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Investigation of Oxidation Reaction Products of 2-Phenylethanol Using Synchrotron Photoionization

机译:二苯基乙醇使用同步辐射光相的氧化反应产物研究

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A photolytically Cl-initiated oxidation reaction of 2-phenylethanol (2PE) was carried out at the Advanced Light Source (ALS) in the Lawrence Berkeley National Laboratory. Using the multiplex photoionization mass spectrometer, coupled with the tunable vacuum ultraviolet radiation of the ALS, data were collected at low pressure (4-6 Torr) and temperature (298-550 K) regimes. Data analysis was performed via characterization of the reaction species photoionization spectra and kinetic traces. Products and reaction pathways are also computed using the CBS-QB3 composite method. The present results suggest primary products m/z = 30 (formaldehyde), 106 (benzaldehyde), and 120 (phenylacetaldehyde) at 298 K, and m/z = 120 (phenylacetaldehyde) at 550 K. Branching fractions at room temperature are 27 +/- 6.5% for formaldehyde, 24 +/- 4.5% for benzaldehyde, and 25 +/- 5.8% for phenylacetaldehyde and 60 +/- 14% for phenylacetaldehyde 550 K.
机译:在劳伦斯伯克利国家实验室的先进光源(ALS)下进行2-苯基乙醇(2PE)的光解Cl-引发的氧化反应。 使用多路复用的光电激素质谱仪,与ALS的可调真空紫外线辐射相结合,在低压(4-6托)和温度(298-550 k)制度下收集数据。 通过表征反应物质的光相谱和动力学痕迹进行数据分析。 还使用CBS-QB3复合方法计算产品和反应途径。 本结果提示初级产物M / Z = 30(甲醛),106(苯甲醛)和120(苯基乙醛)在298K,M / Z = 120(苯乙酰甲醛),在550K时,室温下的支化级分是27 + / - 甲醛的6.5%,苯甲醛的24 +/- 4.5%,苯基乙醛的25 +/- 5.8%,苯甲醛550k的60 +/-14%。

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