Search results for "MANGANESE"

showing 10 items of 666 documents

A Binuclear MnIII Complex of a Scorpiand-Like Ligand Displaying a Single Unsupported MnIII–O–MnIII Bridge

2012

The crystal structure of a binuclear Mn(III) complex of a scorpiand-like ligand (L) displays an unsupported single oxo bridging ligand with a Mn(III)-O-Mn(III) angle of 174.7°. Magnetic susceptibility measurements indicate strong antiferromagnetic coupling between the two metal centers. DFT calculations have been carried out to understand the magnetic behavior and to analyze the nature of the observed Jahn-Teller distortion. Paramagnetic (1)H NMR has been applied to rationalize the formation and magnetic features of the complexes formed in solution.

Models MolecularManganeseMagnetic Resonance SpectroscopyChemistryLigandBridging ligandNuclear magnetic resonance spectroscopyCrystal structureCrystallography X-RayLigandsMagnetic susceptibilityInorganic ChemistryMetalCrystallographyParamagnetismCoordination Complexesvisual_artMagnetsvisual_art.visual_art_mediumProton NMRPhysical and Theoretical ChemistryOxygen CompoundsInorganic Chemistry
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Cubane-Type CuII4 and MnII2MnIII2 Complexes Based on Pyridoxine: A Versatile Ligand for Metal Assembling

2013

By using Vitamin B6 in its monodeprotonated pyridoxine form (PN-H) [PN = 3-hydroxy-4,5-bis(hydroxymethyl)-2-methylpyridine], two tetranuclear compounds of formula [Mn4(PN-H)4(CH3CO2)3Cl2]Cl·2CH3OH·2H2O (1) and [Cu4(PN-H)4Cl2(H2O)2]Cl2 (2) have been synthesized and magneto-structurally characterized. 1 crystallizes in the triclinic system with space group P1 whereas 2 crystallizes in the orthorhombic system with Fdd2 as space group. They exhibit Mn(II)2Mn(III)2 (1) and Cu(II)4 (2) cubane cores containing four monodeprotonated pyridoxine groups simultaneously acting as chelating and bridging ligands (1 and 2), three bridging acetate ligands in the syn-syn conformation (1), and two terminally …

Models MolecularManganeseMolecular StructureStereochemistryLigandPyridoxineTriclinic crystal systemLigandsMagnetic susceptibilitySquare pyramidal molecular geometryInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryOctahedronCubaneOrganometallic CompoundsHydroxymethylOrthorhombic crystal systemPhysical and Theoretical ChemistryCopperInorganic Chemistry
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Polycationic Mn12Single-Molecule Magnets as Electron Reservoirs withS>10 Ground States

2004

Models MolecularManganesePolymersChemistryInorganic chemistryTemperaturechemistry.chemical_elementElectronsGeneral ChemistryManganeseElectronGeneral MedicineCrystallography X-RayCatalysisMagneticsCationsMagnetOrganometallic CompoundsThermodynamicsMoleculeAngewandte Chemie
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Bioinspired manganese(II) complexes with a clickable ligand for immobilisation on a solid support.

2014

International audience; Clickable ligands like N,N′-bis((pyridin-2-yl)methyl)prop-2-yn-1-amine (L1) and N-((1-methyl-1H-imidazol-2-yl)methyl)-N-(pyridin-2-ylmethyl)prop-2-yn-1-amine (L2) have been used to synthesise a series of manganese(II) complexes for grafting onto appropriate solid supports. These ligands mimic the 2-His-1-carboxylate facial chelation present in the active site of the manganese-dependent dioxygenase (MndD), while the alkyne side function allows grafting of the ligand onto an azido-functionalised support using “click chemistry” methodologies. Such synthetic analogues of the MndD crystallise in the solid state as double halide or pseudohalide-bridged dinuclear manganese(…

