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Tripod-shaped molecules: Synthesis and immobilization on Au(1 1 1) substrates

•Synthesis of novel tripod-shaped p-phenylenes with thioacetate anchoring groups.•Optimization of conditions for tridentate self-assembly of the tripods onto Au(1 1 1)•XPS, NEXAFS spectroscopy and AFM characterization of the tripod monolayers.•Functionalization of the assembled tripods with a theoph...

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Bibliographic Details
Published in:Applied surface science 2019-03, Vol.470, p.259-268
Main Authors: Sánchez-Molina, María, Díaz, Amelia, Sauter, Eric, Zharnikov, Michael, López-Romero, J. Manuel
Format: Article
Language:English
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Summary:•Synthesis of novel tripod-shaped p-phenylenes with thioacetate anchoring groups.•Optimization of conditions for tridentate self-assembly of the tripods onto Au(1 1 1)•XPS, NEXAFS spectroscopy and AFM characterization of the tripod monolayers.•Functionalization of the assembled tripods with a theophylline by click reaction.•Specific adsorption of streptavidin onto the tripod-engineered templates. We describe design and synthesis of novel tripod-shaped molecules that are potentially capable of monomolecular assembly on noble metal substrates, maintaining, due to their rigidity and specific geometry, the orientation of the functional arm in a perpendicular fashion with respect to the substrate. Using a combination of X-ray photoelectron spectroscopy, X-ray absorption spectroscopy and atomic force microscopy, the ability of these molecules to form well-defined and densely packed self-assembled monolayers (SAMs) on Au(1 1 1) was demonstrated, with the majority of the molecules adsorbed in the predefined tripodal geometry, relying on the thiolate-gold anchors. The functionality of the respective monomolecular templates was proved by click reaction between the terminal alkyne groups of the monolayers and complementary azide-substituted substituent (theophylline), which served potentially as specific protein receptor. The resulting theophylline-terminated films were successfully tested for specific protein adsorption, verifying the validity and reliability of the presented concept, in terms of the tripod design and its “activation” by the click reaction.
ISSN:0169-4332
1873-5584
DOI:10.1016/j.apsusc.2018.11.013