Search results for "vibrational circular dichroism"

showing 10 items of 32 documents

Circular dichroism in x-ray photoemission from core levels of nonmagnetic species

1992

Circular dichroism in the angular distribution of photoelectrons (CDAD) has been observed in core-level photoemission from spherically symmetric initial states of nonmagnetic species utilizing circularly polarized soft-x-ray radiation from BESSY. Up to now, CDAD was predicted and observed only for aligned initial states. The data for oriented CO molecules prove that circular x-ray dichroism in photoemission from core levels is a general phenomenon that is not restricted to ferromagnets. High asymmetries of 50% suggest future applications as an effective circular x-ray analyzer.

PhysicsCondensed Matter::Materials ScienceCircular dichroismFerromagnetismX-ray magnetic circular dichroismVibrational circular dichroismX-raySynchrotron radiationCondensed Matter::Strongly Correlated ElectronsAtomic physicsDichroismPhotoelectric effectPhysical Review B
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Taming conformational heterogeneity in and with vibrational circular dichroism spectroscopy

2019

Chemical science 10, 7680 -7689 (2019). doi:10.1039/C9SC02866H

PhysicsFlexibility (engineering)FELIX Condensed Matter PhysicsQuantitative Biology::Biomolecules/dk/atira/pure/sustainabledevelopmentgoals/affordable_and_clean_energy010405 organic chemistryMolecular and BiophysicsGeneral ChemistryFunction (mathematics)540010402 general chemistry01 natural sciencesSpectral line3. Good health0104 chemical sciencesHighly sensitiveChemistryddc:540Vibrational circular dichroismStatistical physicsSDG 7 - Affordable and Clean EnergySpectroscopyConformational isomerismReliability (statistics)
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Dominance of the first excitation step for magnetic circular dichroism in near-threshold two-photon photoemission

2012

Magnetic circular dichroism (MCD) in near-threshold photoemission is measured for a perpendicularly magnetized Cs/Co/Pt(111) film with work function adjusted by Cs adsorption. For one-photon photoe ...

PhysicsMagnetic circular dichroismPhysics::OpticsCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsCondensed Matter::Materials ScienceX-ray magnetic circular dichroismTwo-photon excitation microscopyCondensed Matter::SuperconductivityVibrational circular dichroismPerpendicularDominance (ecology)Work functionAtomic physicsExcitationPhysical Review B
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Angular and temperature dependence of the magnetic circular dichroism in4dcore-level photoemission from Gd(0001)

2002

We present experimental and theoretical results for the angular and temperature dependence of magnetic circular dichroism in Gd $4d$ core-level photoelectron emission from a Gd(0001) surface in both normal and off-normal directions and with azimuthal variation. Two theoretical approaches are used to model this data: a single electron theory with full multiple scattering of the outgoing photoelectron and a full-relativistic many-electron theory with single scattering only. Thermal effects due to atomic vibrations and the excitation of initial-state multiplets are also included. For normal emission, we find smooth free-atom-like angular variations in emission intensity, while for off-normal e…

PhysicsMagnetizationCircular dichroismCondensed matter physicsX-ray magnetic circular dichroismScatteringMagnetic circular dichroismVibrational circular dichroismDichroismLinear dichroismMolecular physicsPhysical Review B
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Assignment of the Absolute Configuration and Total Synthesis of (+)-Caripyrin

2014

The antifungal secondary metabolite (+)-caripyrin was studied by vibrational circular dichroism spectroscopy. Analysis of the recorded data, with the Boltzmann weighted-average of the spectra calculated at the B3LYP/6-311G(d,p) level of theory for all relevant conformers, unequivocally proved the (R,R)-configuration for the dextrorotatory natural product. Based on this finding, a short enantioselective synthesis of (+)-caripyrin was developed.

