Search results for "ESOL"

showing 10 items of 2444 documents

Synthesis and Isolation of Enantiomerically Enriched Cyclopenta[b]benzofurans Based on Products from Anodic Oxidation of 2,4-Dimethylphenol

2015

The anodic treatment of 2,4-dimethylphenol offers a powerful and direct method for the construction of a dehydrotetramer with four contiguous stereocentres on a multigram scale. The installation of propellanes on this scaffold using enantiomerically pure carbonyl compounds leads to a mixture of diastereomers. This mixture is easily separable using standard chromatography and gives rise to optically pure cyclopenta[b]benzofurans which are important scaffolds in a variety of natural products. The synthesis is easy to perform and allows a reliable access to chiral compounds with very high enantiomeric excess. It was possible to determine the absolute configuration of these compounds by compari…

ChemistryAnodic oxidationOrganic ChemistryVibrational circular dichroismAbsolute configurationDiastereomerOrganic chemistryPhysical and Theoretical ChemistryEnantiomerEnantiomeric excessElectrochemistryChiral resolutionEuropean Journal of Organic Chemistry
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Thermal oxidative process in extra-virgin olive oils studied by FTIR, rheology and time-resolved luminescence

2011

Abstract With the aim to characterise the antioxidant properties of different extra-virgin olive oils and to understand in more detail the mechanisms of oil degradation, we have made an experimental study on thermal induced oxidative processes of extra-virgin olive oils by using different techniques: Fourier Transform Infrared (FTIR) spectroscopy, rheology and time-resolved luminescence. The oxidation process was followed at three different heating temperatures (30, 60 and 90 °C) as a function of time up to 35 days. Thermal treatment induced changes in the FTIR spectra in the wavenumbers region 3100–3600 cm −1 : in particular, the absorption profiles show an initial formation of hydroperoxi…

ChemistryChemical polarityExtra-virgin olive oilViscosimetryAnalytical chemistryTime-resolved luminescenceGeneral MedicineThermal treatmentPhotochemistrySettore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Analytical ChemistryViscosityFTIRRheologyAntioxidantFourier transform infrared spectroscopyAbsorption (chemistry)SpectroscopyLuminescenceFood ScienceFood Chemistry
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Cover Feature: Highly Enantioselective Kinetic Resolution of Michael Adducts through N-Heterocyclic Carbene Catalysis: An Efficient Asymmetric Route …

2018

ChemistryCyclohexenesOrganic ChemistryEnantioselective synthesisGeneral ChemistryCatalysisCatalysisAdductKinetic resolutionchemistry.chemical_compoundComputational chemistryFeature (computer vision)Cover (algebra)CarbeneChemistry - A European Journal
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The Role of Tissue Pressure and Bulk Flow in the Formation and Resolution of Cold-Induced Edema

1976

The mechanisms responsible for the dynamics of cold-induced edema, its spread and resolution, were examined. The findings indicate that bulk flow and not diffusion should be considered as the main mechanism for the edema spreading through the extracellular spaces of the white matter.

ChemistryDiffusionResolution (electron density)Flow (psychology)Analytical chemistryWhite matterchemistry.chemical_compoundmedicine.anatomical_structureEdemamedicineBiophysicsExtracellularmedicine.symptomTissue pressureEvans Blue
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A POWERFUL TOOL TO STUDY COLLISIONAL PHENOMENA AND FOR COMBUSTION APPLICATIONS : THE HIGH RESOLUTION STIMULATED RAMAN SPECTROSCOPY

1987

ChemistryGeneral EngineeringAnalytical chemistryHigh resolutionStimulated ramanCombustionSpectroscopyLe Journal de Physique Colloques
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The infrared spectrum of CH 3 D between 900 and 3200 cm −1 : extended assignment and modeling

2000

Abstract The high resolution infrared spectrum of CH 3 D in the region from 900 to 3200 cm −1 has been analyzed on the basis of Fourier transform spectra recorded at Kitt Peak and at Giessen. A theoretical model for an effective hamiltonian in terms of irreducible tensor operators recently adapted to symmetric top molecules has been used in order to consider simultaneously all available transitions between the lowest three polyads of the molecule: the Ground State (G.S.), the Triad (three interacting fundamental bands in the 8 μm region) and the Nonad (nine interacting bands in the 4 μm region). A preliminary simultaneous fit of 3467 Triad–G.S., 5208 Nonad–G.S., and 2487 Nonad–Triad (hot ba…

