0000000001309941

AUTHOR

Andrea Mele

showing 20 related works from this author

Solution and solid-state studies on the halide binding affinity of perfluorophenyl-armed uranyl–salophen receptors enhanced by anion–π Interactions

2016

The enhancement of the binding between halide anions and a Lewis acidic uranyl-salophen receptor has been achieved by the introduction of pendant electron- deficient arene units into the receptor skeleton. The association and the occurrence of the elusive anion-p interaction with halide anions (as tetrabutylammonium salts) have been demonstrated in solution and in the solid state, providing unambiguous evidence on the interplay of the concerted interactions responsible for the anion binding.

anion–π interactions; halides; host–guest systems; lewis acid–base interactions; uranyl–salophen; chemistry (all)Solid-stateHalide010402 general chemistry01 natural sciencesCatalysisIonUranyl salophenPolymer chemistryOrganic chemistryReceptorAnion bindingta116Uranyl-salphenlewis acid–base interactionsanion–π interactionsuranyl–salophen010405 organic chemistryChemistryOrganic Chemistryhost–guest systemsGeneral Chemistryinteractions0104 chemical sciencesuranyl-salophen receptorshalideschemistry (all)halide recognitionanions
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Self-assembly and intra-cluster reactions of erbium and ytterbium bis(2-ethylhexyl)sulfosuccinates in the gas phase

2014

RATIONALE The study of surfactant organization in vacuum allows surfactant–surfactant interaction to be unveiled in the absence of surrounding solvent molecules. Knowledge on their chemical-physical properties may also lead to the definition of more efficient gas-phase carriers, air-cleaning agents and nanoreactors. In addition, the presence of lanthanide-group ions adds unique photochemical properties to surfactants. METHODS The structural features, stability and fragmentation patterns of charged aggregates formed by lanthanide-functionalized surfactants, ytterbium and erbium bis(2-ethylhexyl)sulfosuccinate ((AOT)3Yb and (AOT)3Er), have been investigated by electrospray ionization mass spe…

chemistry.chemical_classificationAggregation numberChemistryElectrospray ionizationOrganic ChemistryAnalytical chemistryMass spectrometryPhotochemistryAnalytical ChemistrySupramolecular assemblyMassFragmentation (mass spectrometry)MoleculeSpectroscopyAlkylRapid Communications in Mass Spectrometry
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Chiroptical Phenomena in Reverse Micelles: The Case of (1R,2S)-Dodecyl (2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium Bromide (DMEB)

2014

(1R,2S)-Dodecyl(2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium bromide (DMEB) aggregates dispersed in carbon tetrachloride have been investigated by Fourier transform infrared (FT-IR), vibrational circular dichroism (VCD) and 1H nuclear magnetic resonance (NMR) spectroscopy at various surfactant concentration and water-to-surfactant molar ratio. Experimental data indicate that, even at the lowest investigated concentration and in absence of added water, DMEB molecules associate in supramolecular assemblies. At higher DMEB concentration the aggregates can confine water molecules, making it plausible to think that DMEB form reverse micelles and that water molecules are quite uniformly dist…

PharmacologyHydrogen bondOrganic ChemistrySupramolecular chemistryPhotochemistryMicelleCatalysisAnalytical Chemistrychemistry.chemical_compoundchemistryBromideDrug DiscoveryVibrational circular dichroismProton NMRMoleculeOrganic chemistryChirality (chemistry)SpectroscopyChirality
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Direct experimental observation of mesoscopic fluorous domains in fluorinated room temperature ionic liquids

2017

Fluorinated room temperature ionic liquids (FRTILs) represent a class of solvent media that are attracting great attention due to their IL-specific properties as well as features stemming from their fluorous nature. Medium-to-long fluorous tails constitute a well-defined apolar moiety in the otherwise polar environment. Similarly to the case of alkyl tails, such chains are expected to result in the formation of self-assembled fluorous domains. So far, however, no direct experimental observation has been made of the existence of such structural heterogeneities on the nm scale. We report here the first experimental evidence of the existence of mesoscopic spatial segregation of fluorinated dom…

