TWO-DIMENSIONAL SELF-ASSEMBLY OF SUPRAMOLECULAR STRUCTURES

Author:

BÖHRINGER MATTHIAS1,SCHNEIDER WOLF-DIETER1,BERNDT RICHARD2

Affiliation:

1. Institut de Physique de la Matière Condensèe, Universitè de Lausanne, CH-1015 Lausanne, Switzerland

2. Institut für Experimentelle und Angewandte Physik, Christian-Albrechts-Universität zu Kiel, D-24098 Kiel, Germany

Abstract

We briefly review recent low temperature scanning tunneling microscopy (STM) investigations performed in our laboratory1–5 on the self-assembly of the dipolar organic molecule 1-nitronaphthalene (NN) adsorbed on the reconstructed Au(111) surface. NN becomes chiral upon planar adsorption on the gold surface. We observe several coverage-driven structural transformations which are associated with simultaneous changes in the enantiomeric composition of the self-assembled molecular structures. At low coverages almost exclusively decamers with an 8:2 ratio of the enantiomers are formed. In a medium coverage range enantiopure one-dimensional molecular double chains prevail on the surface. Subsequently, molecules with opposite handedness are admixed until at monolayer coverage racemic one- and two-dimensional structures coexist. Modeling shows that hydrogen bonding causes the observed self-assembly. A subtle interplay between the electrostatic interactions among the molecules and their interaction with the reconstructed metal surface is the origin of the observed coverage-driven chiral phase transition in two dimensions.

Publisher

World Scientific Pub Co Pte Lt

Subject

Materials Chemistry,Surfaces, Coatings and Films,Surfaces and Interfaces,Condensed Matter Physics

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