Department of Chemistry, University of California, Berkeley, California 94720, USA.
School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China.
Nat Chem. 2017 Oct;9(10):950-955. doi: 10.1038/nchem.2804. Epub 2017 Jul 10.
The transition state governs how chemical bonds form and cleave during a chemical reaction and its direct characterization is a long-standing challenge in physical chemistry. Transition state spectroscopy experiments based on negative-ion photodetachment provide a direct probe of the vibrational structure and metastable resonances that are characteristic of the reactive surface. Dynamical resonances are extremely sensitive to the topography of the reactive surface and provide an exceptional point of comparison with theory. Here we study the seven-atom F + CHOH → HF + CHO reaction using slow photoelectron velocity-map imaging spectroscopy of cryocooled CHOHF anions. These measurements reveal spectral features associated with a manifold of vibrational Feshbach resonances and bound states supported by the post-transition state potential well. Quantum dynamical calculations yield excellent agreement with the experimental results, allow the assignment of spectral structure and demonstrate that the key dynamics of complex bimolecular reactions can be captured with a relatively simple theoretical framework.
过渡态决定了化学键在化学反应中形成和断裂的方式,其直接特征化是物理化学中长期存在的挑战。基于负离子光电子俘获的过渡态光谱实验为反应表面的振动结构和亚稳态共振提供了直接探针。动力学共振对反应表面的形貌非常敏感,并提供了与理论进行出色比较的基准。在这里,我们使用低温 CHOHF 阴离子的慢光电电子速度映射成像光谱学研究了七原子 F + CHOH → HF + CHO 反应。这些测量揭示了与后过渡态势阱中支持的多个振动 Feshbach 共振和束缚态相关的光谱特征。量子动力学计算与实验结果非常吻合,允许对光谱结构进行分配,并证明可以用相对简单的理论框架捕捉复杂双分子反应的关键动力学。