Search results for "table"

showing 10 items of 2807 documents

Crystal structure of SrMn2(Si2O7)(OH)2 H2O, a new mineral of the lawsonite type

1992

Crystal with the composition SrMn 2 [Si 2 O 7 ](OH) 2 .H 2 O were found in a sugilite, serandite-pectolite rich sample from the Wessels Mine, Kalahari, South Africa. The crystal structure of the nex compound with space group Cmcm, a = 6.255(1), b = 9.034(2), c = 13.397(2) A, Z = 4 was determined from X-ray single-crystal data (R = 0.048). The structure is of the lawsonite type where Al is completely replaced by Mn 3+ and Ca by Sr. [Mn 3+ O 6 ] octahedra forming edge-sharing chains parallel to a exhibit a Jahn-Teller distortion with four short and two long Mn 3+ -O distances. Sr is in eight-fold coordination and H 2 O is disordered on a split position. Together with orientite, macfallite, ru…

CrystalCrystallographyMaterials scienceRuiziteMineralOctahedronLawsoniteGeochemistry and Petrologylawsonite; soro-silicate; crystal structure; Mn3+ Jahn-Teller distorsionSugiliteMineralogyCrystal structureBlock (periodic table)
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Cs[Ag4Zn2(SCN)9].

2002

Caesium tetrasilver dizinc nona­thio­cyanate, Cs[Ag4Zn2(SCN)9], forms a continuous structure, where the Ag atoms and the S atoms of the thio­cyanate groups form chains which run along [101]. These chains are bonded together through the Cs and Zn atoms. It is not possible to distinguish between space groups P1 and P\overline 1, but, if the latter space group is correct, the structure contains a thio­cyanate group disordered across a centre of inversion. The structure is described in space group P\overline 1, in which the Cs atom also lies on a centre of inversion.

CrystallographyChemistryGroup (periodic table)CaesiumAtomchemistry.chemical_elementSpace groupMoleculeGeneral MedicineCrystal structureSpace (mathematics)Inversion (discrete mathematics)General Biochemistry Genetics and Molecular BiologyActa crystallographica. Section C, Crystal structure communications
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Syntheses, X-ray structures, and redox behaviour of the group 14 bis-boraamidinates M[PhB(μ-N-t-Bu)2]2 (M = Ge, Sn) and Li2M[PhB(μ-N-t-Bu)2]2 (M = Sn…

2009

The solid-state structures of the complexes M[PhB(μ-N-t-Bu)2]2 (1a, M= Ge; 1b, M = Sn) were determined to be spirocyclic with two orthogonal boraamidinate (bam) ligands N,N′-chelated to the group 14 centre. Oxidation of 1b with SO2Cl2 afforded the thermally unstable, blue radical cation {Sn[PhB(μ-N-t-Bu)2]2}•+, identified by electron paramagnetic resonance (EPR) spectroscopy supported by density functional theory (DFT) calculations, whereas the germanium analogue 1a was inert towards SO2Cl2. The reaction between Li2[PhB(μ-N-t-Bu)2]2 and SnCl2 or PbI2 in 2:1 molar ratio in diethyl ether produced the novel heterotrimetallic complexes Li2Sn[PhB(μ-N-t-Bu)2]2 (2b) and (Et2O·Li)LiPb[PhB(μ-N-t-Bu…

CrystallographyGroup (periodic table)ChemistryOrganic ChemistryX-rayGeneral ChemistryRedoxCatalysisNuclear chemistryCanadian Journal of Chemistry
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Crystallographic study of a family of Cs2BX4compounds

1990

Abstract Five compounds of the Cs2BX4 family with B = Zn, Co, Cu and X = Cl, Br were grown and studied. They belong to Pnma space group with 4 formula units per cell. From the full determination of the structure it appears that the ZnX4 tetrahedra are almost regular while the CuX4 tetrahedra are strongly distorted. This seems to be due to a strong Jahn-Teller effect induced by the Cu ions. This remark is extended to other compounds of the general family A2BX4.

