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Kinetische Untersuchungen über die Autoxidation von Olefinen
Authors:M. Futu-Tangu  E. Lawson  W. Pritzkow  V. Voerckel
Abstract:Kinetic Studies on the Autoxidation of Olefins The oxidabilities documentclass{article}pagestyle{empty}begin{document}$ {{{rm k}_{rm p} } mathord{left/ {vphantom {{{rm k}_{rm p} } {sqrt {2{rm k}_{rm t} } }}} right.kern-nulldelimiterspace} {sqrt {2{rm k}_{rm t} } }} $end{document}equation image at 50°C were determined for 37 olefins, using chlorobenzene as the solvent and azodiisobutyronitril as the initiator. In the group of acyclic aliphatic olefins the oxidability rises with increasing number of alkyl groups bound to the double bond. This is also true for cyclic olefins, but in this case the ring size has also a great influence on the oxidability. So the oxidability decreases from five-ring to eight-ring cycloolefins. Particularly high oxidabilities are found in the case of olefins in which a phenyl group is attached directly to the C C-double bond.
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