Search results for "Deute"

showing 10 items of 549 documents

Deuterated Molecular Ruby with Record Luminescence Quantum Yield

2017

The recently reported luminescent chromium(III) complex 13+ ([Cr(ddpd)2]3+; ddpd=N,N’-dimethyl-N,N’-dipyridine-2-yl-pyridine-2,6-diamine) shows exceptionally strong near-IR emission at 775 nm in water under ambient conditions (F=11%) with a microsecond lifetime as the ligand design in 13+ effectively eliminates non-radiative decay pathways, such as photosubstitution, back-intersystem crossing, and trigonal twists. In the absence of energy acceptors, such as dioxygen, the remaining decay pathways are energy transfer to high energy solvent and ligand oscillators, namely OH and CH stretching vibrations. Selective deuteration of the solvents and the ddpd ligands probes the efficiency of these o…

Coordination sphereMaterials science010405 organic chemistryLigandMetal ions in aqueous solutionQuantum yieldGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysis0104 chemical sciencesMicrosecondDeuteriumExcited stateLuminescenceAngewandte Chemie International Edition
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Nuclear Spin Relaxation in Viscous Liquids: Relaxation Stretching of Single-Particle Probes

2021

Spin-lattice relaxation rates R1(ω,T), probed via high-field and field-cycling nuclear magnetic resonance (NMR), are used to test the validity of frequency-temperature superposition (FTS) for the reorientation dynamics in viscous liquids. For several liquids, FTS is found to apply so that master curves can be generated. The susceptibility spectra are highly similar to those obtained from depolarized light scattering (DLS) and reveal an excess wing. Where FTS works, two approaches are suggested to access the susceptibility: (i) a plot of deuteron R1(T) vs the spin-spin relaxation rate R2(T) and (ii) a plot of R1(T) vs an independently measured reference time τref(T). Using single-frequency s…

Coupling constantCouplingHot TemperatureMagnetic Resonance SpectroscopyMaterials scienceViscosityTemperatureViscous liquidMagnetic Resonance ImagingMolecular physicsLight scatteringSpectral lineSurfaces Coatings and FilmsSuperposition principleDeuteriumMaterials ChemistryRelaxation (physics)Physical and Theoretical ChemistryThe Journal of Physical Chemistry B
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Polarizability of the neutron

1990

Abstract A first measurement of quasi-free Compton scattering by the neutron bound in the deuteron has yielded a value for the polarizability of the neutron of αn=(11.7 −11.7+4.3)×10 −4fm 3. This means that a finite value for the polarizability has been obtained, though the result is still consistent with zero. The π0 decay constant Fπ 0γγ and the pion nucleon coupling constant gNNπ have opposite signs.

Coupling constantPhysicsNuclear and High Energy PhysicsAstrophysics::High Energy Astrophysical PhenomenaNuclear TheoryCompton scatteringlcsh:QC1-999Nuclear physicsPionDeuteriumPolarizabilityNeutronAstrophysics::Earth and Planetary AstrophysicsExponential decayAtomic physicsNuclear ExperimentNucleonlcsh:PhysicsPhysics Letters B
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A line-shape analysis for spin-1 NMR signals

1997

An analytic model of the deuteron absorption function has been developed and is compared to experimental NMR signals of deuterated butanol obtained at the SMC experiment in order to determine the deuteron polarization. The absorption function model includes dipolar broadening and a frequency-dependent treatment of the intensity factors. The high-precision TE signal data available are used to adjust the model for Q-meter distortions and dispersion effects. Once the Q-meter adjustment is made, the enhanced polarizations determined by the asymmetry and TE-calibration methods compare well within the accuracy of each method. In analyzing the NMR signals, the quadrupolar coupling constants could …

