Search results for "Azolium"

showing 10 items of 148 documents

Design of POSS-Imidazolium Supported Hybrids for the Conversion of Carbon Dioxide into Cyclic Carbonates

2018

Nowadays, the design of heterogeneous catalysts for the conversion of CO2 into useful chemical products is attracting the attention of the scientific community. The catalytic processes involving carbon dioxide as C1 feedstock are of growing interest for the sustainable development.1 The synthesis of cyclic carbonates by coupling CO2 with epoxides is one of the most interesting pathways for the conversion of carbon dioxide in terms of both atom economy and final products applications. Moreover, ionic liquids emerged as one of the most active catalysts for the production of cyclic carbonates starting from CO2 and epoxides.2 Herein, a series of heterogeneous catalytic systems bearing imidazoli…

carbon dioxide conversionheterogeneous catalysiSettore CHIM/06 - Chimica Organicacyclic carbonatesimidazolium saltPOSS
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Imidazolium Based Cross-Linked Nanostructures from POSS molecular bricks for the Efficient Conversion of Carbon Dioxide

2019

Polyhedral oligomeric silsesquioxanes (POSS) have been employed as molecular bricks for the synthesis of imidazolium cross-linked networks as heterogeneous catalyst for the conversion of carbon dioxide into cyclic carbonates via reaction with epoxides. Two hybrid materials with different nucleophilic species (bromide and iodide) have been prepared and characterized by means of elemental analysis, 13C and 29Si solid state NMR, thermogravimetric analysis and IR spectroscopy. The solids were tested as the sole catalyst under metal- and solvent-free reaction conditions showing full selectivity toward the formation of cyclic carbonates and outstanding productivity values. Several epoxides were r…

carbon dioxide conversionheterogeneous catalysiSettore CHIM/06 - Chimica Organicacyclic carbonatesimidazolium saltPOSS
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Materiali ibridi a base di POSS-Imidazolio per la conversione della CO2 in carbonati ciclici

2018

Lo sviluppo di catalizzatori per i processi di conversione della CO2 è una tematica che sta rivestendo un ruolo di rilevante importanza in ambito non soltanto accademico ma anche industriale grazie alla possibilità di trasformare un rifiuto, quale il diossido di carbonio, in una vasta gamma di prodotti. Nel presente lavoro, nuovi materiali ibridi costituiti da silsesquiossani poliedrici oligomerici (POSS) supportati su silice e funzionalizzati con sali di imidazolio sono stati progettati per la fissazione della CO2. 1 Tutti i solidi sono stati ampiamente caratterizzati e testati per la sintesi di carbonati ciclici tramite reazione tra CO2 ed epossidi in condizioni di reazione solvent-free (…

carbon dioxide conversionhybrid materialheterogeneous catalysiSettore CHIM/06 - Chimica Organicacyclic carbonatesimidazolium saltPOSS
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Materiali catalitici a base di nanoparticelle di palladio immobilizzate su nanoforme di carbonio

2019

carbon nanostructurecarbon nanohornpalladium catalysihybrid materialcarbon nanotubeC-C cross-couplingimidazolium salt
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Supramolecular complexes formed by dimethoxypillar[5]arenes and imidazolium salts: A joint experimental and computational investigation

2017

To gain more insights into the factors acting on the stability of complexes formed by pillar[5]arenes, we investigated the interaction of dimethoxypillar[5]arene with some 1-(n-alkyl)-3-(9-anthracenylmethyl)-imidazolium based organic salts. In particular, we used salts differing in not only the anion nature ([Cl−], [BF4−], [NTf2−] and [SbF6−]) and alkyl chain length (butyl, octyl and dodecylimidazolium derivatives), but also the presence of a hydrogenated or fluorinated tail (octyl and perfluorooctylimidazolium derivatives). Host–guest systems were analysed in solution, solid state and gas phase, using a combined approach of different techniques like fluorescence, 1H NMR, ESI-MS, DSC and DF…

chemistry.chemical_classification010405 organic chemistryChemistryInorganic chemistrySupramolecular chemistrySolid-stateGeneral ChemistrySettore CHIM/06 - Chimica Organica010402 general chemistry01 natural sciencesFluorescenceCatalysis0104 chemical sciencesIonSolventimidazolium salt.CrystallographyChain lengthMaterials ChemistryProton NMRpillar[5]areneAlkylSupramoleculr chemistry
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Aggregation processes of perylene bisimide diimidazolium salts

