Overcrowded Ethylene-Bridged Nanohoop Dimers: Regioselective Synthesis, Multiconfigurational Electronic States, and Global Hückel/Möbius Aromaticity-Reference-Cited by-同舟云学术

Overcrowded Ethylene-Bridged Nanohoop Dimers: Regioselective Synthesis, Multiconfigurational Electronic States, and Global Hückel/Möbius Aromaticity

Published:2021-11-24 Issue:48 Volume:143 Page:20419-20430
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Li Ke¹,Xu Zhuofan¹,Xu Jun²^ORCID,Weng Taoyu¹,Chen Xing¹,Sato Sota³^ORCID,Wu Jishan⁴^ORCID,Sun Zhe¹^ORCID

Affiliation:

1. Institute of Molecular Plus, Tianjin Key Laboratory of Molecular Optoelectronic Sciences, Tianjin University, 92 Weijin Road, Tianjin 300072, China

2. Health Science Platform, Tianjin University, 92 Weijin Road, Tianjin 300072, China

3. Department of Applied Chemistry, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-8656, Japan

4. Department of Chemistry, National University of Singapore, 3 Science Drive 3, Singapore 117543

Funder

Natural Science Foundation of Tianjin City

Japan Society for the Promotion of Science

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.1c10170

Reference68 articles.

1. Redox-active tetraaryldibenzoquinodimethanes

2. Synthesis, Physical Properties, and Reactivity of Stable, π-Conjugated, Carbon-Centered Radicals

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4. The stereochemistry of overcrowded homomerous bistricyclic aromatic enes with alkylidene bridges

5. Breaking Bonds and Forming Nanographene Diradicals with Pressure

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