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 | Physikalisches Institut (PI) |
Fuchs, Harald | Arbeitsgruppe Grenzflächenphysik (Prof. Fuchs) |
Klaasen, Henning | Professur für Organische Chemie (Prof. Studer) |
Liu, Lacheng | Arbeitsgruppe Grenzflächenphysik (Prof. Fuchs) |
Meng, Xiangzhi | Arbeitsgruppe Grenzflächenphysik (Prof. Fuchs) |
Mönig, Harry | Physikalisches Institut (PI) |
Neugebauer, Johannes | Professur für Theoretische Organische Chemie (Prof. Neugebauer) |
Schulze-Lammers, Bertram | Arbeitsgruppe Grenzflächenphysik (Prof. Fuchs) |
Studer, Armido | Professur für Organische Chemie (Prof. Studer) |
Viergutz, Lena | Professur für Organische Chemie (Prof. Studer) |
Witteler, Melanie | Professur für Theoretische Organische Chemie (Prof. Neugebauer) |