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Investigation of the cross-reaction mechanism of C6H5F-HNO2 aqueous solution irradiated at 355 nm by transient absorbance spectrum technique

机译:瞬态吸收光谱技术研究355 nm下C6H5F-HNO2水溶液的交叉反应机理

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摘要

The transient absorption spectrum technique was employed to investigate the cross-reaction mechanism of C6H5F-HNO2 aqueous solution irradiated at 355 nm. The characteristic and the kinetic parameters of transient species were also detected. Hydroxyl radical derived from the photolysis of HNO2 was added to monofluorobenzene with a second-order rate constant of (5.83 +/- 0.17)x10(9) L.mol(-1).s(-1) to form an adduct, C6H5F center dot center dot center dot OH, which was able to react with HNO2 as the main reaction pathway with a rate constant of (8.3 +/- 0.1)x10(7) L.mol(-1)-s(-1). The C6F6 center dot center dot center dot OH adduct can also be decayed by elimination of H2O to yield monofluorophenyl radical C6H4F.. By GC-MS technique, the final products were identified to be monofluorophenol, nitro-monofluorobenzene, nitro-monofluorophenol and para-fluorobiphenyl.
机译:采用瞬态吸收光谱技术研究了在355 nm处辐照的C6H5F-HNO2水溶液的交叉反应机理。还检测了瞬态物质的特性和动力学参数。将来自HNO2的光解的羟基自由基以(5.83 +/- 0.17)x10(9)L.mol(-1).s(-1)的二级速率常数添加到一氟苯中以形成加合物C6H5F中心点中心点OH,能够与HNO2作为主要反应途径反应,速率常数为(8.3 +/- 0.1)x10(7)L.mol(-1)-s(-1)。还可以通过消除H2O来降解C6F6中心点中心点中心点OH加合物,从而生成一氟苯基基团C6H4F。通过GC-MS技术,最终产品被鉴定为一氟苯酚,硝基一氟苯,硝基一氟苯酚和对位氟联苯。

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