Search results for "Iron Compounds"

showing 10 items of 23 documents

Hexanuclear iron(III) salicylaldoximato complexes presenting the [Fe6(mu3-O)2(mu2-OR)2]12+ core: syntheses, crystal structures, and spectroscopic and…

2006

The use of salicylaldehyde oxime (H2salox) in iron(III) carboxylate chemistry has yielded two new hexanuclear compounds [Fe6(mu3-O)2(O2CPh)10(salox)2(L)2].xMeCN.yH2O [L = MeCONH2, x = 6, y = 0 (1); L = H2O, x = 2, y = 3 (2)]. Compound 1 crystallizes in the triclinic space group P with (at 25 degrees C) a = 13.210(8) A, b = 13.87(1) A, c = 17.04(1) A, alpha = 105.79(2) degrees , beta = 96.72(2) degrees , gamma = 116.69(2) degrees , V = 2578.17(2) A(3), and Z = 1. Compound 2 crystallizes in the monoclinic space group C2/c with (at 25 degrees C) a = 21.81(1) A, b = 17.93(1) A, c = 27.72(1) A, beta = 111.70(2) degrees , V = 10070(10) A(3), and Z = 4. Complexes 1 and 2 contain the [Fe6(mu3-O)2(m…

Magnetic Resonance SpectroscopyMolecular StructureChemistryLigandStereochemistryCrystal structureTriclinic crystal systemOximeChemistry InorganicCrystallography X-RayInorganic ChemistryCrystallographychemistry.chemical_compoundMagneticsSpectroscopy MossbauerSalicylaldehydeCarboxylatePhysical and Theoretical ChemistryAcetonitrileIron CompoundsMonoclinic crystal systemInorganic chemistry
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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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Dynamic Tuning of Viscoelastic Hydrogels with Carbonyl Iron Microparticles Reveals the Rapid Response of Cells to Three-Dimensional Substrate Mechani…

2021

Current methods to dynamically tune three-dimensional hydrogel mechanics require specific chemistries and substrates that make modest, slow, and often irreversible changes to their mechanical properties, exclude the use of protein-based scaffolds, or alter hydrogel microstructure and pore size. Here, we rapidly and reversibly alter the mechanical properties of hydrogels consisting of extracellular matrix proteins and proteoglycans by adding carbonyl iron microparticles (MP) and applying external magnetic fields. This approach drastically alters hydrogel mechanics: rheology reveals that application of a 4,000 Oe magnetic field to a 5 mg/mL collagen hydrogel containing 10 wt% MPs increases th…

Materials science02 engineering and technologyCell morphologyMechanotransduction CellularViscoelasticityArticleExtracellular matrix03 medical and health sciencesMagneticsCarbonyl ironRheologyHumansGeneral Materials ScienceMechanotransductionParticle Sizeskin and connective tissue diseasesCells Cultured030304 developmental biologyCell Nucleus0303 health sciencesExtracellular Matrix ProteinsViscositytechnology industry and agricultureHydrogelsDynamic mechanical analysisMechanics021001 nanoscience & nanotechnologyElasticityExtracellular MatrixSelf-healing hydrogelsCalciumCollagen0210 nano-technologyIron CompoundsACS applied materialsinterfaces
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Jarosite and hematite at Meridiani Planum from Opportunity's Mossbauer Spectrometer.

2004

Mössbauer spectra measured by the Opportunity rover revealed four mineralogical components in Meridiani Planum at Eagle crater: jarosite- and hematite-rich outcrop, hematite-rich soil, olivine-bearing basaltic soil, and a pyroxene-bearing basaltic rock (Bounce rock). Spherules, interpreted to be concretions, are hematite-rich and dispersed throughout the outcrop. Hematitic soils both within and outside Eagle crater are dominated by spherules and their fragments. Olivine-bearing basaltic soil is present throughout the region. Bounce rock is probably an impact erratic. Because jarosite is a hydroxide sulfate mineral, its presence at Meridiani Planum is mineralogical evidence for aqueous proc…

Meridiani PlanumGeologic SedimentsExtraterrestrial EnvironmentOutcropMineralogyMagnesium CompoundsMarsengineering.materialFerric CompoundsSpectroscopy MossbauerImpact craterConcretionJarositeComposition of MarsSpacecraftMineralsMultidisciplinaryMineralSulfatesSilicatesWaterHematitevisual_artvisual_art.visual_art_mediumengineeringGeologyIron CompoundsScience (New York, N.Y.)
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Identification of Morphological Biosignatures in Martian Analogue Field Specimens Using In Situ Planetary Instrumentation

