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Large-Cavity Coronoids with Different Inner and Outer Edge Structures.


ABSTRACT: Coronoids, polycyclic aromatic hydrocarbons with geometrically defined cavities, are promising model structures of porous graphene. Here, we report the on-surface synthesis of C168 and C140 coronoids, referred to as [6]- and [5]coronoid, respectively, using 5,9-dibromo-14-phenylbenzo[m]tetraphene as the precursor. These coronoids entail large cavities (>1 nm) with inner zigzag edges, distinct from their outer armchair edges. While [6]coronoid is planar, [5]coronoid is not. Low-temperature scanning tunneling microscopy/spectroscopy and noncontact atomic force microscopy unveil structural and electronic properties in accordance with those obtained from density functional theory calculations. Detailed analysis of ring current effects identifies the rings with the highest aromaticity of these coronoids, whose pattern matches their Clar structure. The pores of the obtained coronoids offer intriguing possibilities of further functionalization toward advanced host-guest applications.

SUBMITTER: Di Giovannantonio M 

PROVIDER: S-EPMC7467669 | biostudies-literature | 2020 Jul

REPOSITORIES: biostudies-literature

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Large-Cavity Coronoids with Different Inner and Outer Edge Structures.

Di Giovannantonio Marco M   Yao Xuelin X   Eimre Kristjan K   Urgel José I JI   Ruffieux Pascal P   Pignedoli Carlo A CA   Müllen Klaus K   Fasel Roman R   Narita Akimitsu A  

Journal of the American Chemical Society 20200702 28


Coronoids, polycyclic aromatic hydrocarbons with geometrically defined cavities, are promising model structures of porous graphene. Here, we report the on-surface synthesis of C168 and C140 coronoids, referred to as [6]- and [5]coronoid, respectively, using 5,9-dibromo-14-phenylbenzo[<i>m</i>]tetraphene as the precursor. These coronoids entail large cavities (>1 nm) with inner zigzag edges, distinct from their outer armchair edges. While [6]coronoid is planar, [5]coronoid is not. Low-temperature  ...[more]

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