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1-十五碳烯与硝酸根自由基反应的产物、机理及α-硝基对烷氧基自由基分解的影响

Products and Mechanism of the Reaction of 1-Pentadecene with NO3 Radicals and the Effect of a -ONO2 Group on Alkoxy Radical Decomposition.

作者信息

Yeh Geoffrey K, Claflin Megan S, Ziemann Paul J

机构信息

Air Pollution Research Center and ‡Department of Chemistry, University of California, Riverside , Riverside, California 92521, United States.

Department of Chemistry and Biochemistry and ∥Cooperative Institute for Research in Environmental Sciences (CIRES), University of Colorado , Boulder, Colorado 80309, United States.

出版信息

J Phys Chem A. 2015 Oct 29;119(43):10684-96. doi: 10.1021/acs.jpca.5b07468. Epub 2015 Oct 16.

Abstract

The linear C15 alkene, 1-pentadecene, was reacted with NO3 radicals in a Teflon environmental chamber and yields of secondary organic aerosol (SOA) and particulate β-hydroxynitrates, β-carbonylnitrates, and organic peroxides (β-nitrooxyhydroperoxides + dinitrooxyperoxides) were quantified using a variety of methods. Reaction occurs almost solely by addition of NO3 to the C═C double bond and measured yields of β-hydroxynitrate isomers indicate that 92% of addition occurs at the terminal carbon. Molar yields of reaction products determined from measurements, a proposed reaction mechanism, and mass-balance considerations were 0.065 for β-hydroxynitrates (0.060 and 0.005 for 1-nitrooxy-2-hydroxypentadecane and 1-hydroxy-2-nitrooxypentadecane isomers), 0.102 for β-carbonylnitrates, 0.017 for organic peroxides, 0.232 for β-nitrooxyalkoxy radical isomerization products, and 0.584 for tetradecanal and formaldehyde, the volatile C14 and C1 products of β-nitrooxyalkoxy radical decomposition. Branching ratios for decomposition and isomerization of β-nitrooxyalkoxy radicals were 0.716 and 0.284 and should be similar for other linear 1-alkenes ≥ C6 whose alkyl chains are long enough to allow for isomerization to occur. These branching ratios have not been measured previously, and they differ significantly from those estimated using structure-activity relationships, which predict >99% isomerization. It appears that the presence of a -ONO2 group adjacent to an alkoxy radical site greatly enhances the rate of decomposition relative to isomerization, which is otherwise negligible, and that the effect is similar to that of a -OH group. The results provide insight into the effects of molecular structure on mechanisms of oxidation of volatile organic compounds and should be useful for improving structure-activity relationships that are widely used to predict the fate of these compounds in the atmosphere and for modeling SOA formation and aging.

摘要

直链C15烯烃1 - 十五碳烯在特氟龙环境舱中与硝酸根自由基发生反应,使用多种方法对二次有机气溶胶(SOA)以及颗粒状β - 羟基硝酸盐、β - 羰基硝酸盐和有机过氧化物(β - 硝基氧基氢过氧化物 + 二硝基氧基过氧化物)的产率进行了定量。反应几乎完全通过硝酸根加成到碳碳双键上发生,所测得的β - 羟基硝酸盐异构体的产率表明,92%的加成发生在末端碳原子上。根据测量结果、提出的反应机理以及质量平衡考虑确定的反应产物的摩尔产率为:β - 羟基硝酸盐为0.065(1 - 硝基氧基 - 2 - 羟基十五烷和1 - 羟基 - 2 - 硝基氧基十五烷异构体分别为0.060和0.005),β - 羰基硝酸盐为0.102,有机过氧化物为0.017,β - 硝基氧基烷氧基自由基异构化产物为0.232,十四醛和甲醛(β - 硝基氧基烷氧基自由基分解产生 的挥发性C14和C1产物)为0.584。β - 硝基氧基烷氧基自由基分解和异构化的分支比分别为0.716和0.284,对于其他碳数≥C6的直链1 - 烯烃,其烷基链足够长以允许异构化发生时,分支比应相似。这些分支比此前尚未测量,且与使用结构 - 活性关系估计的值有显著差异,结构 - 活性关系预测异构化率>99%。似乎与烷氧基位点相邻的 -ONO2基团的存在相对于异构化极大地提高了分解速率,否则异构化可忽略不计,并且这种效应与 -OH基团的效应相似。这些结果为了解分子结构对挥发性有机化合物氧化机理的影响提供了见解,并且对于改进广泛用于预测这些化合物在大气中的归宿以及模拟SOA形成和老化的结构 - 活性关系应是有用的。

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