Search results for "Isostructural"

showing 10 items of 158 documents

High-pressure synthesis of boron-rich chalcogenides B12S and B12Se

2022

The authors thank Drs. I. Dovgaliuk and T. Chauveau for assistance with Rietveld analysis; and Drs. V. Bushlya and A. Jamali for help with EDX/SEM measurements. This work was financially supported by the European Union's Horizon 2020 Research and Innovation Program under Flintstone2020 project (grant agreement No 689279).

Materials sciencePhononFOS: Physical scienceschemistry.chemical_element02 engineering and technologyCrystal structure[CHIM.INOR]Chemical Sciences/Inorganic chemistry01 natural sciencessymbols.namesake0103 physical sciences[CHIM.CRIS]Chemical Sciences/CristallographyMaterials ChemistryIsostructural010306 general physicsBoronCondensed Matter - Materials ScienceRietveld refinementMechanical EngineeringCrystal structureMetals and AlloysMaterials Science (cond-mat.mtrl-sci):NATURAL SCIENCES::Physics [Research Subject Categories][CHIM.MATE]Chemical Sciences/Material chemistry540021001 nanoscience & nanotechnologyCrystallographychemistryMechanics of MaterialsElemental analysisBoron-rich chalcogenidesddc:540symbolsRaman spectraHigh-pressure synthesis0210 nano-technologyRaman spectroscopyStoichiometry
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Two-component self-assembly with solvent leading to "wet" and microcrystalline organogel fibers

2014

Abstract Hypothesis The microcrystalline fibers of N -(2-aminoethyl)-3α-hydroxy-5β-cholan-24-amide 1 provided a useful model system for studying the complex relationship between morphology, experimental parameters, solvent, and the phenomenon of organogelation. The presence of solvents in the solid forms of 1 along with crystallization behavior suggested solvate formation and polymorphic behavior. Experiments Forty solid state- and xerogel samples of 1 formed in organic solvents and in three categories of experimental conditions were analyzed with single crystal X-ray diffraction (XRD), powder X-ray diffraction (PXRD), Raman microscopy, and attenuated total reflection Fourier-transform infr…

Materials sciencecrystallizationbile acid amideInfrared spectroscopylaw.inventioninclusion crystalBiomaterialsCrystalColloid and Surface Chemistrysolvatelawmicrocrystalline fiberCrystallizationIsostructuralta116x-ray crystallographyorganogelxerogelraman microscopySurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsfourier transform infrared spectroscopyCrystallographyMicrocrystallineAttenuated total reflectionSingle crystalPowder diffractionJournal of Colloid and Interface Science
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Cyano-Bridged Bimetallic Assemblies from Hexacyanometalate, [M(CN)6]3- (M = MnIII and FeIII), and [M(N4-macrocycle)]2+ (M = FeIII, NiII and ZnII) Bui…

2001

Reactions between [M(N4-macrocycle)]2+ (M = ZnII and NiII; macrocycle ligands are either CTH = d,l-5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradecane or cyclam = 1,4, 8, 11-tetrazaazaciclotetradecane) and [M(CN)6]3- (M = FeIII and MnIII) give rise to cyano-bridged assemblies with 1D linear chain and 2D honeycomblike structures. The magnetic measurements on the 1D linear chain complex [Fe(cyclam)][Fe(CN)6]·6H2O 1 points out its metamagnetic behavior, where the ferromagnetic interaction operates within the chain and the antiferromagnetic one between chains. The Neel temperature, TN, is 5.5 K and the critical field at 2 K is 1 T. The unexpected ferromagnetic intrachain interaction can…

MineralogyInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryFerromagnetismCyclamOctahedral molecular geometryAntiferromagnetismPhysical and Theoretical ChemistryIsostructuralBimetallic stripCritical fieldNéel temperatureInorganic Chemistry
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Isostructural Dinuclear Phenoxo-/Acetato-Bridged Manganese(II), Cobalt(II), and Zinc(II) Complexes with Labile Sites: Kinetics of Transesterification…

