ChemInform Abstract: HETEROAROMATIC NUCLEOPHILIC SUBSTITUTION. INDUCING A CHANGE FROM AN IONIC TO A RADICAL-CHAIN MECHANISM WITH METHOXIDE ION

1973 ◽  
Vol 4 (50) ◽  
pp. no-no
Author(s):  
JOHN A. ZOLTEWICZ ◽  
TERENCE M. OESTREICH
1970 ◽  
Vol 48 (4) ◽  
pp. 544-545 ◽  
Author(s):  
F. Minisci ◽  
G. P. Gardini ◽  
F. Bertini

The metal ion catalyzed chlorination of 1-chlorobutane, 1-chlorohexane, methyl-pentanoate, and methyl-heptanoate by protonated N-chloroamines proceeds by a free radical chain mechanism and the chain carrying species was shown not to be a chlorine atom, but an amino radical cation.


1959 ◽  
Vol 12 (2) ◽  
pp. 147 ◽  
Author(s):  
NK King ◽  
ME Winfield

A thermodynamical argument is used to support the suggestion made elsewhere that the more common radical chain mechanism for catalysed decomposition of H2O2 need not predominate if the catalyst can readily undergo a reversible 2-electron oxidation. How complete the exclusion of free radical formation may be depends upon the redox characteristics of the catalyst and on whether its oxidation by two single-electron steps is readily reversible along the same path.


2007 ◽  
Vol 122 (3-4) ◽  
pp. 284-291 ◽  
Author(s):  
Pascal Lignier ◽  
Franck Morfin ◽  
Laurent Piccolo ◽  
Jean-Luc Rousset ◽  
Valérie Caps

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