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Article: Building Pentagons into Graphenic Structures by On-Surface Polymerization and Aromatic Cyclodehydrogenation of Phenyl-Substituted Polycyclic Aromatic Hydrocarbons
Title | Building Pentagons into Graphenic Structures by On-Surface Polymerization and Aromatic Cyclodehydrogenation of Phenyl-Substituted Polycyclic Aromatic Hydrocarbons |
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Authors | |
Issue Date | 2016 |
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 Identifier | http://hdl.handle.net/10722/276762 |
ISSN | 2023 Impact Factor: 3.3 2023 SCImago Journal Rankings: 0.957 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Liu, Jia | - |
dc.contributor.author | Dienel, Thomas | - |
dc.contributor.author | Liu, Junzhi | - |
dc.contributor.author | Groening, Oliver | - |
dc.contributor.author | Cai, Jinming | - |
dc.contributor.author | Feng, Xinliang | - |
dc.contributor.author | Müllen, Klaus | - |
dc.contributor.author | Ruffieux, Pascal | - |
dc.contributor.author | Fasel, Roman | - |
dc.date.accessioned | 2019-09-18T08:34:35Z | - |
dc.date.available | 2019-09-18T08:34:35Z | - |
dc.date.issued | 2016 | - |
dc.identifier.citation | Journal of Physical Chemistry C, 2016, v. 120, n. 31, p. 17588-17593 | - |
dc.identifier.issn | 1932-7447 | - |
dc.identifier.uri | http://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.language | eng | - |
dc.relation.ispartof | Journal of Physical Chemistry C | - |
dc.title | Building Pentagons into Graphenic Structures by On-Surface Polymerization and Aromatic Cyclodehydrogenation of Phenyl-Substituted Polycyclic Aromatic Hydrocarbons | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/acs.jpcc.6b05495 | - |
dc.identifier.scopus | eid_2-s2.0-84981523735 | - |
dc.identifier.volume | 120 | - |
dc.identifier.issue | 31 | - |
dc.identifier.spage | 17588 | - |
dc.identifier.epage | 17593 | - |
dc.identifier.eissn | 1932-7455 | - |
dc.identifier.isi | WOS:000381452000048 | - |
dc.identifier.issnl | 1932-7447 | - |