Schmatz Stefan
Institut für Physikalische Chemie, Georg-August-Universität Göttingen Tammannstrasse 6, 37077 Göttingen, Germany.
Chemphyschem. 2004 May 17;5(5):600-17. doi: 10.1002/cphc.200301043.
Understanding the state-resolved dynamics of elementary chemical reactions involving polyatomic molecules, such as the well-known reaction mechanism of nucleophilic bimolecular substitution (SN2), is one of the principal goals in chemistry. In this Review, the progress in the quantum mechanical treatment of SN2 reactions in the gas phase is reviewed. The potential energy profile of this class of reactions is characterized by two relatively deep wells, which correspond to pre- and post-reaction chargedipole complexes. As a consequence, the complex-forming reaction is dominated by Feshbach resonances. Calculations in the energetic continuum constitute a major challenge because the high density of resonance states imposes considerable requirements on the convergence and the energetic resolution of the scattering data. However, the effort is rewarding because new insights into the details of multimode quantum dynamics of elementary chemical reactions can be obtained.
理解涉及多原子分子的基本化学反应的态分辨动力学,例如著名的亲核双分子取代反应(SN2)机理,是化学领域的主要目标之一。在本综述中,我们回顾了气相中SN2反应量子力学处理方面的进展。这类反应的势能面由两个相对较深的势阱表征,它们分别对应反应前和反应后的电荷 - 偶极复合物。因此,复合物形成反应由费什巴赫共振主导。能量连续区的计算是一项重大挑战,因为共振态的高密度对散射数据的收敛性和能量分辨率提出了相当高的要求。然而,这种努力是值得的,因为可以获得对基本化学反应多模量子动力学细节的新见解。