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Article: Building Pentagons into Graphenic Structures by On-Surface Polymerization and Aromatic Cyclodehydrogenation of Phenyl-Substituted Polycyclic Aromatic Hydrocarbons

TitleBuilding Pentagons into Graphenic Structures by On-Surface Polymerization and Aromatic Cyclodehydrogenation of Phenyl-Substituted Polycyclic Aromatic Hydrocarbons
Authors
Issue Date2016
Citation
Journal of Physical Chemistry C, 2016, v. 120, n. 31, p. 17588-17593 How to Cite?
Abstract© 2016 American Chemical Society. Five-membered carbon rings play a crucial role in determining the geometric structures and electronic properties of carbon-based materials. However, incorporating five-membered rings into low-dimensional carbon nanomaterials with atomic precision is still a challenge. Here, we report on the on-surface synthesis of a one-dimensional conjugated polymer comprising fluoranthene subunits obtained by the surface-assisted aromatic cyclodehydrogenation of 1-phenylnaphthalene moieties within the precursor monomers. By using scanning tunneling microscopy (STM), we investigate the formation of the polymer by thermally induced dehalogenative aryl-aryl coupling and subsequent aromatic cyclodehydrogenation on a Au(111) substrate. The formed five-membered carbon rings are directly observed with atomic resolution by noncontact atomic force microscopy (nc-AFM). Our results show that carefully designed phenyl-substituted polycyclic aromatic hydrocarbons can be used for the rational fabrication of five-membered rings in the bottom-up synthesis of carbon-based nanomaterials and thus add a further tool to the emerging field of on-surface synthesis.
Persistent Identifierhttp://hdl.handle.net/10722/276762
ISSN
2023 Impact Factor: 3.3
2023 SCImago Journal Rankings: 0.957
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLiu, Jia-
dc.contributor.authorDienel, Thomas-
dc.contributor.authorLiu, Junzhi-
dc.contributor.authorGroening, Oliver-
dc.contributor.authorCai, Jinming-
dc.contributor.authorFeng, Xinliang-
dc.contributor.authorMüllen, Klaus-
dc.contributor.authorRuffieux, Pascal-
dc.contributor.authorFasel, Roman-
dc.date.accessioned2019-09-18T08:34:35Z-
dc.date.available2019-09-18T08:34:35Z-
dc.date.issued2016-
dc.identifier.citationJournal of Physical Chemistry C, 2016, v. 120, n. 31, p. 17588-17593-
dc.identifier.issn1932-7447-
dc.identifier.urihttp://hdl.handle.net/10722/276762-
dc.description.abstract© 2016 American Chemical Society. Five-membered carbon rings play a crucial role in determining the geometric structures and electronic properties of carbon-based materials. However, incorporating five-membered rings into low-dimensional carbon nanomaterials with atomic precision is still a challenge. Here, we report on the on-surface synthesis of a one-dimensional conjugated polymer comprising fluoranthene subunits obtained by the surface-assisted aromatic cyclodehydrogenation of 1-phenylnaphthalene moieties within the precursor monomers. By using scanning tunneling microscopy (STM), we investigate the formation of the polymer by thermally induced dehalogenative aryl-aryl coupling and subsequent aromatic cyclodehydrogenation on a Au(111) substrate. The formed five-membered carbon rings are directly observed with atomic resolution by noncontact atomic force microscopy (nc-AFM). Our results show that carefully designed phenyl-substituted polycyclic aromatic hydrocarbons can be used for the rational fabrication of five-membered rings in the bottom-up synthesis of carbon-based nanomaterials and thus add a further tool to the emerging field of on-surface synthesis.-
dc.languageeng-
dc.relation.ispartofJournal of Physical Chemistry C-
dc.titleBuilding Pentagons into Graphenic Structures by On-Surface Polymerization and Aromatic Cyclodehydrogenation of Phenyl-Substituted Polycyclic Aromatic Hydrocarbons-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/acs.jpcc.6b05495-
dc.identifier.scopuseid_2-s2.0-84981523735-
dc.identifier.volume120-
dc.identifier.issue31-
dc.identifier.spage17588-
dc.identifier.epage17593-
dc.identifier.eissn1932-7455-
dc.identifier.isiWOS:000381452000048-
dc.identifier.issnl1932-7447-

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