Preparation, solution dynamics and x-ray crystal structure of the anilide-bridged diruthenium complex [(.eta.6-C6Me6)2Ru2(.mu.-NHPh)3][BF4]

1990 ◽  
Vol 29 (10) ◽  
pp. 2027-2030 ◽  
Author(s):  
Gaines C. Martin ◽  
Gus J. Palenik ◽  
James M. Boncella
1985 ◽  
Vol 107 (26) ◽  
pp. 8292-8294 ◽  
Author(s):  
Gerhard W. Klumpp ◽  
Marcel Vos ◽  
Franciscus J. J. De Kanter ◽  
Cees Slob ◽  
Hendrik Krabbendam ◽  
...  

1989 ◽  
Vol 111 (9) ◽  
pp. 3463-3465 ◽  
Author(s):  
Willem Moene ◽  
Marcel Vos ◽  
Franciscus J. J. De Kanter ◽  
Gerhard W. Klumpp ◽  
Anthony L. Spek

1986 ◽  
Vol 17 (16) ◽  
Author(s):  
G. W. KLUMPP ◽  
M. VOS ◽  
F. J. J. DE KANTER ◽  
C. SLOB ◽  
H. KRABBENDAM ◽  
...  

ChemInform ◽  
1989 ◽  
Vol 20 (32) ◽  
Author(s):  
W. MOENE ◽  
M. VOS ◽  
F. J. J. DE KANTER ◽  
G. W. KLUMPP ◽  
A. L. SPEK

2019 ◽  
Vol 2019 (7) ◽  
pp. 1046-1053 ◽  
Author(s):  
Soumyadip Patra ◽  
Mahendra K. Awasthi ◽  
Rohit K. Rai ◽  
Hemanta Deka ◽  
Shaikh M. Mobin ◽  
...  

2017 ◽  
Vol 72 (10) ◽  
pp. 759-762 ◽  
Author(s):  
Marion Graf ◽  
Peter Mayer ◽  
Hans-Christian Böttcher

AbstractTreatment of hydrated ruthenium(III) chloride with tetra-2-pyridyl-1,4-pyrazine (tppz) in refluxing ethoxyethanol afforded the homoleptic dinuclear complex [(tppz)Ru(μ-tppz)Ru(tppz)]4+ (1) besides small amounts of the species [Ru(tppz)2]2+. The title complex 1 was obtained as purple crystals and characterized as its hexafluoridophosphate salt by NMR spectroscopy, mass spectrometry and microanalyses. The molecular structure of 1(PF6)4 has been established by X-ray crystallography.


2001 ◽  
Vol 20 (12) ◽  
pp. 2565-2569 ◽  
Author(s):  
George M. Benedikt ◽  
Brian L. Goodall ◽  
Suri Iyer ◽  
Lester H. McIntosh ◽  
Richard Mimna ◽  
...  

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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