2008

International audience; We have investigated how morphological biosignatures (i.e., features related to life) might be identified with an array of viable instruments within the framework of robotic planetary surface operations at Mars. This is the first time such an integrated lab-based study has been conducted that incorporates space-qualified instrumentation designed for combined in situ imaging, analysis, and geotechnics ( sampling). Specimens were selected on the basis of feature morphology, scale, and analogy to Mars rocks. Two types of morphological criteria were considered: potential signatures of extinct life ( fossilized microbial filaments) and of extant life (crypto-chasmoendolit…

Meridiani PlanumIn situGeologic Sediments010504 meteorology & atmospheric sciencesMOSSBAUER-SPECTROSCOPYInstrumentationOrigin of LifeAntarctic RegionsMarsGUSEV CRATERExploration of MarsCalcium Sulfate01 natural sciencesCRYPTOENDOLITHIC LICHENSCalcium CarbonateAstrobiologyRAMAN-SPECTROSCOPIC DETECTIONGermanyExobiology0103 physical sciences010303 astronomy & astrophysics0105 earth and related environmental sciencesRemote sensingMartianMineralsPlanetary surfaceSpectrometerMERIDIANI-PLANUMWESTERN-AUSTRALIAMars Exploration ProgramAgricultural and Biological Sciences (miscellaneous)YELLOWSTONE-NATIONAL-PARK13. Climate actionSpace and Planetary ScienceMARS EXPLORATIONAmericasANTARCTIC HABITATSIron CompoundsGeologyHAUGHTON IMPACT STRUCTUREAstrobiology
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Microfungal Alkylation and Volatilization of Selenium Adsorbed by Goethite

2009

Selenium adsorbed in the oxyanionic form by Fe-oxides like goethite is considered of benefit for long-term stabilization of (79)Se under near field conditions of radionuclide waste disposal sites. However, microbe-mediated volatilization of the uranium fission product (79)Se has not yet been considered for risk assessment based on the use of the water-solid distribution coefficient K(D). We have performed incubation experiments in a ternary system selenium-microbe-goethite and show that mycobiota including the common black microfungi genera Alternaria alternata are capable of volatilizing the Se even if immobilized by goethite. The microfungi were incubated in a standardized nutrient broth …

MineralsMicrofungiGoethiteVolatilisationAlkylationAlternariachemistry.chemical_elementGeneral ChemistryGas Chromatography-Mass SpectrometryPartition coefficientSeleniumLaboratory flaskAdsorptionchemistryvisual_artvisual_art.visual_art_mediumEnvironmental ChemistryAdsorptionBiomassVolatilizationIron CompoundsSeleniumNuclear chemistryWaste disposalEnvironmental Science & Technology
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Silicic acid competes for dimethylarsinic acid (DMA) immobilization by the iron hydroxide plaque mineral goethite.

2015

Abstract A surface complexation modeling approach was used to extend the knowledge about processes that affect the availability of dimethylarsinic acid (DMA) in the soil rhizosphere in presence of a strong sorbent, e.g., Fe plaques on rice roots. Published spectroscopic and molecular modeling information suggest for the organoarsenical agent to form bidentate-binuclear inner-sphere surface complexes with Fe hydroxides similar to the inorganic As oxyanions. However, since also the ubiquitous silicic acid oxyanion form the same bidentate binuclear surface complexes, our hypothesis was that it may have an effect on the adsorption of DMA by Fe hydroxides in soil. Our experimental batch equilibr…

Models MolecularMineralsEnvironmental EngineeringGoethiteSorbentSurface PropertiesInorganic chemistrySilicic AcidOxyanionPollutionAcid dissociation constantchemistry.chemical_compoundAdsorptionchemistryvisual_artvisual_art.visual_art_mediumEnvironmental ChemistryHydroxideCacodylic AcidSilicic acidPoint of zero chargeAdsorptionWaste Management and DisposalIron CompoundsThe Science of the total environment
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Evidence that steric factors modulate reactivity of tautomeric iron-oxo species in stereospecific alkane C-H hydroxylation

