Search results for "Crystal system"

showing 10 items of 13557 documents

High-pressure structural study of the scheelite tungstatesCaWO4andSrWO4

2005

Angle-dispersive x-ray-diffraction and x-ray-absorption near-edge structure measurements have been performed on ${\mathrm{CaWO}}_{4}$ and ${\mathrm{SrWO}}_{4}$ up to pressures of approximately 20 GPa. Both materials display similar behavior in the range of pressures investigated in our experiments. As in the previously reported case of ${\mathrm{CaWO}}_{4}$, under hydrostatic conditions ${\mathrm{SrWO}}_{4}$ undergoes a pressure-induced scheelite-to-fergusonite transition around 10 GPa. Our experimental results are compared to those found in the literature and are further supported by ab initio total-energy calculations, from which we also predict the instability at larger pressures of the …

Bulk modulusCrystallographyMaterials scienceHafnonAb initio quantum chemistry methodsHydrostatic pressureX-ray crystallographySpace groupOrthorhombic crystal systemCondensed Matter PhysicsFergusonitePhysics::GeophysicsElectronic Optical and Magnetic MaterialsPhysical Review B
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Gold(i) sulfide: Unusual bonding and an unexpected computational challenge in a simple solid

2019

We report the experimental high-pressure crystal structure and equation of state of gold(I) sulfide (Au2S) determined using diamond-anvil cell synchrotron X-ray diffraction. Our data shows that Au2S has a simple cubic structure with six atoms in the unit cell (four Au in linear, and two S in tetrahedral, coordination), no internal degrees of freedom, and relatively low bulk modulus. Despite its structural simplicity, Au2S displays very unusual chemical bonding. The very similar and relatively high electronegativities of Au and S rule out any significant metallic or ionic character. Using a simple valence bond (Lewis) model, we argue that the Au2S crystal possesses two different types of cov…

Bulk modulusMaterials science010405 organic chemistryGold(I) sulfideIonic bondingGeneral ChemistryCubic crystal system010402 general chemistry01 natural sciences0104 chemical sciencesElectronegativitychemistry.chemical_compoundChemical bondchemistryChemical physicsCovalent bondValence bond theory
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Characterization of theTiSiO4structure and its pressure-induced phase transformations: Density functional theory study

2009

Theoretical investigations concerning the possible titanium silicate polymorphs have been performed using density functional theory at B3LYP level. Total-energy calculations and geometry optimizations have been carried out for all phases involved. The following sequence of pressure-driven structural transitions has been found: ${\text{CrVO}}_{4}$-type, $Cmcm$ (in parenthesis the transition pressure), $\ensuremath{\rightarrow}$ zircon-type, $I{4}_{1}/amd$ (0.8 GPa), $\ensuremath{\rightarrow}$ scheelite-type, $I{4}_{1}/a$ (3.8 GPa). At higher pressure the last phase is found to be stable at least up to 25 GPa. The equation of state of the different polymorphs is also reported. We found that t…

Bulk modulusMaterials scienceEquation of state (cosmology)Phase (matter)ThermodynamicsOrthorhombic crystal systemDensity functional theoryDielectricElectronic structureCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsAmbient pressurePhysical Review B
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CCDC 1450587: Experimental Crystal Structure Determination

2016

Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Kari Rissanen|2016|CrystEngComm|18|4971|doi:10.1039/C6CE00240D

C-Methylcalix(4)resorcinarene bis(4-phenylpyridine N-oxide) clathrateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1551402: Experimental Crystal Structure Determination

2017

Related Article: Rakesh Puttreddy, Ngong Kodiah Beyeh, Robin H. A. Ras, John F. Trant, Kari Rissanen|2017|CrystEngComm|19|4312|doi:10.1039/C7CE00975E

C-ethyl-2-bromoresorcinarene bis(pyridine N-oxide) acetone solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Synthesis, Characterization, Thermal and Antimicrobial studies of N-substituted Sulfanilamide derivatives

2014

Abstract Four sulfanilamide derivatives N -[4-(phenylsulfamoyl)phenyl]acetamide (1), 4-amino- N -phenylbenzenesulfonamide (2), N -[4-(phenylsulfamoyl)phenyl]benzamide (3) and N -{4-[(3-chlorophenyl)sulfamoyl]phenylbenzamide (4) were synthesized and characterized by Infra-Red (IR), Nuclear Magnetic Resonance (NMR) and UV–visible (UV–Vis) spectra. Also Liquid Chromatographic (LCMS) and High Resolution Mass Spectrometric (HRMS) methods were used. Crystal structures of 1–4 were determined by single crystal X-ray diffraction (XRD) and their conformational and hydrogen bond (HB) network properties were examined with survey of the literature data. Compounds 1 and 2 crystallize in the same orthorho…