CrystallographyMaterials scienceGroup (periodic table)TetrahedronStructure (category theory)Condensed Matter PhysicsSpace (mathematics)Electronic Optical and Magnetic MaterialsGeneral familyFerroelectrics
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Crystal Structure of the Microwave Dielectric Resonator Ba2Ti9O20

1983

A single-crystal X-ray study of dibarium nonatitanate, Ba2Ti9O20, yielded the triclinic space group P 1 with a=0.7471(1), b= 1.4081(2), c= 1.4344(2) nm, α=89.94(2)°, β= 79.43(2)°, γ= 84.45(2)°, V = 1.476 nm3 Z = 4, and Dx= 4.61 Mg/m3. A refinement of atomic coordinates and isotropic thermal parameters led to a residual of 0.03. The structure consists of hexagonally closest-packed layers of Ba and O atoms in the sequence (hch)3. All Ti atoms reside in octahedral interstices of this closest packing. The various Ti coordination octahedra share only edges and corners with each other. One-half of the Ba atoms is twelve-coordinated by oxygen atoms, the other half is eleven-coordinated.

CrystallographyMaterials scienceOctahedronGroup (periodic table)IsotropyMaterials ChemistryCeramics and CompositesCrystal structureDielectric resonatorAtomic coordinatesTriclinic crystal systemMicrowaveJournal of the American Ceramic Society
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ChemInform Abstract: Crystal Structure of the Microwave Dielectric Resonator Ba2Ti9O20.

1983

A single-crystal X-ray study of dibarium nonatitanate, Ba2Ti9O20, yielded the triclinic space group P 1 with a=0.7471(1), b= 1.4081(2), c= 1.4344(2) nm, α=89.94(2)°, β= 79.43(2)°, γ= 84.45(2)°, V = 1.476 nm3 Z = 4, and Dx= 4.61 Mg/m3. A refinement of atomic coordinates and isotropic thermal parameters led to a residual of 0.03. The structure consists of hexagonally closest-packed layers of Ba and O atoms in the sequence (hch)3. All Ti atoms reside in octahedral interstices of this closest packing. The various Ti coordination octahedra share only edges and corners with each other. One-half of the Ba atoms is twelve-coordinated by oxygen atoms, the other half is eleven-coordinated.

CrystallographyOctahedronChemistryGroup (periodic table)IsotropyGeneral MedicineCrystal structureAtomic coordinatesDielectric resonatorTriclinic crystal systemMicrowaveChemischer Informationsdienst
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Controlling the position of anions relative to a pentafluorophenyl groupw

2012

The position of an anion above an electron-deficient arene can be controlled by the geometry of appended directing groups. Here a series of ammonium substituted pentafluorophenyl derivatives is investigated. The presented results are one step on the way to find the ideal structural features for an effective and superior receptor for anion–π studies.

CrystallographyPosition (vector)StereochemistryGroup (periodic table)ChemistryMaterials ChemistryChemieOne-StepGeneral ChemistryIdeal (ring theory)ta116CatalysisIonNew Journal of Chemistry
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Deduction of the oxidation degree of the group A15 elements at the phthalocyanines on the basis of the Q band

2017

CrystallographyQ band010405 organic chemistryGroup (periodic table)ChemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringBasis (universal algebra)010402 general chemistry01 natural sciences0104 chemical sciencesDegree (temperature)Dyes and Pigments
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Charge-density analysis of 1-nitroindoline: refinement quality using free R factors and restraints. Corrigendum

2011

The D e (dissociation energy) values in Table 6 of the article by Zarychta et al. [(2011). Acta Cryst. B67, 250–262] are corrected.

CrystallographyQuality (physics)ChemistryIntermolecular forceThermodynamicsCharge densityGeneral MedicineTable (information)Bond-dissociation energyGeneral Biochemistry Genetics and Molecular BiologyActa Crystallographica Section B Structural Science
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Electron Crystallography on Polymorphs

2006

Structure analysis via electron diffraction in combination with x-ray powder diffraction and simulation methods has been performed on single crystals of small organic molecules which form polymorphs. For two different examples of pigments and non-linear optical active material data collection, cell parameter and space group determination, structure analysis and refinement are discussed.

CrystallographyStructure analysisElectron diffractionElectron crystallographyGroup (periodic table)Material dataPowder diffractionSimulation methodsOrganic molecules
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