmino AlcoholsCatalysisCatalysisMannich BasesOrganic chemistryProlinePhysical and Theoretical ChemistryMannich reactionOrganic letters
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New Cathepsin Inhibitors to Explore the Fluorophilic Properties of the S 2 Pocket of Cathepsin B: Design, Synthesis, and Biological Evaluation

2011

5 páginas, 1 figura, 2 tablas -- PAGS nros. 5256-5260

Hydrocarbons FluorinatedStereochemistryStereoisomerismhydrolasesstereoselectivityCatalysisCathepsin BCathepsin BNitrilesinhibitorsCombinatorial Chemistry TechniquesHumansMoleculefluorinated ligandsBiological evaluationCathepsinMolecular StructureCombinatorial Chemistry TechniquesligandsChemistryOrganic ChemistryStereoisomerismDipeptidesGeneral Chemistryfluorinated fluorinatedDesign synthesisDrug DesignpeptidesStereoselectivityChemistry – A European Journal
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Dual Hydrogen Bond - Enamine Catalysis Enables a Direct Enantioselective Three-Component Domino Reaction

2011

A dual system, composed of an enantioselective enamine catalyst and a multiple-hydrogen-bond catalyst achieves the three-component enantioselective aldehyde—nitroalkene—aldehyde domino reaction using either two similar or two different aldehydes.

Hydrogen bond catalysisComponent (thermodynamics)Hydrogen bondChemistryEnantioselective synthesisGeneral MedicineGeneral ChemistryCatalysisCatalysisEnaminechemistry.chemical_compoundCascade reactionOrganocatalysisOrganic chemistryta116Angewandte Chemie Intermational Edition
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Ionic liquids as solvents for the Knoevenagel condensation: understanding the role of solvent–solute interactions

2015

The Knoevenagel condensation in ionic liquids has been demonstrated as a strongly solvent-dependent process. The objective of this study was to establish a simple and descriptive trend of solvent–solute interactions that favour the Knoevenagel condensation in ionic liquid media. The reaction between 4-(dimethylamino)benzaldehyde and ethyl cyanoacetate in several imidazolium- and pyrrolidinium-based ionic liquids and one ionic liquid mixture was studied. The rate constants were rationalised by studying the change in the 1H NMR chemical shift of representative starting materials in the ionic liquids and the measurement and consideration of the Kamlet–Taft descriptors for each solvent. The hyd…

Hydrogen bondChemistryGeneral ChemistryCatalysisSolventBenzaldehydechemistry.chemical_compoundReaction rate constantEthyl cyanoacetateIonic liquidMaterials ChemistryProton NMROrganic chemistryKnoevenagel condensationNew Journal of Chemistry
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