Search results for "Nuclear magnetic resonance"

showing 10 items of 1743 documents

Thermal-,Pressure-, and Light-Induced Spin Transition in Novel Cyanide-Bridged FeII-AgI Bimetallic Compounds with Three-Dimensional Interpenetrating …

2002

[EN] Low-spin, high-spin and spin-transition behaviours have been observed for the doubly interpenetrating three-dimensional bimetallic compounds {Fe-II(pz)[Ag(CN)(2)](2)}.pz (pz= pyrazine), {Fe-II(4,4'-bipy)(2)[Ag(CN)(2)](2)} (4,4'-bipy-4,4'-bipyridine), and {Fe-II-(bpe)(2)[Ag(CN)(2)](2)} (bpe = bispyridylethylene), respectively. The single crystals of the bpe derivative undergo a spin transition with a large hysteresis loop at about 95 K. After several warming and cooling cycles, the single crystals become a microcrystalline powder with 50% spin transition. Influence of pressure- as well as light-induced excited spin-state trapping (LIESST) on the thermal 50% spin transition of the microc…

CyanidesSpin statesPyrazineChemistryIronOrganic ChemistrySpin transitionGeneral ChemistrySpin crossoverCooperative phenomenaInterpenetrating 3D structuresCatalysisLIESSTCrystallographychemistry.chemical_compoundBipyridineNuclear magnetic resonanceMicrocrystallineSpin crossoverFISICA APLICADABimetallic strip
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Preparation and structure of pyrrolo[2,1-b]- and isoindolo[1,2-b][3,1]epoxyquinazolines

2007

Abstract Various γ-oxocarboxylic acids [aroylpropionic acids, cis-2-(4-methylbenzoyl)cyclohexanecarboxylic acid, diendo-3-benzoylbicyclo[2.2.1] heptane-2-carboxylic acid, formylbenzoic acid, methanobenzenecyclooctencarboxylic acid and the cyclopentadiene adduct of 3-trans-(4-methylbenzoyl)acrylic acid] were reacted with diexo-3-aminomethyl-7-oxabicyclo[2.2.1]hept-5-en-2-ylamine 2 to result in condensed pyrroloepoxyquinazolines 3–10. The starting 2 retained the diexo configuration, but cis → trans isomerization took place when cis-2-(4-methylbenzoyl)cyclohexanecarboxylic acid was applied. The structures, including the ring annelations and the position of the aryl group on the new chiral cent…

CyclopentadieneStereochemistryArylOrganic ChemistryDiastereomerNuclear magnetic resonance spectroscopyCyclohexanecarboxylic acidMedicinal chemistryAnalytical ChemistryAdductInorganic Chemistrychemistry.chemical_compoundchemistryIsomerizationSpectroscopyAcrylic acidJournal of Molecular Structure
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Study of electrostatic potential surface distribution of wild-type plastocyaninSynechocystissolution structure determined by homonuclear NMR

2003

Plastocyanin is a small (∼10 kDa), type I blue copper protein that works as an electron donor to photosystem I from cytochrome f in both chloroplast systems and in some strains of cyanobacteria. Comparative studies of the kinetic mechanisms of plastocyanins in different organisms show that the electron transfer from photosystem I happens by simple collision in cyanobacteria but through a intermediate transition complex in green algae and superior plants. Previous work has proved that this effect cannot be explained by structural variations across the different plastocyanins but it can be explained by differences in the electrostatic potential distribution at the protein surface. In that cas…

Cytochrome fbiologyChemistryOrganic ChemistrySynechocystisBiophysicsGeneral Medicinebiology.organism_classificationPhotosystem IBiochemistryElectron transport chainHomonuclear moleculeBiomaterialsCrystallographySide chainPlastocyaninTwo-dimensional nuclear magnetic resonance spectroscopyBiopolymers
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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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Correlation between spin structure oscillations and domain wall velocities

2013

Magnetic sensing and logic devices based on the motion of magnetic domain walls rely on the precise and deterministic control of the position and the velocity of individual magnetic domain walls in curved nanowires. Varying domain wall velocities have been predicted to result from intrinsic effects such as oscillating domain wall spin structure transformations and extrinsic pinning due to imperfections. Here we use direct dynamic imaging of the nanoscale spin structure that allows us for the first time to directly check these predictions. We find a new regime of oscillating domain wall motion even below the Walker breakdown correlated with periodic spin structure changes. We show that the e…

DYNAMICSMOTIONMagnetic domainNanowireGeneral Physics and Astronomy02 engineering and technologyNANOWIRESSpin structure01 natural sciencesArticleMAGNETIC-FIELDSGeneral Biochemistry Genetics and Molecular BiologyNuclear magnetic resonancePosition (vector)0103 physical sciencesddc:530010306 general physicsPhysicsMultidisciplinaryCondensed matter physicsDynamics (mechanics)General Chemistry021001 nanoscience & nanotechnologySTATEMagnetic fieldDomain wall (magnetism)Physics and AstronomyDomain (ring theory)0210 nano-technology
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Incoherent quasi-elastic neutron scattering in isomeric alcohols

1992

Abstract Incoherent quasi-elastic neutron scattering (IQENS) data on liquid isomeric alcohols normal-pentanol (n-PeOH) and 2-methyl-2-butanol (2M-2BuOH) and on their mixture are presented. The diffusive motion of protons, as a function of temperature, is analyzed in the framework of the random jump diffusion model. The temperature dependence of the parameters obtained confirms the more “fragile” behaviour of the more sterically hindered 2M-2BuOH with respect to that of the linear n-PeOH.

