Search results for " hydrogen"

showing 10 items of 319 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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Hydrogen bonding in dimers of tritolyl and tritosylurea derivatives of triphenylmethanes.

2006

The crystal structure of the homodimer formed by the tritolylurea 3a proves the existence of a belt of six bifurcated hydrogen bonds between both NH and the O=C groups of the adjacent urea residues. For the tritosylurea 3b, four additional three-center hydrogen bonds, also involving the SO2 oxygen, are found in the crystalline state. Molecular dynamics simulations in a chloroform box confirm these patterns of the hydrogen bonds and the resulting elongation of the dimer 3b. 3b in comparison to 3a x 3a. The calculated complexation energies for the three dimeric combinations are nearly identical in agreement with the simultaneous formation of heterodimer 3a x 3b in a mixture of 3a and 3b.

Models MolecularMagnetic Resonance SpectroscopyDimerLow-barrier hydrogen bondMolecular Conformationchemistry.chemical_elementCrystal structurePhotochemistryCrystallography X-RayBiochemistryOxygenchemistry.chemical_compoundMolecular dynamicsUreaComputer SimulationPhysical and Theoretical ChemistryChloroformHydrogen bondOrganic ChemistryHydrogen BondingTrityl CompoundsCrystallographychemistryUreaThermodynamicsDimerizationOrganicbiomolecular chemistry
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The Molecular and Crystal Structure of tert-Butyl N.ALPHA.-tert-Butoxycarbonyl-L-(S-trityl)cysteinate and the Conformation-Stabilizing Function of We…

2001

The title compound, C31H37NO4S [systematic name: (R)-tert-butyl-2-[(tert-butoxycarbonyl)amino]-3-(tritylsulfanyl)propanoate] is an L-cysteine derivative with three functions: NH2, COOH and SH, blocked by protecting groups tert-butoxycarbonyl, tert-butyl and trityl, respectively. The main chain of the molecule adopts the extended, nearly all-trans C5 conformation with the intramolecular N-H...O=C hydrogen bond. The urethane group is not involved in any intermolecular hydrogen bonding. Only weak intermolecular hydrogen bonds and hydrophobic contacts are observed in the crystal structure. These are C-H...O hydrogen bonds and CH/pi interactions with donor...acceptor distances, C...O ca. 3.5 A a…

Models MolecularStereochemistryPopulationMolecular ConformationCrystallography X-RayRing (chemistry)chemistry.chemical_compoundSpectroscopy Fourier Transform InfraredDrug DiscoveryMoleculeCysteineC5 conformationWeak hydrogen bondseducationConformational isomerismeducation.field_of_studyS-tritylcysteineChemistryHydrogen bondCrystal structureIntermolecular forceHydrogen BondingGeneral ChemistryGeneral MedicineFTIR spectroscopyIntramolecular forceIndicators and ReagentsGasesAb initio calculationsMethyl groupChemical and Pharmaceutical Bulletin
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The Low Barrier Hydrogen Bond in the Photoactive Yellow Protein: A Vacuum Artifact Absent in the Crystal and Solution

2016

Journal of the American Chemical Society 138(51), 16620 - 16631 (2016). doi:10.1021/jacs.6b05609

Models Molecularphotoactive yellow proteinlow-barrier hydrogen bondVacuumHydrogenProtein ConformationLow-barrier hydrogen bondNeutron diffractionchemistry.chemical_elementProtonationCrystallography X-RayPhotoreceptors Microbial010402 general chemistry01 natural sciencesBiochemistryCatalysisColloid and Surface ChemistryProtein structureBacterial Proteins0103 physical sciencesta116Photoactive yellow proteinvetysidokset010304 chemical physicsHydrogen bondChemistryHydrogen BondingGeneral Chemistry5400104 chemical sciencesSolutionsCrystallographyhydrogen bondsddc:540Proton NMRArtifactsJournal of the American Chemical Society
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Enantioselective Synthesis of Tetrahydroprotoberberines and Bisbenzylisoquinoline Alkaloids from a Deprotonated α-Aminonitrile

2011

Under controlled conditions, 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile can be quantitatively deprotonated in the α-position. Its alkylation directly furnishes 3,4-dihydroisoquinolines which can serve as starting materials for the preparation of various alkaloids. Here, the preparation of the benzylisoquinolines (+)-laudanidine, (+)-armepavine, and (+)-laudanosine as well as the tetrahydroprotoberberines (-)-corytenchine and (-)-tetrahydropseudoepiberberine using Noyori's asymmetric transfer hydrogenation are described. The dimeric alkaloids (+)-O-methylthalibrine and (+)-tetramethylmagnolamine were obtained from nonracemic precursors in Ullmann diaryl ether syntheses.

Molecular StructureChemistryBerberine AlkaloidsOrganic ChemistryEnantioselective synthesisStereoisomerismStereoisomerismAlkylationTransfer hydrogenationBenzylisoquinolinesAlkaloidsDeprotonationNitrilesMoleculeOrganic chemistryBenzylisoquinolinesBerberine AlkaloidsThe Journal of Organic Chemistry
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Enantioselective Synthesis of (−)-Dihydrocodeine and Formal Synthesis of (−)-Thebaine, (−)-Codeine, and (−)-Morphine from a Deprotonated α-Aminonitri…

2014

The α-benzylation of a deprotonated bicyclic α-aminonitrile, followed by Noyori's asymmetric transfer hydrogenation combined with the Grewe cyclization onto a symmetrical A-ring precursor, are the key steps of a short and high-yielding enantioselective synthesis of the morphinan (-)-dihydrocodeine. This compound can be converted to (-)-thebaine in high yield by known transformations, while (-)-codeine and (-)-morphine are available from an advanced intermediate.

