Search results for "ionic liquid"

showing 10 items of 432 documents

Cross-Linked Polyamine from Imidazolium-Based Materials: A Simple Route to Useful Catalytic Materials

2018

Cross-linked polyamine-based materials were easily prepared by reduction of the corresponding cross-linked imidazolium-based materials with sodium borohydride in hot ethanol. Overall, the synthetic procedure is based on the polymerization of a suitable bis-vinylimidazolium salt with or without a suitable support, such as silica or silica-coated magnetic nanoparticles (γ-Fe2O3@SiO2), followed by reduction. This simple approach allows the synthesis of materials based on a network of secondary and tertiary amines. Materials were characterized by13C cross-polarization magic angle spinning NMR (13C CPMAS NMR), proton spin-lattice relaxation times in the rotating frame (T1ρH) and thermogravimet…

Heterogeneous catalysiHeterogeneous catalysisPolymersOrganic ChemistrySettore CHIM/06 - Chimica OrganicaIonic liquidPhysical and Theoretical ChemistryAminesPolymerAmineMaterials scienceIonic liquids
researchProduct

Sequential Suzuki/Asymmetric Aldol and Suzuki/Knoevenagel Reactions Under Aqueous Conditions

2012

Here we describe for the first time a sequential Suzuki/asymmetric aldol reaction. Such sequential approach was achieved through the combined use of an ionic liquid supported palladium catalyst and the organocatalyst trans-4-(2,2-diphenylacetoxy)proline. Suzuki and asymmetric aldol reactions were performed under aqueous conditions. The use of a palladium catalyst under basic conditions allowed also the first example of sequential Suzuki/Knoevenagel reaction. Reactions were carried out under aqueous conditions and products were isolated in good to high yields and, in the case of the Suzuki/aldol reaction, with diastereoselectivities up to 91:9 and enantioselectivities up to at least 99 %.

Homogeneous catalysiAqueous solutionSynthetic methodOrganic Chemistrychemistry.chemical_elementHomogeneous catalysisSettore CHIM/06 - Chimica Organicachemistry.chemical_compoundOrganocatalysiAldol reactionschemistrySuzuki reactionAldol reactionOrganocatalysisIonic liquidOrganic chemistryKnoevenagel condensationPhysical and Theoretical ChemistryPalladiumPalladium
researchProduct

Hybrid ionogels as potential antioxidant agents

In the present study, the influence of CNTs on the gelling ability of some carboxylate imidazolium gelators in ionic liquid solutions has been investigated.

Hybrid gels ionic liquids carbon nanotubes antioxidant activitySettore CHIM/06 - Chimica Organica
researchProduct

Ionic liquids as solvents for the Knoevenagel condensation: understanding the role of solvent–solute interactions

2015

The Knoevenagel condensation in ionic liquids has been demonstrated as a strongly solvent-dependent process. The objective of this study was to establish a simple and descriptive trend of solvent–solute interactions that favour the Knoevenagel condensation in ionic liquid media. The reaction between 4-(dimethylamino)benzaldehyde and ethyl cyanoacetate in several imidazolium- and pyrrolidinium-based ionic liquids and one ionic liquid mixture was studied. The rate constants were rationalised by studying the change in the 1H NMR chemical shift of representative starting materials in the ionic liquids and the measurement and consideration of the Kamlet–Taft descriptors for each solvent. The hyd…

Hydrogen bondChemistryGeneral ChemistryCatalysisSolventBenzaldehydechemistry.chemical_compoundReaction rate constantEthyl cyanoacetateIonic liquidMaterials ChemistryProton NMROrganic chemistryKnoevenagel condensationNew Journal of Chemistry
researchProduct

Lewis acid-catalyzed Beckmann rearrangement of ketoximes in ionic liquids

2009

Abstract The Beckmann rearrangement of five ketoximes was done in 17 different ionic liquids by using four Lewis acids. The effect of the type of cation and the type of anion in the ionic liquid on the rate of the rearrangement reaction and product composition is compared and discussed. The effects of the hydrophobicity and the hydrogen bonding ability of ionic liquids on the rearrangement of ketoximes were investigated, as well as the catalytical activity of the Lewis acids.

Hydrogen bondProcess Chemistry and TechnologyGeneral ChemistrySigmatropic reactionCatalysisIonCatalysischemistry.chemical_compoundchemistryBeckmann rearrangementIonic liquidPolymer chemistryOrganic chemistryRearrangement reactionLewis acids and basesCatalysis Communications
researchProduct

Structure and vibrational features of the protic ionic liquid 1,8-diazabicyclo[5.4.0]-undec-7-ene-8-ium bis(trifluoromethanesulfonyl)amide, [DBUH][TF…

2022

Abstract The Protic Ionic Liquid (PIL) formed by neutralization of the super-strong base 1,7-diazabicyclo[5.4.0]undec-7-ene (DBU) with the super-strong acid bis(trifluoromethanesulfonyl)-imide (TFSI), indicated as [DBUH][TFSI], has been investigated. Its chemical physical properties and structural features have been explored using a synergy of experimental and computational tools. Molecular Dynamics-rationalised X-ray diffraction patterns highlight the major role played by hydrogen bonding (HB) in affecting morphology in this PIL. A comparison between HB features in this and in related PILs has been presented, on the base of far-IR experiments and DFT analysis. Indications of a weaker HB in…