2012

Using the dinucleating phenol-based ligand 2,6-bis[3-(pyridin-2-yl)pyrazol-1-ylmethyl]-4-methylphenol] (HL(2)), in its deprotonated form, the six new dinuclear complexes [M(II)(2)(L(2))(μ-O(2)CMe)(2)(MeCN)(2)][PF(6)] (M = Mn (2a), Co (3a), Zn (4a)) and [M(II)(2)(L(2))(μ-O(2)CMe)(2)(MeCN)(2)][BPh(4)] (M = Mn (2b), Co (3b), Zn (4b)) have been synthesized. Crystallographic analyses on 2b·2MeCN, 3b·2MeCN, and 4b·2MeCN reveal that these complexes have closely similar μ-phenoxo bis(μ-carboxylato) structures. The physicochemical properties (absorption and ESI-MS spectral data, 2a,b, 3a,b, and 4a,b; (1)H NMR, 4a,b) of the cations of 2a-4a are identical with those of 2b-4b. Each metal ion is termina…

Models MolecularManganeseEsterificationStereochemistryLigandchemistry.chemical_elementCobaltManganeseZincPyrazoleCrystallography X-RayMedicinal chemistryNitrophenolsInorganic ChemistryZincchemistry.chemical_compoundOrganophosphorus CompoundsDeprotonationchemistryCoordination ComplexesIntramolecular forcePhysical and Theoretical ChemistryIsostructuralCobaltInorganic Chemistry
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New BDH-TTP/[MIII(C5O5)3]3– (M = Fe, Ga) Isostructural Molecular Metals

2012

Two new isostructural molecular metals-(BDH-TTP)(6)[M(III)(C(5)O(5))(3)]·CH(2)Cl(2) (BDH-TTP = 2,5-bis(1,3-dithiolan-2-ylidene)-1,3,4,6-tetrathiapentalene, where M = Fe (1) and Ga (2))-have been prepared and fully characterized. Compound 1 is a molecular conductor showing paramagnetic behavior, which is due to the presence of isolated [Fe(C(5)O(5))(3)](3-) complexes with high-spin S = (5)/(2) Fe(III) metal ions. The conductivity originates from the BDH-TTP organic donors arranged in a κ-type molecular packing. At 4 kbar, compound 1 behaves as a metal down to ∼100 K, showing high conductivity (∼10 S cm(-1)) at room temperature. When applying a pressure higher than 7 kbar, the metal-insulator…

Models MolecularMolecular StructureChemistryIronMetal ions in aqueous solutionGalliumStereoisomerismConductivityLigandsInorganic ChemistryMetalCrystalParamagnetismCrystallographyOctahedronvisual_artOrganometallic Compoundsvisual_art.visual_art_mediumFine structurePhysical and Theoretical ChemistryIsostructuralInorganic Chemistry
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Solid-state NMR and computational investigation of solvent molecule arrangement and dynamics in isostructural solvates of droperidol.

2015

(13)C, (15)N and (2)H solid-state NMR spectroscopy have been used to rationalize arrangement and dynamics of solvent molecules in a set of isostructural solvates of droperidol. The solvent molecules are determined to be dynamically disordered in the methanol and ethanol solvates, while they are ordered in the acetonitrile and nitromethane solvates. (2)H NMR spectra of deuterium-labelled samples allowed the characterization of the solvent molecule dynamics in the alcohol solvates and the non-stoichiometric hydrate. The likely motion of the alcohol molecules is rapid libration within a site, plus occasional exchange into an equivalent site related by the inversion symmetry, while the water mo…

Models MolecularNuclear and High Energy PhysicsMagnetic Resonance SpectroscopyMolecular ConformationSpin–lattice relaxationSolvent dynamicsMotional broadeningCrystallography X-RaySolid-state NMRchemistry.chemical_compoundComputational chemistryMoleculeDroperidolIsostructuralInstrumentationAb initio calculations.RadiationNitromethaneChemistryIsostructural solvatesGeneral ChemistryNuclear magnetic resonance spectroscopyHydrates/solvatesSolventNMR spectra databaseCrystallographySolid-state nuclear magnetic resonanceSolventsHydrate
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Isostructural Inorganic–Organic Piperazine-1,4-diium Chlorido- and Bromidoantimonate(III) Monohydrates: Octahedral Distortions and Hydrogen Bonds

