Search results for "Magnetic study"

showing 7 items of 7 documents

Obsidians of Pantelleria (Strait of Sicily): A Petrographic, Geochemical and Magnetic Study of Known and New Geological Sources

2020

Abstract This paper provides new petrochemical and paleomagnetic data from obsidian sub-sources on the island of Pantelleria, exploited since the Neolithic. Data has been obtained from 14 obsidian samples from 4 locations: Fossa della Pernice (2 sites), Salto la Vecchia and Balata dei Turchi. Here, we aim to better characterize these obsidians using a cross-disciplinary and multi-analytical approach, to further understand their archaeological significance. Major element analyses (EMP) have enabled two compositional super-groups to be distinguished: (i) Fossa della Pernice, less peralkaline and (ii) Balata dei Turchi–Salto la Vecchia, distinctly more peralkaline and having almost identical c…

Bronze ageObsidianArcheology060102 archaeologyGeochemistrySettore GEO/07 - Petrologia E Petrografia06 humanities and the artsConservation010502 geochemistry & geophysics01 natural sciencesLipariEducationPetrographyArchaeologyUstica0601 history and archaeologyMagnetic studyGeologyCC1-960Pantelleria0105 earth and related environmental sciences
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Cyano-bridged structures based on [MnIIN3O2-macrocycle)]2+: a synthetic, structural, and magnetic study.

2005

Reactions between the complex [MnII(L)]2+, where L is a N3O2 macrocyclic ligand, and different cyanometalate precursors such as [M(CN)n]m- (M(III) = Cr, Fe; M(II) = Fe, Ni, Pd, Pt) lead to cyano-bridged molecular assemblies exhibiting a variety of structural topologies. The reaction between [MnII(L)]2+ and [FeII(CN)6]4- forms a trinuclear complex with formula [(MnII(L)(H2O))2(FeII(micro-CN)2(CN)4)] x 2MeOH x 10H2O (1) which crystallizes in the triclinic space group P1. The reaction between [MnII(L)]2+ and [M(II)(CN)4]2-, where M(II) = Ni (2), Pd (3), Pt (4), gives rise to three isostructural linear chain compounds with stoichiometry [(MnII(L))(M(II)(micro-CN)2(CN)2)]n and which crystallize …

Inorganic ChemistryCrystallographyChemistryStereochemistryCyanometalateMacrocyclic ligandPhysical and Theoretical ChemistryMagnetic studyInorganic chemistry
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The first metamagnetic one-dimensional molecular material with nickel(ii) and end-to-end azido bridges

2001

A novel single azido bridged one-dimensional Ni(II) chain, which represents the first metamagnetic one-dimensional metal–azido system with only end-to-end azido bridges, has been synthesised and characterised by a low temperature magnetic study. Lloret Pastor, Francisco, Francisco.Lloret@uv.es

Metamagnetic ; Nickel ; Azido bridges ; SynthesisedSynthesisedMaterials scienceUNESCO::QUÍMICAchemistry.chemical_elementPhotochemistry:QUÍMICA [UNESCO]CatalysisChain (algebraic topology)NickelPolymer chemistryMaterials ChemistryMagnetic studyMolecular materialsazide ligandAzido bridgesUNESCO::QUÍMICA::Química inorgánicaMetals and AlloysGeneral Chemistry:QUÍMICA::Química inorgánica [UNESCO]Surfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsNickelchemistryCeramics and CompositesMetamagnetic
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Mössbauer and magnetic studies of mixed-valence linear chain compounds: Na3Fe2S4 and Na3Fe2Se4

1986

Mossbauer and magnetic data establish the two compounds Na3Fe2X4(X=S, Se) as mixed-valence linear chain compounds with rapid valence fluctuation. The compounds exhibit 1-dimensional antiferromagnetic coupling within the chains, and below a critical temperature a 3-dimensional ferrimagnetic ordering between the chains.

Nuclear and High Energy PhysicsValence (chemistry)Condensed matter physicsChemistryCondensed Matter PhysicsAtomic and Molecular Physics and OpticsAntiferromagnetic couplingCondensed Matter::Materials ScienceFerrimagnetismMössbauer spectroscopyPhysics::Atomic and Molecular ClustersCondensed Matter::Strongly Correlated ElectronsPhysical and Theoretical ChemistryThin filmMagnetic studyHyperfine Interactions
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Magneto-structural correlations and DFT calculations in two rare tetranuclear copper(II)-clusters with doubly phenoxo and end-on azido bridges: Synth…