Coupling constantPhysicsdisNuclear and High Energy PhysicsButanolmedia_common.quotation_subjectsmcpolarized targetQ meterdiPolarization (waves)AsymmetryMolecular physicschemistry.chemical_compoundDipoleNuclear magnetic resonanceDeuteriumchemistrysmc; dis; polarized targetDetectors and Experimental TechniquesInstrumentationShape analysis (digital geometry)media_common
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Quantum effects in the capture of charged particles by dipolar polarizable symmetric top molecules. II. Interplay between electrostatic and gyroscopi…

2013

ally nonadiabatic channel treatment of the capture of charged particles by dipolar polarizable symmetric top molecules with the aim to reveal quantum effects in the collision dynamics. In general, these effects are related to the discrete nature of the intrinsic, orbital, and total angular momenta, to the quantum character of passage of collision partners across effective potential barriers and drops, and to the interplay of two types of anisotropic interactions, the gyroscopic (Coriolis) and the electrostatic ones. The latter feature, in principle, leads to a coupling of capture channels. In the calculation of capture cross sections or rate coefficients, however, this coupling can be ignor…

CouplingSurface PropertiesChemistryStatic ElectricityIntermolecular forceGeneral Physics and AstronomyDeuteriumTritiumResonance (particle physics)Charged particleDipolePolarizabilityQuantum mechanicsQuantum TheoryParticle SizePhysics::Chemical PhysicsPhysical and Theoretical ChemistryAtomic physicsAdiabatic processMethaneQuantumHydrogenThe Journal of Chemical Physics
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Vacuum-ultraviolet absorption of hydrogenated and deuterated silanol groups and interstitial water molecules in amorphousSiO2

2005

Vacuum-ultraviolet (VUV) absorption cross sections of hydrogenated and deuterated silanol groups (SiOX, where $\mathrm{X}=\mathrm{H}$ or D) as well as interstitial water molecules $({\mathrm{X}}_{2}\mathrm{O})$ in amorphous $\mathrm{Si}{\mathrm{O}}_{2}$ $(a\text{\ensuremath{-}}\mathrm{Si}{\mathrm{O}}_{2})$ were determined between photon energies of 7 and $8.2\phantom{\rule{0.3em}{0ex}}\mathrm{eV}$. The absorption bands for the deuterated species are blueshifted compared to those for the hydrogenated ones by $\ensuremath{\sim}0.1\phantom{\rule{0.3em}{0ex}}\text{to}\phantom{\rule{0.3em}{0ex}}0.2\phantom{\rule{0.3em}{0ex}}\mathrm{eV}$ as a result of a decrease in the zero-point energy associat…

CrystallographyMaterials scienceDeuteriumAbsorption spectroscopyHydrogen bondZero-point energyMoleculeAbsorption (logic)Atomic physicsCondensed Matter PhysicsEnergy (signal processing)Electronic Optical and Magnetic MaterialsAmorphous solidPhysical Review B
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1977

Solutions of chain- (PS-d3) and phenyl ring (PS-d5) deuterated polystyrenes in perdeuterated PS-d8 have been investigated with 1H and 2D NMR relaxation and wide line methods. The intra- and intermolecular parts of the 1H second moments at −100°C are 3,7 G2 and 2,0 G2, respectively, for PS-d3, and 14,7 G2 and ca. 0 G2, respectively, for PS-d5. The intermolecular contribution to the 1H spin lattice relaxation rate, determined at 55 MHz between 150°C and 250°C, is about one third of the total rate in PS-d3, and negligible in PS-d5. We suggest that this contribution is caused by rotational fluctuations of the intermolecular H H vectors. The intramolecular 1H- and 2D-relaxation rates indicate th…

Crystallographychemistry.chemical_compoundNuclear magnetic resonanceDeuteriumChemistryIntramolecular forcePolymer chemistryRelaxation (NMR)Intermolecular forceProton NMRSpin–lattice relaxationPhenyl groupTwo-dimensional nuclear magnetic resonance spectroscopyDie Makromolekulare Chemie
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Inverse Conformational Selection in Lipid–Protein Binding

