Search results for "Ionic liquids"

showing 10 items of 186 documents

Functionalised diimidazolium salts: the anion effect on the catalytic ability

2016

The catalytic ability of some functionalised diimidazolium ionic liquids was tested using the Michael addition of malononitrile to t-chalcone as probe reaction. Diimidazolium salts characterized by the presence of 1-(1-imidazolylmethyl)-3,5-di-[1-(3-octylimidazolylmethyl)]benzene cation and differing in the anion structure were used. Both mono- and dianions were employed and among these some chiral anions generally used as organocatalysts were taken into account. Data collected were analysed both as function of ionic liquids structure and basicity, evaluated using the Hammett basicity function. Although the use of chiral anions did not allow performing a stereochemical control of the reacti…

010405 organic chemistryGeneral Chemical EngineeringSettore CHIM/06 - Chimica OrganicaGeneral Chemistry010402 general chemistry01 natural sciencesIonic Liquids Michael Reaction Base catalysis0104 chemical sciencesCatalysisIonchemistry.chemical_compoundchemistryIonic liquidPolymer chemistryMichael reactionOrganic chemistryBenzeneMalononitrileRSC Advances
researchProduct

Catalytic Carbonylative Double Cyclization of 2-(3-Hydroxy-1-yn-1-yl)phenols in Ionic Liquids Leading to Furobenzofuranone Derivatives

2019

A catalytic carbonylative double cyclization method for the synthesis of furo[3,4-b]benzofuran-1(3H)-ones is reported. It is based on the reaction between readily available 2-(3-hydroxy-1-yn-1-yl)phenols, CO, and oxygen carried out in the presence of catalytic amounts of PdI2 (1 mol %) in conjunction with KI (20 mol %) and 2 equiv of diisopropylethylamine at 80 degrees C for 24 h under 30 atm of a 1:4 mixture of CO-air. Interestingly, the process was not selective when carried out in classical organic non-nucleophilic solvents (such as MeCN or DME), leading to a mixture of the benzofurofuranone derivative and the benzofuran ensuing from simple cycloisomerization, whereas it turned out chemo…

010405 organic chemistryOrganic Chemistrychemistry.chemical_elementIonic LiquidsCarbonylationSettore CHIM/06 - Chimica Organica010402 general chemistry01 natural sciencesCarbonylation; Palladium; Cyclization; Ionic Liquids0104 chemical sciencesCatalysischemistry.chemical_compoundIonic liquids palladium catalyst benzofuranchemistryCyclizationIonic liquidOrganic chemistryPhenolsCarbonylationPalladiumPalladium
researchProduct

Imidazolium Based Ionic Liquids: A Promising Green Solvent for Water Hyacinth Biomass Deconstruction.

2018

Water hyacinth (WH) is a troublesome aquatic weed of natural and artificial water bodies of India and other tropical countries and causing severe ecological problems. The WH biomass is low in lignin content and contains high amount of cellulose and hemicellulose, making it suitable material for conversion into liquid fuels for energy production. This study highlighted that, how different imidazolium based ionic liquids (ILs) [1-alkyl-3-methylimidazolium bromide, [Cnmim]Br (n = 2, 4, 6, 8, and 10)] with tunable properties can be employed for the degradation of WH biomass. Different characterizations techniques, such as XRD, FT-IR, SEM, and DSC are used to unravel the interplay between ILs an…

0106 biological sciences020209 energyLignocellulosic biomassBiomass02 engineering and technology01 natural scienceslcsh:Chemistryionic liquidschemistry.chemical_compoundHydrolysisBromide010608 biotechnology0202 electrical engineering electronic engineering information engineeringLigninHemicelluloseCelluloselignocellulosic biomassOriginal ResearchGeneral Chemistrypretreatmentcrystallinity indexChemistrylcsh:QD1-999chemistryhydrolysisIonic liquidwater hyacinthNuclear chemistryFrontiers in chemistry
researchProduct

Room temperature ionic liquids based on cationic porphyrin derivatives and tetrakis(pentafluorophenyl)borate anion

2011

A series of 11 low melting ionic liquids based on meso-substituted A3B -porphyrins and A2B2-porphyrins containing one or two pyridyl substituents have been synthesized in high yields. Three of them are liquids at room temperature. All these porphyrinic salts were characterized by1H NMR,19F NMR, MALDI-TOF mass spectrometry, elemental analysis and UV-visible spectroscopy. The thermal properties and conductivity values of these salt derivatives have been also measured. A specific conductivity value of up to 4 mS.cm-1could be obtained for a compound having the counter-anion B(C6F5)4-.

