Search results for "Paramagnetic"

showing 10 items of 600 documents

The impact of model peptides on structural and dynamic properties of egg yolk lecithin liposomes - experimental and DFT studies.

2015

Electron spin resonance (ESR), 1H-NMR, voltage and resistance experiments were performed to explore structural and dynamic changes of Egg Yolk Lecithin (EYL) bilayer upon addition of model peptides. Two of them are phenylalanine (Phe) derivatives, Ac-Phe-NHMe (1) and Ac-Phe-NMe2 (2), and the third one, Ac-(Z)-ΔPhe-NMe2 (3), is a derivative of (Z)-α,β-dehydrophenylalanine. The ESR results revealed that all compounds reduced the fluidity of liposome's membrane, and the highest activity was observed for compound 2 with N-methylated C-terminal amide bond (Ac-Phe-NMe2). This compound, being the most hydrophobic, penetrates easily through biological membranes. This was also observed in voltage an…

Models Molecularfood.ingredientBioengineeringBiochemistryLecithinlaw.inventionfoodlawLecithinsOrganic chemistryPeptide bondElectron paramagnetic resonanceMolecular BiologyLiposomeMolecular StructureChemistryBilayerBiological membraneGeneral ChemistryGeneral MedicineNuclear magnetic resonance spectroscopyEgg YolkCrystallographyMembraneLiposomesMolecular MedicineQuantum TheoryThermodynamicsPeptidesChemistrybiodiversity
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Effect of tin and lead chlorotriphenyl analogues on selected living cells.

2010

Three kinds of living cells, human embryonic kidney cells, Saccharomyces cerevisiae, and Escherichia coli, were tested for their sensitivity to chlorotriphenyltin and chlorotriphenyllead. The tin compound proved definitely more toxic than the lead derivative, particularly in the case of the human embryonic kidney cells devoid of any protective cell wall. Electron paramagnetic resonance (EPR) comparative studies carried out by using a natural model liposome system (egg yolk lecithin) confirmed considerable changes within the lipid bilayer upon doping by the aforementioned additives, which may be crucial to the mechanism of the observed cell cleavage. The individual dopants revealed diverse i…

Models Molecularfood.ingredientCell SurvivalHealth Toxicology and MutagenesisCellMolecular Conformationchemistry.chemical_elementSaccharomyces cerevisiaeToxicologyCleavage (embryo)BiochemistryLecithinCell wallfoodLecithinsmedicineEscherichia coliOrganometallic CompoundsOrganotin CompoundsHumansChlorotriphenyltinLipid bilayerMolecular BiologyLiposomeElectron Spin Resonance SpectroscopyGeneral MedicineYeastChlorotriphenylleadElectron Paramagnetic Resonancemedicine.anatomical_structureMembraneHEK293 CellsBiochemistrychemistryLeadHuman Embryonic Kidney CellsLiposomesMolecular MedicineTinJournal of biochemical and molecular toxicology
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Copper Uptake Induces Self-Assembly of 18.5 kDa Myelin Basic Protein (MBP)

2010

Myelin basic protein (MBP) is predominantly found in the membranes of the myelin sheath of the central nervous system and is involved in important protein-protein and protein-lipid interactions in vivo and in vitro. Furthermore, divalent transition metal ions, especially Zn(2+) and Cu(2+), seem to directly affect the MBP-mediated formation and stabilization of the myelin sheath of the central nervous system. MBP belongs to the realm of intrinsically disordered proteins, and only fragmentary information is available regarding its partial structure(s) or supramolecular arrangements. Here, using standard continuous wave and modern pulse electron paramagnetic resonance methods, as well as dynam…

Models Molecularinorganic chemicalsLightBiophysicsSupramolecular chemistryIn Vitro TechniquesIntrinsically disordered proteinsBiophysical PhenomenaDivalentlaw.inventionlawAnimalsScattering RadiationMoleculeParticle SizeElectron paramagnetic resonanceIon transporterchemistry.chemical_classificationIon TransportbiologyProteinElectron Spin Resonance SpectroscopyMyelin Basic ProteinMyelin basic proteinSolutionsZincMembranechemistryBiochemistrybiology.proteinBiophysicsCattleProtein MultimerizationCopperBiophysical Journal
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When two become one: Integrating FRET and EPR into one structural model

