Search results for "isomers"

showing 10 items of 64 documents

Hyperpolarized 1H long lived states originating from parahydrogen accessed by rf irradiation

2013

Hyperpolarization has found many applications in Nuclear Magnetic Resonance (NMR) and Magnetic Resonance Imaging (MRI). However, its usage is still limited to the observation of relatively fast processes because of its short lifetimes. This issue can be circumvented by storing the hyperpolarization in a slowly relaxing singlet state. Symmetrical molecules hyperpolarized by Parahydrogen Induced Hyperpolarization (PHIP) provide a straightforward access to hyperpolarized singlet states because the initial parahydrogen singlet state is preserved at almost any magnetic field strength. In these systems, which show a remarkably long 1H singlet state lifetime of several minutes, the conversion of t…

Models MolecularMagnetic Resonance SpectroscopyCiencias FísicasPhysics::Medical PhysicsGeneral Physics and AstronomySpin isomers of hydrogenOtras Ciencias FísicasLong Lived StatesMagnetizationsymbols.namesakeSinglet stateHyperpolarization (physics)Physical and Theoretical ChemistryTriplet statePHIPChemistryObservableMagnetic fieldParaHydrogenMagnetic FieldsHyperpolarizationAlkynessymbolsCondensed Matter::Strongly Correlated ElectronsHydrogenationAtomic physicsHamiltonian (quantum mechanics)CIENCIAS NATURALES Y EXACTAS
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(Trifluoromethoxy)Phenylboronic Acids: Structures, Properties, and Antibacterial Activity.

2021

Three isomers of (trifluoromethoxy)phenylboronic acids were studied in the context of their physicochemical, structural, antimicrobial and spectroscopic properties. They were characterized by 1H, 13C, 11B and 19F NMR spectroscopy. The acidity of all the isomers was evaluated by both spectrophotometric and potentiometric titrations. The introduction of the -OCF3 group influences the acidity, depending, however, on the position of a substituent, with the ortho isomer being the least acidic. Molecular and crystal structures of ortho and para isomers were determined by the single crystal XRD method. Hydrogen bonded dimers are the basic structural motives of the investigated molecules in the sol…

Models MolecularMagnetic Resonance SpectroscopyPotentiometric titrationSubstituentMolecular ConformationPharmaceutical ScienceContext (language use)Crystal structureMicrobial Sensitivity TestsDFTMedicinal chemistryArticleOCF<sub>3</sub>Analytical Chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug StabilityIsomerismtrifluoromethoxyDrug DiscoveryMoleculePhysical and Theoretical ChemistryMolecular StructureHydrogen bondOrganic ChemistryBoronic AcidsNMRAnti-Bacterial AgentsantibacterialchemistryChemistry (miscellaneous)Intramolecular forceX-RayMolecular MedicineisomersOCF3Derivative (chemistry)Molecules (Basel, Switzerland)
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β-turn tendency in N-methylated peptides with dehydrophenylalanine residue: DFT study.

2010

The tendency to adopt β-turn conformation by model dipeptides with α,β-dehydrophenylalanine (ΔPhe) residue in the gas phase and in solution is investigated by theoretical methods. We pay special attention to a dependence of conformational properties on the side-chain configuration of dehydro residue and the influence of N-methylation on β-turn stability. An extensive computational study of the conformational preferences of Z and E isomers of dipeptides Ac-Gly-(E/Z)-ΔPhe-NHMe (1a / 1b) and Ac-Gly-(E/Z)-ΔPhe-NMe(2) (2a/2b) by B3LYP/6-311++G(d,p) and MP2/6-311++G(d,p) methods is reported. It is shown that, in agreement with experimental data, Ac-Gly-(Z)-ΔPhe-NHMe has a great tendency to adopt …

Models MolecularStereochemistryProtein ConformationPhenylalanineBiophysicsdehydrophenylalaninesolvent effectsBiochemistryMethylationBiomaterialschemistry.chemical_compoundResidue (chemistry)Protein structureβ‐turn tendencyAmideE isomersDFT methodsHydrogen bondOrganic ChemistryGeneral Medicinechemistrytheoretical conformational analysisIntramolecular forceTheoretical methodsPolarSolvent effectsPeptidesZBiopolymers
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Toward engineering efficient peptidomimetics. Screening conformational landscape of two modified dehydroaminoacids

