Search results for "SULFUR"

showing 10 items of 545 documents

Reactivity of arsenic compounds on trapping masses and role of the active phase

2019

The aim of the thesis is to study the reactivity of organic arsenic compounds on various recovery masses and to identify the role of the nature of the active phase and the reaction mechanisms involved. The active phase is composed of metals (Ni, Co, Mo, Cu, Zn, Fe, etc.), pure or in a mixture, in the reduced state or in the sulphide state. The selection of the metallic phases will be carried out by molecular modeling "ab initio", and the synthesis by impregnation of metallic salts on mesoporous aluminas). The reactivity of the solids will be studied in a static reactor on simplified model loads, with kinetic monitoring. The advanced characterization of the solids after synthesis and after r…

Heterogeneous catalysisHydrodesulfurization[CHIM.OTHE] Chemical Sciences/OtherReactivityHydrodésulfurationTrapping massRéactivitéAdsorptionCatalyse hétérogène[CHIM.OTHE]Chemical Sciences/OtherMasse de captationArsenic
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A Stereocontrolled Protocol to Highly Functionalized Fluorinated Scaffolds through a Fluoride Opening of Oxiranes

2016

A novel selective and substrate-dependent synthetic protocol has been developed towards the synthesis of various fluorine-containing, highly functionalized cycloalkane derivatives. The method involves the stereoselective epoxidation of some unsaturated cyclic beta-amino acid derivatives as model compounds, followed by a regioselective fluoride opening of oxiranes under various conditions with Deoxofluor and XtalFluor-E reagents, thereby offering an insight into this new epoxide opening methodology with fluoride.

Hydrocarbons FluorinatedPharmaceutical ScienceEpoxideAlkenesstereoselectivity010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441Fluorideschemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoveryOrganic chemistryPhysical and Theoretical Chemistryamino acidsSulfur Compoundsoxirane; fluorination; amino acids; stereoselectivity; regioselectivity010405 organic chemistryOrganic ChemistryRegioselectivityStereoisomerismfluorination0104 chemical sciencesCycloalkanechemistryChemistry (miscellaneous)oxiraneregioselectivityReagentEpoxy CompoundsMolecular MedicineStereoselectivityFluorideMolecules
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Study of the effect of H2S, MeSH and DMS on the sensory profile of wine model solutions by Rate-All-That-Apply (RATA)

2016

The effect of hydrogen sulfide (HS), methanethiol (MeSH) and dimethyl sulfide (DMS) on the odor properties of three wine models-WM- (young white, young red and oaked red wines) was studied. Wine models were built by mixing a pool of common wine volatile and non-volatile compounds and further spiked with eight different combinations of the three sulfur compounds present at two levels (level 0: 0 μg L and level 1: 40 μg L of HS, 12 μg L of MeSH; 55 μg L of DMS). For each wine matrix eight WMs were produced and further submitted to sensory description by Rate-All-That-Apply (RATA) method. Hydrogen sulfide and methanethiol were clearly involved in the formation of reductive aromas and shared th…

Hydrogen sulfide[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritionchemistry.chemical_elementMethanethiolWineperceptionstoragechemistry.chemical_compound0404 agricultural biotechnologyvolatile sulfur-compoundsVolatile Sulfur Compoundshydrogen-sulfideOrganic chemistryFood scienceassimilable nitrogenAromaReductionspanish red winesWinebiologydescriptive analysis04 agricultural and veterinary sciencesWine faultdimethyl sulfide precursorbiology.organism_classification040401 food scienceSulfurchemistryOdoraromaqualityRATA analysisDimethyl sulfideDescriptive analysis[SDV.AEN]Life Sciences [q-bio]/Food and NutritionFood Science
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[Bis(dimethylsulphoxide) protium][trans-bisdimethylsulphoxidetetrachloroiridate(III)]

1988

Abstract [(DMSO)2H]trans-[IrCl4(DMSO)2] (DMSO = dimethylsulphoxide) has been structurally characterized. The hydrogen bonded cation [DMSOHDMSO]+ has a very short OHO bond distance (2.405 A) which compares well with that in the known rhodium analogue. The two DMSO ligands are trans on iridium and coordinate via the sulphur atoms. Earlier work had assigned the cis structure to the anion in this compound.

