Search results for "MANGANESE"

showing 10 items of 666 documents

Oxidative stress protection by manganese complexes of tail-tied aza-scorpiand ligands.

2015

The Mn2+ coordination chemistry of double scorpiand ligands in which two polyazacyclophane macrocycles have been connected by pyridine, phenanthroline and bipyridine spacers has been studied by potentiometry, paramagnetic NMR and electrochemistry. All ligands show high stability with Mn2+ and the complexes were formed in a wide pH range. DFT calculations support the structures and coordination geometries derived from the study. A remarkable antioxidant activity was evidenced for these systems by the McCord-Fridovich assay and in Escherichiacoli sodAsodB deficient bacterial cells. The three systems were tested as anti-inflammatory drugs in human macrophages measuring the accumulation of cyto…

AntioxidantStereochemistrymedicine.medical_treatmentPhenanthrolineInorganic chemistrychemistry.chemical_elementManganese010402 general chemistryElectrochemistry01 natural sciencesBiochemistryAntioxidantsCoordination complexInorganic ChemistrySuperoxide dismutasechemistry.chemical_compoundBipyridineBacterial ProteinsCoordination ComplexesCell Line TumorPyridinemedicineEscherichia coliHumanschemistry.chemical_classificationManganesebiology010405 organic chemistryChemistrySuperoxide DismutaseMacrophagesAnti-Inflammatory Agents Non-Steroidal0104 chemical sciencesOxidative Stressbiology.proteinJournal of inorganic biochemistry
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[Mnii2(bpym)(H2O)8]4+ and [Miv(CN)8]4– (M = Mo and W) as building blocks in designing bpym- and cyanide-bridged bimetallic three-dimensional networks…

2002

One-pot reaction between the dinuclear [MnII2(bpym)(H2O)8]4+ complex and the mononuclear [MIV(CN)8]4− unit (M = Mo and W; bpym = 2,2′-bipyrimidine) in aqueous solution yields the novel heterobimetallic complexes of formula {(μ-bpym)[Mn(H2O)]2-(μ-NC)6M(CN)2} with M = Mo (1) and W (2). 1 and 2 are isostructural three-dimensional compounds where the manganese atoms are bridged by bisbidentate bpym and hexakismonodentate octacyanometalate units. Variable-temperature magnetic susceptibility data of 1 and 2 show the occurrence of a significant antiferromagnetic coupling between the high spin manganese(II) ions through bridging bpym (Jca. −1.1 cm−1, the exchange Hamiltonian being defined as H = −J…

Aqueous solutionCyanidechemistry.chemical_elementGeneral ChemistryManganeseMagnetic susceptibilityCatalysisAntiferromagnetic couplingchemistry.chemical_compoundCrystallographychemistryComputational chemistryMaterials ChemistryIsostructuralBimetallic stripNew Journal of Chemistry
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Thermodynamic parameters for the formation of glycine complexes with magnesium(II), calcium(II), lead(II), manganese(II), cobalt(II), nickel(II), zin…

1995

Abstract Protonation constants and Mg 2+ , Ca 2+ , Pb 2+ , Mn 2+ -, Co 2+ , Ni 2+ , Cu 2+ , Zn 2+  and Cd 2+ glycine complex formation constants have been determined in different aqueous media at different temperatures. Salt effects are explained by a complex formation model which takes into account the formation of weak species. From the temperature dependence of the formation constants, thermodynamic parameters ΔH θ (and in some cases ΔC θ p ) have been obtained. A rigorous analysis of literature data, together with experimental findings, allows recommended formation parameters, in the ranges 0 ≤ I e ≤ 1 mol l −1 ( I e is the effective ionic strength) and 5°C ≤ T ≤ 45°C, to be obt…

Aqueous solutionEnthalpyInorganic chemistrychemistry.chemical_elementIonic bondingProtonationManganeseCondensed Matter PhysicsNickelchemistryStability constants of complexesIonic strengthPhysical chemistryPhysical and Theoretical ChemistryInstrumentationThermochimica Acta
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Screening the bulk properties and reducibility of Fe-doped Mn2O3 from first principles calculations

2017

Abstract Manganese oxides, particularly Mn 2 O 3 , have demonstrated great potential for oxygen carrier materials in chemical looping applications. The application of these materials in the industrial scale is hindered by thermodynamic restrictions related to the reoxidation process. This disadvantage can be overcome by doping the oxide with a guest cation. Iron is one of the most promising dopants, but the atomic-level understanding of its effects on the properties of α-Mn 2 O 3 is incomplete. Herein, we report a systematic GGA+U study of the bulk properties and reducibility of Fe x Mn 2-x O 3 (0 ≤ x ≤ 2) as a function of Fe dopant concentration. In particular, we focus on a representative…

Band gapOxidechemistry.chemical_elementNanotechnology02 engineering and technologyManganeseBulk010402 general chemistry01 natural sciencesOxygenCatalysisCatalysischemistry.chemical_compoundta116density functional theoryFe dopantsDopantta114ChemistrytiheysfunktionaaliteoriaDopingOxygen transportGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesMn2O3Physical chemistry0210 nano-technologyCatalysis Today
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Manganese(II) complexes of scorpiand-like azamacrocycles as MnSOD mimics.

2011

Mn(II) complexes of scorpiand-type azamacrocycles constituted by a tretrazapyridinophane core appended with an ethylamino tail including 2- or 4-quinoline functionalities show very appealing in vitro SOD activity. The observed behaviour is related to structural and electrochemical parameters.

