Chemical selectivity of self-assembled monolayers of calix[4]resorcinarene

Abstract

Selective molecular interactions at an interface formed by self-assembly of a macrocyclic synthetic host, calix[4]resorcinarene with four thiol groups (R4SH), are investigated. The recognition of guest adsorbates from aqueous solutions is monitored using surface plasmon resonance (SPR) and the orientation of the guest-molecule is probed using polarization modulation infrared absorption spectroscopy (PM-IRRAS). The experiments reported here demonstrate that the chemical selectivity of self-assembled monolayers (SAMs) of host molecules such as calix[4]resorcinarenes extends to isomers of several different guest molecules. By using structural isomers of guest molecules such as bipyridine and nitrophenol that are multidentate hydrogen bond acceptors, it is shown that geometric match between guest and host molecules is an integral aspect of the recognition phenomena. Results from SPR and PM-IRRAS experiments reported here highlight the interplay between steric size and forces such as hydrogen bonding and hydrophobic interactions. Competitive and sequential adsorption of guest molecules such as α-hydroxy-γ-butyrolactone and 4,4′-bipyridine shows that these guests compete for the same binding sites on the surface and that the interplay between steric size and molecular forces underlies the preferential selectivity of one guest molecule over another.