Search results for "hydrogenation"

showing 10 items of 155 documents

Polycyclic aromatic chains on metals and insulating layers by repetitive [3+2] cycloadditions

2020

The vast potential of organic materials for electronic, optoelectronic and spintronic devices entails substantial interest in the fabrication of π-conjugated systems with tailored functionality directly at insulating interfaces. On-surface fabrication of such materials on non-metal surfaces remains to be demonstrated with high yield and selectivity. Here we present the synthesis of polyaromatic chains on metallic substrates, insulating layers, and in the solid state. Scanning probe microscopy shows the formation of azaullazine repeating units on Au(111), Ag(111), and h-BN/Cu(111), stemming from intermolecular homo-coupling via cycloaddition reactions of CN-substituted polycyclic aromatic az…

Materials scienceFabricationScienceGeneral Physics and Astronomy02 engineering and technologyConjugated system010402 general chemistry01 natural sciencesArticleGeneral Biochemistry Genetics and Molecular Biologylaw.inventionchemistry.chemical_compoundScanning probe microscopylawDehydrogenationon-surface synthesislcsh:Science13-dipolar cycloadditionschemistry.chemical_classificationMultidisciplinaryalgorithmGrapheneQgrapheneazomethine ylidesGeneral ChemistryPolymer021001 nanoscience & nanotechnologyCycloadditionddc:0104 chemical sciencesCU(111)total-energy calculationschemistryChemical engineeringboron-nitrideBoron nitrideazide-alkyne cycloadditionlcsh:QMaterials chemistrydehalogenation0210 nano-technology
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Shape-Dependence of Pd Nanocrystal Carburization during Acetylene Hydrogenation

2015

This interdisciplinary work combines the use of shape- and size-defined Pd nanocrystals (cubes of 10 and 18 nm, and octahedra of 37 nm) with in situ techniques and DFT calculations to unravel the dynamic phenomena with respect to Pd reconstruction taking place during acetylene hydrogenation. Notably, it was found that the reacting Pd surface evolved at a different pace depending on the shape of the Pd nanocrystals, due to their specific propensity to form carbides under reaction conditions. Indeed, Pd cubes (Pd(100)) reacted with acetylene to form a PdC0.13 phase at a rate roughly 6-fold higher than that of octahedra (Pd(111)), resulting in nanocrystals with different degrees of carburizati…

Reaction conditionsMaterials scienceNanotechnologyPd Nanocrystal Acetylene Hydrogenation DFT structure sensitivitySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsAcetylene hydrogenationCarbidechemistry.chemical_compoundGeneral EnergyAcetylenechemistryNanocrystalOctahedronSettore CHIM/03 - Chimica Generale E InorganicaLattice (order)Physical chemistryPhysical and Theoretical Chemistry
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Enantioselective Synthesis of (−)-Dihydrocodeine and Formal Synthesis of (−)-Thebaine, (−)-Codeine, and (−)-Morphine from a Deprotonated α-Aminonitri…

2014

The α-benzylation of a deprotonated bicyclic α-aminonitrile, followed by Noyori's asymmetric transfer hydrogenation combined with the Grewe cyclization onto a symmetrical A-ring precursor, are the key steps of a short and high-yielding enantioselective synthesis of the morphinan (-)-dihydrocodeine. This compound can be converted to (-)-thebaine in high yield by known transformations, while (-)-codeine and (-)-morphine are available from an advanced intermediate.

MorphinanThebaineMolecular StructureMorphineBicyclic moleculeCodeineStereochemistryOrganic ChemistryEnantioselective synthesisStereoisomerismStereoisomerismTransfer hydrogenationBiochemistryThebainechemistry.chemical_compoundDeprotonationchemistryYield (chemistry)NitrilesmedicineHydrogenationPhysical and Theoretical Chemistrymedicine.drugOrganic Letters
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Relationship between bulk phase, near surface and outermost atomic layer of VPO catalysts and their catalytic performance in the oxidative dehydrogen…

2017

Abstract A set of vanadium phosphorous oxide (VPO) catalysts, mainly consisting of (VO) 2 P 2 O 7 , VO(PO 3 ) 2 or VOPO 4 ·2H 2 O bulk crystalline phases, has been investigated for the oxidative dehydrogenation (ODH) of ethane to ethylene, a key potential reaction for a sustainable industrial and socioeconomic development. The catalytic performance on these VPO catalysts has been explained on the basis of the main crystalline phases and the corresponding surface features found by XPS and LEISS at 400 °C, i.e. within the temperature range used for ODH reaction. The catalysts based on (VO) 2 P 2 O 7 phase presented the highest catalytic activity and productivity to ethylene. Nevertheless, the…

Ethylene010405 organic chemistryInorganic chemistryOxideVanadiumchemistry.chemical_element010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryLow-energy ion scatteringOxidation stateDehydrogenationPhysical and Theoretical ChemistrySelectivity
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A Combination of Visible-Light Organophotoredox Catalysis and Asymmetric Organocatalysis for the Enantioselective Mannich Reaction of Dihydroquinoxal…

2019

[EN] An enantioselective photooxidative Mannich reaction of dihydroquinoxalinones with ketones by the merger of organophotoredox and asymmetric organocatalysis is described. This protocol features very mild reaction conditions using simple and cheap catalysts (Eosin Y and (S)-Proline) for the synthesis of chiral quinoxaline derivatives with good to high yields (up to 94%) and excellent enantioselectivities (up to 99% ee).