2021

Models StructuralPhysicsFörster resonance energy transferNuclear magnetic resonancelawElectron Spin Resonance SpectroscopyFluorescence Resonance Energy TransferBiophysicsElectron paramagnetic resonancelaw.inventionBiophysical Journal
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Synthesis, molecular and electronic structures of a paramagnetic trimetallic cluster containing an unusual Mo3(μ3-Se)2(μ-Se)3 core

2014

Abstract The electron precise [Mo3(μ3-Se)(μ-Se)3(dppe)3Br3]+ incomplete cuboidal complex, with six cluster skeletal electrons (CSE), was converted into the paramagnetic bicapped [Mo3(μ3-Se)2(μ-Se)3(dppe)3]+ cluster (1+), with an unusual seven metal electron population, by treatment with elemental Ga. The cluster core consists of an almost equilateral Mo3 triangle (Mo–Mo distances are in the range 2.7583(7)–2.7748(7) A with an average value of 2.77(3) A), capped by two selenide ligands. The remaining selenium atoms bridge adjacent metal atoms, defining a virtually planar Mo3(μ-Se)3 unit, with the capping Se atoms positioned above and below this plane. The new complex possesses a doublet grou…

MolybdenumCrystal structureCrystal structurelaw.inventionInorganic ChemistrySeleniumchemistry.chemical_compoundCrystallographyDelocalized electronParamagnetismUnpaired electronchemistrylawSelenideMaterials ChemistryCluster (physics)Physical and Theoretical ChemistryElectron paramagnetic resonanceGround stateCluster compoundsESRPolyhedron
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Fullerene as a Platform for Recyclable TEMPO Organocatalysts for the Oxidation of Alcohols

2014

[60]Fullerene has been employed successfully as a molecular platform to anchor 12 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) moieties. Such an octahedrally substituted C60-derivative has been employed as an organocatalyst for the oxidation of primary and secondary alcohols using the Anelli protocol. The reaction showed a general applicability to various alcohols, and the catalyst was recovered easily and could be recycled for at least seven cycles with no loss in catalytic activity. EPR spectroscopy studies revealed that the amount of radicals decreases during the catalytic cycles, even if the recovered material still displays unchanged catalytic activity. This new approach paves the way …

NITROXIDEFullerenePrimary (chemistry)alcoholoxidationChemistryCATALYSISRadicalOrganic ChemistrySettore CHIM/06 - Chimica Organicaorganocatalysiorganic oxidationlaw.inventionCatalysisInorganic ChemistrylawAlcohol oxidationOrganocatalysisOrganic chemistryPhysical and Theoretical ChemistryTEMPOElectron paramagnetic resonanceFULLERENEEPR spectroscopyESR
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A tetranuclear organorhenium(i) complex of the 2,3,5,6-tetrafluoro-7,7,8,8-tetracyano-p-quinodimethane radical anion, TCNQF4˙−

2008

The radical complex {(mu(4)-TCNQF4)[Re(CO)(3)(bpy)](4)}(PF(6))(3), as prepared and isolated from the reaction between TCNQF4 and [Re(CO)(3)(bpy)(MeOH)](PF(6)), was studied electrochemically and by IR vibrational spectroscopy, UV-Vis-NIR absorption spectroscopy, and by EPR at 9.5, 190 and 285 GHz. The isotropic g factor of 2.0058, the detectable g anisotropy, and the (185,187)Re EPR hyperfine coupling of 0.95 mT for four equivalent metal nuclei support predominant, but not exclusive, spin localisation at the bridging ligand. Nitrile and metal carbonyl stretching frequencies as well as the typically structured near infrared absorption band lend further support to (TCNQF4 (-))(Re(I))(4) as the…