2010

International audience; By slightly changing the synthetic conditions, we have prepared two closely related linear tetranuclear CuII complexes with the symmetrical ONNO donor tetradentate Schiff-base ligand [H2L = (OH)C6H4(CH3)Cdouble bond; length as m-dashN(CH2)3Ndouble bond; length as m-dashC(CH3)C6H4(OH)] and with azide ions. These two distinctly coloured crystalline products were characterized by elemental analysis, IR and UV–Vis spectroscopy, CV, EPR spectra and variable temperature magnetic measurements. Single crystal X-ray diffraction studies of the green [Cu4(μ-L)2(μ1,1-N3)2(N3)2] (1) and the red [Cu4(μ-L)2(μ1,1-N3)2(N3)2(H2O)2] (2) crystals show that the coordination environment o…

chemistry.chemical_elementCuII-tetranuclearDFT calculations010402 general chemistry01 natural sciencesSpectral lineIonlaw.inventionInorganic Chemistrychemistry.chemical_compoundlawMaterials Chemistry[CHIM]Chemical SciencesPhysical and Theoretical ChemistrySpectroscopyElectron paramagnetic resonanceLinear-clusters010405 organic chemistryMagnetic studyCopper0104 chemical sciencesCrystallographyMolecular geometrychemistryEPRAzideSingle crystalInorganica Chimica Acta
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Crystal structure and magnetic study of the complex salt [RuCp(PTA)2–μ-CN-1κC:2κN–RuCp(PTA)2][Re(NO)Br4(EtOH)0.5(MeOH)0.5]

2021

A new RuII–ReII complex salt, μ-cyanido-κ2 C:N-bis[(η5-cyclopentadienyl)bis(3,5,7-triazaphosphaadamantane-κP)ruthenium(II)] tetrabromido(ethanol/methanol-κO)nitrosylrhenate(II), [Ru(CN)(C5H5)2(C6H12N3P)4][ReBr4(NO)(CH4O)0.5(C2H6O)0.5] or [RuCp(PTA)2–μ-CN–1κC:2κ2 N-RuCp(PTA)2][Re(NO)Br4(EtOH)0.5(MeOH)0.5] (PTA = 3,5,7-triazaphosphaadamantane) was obtained and characterized by single-crystal X-ray diffraction, elemental analysis and infrared spectroscopy. The title salt was obtained by liquid–liquid diffusion of methanol/DMSO solutions of (NBu4)[Re(NO)Br4(EtOH)] and [(PTA)2CpRu–μ-CN–1κC:2κ2 N-RuCp(PTA)2](CF3SO3). The RuII and ReII independent moieties correspond to a binuclear and mononuclear…

crystal structureSalt (chemistry)Infrared spectroscopychemistry.chemical_element02 engineering and technologyCrystal structure010402 general chemistry01 natural sciencesMedicinal chemistryptachemistry.chemical_compoundGeneral Materials ScienceMagnetic studyQD1-999chemistry.chemical_classificationEthanolChemistryGeneral Chemistry021001 nanoscience & nanotechnologyCondensed Matter Physicsx-ray structure0104 chemical sciencesRutheniumruthenium(ii)ChemistryParameter analysismagnetismrhenium(ii)Methanol0210 nano-technologyActa Crystallographica Section E Crystallographic Communications
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Synthesis, characterization and magnetic study of two new octahedral iron(III) complexes with pendant zwitterionic Schiff bases

2016

Two Schiff bases, HL1 [2-((3-(dimethylamino)propylimino)methyl)-5-bromophenol] and HL2 [2-((2-(diethylamino)ethylimino)methyl)-6-methoxyphenol], have been employed to prepare two new octahedral iron(III) complexes, [Fe(HL1)2(N3)2]ClO4·2H2O (1) and [Fe(HL2)2(NCS)2]ClO4·H2O (2). Both complexes are characterized by spectral and elemental analyses. Single crystal X-ray diffraction studies confirm their structures. In both complexes, Schiff bases are trapped in their zwitterionic forms and coordinated to iron(III) only through the imine nitrogen and phenoxo oxygen, i.e., they behave as bi-dentate ligands, keeping the remaining potential donor sites pendant. The measurement of χM vs. T for both c…

crystal structurevariable temperature magnetic susceptibilityIminechemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciencesOxygenzwiterionicInorganic Chemistrypendantchemistry.chemical_compoundMaterials ChemistryOrganic chemistryPhysical and Theoretical ChemistryMagnetic studyta116010405 organic chemistryNitrogen0104 chemical sciencesCrystallographychemistryOctahedronPotential donorSingle crystaliron(III)Inorganica Chimica Acta
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