General Physics and AstronomyNanotechnology02 engineering and technologyNeutron scattering010402 general chemistryLAYER CAPACITOR APPLICATIONS; PERFLUOROALKYL SIDE-CHAINS; ANGLE NEUTRON-SCATTERING; PARTICLE MESH EWALD; PHYSICOCHEMICAL PROPERTIES; FORCE-FIELD; CATION SYMMETRY; STRUCTURAL-CHARACTERIZATION; AMMONIUM TETRAFLUOROBORATE; MOLECULAR SIMULATION01 natural sciencesionic liquidsionic liquids SANS nanostructuration fluorous domains NMR NOEchemistry.chemical_compoundMolecular dynamicsPhysics and Astronomy (all)nanostructurationMoietyPhysical and Theoretical ChemistryAlkylNOEchemistry.chemical_classificationfluorous domainsMesoscopic physicsSANSNuclear magnetic resonance spectroscopy021001 nanoscience & nanotechnologyNMR0104 chemical sciencesfluorinated ionic liquids neutron scattering x-ray diffraction structurechemistryChemical physicsIonic liquidPolar0210 nano-technology
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Spectroscopic and Structural Investigation of the Confinement of D and L Dimethyl Tartrate in Lecithin Reverse Micelles

2009

The confinement of D and L dimethyl tartrate in lecithin reverse micelles dispersed in cyclohexane has been investigated by FT-IR, polarimetry, electronic and vibrational circular dichroism (ECD and VCD), 1H NMR, and small-angle X-ray scattering (SAXS). Measurements have been performed at room temperature as a function of the solubilizate-to-surfactant molar ratio (R) at fixed lecithin concentration. The analysis of experimental data indicates that the dimethyl tartrate molecules are solubilized within reverse micelles in proximity to the surfactant head groups in the same way for the D and L forms. The encapsulation of dimethyl tatrate within lecithin reverse micelles involves changes in i…

lecithin dimethyl tartrate FT-IR polarimetry circular dichroism NMR SAXSfood.ingredientCyclohexanemicellesTartrateLecithinMicellePolyethylene Glycolschemistry.chemical_compoundfoodLecithinsMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryTartratesModels StatisticalDose-Response Relationship DrugChemistry PhysicalViscosityChemistrySmall-angle X-ray scatteringTemperaturetechnology industry and agricultureElasticitySurfaces Coatings and FilmslecithinModels ChemicalSpectrophotometryVibrational circular dichroismMicellar solutionsPhosphatidylcholinesProton NMRPhysical chemistrylipids (amino acids peptides and proteins)Rheologydimethyl tartrate
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Photocatalysis in dimethyl carbonate green solvent: degradation and partial oxidation of phenanthrene on supported TiO2

2014

Dimethyl carbonate (DMC) is here proposed – for the first time – as a green organic solvent for photocatalytic synthesis. In this work, the photocatalytic partial oxidation of phenanthrene in dimethyl carbonate (DMC) by using anatase TiO2 as the photocatalyst is described as paradigmatic example of a green synthetic process starting from polycyclic aromatic hydrocarbons (PAHs). For comparison, the same reaction carried out also in ethanol, 1-propanol or 2-propanol is reported. The use of DMC as the solvent allowed us to achieve 19% and 23% selectivity towards 9-fluorenone and 6H-benzo[c]chromen- 6-one, respectively. The proposed approach may represent both a new green synthetic process and …