NitrileAbsorption spectroscopyChemistryLigandInfrared spectroscopyBridging ligandMetal carbonylPhotochemistrylaw.inventionInorganic Chemistrychemistry.chemical_compoundElectron transferCrystallographylawElectron paramagnetic resonanceDalton Transactions
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How Hydrogen Bonds Affect Reactivity and Intervalence Charge Transfer in Ferrocenium‐Phenolate Radicals

2016

The ferrocenyl-phenol 2,4-di-tert-butyl-6-(ferrocenylcarbamoyl)phenol (H-1) forms intramolecular hydrogen bonds which are absent in its constitutional isomer 2,6-di-tert-butyl-4-(ferrocenylcarbamoyl)phenol (H-2). Their corresponding bases 1– and 2– show intra- and intermolecular NH···O hydrogen bonds, respectively. The phenolate 1– is reversibly oxidized to 1·, whereas 2– only undergoes a quasi-reversible oxidation to 2·, which suggests a higher reactivity. The radical pools of 1· and 2· formed by the oxidation/deprotonation of H-1 and H-2 have been probed by (rapid-freeze) electron paramagnetic resonance (EPR) spectroscopy and by spin-trapping techniques to elucidate the types of radicals …

Nitroxide mediated radical polymerization010405 organic chemistryChemistryHydrogen bondRadicalIntervalence charge transfer010402 general chemistryPhotochemistry01 natural sciencesMedicinal chemistry0104 chemical scienceslaw.inventionInorganic ChemistryDeprotonationlawValence isomerIntramolecular forceElectron paramagnetic resonanceEuropean Journal of Inorganic Chemistry
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Layered ferromagnets hosting tetraalkylammonium-substituted nitronyl nitroxide free radicals

2008

This paper describes the structural, magnetic and EPR properties of hybrid organic/inorganic magnets formed by anionic heterometallic oxalato-based layers and cationic nitronyl nitroxide (NN) free radicals of the tetraalkylammonium type. A series of compounds of formula nBu3NCH2NN[MCr(ox)3] (M = Mn (1), Ni (2), Zn (3)) has been prepared and studied by AC and DC magnetic susceptibility measurements and EPR spectroscopy. Magnetic order with critical temperatures ranging from 5 K to 15 K was confirmed. EPR measurements show that the organic spin carriers interact significantly with the inorganic network.

Nitroxide mediated radical polymerizationChemistryRadicalInorganic chemistryCationic polymerizationGeneral ChemistryMagnetic susceptibilitylaw.inventionCrystallographyFerromagnetismlawMaterials ChemistryHybrid materialElectron paramagnetic resonanceGroup 2 organometallic chemistryJournal of Materials Chemistry
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Nitronyl Nitroxide Radicals Linked to Exchange‐Coupled Metal Dimers – Studies Using X‐ray Crystallography, Magnetic Susceptibility Measurements, EPR …

2009

To study long-range magnetic interactions between exchange-coupled metal centers and a radical moiety coordinated through a peripheral group, three new homodimetallic complexes with MnII, CoII, and ZnII bridged by a nitronyl nitroxide (NIT) substituted benzoate ligand with the structure [(NIT-C6H4-COO)M2(LR)](ClO4)2 {M = MnII, CoII, and ZnII; NIT = nitronyl nitroxide and LR = N,N,N′,N′-tetrakis(2-benzimidazolylalkyl)-2-hydroxy-1,3-diaminopropane} have been prepared and studied by X-ray crystallography, magnetic susceptibility measurements, EPR spectroscopy, and density functional theory calculations. For comparison, related complexes with MnII and CoII bridged by a diamagnetic nitrobenzoate…

Nitroxide mediated radical polymerizationCoordination sphereChemistryLigandBridging ligandMagnetic susceptibilitylaw.inventionInorganic ChemistryCrystallographyComputational chemistrylawAntiferromagnetismDensity functional theoryElectron paramagnetic resonanceEuropean Journal of Inorganic Chemistry
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