ChemistryInfraredOrganic ChemistryAnalytical chemistryHigh resolutionMolecular physicsStandard deviationHot bandAnalytical ChemistryInorganic Chemistrysymbols.namesakesymbolsWavenumberMoleculeGround stateHamiltonian (quantum mechanics)SpectroscopyJournal of Molecular Structure
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Atomic structure solution of the complex quasicrystal approximant Al77Rh15Ru8 from electron diffraction data

2014

The crystal structure of the novel Al77Rh15Ru8phase (which is an approximant of decagonal quasicrystals) was determined using modern direct methods (MDM) applied to automated electron diffraction tomography (ADT) data. The Al77Rh15Ru8E-phase is orthorhombic [Pbma,a= 23.40 (5),b= 16.20 (4) andc= 20.00 (5) Å] and has one of the most complicated intermetallic structures solved solely by electron diffraction methods. Its structural model consists of 78 unique atomic positions in the unit cell (19 Rh/Ru and 59 Al). Precession electron diffraction (PED) patterns and high-resolution electron microscopy (HRTEM) images were used for the validation of the proposed atomic model. The structure of the E…

ChemistryMetals and AlloysQuasicrystalCrystal structureelectron diffraction tomography; icosahedral and decagonal quasicrystals; modern direct methodsAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsCrystallographyElectron diffractionmodern direct methodsMaterials ChemistryAtomic modelicosahedral and decagonal quasicrystalsPrecession electron diffractionOrthorhombic crystal systemelectron diffraction tomographyHigh-resolution transmission electron microscopyElectron backscatter diffraction
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Installation of Amine Moieties into a Polycyclic Anodic Product Derived from 2,4-Dimethylphenol

2011

When 2,4-dimethylphenol is anodically treated, a dehydrotetramer with four contiguous stereocentres is readily obtained on a multi-gram scale. The substitution of a 2,4-dimethyl-phenoxy fragment by several amines was demonstrated, and the best results were obtained with primary amines. Optically pure α-chiral aliphatic amines yield diastereomeric mixtures that can be separated in most cases. The basic amine causes a partial hemiketal-opening of the bisbenzofuran moiety leading to an equilibrium within an α,β-unsaturated cyclohexenone. This dynamic behaviour occurs on the time scale of NMR spectroscopy and is also found by X-ray analysis providing a consistent picture.

ChemistryOrganic ChemistryDiastereomerGeneral ChemistryNuclear magnetic resonance spectroscopyCatalysisChiral resolutionchemistry.chemical_compoundCyclohexenoneYield (chemistry)MoietyOrganic chemistryAmine gas treatingAminationChemistry - A European Journal
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Up-conversion processes in NaLaF4:Er3+

2009

abstract Structural and spectroscopic investigation of NaLaF 4 :Er 3+ material at different doping concentrations ispresented. X-ray diffraction patterns, up-conversion luminescence spectra and decay curves for 2 H 9/2 ? 4 I 15/2 , 4 S 3/2 ? 4 I 15/2 and 4 F 9/2 ? 4 I 15/2 optical transitions in the material are shown and possibleexcitation routes are discussed. Raman spectrum for the undoped material is presented and the effectivephonon energy of the material is estimated. Based on the obtained results application of rare-earth dopedNaLaF 4 in the field of up-conversion phosphors is evaluated. 2009 Elsevier B.V. All rights reserved. 1. IntroductionFor many years rare-earth (RE) doped materi…

ChemistryOrganic ChemistryDopingAnalytical chemistryNonlinear opticsPhosphorAtomic and Molecular Physics and OpticsPhoton upconversionElectronic Optical and Magnetic MaterialsIonInorganic Chemistrysymbols.namesakesymbolsElectrical and Electronic EngineeringPhysical and Theoretical ChemistryAtomic physicsTime-resolved spectroscopyLuminescenceRaman spectroscopySpectroscopyOptical Materials
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Asymmetric Synthesis of Dihydropyranones with Three Contiguous Stereocenters by an NHC‐Catalyzed Kinetic Resolution

2021

An oxidative NHC-catalyzed kinetic resolution (KR) of racemic mixtures is presented. The developed reaction furnishes tricyclic dihydropyranones with three contiguous stereocenters in excellent dia- and enantioselectivity, with good-to-moderate yields. Mechanistic studies indicate that the rate-determining step of the reaction is the formation of the Breslow intermediate, while the selectivity determining step occurs later in the mechanism. The presented methodology enables rapid synthesis of complex structures in a single step.

ChemistryOrganocatalysisOrganic ChemistryEnantioselective synthesisSingle stepPhysical and Theoretical ChemistrySelectivityCombinatorial chemistryCatalysisKinetic resolutionStereocenterEuropean Journal of Organic Chemistry
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