Search results for " Catalyst"

showing 10 items of 292 documents

Application of palladium complexes bearing acyclic amino(hydrazido)carbene ligands as catalysts for copper-free Sonogashira cross-coupling

2015

Abstract Metal-mediated coupling of one isocyanide in cis-[PdCl2(CNR1)2] (R1 = C6H11 (Cy) 1, tBu 2, 2,6-Me2C6H3 (Xyl) 3, 2-Cl-6-MeC6H3 4) and various carbohydrazides R2CONHNH2 [R2 = Ph 5, 4-ClC6H4 6, 3-NO2C6H4 7, 4-NO2C6H4 8, 4-CH3C6H4 9, 3,4-(MeO)2C6H3 10, naphth-1-yl 11, fur-2-yl 12, 4-NO2C6H4CH2 13, Cy 14, 1-(4-fluorophenyl)-5-oxopyrrolidine-3-yl 15, (pyrrolidin-1-yl)C(O) 16, 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propane-1-yl 17, EtNHC(O) 18] or sulfohydrazides R3SO2NHNH2 [R3 = Ph 19, 4-MeC6H4 20] led to a series of (hydrazido)(amino)carbene complexes cis-[PdCl2{ C (NHNHX) N(H)R1}(CNR1)]; X = COR2, SO2R3 (21–48, isolated yields 60–96%). All prepared species were characterized by elemental…

StereochemistryIsocyanideArylchemistry.chemical_elementSonogashira couplingCopper-free Sonogashira couplingAcyclic diaminocarbenesNuclear magnetic resonance spectroscopyPalladium-(acyclic diminocarbene) catalystsMedicinal chemistryCatalysisCatalysischemistry.chemical_compoundchemistryCatalytic cycleMechanism of catalytic action of Pd-ADCsPhysical and Theoretical Chemistryta116CarbenePalladiumJournal of Catalysis
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Aromatic Nucleophilic Substitution (SNAr) of meso-Nitroporphyrin with Azide and Amines as an Alternative Metal Catalyst Free Synthetic Approach To Ob…

2014

International audience; Aromatic nucleophilic substitution reaction of the nitro group of meso-nitroporphyrins with azide and various amines was achieved and represents an alternative procedure to C-N coupling reactions usually needed to obtain such meso-N-substituted porphyrins in good yields.

Substitution reactionRadical-nucleophilic aromatic substitution010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistryfungi010402 general chemistry01 natural sciencesMedicinal chemistryCoupling reaction0104 chemical sciencescarbohydrates (lipids)chemistry.chemical_compoundchemistryNucleophilic aromatic substitution[ CHIM.ORGA ] Chemical Sciences/Organic chemistryNucleophilic substitutionNitropolycyclic compoundsOrganic chemistryAzideMetal catalyst
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A supercritical-fluid method for growing carbon nanotubes

2007

Large‐scale generation of multiwalled carbon nanotubes (MCNTs) is efficiently achieved through a supercritical fluid technique employing carbon dioxide as the carbon source. Nanotubes with diameters ranging from 10 to 20 nm and lengths of several tens of micrometers are synthesized (see figure). The supercritical‐fluid‐grown nanotubes also exhibit field‐emission characteristics similar to MCNTs grown by chemical‐vapor deposition.

Supercritical fluidsMaterials scienceCarbon nanofiberMechanical EngineeringCarbon nanotubesCarbon nanotubeChemical vapor depositionCondensed Matter::Mesoscopic Systems and Quantum Hall EffectSupercritical fluidlaw.inventionCarbon nanotubes multiwalledCondensed Matter::Materials ScienceNanofluidIndustrial technologyChemical engineeringMechanics of MaterialslawFrit compressionChemical vapor depositionGeneral Materials ScienceCarbon nanotube supported catalyst
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Sali di imidazolio multistrato supportati covalentemente: attività catalitica per la produzione di carbonati ciclici in scCO2 e nuovi supporti per ca…

