Abstract

We report the observation of electron-induced unidirectional planar molecular rotation of para-chlorostyrene on Si(100), studied by scanning tunneling microscopy (STM) at room temperature and by ab initio theory. This bifunctional molecule is shown to be favorable to the electron-induced rotation since the phenyl group acts as a pivot and the vinyl as a lever arm. In the initial configuration, both phenyl and vinyl are attached to silicon dimers along the same row of the substrate. The first electron from the STM tip is observed to induce a lateral shift of the vinyl to “state 1” in which the vinyl is bound asymmetrically to one side of a silicon dimer. The second electron is found to give rise to a ∼60° rotation to “state 2”, a configuration in which the vinyl has swung around the phenyl to an adjacent dimer row. The impulsive two-state (I2S) model was employed to explain the conversion of the initial state to state 1 and the conversion of state 1 to state 2. These two successive impulses were computed b...

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