Search results for "x-ray crystallography"
showing 10 items of 544 documents
Structural properties of phosphatidylcholine in a monolayer at the air/water interface
1991
Neutron reflectivities of phosphatidylcholine monolayers in the liquid condensed (LC) phase on ultrapure H 2 O and D 2 O subphases have been measured on a Langmuir film balance. Using a dedicated liquid surface reflectometer, reflectivities down to R = 10 -6 in the momentum transfer range Q z = 0–0.4A -1 were accessed. In a new approach, by refining neutron reflectivity data from chain-perdeuterated DPPC-d 62 in combination with x-ray measurements on the same monolayer under similar conditions it is shown that the two techniques mutually complement one another. This analysis leads to a detailed conception of the interface structure. It is found that in the LC phase (which is analogous to th…
Structure, properties and comparison of C,N-chelated and amido-stabilized plumbylenes
2010
The molecular structure of {2-[(CH3)2NCH2]C6H4}2Pb (1) in the solid state was determined by X-ray diffraction techniques on a single crystalline material. Bulky amido ligand stabilized complexes [(i-C3H7)2C6H3]NHLi (2) and [(i-C3H7)2C6H3N(Me3Si)]2Pb (3) were synthesized and characterized both in the solid state and solution by 1H, 13C, 15N and 207Pb NMR and XRD techniques. The structure of both C,N-chelated and bulky amido plumbylenes is compared.
Peculiarities of X-Ray Diffraction in Crystals with Diffuse Boundaries of Twin on System {011}, <011>
2000
X-ray diffraction on (KBr)1−x(KCN)xmixed crystals
1985
Crystallography and Crystal Engineering
2007
Structural characterization, thermal, dielectric and vibrational properties of tris(allylammonium) hexabromoantimonate(III), (C3H5NH3)3SbBr6
2010
Abstract The novel inorganic–organic hybrid material, allylammonium hexabromoantimonate(III), (C3H5NH3)3SbBr6, has been synthesized and its structure has been determined by means of the single-crystal X-ray diffraction studies at five temperatures (273, 248, 220, 170 and 100 K). At room temperature the compound crystallizes in the monoclinic space group, C2/m. Its crystal structure is composed of the discrete SbBr 6 3 - anions and three non-equivalent allylammonium, (C3H5NH3)+, cations. In (C3H5NH3)3SbBr6 three solid–solid structural phase transitions are detected: a continuous one at 260/256 K (on heating–cooling) from phase I to II, a discontinuous one at 227/208 K (II→III) and another di…
Front Cover: The Important Role of the Nuclearity, Rigidity, and Solubility of Phosphane Ligands in the Biological Activity of Gold(I) Complexes (Che…
2018
Contribution of X-Ray diffraction to the study of spin transitions in some iron (II) complexes
1991
Abstract A review of recent single crystal investigations under constraint of iron (II) spin crossover complexes is given. The systems covered are Fe L2 (NCS)2 complexes (L = Phen, Btz) and some analogous derivatives. Emphasis is laid on the correlations between structural changes associated with spin transitions and the experimentally determined characteristics of these transitions.
Structural and Magnetic Characterization of a Novel Heptanuclear Hydroxo-Bridged Copper(II) Cluster of the Corner-Sharing Dicubane Type
1994
Hexakis(dimethylformamide)iron(II) complex cation in hexahalorhenate(IV)-based salts: synthesis, X-ray structure and magnetic properties
2018
Two iron(II)-rhenium(IV) compounds of general formula [FeII(dmf)6][ReIVX6] [X = Cl (1) and Br (2); dmf = N,N-dimethylformamide] have been prepared and characterized. X-ray powder diffraction measurements on samples of 1 and 2 support the same structure for both systems. The crystal structure of 1 was determined by single-crystal X-ray diffraction. 1 crystallizes in the triclinic system with space group Pī. Each iron(II) is six-coordinate and bonded to six oxygens from six dmf molecules building a distorted octahedral environment. Rhenium(IV) is six-coordinate by six halide anions in an almost regular octahedral geometry. The magnetic properties were investigated from variable-temperature ma…