Search results for "X-ray Diffraction"

showing 10 items of 280 documents

Preparation and structural characterization of Ph3Sn(IV)+ complexes with pyridinecarboxylic acids or hydroxypyridene, -pyrimidine and –quinoline.

2006

A number of [Ph3Sn(IV)](+) complexes formed with ligands containing -OH (-C=O), or -COOH group(s) and aromatic IN) donor atom have been prepared. The binding sites of the ligands were identified by FT-IR spectroscopic measurements. In the complexes containing hydroxy and carboxylate functions, the carboxylato group is coordinated to the organotin(IV) centres in monodentate or bridging bidentate manner. It was also found that in the hydroxypyridine and -pyrimidine complexes the [Ph3Sn(IV)]+ moiety in most cases reacts with the phenolic form of the ligands. The rationalisation of the experimental Sn-119 Mossbauer nuclear quadrupole splittings, vertical bar Delta(exp)vertical bar - according t…

DenticityPyrimidineStereochemistrytriphenyltin(IV)BiochemistryMedicinal chemistryInorganic ChemistryMossbauerchemistry.chemical_compound2-HYDROXYPYRIDINEPyridineMaterials ChemistryMoietyCarboxylatePhysical and Theoretical ChemistryCOORDINATIONDERIVATIVESOrganic ChemistryQuinolineX-ray diffraction DICARBOXYLIC-ACIDShydroxypyridine -pyrimidine and pyridinecarboxylato complexeFT-IRTrigonal bipyramidal molecular geometryOctahedronchemistryLIGANDS
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Preparation and structural studies on the tBu2Sn(IV) complexes with aromatic mono- and dicarboxylic acids containing hetero {N} donor atom

2004

Nine complexes of 'Bu2Sn(IV)(2+) were obtained in the solid state with ligands containing -COOH group(s) and aromatic (N) donor atom. The binding sites of the ligands were identified by FT-IR spectroscopic measurements. It was found that in most cases the -COO- groups are co-ordinated in monodentate manner. Nevertheless, in some of our complexes, the -COO- group forms bridges between two central {Sn} atoms resulting in the formation of an oligomeric structure, a motif that is characteristic only to the nicotinate compound. These pieces of information and the rationalisation of the experimental Sn-119 Mossbauer nuclear quadrupole splittings, Delta, - according to the point charge model forma…

DenticitygeometryX ray diffractionCrystal structureOrganotin(IV)nicotinic acid derivativeBiochemistryInorganic Chemistrycomplex formationMaterials ChemistryMoleculeorganotin compoundcontrolled studyPhysical and Theoretical Chemistryinfrared spectroscopychemical bindinghydrogen bondHydrogen bondChemistryMössbauer spectroscopybinding siteOrganic ChemistryarticleSquare pyramidal molecular geometryX-ray diffractionFT-IRtin derivativeTrigonal bipyramidal molecular geometryCrystallographyOctahedrondicarboxylic acidSettore CHIM/03 - Chimica Generale E Inorganicachemical structureMolecular modellingcarboxylic acidsynthesimolecular modelchemical analysiSingle crystal
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Optimization of sample preparation conditions for detecting trace amounts of β-tegafur in α- and β-tegafur mixture.

2012

We report a semiquantitative method for determining trace amounts (<1%) of thermodynamically stable forms in polymorphic mixtures, focusing on sample preparation ef- fects on solid phase transitions. Tegafur (5-fluoro-1-(oxolan-2-yl)-1,2,3,4-tetrahydropyrimidine- 2,4-dione) was used as a model material in this study. The amounts of the thermodynamically stable $ tegafur were increased to levels detectable by powder X-ray diffractometry by grind- ing the samples in a ball mill in the presence of water. The limit of detection for this method was as low as 0.0005% of $ tegafur in " and $ tegafur mixtures. The amount of $ tegafur after sample preparation was found to be proportional to the init…

Detection limitLangmuirAntimetabolites AntineoplasticTrace AmountsChemistryAnalytical chemistryPharmaceutical ScienceTegafurPhase TransitionPolymorphism (materials science)IsomerismX-Ray DiffractionLimit of DetectionmedicineThermodynamicsSample preparationBall millMass fractionPowder Diffractionmedicine.drugTegafurJournal of pharmaceutical sciences
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Inhibition of skin inflammation in mice by diclofenac in vesicular carriers: Liposomes, ethosomes and PEVs