2011

I liquidi ionici supportati (SILP) hanno trovato interessanti applicazioni sia nel campo delle reazioni catalizzate da metalli che in organocatalisi [1]. Inoltre, i SILP sono stati efficacemente impiegati in reazioni di apertura di epossidi in CO2 supercritica per fornire carbonati ciclici [2]. I liquidi ionici vengono generalmente supportati covalentemente attraverso la modificazione dei gruppi funzionali presenti sulla superficie del supporto, conducendo in tal modo alla formazione di un monostrato di liquido ionico supportato. Gli esempi di SILP legati covalentemente, in maniera tale da ottenere dei multistrato, sono rari. In questa comunicazione viene riportato un metodo per preparare d…

Supported catalystSettore CHIM/06 - Chimica OrganicaIonic liquid
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Studium zum Vorgang der Wasserstoffübertragung, 50. Elektroreduktion und phasentransferkatalysierte Borhydrid-reduktion prochiraler Ketone

1978

Prochirale Carbonylverbindungen wurden in die entsprechenden sekundaren Alkohole ubergefuhrt a) durch Elektroreduktion und b) mit NaBH4, in beiden Fallen mit den gleichen Ephedriniumsalzen, und zwar fur a) als optisch aktive Leitsalze und fur b) als optisch aktive Phasentransfer-Katalysatoren. Es wurden bei der Elektroreduktion und bei der Phasentransfer-Katalyse die Ausbeuten an Carbinol (und Pinakol)3), die optische Ausbeute und die absolute Konfiguration des bevorzugt gebildeten Enantiomeren bestimmt. In der uberwiegenden Mehrzahl der untersuchten Beispiele besitzen die unter Mitwirkung optisch aktiver Ephedriniumsalze nach beiden Methoden erhaltenen Uberschusenantiomeren die entgegenges…

Supporting electrolyteChemistryHydrideOrganic ChemistryPolymer chemistryAbsolute configurationChiral phasePhysical and Theoretical ChemistryOptically activeEnantiomerPhase-transfer catalystCatalysisJustus Liebigs Annalen der Chemie
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α-d-Glucopyranose Adsorption on a Pd30 Cluster Supported on Boron Nitride Nanotube

2016

Boron nitride nanotube (BNNT) as an innovative support for carbohydrate transformation processes was evaluated, using density functional theory. The α-d-glucopyranose adsorption on a Pd30 cluster, supported on BNNT, was used to check both the local activity of topologically different metallic sites and the effects of the proximity of the BNNT surface to the same metallic sites. Detailed geometrical and electronic analyses performed on Pd30/BNNT and α-d-glucopyranose/Pd30/BNNT systems were discussed. It was observed that the deposition of the Pd30 cluster onto the BNNT support gives rise to an electronic rearrangement, determining a charge transfer from the support to the adsorbed metal clus…

Surface site reactivityChemical substanceNanotechnologyElectron donor02 engineering and technology010402 general chemistryDFT01 natural sciencesBoron nitride nanotubeCatalysisCatalysiCatalysisMetalchemistry.chemical_compoundAdsorptionSupported palladium catalystCluster (physics)Chemistry (all)Molecular electrostatic potentialGeneral Chemistry021001 nanoscience & nanotechnologyBoron nitride nanotube; DFT; Molecular electrostatic potential; Supported palladium catalyst; Surface site reactivity; α-d-Glucopyranose adsorption; Catalysis; Chemistry (all)0104 chemical scienceschemistryChemical physicsvisual_artα-d-Glucopyranose adsorptionvisual_art.visual_art_mediumDensity functional theory0210 nano-technologyScience technology and societyTopics in Catalysis
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In Situ Regeneration of Copper-Coated Gas Diffusion Electrodes for Electroreduction of CO2 to Ethylene

2021

This research was funded by the European Union’s Horizon 2020 research and innovation program under grant agreement No 768789 as well as by the Polish National Centre of Science under grant no 2017/26/D/ST8/00508. The Institute of Solid State Physics, University of Latvia, as a center of excellence, has received funding from the European Union’s Horizon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-TeamingPhase2 under grant agreement no. 739508, project CAMART2.

