Department of Chemistry, University of California, Irvine, California 92697, United States.
J Phys Chem A. 2012 Jun 21;116(24):6068-77. doi: 10.1021/jp211304v. Epub 2012 Jan 25.
Methyl peroxide (CH(3)OOH) is commonly found in atmospheric waters and ices in significant concentrations. It is the simplest organic peroxide and an important precursor to hydroxyl radical. Many studies have examined the photochemical behavior of gaseous CH(3)OOH; however, the photochemistry of liquid and frozen water solutions is poorly understood. We present a series of experiments and theoretical calculations designed to elucidate the photochemical behavior of CH(3)OOH dissolved in liquid water and ice over a range of temperatures. The molar extinction coefficients of aqueous CH(3)OOH are different from the gas phase, and they do not change upon freezing. Between -12 and 43 °C, the quantum yield of CH(3)OOH photolysis is described by the following equation: Φ(T) = exp((-2175 ± 448)1/T) + 7.66 ± 1.56). We use on-the-fly ab initio molecular dynamics simulations to model structures and absorption spectra of a bare CH(3)OOH molecule and a CH(3)OOH molecule immersed inside 20 water molecules at 50, 200, and 220 K. The simulations predict large sensitivity in the absorption spectrum of CH(3)OOH to temperature, with the spectrum narrowing and shifting to the blue under cryogenic conditions because of constrained dihedral motion around the O-O bond. The shift in the absorption spectrum is not observed in the experiment when the CH(3)OOH solution is frozen suggesting that CH(3)OOH remains in a liquid layer between the ice grains. Using the extinction coefficients and photolysis quantum yields obtained in this work, we show that under conditions with low temperatures, in the presence of clouds with a high liquid-water content and large solar zenith angles, the loss of CH(3)OOH by aqueous photolysis is responsible for up to 20% of the total loss of CH(3)OOH due to photolysis. Gas phase photolysis of CH(3)OOH dominates under all other conditions.
过氧甲烷(CH(3)OOH)在大气水和冰中以高浓度普遍存在。它是最简单的有机过氧化物,也是羟基自由基的重要前体。许多研究都考察了气态 CH(3)OOH 的光化学反应;然而,液态和冻结水溶剂的光化学性质还了解甚少。我们进行了一系列实验和理论计算,旨在阐明 CH(3)OOH 在液态水和冰中的光化学反应行为,实验温度范围较宽。水相 CH(3)OOH 的摩尔消光系数与气相不同,且在冻结时不会改变。在-12 到 43°C 之间,CH(3)OOH 光解的量子产率由以下方程描述:Φ(T) = exp((-2175 ± 448)1/T) + 7.66 ± 1.56)。我们使用即时从头算分子动力学模拟来模拟裸露的 CH(3)OOH 分子和沉浸在 20 个水分子中的 CH(3)OOH 分子的结构和吸收光谱,温度分别为 50、200 和 220 K。模拟预测 CH(3)OOH 的吸收光谱对温度非常敏感,低温下由于 O-O 键的二面角运动受限,光谱变窄并蓝移。当 CH(3)OOH 溶液冻结时,实验中并未观察到吸收光谱的移动,这表明 CH(3)OOH 仍留在冰粒之间的液层中。利用本工作中获得的消光系数和光解量子产率,我们表明在低温条件下,当云液水含量高且太阳天顶角大时,水相光解导致 CH(3)OOH 的损失可达 CH(3)OOH 总光解损失的 20%。在所有其他条件下,CH(3)OOH 的气相光解都占主导地位。