Fernandes Ravi X, Giri Binod Raj, Hippler Horst, Kachiani Chatuna, Striebel Frank
Institut für Physikalische Chemie, Lehrstuhl fur Molekulare Physikalische Chemie, Fritz Haber Weg 4, 76131 Karlsruhe, Germany.
J Phys Chem A. 2005 Feb 17;109(6):1063-70. doi: 10.1021/jp047482b.
We present the first direct study on the thermal unimolecular decomposition of allyl radicals. Experiments have been performed behind shock waves, and the experimental conditions covered temperatures ranging from 1125 K up to 1570 K and pressures between 0.25 and 4.5 bar. Allyl radicals have been generated by thermal decomposition of allyl iodide, and H-atom resonance absorption spectroscopy has been used to monitor the reaction progress. A marked pressure dependence of the rate constant has been observed which is in agreement with the results from a master equation analysis. However, our experimental results as well as our Rice-Ramsperger-Kassel-Marcus calculations seem to contradict the results of Deyerl et al. (J. Chem. Phys. 1999, 110, 1450) who investigated the unimolecular decomposition of allyl radicals upon photoexcitation and tried to deduce specific rate constants for the unimolecular dissociation in the electronic ground state. At pressures around 1 bar we extracted the following rate equation: k(T) = 5.3 x 10(79)(T/K)(-19.29) exp[(-398.9 kJ/mol)/RT] s(-1). The uncertainty of the rate constant calculated from this equation is estimated to be 30%.
我们展示了关于烯丙基自由基热单分子分解的首次直接研究。实验是在激波后进行的,实验条件涵盖了从1125 K到1570 K的温度范围以及0.25至4.5巴的压力范围。烯丙基自由基通过烯丙基碘的热分解产生,并且氢原子共振吸收光谱法已被用于监测反应进程。观察到速率常数对压力有显著依赖性,这与主方程分析的结果一致。然而,我们的实验结果以及我们的赖斯 - 拉姆施泰格 - 卡斯尔 - 马库斯计算结果似乎与戴尔等人(《化学物理杂志》,1999年,第110卷,第1450页)的结果相矛盾,他们研究了光激发下烯丙基自由基的单分子分解,并试图推导电子基态下单分子解离的特定速率常数。在约1巴的压力下,我们得出以下速率方程:k(T) = 5.3 x 10(79)(T/K)(-19.29) exp[(-398.9 kJ/mol)/RT] s(-1)。由该方程计算出的速率常数的不确定度估计为30%。