Department of Chemistry and Institute for Optical Sciences, University of Toronto, 80 St George Street, Toronto, Ontario, M5S 3H6, Canada.
Nat Chem. 2011 May;3(5):400-8. doi: 10.1038/nchem.1029. Epub 2011 Apr 17.
The recoil of adsorbates away (desorption) and towards (reaction) surfaces is well known. Here, we describe the long-range recoil of adsorbates in the plane of a surface, and accordingly the novel phenomenon of reactions occurring at a substantial distance from the originating event. Three thermal and three electron-induced surface reactions are shown by scanning tunnelling microscopy to propel their physisorbed ethylenic products across the rough surface of Si(100) over a distance of up to 200 Å before an attachment reaction. The recoil energy in the ethylenic products comes from thermal exoergicity or from electronic excitation of chemisorbed alkenes. We propose that the mechanism of migration is a rolling motion, because the recoiling molecule overcomes raised surface obstacles. Electronic excitation of propene causes directional recoil and often end-to-end inversion, suggesting cartwheeling. Ab initio calculations of the halogenation and electron-induced reactions support a model in which asymmetric forces between the molecule and the surface induce rotation and therefore migration.
吸附物远离(解吸)和朝向(反应)表面的反冲是众所周知的。在这里,我们描述了吸附物在表面平面上的长程反冲,以及由此产生的在远离起始事件的位置发生反应的新现象。通过扫描隧道显微镜,我们展示了三个热和三个电子诱导的表面反应,它们将其物理吸附的乙烯产物在附着反应之前,在粗糙的 Si(100)表面上跨越长达 200 Å 的距离推进。在乙烯产物中的反冲能量来自热放能或化学吸附烯烃的电子激发。我们提出迁移的机制是滚动运动,因为反冲分子克服了凸起的表面障碍物。丙烯的电子激发导致定向反冲,并且经常发生端到端反转,表明是侧翻运动。卤化和电子诱导反应的从头算计算支持了这样一种模型,即分子和表面之间的不对称力诱导旋转,从而导致迁移。