Search results for "isomers"

showing 10 items of 64 documents

Binding abilities of dehydropeptides towards Cu(II) and Ni(II) ions. Impact of Z–E isomerization on metal ion binding

2002

The study on the binding ability of dehydro-tri- and tetrapeptides has shown that the alpha,beta-double bond has a critical effect on the peptide coordination to metal ions. It may affect the binding of the vicinal amide nitrogens by the electronic effect and stabilize the complex due to steric effects. The (Z) isomer is the most effective in stabilizing of the complexes formed. The presence of large side chain in the dehydroamino acid residue may also be critical for the coordination mode in the metallopeptide systems.

Steric effectsNickel(II) complexesE–Z isomersMetal ion bindingChemistryMetal ions in aqueous solutionPhotochemistryBiochemistryisomerizationInorganic ChemistryMetalCrystallographychemistry.chemical_compounddehydropeptidesAmidevisual_artSide chainvisual_art.visual_art_mediumElectronic effectCopper(II) complexesIsomerizationVicinalJournal of Inorganic Biochemistry : an interdisciplinary journal
researchProduct

Substrate-dependent fluorinations of highly functionalized cycloalkanes

2016

Abstract Substrate-dependent fluorinations of several highly functionalized cycloalkanes with multiple stereocentres were investigated. The synthetic transformations were based on selective functionalization of the ring C C bonds of the readily available bicyclic β-lactams by epoxidation and regioselective nucleophilic oxirane opening with azide or cyanide, followed by hydroxy–fluorine exchange with Deoxofluor. Depending on the substituents and their relative steric arrangement, the attempted fluorinations produced different types of substituted cycloalkanes. These selective, substrate-directed synthetic procedures and their presumed pathways towards interesting highly functionalized fluori…

Steric effectsamino acidsBicyclic molecule010405 organic chemistryChemistryOrganic ChemistryselectivityRegioselectivitydeoxygenation010402 general chemistryRing (chemistry)01 natural sciencesBiochemistryfluorination0104 chemical sciencesCycloalkanechemistry.chemical_compoundNucleophileDrug DiscoveryOrganic chemistrystereoisomersAzideSelectivityta116Tetrahedron
researchProduct

Toward a density functional description of liquid pH2.

2010

A finite-temperature density functional approach to describe the properties of parahydrogen in the liquid-vapor coexistence region is presented. The first proposed functional is zero-range, where the density-gradient term is adjusted so as to reproduce the surface tension of the liquid-vapor interface at low temperature. The second functional is finite-range and, while it is fitted to reproduce bulk pH2 properties only, it is shown to yield surface properties in good agreement with experiments. These functionals are used to study the surface thickness of the liquid-vapor interface, the wetting transition of parahydrogen on a planar Rb model surface, and homogeneous cavitation in bulk liquid…

Surface (mathematics)Chemical Physics (physics.chem-ph)Statistical Mechanics (cond-mat.stat-mech)Yield surfaceChemistryThermodynamicsFOS: Physical sciencesFísicaCondensed Matter - Soft Condensed MatterSpin isomers of hydrogenFunctional descriptionSurface tensionPhysics::Fluid DynamicsPlanarWetting transitionPhysics - Chemical PhysicsCavitationPhysics::Atomic and Molecular ClustersSoft Condensed Matter (cond-mat.soft)Physical and Theoretical ChemistryCondensed Matter - Statistical MechanicsThe journal of physical chemistry. A
researchProduct

Real-Time Nuclear Magnetic Resonance Detection of Fumarase Activity Using Parahydrogen-Hyperpolarized [1- 13 C]Fumarate

2019

Hyperpolarized fumarate can be used as a probe of real-time metabolism in vivo, using carbon-13 magnetic resonance imaging. Dissolution dynamic nuclear polarization is commonly used to produce hyperpolarized fumarate, but a cheaper and faster alternative is to produce hyperpolarized fumarate via PHIP (parahydrogen-induced polarization). In this work, we trans-hydrogenate [1-13C]acetylene dicarboxylate with para-enriched hydrogen using a commercially available Ru catalyst in water to produce hyperpolarized [1-13C]fumarate. We show that fumarate is produced in 89% yield, with succinate as a side product in 11% yield. The proton polarization is converted into 13C magnetization using a constant…

Time FactorsHydrogenNuclear Magnetic Resonancechemistry.chemical_element010402 general chemistrySpin isomers of hydrogenPhotochemistry01 natural sciencesBiochemistryCatalysisFumarate HydrataseCatalysisMagnetizationchemistry.chemical_compoundColloid and Surface ChemistryFumaratesMoleculeCarbon IsotopesMolecular StructureFumarase activityCarbon Isotopes; Fumarate Hydratase; Fumarates; Molecular Structure; Time Factors; Nuclear Magnetic Resonance BiomolecularGeneral Chemistry0104 chemical sciencesAcetylenechemistryFumaraseBiomolecularJournal of the American Chemical Society
researchProduct

Polarization transfer via field sweeping in parahydrogen-enhanced nuclear magnetic resonance.

