Search results for " Liquid"

showing 10 items of 3037 documents

Cathodic behaviour of dicationic imidazolium bromides: the role of the spacer

2019

The cathodic reduction of dicationic imidazolium bromides, whose spacer is either an aliphatic chain or a xylyl group, leads to the formation of the corresponding N-heterocyclic carbenes (NHCs), which were isolated as the corresponding thiones, after reaction with elemental sulfur. The behaviour of the dications was compared with the corresponding monocations. The behaviour of dicarbenes depends on the nature of the spacer. This study evidenced that dicarbenes deriving from xylyl dications are less stable than the corresponding aliphatic ones (giving lower yields in thiones), due to a debenzylation reaction. On the other hand, the yields in thiones starting from aliphatic dications are high…

chemistry.chemical_compoundchemistryimidazolium dications; cathodic reduction; imidazole-2-thione; N-heterocyclic carbene; electroorganic chemistryIonic liquidInorganic chemistryElectrochemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologieSettore CHIM/06 - Chimica OrganicaCyclic voltammetryCatalysisionic liquids electrochemistry cyclic voltammetryCathodic protection
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Donor-Stabilized Phosphenium Adducts as New Efficient and Immobilizing Ligands in Palladium-Catalyzed Alkynylation and Platinum-Catalyzed Hydrogenati…

2009

The straightforward synthesis of a new donor-stabilized phosphenium ligand 3d by addition of bromodifurylphosphine to 1,3-dimethylimidazolium-2-carboxylate 1 is described. The obtained ligand exhibits a very strong π-acceptor character, comparable to that of triphenyl phosphite [P(OPh) 3 ] or of tris-halogenophosphines, with a v CO (A 1 ) at 2087 cm ―1 for its nickel tricarbonyl complex. This ligand, as well as the related 3a which was obtained from chlorodiphenylphosphine, were tested in palladium-catalyzed aryl alkynylation and in the platinum-catalyzed selective hydrogenation of chloronitrobenzenes, both in an ionic liquid phase. In C―C bond cross-coupling we observed that the increase o…

chemistry.chemical_element010402 general chemistryPhotochemistry01 natural sciencesCatalysisionic liquids[ CHIM.CATA ] Chemical Sciences/Catalysischemistry.chemical_compoundphosphenium saltsPolymer chemistryplatinumTriphenylphosphineComputingMilieux_MISCELLANEOUScatalyst recyclingcatalysis010405 organic chemistryLigandTriphenyl phosphite[CHIM.CATA]Chemical Sciences/CatalysisGeneral Chemistrypalladium0104 chemical scienceschemistryPhenylacetyleneIonic liquidPlatinumPalladiumAdvanced Synthesis & Catalysis
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Selective Cobalt over Nickel separation using neat and confined ionic liquids

2020

International audience; Task Specific Ionic Liquids (TSILs) generated by association between tetraalkylammonium cations and coordinating anions such as dicyanamide (Dca-) and thiocyanate (SCN-) were used for the selective separation of Ni(II) over Co(II). SCN-based TSIL presents higher extraction efficiency than the Dca-based one towards Co(II) (E = 85.4 % vs 54.6 %) and Ni (II) (E = 22 % vs 0.5%) but lower separation factors (βCo/Ni = 21 vs 239). Interestingly, extraction of Co(II) and Ni(II) in Dca-based TSIL can be enhanced using salts with chaotropic anions such as NaNO3 (E > 90 % for Co(II) and E = 85% for Ni(II)). The use of NaCl allows, moreover, the efficient separation of both ions…

chemistry.chemical_element02 engineering and technology010501 environmental sciences01 natural sciencesMetalchemistry.chemical_compoundTSIL[CHIM.GENI]Chemical Sciences/Chemical engineeringRecyclabilityNickelChemical Engineering (miscellaneous)IonogelWaste Management and DisposalDicyanamide0105 earth and related environmental sciencesAqueous solutionThiocyanateProcess Chemistry and TechnologyExtraction (chemistry)Cobalt021001 nanoscience & nanotechnologyPollutionNickelchemistryvisual_artIonic liquidvisual_art.visual_art_medium0210 nano-technologyCobaltNuclear chemistry
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All-trans to 11-cis retinol isomerization in nuclear membrane fraction from bovine retinal pigment epithelium

1991

Abstract Isomerization of all-trans to 11-cis retinol has been studied in a membrane preparation from the nuclear fraction of bovine retinal pigment epithelium. When the nuclear membrane preparation deprived of endogenous retinoids is incubated with 4·5 μ m all-trans-retinol, the mean value calculated for the isomerase activity is 1·32 nmol 11-cis retinol formed hr−1 mg protein−1. Simultaneous formation of all-trans and 11-cis retinyl esters is also observed in the nuclear preparation. When assayed under the same experimental condition, RPE 150 000 g post-nuclear sediment shows about 70% of the isomerase activity found in the nuclear membrane fraction. Treatment of the nuclear membrane frac…

cis-trans-IsomerasesIsomerase activityNuclear EnvelopeDetergentsIsomeraseCellular and Molecular Neurosciencechemistry.chemical_compoundIsomerismChapsmedicineAnimalsBovine serum albuminNuclear membraneIsomerasesPigment Epithelium of EyeVitamin AChromatography High Pressure LiquidCell NucleusChromatographybiologyRetinolCholic AcidsSensory SystemsEnzyme assayOphthalmologyMembranemedicine.anatomical_structureSolubilityBiochemistrychemistrybiology.proteinCattleExperimental Eye Research
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Città liquide: un manifesto-progetto per la nuova città creativa

