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- W1998056356 abstract "We report the study of the isomeric selective OH-initiated oxidation of 1,3-butadiene in the presence of O2 and NO using the LP/LIF technique. The photolysis of monodeuterated 1-iodo-3-buten-2-ol provides only one of the possible OD-butadiene adducts, the minor addition channel product, simplifying the oxidation mechanism. We find, based on analysis of OD time-dependent traces that prompt rearrangement of initial beta-hydroxyalkyl radicals to alpha-hydroxyalkyl radicals occurs in agreement with RRKM/ME theoretical predictions. We report a rate constant of (3.3+/-1.0) x 10(-11) cm3 molecules(-1) s(-1) for deuterium abstraction from the alpha-hydroxyalkyl radical at 298 +/-2 K. Our approach demonstrates the feasibility of isomeric selective kinetic studies of the OH-initiated oxidation of unsaturated hydrocarbons." @default.
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- W1998056356 date "2005-08-13" @default.
- W1998056356 modified "2023-10-14" @default.
- W1998056356 title "The OH-Initiated Oxidation of 1,3-Butadiene in the Presence of O<sub>2</sub> and NO: A Photolytic Route To Study Isomeric Selective Reactivity" @default.
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- W1998056356 doi "https://doi.org/10.1021/jp051545o" @default.
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