Lai Yi-Fang, Leung Lydie, Timm Matthew J, Walker Gilbert C, Polanyi John C
Lash Miller Chemical Laboratories, Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario, M5S 3H6, Canada.
Department of Physical Chemistry, University of Graz, Heinrichstrasse 28, 8010 Graz, Austria.
Faraday Discuss. 2024 Aug 27;251(0):448-456. doi: 10.1039/d3fd00167a.
Electron-induced dissociation of a fluorocarbon adsorbate CF (ad) at 4.6 K is shown by Scanning Tunnelling Microscopy (STM) to form directed energetic F-atom 'projectiles' on Cu(110). The outcome of a collision between these directed projectiles and stationary co-adsorbed allyl 'target' molecules was found through STM to give rotational excitation of the target allyl, clockwise or anti-clockwise, depending on the chosen collision geometry. Molecular dynamics computation linked the collisional excitation of the allyl target to an 'abortive chemical reaction', in which the approach of the F-projectile stretched an H-C bond lifting the allyl above the surface, facilitating isomerization from 'Across' to 'Along' a Cu row.
扫描隧道显微镜(STM)显示,在4.6K温度下,电子诱导的氟碳吸附物CF(ad)在铜(110)表面解离,形成定向高能氟原子“射弹”。通过STM发现,这些定向射弹与静止的共吸附烯丙基“靶”分子之间的碰撞结果会使靶烯丙基产生顺时针或逆时针的旋转激发,这取决于所选择的碰撞几何结构。分子动力学计算将烯丙基靶的碰撞激发与“未遂化学反应”联系起来,在该反应中,氟射弹的接近拉伸了一个H-C键,将烯丙基提升到表面上方,促进了从“跨”铜排到“沿”铜排的异构化。