2013

Effective peptidomimetics should posses structural rigidity and appropriate interaction pattern leading to potential spatial and electronic matching to the target receptor site. Rational design of such small bioactive molecules could push chemical synthesis and molecular modeling toward faster progress in medicinal chemistry. Conformational properties of N-t-butoxycarbonyl-glycine-(E/Z)-dehydrophenylalanine N′,N′-dimethylamides (Boc-Gly-(E/Z)-ΔPhe-NMe2) in chloroform were studied by NMR and IR spectroscopy. The experimental findings were supported by extensive calculations at DFT(B3LYP, M06-2X) and MP2 levels of theory and the β-turn tendency for both isomers of the studied dipeptide were d…

Models MolecularspectroscopyMagnetic Resonance SpectroscopyMolecular modelProtein ConformationBiophysicsInfrared spectroscopydehydrophenylalanineBiochemistryBiomaterialschemistry.chemical_compoundComputational chemistryAmideStructural rigidityE isomersDipeptideOrganic Chemistryconformational analysisß-turn tendencyRational designGeneral MedicineCarbon-13 NMRSolutionschemistryDFT-GIAO calculationsIRProton NMRPeptidomimeticsPeptides13 C-NMRH-NMRZBiopolymers
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Recoil isomer tagging in the proton-rich odd-odd N = 77 isotones, 142Tb and 144Ho

2001

A fusion-evaporation reaction has been employed to search for isomeric states in the near-proton drip-line N577 isotones, 65 142Tb and 67 144Ho. The recoiling nuclei were implanted into a silicon detector at the focal plane of a gas-filled separator, where a recoil isomer tagging technique was employed to correlate prompt and delayed g-ray transitions across isomeric states. New states were observed to be built upon a known 15-ms isomer in 142Tb and the feeding and decay of a new 500(20)-ns isomeric state was established in 144Ho. This measurement represents the first observation of excited states in 144Ho. The behavior of the new states above the isomers suggests that they are built upon l…

Nuclear TheoryPhysics::Atomic and Molecular ClustersisomerstaggingNuclear Experiment
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Magnetic resonance imaging of (1)H long lived states derived from parahydrogen induced polarization in a clinical system.

2015

Hyperpolarization is a powerful tool to overcome the low sensitivity of nuclear magnetic resonance (NMR). However, applications are limited due to the short lifetime of this non equilibrium spin state caused by relaxation processes. This issue can be addressed by storing hyperpolarization in slowly decaying singlet spin states which was so far mostly demonstrated for non-proton spin pairs, e.g. 13C-13C. Protons hyperpolarized by parahydrogen induced polarization (PHIP) in symmetrical molecules, are very well suited for this strategy because they naturally exhibit a long-lived singlet state. The conversion of the NMR silent singlet spin state to observable magnetization can be achieved by ma…

Nuclear and High Energy PhysicsMagnetic Resonance SpectroscopyVinyl CompoundsSpin statesProtonRadio WavesCiencias FísicasBiophysics010402 general chemistrySpin isomers of hydrogen01 natural sciencesBiochemistryMagnetizationNuclear magnetic resonanceElectromagnetic FieldsPARAHYDROGENHyperpolarization (physics)Singlet stateHYPERPOLARIZATIONPHIP010405 organic chemistryChemistryPULSE SEQUENCEPulse sequenceNuclear magnetic resonance spectroscopyCondensed Matter PhysicsMagnetic Resonance Imaging0104 chemical sciencesAstronomíaLONG LIVED STATECondensed Matter::Strongly Correlated ElectronsProtonsCIENCIAS NATURALES Y EXACTASHydrogenJournal of magnetic resonance (San Diego, Calif. : 1997)
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Zero- to Ultralow-Field Nuclear Magnetic Resonance $J$-Spectroscopy with Commercial Atomic Magnetometers

2019

Zero- to ultralow-field nuclear magnetic resonance (ZULF NMR) is an alternative spectroscopic method to high-field NMR, in which samples are studied in the absence of a large magnetic field. Unfortunately, there is a large barrier to entry for many groups, because operating the optical magnetometers needed for signal detection requires some expertise in atomic physics and optics. Commercially available magnetometers offer a solution to this problem. Here we describe a simple ZULF NMR configuration employing commercial magnetometers, and demonstrate sufficient functionality to measure samples with nuclear spins prepolarized in a permanent magnet or initialized using parahydrogen. This opens …

