A new armchair carbon nanobelt synthesized by tuning the regioselectivity of the Scholl reaction of quinquephenyl

Zeming Xia; Ka Man Cheung; Han Chen; Sai Ho Pun; Qian Miao

doi:10.1039/D4CC00979G

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A new armchair carbon nanobelt synthesized by tuning the regioselectivity of the Scholl reaction of quinquephenyl†

Zeming Xia,

^a Ka Man Cheung,^a Han Chen,

^a Sai Ho Pun^a and Qian Miao

*^a

Author affiliations

* Corresponding authors

^a Department of Chemistry and State Key Laboratory of Synthetic Chemistry, The Chinese University of Hong Kong Shatin, New Territories, Hong Kong, China
E-mail: miaoqian@cuhk.edu.hk

Abstract

A new armchair carbon nanobelt is successfully synthesized by tuning the regioselectivity of the Scholl reaction of 1,1′:2′,1′′:4′′,1′′′:2′′′,1′′′′-quinquephenyl. This nanobelt exhibits a preferential binding affinity towards C₇₀ over C₆₀ as found from photoluminescence titration experiments.

This article is part of the themed collections: Chemical Communications HOT Articles 2024 and ChemComm 60th Anniversary Collection

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Article information

DOI: https://doi.org/10.1039/D4CC00979G
Article type: Communication
Submitted: 29 Feb 2024
Accepted: 21 Mar 2024
First published: 21 Mar 2024

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Chem. Commun., 2024,60, 4314-4317

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A new armchair carbon nanobelt synthesized by tuning the regioselectivity of the Scholl reaction of quinquephenyl

Z. Xia, K. M. Cheung, H. Chen, S. H. Pun and Q. Miao, Chem. Commun., 2024, 60, 4314 DOI: 10.1039/D4CC00979G

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Chemical Communications

A new armchair carbon nanobelt synthesized by tuning the regioselectivity of the Scholl reaction of quinquephenyl†

Abstract

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A new armchair carbon nanobelt synthesized by tuning the regioselectivity of the Scholl reaction of quinquephenyl

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