Liu, Jia; Dienel, Thomas; Liu, Junzhi; Groening, Oliver; Cai, Jinming; Feng, Xinliang; Müllen, Klaus; Ruffieux, Pascal; Fasel, Roman (2016). Building Pentagons into Graphenic Structures by On-Surface Polymerization and Aromatic Cyclodehydrogenation of Phenyl-Substituted Polycyclic Aromatic Hydrocarbons. Journal of physical chemistry. C, 120(31), pp. 17588-17593. American Chemical Society 10.1021/acs.jpcc.6b05495
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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.
Item Type: |
Journal Article (Original Article) |
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Division/Institute: |
08 Faculty of Science > Department of Chemistry, Biochemistry and Pharmaceutical Sciences (DCBP) |
UniBE Contributor: |
Fasel, Roman |
Subjects: |
500 Science > 570 Life sciences; biology 500 Science > 540 Chemistry 500 Science > 530 Physics |
ISSN: |
1932-7447 |
Publisher: |
American Chemical Society |
Language: |
English |
Submitter: |
Roman Fasel |
Date Deposited: |
05 Jan 2017 14:33 |
Last Modified: |
05 Dec 2022 15:00 |
Publisher DOI: |
10.1021/acs.jpcc.6b05495 |
BORIS DOI: |
10.7892/boris.90589 |
URI: |
https://boris.unibe.ch/id/eprint/90589 |