Search results for "Inorganic chemist"

showing 10 items of 7340 documents

Supported Ionic Liquid Asymmetric Catalysis. A New Method for Chiral Catalysts Recycling. The Case of Proline-Catalyzed Aldol Reaction.

2004

A new method for chiral catalysts recycling, based on the supported ionic liquid asymmetric catalysis concept, has been developed. This concept involves the treatment of a monolayer of covalently attached ionic liquid on the surface of silica gel with additional ionic liquid. These layers serve as the reaction phase in which the homogeneous chiral catalyst is dissolved. As first application of this concept the L-proline-catalyzed aldol reaction has been carried out. Good yields and ee values, comparable with those obtained under homogeneous conditions have been obtained. Moreover, this material shows high regenerability.

inorganic chemicalsChemistrySilica gelorganic chemicalsOrganic ChemistryInorganic chemistryEnantioselective synthesisGeneral MedicineBiochemistryCombinatorial chemistryCatalysischemistry.chemical_compoundAldol reactionCovalent bondPhase (matter)Drug DiscoveryMonolayerIonic liquidChemInform
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TAP reactor study of the deep oxidation of propane using cobalt oxide and gold-containing cobalt oxide catalysts

2009

Abstract A transient reactor study of the oxidation of propane to CO 2 on gold-free and gold-doped CoO x catalysts has been carried out. It has been demonstrated that the presence of gold markedly promotes the catalytic reactivity of cobalt oxide in the total oxidation of propane. Both catalysts oxidised propane directly to CO 2 via a Mars–Van Krevelen mechanism, and this was confirmed using isotopically labelled oxygen experiments. The increased activity of the gold catalyst is related to the faster reoxidation of the cobalt oxide when gold is present in the catalyst, since the reaction step in which the catalyst is reduced, due to propane oxidation, is similar for both catalysts. The fast…

inorganic chemicalsChemistryorganic chemicalsProcess Chemistry and TechnologyCatalyst supportInorganic chemistrychemistry.chemical_elementHeterogeneous catalysisOxygenCatalysisCatalysischemistry.chemical_compoundCatalytic oxidationTransition metalPropaneheterocyclic compoundsCobalt oxideApplied Catalysis A: General
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Crystal structure of a CsF-uranyl-salen complex. An unusual cesium-chlorine coordination.

2006

Complexation of CsF with the ditopic uranyl-salen receptor results in a solid-state structure, in which the coordination sphere of cesium is filled by ligation to one of the chlorine atoms of the solvent chloroform. This X-ray structure is the first example of chloroform ligation to an alkali-metal ion.

inorganic chemicalsChloroformCoordination sphereInorganic chemistrychemistry.chemical_elementCrystal structureUranylIonInorganic ChemistrySolventchemistry.chemical_compoundchemistryCaesiumPolymer chemistryChlorinePhysical and Theoretical ChemistryInorganic chemistry
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The effect of gold addition on the catalytic performance of copper manganese oxide catalysts for the total oxidation of propane

2011

Mixed copper manganese oxide catalysts (Hopcalite) have been studied for the total oxidation of propane, as a model for hydrocarbon volatile organic compound emission control. Catalysts were prepared using coprecipitation with and without gold. Calcination temperature influenced the catalyst activity and those prepared at 300 °C were the most active. Characterization showed that the catalysts had a nanowire-type morphology, and for those containing gold it was present as metallic particles occluded within the nanowires. The incorporation of gold into the catalyst enhanced the activity for propane conversion, but the presence of gold did not noticeably enhance the light-off activity. Althou…

inorganic chemicalsCoprecipitationorganic chemicalsProcess Chemistry and TechnologyInorganic chemistrychemistry.chemical_elementCatalysislaw.inventionCatalysisMetalchemistry.chemical_compoundHopcalitechemistryCatalytic oxidationlawPropanevisual_artvisual_art.visual_art_mediumheterocyclic compoundsCalcinationGeneral Environmental SciencePalladiumApplied Catalysis B: Environmental
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The reduction of molecular oxygen by iron porphyrins

2002

Abstract Molecular assemblies have been synthesised to reproduce the structure of the cytochrome c oxidase (C c O) active site and to explore the roles played by its different features. It was discovered that a single iron porphyrin, adsorbed at the surface of a graphite electrode, is a selective catalyst for the four-electron reduction of dioxygen to water, at pH 7. To cite this article: D. Ricard et al., C. R. Chimie 5 (2002) 33–36

inorganic chemicalsCytochromebiology010405 organic chemistryGeneral Chemical EngineeringInorganic chemistryActive sitechemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrochemistryElectrocatalyst01 natural sciencesPorphyrinOxygen[ CHIM ] Chemical Sciences0104 chemical scienceschemistry.chemical_compoundchemistryPolymer chemistry[CHIM] Chemical Sciencesbiology.proteinCytochrome c oxidase[CHIM]Chemical SciencesGraphite
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Substituent Effects on the [N-I-N](+) Halogen Bond

2016

We have investigated the influence of electron density on the three-center [N-I-N](+) halogen bond. A series of [bis(pyri din e) io dine](+) and [1,2-bis ( (pyridin e-2-71 ethynyl)b e nze n e)io dine](+) BF4- complexes substituted with electron withdrawing and donating functionalities in the para-position of their pyridine nitrogen were synthesized and studied by spectroscopic and computational methods. The systematic change of electron density of the pyridine nitrogens upon alteration of the para-substituent (NO2, CF3, H, F, Me, OMe, NMe2) was confirmed by N-15 NMR and by computation of the natural atomic population and the pi electron population of the nitrogen atoms. Formation of the [N-…

inorganic chemicalsElectron densityPopulationInorganic chemistryhalogen bondsSubstituent010402 general chemistry01 natural sciencesBiochemistryCatalysisArticlechemistry.chemical_compoundColloid and Surface ChemistryPyridineeducationBenzeneta116education.field_of_studyHalogen bond010405 organic chemistryChemical shiftGeneral ChemistryKemi0104 chemical sciencesCrystallographychemistryChemical SciencesPolar effect
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Oxidative dehydrogenation of ethane: A study over the structure and robustness of Ni–W–O catalysts

