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Reactivity of adrenaline toward alkoxyl radicals and carbonyl triplet states
Gonzalo Cosa,J. C. Scaiano
Organic & Biomolecular Chemistry Pub Date : 10/31/2008 00:00:00 , DOI:10.1039/B810765C
Abstract

The reactivities of adrenaline toward hydrogen abstraction by the tert-butoxyl radical and the excited triplet state of benzophenone have been examined in solution using laser flash photolysis techniques. The rate constants obtained in acetonitrile-rich solvents are 13 and 1.5 × 108 M−1 s−1 for benzophenone triplet and the tert-butoxyl radical, respectively. Adrenaline is a better hydrogen donor than phenol, but not as efficient as α-tocopherol.

Graphical abstract: Reactivity of adrenaline toward alkoxyl radicals and carbonyl triplet states
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