Settore ING-IND/24 - Principi Di Ingegneria ChimicaAnataseGeneral Chemical EngineeringGeneral ChemistryPhenanthreneaaSolventchemistry.chemical_compoundchemistryPhotocatalysisDegradation (geology)Organic chemistrySettore CHIM/07 - Fondamenti Chimici Delle TecnologiePartial oxidationDimethyl carbonatephenanthrene supported TiO2 partial oxidation green solventSelectivityRSC Adv.
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Orientation and molecular contacts of melatonin confined into AOT and lecithin reversed micellar systems

2008

Abstract The state of increasing amounts of melatonin (MLT) confined in dry AOT or lecithin reversed micelles dispersed in CCl 4 has been investigated by UV–vis and 1 H NMR spectroscopies. The experimental results are consistent with MLT totally entrapped in reversed micelles, as a consequence of specific melatonin/surfactant interaction; the main driving force of the MLT solubilization in the core of reversed micelles is the establishment of H-bonding between the MLT NH groups (both indolic and amidic) and the head group of surfactants. The short contacts deduced from intermolecular NOEs are accounted for by favourable interactions between the surfactant's polar head and the H7–NH–H2 fragm…

food.ingredientIntermolecular forceReversed micelleLecithinNuclear Overhauser enhancementPhotochemistryLecithinMicelleMelatoninchemistry.chemical_compoundconfinement melatonin reverse micellesColloid and Surface ChemistryfoodchemistryPulmonary surfactantPhosphatidylcholineProton NMRmedicineOrganic chemistryMoleculeAOTMelatoninmedicine.drug
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Self-assembly in surfactant-based liquid mixtures: Bis(2-ethylhexyl)phosphoric acid/bis(2-ethylhexyl)amine systems

2010

Surfactant-based liquid mixtures constitute an interesting class of nanostructured materials with promising potential in specialized applications. Here, structural and conductometric properties of liquid mixtures composed of bis(2-ethylhexyl)amine (BEEA) and bis(2-ethylhexyl)phosphoric acid (HDEHP) have been thoroughly investigated with the aim to correlate structural features with system charge transport capability. The evolution of self-assembled local nanostructures with system composition has been investigated by FT-IR and XRD while the conductometric properties were probed by conventional AC complex impedance. Both pure components exhibit nano-segregation due to their amphiphilic natur…

ChemistryAnalytical chemistryInfrared spectroscopyConductivitySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistryPulmonary surfactantChemical engineeringAmphiphileX-ray crystallographyAmine gas treatingSelf-assemblyPhosphoric acidSurfactants Conducting materials Self-assembly Liquid mixturesSettore CHIM/02 - Chimica Fisica
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Gas-phase ion chemistry of protonated melatonin

2009

The gas-phase ion chemistry of protonated melatonin has been investigated by mass spectrometric (MS) techniques involving chemical ionisation, fast atom bombardment and electrospray ionisation. Either naturally-occurring or collision-induced decomposition experiments have been carried out using side chain tetra-deuterium-labelled derivatives, as well as the corresponding N–D derivatives obtained by exchange with D2O. The analysis of experimental results allows definite pathways for the formation of the ion at m/z 174 to be assigned and sheds some more light on the overall fragmentation pathways. Experiments on labelled derivatives evidenced H–D scrambling processes during fragmentation.

IonsElectrospraySpectrometry Mass Electrospray IonizationChemistryElectrospray ionizationInorganic chemistryDeuterium Exchange MeasurementProtonationmelatonin ESI/MS ESI/MS/MSion chemistryGeneral MedicineFast atom bombardmentPhotochemistryAtomic and Molecular Physics and OpticsIonFragmentation (mass spectrometry)AmmoniaTandem Mass SpectrometryAcetamidesProton affinityQuantum TheoryGasesProtonsSpectroscopyGas-phase ion chemistryMelatonin
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Guest-to-host proton transfer in melatonin-beta-cyclodextrin inclusion complex by ionspray, fast atom bombardment and tandem mass spectrometry.