A(2)B(2)-porphyrinsMediaInorganic chemistrySalt (chemistry)tetrakis(pentafluorophenyl)borate anionExtractionConductivityElectrochemistryCatalysisIonDscchemistry.chemical_compoundElectrolyteElectrochemistryMolten-Saltschemistry.chemical_classificationTgaCationic polymerizationGeneral ChemistryA(3)B-porphyrinsPorphyrinRT ionic liquidschemistrySensitized Solar-CellsIonic liquidProton NMRconductivity
researchProduct

Performance of amines as silanol suppressors in reversed-phase liquid chromatography

2016

In reversed-phase liquid chromatography, cationic basic compounds yield broad and asymmetrical peaks, as a result of their ionic interaction with the anionic free silanol groups present in the silica-based stationary phases (commonly derivatised with C18 groups). A simple way to improve the peak shape is the addition to the hydro-organic mobile phase of a reagent (usually called additive) with cationic character. This associates with the stationary phase to prevent the access of analytes to the free silanol groups. Cationic additives may interact electrostatically with the anionic silanols. The hydrophobic region of the additive may also associate with the alkyl chains bound to the stationa…

Adrenergic beta-AntagonistsIonic Liquids010402 general chemistry01 natural sciencesBiochemistryAnalytical Chemistrychemistry.chemical_compoundHexylamineEndcappingPhase (matter)BoratesAminesChromatography Reverse-PhaseChromatography010401 analytical chemistryOrganic ChemistryImidazolesCationic polymerizationGeneral MedicineReversed-phase chromatographySilanes0104 chemical sciencesSilanolchemistryIonic liquidPentylamineHydrophobic and Hydrophilic InteractionsJournal of Chromatography A
researchProduct

Suitability of 1-hexyl-3-methylimidazolium ionic liquids for the analysis of pharmaceutical formulations containing tricyclic antidepressants

2018

Abstract The reversed-phase chromatographic behaviour of six tricyclic antidepressants (amitryptiline, clomipramine, doxepin, imipramine, nortryptiline and maprotiline) was examined in this work with acetonitrile-water mobile phases, in the absence and presence of the ionic liquids 1-hexyl-3-methylimidazolium chloride and 1-hexyl-3-methylimidazolium tetrafluoroborate, which have interesting features for the separation of basic compounds, in terms of peak shape combined with reduced retention. Tricyclic antidepressants are low polarity drugs that strongly associate to the alkyl chains of conventional stationary phases. They are also positively charged in the usual working pH range (2–8) in r…

AmitriptylineDrug CompoundingIonic LiquidsNortriptyline02 engineering and technologyAntidepressive Agents Tricyclic01 natural sciencesBiochemistryChlorideAnalytical Chemistrychemistry.chemical_compoundLimit of DetectionBoratesmedicineSample preparationMaprotilineAcetonitrileAlkylchemistry.chemical_classificationChromatography Reverse-PhaseChromatography010401 analytical chemistryOrganic ChemistryImidazolesGeneral Medicine021001 nanoscience & nanotechnologyDoxepin0104 chemical scienceschemistryIonic liquidSpectrophotometry UltravioletDoxepin0210 nano-technologymedicine.drugTricyclicJournal of Chromatography A
researchProduct

Graphene and ionic liquids new gel paste electrodes for caffeic acid quantification

2015

Abstract Graphene/ionic liquids nanocomposite gels were synthesized by an electrochemical etching approach and fully characterized under a morphological and structural point of view. For this purpose, several analytical techniques were applied, as HR-TEM/EDX (High Resolution-Transmission Electron Microscopy/Energy Dispersive X-Ray Analysis); FE-SEM/EDX (Field Emission-Scanning Electron Microscopy/Energy Dispersive X-Ray Analysis); XPS (X-Ray Photoelectron Spectroscopy); FT-IR (Fourier Transform-Infrared Spectroscopy) and electrochemical techniques. After the characterization study, nanocomposite-gel paste electrodes were assembled, exhibiting a selective and specific detection toward the ca…