Biomimetic materialsAza CompoundsManganeseMacrocyclic CompoundsStereochemistrySuperoxide DismutaseMetals and AlloysMolecular Conformationchemistry.chemical_elementGeneral ChemistryManganeseElectrochemistryCrystallography X-RayCatalysisMolecular conformationSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryBiomimetic MaterialsCoordination ComplexesMaterials ChemistryCeramics and CompositesQuinolinesAza CompoundsChemical communications (Cambridge, England)
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XAFS Studies of High-Valent Porphyrinato Manganèse Complexes with Ozone

1997

We produce strong evidence of the interaction of ozone with a series of Manganese (III) porphyrinato complexes to form a well defined reactive intermediate. In the latter species, the Manganese atom which is formally in a tetravalent (IV) state, is (at least) hexacoordinated with the metal unambiguously lying in the basal plane of the four pyrrolic nitrogens of the porphyrin macrocycle. Substitution of Bromine or Chlorine axial ligands by ozonids is most likely to happen. This conclusion is also supported by XANES and EXAFS spectra recorded at the Chlorine K-edge which suggest that ozone may even form with chlorine a complex anion.

BromineExtended X-ray absorption fine structureReactive intermediateInorganic chemistryGeneral Physics and Astronomychemistry.chemical_elementManganesePorphyrinX-ray absorption fine structureMetalchemistry.chemical_compoundchemistryvisual_artpolycyclic compoundsChlorinevisual_art.visual_art_mediumLe Journal de Physique IV
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Sorption properties of algae Spirogyra sp. and their use for determination of heavy metal ions concentrations in surface water.

2010

Abstract Kinetics of heavy-metal ions sorption by alga Spirogyra sp. was evaluated experimentally in the laboratory, using both the static and the dynamic approach. The metal ions – Mn2+, Cu2+, Zn2+ and Cd2+ – were sorbed from aqueous solutions of their salts. The static experiments showed that the sorption equilibria were attained in 30 min, with 90-95% of metal ions sorbed in first 10 min of each process. The sorption equilibria were approximated with the Langmuir isotherm model. The algae sorbed each heavy metal ions proportionally to the amount of this metal ions in solution. The experiments confirmed that after 30 min of exposition to contaminated water, the concentration of heavy meta…

CadmiumAqueous solutionMetal ions in aqueous solutionInorganic chemistryBiophysicschemistry.chemical_elementLangmuir adsorption modelWaterSorptionGeneral MedicineManganeseSpirogyraCopperIonSolutionssymbols.namesakeKineticschemistryCationsMetals HeavyElectrochemistrysymbolsAdsorptionPhysical and Theoretical ChemistryBioelectrochemistry (Amsterdam, Netherlands)
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Investigation of manganese in salt- and freshwater pearls

2001

Abstract The trace element distribution in natural and cultured pearls is analysed by micro-PIXE, cathodoluminescence (CL) microscopy and spectroscopy and electron spin resonance (ESR) spectroscopy to develop a new method to distinguish cultured from natural pearls. These different kinds of pearls can be identified by their manganese content and its distribution in aragonite and calcite structure, respectively. Manganese content of natural freshwater pearls from Persian Gulf was compared to that of natural freshwater pearls from the Mississippi river (USA). Moreover manganese content of tissue-graft freshwater pearls from Chansu (China) was compared to that of natural freshwater pearls from…

CalciteNuclear and High Energy PhysicsMicro pixeAragoniteTrace elementchemistry.chemical_elementMineralogyManganeseengineering.materialchemistry.chemical_compoundchemistryEnvironmental chemistryengineeringInstrumentationNuclear Instruments and Methods in Physics Research Section B: Beam Interactions with Materials and Atoms
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Carbon-isotope record and palaeoenvironmental changes during the early Toarcian oceanic anoxic event in shallow-marine carbonates of the Adriatic Car…

2013

AbstractGeochemical (δ13C, δ18O and Mn) compositions of Lower Jurassic shallow-water carbonates cropping out in Croatia were analyzed to elucidate the impact of the early Toarcian oceanic anoxic event (T-OAE) on the Adriatic Carbonate Platform (AdCP). The bulk-rock carbon-isotope records through the studied sections (Velebit-A, Velebit-B and Gornje Jelenje) are characterized by two significant excursions: (i) an initial positive trend interrupted by a pronounced negative shift (c. 2.5‰) that is followed by (ii) an increasing trend of positive values (up to 4.5‰). A comparison with δ13C trends obtained from well-calibrated sections from other localities in Europe shows that the overall chara…

Calciteδ18OCarbonate platformCroatiaOceanic Anoxic EventSedimentGeologyDiachronouscarbon-isotope stratigraphy; carbonate platform; Croatia; T-OAEstable isotope stratigraphyDiagenesisPaleontologychemistry.chemical_compoundlower ToarcianchemistryAdriatic Carbonate PlatformmanganeseCarbonateSedimentary rockGeology
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Manganese carbonyl terpyridyl complexes: their synthesis, characterization and potential application as CO-release molecules

2014

MnI carbonyl terpyridyl complexes have been synthesized and characterized. The tricarbonyl derivative exhibits interesting behaviors for controlled CO-release by both thermal and photosynthetic pathways.

Carbon MonoxideManganeseLightMetals and Alloyschemistry.chemical_elementGeneral ChemistryManganesePhotosynthesisPhotochemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCharacterization (materials science)chemistry.chemical_compoundchemistryCoordination ComplexesMaterials ChemistryCeramics and CompositesMolecule[CHIM]Chemical SciencesCo releaseta116Derivative (chemistry)ComputingMilieux_MISCELLANEOUSChemical Communications
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