Search results for "medium"

showing 10 items of 3746 documents

The dynamic properties of the M121H azurin metal site as studied by NMR of the paramagnetic Cu(II) and Co(II) metalloderivatives

1998

The M121H azurin mutant in solution presents various species in equilibrium that can be detected and studied by 1H NMR of the Cu(II) and Co(II) paramagnetic metalloderivatives. In both cases up to three species are observed in slow exchange, the proportions of which are different for the two metalloderivatives. Above pH 5 the major species displays a tetrahedral coordination in which the His121 can be observed as a coordinated residue. Its metal site corresponds to a new type of site that is defined as a type 1.5 site. The second and third species resemble the wild type (type 1) azurin and, above pH 4.5, they are present only at a low concentration. At low pH a protonation process increases…

Magnetic Resonance SpectroscopyChemistryInorganic chemistryWild typeElectron Spin Resonance SpectroscopyTemperatureProtonationCell BiologyNuclear magnetic resonance spectroscopyCobaltHydrogen-Ion ConcentrationBiochemistryMetalParamagnetismCrystallographyResidue (chemistry)Azurinvisual_artvisual_art.visual_art_mediumSpectrophotometry UltravioletAzurinMolecular BiologyCopperCoordination geometry
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Paramagnetic Cobalt and Nickel Derivatives of Alcaligenes denitrificans Azurin and Its M121Q Mutant. A 1H NMR Study

1996

Using cobalt or nickel to replace copper in native azurin allows one to fingerprint the metal coordination site of the protein. The metal sites of wild type Alcaligenes denitrificans azurin and its M121Q mutant are clearly distinguishable through the paramagnetic 1H NMR spectra of the Ni(II) and Co(II) derivatives. In the wild type azurin, Gly45 coordinates to nickel or cobalt, while Met121 appears as a weak metal ligand. On the contrary, in the M121Q azurin mutant, the metal exhibits a clear preference for the Gln121, which coordinates through the side chain carbonyl oxygen, and Gly45 is not a ligand. Changes in the isotropic shifts and relaxation properties of signals from the Cys112, His…

Magnetic Resonance SpectroscopyProtein ConformationStereochemistryAlcaligenes denitrificanschemistry.chemical_elementBiochemistryElectron TransportMetalAzurinNickelMetalloproteinsPoint MutationAlcaligenesPlant ProteinsBinding SitesStellacyaninMolecular StructurebiologyLigandCobaltbiology.organism_classificationNMR spectra databaseNickelchemistrySpectrophotometryvisual_artvisual_art.visual_art_mediumbiology.proteinSpectrophotometry UltravioletAzurinCobaltBiochemistry
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Metal complexes of phenobarbituric acid. Chelating behavior of the phenobarbiturate ring. Anticonvulsant properties of the K2[Cu(N-methylphenobarbitu…

1992

Abstract Na2Ni(phenobarbiturato)4·3H2O, Na2Ni3(phenobarbiturato)2(OH)6·4H2O, and NaZn(phenobarbiturato)2(OH)·H2O derivatives were prepared from Ni(II) and Zn(II) and phenobarbital. The Na2Ni(phenobarbiturato)4·3H2O complex is diamagnetic and isostructural with the complex previously reported, Na2Cu(phenobarbiturato)4, suggesting a square-planar environment around the Ni(II) ion. The DMF solutions of this complex show the existence of two species. The EPR spectra of the Cu(II) doped complex show the hyperfine and superhyperfine structures. The covalence parameters α2, β2, and δ2 show a strong bonding in the equatorial plane and suggests the formation of a [CuN4] chromophore. The anticonvulsa…

Magnetic Resonance SpectroscopyStereochemistryMephobarbitalBiochemistrylaw.inventionIonInorganic ChemistryMetalStructure-Activity RelationshiplawSeizuresAnimalsChelationIsostructuralElectron paramagnetic resonanceHyperfine structureChelating AgentsElectroshockMolecular StructureChemistryElectron Spin Resonance SpectroscopyChromophoreCrystallographyCovalent bondMetalsvisual_artPhenobarbitalvisual_art.visual_art_mediumAnticonvulsantsCopperJournal of inorganic biochemistry
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Mechanisms of Water Interaction with Pore Systems of Hydrochar and Pyrochar from Poplar Forestry Waste

