Search results for " Crystal"

showing 10 items of 3073 documents

Charge Transfer Salts Based on Polyoxometalates and Seleno-Substituted Organic Donors. Synthesis, Structure, and Magnetic Properties of (BEST)3H[PMo1…

1998

Electrochemical oxidation of the tetrathiafulvalene (TTF) type organic donor bis(ethylenediseleno)tetrathiafulvalene (BEST) in the presence of the Keggin polyoxometalate [PMo12O40]3- affords the radical salt formulated as (BEST)3H[PMo12O40] (crystal data:  triclinic, space group P1 with a = 13.056(1) A, b = 13.957(1) A, c = 22.302(3) A, α = 97.019(9)°, β = 94.17(1)°, γ = 95.847(9)°, and Z = 2). This is the first salt of a selenium-containing donor with a polyoxometalate cluster. The structure of this organic/inorganic hybrid consists of layers of the organic donors that alternate with polyoxometalate layers in the c direction. The organic molecules, which are completely ionized, form two ty…

chemistry.chemical_classificationRadicalInorganic chemistrySalt (chemistry)Triclinic crystal systemElectrochemistryMagnetic susceptibilityInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryPolyoxometalateCluster (physics)Physical and Theoretical ChemistryTetrathiafulvaleneInorganic Chemistry
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Conformational investigation of α, β-dehydropeptides

2009

The crystal structure of Ac-Pro-delta Val-NHCH3 was examined to determine the influence of the alpha,beta-dehydrovaline residue on the nature of peptide conformation. The peptide crystallizes from methanol-diethyl ether solution at 4 degrees in needle-shaped form in orthorhombic space group P2(1)2(1)2(1) with a = 11.384(2) A, b = 13.277(2) A, c = 9.942(1) A, V = 1502.7(4) A3, Z = 4, Dm = 1.17 g.cm-3 and Dc = 1.18 g.cm-3. The structure was solved by direct methods using SHELXS-86 and refined to an R value of 0.057 for 1922 observed reflections. The peptide is found to adopt a beta-bend between the type I and the type III conformation with phi 1 = -68.3(4) degrees, psi 1 = -20.1(4) degrees, p…

chemistry.chemical_classificationResidue (chemistry)chemistryStereochemistryHydrogen bondIntramolecular forceOrthorhombic crystal systemPeptideCrystal structureMethylamideBiochemistryPeptide ConformationInternational Journal of Peptide and Protein Research
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Semicarbazides as gel forming agents for common solvents and liquid crystals

2006

This paper describes the synthesis of 14 new gelling agents with semicarbazide groups as H-bonding motifs and alkyl- and/or azobenzene side groups. They gel solvents like decaline, 1,2-dichlorobenzene and toluene and liquid crystalline mixtures. X-Ray structure analysis shows that the semicarbazides are connected by H-bonds, each molecule to four neighbours. As a result a ribbon is formed with a core of H-bonded semicarbazide groups and alkyl chains sticking to the side. IR measurements show an unchanged H-bonding motif in large crystals and in the gel fibres, even in LC-mixture. During heating the gel melts (rheology), while the H-bonding motif of the crystal disappears (IR and DSC measure…

chemistry.chemical_classificationSemicarbazideSemicarbazidesStereochemistryInfrared spectroscopyGeneral Chemistrychemistry.chemical_compoundDifferential scanning calorimetryAzobenzenechemistryLiquid crystalPolymer chemistryMaterials ChemistryGlass transitionAlkylJ. Mater. Chem.
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On the reaction of [Ph2(OH)Si]2O with t-Bu2SnCl2: Synthesis and characterization of the first well defined polystannasiloxane [(t-Bu2SnO)(Ph2SiO)2]n

1997

Abstract The high yield synthesis of [(t-Bu2SnO)(Ph2SiO)2], 1 is reported. Compound 1 is a linear polymer in the solid state but a six-membered ring in solution.

chemistry.chemical_classificationSiliconOrganic Chemistrychemistry.chemical_elementPolymerCharacterization (mathematics)Ring (chemistry)BiochemistryInorganic ChemistryCrystallographychemistryYield (chemistry)X-ray crystallographyMaterials ChemistryPhysical and Theoretical ChemistryWell-definedTinJournal of Organometallic Chemistry
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FT-IR and dielectric study of water/AOT liquid crystals

2000

Abstract In order to explore the influence of microwave radiation on highly viscous microheterogeneous systems, the evolution of structural and dynamical properties of the water/sodium bis(2-ethylhexyl) sulfosuccinate (AOT) liquid crystals as a function of the molar ratio R (R=[water]/[AOT]) has been investigated by FT-IR spectroscopy and time domain reflectometry. The study emphasises how the progressive hydration of the surfactant head groups is mainly responsible for the structural and dynamical evolution of water/AOT liquid crystals. In particular, it has been found that the state of water at lower R values is strongly perturbed, bulk-like water appears only at R>23 and the water/AOT in…

chemistry.chemical_classificationSodiumOrganic ChemistryAnalytical chemistryIonic bondingchemistry.chemical_elementDielectricAnalytical ChemistryInorganic ChemistrychemistryPulmonary surfactantLiquid crystalCounterionFourier transform infrared spectroscopySpectroscopySpectroscopyJournal of Molecular Structure
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Liquid-crystalline ordering as a concept in materials science: from semiconductors to stimuli-responsive devices.