TechnologyEthyleneInorganic chemistrychemistry.chemical_element02 engineering and technologyElectrolyte010402 general chemistryElectrocatalyst7. Clean energy01 natural sciencesArticleCatalysischemistry.chemical_compoundEthyleneCopper catalystsethyleneelectrocatalysisGaseous diffusionGeneral Materials Sciencecopper complexesElectrochemical reduction of carbon dioxideMicroscopyQC120-168.85TQH201-278.5carbon dioxideEngineering (General). Civil engineering (General)021001 nanoscience & nanotechnologyCopperTK1-99710104 chemical sciencesDescriptive and experimental mechanicschemistryCarbon dioxide13. Climate action:NATURAL SCIENCES [Research Subject Categories]copper catalystsElectrical engineering. Electronics. Nuclear engineeringTA1-2040GDE0210 nano-technologyElectrocatalysisFaraday efficiencyCopper complexes
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Recyclable Heterogeneous and Low-Loading Homogeneous Chiral Imidazolidinone Catalysts for α-Alkylation of Aldehydes

2014

Two polystyrene-supported and six homogeneous MacMillan imidazolidinone catalysts were prepared and tested for the asymmetric α-alkylation of propanal with benzodithiolylium tetrafluoroborate. The chiral imidazolidinone was linked to polystyrene through the N-3 atom or through the phenyl ring and their catalytic activity was compared with that of their unsupported precursors. This comparison has allowed us to find an unsupported catalyst that displays high catalytic activity down to 5 or 2 mol % at room temperature with a high level of enantioselectivity also when used with hexanal and 3-phenylpropanal. In addition, one of the heterogeneous materials was revealed to be highly recyclable for…

TetrafluoroborateImidazolidinoneasymmetric synthesiEnantioselective synthesisSettore CHIM/06 - Chimica OrganicaGeneral ChemistryorganocatalysiAlkylationHexanalCatalysischemistry.chemical_compoundchemistryOrganocatalysisOrganic chemistryPolystyrenesupported catalystsalkylationheterocycleChemPlusChem
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Biomass-based composite catalysts for catalytic wet peroxide oxidation of bisphenol A : preparation and characterization studies

2019

Abstract The wet granulation process was used to prepare new, efficient, and cost-effective granular biomass-based composite catalysts for catalytic wet peroxide oxidation (CWPO) of bisphenol A (BPA). The most stable composite granules was prepared by mixing biomass-based carbon residue (CR) with metakaolin (MK) combined with calcium oxide (CaO) or cement and a solvent (NaOH or KOH). For all the prepared composite granules, the optimized binding agents to carbon ratio was 0.3, the solvent to carbon ratio 1.2, and the agitation rate 1200 rpm. The specific surface area of the prepared catalysts was 152–205 m2/g. The composite granular catalyst (CR + MK + CaO + NaOH) had the most durable and s…

Thermal desorption spectroscopybiomassacomposite catalystComposite numbergranular activated carbon02 engineering and technologyjätevesi010501 environmental sciences01 natural sciencesPeroxidewastewater purificationCatalysisGranulationchemistry.chemical_compoundSpecific surface areaChemical Engineering (miscellaneous)Calcium oxideWaste Management and Disposalta116komposiitit0105 earth and related environmental sciencesjäteveden käsittelybiomassProcess Chemistry and Technology021001 nanoscience & nanotechnologyPollutionSolventchemistryaktiivihiilioxidation of bisphenol A0210 nano-technologyNuclear chemistryJournal of Environmental Chemical Engineering
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A highly reduced graphene oxide/ZrOx–MnCO3 or –Mn2O3 nanocomposite as an efficient catalyst for selective aerial oxidation of benzylic alcohols

2017

Highly reduced graphene oxide (HRG) nanocomposites of manganese carbonate doped with (1%) zirconia (ZrOx) nanoparticles [ZrOx(1%)–MnCO3/(X%)HRG (where X = 0–7)] were prepared employing a facile co-precipitation method in which the percentage of HRG was varied. The resulting nanocomposite was calcined at 300 °C. Further calcination of the catalyst at 500 °C resulted in the conversion of manganese carbonate to manganese oxide [ZrOx(1%)–Mn2O3/(X%)HRG]. The effect of the inclusion of HRG on the catalytic activity along with its comparative performance between carbonates and their respective oxides was studied for the liquid-phase selective oxidation of benzylic alcohols into corresponding aldeh…

Thermogravimetric analysisGeneral Chemical EngineeringOxide02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesNanomaterial-based catalyst0104 chemical scienceslaw.inventionCatalysischemistry.chemical_compoundchemistrylawBenzyl alcoholAlcohol oxidationCalcination0210 nano-technologySelectivityNuclear chemistryRSC Advances
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