Search results for "Crystal Structure"

showing 10 items of 15036 documents

CCDC 1575390: Experimental Crystal Structure Determination

2017

Related Article: V. Piccialli, A. Tuzi, R. Centore|2017|Acta Crystallogr.,Sect.E:Cryst.Commun.|73|1603|doi:10.1107/S2056989017013391

9alpha11alpha-epoxy-5alpha-cholest-7-ene-3beta56alpha-triol 36-diacetateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Ferromagnetic coupled μ-phenoxo-μ-carboxylato heterodinuclear complexes based on the Cr(salen) moiety: Structural and magnetic characterization

2009

The synthesis, crystal structure, and magneto-chemical characterization of two new unprecedented μ-phenoxo-μ-carboxylato heterodinuclear complexes based on the Cr(salen) moiety (salen = N,N′-bis(salicylidene)ethylenediamine), [MII(O2C(CH3)3)(OH2)2(μ-O2C(CH3)3)(μ-salen)CrIII(O2C(CH3)3)], M = Ni (2), Co(3) are reported. The dinuclear complexes were obtained starting from the mononuclear trans-[Cr(salen)(CN)2]PPh4 (1), whose crystal structure is also reported. They show a trans arrangement of the Cr(salen) unit, bridging through the phenolate O atoms to a second metal center. An additional μ2-O2-carboxylato bridge and a further monodentating carboxylate ligand complete the roughly octahedral C…

ANISOTROPYCoordination sphereChemistryOtras Ciencias QuímicasExchange interactionCiencias QuímicasEthylenediamineCrystal structureSINGLE-MOLECULE MAGNETSInorganic ChemistryMagnetizationCrystallographychemistry.chemical_compoundCOBALT(II) COMPLEXESOctahedronFerromagnetismCarboxylatePIVALATE COMPLEXESCIENCIAS NATURALES Y EXACTAS
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Pressure dependence of the optical properties of wurtzite and rock-salt Zn1–xCoxO thin films

2007

In this paper we investigate the electronic structure of Zn 1-x Co x O by means of optical absorption measurements under pressure. Thin films of Zn 1-x Co x O with different Co content (from 1 to 30%) were prepared by pulsed laser deposition on mica substrates. Absorption spectra exhibit three main features that are clearly correlated to the Co content in the films: (i) absorption peaks in the infrared associated to crystal-field-split internal transitions in the Co 3d shell, with very small pressure coefficients due to their atomic character; (ii) a broad absorption band below the fundamental edge associated to charge transfer transitions, that exhibit relatively large pressure coefficient…

Absorption edgeAbsorption spectroscopyChemistryAbsorption bandPhase (matter)Analytical chemistryThin filmCondensed Matter PhysicsAbsorption (electromagnetic radiation)Electronic Optical and Magnetic MaterialsWurtzite crystal structurePulsed laser depositionphysica status solidi (b)
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Molybdenum oxide nitrides of the Mo_{2}(O,N,\square)_{5}$ type : on the way to Mo_{2}O_{5}$

2017

Abstract: Blue-colored molybdenum oxide nitrides of the Mo-2(O,N,square)(5) type were synthesized by direct nitridation of commercially available molybdenum trioxide with a mixture of gaseous ammonia and oxygen. Chemical composition, crystal structure, and stability of the obtained and hitherto unknown compounds are studied extensively. The average oxidation state of +5 for molybdenum is proven by Mo K near-edge X-ray absorption spectroscopy; the magnetic behavior is in agreement with compounds exhibiting (MoO6)-O-v units. The new materials are stable up to similar to 773 K in an inert gas atmosphere. At higher temperatures, decomposition is observed. X-ray and neutron powder diffraction, e…

Absorption spectroscopyChemistryInorganic chemistryOxidechemistry.chemical_element02 engineering and technologyCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesMolybdenum trioxideInorganic Chemistrychemistry.chemical_compoundChemistryElectron diffractionOxidation stateMolybdenumPhysical and Theoretical Chemistry0210 nano-technologyInert gasInorganic chemistry
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Probing NiO nanocrystals by EXAFS spectroscopy

2010

Abstract The structure relaxation in nanocrystalline NiO (nano-NiO, 13 nm crystallite size) has been studied by X-ray absorption spectroscopy at the Ni K-edge at 300 K. Conventional single-scattering analysis of the EXAFS signals from the first two coordination shells showed a lattice volume expansion by about 1% and a contraction of the Ni–O bonds by about 0.5% in nano-NiO compared to microcrystalline NiO. A more sophisticated approach, based on a combination of classical molecular dynamics and ab initio multiple-scattering EXAFS theory, allowed us to interpret both static relaxation and lattice dynamics in nano-NiO.