2015

The supramolecular aggregation of three diimidazolium- functionalized perylene bisimides, differing in the alkyl chain length was investigated. These salts form aggregates in solvents like chloroform, dichloromethane, and glycerol. Solvent-, concentration-, and temperature-dependent spectroscopic studies were carried out, evidencing the occurrence of an isodesmic, enthalpy-driven aggregation process, underpinned by p–p stacking and hydrogen bonding. Moreover, dynamic light scattering (DLS) measurements and SEM images revealed that these salts aggregate in chloroform into elongated structures.

chemistry.chemical_classificationIsodesmic reactionChloroformOrganic ChemistrySupramolecular chemistryGeneral ChemistrySettore CHIM/06 - Chimica OrganicaCatalysisSolventchemistry.chemical_compoundchemistryDynamic light scatteringPolymer chemistryOrganic chemistrydiimidazolium salts perylene bisimide self-assemblyAlkylPeryleneDichloromethaneSettore CHIM/02 - Chimica Fisica
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Self-assembly of fluorescent diimidazolium salts: tailor properties of the aggregates changing alkyl chain features

2016

Searching for new fluorescent organic salts to be used in biomedical and electrochemical field, we conjugated properties of imidazolium salts with the ones of naphthalene diimide core and we obtained some N,N′-bis-(1-alkyl-3-propylimidazolium)naphthalene diimide diiodides. We took into account alkyl chains going from hexyl to dodecyl, as well as hydrogenated and fluorinated alkyl tails. After determination of their thermal behaviour by differential scanning calorimetry, concentration-, and temperature-dependent spectroscopic studies (UV-vis and fluorescence) were performed evidencing the occurrence of isodesmic and enthalpy-driven self-assembly processes. Properties of aggregates were also …

chemistry.chemical_classificationIsodesmic reactionScanning electron microscopeGeneral Chemical EngineeringDiimidazolium salts self-assembly H-aggregatesSettore CHIM/06 - Chimica Organica02 engineering and technologyGeneral ChemistryConjugated system010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesFluorescenceFluorescence spectroscopy0104 chemical sciencesDifferential scanning calorimetrychemistrySelf-assembly0210 nano-technologyAlkylRSC Advances
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π-Conjugated diimidazolium salts: rigid structure to obtain organized materials.

2015

Phenylene ethynylene based diimidazolium salts differing in the alkyl chain length borne on the imidazolium ion and anion nature were synthesized. Their properties were studied both in solution and in the solid state. Salts obtained were able to aggregate in organic solvent solution. Aggregate formation was studied by performing concentration dependent measurements using UV-vis, fluorescence and Resonance Light Scattering. Furthermore, features of the aggregates were also investigated in the solid state by means of fluorescence and Scanning Electron Microscopy measurements. Finally, Density Functional Theory calculations were performed to obtain insights into the interaction geometry in the…

chemistry.chemical_classificationdiimidazolium salts self-assembly DFT investigationChemistryGeneral Physics and AstronomySalt (chemistry)Settore CHIM/06 - Chimica OrganicaConjugated systemResonance (chemistry)IonSolventPhenylenePhysical chemistryOrganic chemistryDensity functional theoryPhysical and Theoretical ChemistryAlkylSettore CHIM/02 - Chimica FisicaPhysical chemistry chemical physics : PCCP
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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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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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