2001

Ionspray (IS) and fast atom bombardment (FAB) positive ionization mass spectrometry (MS) of 1:1 β-cyclodextrin (β-CD)-melatonin (MLT) host-guest complex allowed the detection of gaseous protonated 1:1 β-CD-MLT. Tandem MS collision-induced dissociation (CID) of such protonated 1:1 β-CD-MLT species showed the proton (charge) to be retained to a significant extent by the host and by its cage fragmentation products, in spite of the higher proton affinity of MLT with respect to that of β-CD. This requires an endothermic guest-to-host proton transfer to occur within the gaseous association. Collisional activation could be accounted for by the promotion of such an endothermic process; however…

Spectrometry Mass Electrospray IonizationFast atom bombardmentTandem mass spectrometryAnalytical chemistryBeta-CyclodextrinsProtonationSpectrometry Mass Fast Atom BombardmentPhotochemistryTandem mass spectrometryDissociation (chemistry)Inclusion compoundchemistry.chemical_compoundFragmentation (mass spectrometry)CyclodextrinSpectroscopyβ-cyclodextrin host-guest complexeMelatoninCyclodextrinsbeta-Cyclodextrinsbeta-CyclodextrinFast atom bombardmentElectrosprayEndothermic guest-to-host proton transferAlgorithmchemistryIonsprayProton affinityAlgorithmsJournal of mass spectrometry : JMS
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Interactions of α-tocopherol with biomembrane models: Binding to dry lecithin reversed micelles

2005

Abstract The state of α-tocopherol (Vitamin E) in solutions of dry lecithin reversed micelles dispersed in an apolar medium has been investigated as a function of the Vitamin E to surfactant molar ratio (RVE) at fixed surfactant concentration by FT-IR, 1H NMR and SAXS with the aim to emphasize the role played by anisotropic intermolecular interactions and confinement effects as driving forces of its partitioning between apolar bulk solvent and polar nanodomains and of mutual Vitamin E/reversed micelle effects. It has been found that its binding strength to reversed micelles, triggered by steric and orientational constrains, is mainly regulated by specific interactions between the hydrophili…

Magnetic Resonance Spectroscopyfood.ingredientreversed micelleChemistry Pharmaceuticalmedicine.medical_treatmentPharmaceutical Sciencevitamin EMicelleLecithinDrug IncompatibilitySurface-Active Agentschemistry.chemical_compoundfoodPulmonary surfactantalpha-tocopherolPhosphatidylcholineSpectroscopy Fourier Transform InfraredmedicineOrganic chemistryTocopherolCarbon TetrachlorideMicellesVitamin EBiological membraneVitaminsintermolecular interactionlecithinchemistryPhosphatidylcholinesBiophysicslipids (amino acids peptides and proteins)solubilization.alpha-TocopherolInternational Journal of Pharmaceutics
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Partial photocatalytic oxidation of glycerol in TiO2 water suspensions

2010

2nd European Conference on Environmental Applications of Advanced Oxidation Processes -- SEP 09-11, 2009 -- Nicosia, CYPRUS

Settore ING-IND/24 - Principi Di Ingegneria ChimicaAnataseTitanium DioxideAqueous solutionFormic acidElectrospray ionizationGlycerol partial oxidation Selective photocatalytic oxidation Titanium dioxide Reaction pathwaysInorganic chemistryAqueous two-phase systemGeneral ChemistryCatalysischemistry.chemical_compoundchemistryGlyceraldehydeTitanium dioxideGlycerolSettore CHIM/07 - Fondamenti Chimici Delle TecnologieSelective Photocatalytic OxidationGlycerol Partial OxidationReaction Pathways
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Gas-phase ion chemistry of protonated melatonin: naturally occurring and collision induced fragmentation

2007

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FT-IR and nuclear overhauser enhancement study of the state of urea confined in AOT-reversed micelles

