Chemical Activation of a Single Melamine Molecule via Isomerization Followed by Metalation with a Copper Atom
Scanning probe methods have very successfully been used for inducing on-surface reactions and imaging with high resolution the reaction partners at the single-molecule level. However, the entire sequence of chemically activating an educt, identifying its reactive site, running a chemical reaction, and quantifying the involved forces and energies has been missing to date. Here, the organic molecule melamine adsorbed on Cu(100) serves as a single-molecule model system for activation via tautomerization and subsequent metalation with a single Cu atom. An atomic force microscope with a CO-decorated tip probes the most reactive intramolecular site of the tautomer, while a Cu-terminated tip transfers a single Cu atom to this site. Following the interaction between the mutually approached reaction partners up to the verge of chemical-bond formation enables access to the force and energy involved in the single-molecule metalation process. Total-energy calculations from density functional theory support the experimental findings and illustrate the structure of the reactants.
Authors
- Karl Rothe (ORCID: https://orcid.org/0000-0001-6672-398X)
- N. Néel (ORCID: https://orcid.org/0000-0003-0498-9138)
- Thomas Frederiksen (ORCID: https://orcid.org/0000-0001-7523-7641)
- J. Kröger (ORCID: https://orcid.org/0000-0002-6452-5864)
- Manex Alkorta (ORCID: https://orcid.org/0009-0003-8109-9216)
Institutions
- Ikerbasque (ES)
- Technische Universität Ilmenau (DE)
- University of the Basque Country (ES)
- Material Physics Center (ES)
- Donostia International Physics Center (ES)
Publication Details
- Journal
- ACS Nano
- Published
- 2025-02-26
- DOI
- https://doi.org/10.1021/acsnano.4c18832
- Primary Topic
- Molecular Junctions and Nanostructures
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Ministerio de Ciencia, Innovación y Universidades
- Hezkuntza, Hizkuntza Politika Eta Kultura Saila, Eusko Jaurlaritza
- Deutsche Forschungsgemeinschaft
- Bundesministerium für Bildung und Forschung