Allyl radicals from 3,3′-azo-1-propene

3,3′-Azo-1-propene (4), 3,3′-azo-1-propene-3,3′-d 2 (5) and 3,3′-azo-1-propene-3,3,3′3′-d 4 (6) have been synthesized and characterized. Thermolysis of 4, at 40–300 Torr, and in the region 150–170°, followed first order kinetics (E a = 36.1 ± 0.2 kcal mole −1 , log A = 15.54 ± 0.10) the major product, >99.9%, being 1,5-hexadiene (9). The presence of less than 0.1% propene suggests that the allyl radical is unable to abstract hydrogen from 4 or 9. Statistical scrambling of deuterium, in the products of thermolysis of 5 and 6, was observed. These results are interpreted in terms of a mechanism wherein allyl radicals are generated. Comparison of the activation energies for azoalkanes and 4 with the bond dissociation energies of hydrocarbons suggest that a good Polanyi plot is possible.