Inorgano-Grignard reagents. Preparation, reactions, and X-ray crystal structure of bis-(η-cyclopentadienyl)hydromolybdenum[bromo(bistetrahydrofuran)magnesium]

1977 ◽  
pp. 135-136 ◽  
Author(s):  
Stephen G. Davies ◽  
Malcolm L. H. Green ◽  
Keith Prout ◽  
Alessandro Coda ◽  
Vittorio Tazzoli
Keyword(s):  
Crystal Structure ◽  
Grignard Reagents ◽  
X Ray

Reactions of conjugated arylazocyclohexenes with Grignard reagents; X-ray crystal structure of 1-hydroperoxy-1-(o-methoxyphenylazo)-2-phenylcyclohexane

1977 ◽  
pp. 1377 ◽  
Author(s):  
Silvano Bozzini ◽  
Sergio Grattion ◽  
Amerigo Risaliti ◽  
Antonia Stener ◽  
Mario Calligaris ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Grignard Reagents ◽  
X Ray

scholarly journals Selective access to p-dialkyl-carbo-benzenes from a [6]pericyclynedione: the n-butyl nucleophile model for a metal switch study

2017 ◽  
Vol 95 (4) ◽  
pp. 454-459 ◽  
Author(s):  
Chongwei Zhu ◽  
Carine Duhayon ◽  
Alix Saquet ◽  
Valérie Maraval ◽  
Remi Chauvin
Keyword(s):  
Crystal Structure ◽  
Electrochemical Behavior ◽  
Spectroscopic Properties ◽  
Grignard Reagents ◽  
Cyclic Voltammograms ◽  
Redox Processes ◽  
Metal Centers ◽  
X Ray ◽  
Selective Access ◽  
Switch Study

The synthesis, spectroscopic properties, comparative electrochemical behavior in CHCl3 vs CH2Cl2, and X-ray crystal structure of p-di-n-butyl-tetraphenyl-carbo-benzene are described. The selectivity of preparation of the ultimate [6]pericyclynediol precursor has been examined by comparing the reactivity of the [6]pericyclynedione substrate with four n-Bu-MXn nucleophiles involving more or less halogenated metal centers MXn (0 ≤ n ≤ 2): Li, MgBr, MgCl, CeCl2/LiCl. The cerium reagent is found to be the most efficient, giving approximately twice the yield given by Grignard reagents in the target diadduct (90% vs 51%–53%). The dibutyl-carbo-benzene product happens to be soluble in both CHCl3 and CH2Cl2: cyclic voltammograms of either solution exhibit almost identical peak potentials with reduced reversibility of the redox processes in CHCl3.

A study on α-RuCl3 crystal structure by scanning tunneling microscopy

1989 ◽  
Vol 47 ◽  
pp. 30-31
Author(s):  
H.-J. Cantow ◽  
H. Hillebrecht ◽  
S. Magonov ◽  
H. W. Rotter ◽  
G. Thiele
Keyword(s):  
Crystal Structure ◽  
Density Distribution ◽  
Scanning Tunneling Microscopy ◽  
Electron Density ◽  
Structure Determination ◽  
Electron Density Distribution ◽  
Scanning Tunneling ◽  
Monoclinic Space Group ◽  
Tunneling Microscopy ◽  
X Ray

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.

X-ray Crystal Structure of ?9-THC-tosylate

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

Crystal structure of an inclusion complex between chiral monoaza-15-crown-5 and S(–)-1-phenyl-ethyl ammonium percholorate

2003 ◽  
Vol 218 (5) ◽  
Author(s):  
Süheyla Özbey ◽  
F. B. Kaynak ◽  
M. Toğrul ◽  
N. Demirel ◽  
H. Hoşgören
Keyword(s):  
Crystal Structure ◽  
Inclusion Complex ◽  
Single Crystal ◽  
X Ray Diffraction ◽  
Space Group ◽  
X Ray ◽  
New Type

AbstractA new type of inclusion complex, S(–)-1 phenyl ethyl ammonium percholorate complex of R-(–)-2-ethyl - N - benzyl - 4, 7, 10, 13 - tetraoxa -1- azacyclopentadecane, has been prepared and studied by NMR, IR and single crystal X-ray diffraction techniques. The compound crystallizes in space group

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