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Two-Leg Molecular Ladders Formed by Hierarchical Self-Assembly of an Organic Radical

Nuria Crivillers, Shuhei Furukawa,, Andrea Minoia, An Ver Heyen,Marta Mas-Torrent, Christian Sporer, Mathieu Linares, Alexander Volodin, Chris Van Haesendonck, Mark Van der Auweraer, Roberto Lazzaroni, Steven De Feyter, Jaume Veciana, and Concepcio Rovira, Washington (2009)

The supramolecular organization of a new polychlorotriphenyl (PTM) radical bearing three long alkyl chains has been studied by scanning tunneling microscopy (STM) at the liquid-solid interface. This radical hierarchically self-assembles on graphite forming head-to-head dimers that organize in rows following an interesting spin-containing two-leg molecular ladder topology, in which the alkyl chains determine the space between the radical rows and act as diamagnetic barriers. In addition, these double-rows also selfassemble three-dimensionally, leading to a multilayer organization which is still influenced by the HOPG substrate symmetry. The observed nanostructures are sustained by different intermolecular interactions such as Cl · · · Cl, Cl · · · Ph, π-π, van der Waals, and CH· · ·π interactions. Theoretical calculations were used to model the observed assemblies, and the results were in complete agreement with the experimental data. Remarkably, atomic force microscopy (AFM) studies confirmed that this tendency to form double rows composed by the PTM magnetic heads surrounded by the alkyl chains is maintained after the complete evaporation of the solvent. The electrochemical and magnetic properties of these PTM nanostructures were also demonstrated.

Partners : CSIC UMons

Place of Publication : Washington

Date of Publication : 2009/04/10

Additional Data : J. AM. CHEM. SOC. 2009, 131, 6246–6252

Link to the online version of the article.