2008

città liquidecittà creativaSettore ICAR/21 - Urbanisticawaterfront
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Increased conformational rigidity of humic substances by oxidative biomimetic catalysis

2005

A synthetic water-soluble meso-tetra(2,6-dichloro-3-sulfonatophenyl)porphyrinate of iron(III) chloride, Fe(TDCPPS)Cl, was employed as a biomimetic catalyst in the oxidative coupling of terrestrial humic materials. High-performance size-exclusion chromatography (HPSEC), solid-state nuclear magnetic resonance (CPMAS-(13)C NMR), electron paramagnetic resonance (EPR), and diffuse reflectance infrared spectroscopy (DRIFT) were used to follow conformational and structural changes brought about in different humic materials by the oxidative coupling. Increase in apparent weight-average molecular weight (Mw(a)) occurred invariably for all humic substances with the oxidative polymerization catalyzed …

conformationMagnetic Resonance SpectroscopySpectrophotometry InfraredPolymers and PlasticsDiffuse reflectance infrared spectroscopy (DRIFT)Biomimetic materialsaromatic compoundgel permeation chromatographyMolecular ConformationPhotochemistryIron compoundslaw.inventionPolymerizationenvironmental managementcovalent bondlawSize exclusion chromatographyBiomimetic catalysisBiomimeticsMaterials ChemistryOrganic chemistryHumic acidElectron paramagnetic resonanceInfrared spectroscopyChromatography High Pressure Liquidchemistry.chemical_classificationSettore CHIM/03 - Chimica Generale e InorganicaCarbon IsotopesChromatographyindustryCatalystsChemistrytetra(2articleelectrophoretic mobilitybiomimetic materialNuclear magnetic resonance spectroscopyunclassified drugConformationsacetic acidpriority journalCovalent bondSpectrophotometrySynthesis (chemical)High Pressure Liquidtechnology6 dichloro 3 sulfonatophenyl)porphyrinic acid derivativeInfraredOxidation-Reductionmolecular stabilityHumic materialsoxidationSettore AGR/13 - Chimica AgrariaSupramolecular chemistryBioengineeringcomplex mixturesCatalysisCatalysisdiffuse reflectance spectroscopyhumic substanceBiomaterialsalkyl etherElectron spin resonance spectroscopycomplex formationParticle SizeNuclear magnetic resonance spectroscopyHumic Substancesfree radicalbiomimetic oxidative humicelectron spin resonanceHigh performance size exclusion chromatography (HPSEC)ferrous chloridemolecular weightsolid statecarbon nuclear magnetic resonancePolymerizationSolubilitychemical structureOxidative coupling of methaneCatalysts; Conformations; Electron spin resonance spectroscopy; Infrared spectroscopy; Iron compounds; Nuclear magnetic resonance spectroscopy; Oxidation; Polymerization; Size exclusion chromatography; Solubility; Synthesis (chemical); Biomimetic catalysis; Diffuse reflectance infrared spectroscopy (DRIFT); High performance size exclusion chromatography (HPSEC); Humic materials; Biomimetic materials; acetic acid; alkyl ether; aromatic compound; biomimetic material; ferrous chloride; free radical; tetra(26 dichloro 3 sulfonatophenyl)porphyrinic acid derivative; unclassified drug; article; carbon nuclear magnetic resonance; catalysis; catalyst; chemical structure; complex formation; conformation; covalent bond; diffuse reflectance spectroscopy; electron spin resonance; electrophoretic mobility; environmental management; gel permeation chromatography; humic substance; industry; molecular stability; molecular weight; oxidation; polymerization; priority journal; solid state; technology; Biomimetics; Carbon Isotopes; Catalysis; Chromatography High Pressure Liquid; Electron Spin Resonance Spectroscopy; Humic Substances; Magnetic Resonance Spectroscopy; Molecular Conformation; Oxidation-Reduction; Particle Size; Spectrophotometry Infraredcatalyst
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Heparan sulfate levels in mucopolysaccharidoses and mucolipidoses.