2013

Diclofenac-loaded phospholipid vesicles, namely conventional liposomes, ethosomes and PEVs (penetration enhancer-containing vesicles) were developed and their efficacy in TPA (phorbol ester) induced skin inflammation was examined. Vesicles were made from a cheap and unpurified mixture of phospholipids and diclofenac sodium; Transcutol P and propylene glycol were added to obtain PEVs, and ethanol to produce ethosomes. The structure and lamellar organization of the vesicle bilayer were investigated by transmission electron microscopy and small and wide angle X-ray scattering, as well as the main physico-chemical features. The formulations, along with a diclofenac solution and commercial Volta…

DiclofenacSurface PropertiesDrug CompoundingSkin AbsorptionLipid BilayersPharmaceutical ScienceIn Vitro TechniquesDermatitis ContactMiceDiclofenacMicroscopy Electron TransmissionX-Ray DiffractionmedicineAnimalsSkinDrug CarriersLiposomeChromatographyEthanolChemistryBilayerVesicleAnti-Inflammatory Agents Non-SteroidalDiclofenac SodiumPenetration (firestop)PermeationPropylene GlycolLiposomesBiophysicsNanoparticlesNanocarriersmedicine.drugInternational Journal of Pharmaceutics
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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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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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Structural and electrical study of the topological insulator SnBi2Te4 at high pressures

2016

We report high-pressure X-ray diffraction and electrical measurements of the topological insulator SnBi2Te4 at room temperature. The pressure dependence of the structural properties of the most stable phase of SnBi2Te4 at ambient conditions (trigonal phase) have been experimentally determined and compared with results of our ab initio calculations. Furthermore, a comparison of SnBi2Te4 with the parent compound Bi2Te3 shows that the central TeSnTe trilayer, which substitutes the Te layer at the center of the TeBiTeBiTe layers of Bi2Te3, plays a minor role in the compression of SnBi2Te4. Similar to Bi2Te3, our resistance measurements and electronic band structure simulations in SnBi2Te4 at hi…

DiffractionElectronic topological transitionMaterials science02 engineering and technology01 natural sciencesAb initio quantum chemistry methodsPhase (matter)0103 physical sciencesMaterials ChemistryElectrical measurementsTopological insulators010306 general physicsElectronic band structureCondensed matter physicsMechanical EngineeringMetals and Alloys021001 nanoscience & nanotechnologyX-ray diffractionHigh pressureMechanics of MaterialsHigh pressureTopological insulatorFISICA APLICADAX-ray crystallographyTransport properties0210 nano-technology
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Crystal structure of 4,6-O-ethylidene-N-(2-hydroxybenzylidene)-β-D-glucopyranosylamine

2002

4,6-O-Ethylidene-N-(2-hydroxybenzylidene)-β-D-glucopyranosylamine was synthesized and characterized using analytical, spectral and single-crystal X-ray diffraction methods. The anomeric nature of the saccharide moiety was proposed based on 1H NMR studies and was confirmed by the crystal structure. The lattice structure of this compound was compared with that of its analogues.

DiffractionGlucosamineMagnetic Resonance SpectroscopyAnomerSingle CrystalsMolecular StructureChemistryStereochemistryOrganic ChemistrySynthesis (Chemical)Saccharide MoietyH-1 Nmr StudiesGeneral MedicineCrystal structureBiochemistryAnalytical ChemistryCrystallographyX-Ray DiffractionLattice StructureProton NMRCrystal StructureMoietyCrystallizationIndraStra Global
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Pressure-induced amorphization of the Y3Ga5O12 garnet studied to 1 Mbar

2020

We use micro-beam synchrotron x-ray diffraction to study the pressure-induced amorphization of nano-sized and single crystals of Y3Ga5O12 up to pressures exceeding 1 Mbar in static compression. The abrupt pressure-induced amorphization found for both 56 nm and bulk micrometric crystals at around 76 GPa independently of the pressure transmitting medium employed demonstrates its intrinsic nature, previously predicted at 79 GPa by ab initio calculations. The single crystal structural solution at 50 GPa shows that the contraction of the unit-cell, mostly accommodated by the compressible YO8 dodecahedra, gives rise to a regularization and tilting increase of the GaO6 polyhedra with the Y?O-Ga an…

DiffractionMaterials science02 engineering and technology010402 general chemistry01 natural scienceslaw.inventionDodecahedronAb initio quantum chemistry methodslawMaterials ChemistryPressureBulk modulusCondensed matter physicsMechanical EngineeringMetals and AlloysGarnets021001 nanoscience & nanotechnologySynchrotronAmorphization0104 chemical sciencesX-ray diffractionNanocrystalMechanics of MaterialsX-ray crystallography0210 nano-technologySingle crystal
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