2013

While the unique optical properties of liquid crystals (LCs) are already well exploited for flat-panel displays, their intrinsic ability to self-organize into ordered mesophases, which are intermediate states between crystal and liquid, gives rise to a broad variety of additional applications. The high degree of molecular order, the possibility for large scale orientation, and the structural motif of the aromatic subunits recommend liquid-crystalline materials as organic semiconductors, which are solvent-processable and can easily be deposited on a substrate. The anisotropy of liquid crystals can further cause a stimuli-responsive macroscopic shape change of cross-linked polymer networks, w…

chemistry.chemical_classificationSolid-state chemistryMaterials scienceNanotechnologyGeneral ChemistryPolymerCatalysisCrystalOrganic semiconductorchemistryLiquid crystalArtificial muscleSelf-assemblyAnisotropyAngewandte Chemie (International ed. in English)
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Structural study of NaNdGa4S8, a luminescent material with low-concentration quenching

1988

Abstract Single-crystal X-ray diffraction analysis and optical investigations of NaNdGa 4 S 8 show that Nd 3+ ions are essentially distributed in two of the three square antiprismatic sites of a CaGa 2 S 4 -type lattice. The NdS 8 polyhedra are isolated (minimum NdNd distance: 6.07 A) so the interactions responsible for concentration quenching of the luminescence are considerably reduced

chemistry.chemical_classificationSquare antiprismatic molecular geometryChemistryInorganic chemistryCrystal structureCondensed Matter PhysicsElectronic Optical and Magnetic MaterialsIonInorganic ChemistryBond lengthCrystallographyMolecular geometryX-ray crystallographyMaterials ChemistryCeramics and CompositesPhysical and Theoretical ChemistryLuminescenceInorganic compoundJournal of Solid State Chemistry
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Experimental Investigations and ab Initio Studies on Hexacoordinated Complexes of Dichlorosilane

1998

Dichlorosilane, SiH2Cl2, forms two different kinds of coordination compounds with pyridine and 3-picoline:  the simple adduct trans-SiH2Cl2(L)2 and the ionic complex [SiH2(L)4]Cl2·4CHCl3 (L = pyridine, 3-picoline). The adducts trans-SiH2Cl2(py)2, 1, and trans-SiH2Cl2(3pic)2, 2, form directly from the reaction of bis(dichlorosilyl)methylamine, NMe(SiHCl2)2 with pyridine (py), and 3-picoline (3pic). Reaction of 1 with an excess of pyridine in chloroform yielded [SiH2(py)4]Cl2·4CHCl3, 3. The molecular and crystal structures of 1−3 were investigated by single-crystal X-ray diffraction. The Si atoms of all three compounds are hexacoordinated and lie on centers of inversion. The basic structural …

chemistry.chemical_classificationStereochemistryAb initioDichlorosilaneGeneral ChemistryCrystal structureTriclinic crystal systemBiochemistryCatalysisCoordination complexAdductchemistry.chemical_compoundCrystallographyColloid and Surface ChemistrychemistryPyridineMonoclinic crystal systemJournal of the American Chemical Society
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TaNi 2 .05Te 3 , eine Verbindung mit “aufgefüllter” TaFe 1+ x Te 3 ‐Struktur

1994

TaNi2.05Te3, a Novel Telluride with “Stuffed” TaFe1+xTe3 Structure The novel metal-rich layer compound TaNi2.05Te3 was synthesized from the elements. Its structure contains TaNi2Te3 layers which are interconnected by Ni atoms on partially occupied tetragonal-pyramidal sites located between the layers. The title compound and the related telluride TaFe1.14Te3 form a pair of compounds differing only in the occupation or nonoccupation of one 3d-material atom site. Therefore, the structure of TaNi2.05Te3, which is stabilized by interstial Ni atoms, can be regarded as a “stuffed” TaFe1.14Te3 type. Pairs of compounds with a similar structural relationship seem to be of general importance in early …

chemistry.chemical_classificationStereochemistryChalcogenideCrystal structureInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryTernary compoundTellurideX-ray crystallographyAtomMoleculeInorganic compoundChemische Berichte
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Über tetraaryl-methan-analoga in der gruppe 14

1994

Abstract The title compounds have been synthesized by Grignard reactions or pyrolysis of diplumbanes respectively. The crystal structures of m -Tol 4 Pb and Ph 4 Pb (redetermination) have been determined. All eight compounds (Ph/Tol) 4 (Sn/Pb) are S 4 symmetric and contracted along this unique axis. The 13 C-NMR chemical shifts and the couplings 1 J ( 119 Sn/ 207 Pb 13 C) as well depend additively upon the methyl substituents. The ratios 1 K ( 207 Pb 13 C): 1 K ( 119 Sn 13 C) of the reduced coupling constants are all near to 1.61; a comparison with values from the literature for alkyl, alkenyl and alkinyl substituents is given. The ratio δ( 207 Pb):δ( 119 Sn) results in 2.28. IR (700 dow…

chemistry.chemical_classificationStereochemistryChemical shiftOrganic ChemistryNuclear magnetic resonance spectroscopyCrystal structureGrignard reagentBiochemistryMedicinal chemistryInorganic Chemistrysymbols.namesakechemistryX-ray crystallographyMaterials ChemistrysymbolsMoleculePhysical and Theoretical ChemistryRaman spectroscopyAlkylJournal of Organometallic Chemistry
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