Search results for " diffraction"

showing 10 items of 896 documents

trans-4-Bromo-ONN-azoxybenzene at 100 K.

2004

The crystal structure of the alpha isomer of trans-4-bromoazoxybenzene [systematic name: trans-1-(bromophenyl)-2-phenyldiazene 2-oxide], C(12)H(9)BrN(2)O, has been determined by X-ray diffraction. The geometries of the two molecules in the asymmetric unit are slightly different and are within approximately 0.02 A for bond lengths, approximately 2 degrees for angles and approximately 3 degrees for torsion angles. The azoxy bridges in both molecules have the typical geometry observed for trans-azoxybenzenes. The crystal network contains two types of planar molecules arranged in columns. The torsion angles along the Ar-N bonds are only 7 (2) degrees, on either side of the azoxy group.

DiffractionAzoxyCrystal structureIsomersTorsion (mechanics)X ray diffraction analysisGeneral MedicineCrystal structureMolecular dynamicsGeneral Biochemistry Genetics and Molecular BiologyBond lengthCrystalchemistry.chemical_compoundCrystallographyTorsional stressMolecular geometrychemistrySubstitution reactionsOxidationMoleculeActa crystallographica. Section C, Crystal structure communications
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Anisotropic lattice distortions in biogenic calcite induced by intra-crystalline organic molecules.

2006

9 pages; International audience; We have performed precise structural measurements on five different calcitic seashells by high-resolution X-ray powder diffraction on a synchrotron beam line and by laboratory single crystal X-ray diffraction. The unit cell parameters a and c of biogenic calcite were found to be systematically larger than those measured in the non-biogenic calcite. The maximum lattice distortion (about 2.10(-3)) was detected along the c-axis. Under heat treatment above 200 degrees C, a pronounced lattice relaxation was observed, which allowed us to conclude that anisotropic lattice swelling in biogenic calcite is induced by organic macromolecules incorporated within the sing…

DiffractionBiomineralizationMESH : Calcium CarbonateMESH: Bivalvia02 engineering and technologyCrystallography X-Ray01 natural scienceslaw.inventionchemistry.chemical_compoundStructural BiologylawMESH : BivalviaOstreaMESH : AnisotropyMESH: AnimalsOrganic ChemicalsCrystallizationAnisotropyMESH: CrystallizationCalciteMESH: OstreaSynchrotron radiationCalciteCrystal growth and nucleationMESH : Organic Chemicals021001 nanoscience & nanotechnologyMESH: Calcium CarbonateMESH : CrystallizationX-ray crystallographyCrystallization0210 nano-technologyMaterials scienceMESH : Crassostrea010402 general chemistryCalcium CarbonateAnimalsCrassostreaIntra-crystalline organic molecules[SDV.IB.BIO]Life Sciences [q-bio]/Bioengineering/BiomaterialsBiogenic crystalsMESH : OstreaMESH: Organic ChemicalsMESH: Crystallography X-Ray[ SDV.IB.BIO ] Life Sciences [q-bio]/Bioengineering/BiomaterialsBivalvia0104 chemical sciencesX-ray diffractionCrystallographyMESH: CrassostreachemistryMESH: AnisotropyAnisotropyMESH : AnimalsMESH : Crystallography X-RaySingle crystalPowder diffractionBiomineralization
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A Novel High‐Pressure Tin Oxynitride Sn 2 N 2 O

2020

Chemistry - a European journal in Press(in Press), chem.201904529 (2019). doi:10.1002/chem.201904529

DiffractionBulk modulusSilicon oxynitride010405 organic chemistryChemistryOrganic ChemistryAnalytical chemistrychemistry.chemical_elementGermaniumGeneral ChemistryCrystal structure540010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundElectron diffractionddc:540Electronic band structureTinChemistry – A European Journal
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In situ high-pressure synchrotron X-ray diffraction study of the structural stability in NdVO4 and LaVO4