2004

Glycosaminoglycans are accumulated in both mucopolysaccharidoses (MPS) and mucolipidoses (ML). MPS I, II, III and VII and ML II and ML III patients cannot properly degrade heparan sulphate (HS). In spite of the importance of HS storage in the metabolic pathway in these diseases, blood and urine HS levels have not been determined systematically using a simple and economical method. Using a new ELISA method using anti-HS antibodies, HS concentrations in blood and urine were determined in MPS and ML II and ML III patients. HS concentrations were determined in 156 plasma samples from MPS I (n = 23), MPS II (n = 26), MPS III (n = 24), MPS IV (n = 62), MPS VI (n = 5), MPS VII (n = 5), ML II (n = …

congenital hereditary and neonatal diseases and abnormalitiesAdolescentMucopolysaccharidosisEnzyme-Linked Immunosorbent AssayUrineSignificant elevationGlycosaminoglycanchemistry.chemical_compoundMucolipidosesGeneticsmedicineHumansElisa methodskin and connective tissue diseasesChildGenetics (clinical)Chromatography High Pressure LiquidGlycosaminoglycansDose-Response Relationship DrugChemistryHeparinInfant Newbornnutritional and metabolic diseasesMucolipidosesInfantHeparan sulfateMucopolysaccharidosesmedicine.diseaseMolecular biologyDose–response relationshipBiochemistryChemistry ClinicalChild PreschoolHeparitin SulfateBiomarkersJournal of inherited metabolic disease
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Ethical Versus Conventional Banking: A Case Study

2018

The 2008 financial crisis has changed the structure of banking, generating public distrust in the conventional financial system. An alternative has emerged as a result of this lack of confidence. This alternative is known as ethical banking. A growing number of investors, asset managers, and financial intermediaries have incorporated sustainability considerations into their business practices. This paper discusses the origins of ethical banking and describes its primary characteristics. The goal is to determine whether ethical banking can be as profitable as conventional banking despite only investing in projects based on social values. A comparative analysis is performed to identify differ…

conventional bankingTransparency (market)media_common.quotation_subjectGeography Planning and DevelopmentFinancial intermediarylcsh:TJ807-830social valueslcsh:Renewable energy sourcesFinancial systemManagement Monitoring Policy and Law:CIENCIAS ECONÓMICAS [UNESCO]Profit (economics)0502 economics and businessBalance sheetlcsh:Environmental sciencesmedia_commonlcsh:GE1-350050208 financeDistrustRenewable Energy Sustainability and the Environmentsocial economylcsh:Environmental effects of industries and plants05 social sciencesUNESCO::CIENCIAS ECONÓMICASMarket liquidityethical bankinglcsh:TD194-195SustainabilityFinancial crisissocial bankingBusiness050203 business & managementSustainability
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The first catalytic method for Heck alkynylation of unactivated aryl bromides (copper-free Sonogashira) in an ionic liquid: 1 mol-percent palladium/t…

2007

Herein we report the studies of Heck alkynylation (copper-free Sonogashira) with aryl halides (I, Br, Cl) employing various metallic precursors, tertiary phosphanes and bases in [BMIM][BF4] as the solvent. As a result, we provide the first method that allows the coupling of a large array of substrates, either activated or deactivated bromides in an ionic liquid. Furthermore, the system of highest efficiency is unexpectedly the simplest and cheaper combination that employs [Pd(η3-C3H5)Cl]2/PPh3 at only a 1 mol-% loading with pyrrolidine as the base and in the absence of a copper salt. The coupling of sterically and electronically deactivated bromides bearing different functional groups to ar…

copper-free SonogashiraIonic bondingchemistry.chemical_elementSonogashira coupling010402 general chemistry01 natural sciences7. Clean energyHeck alkynylationPyrrolidineCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/CatalysisHeck reactiontriphenylphosphaneOrganic chemistryPhysical and Theoretical ChemistryAlkylComputingMilieux_MISCELLANEOUSionic liquidchemistry.chemical_classificationcatalysis010405 organic chemistryArylOrganic ChemistryGeneral Medicine[CHIM.CATA]Chemical Sciences/CatalysispalladiumCombinatorial chemistrymethylimidazolium0104 chemical sciencesSolventchemistryIonic liquidPalladium
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Poly[1-ethyl-3-methylimidazolium [tri-μ-isothiocyanato-manganate(II)]]

2019

The title compound, {(C9H11N2)[Mn(NCS)3]} n , has been obtained as a side product of the salt metathesis reaction of 1-ethyl-3-methylimidazolium bromide, (EMIm)Br, and K2[Mn(NCS)4]. The structure consists of discrete 1-ethyl-3-methylimidazolium cations and an anionic two-dimensional network of manganese(II)-based complex anions, interconnected by thiocyanate ions. Every Mn2+ ion is coordinated by three S atoms of three NCS− ions and three N atoms of further three NCS− ions in a meridional octahedral fashion.

crystal structurethiocyanateThiocyanateManganatechemistry.chemical_elementThio-02 engineering and technologyCrystal structureManganese010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesMedicinal chemistry0104 chemical scienceschemistry.chemical_compoundnetwork structurechemistryBromideIonic liquidmanganeselcsh:QD901-999Salt metathesis reactionlcsh:Crystallography0210 nano-technologyionic liquidIUCrData
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