2020

Halogenidoantimonate(III) monohydrates of the (C4H12N2)[SbX5]&middot

Models Molecularcrystal structureMaterials scienceHydrogenSurface PropertiesMolecular ConformationPharmaceutical Sciencechemistry.chemical_elementCrystal structurelow temperatureArticleAnalytical Chemistrylcsh:QD241-441lcsh:Organic chemistryDrug DiscoveryMoleculeHirshfeld surface analysisPhysical and Theoretical ChemistryIsostructuralOrganic Chemicalsoctahedral distortionPiperazineHydrogen bondOrganic Chemistryhydrogen bondinginorganic–organic hybrid materialsCrystallographyOctahedronchemistryChemistry (miscellaneous)Inorganic ChemicalsMolecular MedicineWater of crystallizationhalogenidoantimonates(III)Monoclinic crystal systemMolecules
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First principles modelling of oxygen impurities in UN nuclear fuels

2008

We report results of first principles VASP supercell calculations of O impurity in UN fuels placed either at an interstitial tetrahedral position or as a substitution for a host N ion. In the latter case O perfectly fits into N site producing no lattice distortion. Such the O substitutional impurity only slightly affects the formation energies of U and N vacancies nearby. In both interstitial and substitutional positions O atom attracts the additional electron density and transforms into the negatively charged ion. Oxygen incorporation into pre-existing N vacancy is energetically more favourable than into the interstitial position. The O impurities produce an additional peak at the low ener…

Nuclear and High Energy PhysicsElectron densityChemistrychemistry.chemical_elementUraniumOxygenIonNuclear Energy and EngineeringImpurityVacancy defectPhysical chemistryGeneral Materials ScienceAtomic physicsIsostructuralSpectroscopyJournal of Nuclear Materials
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Hybrid Molecular Magnets Obtained by Insertion of Decamethylmetallocenium Cations into Layered, Bimetallic Oxalate Complexes: [ZIIICp*2][MIIMIII(ox)3…

2000

A new series of hybrid organometallic - inorganic layered magnets with the formula [Z(III)Cp*2][M(II)M(III)(ox)3] (Z(III) = Co, Fe; M(III) = Cr, Fe; M(II) = Mn, Fe, Co, Cu, Zn; ox = oxalate; Cp* = pentamethylcyclopentadienyl) has been prepared. All of these compounds are isostructural and crystallize in the monoclinic space group C2/m, as found by X-ray structure analysis. Their structure consists of an eclipsed stacking of the bimetallic oxalate-based extended layers separated by layers of organometallic cations. These salts show spontaneous magnetization below To, which corresponds to the presence of ferro-, ferri-, or canted antiferromagnetism. Compounds in which the paramagnetic deca-me…

Organic ChemistryGeneral ChemistryCatalysisOxalateParamagnetismchemistry.chemical_compoundCrystallographyNuclear magnetic resonancechemistryFerromagnetismMössbauer spectroscopyAntiferromagnetismDiamagnetismIsostructuralSpontaneous magnetizationChemistry - A European Journal
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Interlocking inorganic screw helices: synthesis, structure, and magnetism of the novel framework uranium orthothiophoshates A11U7(PS4)13 (A = K, Rb).

2002

The novel quaternary uranium thiophosphate K11U7(PS4)13 has been synthesized by reacting uranium metal, K2S, S, and P2S5 at 700 degrees C in an evacuated silica tube. The crystal structure was determined by single crystal X-ray diffraction techniques. K11U7(PS4)13 crystallizes in the tetragonal space group I42d (a = 32.048(2) A, c = 17.321(1) A, Z = 8). The structure contains a tunnel framework composed of eight interlocking uranium U7(PS4)13 screw helices, with alkali metal cations residing inside the framework channels. The uranium atoms are coordinated in a bi- or tricapped trigonal prismatic fashion. The screw helices are built up from uranium atoms interconnected by PS4 tetrahedral uni…

Organic Chemistrychemistry.chemical_elementGeneral ChemistryCrystal structureUraniumTrigonal prismatic molecular geometryAlkali metalMagnetic susceptibilityCatalysisTetragonal crystal systemCrystallographychemistryIsostructuralSingle crystalChemistry (Weinheim an der Bergstrasse, Germany)
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