Models MolecularStereochemistryMolecular ConformationAlkynechemistry.chemical_elementManganese[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistryCrystallography X-RayLigands01 natural scienceslaw.inventionDioxygenasesInorganic ChemistrylawCoordination ComplexesCatalytic DomainPolymer chemistryChelationElectron paramagnetic resonanceSolid-Phase Synthesis Techniqueschemistry.chemical_classificationManganesebiology010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryElectron Spin Resonance SpectroscopyActive site[CHIM.CATA]Chemical Sciences/Catalysis[CHIM.MATE]Chemical Sciences/Material chemistrySilicon Dioxide0104 chemical scienceschemistrySuperexchangebiology.proteinClick chemistryClick ChemistryDalton transactions (Cambridge, England : 2003)
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Solid-State Aggregation of Metallacyclophane-Based MnIICuII One-Dimensional Ladders

2012

Two distinct one-dimensional (1) and two-dimensional (2) mixed-metal-organic polymers have been synthesized by using the "complex-as-ligand" strategy. The structure of 1 consists of isolated ladderlike Mn(II)(2)Cu(II)(2) chains separated from each other by neutral Mn(II)(2) dimers, whereas 2 possesses an overall corrugated layer structure built from additional coordinative interactions between adjacent Mn(II)(2)Cu(II)(2) ladders. Interestingly, 1 and 2 show overall ferri- and antiferromagnetic behavior, respectively, as a result of their distinct crystalline aggregation in the solid state.

Models Molecularchemistry.chemical_classificationManganeseMolecular StructureTemperatureSolid-statePolymerCrystallography X-RayInorganic ChemistryCrystallographychemistryOrganometallic CompoundsAntiferromagnetismPhysical and Theoretical ChemistryLayer (electronics)CopperInorganic Chemistry
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Mn, Fe, Zn and As speciation in a fast-growing ferromanganese marine nodule

2004

The speciation of Mn, Fe, As and Zn in a fast-growing (0.02mm/yr), shallow-marine ferromanganese nodule has been examined by micro X-ray fluorescence, micro X-ray diffraction, and micro X-ray absorption spectroscopy. This nodule exhibits alternating Fe-rich and Mn-rich layers reflecting redox variations in water chemistry. Fe occurs as two-line ferrihydrite. The As is strictly associated with Fe and is mostly pentavalent, with an environment similar to that of As sorbed on or coprecipitated with synthetic ferrihydrite. The Mn is in the form of turbostratic birnessite with ~;10 percent trivalent manganese in the layers and probably ~;8 percent corner-sharing metal octahedra in the interlayer…

Nodule (geology)BirnessiteXASInorganic chemistrychemistry.chemical_elementManganese010501 environmental sciencesengineering.material010502 geochemistry & geophysics01 natural sciencesFerromanganeseMetalFerrihydriteXAS EXAFS marine ferromanganese nodule Baltic sea speciation[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/GeochemistryGeochemistry and Petrology0105 earth and related environmental sciencesX-ray absorption spectroscopyBaltic seaExtended X-ray absorption fine structureRadiochemistrymarine ferromanganese nodule6. Clean waterEXAFSspeciationchemistryvisual_artEarth Sciencesvisual_art.visual_art_mediumengineeringEnvironmental scienceGeochimica et Cosmochimica Acta
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Changes in nuclear structure along the Mn isotopic chain studied via charge radii

2016

The hyperfine spectra of $^{51,53-64}$Mn were measured in two experimental runs using collinear laser spectroscopy at ISOLDE, CERN. Laser spectroscopy was performed on the atomic $3d^5\ 4s^2\ ^{6}\text{S}_{5/2}\rightarrow 3d^5\ 4s4p\ ^{6}\text{P}_{3/2}$ and ionic $3d^5\ 4s\ ^{5}\text{S}_2 \rightarrow 3d^5\ 4p\ ^{5}\text{P}_3$ transitions, yielding two sets of isotope shifts. The mass and field shift factors for both transitions have been calculated in the multiconfiguration Dirac-Fock framework and were combined with a King plot analysis in order to obtain a consistent set of mean-square charge radii which, together with earlier work on neutron-deficient Mn, allow the study of nuclear struc…