2014

The aim of this study was to understand the water-surface interactions of two chars obtained by gasification (pyrochar) and hydrothermal carbonization (hydrochar) of a poplar biomass. The two samples revealed different chemical compositions as evidenced by solid state (13)C NMR spectroscopy. In fact, hydrochar resulted in a lignin-like material still containing oxygenated functionalities. Pyrochar was a polyaromatic system in which no heteronuclei were detected. After saturation with water, hydrochar and pyrochar were analyzed by fast field cycling (FFC) NMR relaxometry. Results showed that water movement in hydrochar was mainly confined in very small pores. Conversely, water movement in py…

Magnetic Resonance SpectroscopyWater flowSettore AGR/13 - Chimica Agraria1600 General Chemistry1100 General Agricultural and Biological SciencesHydrothermal carbonizationAdsorptionBiocharmedicine910 Geography & travelPorosityWaste ProductsChemistryTemperatureWaterForestryGeneral Chemistry10122 Institute of GeographyPopulusAgronomyChemical engineeringCharcoalGeneral Agricultural and Biological SciencesPorous mediumSaturation (chemistry)Porosityfast field cycling NMR relaxometry hydrochar pyrochar biochar water dynamicsActivated carbonmedicine.drug
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Single-ion magnet behaviour in mononuclear and two-dimensional dicyanamide-containing cobalt(ii) complexes.

2016

Three cobalt(II) complexes of formulae [Co(dca)2(bim)4] (1), [Co(dca)2(bim)2]n (2) and [Co(dca)2(bmim)2]n (3) [dca = dicyanamide, bim = 1-benzylimidazole and bmim = 1-benzyl-2-methylimidazole] were prepared and structurally analyzed by single-crystal X-ray crystallography. Compound 1 is a mononuclear species where the cobalt(II) ion is six-coordinate with four bim molecules in the equatorial positions [Co–Nbim = 2.1546(15) and 2.1489(15) A] and two trans-positioned dca ligands [Co–Ndca = 2.1575(18) A] in the axial sites of a somewhat distorted octahedral surrounding. The structures of 2 and 3 consist of two-dimensional grids of cobalt(II) ions where each metal atom is linked to the other fo…

Magnetic moment010405 organic chemistryChemistryStereochemistrychemistry.chemical_element010402 general chemistry01 natural sciencesMagnetic susceptibility0104 chemical sciencesIonInorganic ChemistryMetalchemistry.chemical_compoundCrystallographyOctahedronvisual_artvisual_art.visual_art_mediumMoleculeCobaltDicyanamideDalton transactions (Cambridge, England : 2003)
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Hybrid materials containing organometallic cations and 3-D anionic metal dicyanamide networks of type [Cp*2M][M′(dca)3]

2004

A new series of hybrid materials of type [Cp*2M][M′(dca)3] has been prepared by cation templation and structurally characterised (M = Fe(III), Co(III); M′ = Mn(II), Fe(II), Co(II), Ni(II), Cd(II); dca− = N(CN)2−). The crystallographic analysis of [Cp*2Fe][Cd(dca)3] showed that the [Cd(dca)3]− anionic framework is of a symmetrical 3-D α-polonium type, containing octahedral Cd nodes and μ1,5-dca bridging ligands. The [Cp*2Fe]+ cations occupy the cube-like cavities within the framework. The cationic and anionic-framework sublattices remain magnetically independent and display susceptibilities, over the range 300 to 2 K, of a Curie–Weiss nature obtained by adding a S = 1/2 (Cp*2Fe+) or a S = 0 …

Magnetic orderChemistryStereochemistryCationic polymerizationInorganic ChemistryMetalCrystallographychemistry.chemical_compoundOctahedronvisual_artRelaxation effectMössbauer spectroscopyvisual_art.visual_art_mediumHybrid materialDicyanamideDalton Trans.
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Coordination Complexes of a Neutral 1,2,4-Benzotriazinyl Radical Ligand: Synthesis, Molecular and Electronic Structures, andMagnetic Properties

2015

A series of d-block metal complexes of the recently reported coordinating neutral radical ligand 1-phenyl-3-(pyrid-2-yl)-1,4-dihydro-1,2,4-benzotriazin-4-yl (1) was synthesized. The investigated systems contain the benzotriazinyl radical 1 coordinated to a divalent metal cation, MnII, FeII, CoII, or NiII, with 1,1,1,5,5,5-hexafluoroacetylacetonato (hfac) as the auxiliary ligand of choice. The synthesized complexes were fully characterized by single-crystal X-ray diffraction, magnetic susceptibility measurements, and electronic structure calculations. The complexes [Mn(1)(hfac)2] and [Fe(1)(hfac)2] displayed antiferromagnetic coupling between the unpaired electrons of the ligand and the meta…

