Regensburg 2010 – scientific programme
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O: Fachverband Oberflächenphysik
O 14: Metal substrates: Adsorption of organic / bio molecules II
O 14.2: Talk
Monday, March 22, 2010, 15:15–15:30, H36
On the Scalability of Supramolecular Networks - High Packing Density vs. Optimized Hydrogen Bonds in Tricarboxylic Acid Monolayers — •Jürgen F. Dienstmaier1, Kingsuk Mahata2, Wolfgang M. Heckl3, Michael Schmittel2, and Markus Lackinger1 — 1LMU München, Sektion Kristallographie — 2Universität Siegen, Organische Chemie I — 3Deutsches Museum
We present a Scanning Tunneling Microscopy (STM) based study of 1,3,5-tris[4*-carboxy(1,1*-biphenyl-4-yl)]benzene (TCBPB) monolayers at the liquid-solid interface. In analogy to smaller aromatic threefold symmetric tricarboxylic acids, this compound was aimed to yield two-dimensional nanoporous networks with large cavities. Depending on the solute concentration, three crystallographically distinct phases with pores of different size and shape were observed on graphite (001) with heptanoic acid as solvent. All three phases have the same dimer motif as basic building block in common. Yet, as opposed to other carboxylic acid assemblies, these dimers are not interconnected by O-H...O hydrogen bonds as anticipated, but by two energetically inferior C-H...O hydrogen bonds. Instead of the common head-to-head arrangement, this bonding pattern results in displaced dimers, which exhibit lower symmetry, allow for higher packing density, and give rise to chirality of all polymorphs. In accordance with studies of comparable systems, a positive correlation between solute concentration and average surface packing density is identified, which is rationalized by thermodynamic arguments.