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Statistical theory for the kinetics and dynamics of roaming reactions

机译:漫游反应动力学的统计理论

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摘要

We present a statistical theory for the effect of roaming pathways on product branching fractions in both unimolecular and bimolecular reactions. The analysis employs a separation into three distinct steps: (i) the formation of weakly interacting fragments in the longrange/van der Waals region of the potential via either partial decomposition (for unimolecular reactants) or partial association (for bimolecular reactants), (ii) the roaming step, which involves the reorientation of the fragments from one region of the long-range potential to another, and (iii) the abstraction, addition, and/or decomposition from the long-range region to yield final products. The branching between the roaming induced channel(s) and other channels is obtained from a steady-state kinetic analysis for the two (or more) intermediates in the long-range region of the potential. This statistical theory for the roaming-induced product branching is illustrated through explicit comparisons with reduced dimension trajectory simulations for the decompositions of H_2CO, CH_3CHO, CH_3OOH, and CH_3CCH. These calculations employ high-accuracy analytic potentials obtained from fits to wide-ranging CASPT2 ab initio electronic structure calculations. The transition-state fluxes for the statistical theory calculations are obtained from generalizations of the variable reaction coordinate transition state theory approach. In each instance, at low energy the statistical analysis accurately reproduces the branching obtained from the trajectory simulations. At higher energies, e.g., above 1 kcal/mol, increasingly large discrepancies arise, apparently due to a dynamical biasing toward continued decomposition of the incipient molecular fragments (for unimolecular reactions). Overall, the statistical theory based kinetic analysis is found to provide a useful framework for interpreting the factors that determine the significance of roaming pathways in varying chemical environments. (Figure presented)
机译:我们提出了一种统计理论,用于在单分子和双分子反应中,漫游路径对产物分支分数的影响。该分析将分离分为三个不同的步骤:(i)通过部分分解(对于单分子反应物)或部分缔合(对于双分子反应物)在电位的长程/范德华斯区域形成弱相互作用的片段,(ii )漫游步骤,其中涉及将片段从远程电位的一个区域重新定向到另一个区域,以及(iii)从远程区域进行抽象,添加和/或分解以生成最终产品。漫游诱导通道与其他通道之间的分支是通过对电位的长距离区域中的两个(或多个)中间体的稳态动力学分析获得的。通过与H_2CO,CH_3CHO,CH_3OOH和CH_3CCH分解的降维轨迹模拟进行显式比较,说明了这种漫游诱导产品分支的统计理论。这些计算采用从拟合到广泛的CASPT2从头算电子结构计算中获得的高精度分析潜能。统计理论计算的过渡态通量是从可变反应坐标过渡态理论方法的概括中获得的。在每种情况下,在低能量情况下,统计分析都会准确地再现从轨迹模拟获得的分支。在较高的能量下,例如高于1kcal / mol,出现越来越大的差异,这显然是由于对初始分子片段的持续分解的动态偏见(对于单分子反应而言)。总体而言,发现基于统计理论的动力学分析为解释决定在不同化学环境中漫游路径的重要性的因素提供了有用的框架。 (图示)

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