0000000000043126

AUTHOR

Marco Passarello

showing 7 related works from this author

Fast proton conduction in hydrogen bonded microheterogeneous systems: Bis(2-ethylhexyl)phosphoric acid/N-methyl formamide liquid mixtures

2009

Structural and dynamical properties of bis(2-ethylhexyl)phosphoric acid (HDEHP)/N-methyl formamide (NMF) liquid mixtures in the whole composition range have been investigated by Fourier Transform Infrared spectroscopy (FT-IR), X-rays Diffraction (XRD), and AC complex impedance spectroscopy. Driven by hydrogen bond interactions among HDEHP PO(4)H group and NMF CO and NH groups, and also by steric effects among the HDEHP alkyl chains, the system microstructure is mainly characterized by the coexistence of spatially separated hydrophilic and hydrophobic nanodomains showing local organization and short-range order. The evolution of this structural feature with system composition has been highli…

chemistry.chemical_classificationFormamideHydrogen bondAnalytical chemistryInfrared spectroscopyFast proton conduction systems Microheterogeneous liquid mixtures Bis(2-ethylhexyl)phosphoric acid N-methyl formamidePercolation thresholdSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsBiomaterialschemistry.chemical_compoundColloid and Surface ChemistrychemistryX-ray crystallographyFourier transform infrared spectroscopyPhosphoric acidAlkylSettore CHIM/02 - Chimica FisicaJournal of Colloid and Interface Science
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Investigations of methyl lactate in the presence of reverse micelles by vibrational spectroscopy and circular dichroism

2012

Abstract The FT-IR and vibrational circular dichroism (VCD) spectra of ( S )- and -( R )-methyl lactate have been recorded for neat samples and at various concentrations in CCl 4 and DMSO solutions. These spectra are used to analyse the FT-IR and VCD spectra of methyl lactates in presence of sodium bis(2-ethylhexyl)sulfosuccinate (AOT) in CCl 4 , where the surfactant molecules are known to form reverse micelles. Some tendency of methyl lactate to interact with AOT micellar aggregates is observed, but not as well defined as previously observed for dimethyl tartrate in analogous circumstances. Besides, near infrared (NIR) absorption and VCD data have been obtained for most of the above system…

endocrine systemCircular dichroismChemistryHydrogen bondAnalytical chemistryInfrared spectroscopyMethyl lactateMicellechemistry.chemical_compoundVibrational circular dichroismMoleculePhysical chemistryAbsorption (chemistry)Methyl lactate Sodium bis(2-ethylhexyl)sulfosuccinate (AOT) Reverse micelles VCD NIR AnharmonicitySpectroscopyVibrational Spectroscopy
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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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Triggering dissymmetry in achiral dye molecules by chiral solvents: Circular dichroism experiments and DFT calculations

2011

The electronic circular dichroism spectra of achiral product “Lumogen F Red” (ROT-300) in four different chiral solvents are recorded at different temperatures. DFT calculations allow to identify two enantiomeric conformers for ROT-300. In vacuo they are equally populated; in chiral solvents one enantiomer prevails. Thermodynamic quantities involved in the chiral preference are derived. Chirality, 2011. © 2011 Wiley-Liss, Inc.

Models MolecularCircular dichroismMolecular ConformationPhotochemistryCatalysisAnalytical ChemistryProchiralityComputational chemistryDrug Discoverycircular dichroism (CD)time-dependent density functional theory (TDDFT)MoleculeColoring AgentsConformational isomerismSpectroscopySettore CHIM/02 - Chimica FisicaPharmacologyChemistryCircular DichroismOrganic ChemistryStereoisomerismCircular dichroism spectradye molecules solvent effectSolventsQuantum TheoryEnantiomerChirality (chemistry)Chirality
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Sintesi e caratterizzazione di nuovi sistemi fotoluminescenti nanostrutturati.

2012

Nuovi sistemi fotoluminescenti nanostrutturati.
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Triggering Dissymmetry in Achiral Dye Molecules by Chiral Solvents:Circular Dichroism Experiments and DFT Calculations

2011

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EXAFS and SAXS Investigation of Frozen Metal-Containing Reverse Micelles Dispersed in n-Heptane

2008

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