Center for Advanced Reaction Dynamics, Institute for Basic Science (IBS), Daejeon, Republic of Korea.
Department of Chemistry and KI for the BioCentury, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, Republic of Korea.
Nature. 2024 Jan;625(7996):710-714. doi: 10.1038/s41586-023-06909-5. Epub 2024 Jan 10.
Molecular ions are ubiquitous and play pivotal roles in many reactions, particularly in the context of atmospheric and interstellar chemistry. However, their structures and conformational transitions, particularly in the gas phase, are less explored than those of neutral molecules owing to experimental difficulties. A case in point is the halonium ions, whose highly reactive nature and ring strain make them short-lived intermediates that are readily attacked even by weak nucleophiles and thus challenging to isolate or capture before they undergo further reaction. Here we show that mega-electronvolt ultrafast electron diffraction (MeV-UED), used in conjunction with resonance-enhanced multiphoton ionization, can monitor the formation of 1,3-dibromopropane (DBP) cations and their subsequent structural dynamics forming a halonium ion. We find that the DBP cation remains for a substantial duration of 3.6 ps in aptly named 'dark states' that are structurally indistinguishable from the DBP electronic ground state. The structural data, supported by surface-hopping simulations and ab initio calculations, reveal that the cation subsequently decays to iso-DBP, an unusual intermediate with a four-membered ring containing a loosely bound bromine atom, and eventually loses the bromine atom and forms a bromonium ion with a three-membered-ring structure. We anticipate that the approach used here can also be applied to examine the structural dynamics of other molecular ions and thereby deepen our understanding of ion chemistry.
分子离子无处不在,在许多反应中起着关键作用,特别是在大气和星际化学的背景下。然而,由于实验困难,它们的结构和构象转变,特别是在气相中,比中性分子的研究要少。卤鎓离子就是一个很好的例子,其高反应性和环张力使其成为短寿命中间体,即使是弱亲核试剂也很容易攻击它们,因此在它们进一步反应之前,很难将它们分离或捕获。在这里,我们展示了兆电子伏特超快电子衍射(MeV-UED)与共振增强多光子电离相结合,可以监测 1,3-二溴丙烷(DBP)阳离子的形成及其随后形成卤鎓离子的结构动力学。我们发现,DBP 阳离子在恰如其名的“暗态”中持续存在相当长的 3.6 ps,其结构与 DBP 的电子基态无法区分。结构数据得到表面跳跃模拟和从头算计算的支持,揭示了阳离子随后衰变到 iso-DBP,这是一种具有四元环的不寻常中间体,其中含有一个松散结合的溴原子,最终失去溴原子并形成具有三元环结构的溴鎓离子。我们预计,这里使用的方法也可以应用于检查其他分子离子的结构动力学,从而加深我们对离子化学的理解。