Nuclear and High Energy PhysicsMaterials scienceZero field NMRPhysics - Instrumentation and DetectorsMagnetometerBiophysicsFOS: Physical sciences010402 general chemistrySpin isomers of hydrogen01 natural sciencesBiochemistry030218 nuclear medicine & medical imaginglaw.invention03 medical and health sciences0302 clinical medicineNuclear magnetic resonancelawPhysics - Chemical PhysicsHyperpolarization (physics)SpectroscopyChemical Physics (physics.chem-ph)SpinsInstrumentation and Detectors (physics.ins-det)Condensed Matter Physics0104 chemical sciencesMagnetic fieldMagnet
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Three beta-decaying states in 128In and 130In resolved for the first time using Penning-trap techniques

2020

Isomeric states in 128In and 130In have been studied with the JYFLTRAP Penning trap at the IGISOL facility. By employing state-of-the-art ion manipulation techniques, three different beta-decaying states in 128In and 130In have been separated and their masses measured. JYFLTRAP was also used to select the ions of interest for identification at a post-trap decay spectroscopy station. A new beta-decaying high-spin isomer feeding the isomer in 128Sn has been discovered in 128In at 1797.6(20) keV. Shell-model calculations employing a CD-Bonn potential re-normalized with the perturbative G-matrix approach suggest this new isomer to be a 16⁺ spin-trap isomer. In 130In, the lowest-lying (10⁻) isom…

Nuclear and High Energy PhysicsPenning trapAstronomy & Astrophysics01 natural sciencesIonPhysics Particles & Fieldsbeta-decay spectroscopyIsomersShell model0103 physical sciencesPhysics::Atomic and Molecular ClustersNuclear Experiment010306 general physicsSpectroscopyCouplingPhysicsScience & TechnologyNUCLEI010308 nuclear & particles physicsPhysicsPRECISION MASS-SPECTROMETRYNuclear shell modelR-PROCESSshell modelpenning trapRAMSEY METHODPenning traplcsh:QC1-999Physics NuclearExcited stateBeta (plasma physics)Physical SciencesSHELL-MODELTRANSITION-PROBABILITIESisomersAtomic physicsBeta-decay spectroscopylcsh:PhysicsIon cyclotron resonancePhysics Letters B
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A facility for production and laser cooling of cesium isotopes and isomers

2018

We report on the design, installation, and test of an experimental facility for the production of ultra-cold atomic isotopes and isomers of cesium. The setup covers a broad span of mass numbers and nuclear isomers, allowing one to directly compare chains of isotopes and isotope/isomer pairs. Cesium nuclei are produced by fission or fusion-evaporation reactions using primary proton beams from a 130 MeV cyclotron impinging upon a suitable target. The species of interest is ejected from the target in ionic form, electrostatically accelerated, mass separated, and routed to a science chamber. Here, ions are neutralized by implantation in a thin foil, and extracted by thermal diffusion. A neutral…

Nuclear and High Energy PhysicsPhysics - Instrumentation and DetectorsProtonCesium IsotopesAtomic Physics (physics.atom-ph)FissiontutkimuslaitteetCyclotronFOS: Physical scienceschemistry.chemical_element7. Clean energy01 natural sciencesPhysics - Atomic Physicslaw.inventionIonlaser coolinglawLaser cooling0103 physical sciencesPhysics::Atomic and Molecular ClustersPhysics::Atomic PhysicsNuclear Experiment (nucl-ex)Nuclear Experiment010306 general physicsNuclear ExperimentInstrumentationPhysicsultra-cold nucleita114Isotope010308 nuclear & particles physicsInstrumentation and Detectors (physics.ins-det)3. Good healthchemistryCaesiumAtomic physicsydinfysiikkaisotopes and isomersNuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
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Assignment of1H and13C NMR data for (−)-methyl thyrsiflorin A and some scopadulan precursors

2001

The 1H and 13C NMR spectral analysis of synthetic (−)-methylthyrsiflorin A and 10 scopadulan precursors is reported. Resonance assignments were based on one- and two-dimensional NMR techniques, which included 1H, 13C, DEPT and HMQC and also 1D NOE difference spectroscopy. Copyright © 2001 John Wiley & Sons, Ltd.

Nuclear magnetic resonanceChemistryNMR spectroscopy of stereoisomersProton NMRResonancePhysical chemistryGeneral Materials ScienceGeneral ChemistryFluorine-19 NMRCarbon-13 NMRDEPTSpectroscopyMethyl thyrsiflorin AMagnetic Resonance in Chemistry
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