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首页> 外文期刊>The Journal of Chemical Physics >Microcanonical rates for the unimolecular dissociation of the ethyl radical
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Microcanonical rates for the unimolecular dissociation of the ethyl radical

机译:乙基单分子解离的微规范速率

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摘要

We report results on the photodissociation dynamics of the ethyl radical, C_2H_5. A beam of internally cold radicals is generated by supersonic jet flash pyrolysis of ethyl iodide or n-propylnitrite, respectively. Upon excitation into the A~2A_13s Rydberg state ethyl dissociates, presumably on the ground-state surface, into ethylene and a hydrogen atom that is detected by time-resolved photoionization. By varying the excitation energy between 264 and 245 nm, microcanonical rates are obtained as a function of excitation energy. The reaction rates are on the order of 10~7s~(-1), several orders of magnitude slower than expected from simple Rice-Ramsperger-kassel-Marcus calculations.
机译:我们报告了乙基C_2H_5的光解离动力学的结果。分别通过碘乙烷或正丙基亚硝酸盐的超音速喷射热解产生内部冷自由基束。激发进入A〜2A_13s的Rydberg态后,乙基可能在基态表面上离解为乙烯和一个氢原子,该氢原子可通过时间分辨光电离检测到。通过在264 nm和245 nm之间改变激发能,可以得到微规范速率,它是激发能的函数。反应速率约为10〜7s〜(-1),比Rice-Ramsperger-kassel-Marcus的简单计算所预期的要慢几个数量级。

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