scholarly journals Absolute Rate Constants for Hydrogen Atom Transfer from Tertiary Amides to the Cumyloxyl Radical: Evaluating the Role of Stereoelectronic Effects

2014 ◽  
Vol 79 (15) ◽  
pp. 7179-7184 ◽  
Author(s):  
Michela Salamone ◽  
Michela Milan ◽  
Gino A. DiLabio ◽  
Massimo Bietti





1979 ◽  
Vol 57 (18) ◽  
pp. 2484-2490 ◽  
Author(s):  
J. A. Howard ◽  
J. H. B. Chenier

Rate constants and Arrhenius parameters for reaction of the tert-butylperoxy radical with 1-bromo-2-methylbutane and 1-bromo-3-methylbutane in solution from 30–80 °C have been estimated. The magnitude of these kinetic parameters are consistent with activation of the tertiary hydrogen vicinal to the bromine substituent and the involvement of a "bridged" transition state in the hydrogen atom transfer reaction.Chloro, trimethylsilyl, and trimethylstannyl substituents also activate a vicinal tertiary hydrogen and activation increases in the order trimethylsilyl ∼ trimethylstannyl < chloro < bromo.



2019 ◽  
Vol 53 (10) ◽  
pp. 5816-5827 ◽  
Author(s):  
Jimmy Murillo-Gelvez ◽  
Kevin P. Hickey ◽  
Dominic M. Di Toro ◽  
Herbert E. Allen ◽  
Richard F. Carbonaro ◽  
...  


2016 ◽  
Vol 49 (5) ◽  
pp. 877-883 ◽  
Author(s):  
Manoj Kumar ◽  
Amitabha Sinha ◽  
Joseph S. Francisco




Author(s):  
Hunter B. Vibbert ◽  
Hagen Neugebauer ◽  
Jack R Norton ◽  
Andreas Hansen ◽  
Markus Bursch ◽  
...  

The H• transfer rate constants for a series of group 6 molybdenum and tungsten pyrazolyl borate complexes are described. The rate constants for these complexes were found to span a range over 1 magnitude. Analysis of the H• transfer rate constants suggests that a combination of steric, electronic, and enthalpic factors are important in these reactions. Further analysis of the components suggests that the generated 17 e– radicals of these complexes are less electrophilic than the more commonly used CpCr(CO)3H complexes. General implications for H• transfer reactions are discussed.



2019 ◽  
Vol 55 (36) ◽  
pp. 5227-5230 ◽  
Author(s):  
Teo Martin ◽  
Michela Salamone ◽  
Massimo Bietti

Strong C–H bond deactivation toward HAT has been observed in the reactions of the cumyloxyl radical with 1,2- and 1,3-diols, following addition of Li+ and Ca2+. Weaker effects have been observed with Mg2+. The role of substrate structure and of the metal ion is discussed.



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