2003

Abstract The system urea/sodium-bis(2-ethylhexyl)sulfosuccinate (AOT) dispersed in CCl 4 and benzene-d6 was investigated by viscosimetry, FT-IR and high-resolution 1 H NMR spectroscopy, as a function of urea/AOT molar ratio ( R urea ) at fixed AOT molal concentration (0.3467 mol kg −1 ) and as a function of AOT concentration at fixed R urea (0.5) at 25 °C. The experimental data are consistent with the hypothesis that urea is encapsulated as small-size hydrogen-bonded cluster in the hydrophilic micellar core of the AOT-reversed micelles and that this structure is maintained well above the volume fraction of the dispersed phase, where a percolative transition occurs. Intermolecular nuclear ov…

chemistry.chemical_classificationMolalityInorganic chemistryMicellechemistry.chemical_compoundColloid and Surface ChemistrySulfonatechemistryPulmonary surfactantUreaProton NMRPhysical chemistryAlkylMethyl groupColloids and Surfaces A: Physicochemical and Engineering Aspects
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Multiple points of view of heteronuclear NOE: long range vs short range contacts in pyrrolidinium based ionic liquids in the presence of Li salts.

2015

The nuclear Overhauser enhancement (NOE) is a powerful tool of NMR spectroscopy extensively used to gain structural information in ionic liquids (ILs). A general model for the distance dependence of intermolecular NOE in ILs was recently proposed showing that NOE spots beyond the first solvation shell and accounts for long-range effects. This conclusion prompted for a deep rethinking of the NOE data interpretation in ILs. In this paper we present an extensive and quantitative study of N-propyl-N-methyl pyrrolidinium bis(trifluoromethanesulfonyl)imide (PYR13TFSI), the homologue with bis(fluorosulfonyl)imide (PYR13FSI), and their mixtures with LiTFSI based on 1H-19F and 1H-7LiNOE correlation …

Materials Chemistry2506 Metals and AlloysAtomic and Molecular Physics and OpticAnalytical chemistryCondensed Matter PhysicIonic liquidLithiumchemistry.chemical_compoundMaterials ChemistryPhysical and Theoretical ChemistryImideHeteronuclear NOESpectroscopyIntermolecular NOE;Fluorosulfonylimide;Ionic liquids;NMR;Trifluoromethanesulfonimide;Pyrrolidinium;Lithium;Heteronuclear NOELarmor precessionFluorosulfonylimideIntermolecular NOEElectronic Optical and Magnetic MaterialIntermolecular forceHeteronuclear NOE NMR Ionic liquids Pyrrolidinium Fluorosulfonylimide Trifluoromethanesulfonimide Lithium Intermolecular NOENuclear magnetic resonance spectroscopyCondensed Matter PhysicsAtomic and Molecular Physics and OpticsNMRElectronic Optical and Magnetic MaterialsIonic liquidsCrystallographyTrifluoromethanesulfonimideSolvation shellHeteronuclear moleculechemistryIonic liquidPolarPyrrolidinium
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Self-assembly and intra-cluster reactions of erbium and ytterbium bis(2-ethylhexyl)sulfosuccinates in the gas phase.

2014

RATIONALE: The study of surfactant organization in vacuum allows surfactant–surfactant interaction to be unveiled in the absence of surrounding solvent molecules. Knowledge on their chemical-physical properties may also lead to the definition of more efficient gas-phase carriers, air-cleaning agents and nanoreactors. In addition, the presence of lanthanide-group ions adds unique photochemical properties to surfactants. METHODS: The structural features, stability and fragmentation patterns of charged aggregates formed by lanthanide- functionalized surfactants, ytterbium and erbium bis(2-ethylhexyl)sulfosuccinate ((AOT) 3 Yb and (AOT) 3 Er), have been investigated by electrospray ionization m…

Spectrometry Mass Electrospray IonizationSurface-Active AgentsSuccinatesself Assembly Mass spectrometry Lanthanides AOT Er YbGasesYtterbiumErbiumRapid communications in mass spectrometry : RCM
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Distinct patterns of Fos immunoreactivity in striatum and hippocampus induced by different kinds of novelty in mice.

