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Picosecond Addition and β-Scission Reactions of Thiyl Radicals with Unsaturated Hydrocarbons

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Abstract

It is well known that free radical reactions exhibit extreme product diversity through the action of a limited number of elementary steps. The most facile elementary reaction between sulfur centered thiyl radicals and hydrocarbon liquids is free radical addition to carbon-carbon double bonds (1). This is a rapid exothermic reaction which is generally reversible.

© 1986 Optical Society of America

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