Abstract
As a continuation of our work employing polyphenylene-dicarbonitrile molecules and in particular the terphenyl derivative 1 (TDCN), we have synthesized a novel ditopic terphenyl-4,4"-di(propiolonitrile) (2) linker for the self-assembly of organic monolayers and metal coordination at interfaces. The structure of the organic linker 2 was confirmed by single crystal X-ray diffraction analysis (XRD). On the densely packed Ag(111) surface, the terphenyl-4,4"-di(propiolonitrile) linkers self-assemble in a regular, molecular chevron arrangement exhibiting a Moiré pattern. After the exposure of the molecular monolayer to a beam of Gd atoms, the propiolonitrile groups get readily involved in metal-ligand coordination interactions. Distinct coordination motifs evolve with coordination numbers varying between three and six for the laterally-bound Gd centers. The linker molecules retain an overall flat adsorption geometry. However, only networks with restricted local order were obtained, in marked contrast to previously employed, simpler polyphenylene-dicarbonitrile 1 linkers.
Original language | English |
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Pages (from-to) | 327-335 |
Number of pages | 9 |
Journal | Beilstein Journal of Nanotechnology |
Volume | 6 |
Issue number | 1 |
DOIs | |
State | Published - 2015 |
Keywords
- Lanthanides
- Metal-organic networks
- Molecular self-assembly
- Organic monolayers
- Single crystal X-ray diffraction analysis
- UHV-STM
- di(propiolonitrile) linker