HydrogenChemistryStereochemistrychemistry.chemical_elementNuclear magnetic resonance spectroscopyCrystal structureMedicinal chemistrySulfurRhodiumInorganic ChemistryBond lengthX-ray crystallographyMaterials ChemistryIridiumPhysical and Theoretical ChemistryPolyhedron
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Hydrogen trapping: Synergetic effects of inorganic additives with cobalt Sulfide absorbers and reactivity of cobalt polysulfide

2012

International audience; The biphasic product CoS2 + Co(OH)(2) obtained by oxidation of cobalt sulfide is known to trap hydrogen at room temperature and low pressure according to a balanced reduction equation. Adding various inorganic compounds to this original absorber induces their reduction by hydrogen in the same conditions at a significant rate: (i) excess cobalt hydroxide is reduced to metallic cobalt; (ii) nitrate ions are reduced to ammonia; (iii) sulfur and sodium thiosulfate are reduced to H2S or NaHS and Na2S, respectively. Without a hydrogen absorber these inorganic compounds are not reduced by H-2, suggesting synergetic effects involving H-2 and the hydrogen absorber. Amorphous …

HydrogenCobalt hydroxideHydrogen sulfideInorganic chemistryDRINKING-WATEREnergy Engineering and Power Technologychemistry.chemical_elementCATALYSTS02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundREMOVALOXYSULFIDECHEMISTRYPolysulfideRenewable Energy Sustainability and the EnvironmentNITRITE021001 nanoscience & nanotechnologyCondensed Matter PhysicsSulfurCobalt sulfide0104 chemical sciencesCobalt extraction techniquesREDUCTIONFuel Technologychemistry13. Climate action0210 nano-technologyCobaltNITRATE
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A laboratory and theoretical study on the uptake of sulfur dioxide gas by small water drops containing hydrogen peroxide under laminar and turbulent …

2000

Abstract Laboratory experiments are described where the uptake of SO2 gas by water drops containing H2O2 is investigated where the taken up S(IV) is quickly converted to S(VI). During the gas uptake the drops were freely suspended at their terminal velocity by means of the Mainz vertical wind tunnel. Two series of experiments were carried out, one with a laminar air flow in the wind tunnel, one with a turbulent air flow in the wind tunnel. Afterwards, the experimental results were compared against model computations using the so-called fully mixed convective diffusion model. The experimental results for laminar flow conditions showed that the fully mixed convective diffusion model for the u…

HydrologyAtmospheric ScienceTerminal velocityTurbulenceChemistryAirflowSulfuric acidLaminar flowMechanicsPhysics::Fluid Dynamicschemistry.chemical_compoundAtmospheric chemistryPhysics::Atmospheric and Oceanic PhysicsSulfur dioxideGeneral Environmental ScienceWind tunnelAtmospheric Environment
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Chromo-Fluorogenic Detection of Nitroaromatic Explosives by Using Silica Mesoporous Supports Gated with Tetrathiafulvalene Derivatives

2013

[EN] Three new hybrid gated mesoporous materials (SN3-1, SNH2-2, and SN3-3) loaded with the dye [Ru(bipy)(3)](2+) (bipy=bipyridine) and capped with different tetrathiafulvalene (TTF) derivatives (having different sizes and shapes and incorporating different numbers of sulfur atoms) have been prepared. The materials SN3-1 and SN3-3 are functionalized on their external surfaces with the TTF derivatives 1 and 3, respectively, which were attached by employing the click chemistry reaction, whereas SNH2-2 incorporates the TTF derivative 2, which was anchored to the solid through an amidation reaction. The final gated materials have been characterized by standard techniques. Suspensions of these s…

INGENIERIA DE LA CONSTRUCCIONInorganic chemistrychemistry.chemical_elementmesoporous materials010402 general chemistrysensors01 natural sciencesCatalysisgated materialschemistry.chemical_compoundBipyridineNitroaromatic explosivesQUIMICA ORGANICAtetrathiafulvalenePolymer chemistryQUIMICA ANALITICAnitroaromatic explosivesAcetonitrileTtf derivatives010405 organic chemistryOrganic ChemistryQUIMICA INORGANICAGeneral ChemistryTetryloptical detectionSulfur0104 chemical scienceschemistryMesoporous materialTetrathiafulvalene
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Structure and function of the vacuolar Ccc1/VIT1 family of iron transporters and its regulation in fungi