Nuclear and High Energy PhysicsField (physics)N=28FOS: Physical sciences114 Physical sciences01 natural sciencesSpectral line0103 physical sciencesPROGRAMNuclear Physics - ExperimentNeutronNuclear Experiment (nucl-ex)LASER SPECTROSCOPY010306 general physicsSpectroscopyCALCIUM ISOTOPESNuclear ExperimentHyperfine structureisotopesPhysicsisotoopitta114010308 nuclear & particles physicsNuclear structureSHIFTShyperfine spectraOrder (ring theory)Charge (physics)mangaaniQUADRUPOLE-MOMENTSnuclear structuremanganeseSHELL-MODELlaser spectroscopyNEUTRONPräzisionsexperimente - Abteilung BlaumAtomic physicsPhysical Review C
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Mössbauer Study of Lanthanum–Strontium Ferromanganite Oxides

2004

The La0.88Sr0.2Mn(1−y)Fey0(3±δ, i (LSMF with y = 0, 0.2, 0.5, 0.8, 1) compounds are prospective cathode materials for advanced solid oxide fuel cells (SOFC) application operating at 700° C. Usual analysis methods like thermogravimetric analysis or redox titration enable to determine the average oxidation state of both manganese and iron cations. The comparative role of iron and manganese in B-site was evaluated by 57Fe Mossbauer spectroscopy. Spectra revealed that the complete substitution of iron for manganese induces the formation of Fe5+ for the compound with y = 1. However, no tetravalent iron cation was observed in air for the LSMF compounds with y = 0.2, 0.5 and 0.8. This means that o…

Nuclear and High Energy PhysicsInorganic chemistryOxidechemistry.chemical_elementDisproportionation02 engineering and technologyManganese010402 general chemistry01 natural sciences7. Clean energychemistry.chemical_compoundOxidation stateRedox titrationMössbauer spectroscopyLanthanum[CHIM]Chemical SciencesPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUSValence (chemistry)021001 nanoscience & nanotechnologyCondensed Matter PhysicsAtomic and Molecular Physics and Optics0104 chemical scienceschemistry13. Climate action0210 nano-technology
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Evidence for Increased neutron and proton excitations between 51−63 Mn

2015

The hyperfine structures of the odd-even 51−63Mnatoms (N=26 −38) were measured using bunched beam collinear laser spectroscopy at ISOLDE, CERN. The extracted spins and magnetic dipole moments have been compared to large-scale shell-model calculations using different model spaces and effective interactions. In the case of 61,63Mn, the results show the increasing importance of neutron excitations across the N=40subshell closure, and of proton excitations across the Z=28shell gap. These measurements provide the first direct proof that proton and neutron excitations across shell gaps are playing an important role in the ground state wave functions of the neutron-rich Mn isotopes. publisher: Els…

Nuclear and High Energy PhysicsProtonNuclear TheoryMagnetic dipole momentsMagnetic dipole momentNuclear Physics - ExperimentNeutronPhysics::Atomic PhysicsNuclear ExperimentWave functionHyperfine structurePhysicsManganeseta114SpinsMagnetic momentMagnetic dipole moment; Manganese; Spin determination; Nuclear and High Energy Physicsmangaanilcsh:QC1-999Spin determinationPhysics::Accelerator PhysicsPräzisionsexperimente - Abteilung BlaumAtomic physicsGround stateMagnetic dipolelcsh:PhysicsPhysics Letters B
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Classical-spin approach to a magnetic comb-like chain: application to the two-sublattice chain compound MnMn(CDTA)·7H2O

1991

Abstract We report on the magnetic properties of the two-sublattice manganese chain MnMn(CDTA)·7H 2 O. In view of the structural features, this compound may give rise to a novel type of one-dimensional magnetic network formed by a chain of exchange coupled triangles. A classical-spin model that considers two magnetic sites coupled through two different and isotropic exchange interactions is developed and used in order to analyze the magnetic properties of this compound. The possibility of having a spinfrustration is also examined.

Nuclear magnetic resonancechemistryChain (algebraic topology)Chemical physicsIsotropyGeneral Physics and Astronomychemistry.chemical_elementCondensed Matter::Strongly Correlated ElectronsManganesePhysical and Theoretical ChemistrySpin (physics)Chemical Physics Letters
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