2014

Abstract Room-temperature angle-dispersive X-ray diffraction measurements on zircon-type NdVO 4 and monazite-type LaVO 4 were performed in a diamond-anvil cell up to 12 GPa. In NdVO 4 , we found evidence for a non-reversible pressure-induced structural phase transition from zircon to a monazite-type structure at 6.5 GPa. Monazite-type LaVO 4 also exhibits a phase transition but at 8.6 GPa. In this case the transition is reversible and isomorphic. In both compounds the pressure induced transitions involve a large volume collapse. Finally, the equations of state and axial compressibilities for the low-pressure phases are also determined.

DiffractionCeramicsPhase transitionMaterials scienceHigh-pressureMechanical EngineeringAnalytical chemistryCrystal structureCondensed Matter PhysicsX-ray diffractionCrystallographyVolume (thermodynamics)Mechanics of MaterialsStructural stabilityvisual_artX-ray crystallographyvisual_art.visual_art_mediumCompressibilityGeneral Materials ScienceCeramicCeramics; High-pressure; X-ray diffractionMaterials Research Bulletin
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Structural properties of magnesium stearate pseudopolymorphs: effect of temperature.

2003

A thorough review of the relevant literature reveals that the interaction between water vapour and magnesium stearate, in contrast to many other metal soaps, is not properly understood. The structural modifications associated with the up-take or loss of water of vegetable-derived commercial magnesium stearate powders exposed to humid air or vacuum at room temperature are investigated using standard powder X-ray diffractometry. It is found that in such conditions magnesium stearate reacts reversibly with the vapour phase with structural consequences very similar to the high temperature transition between the crystalline and rotator phases of other anhydrous metal soaps. When temperature is i…

DiffractionChemical PhenomenaChemistry PhysicalAnalytical chemistryPharmaceutical ScienceWaterMetalHeatingCrystallographychemistry.chemical_compoundLattice constantchemistryDrug StabilityX-Ray Diffractionvisual_artX-ray crystallographyAnhydrousvisual_art.visual_art_mediumTechnology PharmaceuticalMagnesium stearateHydratePowder diffractionStearic AcidsInternational journal of pharmaceutics
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High-pressure powder x-ray diffraction study of EuVO4

2015

The high-pressure structural behavior of europium orthovanadate has been studied using in-situ, synchrotron based, high-pressure x-ray powder diffraction technique. Angle-dispersive x-ray diffraction measurements were carried out at room temperature up to 34.7 GPa using a diamond-anvil cell, extending the pressure range reported in previous experiments. We confirmed the occurrence of zircon-scheelite phase transition at 6.8 GPa and the coexistence of low- and high-pressure phases up to 10.1 GPa. In addition, clear evidence of a scheelite-fregusonite transition is found at 23.4 GPa. The fergusonite structure remains stable up to 34.7 GPa, the highest pressure reached in the present measureme…

DiffractionChemical Physics (physics.chem-ph)Phase transitionCondensed Matter - Materials ScienceChemistrychemistry.chemical_elementMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesCrystal structureCondensed Matter PhysicsFergusoniteSynchrotronElectronic Optical and Magnetic Materialslaw.inventionInorganic ChemistryCrystallographylawPhysics - Chemical PhysicsX-ray crystallographyMaterials ChemistryCeramics and CompositesPhysical and Theoretical ChemistryEuropiumPowder diffraction
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"Ab initio" structure solution from electron diffraction data obtained by a combination of automated diffraction tomography and precession technique

2009

Using a combination of our recently developed automated diffraction tomography (ADT) module with precession electron technique (PED), quasi-kinematical 3D diffraction data sets of an inorganic salt (BaSO(4)) were collected. The lattice cell parameters and their orientation within the data sets were found automatically. The extracted intensities were used for "ab initio" structure analysis by direct methods. The data set covered almost the complete set of possible symmetrically equivalent reflections for an orthorhombic structure. The structure solution in one step delivered all heavy (Ba, S) as well as light atoms (O). Results of the structure solution using direct methods, charge flipping …

