Structure and Reactivity of Self Assembled Monolayers

STEVEN L. BERNASEK
Department of Chemistry
Princeton University


Long chain hydrocarbons self-assemble on various substrates to make highly ordered, robust organic thin films.  The most studied prototype self-assembled monolayer (SAM) system is the class of SAMs consisting of long chain n-alkyl thiols adsorbed upright on gold surfaces.  In contrast, long chain hydrocarbons and substituted hydrocarbons self-assemble parallel to the graphite surface, forming well ordered overlayers exhibiting chirality and nano-scaled patterns.  We will discuss our recent studies of both of these types of monolayer systems.  Low energy ion scattering has been used to probe the structure and reactivity of a series of n-alkyl thiol monolayers.  An odd-even structural effect has been observed for the reaction of the monolayers with the incident probe ions, pyrazine and benzene.  Substituted long chain alkane molecules adsorbed on pyrolytic graphite have also been examined, in this instance using atomic resolution scanning tunneling microscopy.  Examples of chiral structures and monolayer structures that probe both molecule-molecule and molecule-substrate bonding interactions will be discussed.  Several new types of chiral monolayer formation will be described.  Efforts to understand the molecule-molecule and molecule-substrate interactions that govern structure formation will be discussed.

Date:   Thursday, April 8, 2004

12:00 Noon, Room 260, Wright-Rieman Chemistry Laboratory
Lunch at 11:45 A.M.