Mofidfar Mohammad, Mehrgardi Masoud A, Zare Richard N
Department of Chemistry, Stanford University, Stanford, California 94305, United States.
Department of Chemistry, University of Isfahan, Isfahan 81743, Iran.
J Am Chem Soc. 2024 Jul 10;146(27):18498-18503. doi: 10.1021/jacs.4c04092. Epub 2024 Jun 27.
Using real-time mass spectrometric (MS) monitoring, we demonstrate one-step, catalyst-free spontaneous oxidation of various alcohols (ROH) to key reactive intermediates for the formation of ROO compounds on the surface of water microdroplets surrounded by alcohol vapor, carried out under ambient conditions. These organic peroxides (POs) can act as important secondary organic aerosols (SOA). We used hydrogen-deuterium exchange by spraying DO instead of HO to learn about the reaction mechanism, and the results demonstrate the crucial role of the water-air interface in microdroplet chemistry. We find that the formation of POs relies on electron transfer occurring at the microdroplet interface, which generates hydrogen atoms and hydroxyl radicals that lead to a cascade of radical reactions. This electron transfer is believed to be driven by two factors: (1) the emergence of a strong electrostatic potential on the microdroplet's surface; and (2) the partial solvation of ions at the interface. Mass spectra reveal that the formation of POs is dependent on the alcohol structure, with tertiary alcohols showing a higher tendency to form organic peroxides than secondary alcohols, which in turn are more reactive than primary alcohols.
通过实时质谱(MS)监测,我们展示了在环境条件下,各种醇类(ROH)在被醇蒸气包围的水微滴表面一步无催化剂自发氧化为形成ROO化合物的关键反应中间体的过程。这些有机过氧化物(POs)可作为重要 的二次有机气溶胶(SOA)。我们通过喷洒D₂O而非H₂O进行氢-氘交换来了解反应机理,结果证明了水-空气界面在微滴化学中的关键作用。我们发现POs的形成依赖于在微滴界面发生的电子转移,该电子转移产生氢原子和羟基自由基,进而引发一系列自由基反应。据信这种电子转移由两个因素驱动:(1)微滴表面出现强静电势;(2)界面处离子的部分溶剂化。质谱显示POs的形成取决于醇的结构,叔醇形成有机过氧化物的倾向高于仲醇,而仲醇又比伯醇更具反应性。