DiffractionChemistryAb initioMolecular physicsAtomic and Molecular Physics and OpticsElectronic Optical and Magnetic MaterialsDiffraction tomographyCrystallographyElectron diffractionLattice (order)Direct methodsElectron diffractionSTEMNanodiffractionAutomationTomographyPrecession electron techniqueStructure solutionPrecession electron diffractionOrthorhombic crystal systemInstrumentation
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Crystal structure analysis of a star-shaped triazine compound: a combination of single-crystal three-dimensional electron diffraction and powder X-ra…

2017

The solid-state structure of star-shaped 2,4,6-tris{(E)-2-[4-(dimethylamino)-phenyl]ethenyl}-1,3,5-triazine is determined from a powder sample by exploiting the respective strengths of single-crystal three-dimensional electron diffraction and powder X-ray diffraction data. The unit-cell parameters were determined from single crystal electron diffraction data. Using this information, the powder X-ray diffraction data were indexed, and the crystal structure was determined from the powder diffraction profile. The compound crystallizes in a noncentrosymmetric space group,P212121. The molecular conformation in the crystal structure was used to calculate the molecular dipole moment of 3.22 Debye,…

DiffractionChemistryMetals and Alloys02 engineering and technologyCrystal structure010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic MaterialsDipolesymbols.namesakeCrystallographyElectron diffractionX-ray crystallographyMaterials Chemistrysymbols0210 nano-technologySingle crystalPowder diffractionDebyeActa crystallographica Section B, Structural science, crystal engineering and materials
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Fast algorithms for free-space diffraction patterns calculation

1999

Here we present a fast algorithm for Fresnel integral calculation. Some fast algorithms using the fast Fourier transform are analysed and their performance has been checked. These methods are of easy implementation, but are only valid for a specific range of distances. Fast algorithms based on the Fractional Fourier transform allow accurate evaluation of the Fresnel integral from object to Fraunhofer domain in a single step.

DiffractionComputer sciencebusiness.industryFast Fourier transformPhysics::OpticsFresnel integralAtomic and Molecular Physics and OpticsDiscrete Fourier transformFractional Fourier transformElectronic Optical and Magnetic MaterialsDiscrete Fourier transform (general)symbols.namesakeCyclotomic fast Fourier transformOpticsFourier transformsymbolsPseudo-spectral methodElectrical and Electronic EngineeringPhysical and Theoretical ChemistryHarmonic wavelet transformbusinessAlgorithmFresnel diffractionOptics Communications
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Elektrónová a pásová štruktúra CuMnAs študovaná optickou a fotoemissinou spektroskopiou

2017

Tetragonal phase of CuMnAs progressively appears as one of the key materials for antiferromagnetic spintronics due to efficient current-induced spin-orbit torques whose existence can be directly inferred from crystal symmetry. Theoretical understanding of spintronic phenomena in this material, however, relies on the detailed knowledge of electronic structure (band structure and corresponding wave functions) which has so far been tested only to a limited extent. We show that AC permittivity (obtained from ellipsometry) and UV photoelectron spectra agree with density functional calculations. Together with the x-ray diffraction and precession electron diffraction tomography, our analysis confi…

DiffractionCondensed Matter - Materials ScienceMaterials scienceSpintronicsCondensed matter physicsPhotoemission spectroscopyMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesspintronics DFT photoemission optical properties CuMnAs02 engineering and technologyCrystal structureElectronic structure021001 nanoscience & nanotechnology01 natural sciences3. Good healthTetragonal crystal systemCondensed Matter::Materials ScienceSpintronika DFT fotoemissia optické vlastnosti CuMnAs0103 physical sciencesPrecession electron diffraction010306 general physics0210 nano-technologyElectronic band structure
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