Analytical chemistrySurfaces Coatings and FilmAnti-oxidant agentsCondensed Matter PhysicAnti-oxidant agentIonic liquidElectrochemistrylaw.inventionNanocompositeschemistry.chemical_compoundX-ray photoelectron spectroscopylawgraphene Ionic liquids; nanocomposites; electrochemistry; caffeic acid; anti-oxidant agentsMaterials ChemistryElectrochemistryMoleculeElectrical and Electronic EngineeringInstrumentationSettore CHIM/02 - Chimica FisicaMaterials Chemistry2506 Metals and AlloySettore CHIM/03 - Chimica Generale e InorganicaDetection limitCaffeic acidNanocompositeNanocompositeGrapheneElectronic Optical and Magnetic MaterialMetals and AlloysCondensed Matter Physicsgraphene Ionic liquidsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIonic liquidschemistryChemical engineeringIonic liquidElectrode2506Graphene
researchProduct

Liquid structure of a water-in-salt electrolyte with a remarkably asymmetric anion

2021

Water-in-salt systems, i.e., super-concentrated aqueous electrolytes, such as lithium bis(trifluoromethanesulfonyl)imide (21 mol/kgwater), have been recently discovered to exhibit unexpectedly large electrochemical windows and high lithium transference numbers, thus paving the way to safe and sustainable charge storage devices. The peculiar transport features in these electrolytes are influenced by their intrinsically nanoseparated morphology, stemming from the anion hydrophobic nature and manifesting as nanosegregation between anions and water domains. The underlying mechanism behind this structure-dynamics correlation is, however, still a matter of strong debate. Here, we enhance the apol…

AnionsDYNAMICSLI+MOLECULAR-FORCE FIELDLOCAL-STRUCTUREWaterLithiumMolecular Dynamics Simulationmolecular-force field; particle meshewald; local-structure; ionic liquids; dynamics; viscosity; conductivity dependence; LI+PARTICLE MESH EWALElectrolytesIONIC LIQUIDSDEPENDENCECONDUCTIVITYVISCOSITY
researchProduct

Micro magnetofluidics: droplet manipulation of double emulsions based on paramagnetic ionic liquids

2013

The ability to control and manipulate discrete fluid droplets by magnetic fields offers new opportunities in microfluidics. A surfactant-free and easy to realize technique for the continuous generation of double emulsion droplets, composed of an organic solvent and a paramagnetic ionic liquid, is applied. The inner phase of the emulsion droplet consists of imidazolium-based ionic liquids with either iron, manganese, nickel or dysprosium containing anions which provide paramagnetic behaviour. The double emulsion droplets are dispersed in a continuous phase of FC-40. All substances - the organic phase, the paramagnetic ionic liquid and the continuous phase -are immiscible. The magnetic proper…

AnionsIronMicrofluidicsMicrofluidicsBiomedical EngineeringMixing (process engineering)Analytical chemistryIonic LiquidsBioengineeringBiochemistryPhysics::Fluid DynamicsMagneticsParamagnetismchemistry.chemical_compoundNickelPhase (matter)DysprosiumPhysics::Atomic and Molecular ClustersCoalescence (physics)ManganeseChemistryImidazolesGeneral ChemistryMagnetic fieldCondensed Matter::Soft Condensed MatterChemical engineeringMagnetIonic liquidEmulsionshuman activitiesLab on a Chip
researchProduct

Aryl azides formation under mild conditions: a kinetic study in some ionic liquid solutions.

2009

The kinetics of nucleophilic aromatic substitution of three nitrothiophene derivatives in different [1-butyl-3-methylimidazolium][N(3)]/ionic liquid binary mixtures was studied spectrophotometrically at 298 K. Ionic liquids differing for cation structure (imidazolium or pyrrolidinium) and for size, shape, and coordination ability of the anion ([BF(4)(-)], [PF(6)(-)], [SbF(6)(-)], and [NTf(2)(-)]) were used. Furthermore, in order to have a comparison with conventional organic solvents, the target reaction was also carried out in DMF solution at increasing concentration of NaN(3) or [bmim][N(3)]. Data collected show that the reaction occurs faster in DMF than in ionic liquid solution. Further…

ArylOrganic ChemistryInorganic chemistryionic liquids aryl azides kinetic measurementsLeaving groupSolventchemistry.chemical_compoundchemistryNucleophileNucleophilic aromatic substitutionHexafluorophosphateIonic liquidNucleophilic substitutionPhysical chemistryThe Journal of organic chemistry
researchProduct