Chiral ordering and conformational dynamics for a class of oligo-phenylene-ethynylenes on Au(111)

Busse C, Weigelt S, Petersen L, Lægsgaard E, Besenbacher F, Linderoth T, Thomsen A, Nielsen M, Gothelf K

Research article (journal)

Abstract

Adsorption structures formed from a class of planar organic molecules on the Au(111) surface under ultrahigh vacuum conditions have been characterized using scanning tunneling microscopy (STM). The molecules have different geometries, linear, bent, or three-spoke, but all consist of a conjugated aromatic backbone formed from three or four benzene rings connected by ethynylene spokes and functionalized at all ends with an aldehyde, a hydroxyl, and a bulky tert-butyl group. Upon adsorption, the molecules adopt different surface conformations some of which are chiral. For the majority of the observed adsorption structures, chirality is expressed also in the molecular tiling pattern, and the two levels of chirality display a high degree of correlation. The formation and chiral ordering of the self-assembled structures are shown to result from dynamic interchanges between a diffusing lattice gas and the nucleated islands, as well as from a chiral switching process in which molecules alter their conformation by an intramolecular rotation around a molecular spoke, enabling them to accommodate to the tiling pattern of the surrounding molecular structures. The kinetics of the conformational switching is investigated from time-resolved, variable temperature STM, showing the process to involve an activation energy of ∼0.3 eV depending on the local molecular environment. The molecule-molecule interactions appear primarily to be of van der Waals character, despite the investigated compounds having functional moieties capable of forming intermolecular hydrogen bonds. © 2007 American Chemical Society.

Details zur Publikation

Release year: 2007
Language in which the publication is written: English
Link to the full text: http://www.scopus.com/inward/record.url?eid=2-s2.0-34250335292&partnerID=40&md5=e3d5c90f47d862f869c5f6f14cd2f3dd