2014

[EN] The robustness of one selected Ni-W-O catalyst has been studied in the oxidative dehydrogenation of ethane. This catalyst initially deactivates for the first 10 h online decreasing 15% of its catalytic activity compared to its initial stable catalytic activity. However from 10 to 60 h online the catalytic activity keeps almost stable. On the other hand, it has been shown that the Ni-W-O catalyst cannot tolerate an oxygen-free atmosphere (C-2 and He) as nickel oxide is transformed into metallic nickel. Methane and hydrogen as well as abundant coke were formed on the surface of the catalyst in these O-free conditions. However a re-calcination in air leads to the removal of coke, the cata…

inorganic chemicalsEthyleneHydrogenGeneral Chemical EngineeringCatalyst supportInorganic chemistryEnergy Engineering and Power Technologychemistry.chemical_elementCatalysisMethaneCatalysisEthylenechemistry.chemical_compoundDehydrogenationNickel tungstenOxidative dehydrogenation of ethaneOxide catalystsEthaneChemistryorganic chemicalsNickel oxideCokeFuel TechnologyNi-W-OHydrogenOxidative dehydrogenationFuel Processing Technology
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An Off-On-Off Fluorescent Sensor for pH Windows Based on the 13aneN4-Zn 2+ System

2016

International audience; The new ligand L was prepared and features a 13-membered tetraaza macrocyclic ring with a 1,8-naphthalimide fluorophore appended to a C atom of its backbone. The protonation constants of L as well as its complexation constants with Zn2+ ions were determined in 1:1 water/methanol solutions by potentiometric titrations. Fluorimetric pH titrations were performed with L alone and L in the presence of Zn2+ ions (1:1), and the species distributions (%) versus pH were compared. A window-shaped fluorescence trend was observed with pH for the L/Zn2+ system, which behaves as an off-on-off pH sensor. The on window is centred in the 6.5-7.5 pH range, in correspondence with the f…

inorganic chemicalsFluorophorePotentiometric titrationInorganic chemistryProtonationYeast cellsSensors; Fluorescence; Zinc; Yeast cells; Macrocyclic ligands010402 general chemistry01 natural sciencesMicelleFluorescenceInorganic Chemistrychemistry.chemical_compoundMacrocyclic ligandsCyclamLipophilicity[SDV.IDA]Life Sciences [q-bio]/Food engineeringEquilibriaMicellesIonsChemosensors010405 organic chemistryLigandSensorsChelation-enhanced fluorescencezinc[ SDV.IDA ] Life Sciences [q-bio]/Food engineeringMetal-complexesFluorescence0104 chemical scienceschemistryCyclamTitrationMacrocycles
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Porous clays heterostructures as supports of iron oxide for environmental catalysis

2018

[EN] Porous Clays Heterostructures (PCH) from natural pillared clays (bentonite with a high proportion of montmorillonite) have been used as supports of iron oxide for two reactions of environmental interest: i) the elimination of toluene (a representative compound of one of the most toxic subsets of volatile organic compounds, aromatics) by total oxidation and ii) the selective oxidation of H2S to elemental sulfur. For both reactions these catalysts have resulted to be remarkably more efficient than similar catalysts prepared using conventional silica as a support. Thus, in the total oxidation of toluene it has been observed that the catalytic activity obtained using siliceous PCH is two o…

inorganic chemicalsGeneral Chemical EngineeringInorganic chemistryIron oxidechemistry.chemical_element02 engineering and technology010402 general chemistry01 natural sciencesIndustrial and Manufacturing EngineeringCatalysischemistry.chemical_compoundH2S to STotal and selective oxidationIron oxideEnvironmental ChemistrySulfatePorous Clays Heterostructures (PCH)ChemistryVOCGeneral Chemistry021001 nanoscience & nanotechnologySulfurToluene0104 chemical sciencesMontmorilloniteBentonite0210 nano-technologySelectivityTolueneChemical Engineering Journal
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Phosphororganische Verbindungen, 68. Darstellung und Eigenschaften von Tetrakis(diphenylphosphin)‐nickel(0)

1971

Die Titelsubstanz 1 wurde durch Einwirkung von Diphenylphosphin auf Bis-π-allyl-nickel, Tetrakis(triphenylphosphin)-nickel(0) (2), Nickelpulver oder Nickel(II)-bromid dargestellt. Ihre Struktur wurde durch Zerewitinoff-Bestimmung, IR- und NMR-Spektren abgesichert. Eine Alkylierung von metalliertem 1 gelang nicht. Organic Phosphorus Compounds, 68. Preparation and Properties of Tetrakis(diphenylphosphine)nickel(0) The title compound, 1, was prepared by reacting of diphenylphosphine with bis(π-allyl)nickel, tetrakis(triphenylphosphine)nickel(0) (2), nickel-powder, or nickel(II) bromide. The structure of 1 was elucidated by Zerewitinoff method, i. r. and n. m. r. spectra. The alkylation of meta…

inorganic chemicalsInorganic Chemistrychemistry.chemical_compoundNickelDiphenylphosphinechemistryBromidePolymer chemistryotorhinolaryngologic diseasesOrganic phosphoruschemistry.chemical_elementAlkylationTriphenylphosphineChemische Berichte
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