Hydrogen bondingMaterials scienceProtic Ionic LiquidBase (chemistry)DFT calculationMolecular Dynamics010402 general chemistry01 natural scienceschemistry.chemical_compoundDFT calculation; Far-ir spectroscopy; Hydrogen bonding; Molecular Dynamics; Protic Ionic Liquid; X-ray scatteringPhase (matter)Materials ChemistryFar-ir spectroscopyPhysical and Theoretical ChemistryConformational isomerismSpectroscopychemistry.chemical_classification010405 organic chemistryHydrogen bondX-ray scatteringCondensed Matter PhysicsAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsCrystallography18-Diazabicyclo[5.4.0]undec-7-enechemistryAbsorption bandIonic liquidDispersion (chemistry)Journal of Molecular Liquids
researchProduct

Bio-based 1,3-diisobutyl imidazolium hydrogen oxalate [iBu 2 IM](HC 2 O 4 ) as CO 2 shuttle

2017

International audience; This manuscript describes the using of biosourced L-valine, oxalic acid and glyoxal to produce a biobased imidazolium hydrogen oxalate [iBu(2)IM](HC2O4) which is converted to its related hydrogen carbonate salt by a simple electrolysis without using strong base. The addition of weak protic acids to the latter compound leads to a rapid and quantitative CO2 release with formation of the starting hydrogen oxalate salt or a new halide free bio-based ionic liquid [iBu(2)IM](AcO) which is able to adsorb reversibly the CO2 at room temperature. The protonation reactions, combined with electrolysis, could then be a promising alternative solution for storage and transport of C…

HydrogenOxalic acidInorganic chemistryHalideSalt (chemistry)chemistry.chemical_elementProtonation010402 general chemistrycarbon-dioxide01 natural sciences[ CHIM ] Chemical SciencesOxalatelaw.inventionefficientionic liquidschemistry.chemical_compoundlawstabilized phosphenium adductsEnvironmental Chemistry[CHIM]Chemical Scienceselectrochemical reductioncaptureacidsmethanolchemistry.chemical_classificationElectrolysis010405 organic chemistrycrystal-structurePollution0104 chemical scienceschemistrydimethyl-sulfoxideIonic liquid
researchProduct

Liquid structure and dynamics in the choline acetate:urea 1:2 deep eutectic solvent

2021

We report on the thermodynamic, structural, and dynamic properties of a recently proposed deep eutectic solvent, formed by choline acetate (ChAc) and urea (U) at the stoichiometric ratio 1:2, hereinafter indicated as ChAc:U. Although the crystalline phase melts at 36-38 degrees C depending on the heating rate, ChAc:U can be easily supercooled at sub-ambient conditions, thus maintaining at the liquid state, with a glass-liquid transition at about -50 degrees C. Synchrotron high energy x-ray scattering experiments provide the experimental data for supporting a reverse Monte Carlo analysis to extract structural information at the atomistic level. This exploration of the liquid structure of ChA…

IONIC LIQUIDMONTE-CARLO CHLORIDE SCATTERING WATER NANOSTRUCTURE NANOSCALEsynchrotron radiationeutecticnuclear relaxationX-ray scatteringhydrogen bondingNMRcholine acetatemolecular dynamicsX-rayMOLECULAR-DYNAMICScholinedeep eutectic solvents X-ray scattering synchrotron radiation NMR nuclear relaxation molecular dynamics choline acetateNUCLEAR-MAGNETIC-RESONANCE MOLECULAR-DYNAMICS IONIC LIQUID SFREE ANALYZER MONTE-CARLO CHLORIDE SCATTERING WATER NANOSTRUCTURE NANOSCALESFREE ANALYZERdeep eutectic solvent thermodynamic properties structural properties dynamic propertiesNUCLEAR-MAGNETIC-RESONANCEdeep eutectic solventsSettore CHIM/02 - Chimica Fisica
researchProduct

Experimental and theoretical studies on polar Diels–Alder reactions of 1-nitronaphathalene developed in ionic liquids

2013

The reactions between 1-nitronaphthalene 1 and two nucleophilic dienes, Danishefsky´s diene 2 and 1-trimethylsilyloxy-1,3-butadiene 3, to yield phenanthrenols 7 and 8 developed in protic and aprotic ionic liquids (ILs) with an imidazolium cation base permit to conclude that the reactions occur in better experimental conditions than in molecular solvents. The yields obtained with protic ILs are better than those observed with aprotic ILs. In this sense, the higher yields obtained with aprotic ILs, (working at 60ºC, 48 h) are comparable with the lower yields observed in protic ILs (60 ºC, 24 h). DFT calculations for the reaction of 1-nitronaphthalene 1 with diene 3, in the absence and in the …

IONIC LIQUIDTetrafluoroborateDieneGeneral Chemical EngineeringSolvationCiencias QuímicasGeneral ChemistryNitrosoPhotochemistryNITRONAPHTHALENESDFTDIELS-ALDERCatalysischemistry.chemical_compoundQuímica OrgánicachemistryNucleophileComputational chemistryIonic liquidSolvent effectsCIENCIAS NATURALES Y EXACTAS
researchProduct

Probing the chemical interaction between iridium nanoparticles and ionic liquid by XPS analysis

2009

Abstract In situ X-ray photoelectron spectroscopy analysis of Ir(0) nanoparticles (1.6 ± 0.3 nm) dispersed in imidazolium ionic liquid (EMI.EtSO4) shows evidences of the effective interaction between the metallic clusters and the surrounding liquid. By monitoring the C 1s signal of the ionic liquid one observes a change of the binding energy in one of its components (C2) when in the presence of Ir nanoparticles. This result was corroborated by isotope labeling experiments.

In situIsotopeBinding energyInorganic chemistryGeneral Physics and AstronomyNanoparticlechemistry.chemical_elementChemical interactionchemistry.chemical_compoundchemistryX-ray photoelectron spectroscopyIonic liquidIridiumPhysical and Theoretical ChemistryChemical Physics Letters
researchProduct