Sanchez-Sanchez C, Dienel T, Deniz O, Ruffieux P, Berger R, Peng X, Muellen K, Fasel R (2016)
Publication Type: Journal article
Publication year: 2016
Book Volume: 10
Pages Range: 8006-8011
Journal Issue: 8
We report on the atomic structure of graphene nanoribbons (GNRs) formed via on-surface synthesis from 10,10′-dibromo-9,9′-bianthryl (DBBA) precursors on Cu(111). By means of ultrahigh vacuum noncontact atomic force microscopy with CO-functionalized tips we unveil the chiral nature of the so-formed GNRs, a structure that has been under considerable debate. Furthermore, we prove that - in this particular case - the coupling selectivity usually introduced by halogen substitution is overruled by the structural and catalytic properties of the substrate. Specifically, we show that identical chiral GNRs are obtained from 9,9′-bianthryl, the unsubstituted sister molecule of DBBA.
APA:
Sanchez-Sanchez, C., Dienel, T., Deniz, O., Ruffieux, P., Berger, R., Peng, X.,... Fasel, R. (2016). Purely Armchair or Partially Chiral: Noncontact Atomic Force Microscopy Characterization of Dibromo-Bianthryl-Based Graphene Nanoribbons Grown on Cu(111). ACS nano, 10(8), 8006-8011. https://dx.doi.org/10.1021/acsnano.6b04025
MLA:
Sanchez-Sanchez, Carlos, et al. "Purely Armchair or Partially Chiral: Noncontact Atomic Force Microscopy Characterization of Dibromo-Bianthryl-Based Graphene Nanoribbons Grown on Cu(111)." ACS nano 10.8 (2016): 8006-8011.
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