Exchange reactions between alkanethiolates and alkaneselenols on Au{111}
J Nathan Hohman1, John C Thomas, Yuxi Zhao
1California NanoSystems Institute and Department of Chemistry and Biochemistry, University of California , Los Angeles, California 90095, United States.
Abstract:
When alkanethiolate self-assembled monolayers on Au{111} are exchanged with alkaneselenols from solution, replacement of thiolates by selenols is rapid and complete, and is well described by perimeter-dependent island growth kinetics. The monolayer structures change as selenolate coverage increases, from being epitaxial and consistent with the initial thiolate structure to being characteristic of selenolate monolayer structures. At room temperature and at positive sample bias in scanning tunneling microscopy, the selenolate-gold attachment is labile, and molecules exchange positions with neighboring thiolates. The scanning tunneling microscope probe can be used to induce these place-exchange reactions.
Related Concept Videos
Preparation and Reactions of Thiols
Introduction to Electrophilic Addition Reactions of Alkenes
Addition and elimination...
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Preparation and Reactions of Sulfides
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...


