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Azo bond formation on metal surfaces.

Xiangzhi MengHenning KlaasenLena ViergutzBertram Schulze LammersMelanie C BörnerHarry MönigSaeed AmirjalayerLacheng LiuJohannes NeugebauerHong Ying GaoArmido StuderHarald Fuchs
Published in: Angewandte Chemie (International ed. in English) (2020)
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.
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