Articolo in rivista, 2019, ENG, 10.1021/jacs.9b03554
Xu, Kun; Urgel, José I.; Eimre, Kristjan; Di Giovannantonio, Marco; Keerthi, Ashok; Komber, Hartmut; Wang, Shiyong; Narita, Akimitsu; Berger, Reinhard; Ruffieux, Pascal; Pignedoli, Carlo A.; Liu, Junzhi; Müllen, Klaus; Fasel, Roman; Feng, Xinliang
Okinawa Institute of Science and Technology Graduate University; Max Planck Institute for Polymer Research; University of Bern; Empa - Swiss Federal Laboratories for Materials Science and Technology; Technische Universität Dresden; Leibniz-Institut für Polymerforschung Dresden e.V.; The University of Manchester
On-surface synthesis provides an effective approach toward the formation of graphene nanostructures that are difficult to achieve via traditional solution chemistry. Here, we report on the design and synthesis of a nonplanar porous nanographene with 78 sp carbon atoms, namely C78. Through a highly selective oxidative cyclodehydrogenation of 2,3,6,7,10,11-hexa(naphthalen-1-yl)triphenylene (2), propeller nanographene precursor 1 was synthesized in solution. Interestingly, although 1 could not be cyclized further in solution, porous nanographene C78 was successfully achieved from 1 by on-surface assisted cyclodehydrogenation on Au(111). The structure and electronic properties of C78 have been investigated by means of scanning tunneling microscopy, noncontact atomic force microscopy, and scanning tunneling spectroscopy, complemented by computational investigations. Our results provide perspectives for the on-surface synthesis of porous graphene nanostructures, offering a promising strategy for the engineering of graphene materials with tailor-made properties.
Journal of the American Chemical Society (Print) 141 (19), pp. 7726–7730
ID: 426527
Year: 2019
Type: Articolo in rivista
Creation: 2020-07-31 15:39:56.000
Last update: 2020-07-31 15:39:56.000
CNR authors
External links
OAI-PMH: Dublin Core
OAI-PMH: Mods
OAI-PMH: RDF
DOI: 10.1021/jacs.9b03554
URL: http://www.scopus.com/record/display.url?eid=2-s2.0-85065769072&origin=inward
External IDs
CNR OAI-PMH: oai:it.cnr:prodotti:426527
DOI: 10.1021/jacs.9b03554
Scopus: 2-s2.0-85065769072