Reactivity of transition metal fluorides. Vi. Halogen-exchange reactions of vanadium pentafluoride

1968 ◽  
Vol 21 (6) ◽  
pp. 1421 ◽  
Author(s):  
JH Canterford ◽  
TA O'Donnell

In an earlier paper in this series, it was indicated that halogen-exchange reactions between vanadium pentafluoride and covalent chlorides are very complex. The present work shows that the results may be rationalized on the basis of an initial halogen-exchange reaction, producing vanadium tetrachloride, chlorine, and the appropriate fluoride. As soon as some vanadium tetrachloride is formed, competitive reactions commence, thus making the exact elucidation of the reaction schemes very difficult. In order to clarify the situation, some reactions of vanadium tetrachloride itself were studied.

1971 ◽  
Vol 24 (2) ◽  
pp. 243 ◽  
Author(s):  
JH Canterford ◽  
TA O'Donnell ◽  
AB Waugh

Oxidation-reduction and halogen-exchange reactions of the higher fluorides of rhenium with a series of selected reagents have been investigated. The results correlate with studies of reactivities of higher fluorides of other transition metals previously reported. The reactions reported provide markedly improved preparative routes to the hexachloride, pentabromide, and pentafluoride of rhenium.


1969 ◽  
Vol 22 (9) ◽  
pp. 1877 ◽  
Author(s):  
TA O'Donnell ◽  
PW Wilson

Following similar, previously reported studies of reactions of uranium hexafluoride, selected oxidation-reduction and halogen-exchange reactions of the tetra- fluoride, pentafluoride, and intermediate fluorides of uranium have been investigated.


Molbank ◽  
10.3390/m1289 ◽  
2021 ◽  
Vol 2021 (4) ◽  
pp. M1289
Author(s):  
Sukanta Bar

5-propyl-2-((trityloxy)methyl)thiophene-3-carbaldehyde was synthesized by using the concept of chemo- and regioselective Br/Li exchange reaction from 3-bromo-5-propyl-2-((trityloxy)methyl)thiophene. This is a five-step protocol starting from thiophene with an overall yield of 33%. These lithium/halogen exchange reactions were carried out at −78 °C to rt over the period of 1 to 18 h depending on the reactivity of electrophiles.


1989 ◽  
Vol 45 (1) ◽  
pp. 51
Author(s):  
J.H. Holloway ◽  
E.G. Hope ◽  
A.K. Brisdon ◽  
P.J. Jones ◽  
W. Levason ◽  
...  

2019 ◽  
Vol 55 (86) ◽  
pp. 12984-12987
Author(s):  
Carlos Marquez ◽  
Matthieu Corbet ◽  
Simon Smolders ◽  
Philippe Marion ◽  
Dirk De Vos

A series of transition metal-based double metal cyanides (DMCs) were studied as catalysts for the synthesis of nitriles via acid-nitrile exchange reaction.


2007 ◽  
Vol 162 (7-8) ◽  
pp. 613-620 ◽  
Author(s):  
José Jiménez-Mier ◽  
Guillermo M. Herrera-Pérez ◽  
Paul Olalde-Velasco ◽  
Elizabeth Chavira ◽  
Ioscani Jiménez ◽  
...  

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