Abstract
Until now the reactions of organic peroxy radicals (RO(2)) with alkenes in the gas phase have been essentially studied at high temperature (T ≥ 360 K) and in the context of combustion processes, while considered negligible in the Earth's atmosphere. In this work, the reactions of methyl-, 1-pentyl- and acetylperoxy radicals (CH(3)O(2), C(5)H(11)O(2), and CH(3)C(O)O(2), respectively) with 2-methyl-2-butene, 2,3-dimethyl-2-butene and for the first time the atmospherically relevant isoprene, α-pinene, and limonene were studied at room temperature (298 ± 5 K). Monitoring directly the radicals with chemical ionization mass spectrometry led to rate coefficients larger than expected from previous combustion studies but following similar trends in terms of alkenes, with (in molecule(-1) cm(3) s(-1)) = 10(-18) to 10(-17) × 2/2 and = 10(-14) to 10(-13) × 5/5. While these reactions would be negligible for CH(3)O(2) and aliphatic RO(2) at room temperature, this might not be the case for acyl-, and perhaps hydroxy-, allyl- and other substituted RO(2). Combining our results with the Structure-Activity Relationship (SAR) predicts k (II)(298 K) ∼10(-14) molecule(-1) cm(3) s(-1) for hydroxy- and allyl-RO(2) from isoprene oxidation, potentially accounting for up to 14% of their sinks in biogenic-rich regions of the atmosphere and much more in laboratory studies.