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- W2467501900 abstract "One strategy for controlling selectivity in surface-catalyzed reactions is to precisely control the types of surface sites available for reaction. Here, we show that such control can be achieved on Pd/Al2O3 catalysts modified by alkanethiol self-assembled monolayers (SAMs) by changing the length of the modifier’s alkyl tail. Density functional theory (DFT) calculations show that thiolates with short alkyl chains preferentially bind to undercoordinated Pd step sites but that adsorption on (111) terrace sites is more favorable at higher chain lengths due to greater stabilization by van der Waals interactions. Linear alkanethiol SAMs with chain lengths ranging from six to 18 carbon atoms were deposited on Pd/Al2O3 catalysts to probe this predicted effect experimentally. Infrared spectroscopy measurements conducted after CO adsorption confirmed that increases in alkyl chain length resulted in increasing specificity in poisoning of terrace sites. The catalysts were also evaluated for furfuryl alcohol hydrogena..." @default.
- W2467501900 created "2016-07-22" @default.
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- W2467501900 date "2016-07-06" @default.
- W2467501900 modified "2023-09-29" @default.
- W2467501900 title "Catalyst Site Selection via Control over Noncovalent Interactions in Self-Assembled Monolayers" @default.
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- W2467501900 doi "https://doi.org/10.1021/acscatal.6b01074" @default.
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