2010

In this study the immediate-early gene Fos was used to investigate the response to different novel stimuli in a wide array of brain regions including the hippocampus, the rhinal cortex, the frontal cortex and different components of the striatal complex. Independent groups of CD-1 mice were exposed to three different novelty conditions: (1) novel environment (empty open field); (2) complex novel environment (i.e. open field containing objects); and (3) identity-based detection of novel objects. We observed that a complex novel environment and a knowledge-based novelty modulated Fos levels in both the dorsal and the ventral components of the striatum, while Fos immunoreactivity in the medial…

MaleCognitive NeuroscienceRhinal cortexHippocampusExperimental and Cognitive PsychologyCell CountStriatumEnvironmentMotor ActivityHippocampusOpen fieldTemporal lobeBehavioral NeuroscienceMiceBasal gangliaAnimalsPrefrontal cortexmedial temporal lobe; striatum; prefrontal cortex; object novelty; environmental noveltyNeuronsAnalysis of VarianceBehavior AnimalNoveltyImmunohistochemistryCorpus StriatumPsychologyNeuroscienceProto-Oncogene Proteins c-fosNeurobiology of learning and memory
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Structural and physicochemical characterization of the inclusion complexes of cyclomaltooligosaccharides (cyclodextrins) with melatonin

2002

The stoichiometry, geometry, stability, and solubility of the inclusion complexes of melatonin (MLT) with native cyclomaltooligosaccharides (α-, β- or γ-cyclodextrins, CDs) are determined experimentally by high-resolution NMR spectroscopy, calorimetric and solubility measurements, and mass spectrometry. The observed differences are discussed in terms of molecular recognition expression of the host-guest (h-g) interactions within the hydrophobic CDs cavities of different size. The 1:1 h-g stoichiometry in water solution prevails at low CD concentrations; the trend to form higher order associations is observed at increasing CD concentrations. The stability order β-CD>γ-CD>α-CD for the c…

Models MolecularSpectrometry Mass Electrospray IonizationElectrospray ionizationProtonationCalorimetryCalorimetryMass spectrometryBiochemistryInclusion complexeAnalytical ChemistryExcipientsMolecular recognitionCyclodextrinSolubilityNuclear Magnetic Resonance BiomolecularMelatoninCyclodextrinsMass spectrometryChemistryOrganic ChemistryGeneral MedicineNuclear magnetic resonance spectroscopyNMRCrystallographySolubilityThermodynamicsStoichiometry
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CCDC 1427937: Experimental Crystal Structure Determination

2017

Related Article: Luca Leoni, Rakesh Puttreddy, Ondřej Jurček, Andrea Mele, Ilaria Giannicchi, Francesco Yafteh Mihan, Kari Rissanen, Antonella Dalla Cort|2016|Chem.-Eur.J.|22|18714|doi:10.1002/chem.201604313

Space GroupCrystallographytetrabutylammonium bromo-(dioxo)-(2'3'4'5'6'-pentafluoro-3-(((2-((2-(hydroxy)benzylidene)amino)phenyl)imino)methyl)biphenyl-2-olato)-uraniumCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1427936: Experimental Crystal Structure Determination

2017

Related Article: Luca Leoni, Rakesh Puttreddy, Ondřej Jurček, Andrea Mele, Ilaria Giannicchi, Francesco Yafteh Mihan, Kari Rissanen, Antonella Dalla Cort|2016|Chem.-Eur.J.|22|18714|doi:10.1002/chem.201604313

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameterstetrabutylammonium chloro-(dioxo)-(2'3'4'5'6'-pentafluoro-3-(((2-((2-oxybenzylidene)amino)phenyl)imino)methyl)biphenyl-2-olato)-uraniumExperimental 3D Coordinates
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