Heptene end-capped Thiele hydrocarbons with tunable configuration and emission and on-surface transformation via annulation.

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemical Communications Pub Date : 2025-02-13 DOI:10.1039/d5cc00053j
Yilin Shu, Jianmin Huang, Junfang Yang, Zhichun Shangguan, Junlong Ma, Cheng Li, Guanxin Zhang, Qian Peng, Xi-Sha Zhang, Qitang Fan, Bing Wang, Deqing Zhang
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引用次数: 0

Abstract

We report a para-quinodimethane skeleton (p-QDM)-based polycyclic aromatic hydrocarbon (PAH) with heptenes as end-capping groups and F-substituents in the central six-membered ring. This compound shows the syn-configuration in one crystal form with relative strong emission (ΦF = 0.25), and the anti-configuration in another crystal form with weak emission. Furthermore, this compound was transformed into the more annulated PAHs via on-surface C-F bond activations.

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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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