Theoretical Investigation of 6-Mercaptopurine Isomers’ Adsorption on the Au(001) Surface: Revealing the Fate of Different Isomers

摘要

Density functional theory (DFT) calculations were performed for the adsorption of different isomers of 6-mercaptopurine on the Au(001) surface. All of the configurations of four thione and two thiol isomers were considered. The results show that the thione isomers adsorbed more strongly on the Au(001) surface compared with the thiol ones. In all of the configurations, the calculated binding energy of ma-8 is the largest, in which the S atom of 6-mercaptopurine binds strongly with one Au atom on the monodentate sites and 6-mercaptopurine retains a flat geometry, predominantly with an approximately 30° orientation between the C–S bond and the Au–Au bond of the catalyst. Additionally, the 6-mercaptopurines in ma-2, mb-5, and mc-3 also bind more strongly onto the surface, which show relatively higher stability on the surfaces, indicating a high preference for adsorption. Charge density differences and TDOS analyses for the four configurations also show that the electronic charges are accumulated between Au and S atoms in the Au–S bonds, indicating occurrence of adsorption and chemical-bond formation.