溶剂分解
化学
质子化
动力学同位素效应
化学物理
分子
质子
化学反应
反应中间体
计算化学
氘
催化作用
有机化学
物理
原子物理学
水解
核物理学
离子
作者
Xinmiao Xie,Jiajia Yang,Yong Yan,Jie Hao,Chen Yang,Yilin Guo,Haobin Wang,Bao‐Liang Zhong,Wei Huang,Ganglong Cui,Wei‐Hai Fang,Linghai Xie,Xuefeng Guo
标识
DOI:10.1002/anie.202425097
摘要
A central goal of chemical mechanism research is to provide a comprehensive interpretation of chemical reaction pathways to clarify the evolution patterns of reactions. In this work, we present an unprecedented comprehensive monitoring of the elementary reaction pathways of the SN1 solvolysis on an in-situ real-time single-molecule electrical detection platform. Through the precise control of an oriented external electric field, we capture two short-lived protonated intermediates at the single-molecule level and elucidate their roles in the solvolysis reaction. Both temperature- and isotope-dependent experiments, in combination with theoretical simulations, reveal crucial roles for the hydrogen-bonded acetic-acid-mediated triple-proton-transfer and the proton-tunneling effect in the interconversion of these two intermediates. This work highlights the precise manipulation of chemical reactions by electrostatic field and opens up a universal route to discover unknown intermediates or novel phenomena in the processes of material transformation and life activities.
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