Articolo in rivista, 2020, ENG, 10.1002/anie.202001939
Urgel, Jose, I; Di Giovannantonio, Marco; Eimre, Kristjan; Lohr, Thorsten G.; Liu, Junzhi; Mishra, Shantanu; Sun, Qiang; Kinikar, Amogh; Widmer, Roland; Stolz, Samuel; Bommert, Max; Berger, Reinhard; Ruffieux, Pascal; Pignedoli, Carlo A.; Muellen, Klaus; Feng, Xinliang; Fasel, Roman
Empa Swiss Fed Labs Mat Sci & Technol; Tech Univ Dresden; Tech Univ Dresden; Ecole Polytech Fed Lausanne; Max Planck Inst Polymer Res; Univ Bern
Cumulene compounds are notoriously difficult to prepare and study because their reactivity increases dramatically with the increasing number of consecutive double bonds. In this respect, the emerging field of on-surface synthesis provides exceptional opportunities because it relies on reactions on clean metal substrates under well-controlled ultrahigh-vacuum conditions. Here we report the on-surface synthesis of a polymer linked by cumulene-like bonds on a Au(111) surface via sequential thermally activated dehalogenative C-C coupling of a tribenzoazulene precursor equipped with two dibromomethylene groups. The structure and electronic properties of the resulting polymer with cumulene-like pentagon-pentagon and heptagon-heptagon connections have been investigated by means of scanning probe microscopy and spectroscopy methods and X-ray photoelectron spectroscopy, complemented by density functional theory calculations. Our results provide perspectives for the on-surface synthesis of cumulene-containing compounds, as well as protocols relevant to the stepwise fabrication of carbon-carbon bonds on surfaces.
Angewandte Chemie (Int. ed., Print)
carbon nanostructures, cumulenes, nonbenzenoid hydrocarbons, sequential dehalogenation, surface chemistry
ID: 426496
Year: 2020
Type: Articolo in rivista
Creation: 2020-07-31 15:11:10.000
Last update: 2020-07-31 15:11:10.000
CNR authors
External IDs
CNR OAI-PMH: oai:it.cnr:prodotti:426496
DOI: 10.1002/anie.202001939
ISI Web of Science (WOS): 000535955400001