AVS 56th International Symposium & Exhibition
    Surface Science Thursday Sessions
       Session SS2-ThA

Paper SS2-ThA8
Surface Supported Chain Formation of Magnetic Molecules

Thursday, November 12, 2009, 4:20 pm, Room N

Session: Supramolecular Interfaces by Design
Presenter: S. Kuck, University of Hamburg, Germany
Authors: S. Chang, University of Hamburg, Germany
K. Clark, Ohio University
A. Dilullo, Ohio University
S. Kuck, University of Hamburg, Germany
S.-W. Hla, Ohio University
G. Hoffmann, University of Hamburg, Germany
R. Wiesendanger, University of Hamburg, Germany
Correspondent: Click to Email

The last years showed a tremendous development into accessing and understanding the physics of metal-organic complexes in contact to a surface on a single molecule level. Molecular classes in the focus are often specialized but commercially available systems. Further progress towards device development requires molecular classes with a more flexible structure for functionalization.

In our contribution we introduce such a promising candidate, the so called Salens, and present first results on the local investigation by Scanning Tunneling Microscopy (STM). Salens are volatile metal-organic complexes with the metallic ion caged from three sides. Salens are chemically easily modified to tune the interaction with a substrate, with neighboring molecules, or to establish an intramolecular electronic and magnetic communication between two metallic centers through the organic periphery. Based on the paramagnetic Co-Salen, which shows no self-assembly on metallic substrates, we demonstrate that the exchange of a single atom in the molecular structure the interaction can be tuned from repulsive to attractive interaction[1]. Even surface-supported covalent bonding can be initiated to form larger entities. By means of STM, STS, and STM induced manipulation we will discuss the adsorption and the electronic properties of the parent Co-Salen and modified Salens on metallic and isolating surfaces.

Acknowledgements: This work was supported by the DFG within the GrK 611 and the SFB 668-A5, by the EU in the project “SPiDMe”, and the NSF-PIRE program.

[1] S. Kuck et al., “Steering two dimensional molecular growth via dipolar interaction“, accepted for publication in ChemPhysChem (2009).