Darstellung und Einkristall-Röntgenstrukturanalyse einiger Fluorphosphite und Phosphitester / Preparation and Single Crystal X-Ray Diffraction Study of Some Fluorophosphites and Phosphite Esters

1993 ◽  
Vol 48 (5) ◽  
pp. 659-671 ◽  
Author(s):  
Thomas G. Meyer ◽  
Axel Fischer ◽  
Peter G. Jones ◽  
Reinhard Schmutzler

The synthesis of some monofluorophosphite esters from the appropriate hydroxy compound and PCl2F in the presence of a tertiary amine is described. The reaction of 2,2′-dihydroxy-biphenyl with PCl3 in the presence of triethylamine did not furnish the expected chlorophosphite 9; instead, the bridged bisphosphite ester, 10, was obtained. Reaction of the fluorophosphite ester 8 with 3,5-di-tert-butyl-benzoquinone furnished the spiromonofluorophosphorane 12 in which λ5P is part of a five-membered and a seven-membered ring system. Single crystal X-ray diffraction studies were conducted on compounds 2, 10 and 13. In the case of 2, crystallographic 2/m symmetry and short intermolecular P · · · O distances were observed. Compound 10 shows short intramolecular P · · · O contacts. The catechyl phosphate 13, similarly to other dialkylphosphate esters, was found to be a hydrogen-bonded dimer.

2019 ◽  
Vol 43 (33) ◽  
pp. 13282-13293
Author(s):  
J.-B. Regnouf-de-Vains ◽  
B. Malaman ◽  
S. Bouguet-Bonnet ◽  
Sophie Poinsignon ◽  
Sébastien Leclerc ◽  
...  

An original M4L2 “hand-to-hand” copper(i)/tetra-bipyridyl-calix[4]arene complex was obtained and characterized in the solid state by X-ray diffraction. It changes in MeCN solution to its M2L analogue.


1986 ◽  
Vol 64 (1) ◽  
pp. 174-179 ◽  
Author(s):  
Michael D. Fryzuk ◽  
May-Ling Jang ◽  
Terry Jones ◽  
Frederick W. B. Einstein

The reaction of phenol with the binuclear rhodium hydride [{(i-Pr)2PCH2CH2P(i-Pr)2}Rh]2(μ-H)2 generates [{(i-Pr)2PCH2CH2P(i-Pr)2}Rh]2(μ-H)(μ-OC6H5), 2, which was characterized by both solution spectroscopic techniques and a single crystal X-ray diffraction study. The structure was solved using Patterson and Fourier methods and refined to R = 0.019 (Rw = 0.027) for 6062 reflections; crystals of the compound are triclinic, space group [Formula: see text], with a = 9.018(2), b = 12.988(2), c = 17.558(3) Å, α = 99.42(1), β = 92.62(2), γ = 91.85(2)°, and Z = 2. Further reaction with excess phenol leads to the mononuclear complex (η5-C6H5O)Rh{(i-Pr)2PCH2CH2P(i-Pr)2}•2C6H5OH, which contains two phenol units hydrogen bonded to the oxygen of the η5-cyclohexy]dienylone ligand. The presence of the bridging phenoxide ligand in 2 results in reduced reactivity as compared to the starting binuclear hydride dimer.


1992 ◽  
Vol 45 (12) ◽  
pp. 2089 ◽  
Author(s):  
EL Ghisalberti ◽  
BW Skelton ◽  
AH White

The structure of the compound obtained on heating the naturally occurring clerodane furanoditerpene (1) had been formulated as (2) on the basis of spectroscopic studies. A single-crystal X-ray diffraction study on the dihydro derivative of (2) has confirmed this and provides support for the stereochemistry previously assigned to (1) on the basis of chemical evidence.


1996 ◽  
Vol 271 (3-4) ◽  
pp. 189-196 ◽  
Author(s):  
P Bordet ◽  
F Duc ◽  
S LeFloch ◽  
J.J Capponi ◽  
E Alexandre ◽  
...  

Author(s):  
Innokenty Kantor ◽  
Alexander Kurnosov ◽  
Catherine McCammon ◽  
Leonid Dubrovinsky

AbstractA high-pressure quasi-single crystal X-ray diffraction study of a synthetic iron oxide Fe


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