Analytical Chemistry Laboratory, National Institute of Chemistry , 1000 Ljubljana, Slovenia.
Division for Marine and Environmental Research, Ruđer Bošković Institute , 10000 Zagreb, Croatia.
Environ Sci Technol. 2016 Jun 7;50(11):5526-35. doi: 10.1021/acs.est.6b00823. Epub 2016 May 12.
Methylnitrocatechols (MNCs) are secondary organic aerosol (SOA) tracers and major contributors to atmospheric brown carbon; however, their formation and aging processes in atmospheric waters are unknown. To investigate the importance of aqueous-phase electrophilic substitution of 3-methylcatechol with nitronium ion (NO2(+)), we performed quantum calculations of their favorable pathways. The calculations predicted the formation of 3-methyl-5-nitrocatechol (3M5NC), 3-methyl-4-nitrocatechol (3M4NC), and a negligible amount of 3-methyl-6-nitrocatechol (3M6NC). MNCs in atmospheric PM2 samples were further inspected by LC/(-)ESI-MS/MS using commercial as well as de novo synthesized authentic standards. We detected 3M5NC and, for the first time, 3M4NC. In contrast to previous reports, 3M6NC was not observed. Agreement between calculated and observed 3M5NC/3M4NC ratios cannot unambiguously confirm the electrophilic mechanism as the exclusive formation pathway of MNCs in aerosol water. However, the examined nitration by NO2(+) is supported by (1) the absence of 3M6NC in the ambient aerosols analyzed and (2) the constant 3M5NC/3M4NC ratio in field aerosol samples, which indicates their common formation pathway. The magnitude of error one could make by incorrectly identifying 3M4NC as 3M6NC in ambient aerosols was also assessed, suggesting the importance of evaluating the literature regarding MNCs with special care.
甲硝草酚(MNCs)是二次有机气溶胶(SOA)示踪剂,也是大气棕色碳的主要贡献者;然而,其在大气水中的形成和老化过程尚不清楚。为了研究与硝鎓离子(NO2(+))的水相中亲电取代 3-甲基儿茶酚的重要性,我们进行了它们有利途径的量子计算。计算预测了 3-甲基-5-硝基儿茶酚(3M5NC)、3-甲基-4-硝基儿茶酚(3M4NC)和少量 3-甲基-6-硝基儿茶酚(3M6NC)的形成。通过使用商业和新合成的真实标准品的 LC/(-)ESI-MS/MS 进一步检查大气 PM2 样品中的 MNCs。我们检测到 3M5NC,并首次检测到 3M4NC。与先前的报告相反,未观察到 3M6NC。计算出的 3M5NC/3M4NC 比值与观察到的比值之间的一致性并不能明确证实亲电机制是气溶胶水中 MNCs 的唯一形成途径。然而,通过 NO2(+)进行的硝化作用得到了支持:(1)在所分析的环境气溶胶中不存在 3M6NC;(2)在现场气溶胶样品中 3M5NC/3M4NC 比值恒定,这表明它们具有共同的形成途径。在环境气溶胶中错误地将 3M4NC 鉴定为 3M6NC 可能会造成的误差大小也进行了评估,这表明特别需要谨慎评估有关 MNCs 的文献。