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It has been shown that well-defined, ordered organic layers can be formed on the silicon (100) surface. This is achieved through the interaction of unsaturated C=C bonds with the oriented dimers of the reconstructed Si(100)-(2×1) surface. In this article, we present an investigation of the structure and chemical bonding of organic films prepared using different organic precursors. Data were obtained using scanning tunneling microscopy, Fourier-transform infrared spectroscopy, and x-ray photoelectron spectroscopy. The molecules investigated are cyclopentene, 3-pyrroline, and norbornadiene, representing prototypical cyclic, heterocyclic, and bicyclic unsaturated organic molecules, respectively. Each molecule has at least one unsaturated C=C bond.
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Hovis et al. (1997) studied this question.
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