2014

A new iron complex mediates stereospecific hydroxylation of alkyl C-H bonds with hydrogen peroxide, exhibiting excellent efficiency. Isotope labelling studies provide evidence that the relative reactivity of tautomerically related oxo-iron species responsible for the C-H hydroxylation reaction is dominated by steric factors This work has been supported by the European Union (the Erasmus Mundus program), the International Research Training Group Metal Sites in Biomolecules: Structures, Regulation and Mechanisms (www.biometals.eu), and COST Action CM1003. M.C. acknowledges ERC-29910, MINECO of Spain for CTQ2012- 37420-C02-01/BQU and CSD2010-00065, catalan DIUE (2009SGR637) and an ICREA academ…

Steric effectsStereochemistryIronrautaHydroxylationOxidacióIron compoundsCatalysisCatalysisHydroxylationchemistry.chemical_compoundStereospecificityCatàlisiCoordination ComplexesAlkanesOxidationMaterials ChemistryReactivity (chemistry)Hydrogen peroxideta116Alkylchemistry.chemical_classificationMolecular StructurekoordinaatioyhdisteetMetals and AlloysStereoisomerismcoordination compundsFerro -- CompostosGeneral ChemistryHydrogen PeroxideTautomer3. Good healthSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryCeramics and CompositesOxygenases
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Distinct photodynamics of κ-N and κ-C pseudoisomeric iron(ii) complexes

2021

Two closely related FeII complexes with 2,6-bis(1-ethyl-1H-1,2,3-triazol-4yl)pyridine and 2,6-bis(1,2,3-triazol-5-ylidene)pyridine ligands are presented to gain new insights into the photophysics of bis(tridentate) iron(II) complexes. The [Fe(N^N^N)2]2+ pseudoisomer sensitizes singlet oxygen through a MC state with nanosecond lifetime after MLCT excitation, while the bis(tridentate) [Fe(C^N^C)2]2+ pseudoisomer possesses a similar 3MLCT lifetime as the tris(bidentate) [Fe(C^C)2(N^N)]2+ complexes with four mesoionic carbenes. Financial support from the Deutsche Forschungsge-meinschaft [DFG, Priority Program SPP 2102] "Light-controlled reactivity of metal complexes" (BA 4467/7-1, LO 714/11-1, …

TrisDenticitysynthesisPyridinepyridine derivativecarbenoidIron compoundsCatalysisexperimental studychemistry.chemical_compoundPyridineMaterials Chemistryphysical chemistrycontrolled studyChemistrySinglet oxygenPyridine ligandsSinglet oxygenMetals and AlloysMesoionicGeneral ChemistryNanosecondPyridine ligandSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsunclassified drugCrystallographyPhotophysicsiron complexisomerCeramics and CompositesCarbeneschemical structurephotodynamicsphysicsExcitationchemical parameters
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Iron’s Wake: The Performance of Quantum Mechanical-Derived Versus General-Purpose Force Fields Tested on a Luminescent Iron Complex

2020

Recently synthetized iron complexes have achieved long-lived excited states and stabilities which are comparable, or even superior, to their ruthenium analogues, thus representing an eco-friendly and cheaper alternative to those materials based on rare metals. Most of computational tools which could help unravel the origin of this large efficiency rely on ab-initio methods which are not able, however, to capture the nanosecond time scale underlying these photophysical processes and the influence of their realistic environment. Therefore, it exists an urgent need of developing new low-cost, but still accurate enough, computational methodologies capable to deal with the steady-state and trans…

Work (thermodynamics)AcetonitrilesLuminescenceIronPharmaceutical ScienceMolecular Dynamics Simulation010402 general chemistry01 natural sciencesArticleAnalytical Chemistrylcsh:QD241-441Molecular dynamicschemical environmentlcsh:Organic chemistry0103 physical sciencesDrug Discoverytime-dependent density functional theory.Statistical physicsPhysical and Theoretical ChemistryQuantumComputingMilieux_MISCELLANEOUSPhysics010304 chemical physicsSpectrum AnalysisScale (chemistry)Organic ChemistryTime-dependent density functional theoryNanosecond0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistrytime-dependent density functional theoryiron complexChemistry (miscellaneous)Excited stateSolventsQuantum TheoryMolecular MedicineLuminescenceIron Compoundsforce field molecular dynamicsMolecules
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