Hydrotelluration of acetylenic esters: structural characterization of stereoisomers of methyl/ethyl β-(aryltelluro)acrylates

RSC Advances ◽  
2015 ◽  
Vol 5 (72) ◽  
pp. 58246-58254 ◽  
Author(s):  
Bandana Singh ◽  
Ashok K. S. Chauhan ◽  
Ramesh C. Srivastava ◽  
Andrew Duthie ◽  
R. J. Butcher

Synthesis of tellurated acrylates, ArTeCHCHCOOR and their solid state structures have been explored. The 125Te chemical shift and 2J(1H–125Te) are useful indicators of their geometry in solution.

2019 ◽  
Vol 9 (21) ◽  
pp. 6180-6190 ◽  
Author(s):  
Marcos de Oliveira ◽  
Dominik Seeburg ◽  
Jana Weiß ◽  
Sebastian Wohlrab ◽  
Gerd Buntkowsky ◽  
...  

Advanced analysis of 51V NMR chemical shift and quadrupolar tensor parameters revealed novel insights into the structure of vanadium species in MCM-41-based catalysts.


1999 ◽  
Vol 121 (10) ◽  
pp. 2307-2308 ◽  
Author(s):  
T. Beringhelli ◽  
G. D'Alfonso ◽  
M. Panigati ◽  
F. Porta ◽  
P. Mercandelli ◽  
...  

2012 ◽  
Vol 16 (01) ◽  
pp. 154-162 ◽  
Author(s):  
Edwin W.Y. Wong ◽  
Daniel B. Leznoff

The reduction of magnesium phthalocyanine (MgPc) with 2.2 equivalents of potassium graphite in 1,2-dimethoxyethane (DME) gives [K2(DME)4]PcMg(OH)(1) in 67% yield. Compound 1 was structurally characterized using single crystal X-ray crystallography and was found to be a monomeric, heterometallic complex consisting of a μ3-OH ligand that bridges a [MgIIPc3-]- anion to two potassium cations solvated by four DME molecules. An absorption spectrum of 1 confirms the Pc ligand is singly reduced and has a 3–charge. The solid-state structure of 1 does not indicate breaking of the aromaticity of the Pc ligand. Compound 1 is only the second Pc3- complex and the first reduced MgPc to be isolated and structurally characterized.


2005 ◽  
pp. 171-180 ◽  
Author(s):  
Leigh A. Graham ◽  
Alison R. Fout ◽  
Karl R. Kuehne ◽  
Jennifer L. White ◽  
Bhaskar Mookherji ◽  
...  

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