Magnetic susceptibility measurementsAntiferromagnetic couplingIron compoundsLigands01 natural sciencesNickelheterosyklitMetal ionsta116Cobalt compoundsChelationChemistryMetal–radical interactionsMagnetismSingle crystal x-ray diffractionRadicals[CHIM.MATE]Chemical Sciences/Material chemistrymetal-radical interactionsradicalsexchange interactionsChemistrykoordinaatiokemiaUnpaired electronPositive ionsMetalsSynthesis (chemical)visual_artradikaalitvisual_art.visual_art_mediumElectronic structureCoordinating propertiesmagneettiset ominaisuudetX ray diffractionRadicalInorganic chemistryRadical interactionsElectronic structureHeterocycles010402 general chemistryCatalysisMagnetic susceptibilityMetalElectronic structure calculationsMetal complexesMagnetic properties[CHIM.COOR]Chemical Sciences/Coordination chemistrymetalli-radikaali -vuorovaikutuksetManganeseheterocycles010405 organic chemistryLigandCrystal structureOrganic ChemistryGeneral ChemistryMagnetic susceptibility0104 chemical sciencesCrystallographyOctahedronFerromagnetismExchange interactionscoordination chemistrySingle crystalsmagnetic propertiesCoordination reactions
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Magnetism and Molecular Nonlinear Optical Second-Order Response Meet in a Spin Crossover Complex

2012

International audience; The quadratic hyperpolarizability of two inorganic Schiff base metal complexes which differ from each other by the nature of the central metal ion (FeII or ZnII) is estimated using hyper-Rayleigh light-scattering (HRS) measurements. The investigated FeII microcrystals exhibit a thermal spin-crossover (SCO) from a diamagnetic to a paramagnetic state centered at T1/2 = 233 K that can be reproduced by the HRS signal whose modest intensity is mainly due to their centrosymmetric packing structure. Diamagnetic ZnII microcrystals even lead to much weaker (∼400 times) HRS intensities which are in addition temperature-independent. These observations allow us to ascribe the ch…

MagnetismHyperpolarizability02 engineering and technology010402 general chemistry01 natural sciencesMolecular physicsMetalParamagnetismchemistry.chemical_compoundNuclear magnetic resonanceSpin crossover[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistrySchiff basebusiness.industry021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral Energychemistryvisual_artvisual_art.visual_art_mediumDiamagnetismPhotonics0210 nano-technologybusiness
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Ferromagnetism in [Mn(Cp*) 2 ] + ‐Derived Complexes: the “Miraculous” Stacking in [Mn(Cp*) 2 ][Ni(dmit) 2 ]

2003

The synthesis and characterisation (X-ray structure and magnetism) of metal complexes (Ni, Au) with the [Mn(Cp*)2]+ cation and the dmit2− and dmid2− ligands are reported. [Mn(Cp*)2][Ni(dmit)2] (1) and [Mn(Cp*)2][Au(dmit)2] (2) exhibit the same structural arrangement, built on stacks of [Ni(dmit)2]− pairs separated by two [Mn(Cp*)2]+ cations, showing a ···D+D+A−A−D+D+A−A−··· motif. On the contrary, the dmid2− derivative [Mn(Cp*)2][Ni(dmid)2]·CH3CN (3) exhibits a totally different structure, built on mixed layers composed of one [Ni(dmid)2]− unit separated by two [Mn(Cp*)2]+ cations, showing a ···D+D+A−D+D+A−···motif. The layers are separated from each other by perpendicular [Ni(dmid)2]− unit…

MagnetismLigandchemistry.chemical_elementManganeseMagnetic susceptibilityInorganic ChemistryMetalCrystallographyNuclear magnetic resonanceFerromagnetismchemistryFerrimagnetismvisual_artvisual_art.visual_art_mediumAntiferromagnetismEuropean Journal of Inorganic Chemistry
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Molecular Magnetic Materials from Polyoxometalates

1994

The significance of polyoxometalates in the field of molecular magnetism is discussed. We show that this kind of inorganic complexes provides remarkable examples for the study of the exchange interactions in clusters. On the other hand, we examine the possibility of using these metal oxide anions as magnetic components of molecular materials containing organic tetrathiafulvalenes as electron donor molecules.

MagnetismOxideElectron donorequipment and suppliesMagnetic exchangeMetalchemistry.chemical_compoundchemistryChemical physicsComputational chemistryvisual_artMagnetic componentsvisual_art.visual_art_mediumMoleculeMolecular materialshuman activities
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