Theoretical analysis of the coverage dependence of enantioselective chemisorption on a chirally templated surface

The effect of the formation of ensembles of chiral templates on the enantioselectivity of model heterogeneous catalysts is studied theoretically in the framework of a cooperative sequential adsorption model. Analytical solutions are presented for random adsorption onto a chirally templated surface which indicate that the surface exhibits a maximum enantioselectivity of ;2.5, in agreement with results of enantioselective chemisorption experiments carried out in ultrahigh vacuum. It is suggested that the high enantioselectivity (*90%) encountered in commercial catalysts could be due to correlated adsorption of the template molecules, and that these effects can be modeled using Monte Carlo calculations. © 2003 American Institute of Physics. @DOI: 10.1063/1.1556077#