AlkylationActivation010402 general chemistry01 natural sciencesBiochemistryCatalysisReaccions químiqueschemistry.chemical_compoundQuinoxalineCatàlisiComplexesTertiary-AminesAcidOrganic chemistryPhysical and Theoretical ChemistryEosin YFunctionalizationMannich reactionReaction conditions010405 organic chemistryOrganic ChemistryEnantioselective synthesisMethodology0104 chemical sciencesPhotoredox catalysisEfficientchemistryOrganocatalysisFISICA APLICADAHydrogenationQuímica orgànicaVisible spectrum
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ChemInform Abstract: New Electrophilic Reactions of 2,2′-Bisindolyls with Acid Chlorides and Carbodienophiles.

2010

Some new acylation and cyclization reactions of 2,2′-bisindolyls 1, 2 are described. The product patterns constitute acyl derivatives 3, 4, 5 and an aldehyde 7, indolo[2,3-a]carbazoles 6, 14, 17, 19, 20 and cyclopentadiindoles 22 and 24. In the reaction with aryne or diazotated anthranilic acid, a 3-benzoylindole derivative 9 and phenylindolyl azo dye 10 are formed. N-methylmaleimide reacts with 2,2′-bisindolyl 2 via Michael type addition, dehydrogenation and cyclization to several functionalized or anellated indole derivatives 11, 12, 13 and 14, respectively.

AcylationIndole testchemistry.chemical_classificationchemistry.chemical_compoundchemistryElectrophileAnthranilic acidOrganic chemistryDehydrogenationGeneral MedicineAldehydeAryneChemInform
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Oxidative dehydrogenation of ethane over NiO–CeO2 mixed oxides catalysts

2012

[EN] In this paper we present the synthesis, characterization and catalytic behaviour in the oxidative dehydrogenation of ethane of NiO-CeO2 mixed oxides. The addition of cerium oxide to NiO strongly modifies its catalytic performance, although the changes in the catalytic behaviour depend on the catalyst composition. The incorporation of low amounts of cerium oxide to NiO multiplies the productivity to ethylene in the oxidative dehydrogenation of ethane by a factor of ca. 7, which is the result of an increase in both catalytic activity and selectivity to ethylene. The enhanced activity has been related to the remarkable increase of the surface area of catalyst and the low crystal sizes of …

Cerium oxideEthyleneCatalyst characterization (XPS TPR XRD Raman FTIR of adsorbed CO oxygen isotopic-exchange)Inorganic chemistryNon-blocking I/Ochemistry.chemical_elementCerium oxideGeneral ChemistryCatalysisCatalysisCerium(IV) oxide–cerium(III) oxide cycleEthylenechemistry.chemical_compoundCeriumchemistryDehydrogenationOxidative dehydrogenation of ethaneNickel oxideSelectivityCatalysis Today
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Cis-15 intermediates of biohydrogenation in the duodenal flow of cows receiving linseed

2006

Duodenal samples from a previous experiment (Akraim et al., 2006) were reanalysed for determination of cis-15 intermediates of ruminal biohydrogenation (BH). Three dry Holstein cows fitted with a duodenal cannula received a diet with 14% (dry matter basis) raw linseed. C18 fatty acids (C18FA) represented 6.3% of dietary dry matter, and contained 57.8% of C18:3. After 18 days adaptation, on each cow, twelve samples of duodenal flow were taken over 3 days, composited, and analysed for FA composition. Cis-9,trans-11,cis-15C18:3 and trans-11,cis-15C18:2 (CLnA) were identified by GC-MS. The proportion of CLnA was low, in spite of the high C18:3 intake. The first step of C18:3 BH, isomerisation t…

Linolenic acid[SPI.GPROC] Engineering Sciences [physics]/Chemical and Process EngineeringBiohydrogenationLinseed[SDV]Life Sciences [q-bio]food and beverages[INFO] Computer Science [cs][SDV.IDA] Life Sciences [q-bio]/Food engineering[SDV] Life Sciences [q-bio]Médecine vétérinaire et santé animal[SDV.IDA]Life Sciences [q-bio]/Food engineeringDairy cow[INFO]Computer Science [cs][SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringBIOHYDROGENATIONDUODENAL FLOW
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Carbons from second generation biomass as sustainable supports for catalytic systems

2018

In this study activated carbons were produced from the wood of three different wood species (pine, birch, spruce). The resulting activated carbons were characterized in bulk for ash content, carbon content (elemental analyses), specific surface area, and pore size distribution, and at the surface by measuring the autogenerated pH and studying their structure by XPS. All the samples presented high surface areas and appeared to be mesoporous materials (mesopores >80%). The carbons were then used as support for AuPt nanoparticles and tested in the liquid phase oxidation of glycerol (GLY) and in the hydrogenation of levulinic acid (LA), two important chemicals from cellulose-based biomass. The …

Activated mesoporous carbonskatalyytitaktiivihiiliLevulinic acid hydrogenationbiomassa (teollisuus)Carbon supported catalystsGlycerol oxidationGVL production
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The effect of β-mercaptoethanol on lactate dehydrogenase from rat brain

1963

Abstract Catalytic studies on lactate dehydrogenase from rat brain in the presence of β-mercaptoethanol have been performed. It has been found that pyruvate reduction and lactate dehydrogenation were differently affected by the addition of the sulfhydryl compound to the reaction mixture. The effect of β-mercaptoethanol on the catalyzed reaction has been shown to be dependent on the hydrogen ion concentration. When lactate dehydrogenation is measured, β-mercaptoethanol causes a net enhancement of the reaction rate at the more acidic pH values.

PharmacologyHydrogen ionL-Lactate DehydrogenaseResearchBrainL-Lactate dehydrogenaseRat brainBiochemistryRatsCatalysisReaction ratechemistry.chemical_compoundchemistryBiochemistryLactate dehydrogenaseDehydrogenationSulfhydryl CompoundsMercaptoethanolNuclear chemistryBiochemical Pharmacology
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