Stereo-isomerism controls surface reactivity: 1-chloropentane-pairs on Si(100)-2×1.
نویسندگان
چکیده
Chloropentane forms asymmetric ('A') and symmetric ('S') pairs on Si(100)-2×1, differing in the direction of curvature of one pentane tail. Surprisingly this renders the rate of thermal reaction of 'A' fifteen times greater than 'S' in chlorinating room-temperature silicon. Correspondingly, for electron-induced reaction the energy threshold for A is 1 eV less than for S.
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ورودعنوان ژورنال:
- Chemical communications
دوره 47 44 شماره
صفحات -
تاریخ انتشار 2011