Synthesis and X-ray crystal structure of the asymmetric trinuclear complex [Ni3(µ3-S)2(H2O)(PPh3)5][PF6]2

Author(s):  
Carlo A. Ghilardi ◽  
Paolo Innocenti ◽  
Stefano Midollini ◽  
Annabella Orlandini
2010 ◽  
Vol 65 (10) ◽  
pp. 1240-1244 ◽  
Author(s):  
Bao Lin Liu ◽  
Juan Dang ◽  
Shuang Quan Zang ◽  
Qing Lun Wang ◽  
Ruo Jie Tao

A new dissymmetrical oxamidate ligand has been used to construct a metal-organic network. Using this ligand, a novel coordination polymer, namely {[Cu(obea)]2Cu・CH3OH・H2O}n (1) [H3obea = N1-(2-carboxyphenyl)-N2-(2-hydroxyethyl)oxalamide] has been synthesized and characterized by single-crystal X-ray analysis. The structure of complex 1 consists of neutral trinuclear complex units. Through syn-anti carboxylate bridges, the complex features a 2D structure with a helical substructure. Its magnetic properties have been investigated.


1990 ◽  
Vol 170 (1) ◽  
pp. 23-26 ◽  
Author(s):  
Hilary J. Banbery ◽  
Ferida S. McQuillan ◽  
Thomas A. Hamor ◽  
Christopher J. Jones ◽  
Jon.A. McCleverty

1979 ◽  
Vol 34 (12) ◽  
pp. 1698-1702 ◽  
Author(s):  
Achim Müller ◽  
Hartmut Bögge ◽  
Elisabeth Königer-Ahlborn

The title compound was prepared by reaction of AgNO3, P(C6H5)3 and (NH4)2WS4 in a dichloromethane/water system. The crystal structure was determined from single crystal X-ray diffraction data (monoclinic, space group P21/c, with a = 1811,1(2), b = 1735.6(2), c = 1779,7(2) pm, β = 95,02(1)°, V = 5572,7 · 106 pm3, Z = 4). The compound contains a tetradentate WS42- ligand and two silver atoms, having a tetrahedral and trigonal planar coordination.


1993 ◽  
Vol 461 (1-2) ◽  
pp. C4-C6 ◽  
Author(s):  
Carlo A. Ghilardi ◽  
Stefano Midollini ◽  
Annabella Orlandini ◽  
Giancarlo Scapacci ◽  
Alberto Vacca

Author(s):  
Sefa Durmus ◽  
B. Meltem Ates ◽  
Orhan Atakol ◽  
Filiz Ercan

AbstractA tetradentate ONNO type Schiff base was synthesized from salicyaldehyde and 1,4-diaminobutane. Thermogravimetric analysis, elemental analysis and X-ray diffraction results showed this Schiff base to give a trinuclear complex with Ni(II) ions in presence of acetate ions. The complex crystallizes in the triclinic


Author(s):  
H.-J. Cantow ◽  
H. Hillebrecht ◽  
S. Magonov ◽  
H. W. Rotter ◽  
G. Thiele

From X-ray analysis, the conclusions are drawn from averaged molecular informations. Thus, limitations are caused when analyzing systems whose symmetry is reduced due to interatomic interactions. In contrast, scanning tunneling microscopy (STM) directly images atomic scale surface electron density distribution, with a resolution up to fractions of Angstrom units. The crucial point is the correlation between the electron density distribution and the localization of individual atoms, which is reasonable in many cases. Thus, the use of STM images for crystal structure determination may be permitted. We tried to apply RuCl3 - a layered material with semiconductive properties - for such STM studies. From the X-ray analysis it has been assumed that α-form of this compound crystallizes in the monoclinic space group C2/m (AICI3 type). The chlorine atoms form an almost undistorted cubic closed package while Ru occupies 2/3 of the octahedral holes in every second layer building up a plane hexagon net (graphite net). Idealizing the arrangement of the chlorines a hexagonal symmetry would be expected. X-ray structure determination of isotypic compounds e.g. IrBr3 leads only to averaged positions of the metal atoms as there exist extended stacking faults of the metal layers.


Planta Medica ◽  
2008 ◽  
Vol 74 (03) ◽  
Author(s):  
W Gul ◽  
P Carvalho ◽  
D Slade ◽  
M Avery ◽  
JR Duchek ◽  
...  
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