CARBONIC-ANHYDRASE INHIBITORSStereochemistryCrystal structureAntimicrobial activitySOLUBILITYTriclinic crystal systemAnalytical ChemistryInorganic ChemistrySynthesischemistry.chemical_compoundDESIGNSulfanilamidesmedicineSUBLIMATIONCRYSTAL-STRUCTUREThermal analysista116SpectroscopySULFONAMIDE DERIVATIVESHydrogen bondCrystal structureOrganic ChemistryThermal decompositionSulfanilamideX-ray diffractionCrystallographySOLVATIONchemistryACIDOrthorhombic crystal systemAcetamidemedicine.drugMonoclinic crystal systemJournal of Molecular Structure
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Photochemical ligand rearrangement in dirhodium(II) compounds. Structure of Rh2(O2CCH3)2(η2-O2CCH3)[(C6H4)PPh2] (η2-PCCl)(PCClP-ClC6H4)Ph2

1995

Abstract The photochemical reaction of the adducts Rh2(O2CCH3)3[(C6H4)P(o-ClC6H4)Ph]· (P(p-XC6H4)3) (X=H, Me, Cl), yield the compounds Rh2(O2CCH3)2(η2-O2CCH3)[(p-XC6H3)P (p-XC6H4)2](η2-PCCl), (PCCl=P(o-ClC6H4)Ph2) in a ligand rearrangement reaction that involves activation of CH and RhC bonds. The factors that favour this process are studied by carrying out photochemical reactions with different phosphines. The structures of Rh2(O2CCH3)2(η2-O2CCH3) [(C6H4)PPh2](η2-PCCl) has been determined by X-ray diffraction. Mr=1321.1, orthorhombic, space group Pbcn, a=20.339(8), b=20.07(6), c=23.07(3) A , V=9413(3) A 3 , Z=8, D x =1.86 g cm −3 . Mo Kα radiation (graphite crystal monochromator, λ=0.071…

Chelating ligandsChemistryLigandCrystal structurePhotochemistryAdductInorganic ChemistryBond lengthchemistry.chemical_compoundMaterials ChemistryRearrangement reactionOrthorhombic crystal systemPhysical and Theoretical ChemistryTriphenylphosphineInorganica Chimica Acta
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Synthesis and X-ray crystal structure of manganese(II) pyridine-2-thiolate

1997

2:1 complexes of pyridine-2(1H)-thione (LH) with manganese(II) were prepared: (LH)2MnCl2, (LH)2MnBr2 and [L2Mn]n. The polymeric chain structure of [L2Mn]n contains a distorted octahedrally coordinated manganese (MnN2S4) with chelating ligands, the N-atoms are in cis positions and the S-atoms of the pyridine-2-thiolates bridging; crystallographic data for [C10H8MnN2S2]n: space group C2/c (monoclinic), and R1 = 0.0571 for 1326 reflexes with Fo4σ(Fo).

Chelating ligandsX-raychemistry.chemical_elementCrystallographic dataCrystal structureManganeseInorganic ChemistryChain structureCrystallographychemistryPyridine-2-thiolateMaterials ChemistryPhysical and Theoretical ChemistryMonoclinic crystal systemInorganica Chimica Acta
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Anomalous High-Pressure Jahn-Teller Behavior inCuWO4

2012

High-pressure optical-absorption measurements performed in CuWO4 up to 20 GPa provide experimental evidence of the persistence of the Jahn-Teller (JT) distortion in the whole pressure range both in the low-pressure triclinic and in the highpressure monoclinic phase. The electron-lattice coupling associated with the eg(Exe) and t2g(Txe) orbitals of Cu2+ in CuWO4 are obtained from correlations between the JT distortion of the CuO6 octahedron and the associated structure of Cu2+ d-electronic levels. This distortion and its associated JT energy (EJT) decrease upon compression in both phases. However, both the distortion and associated EJT increase sharply at the phase transition pressure (PT = …

Chemical Physics (physics.chem-ph)Condensed Matter - Materials ScienceMaterials scienceStrongly Correlated Electrons (cond-mat.str-el)Condensed matter physicsJahn–Teller effectMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesGeneral Physics and AstronomyTriclinic crystal systemCondensed Matter - Strongly Correlated ElectronsAtomic orbitalOctahedronPhysics - Chemical PhysicsDistortionPhase (matter)MultiferroicsMonoclinic crystal systemPhysical Review Letters
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High-pressure study of substrate material ScAlMgO4

2011

We report on the structural properties of ScAlMgO4 studied under quasi-hydrostatic pressure using synchrotron high-pressure x-ray diffraction up to 40 GPa. We also report on single-crystal studies of ScAlMgO4 performed at 300 K and 100 K. We found that the low-pressure phase remains stable up to 24 GPa. At 28 GPa, we detected a reversible phase transformation. The high-pressure phase is assigned to a monoclinic distortion of the low-pressure phase. No additional phase transition is observed up to 40 GPa. In addition, the equation of state, compressibility tensor, and thermal expansion coefficients of ScAlMgO4 are determined. The bulk modulus of ScAlMgO4 is found to be 143(8) GPa, with a str…

Chemical Physics (physics.chem-ph)Condensed Matter - Materials SciencePhase transitionBulk modulusMaterials scienceCondensed matter physicsMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciencesCondensed Matter PhysicsThermal expansionElectronic Optical and Magnetic MaterialsCondensed Matter::Materials SciencePhysics - Chemical PhysicsX-ray crystallographyCompressibilityAnisotropyMonoclinic crystal systemWurtzite crystal structurePhysical Review B
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