Dv. Avila et al., PERFLUORO-TERT-BUTYL, A REACTIVE, NEUTRAL, ELECTROPHILIC CARBON-CENTERED RADICAL PAR EXCELLENCE, Tetrahedron, 52(38), 1996, pp. 12351-12356
Absolute rate constants for (CF3)(3)C-. addition to terminal olefins i
ncrease by roughly a factor of 30 for every 1 eV decrease in the ioniz
ation potential (IF) of the alkene. A similar decrease in IP increases
the rate of addition of CF3. and n-C3F7. by a factor of only 3 or 4.
The perfluoro-tert-butyl radical is, therefore, the most electrophilic
, neutral carbon-centered radical to have been studied to date. Copyri
ght (C) 1996 Elsevier Science Ltd