2020

Iron is an essential micronutrient for most living beings since it participates as a redox active cofactor in many biological processes including cellular respiration, lipid biosynthesis, DNA replication and repair, and ribosome biogenesis and recycling. However, when present in excess, iron can participate in Fenton reactions and generate reactive oxygen species that damage cells at the level of proteins, lipids and nucleic acids. Organisms have developed different molecular strategies to protect themselves against the harmful effects of high concentrations of iron. In the case of fungi and plants, detoxification mainly occurs by importing cytosolic iron into the vacuole through the Ccc1/V…

ISC Iron-sulfur lusterCS Consistency scoreCcc1Ribosome biogenesisVacuoleReview ArticleYRE Yap response elementsBiochemistryBiotecnologia0302 clinical medicineStructural BiologyCg Candida glabrata0303 health sciencesMAFFT Multiple Alignment using Fast Fourier TransformNRAMP Natural Resistance-Associated Macrophage ProteinbiologyVIT1ChemistryMBD Metal-binding domainPlantsComputer Science ApplicationsBiochemistry030220 oncology & carcinogenesisCRD Cysteine-rich domainEg Eucalyptus grandisIron detoxificationBiotechnologyCBC CCAAT-binding core complexlcsh:BiotechnologySaccharomyces cerevisiaeVTL Vacuolar iron transporter-likeBiophysicsVIT Vacuolar iron transporterbZIP basic leucine-zipper03 medical and health sciencesFongsLipid biosynthesislcsh:TP248.13-248.65GeneticsFe IronIron transportTranscription factor030304 developmental biologyComputingMethodologies_COMPUTERGRAPHICSBLOSUM BLOcks SUbstitution MatrixTMD Transmembrane domainML Maximum-likelihoodIron regulationDNA replicationFungibiology.organism_classificationYeastYeastMetabolic pathwayH HelixHap Heme activator proteinVacuoleROS Reactive oxygen speciesFerroComputational and Structural Biotechnology Journal
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Complexes of organometallic compounds

1974

Abstract Novel complexes RClSntrid, where R is Me, Ph, n-Oct, and trid 2− are dianions of tridentate “planar” ligands with ONO and SNO donor atoms, were synthesized and investigated in the solid state by infrared and Mossbauer spectroscopy. Possible configurations are discussed; polymeric trigonal bipyramidal structures seem to occur, although five-coordinated monomers as well as octahedral dimers (via oxygen or sulfur bridges) are not excluded.

InfraredStereochemistryOrganic Chemistrychemistry.chemical_elementBiochemistryOxygenSulfurInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundCrystallographyMonomerOctahedronchemistryMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryGroup 2 organometallic chemistryJournal of Organometallic Chemistry
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Isomerism and Ligand Rearrangement within the cyclo-P2S3 Middle Deck in Dimolybdenum Triple-Decker Complexes

2009

The molecular structure of [Cp*2Mo2P2S3] (1; Cp* = η5-C5Me5) has been reinvestigated. In DFT studies a series of various positional isomers A−E have been calculated for the model complex [(C5H5)2Mo2P2S3]. The energetically favored isomer [Cp*2Mo2(μ,η2:2-PS)2(μ-S)] (1B) reacts with W(CO)5THF to give [Cp*2Mo2P2S3·W(CO)5] (2). X-ray diffraction analysis of 2 confirms the presence of two η2:2-PS dumbbells and one singly bridging sulfur ligand, the W(CO)5 fragment being coordinated at one of the P atoms. Arrangement B is also found in the structure of the diadduct [Cp°2Mo2P2S3{W(CO)5}2] (3; Cp° = t-BuMe2C5H2), which is more stable than its Cp* analogue. 31P solid-state MAS NMR spectroscopic stud…

Inorganic ChemistryChemistryLigandStereochemistryOrganic ChemistryStructural isomerCluster (physics)Solid-stateMoleculePhysical and Theoretical ChemistrySulfur ligandOrganometallics
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