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Reactivity of amines toward tert-butoxy radicals: Effect of solvent and amine structure

✍ Scribed by M. V. Encina; S. Díaz; E. Lissi


Publisher
John Wiley and Sons
Year
1981
Tongue
English
Weight
235 KB
Volume
13
Category
Article
ISSN
0538-8066

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✦ Synopsis


Abstract

The reactivity of amines towards tert‐butoxy radicals depends upon the amine ionization potential and the solvent, indicating that polar structures contribute to the reactivity of these compounds. Nevertheless, the dependence with the amine potential is smaller than the one obtained for the quenching of carbonyl excited states by amines and other factors as the strength of the broken hydrogen bond and steric hindrance are also significant in determining the rate of the process.


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