MorphinanThebaineMolecular StructureMorphineBicyclic moleculeCodeineStereochemistryOrganic ChemistryEnantioselective synthesisStereoisomerismStereoisomerismTransfer hydrogenationBiochemistryThebainechemistry.chemical_compoundDeprotonationchemistryYield (chemistry)NitrilesmedicineHydrogenationPhysical and Theoretical Chemistrymedicine.drugOrganic Letters
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Complete Measurement of the Λ Electromagnetic Form Factors.

2019

The exclusive process e+e−→ΛΛ¯, with Λ→pπ− and Λ¯→p¯π+, has been studied at s=2.396 GeV for measurement of the timelike Λ electric and magnetic form factors, GE and GM. A data sample, corresponding to an integrated luminosity of 66.9 pb−1, was collected with the BESIII detector for this purpose. A multidimensional analysis with a complete decomposition of the spin structure of the reaction enables a determination of the modulus of the ratio R=|GE/GM| and, for the first time for any baryon, the relative phase ΔΦ=ΦE−ΦM. The resulting values are R=0.96±0.14(stat)±0.02(syst) and ΔΦ=37°±12°(stat)±6°(syst), respectively. These are obtained using the recently established and most precise value of …

Multi-dimensional analysisElectron–positron annihilationRelative phaseHadronAnalytical chemistryGeneral Physics and AstronomyHadronsOBSERVABLESLambdaBaryon01 natural sciencesArticleNOHigh Energy Physics - ExperimentSubatomär fysikGermanium compoundsElectromagnetic form factorsSubatomic Physics0103 physical sciencesMagnetic form factorTwo-photon exchangePiddc:530010306 general physicsAsymmetry parameterProton Scattering; Nucleons; HydrogenPhysicsIntegrated luminosityDecompositionPhysicsHigh Energy Physics::PhenomenologyApproximation theoryPhysics multidisciplinaryPhotonHigh Energy Physics - Experiment; High Energy Physics - ExperimentBaryonLuminanceSpin structuresHigh Energy Physics::ExperimentMagnetic form factorMulti dimensional analysisBar (unit)Physical review letters
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Synthesis and characterization of nanocrystalline LaNi5 hydrogen storage materials

2009

With the growing environmental concerns of greenhouse gas emissions from the burning of fossil fuels, it is becoming increasingly important to switch to cleaner alternative fuels such as hydrogen [1]. Inter-metallic LaNi5 is one of the most widely used and studied solid-state hydrogen storage material – a pet material for the prototype systems using hydrogen fuel. However, nanostructuring effects on this systems are not yet fully explored. Recently we have carried out systematic studies regarding the effect of nanostructuring on the hydrogen sorption properties of this material [2]. Unlike some other potential hydrogen storage materials, which shows faster kinetics upon nanostructuring, the…

Nanostructuring ball milling hydrogen storage LaNi5
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Ni alloy nanowires as high efficiency electrode materialsnfor alkaline electrolysers

2020

Hydrogen production by water electrolysis (WE) is a very promising technology because it is a pollution-free process especially if renewable sources are employed to energy supply. Nowadays, the cost of hydrogen production by WE is higher than other available technologies, which makes WE not competitive. Many efforts have been made to improve WE performance, through the use of electrodes made of transition metal alloys as cathode and compound of metal oxide as anode [1]. In the field of water-alkaline electrolyzer, the development of cheap nanoporous based nickel electrodes with high electrocatalytic features is one of the potential approaches to increase the WE performance [2]. A facile met…

Nanowires electrolyzers water splitting oxygen evolution hydrogen evolution electrocatalystisSettore ING-IND/23 - Chimica Fisica ApplicataSettore ING-IND/17 - Impianti Industriali Meccanici
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Development of a nanostructured sensor for monitoring oxidative stress in living cells

2018

Oxidative burden is elevated in the lung of COPD patients and is associated with aging and chronic inflammation. When overcoming physiological levels, reactive oxygen species (ROS) cause cell damage and sustain inflammation. Both lung epithelium and alveolar macrophages contribute to ROS generation. Currently, ROS generation is measured using fluorescent probes and colorimetric/fluorimetric assays. We present an amperometric nanostructured sensor for real-time detection of hydrogen peroxide (H2O2) released by living cells. The H2O2 sensing performance was evaluated through the current vs time response of platinum rod at a working potential of −0.45 V vs saturated calomel electrode acting as…

Nigericin02 engineering and technology010402 general chemistrymedicine.disease_cause01 natural sciencesFlow cytometrychemistry.chemical_compoundIn vivoelectrochemical sensors hydrogen peroxide COPD ROSmedicineHydrogen peroxideCell damagechemistry.chemical_classificationReactive oxygen speciesmedicine.diagnostic_testbusiness.industryCell growth021001 nanoscience & nanotechnologymedicine.disease0104 chemical sciencesSettore ING-IND/23 - Chimica Fisica ApplicatachemistryBiophysics0210 nano-technologybusinessOxidative stress
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