Meng X, Klaasen H, Viergutz L, Schulze Lammers B, Witteler MC, Mönig H, Amirjalayer S, Liu L, Neugebauer J, Gao H, Studer A, Fuchs H
Forschungsartikel (Zeitschrift) | Peer reviewedAbstract The formation of azo compounds via redox cross-coupling of nitroarenes and arylamines, challenging in solution phase chemistry, is achieved by on-surface chemistry. Reaction products are analyzed with a cryogenic scanning tunneling microscope (STM) and X-ray photoelectron spectroscopy (XPS). By using well-designed precursors containing both an amino and a nitro functionality, azo polymers are prepared on surface via highly efficient nitro-amino cross-coupling. Experiments conducted on other substrates and surface orientations reveal that the metal surface has a significant effect on the reaction efficiency. The reaction was further found to proceed from partially oxidized/reduced precursors in dimerization reactions, shedding light on the mechanism that was studied by DFT calculations.
| Amirjalayer, Saeed | |
| Fuchs, Harald | |
| Klaasen, Henning | |
| Liu, Lacheng | |
| Meng, Xiangzhi | |
| Mönig, Harry | |
| Neugebauer, Johannes | |
| Schulze-Lammers, Bertram | |
| Studer, Armido | |
| Viergutz, Lena | |
| Witteler, Melanie |