2019

<div><br></div><div><table><tr><td>We show that in a spin system of two magnetically inequivalent protons coupled to a heteronucleus such as 13C, an adiabatic magnetic field sweep, passing through zero field, transfers proton singlet order into magnetization of the coupled heteronucleus. This effect is potentially useful in parahydrogen-enhanced nuclear magnetic resonance, and is demonstrated on singlet-hyperpolarized [1-13C]maleic acid, which is prepared via the reaction between [1-13C]acetylene dicarboxylic acid and para-enriched hydrogen gas. The magnetic field sweeps are of microtesla amplitudes, and have durations on the order of seconds. We sh…

Zero field NMRMaterials science010304 chemical physicsMaleic acidHydrogenField (physics)ProtonGeneral Physics and Astronomychemistry.chemical_element010402 general chemistryPolarization (waves)Spin isomers of hydrogen01 natural sciences0104 chemical sciencesMagnetic fieldchemistry.chemical_compoundMagnetizationNuclear magnetic resonancechemistry0103 physical sciencesSinglet statePhysical and Theoretical ChemistryThe Journal of chemical physics
researchProduct

Decay and Fission Hindrance of Two- and Four-Quasiparticle K Isomers in 254Rf

2015

International audience; Two isomers decaying by electromagnetic transitions with half-lives of 4.7(1.1) and 247(73) mu s have been discovered in the heavy (254)Rf nucleus. The observation of the shorter-lived isomer was made possible by a novel application of a digital data acquisition system. The isomers were interpreted as the K-pi = 8(-), nu(2)(7/2(+)[624]; 9/2(-)[734]) two-quasineutron and the K-pi = 16(+), 8(-)nu(2)(7/2(+)[624]; 9/2(-)[734] circle times 8(-)pi(2) (7/2(-)[514]; 9/2(+)[624]) four-quasiparticle configurations, respectively. Surprisingly, the lifetime of the two-quasiparticle isomer is more than 4 orders of magnitude shorter than what has been observed for analogous isomer…

[PHYS]Physics [physics]General PhysicsNO-254nuclear isomersEngineeringNUCLEISTATESPhysical Sciencesrutherfordium[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]FM-250Mathematical Sciences
researchProduct

Computational investigations of 18-electron triatomic sulfur–nitrogen anions

2018

MRCI-SD/def2-QZVP and PBE0/def2-QZVP calculations have been employed for the analysis of geometries, stabilities, and bonding of isomers of the 18-electron anions N2S2−, NS2−, and NSO−. Isomers of the isoelectronic neutral molecules SO2, S2O, S3, and O3 are included for comparison. The sulfur-centered acyclic NSN2−, NSS−, and NSO− anions are the most stable isomers of their respective molecular compositions. However, the nitrogen-centered isomers SNS− and SNO− lie close enough in energy to their more stable counterparts to allow their occurrence. The experimental structural information, where available, is in good agreement with the optimized bond parameters. The bonding in all investigate…

anionit010405 organic chemistryisomeriaTriatomic moleculeOrganic Chemistrychemistry.chemical_elementGeneral ChemistryElectron010402 general chemistrylaskennallinen kemia01 natural sciencesSulfurNitrogenCatalysis0104 chemical scienceselectronic structureschemistry18-electron triatomicssulfur–nitrogen anionsrikkiyhdisteetPhysical chemistryisomerstyppiyhdisteettheoretical calculations
researchProduct

Experimental study of isomeric intruder ½+ states 197,203At

2017

A newly observed isomeric intruder ½ + state [ T ½ = 3.5 ( 6 ) ms ] is identified in 203 At using a gas-filled recoil separator and fusion-evaporation reactions. The isomer is depopulated through a cascade of E 3 and mixed M 1 / E 2 transitions to the 9 / 2 − ground state, and it is suggested to originate from the π ( s ½ ) − 1 configuration. In addition, the structures above the ½ + state in 203 At and 197 At are studied using in-beam γ -ray spectroscopy, recoil-decay tagging, and recoil-isomer decay tagging methods. The ½ + state is fed from 3 / 2 + and 5 / 2 + states, and the origin of these states are discussed. peerReviewed

astatiiniisomersintruder states
researchProduct

Palladium(II)-Mediated Addition of Benzenediamines to Isocyanides: Generation of Three Types of Diaminocarbene Ligands Depending on the Isomeric Stru…

2016

Coupling of the palladium-bis(isocyanide) complexes cis-[PdCl2(CNR)2] (R = 2,6-Me2C6H3 1, 2-Cl-6-MeC6H3 2) with benzene-1,3-diamine (BDA1) leads to the diaminocarbene species cis-[PdCl2(CNR){C(NHR)═NH(1,3-C6H4NH2)}] (5 and 6, respectively). In this reaction, BDA1 behaves as a monofunctional nucleophile that adds to one of the RNC ligands by one amino group. By contrast, the reaction of 1 and 2 with benzene-1,4-diamine (BDA2) involves both amino functionalities of the diamine and leads to the binuclear species [cis-PdCl2(CNR){μ-C(NHR)═NH(1,4-C6H4)NH═C(NHR)}-(cis)-PdCl2(CNR)] (6 and 7) featuring two 1,4-bifunctional diaminocarbene ligands. The reaction of cis-[PdCl2(CNR)2] (R = cyclohexyl 3) …

benzenediamines010405 organic chemistryStereochemistryIsocyanideOrganic Chemistrychemistry.chemical_elementdiaminocarbenespalladium complexes010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryNucleophileDiamineisomersPhysical and Theoretical ChemistryCarbeneta116PalladiumOrganometallics
researchProduct

Comparative investigations of hydroxyamine carane derivative and its R,S-diastereoisomers with strong local anesthetic activity

2001

Our previously conducted pharmacological screening led as to the discovery of the strong local anesthetic activity of the compound designated as KP-23. Earlier crystallographic studies revealed that the compound KP-23 crystallized in diastereoisomeric form in lowest symmetry. The aim of these comparative investigations was to evaluate anesthetic activity of KP-23 and its R,S-diastereoisomers, which were synthesized at the Institute of Organic Chemistry, Biochemistry and Biotechnology, Wroclaw University of Technology.

carane derivativesanesthetic activitylidocainediastereoisomersPolish Journal of Pharmacology
researchProduct