DYNAMICSMaterials scienceNuclear magnetic resonanceJump diffusionFunction (mathematics)Physics::Chemical PhysicsElectrical and Electronic EngineeringNeutron scatteringCondensed Matter PhysicsTEMPERATURESmall-angle neutron scatteringMolecular physicsElectronic Optical and Magnetic MaterialsPhysica B: Condensed Matter
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Slow Magnetic Relaxation in a Co (II)–Y (III) Single‐Ion Magnet with Positive Axial Zero‐Field Splitting

2013

This work was supported by the MINECO (Spain) (Project CTQ2011-24478), the Junta de Andalucía (FQM-195 and Project of excellence P08-FQM-03705), and the University of Granada. E.R. and E.Cr. thank MINECO grant No. CTQ2011-23862-C02-01 and Generalitat de Catalunya grant No. 2009SGR-1459, for financial support. We would like to thank Prof. Liviu Chibotaru for providing us the SINGLE_ANISO program and Dr. Andrew Ozarowski for the EPR simulation software. E.K.B. thanks the EPSRC and Leverhulme Trust for financial support. The NHMFL is funded by the NSF, DoE, and the state of Florida. J.C. acknowledges financial support by the Spanish Ministerio de Ciencia e Innovación through projects CTQ2010-1…

DYNAMICSModels Molecularpositive zero-field splittingINSchemistry.chemical_elementZero field splitting010402 general chemistry01 natural sciences7. Clean energyCatalysisO ligandsMOLECULE MAGNETNuclear magnetic resonancesingle ion magnetsYttriumMagnetic relaxationCompartmental ligandAnisotropyHYSTERESISComputingMilieux_MISCELLANEOUSANISOTROPY[PHYS]Physics [physics]IonsMolecular StructureCondensed matter physicsSingle ion010405 organic chemistryChemistryCobaltGeneral ChemistryYttriumNBARRIERcobaltCo(II)FAMILY0104 chemical sciencesyttriumHysteresisPositive axial ZFSDYSPROSIUM(III)TBMagnetic FieldsMagnetMagnetsSingle ion magnetCOMPLEXESCobaltBEHAVIOR
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Cytotoxic drimane meroterpenoids from the Indonesian marine sponge Dactylospongia elegans

2017

Abstract Chemical investigation of the methanol extract of an Indonesian marine sponge Dactylospongia elegans (family Thorectidae) afforded two undescribed drimane meroterpenoidal metabolites, dactylospongenones G and H (1 and 2) together with thirteen known compounds (3–15) including pelorol, 5-epi-ilimaquinone, 5-epi-smenospongine, 5-epi-smenospongidine, nakijiquinone D, smenospongine C, isospongiaquinone, isosmenospongine, nakijiquinones A-C, G and 5-epi-nakijiquinone Q. The structures of the new metabolites were unambiguously determined by 1D and 2D NMR spectroscopy and by HRESIMS. All isolated compounds were assessed for their antimicrobial, antitubercular and cytotoxic activities. Sev…

Dactylospongia elegansbiology010405 organic chemistryStereochemistrySmenospongine CPlant Sciencebiology.organism_classificationAntimicrobial01 natural sciencesBiochemistry0104 chemical sciences010404 medicinal & biomolecular chemistrySpongeCytotoxic T cellCytotoxicityAgronomy and Crop ScienceTwo-dimensional nuclear magnetic resonance spectroscopyIsospongiaquinoneBiotechnologyPhytochemistry Letters
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Ac field dependence of the susceptibility of Bi2Sr2CaCu2O8 thin films at low dc fields

1996

We have measured the ac field dependence of the ac susceptibility of 400 nm thick Bi2212 thin films at low dc fields 0 ≤μ0Ha ≤ 1 mT in transverse geometry. We show that at reduced temperaturest≤0.85 the ac field dependence can be described by the non-linear Bean model after Brandt as in Y123 thin films. Att>0.85, however, we observe a decrease of the energy dissipation and shielding capability. The critical current density at zero dc field is given byjc−4×1010(1−(T/Tc))2.8±0.1 A/m2.

Dc fieldPhysicsTransverse planeNuclear magnetic resonanceCondensed matter physicsAc fieldElectromagnetic shieldingGeneral Physics and AstronomyCritical currentDissipationThin filmCzechoslovak Journal of Physics
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Enhanced β-turn conformational stability of tripeptides containing Δphe in cis over trans configuration

2013

Conformations of three pairs of dehydropeptides with the opposite configuration of the Delta Phe residue, Boc-Gly-Delta(Z/E)Phe-Phe-p-NA (Z- p -NA and E- p -NA), Boc-Gly-Delta(Z/E)Phe-Phe-OMe (Z-OMe and E-OMe), and Boc-Gly-Delta(Z/E)Phe-Phe-OH (Z-OH and E-OH) were compared on the basis of CD and NMR studies in MeOH, TFE, and DMSO. The CD results were used as the additional input data for the NMR-based calculations of the detailed solution conformations of the peptides. It was found that Z- p -NA, E- p -NA, Z-OMe, and Z-OH adopt the beta-turn conformations and E-OMe and E-OH are unordered. There are two overlapping type III beta-turns in Z- p -NA, type II' beta-turn in E- p -NA, and type II …

Dehydropeptide conformationCircular dichroismMagnetic Resonance SpectroscopyStereochemistryProtein ConformationPhenylalanineClinical BiochemistryTripeptideCircular dichroismTemperature coefficients of amide protonsBiochemistryNuclear magnetic resonancechemistry.chemical_compoundResidue (chemistry)Trans configurationchemistry [Oligopeptides]Amideotorhinolaryngologic diseasesHydrogen bondProtein StabilityDehydropeptidesCircular DichroismOrganic ChemistryStereoisomerismchemistryIntramolecular forceddc:540Dehydrophenylalanine configurationchemical synthesis [Oligopeptides]Conformational stabilitychemistry [Phenylalanine]OligopeptidesAmino Acids
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