Absorption spectroscopyExtended X-ray absorption fine structureChemistryNon-blocking I/OAb initio02 engineering and technologyGeneral ChemistryCrystal structure021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciencesNanocrystalline materialCondensed Matter::Materials ScienceAb initio quantum chemistry methodsComputational chemistry0103 physical sciencesMaterials ChemistryPhysical chemistryCondensed Matter::Strongly Correlated ElectronsCrystallite010306 general physics0210 nano-technologySolid State Communications
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External pressure and composition effects on the atomic and electronic structure of SnWO4

2015

The atomic and electronic structure of tin tungstates, α-SnWO4, α-Sn1.03W0.99O4 and β-SnWO4 ,w as studied by the W L3-edge X-ray absorption spectroscopy and first-principles linear combination of atomic orbital (LCAO) calculations based on the hybrid exchange-correlation density functional (DFT)/ Hartree–Fock (HF) scheme. It was found that the crystal structure of both α-phases is built up of strongly distorted WO6 octahedra, whereas that of β-SnWO4 is composed of nearly regular WO4 tetrahedra. In addition, there are distorted SnO6 octahedra in both α- and β-phases. The metal–oxygen octahedra distortion is explained by the second-order Jahn–Teller effect. The influence of pressure on the st…

Absorption spectroscopyExtended X-ray absorption fine structureRenewable Energy Sustainability and the EnvironmentBand gapChemistryElectronic structureCrystal structureMolecular physicsSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCrystallographyAtomic orbitalOctahedronLinear combination of atomic orbitalsddc:530
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[Cu32(PET)24H8Cl2](PPh4)2: A Copper Hydride Nanocluster with a Bisquare Antiprismatic Core

2020

Atomically precise coinage metal (Au, Ag, and Cu) nanoclusters (NCs) have been the subject of immense interest for their intriguing structural, photophysical, and catalytic properties. However, the synthesis of Cu NCs is highly challenging because of low reduction potential and high reactivity of copper, demonstrating the need for new synthetic methods using appropriate ligand combinations. By designing a diamine-assisted synthetic strategy, here we report the synthesis and total structure characterization of a box-like dianionic Cu NC [Cu32(PET)24H8Cl2](PPh4)2 coprotected by 2-phenylethanethiolate (PET), hydride, and chloride ligands. Its crystal structure comprises a rare bisquare antipri…

Absorption spectroscopyHydrideChemistryLigandGeneral ChemistryElectronic structureCrystal structure010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical sciencesNanoclustersCrystallographychemistry.chemical_compoundColloid and Surface ChemistryCopper hydrideDensity functional theoryJournal of the American Chemical Society
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Derivatisation of Pyrogallarenes

2005

Derivatisation of upper-rim hydroxy groups of pyrogallarenes produced completely acylated and tosylated pyrogallarene derivatives. Mesitylation of pyrogallarene, however, resulted in a regioselective derivatisation of hydroxy groups, i.e. eight OH groups out of 12 were mesitylated. Crystal structures of the synthesised pyrogallarene derivatives indicate that completely substituted pyrogallarenes exist in a distorted crown conformation despite of the lack of stabilising intramolecular hydrogen bonds. In contrast, the partially substituted pyrogallarene adopts a boat conformation and has an open cavity for the inclusion of small guest molecules. © Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinh…

AcylationOpen cavityHydrogen bondStereochemistryChemistryIntramolecular forceOrganic ChemistryCyclohexane conformationMoleculeRegioselectivityCrystal structurePhysical and Theoretical ChemistryMedicinal chemistryEuropean Journal of Organic Chemistry
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Multivariate Metal-Organic Frameworks for the Simultaneous Capture of Organic and Inorganic Contaminants from Water

2019

We report a new water-stable multivariate (MTV) Metal-Organic Framework (MOF) prepared by combining two different oxamide-based metalloligands derived from the natural amino acids L-serine and L-methionine. This unique material features hexagonal channels decorated with two types of flexible and functional 'arms' (-CH2OH and -CH2CH2SCH3) capable to act, synergistically, for the simultaneous and efficient removal of both inorganic (heavy metals like Hg2+, Pb2+ and Tl+) and organic (dyes such as Pyronin Y, Auramine O, Brilliant Green and Methylene Blue) contaminants and, in addition, this MTV-MOF is completely reusable. Single-crystal X-ray diffraction (SCXRD) measurements allowed to solve th…

Aigua ContaminacióAuramine OChemistryOxamideInorganic chemistryfungiQuímica organometàl·licaHeavy metalsGeneral ChemistryCrystal structure010402 general chemistry01 natural sciencesBiochemistryCatalysis0104 chemical scienceschemistry.chemical_compoundColloid and Surface ChemistryBrilliant greenInorganic contaminantsMetal-organic frameworkMethylene blue
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2001

A new manganese(III) oxamato dimer possesing an unprecedented Mn2(μ-O2CR)(μ-OH2⋯O2 CR) core has been synthesised, structurally and magnetically characterised, and used as a catalyst for the oxidation of alkanes to alcohols and ketones by ButO2H and O2 in CH2Cl2 at rt.

Alkanechemistry.chemical_classificationChemistryDimerMetals and Alloyschemistry.chemical_elementGeneral ChemistryCrystal structureManganeseCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCatalysischemistry.chemical_compoundPolymer chemistryMaterials ChemistryCeramics and CompositesOrganic chemistryCarboxylateChemical Communications
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