StereochemistryChemistryOrganic ChemistryVibrational circular dichroismEnantioselective synthesisAbsolute configurationInfrared spectroscopyTotal synthesisPhysical chemistryPhysical and Theoretical ChemistrySpectroscopyConformational isomerismDextrorotatoryEuropean Journal of Organic Chemistry
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Resolution and Determination of the Absolute Configuration of a Twisted Bis-Lactam Analogue of Tröger's Base: A Comparative Spectroscopic and Computa…

2015

The first reported twisted bis-lactam, a racemic Tröger's base (TB) analogue (2), was resolved into its enantiomers on a chiral stationary phase HPLC column. The absolute configuration of (+)-2 was determined to be (R,R)-2 by comparing experimental and calculated vibrational circular dichroism (VCD) and electronic circular dichroism (ECD) spectra. The absolute configuration of (-)-2 was determined by comparing experimental and calculated electronic circular dichroism (ECD) spectra. The corresponding theoretical spectra were calculated using the lowest energy conformation of (R,R)-2 and (S,S)-2 at the B3LYP/6-31G(d,p) level of theory. The absolute configuration of (+)-2 was also determined t…

Tröger's BaseCircular dichroismtwisted Bis-Lactam AnalogueStereochemistryOrganic ChemistryResolution (electron density)Absolute configurationchemistrychemistry.chemical_compoundCrystallographychemistryVibrational circular dichroismLactamFlack parameterEnantiomerta116Tröger's baseThe Journal of organic chemistry
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Analytical chemistry on many-center chiral compounds based on vibrational circular dichroism: Absolute configuration assignments and determination of…

2019

The absolute configuration of a chiral molecule is key to its biological activity. Being able to find out what this configuration is, is thus crucial for a wide range of applications. The difficulties associated with such a determination steeply rise as the number of chiral centers in a given compound becomes larger. Concurrently, it becomes increasingly more challenging to determine the levels and identity of potential stereochemical contaminants in a given sample with one and the same technique, leading in practice to extensive and laborious efforts employing multiple analytical techniques. Here, experimental and theoretical studies based on Vibrational Circular Dichroism (VCD) are presen…

Vibrational optical activity02 engineering and technologyCenter (group theory)01 natural sciencesBiochemistrySpectral lineAnalytical ChemistrySynthetic drugsSDG 3 - Good Health and Well-beingComputational chemistryStereochemistryEnvironmental ChemistryAbsolute configurationSpectroscopyFELIX Condensed Matter PhysicsChemistryDiastereomeric impurity levelsPharmaceutics010401 analytical chemistryAbsolute configurationDiastereomer021001 nanoscience & nanotechnology0104 chemical sciencesDensity functional calculationVibrational circular dichroism/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being0210 nano-technologyDensity functional calculation
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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, DMEBmolecules associate in supramolecular assemblies. At higherDMEBconcentration the aggregates can confine watermolecules,making it plausible to think thatDMEB form reverse micelles and that watermolecules are quite uniformly distributed…

confinement effects2S)-dodecyl(2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium bromide (DMEB)reverse micellegenetic structures(1RPGSE-NMR(1R; 2S)-dodecyl(2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium bromide (DMEB) reverse micelles confinement effects hydrogen bonding vibrational circular dichroism (VCD) PGSE-NMR(1R2S)-dodecyl(2-hydroxy-1-methyl-2-phenylethyl)dimethylammonium bromide (DMEB)confinement effectreverse micellesvibrational circular dichroism (VCD)hydrogen bondingSettore CHIM/02 - Chimica Fisica
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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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A Tunable, Fullerene‐Based Molecular Amplifier for Vibrational Circular Dichroism

2019

Abstract Vibrational circular dichroism (VCD) studies are reported on a chiral compound in which a fullerene C60 moiety is used as an electron acceptor and local VCD amplifier for an alanine‐based peptide chain. Four redox states are investigated in this study, of which three are reduced species that possess low‐lying electronic states as confirmed by UV/Vis spectroelectrochemistry. VCD measurements in combination with (TD)DFT calculations are used to investigate (i) how the low‐lying electronic states of the reduced species modulate the amplification of VCD signals, (ii) how this amplification depends on the distance between oscillator and amplifier, and (iii) how the spatial extent of the…

endocrine systemFullerenechirality010402 general chemistry01 natural sciencesRedoxCatalysisAnalytical ChemistryElectronic statesMoietychemistry.chemical_classificationFull Paper010405 organic chemistryAmplifierOrganic ChemistryfullerenesspectroelectrochemistryGeneral ChemistryFull PapersElectron acceptorvibrational circular dichroism0104 chemical sciencesCrystallographychemistrydensity functional calculationsVibrational circular dichroismChirality (chemistry)Chemistry – A European Journal
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