2021

International audience; Interest in lipid interactions with proteins and other biomolecules is emerging not only in fundamental biochemistry but also in the field of nanobiotechnology where lipids are commonly used, for example, in carriers of mRNA vaccines. The outward-facing components of cellular membranes and lipid nanoparticles, the lipid headgroups, regulate membrane interactions with approaching substances, such as proteins, drugs, RNA, or viruses. Because lipid headgroup conformational ensembles have not been experimentally determined in physiologically relevant conditions, an essential question about their interactions with other biomolecules remains unanswered: Do headgroups excha…

DYNAMICSELECTRIC CHARGEBILAYERSPHOSPHATIDYLCHOLINE HEADGROUPMembrane lipidsDEUTERIUMPlasma protein bindingMolecular Dynamics Simulationlipidit010402 general chemistry01 natural sciencesBiochemistrybiomolekyylitCatalysis03 medical and health sciencesMolecular dynamicskemialliset sidoksetColloid and Surface ChemistryProtein structurePHOSPHOLIPID-BINDINGMAGNETIC-RESONANCE[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologySEGMENTAL ORDER[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyConformational ensemblesNuclear Magnetic Resonance Biomolecular030304 developmental biologychemistry.chemical_classification0303 health sciencesChemistryBiomoleculeMEMBRANE-LIPIDSProteinsPhosphatidylglycerolsGeneral Chemistrycomputer.file_formatProtein Data BankLipids0104 chemical sciencesBiophysicsPhospholipid BindingPhosphatidylcholinesMAS NMR1182 Biochemistry cell and molecular biologylipids (amino acids peptides and proteins)proteiinitcomputerProtein Binding
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Direct determination of lead in human milk by electrothermal atomic absorption spectrometry

1999

Abstract Infants are particularly sensitive to the toxic effects of lead. Since milk is their only or main food it is important to know the contribution of milk to lead intake. The purpose of this study was to develop a direct method for determining the lead content of human milk by electrothermal atomic absorption spectrometry when a deuterium lamp is the only background correction available. The optimum conditions for lead determination in breast milk: sample dilution in Triton ×-100, modifier (75 μg of palladium) and nitric acid contents (2%) and the graphite furnace program (mineralization: 1100°C; atomization: 2300°C) were selected. The analytical parameters are: linearity (20–300 ng m…

Detection limitChromatographyChemistryAnalytical chemistryGeneral MedicineBreast milkAnalytical Chemistrylaw.inventionchemistry.chemical_compoundDeuteriumNitric acidlawGraphiteLead (electronics)Atomic absorption spectroscopyQuantitative analysis (chemistry)Food ScienceFood Chemistry
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Pulsed EPR determination of water accessibility to spin-labeled amino acid residues in LHCIIb.

2009

Membrane proteins reside in a structured environment in which some of their residues are accessible to water, some are in contact with alkyl chains of lipid molecules, and some are buried in the protein. Water accessibility of residues may change during folding or function-related structural dynamics. Several techniques based on the combination of pulsed electron paramagnetic resonance (EPR) with site-directed spin labeling can be used to quantify such water accessibility. Accessibility parameters for different residues in major plant light-harvesting complex IIb are determined by electron spin echo envelope modulation spectroscopy in the presence of deuterated water, deuterium contrast in …

DetergentsBiophysicsLight-Harvesting Protein ComplexesSpectroscopy Imaging and Other TechniquesBuffersCrystallography X-RaySpectral linelaw.inventionlawMoleculeHumansAmino AcidsElectron paramagnetic resonanceProtein Structure QuaternaryHyperfine structureAlkylPlant Proteinschemistry.chemical_classificationPulsed EPRChemistryElectron Spin Resonance SpectroscopyPeasTemperatureWaterSite-directed spin labelingCrystallographyDeuteriumSolubilityMutationSolventsSpin LabelsProtein MultimerizationBiophysical journal
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