Deprotonation and anionic rearrangements of organometallic compounds. Reactions of the hydride complex (η5-C5H5)Re(NO)(PPh3)(H) with n-butyl-lithium–tetramethylethylenediamine

Author(s):  
Guy L. Crocco ◽  
J. A. Gladysz
1985 ◽  
Vol 40 (11) ◽  
pp. 1490-1494 ◽  
Author(s):  
Herbert Schumann ◽  
Gerald Jeske

Tricyclopentadienylneodymium and -lutetium react with sec-butyl lithium and terf-butyl lithium to form sec-butyl- and tert-butyl(dicyclopentadienyl)neodymium and -lutetium, which decompose to the corresponding dicyclopentadienyllanthanide hydride complexes. Dicyclopentadienyl-bis-(trimethylsilyl)methylsamarium and -lutetium are made from dicyclopentadienylsamarium or -lutetium chloride and bis(trimethylsilyl)methyl lithium. They react with hydrogen to form the corresponding dicyclopentadienyllanthanide hydride complexes.


1965 ◽  
Vol 38 (4) ◽  
pp. 991-998
Author(s):  
B. L. Erusalimskii ◽  
I. G. Krasnoselskaya ◽  
V. V. Mazurek

Abstract In the polymerization of chloroprene in the presence of butyl lithium, a substantial role is ascribed to reactions of deactivation of growing chains, which prevents the possibility of attaining a high degree of conversion. Kinetic data indicate the anionic mechanism of the process.


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