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soln). In the formation of mixed monolayers of alkanethiolates from a solution containing alkanethiols, the chemisorption of alkanethiols onto noble metal surfaces results in the displacement of the terminal H atom so that the resulting adsorbate molecule (alkanethiolate) is quite different from its solution counterpart (alkanethiol). However, because most organic thiols of practical interest usually consist of six or more backbone atoms, the difference between these two values is negligible
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soln). In the formation of mixed monolayers of alkanethiolates from a solution containing alkanethiols, the chemisorption of alkanethiols onto noble metal surfaces results in the displacement of the terminal H atom so that the resulting adsorbate molecule (alkanethiolate) is quite different from its solution counterpart (alkanethiol). However, because most organic thiols of practical interest usually consist of six or more backbone atoms, the difference between these two values is negligible
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