Please use this identifier to cite or link to this item: https://doi.org/https://pubs.acs.org/doi/abs/10.1021/acs.orglett.3c00870
Title: Bisazapentalene Dication: Global Aromaticity and Open-Shell Singlet Ground State
Authors: Yi Han 
Jun Zhu
Shaoqiang Dong 
Yijie Eng
Tao tao
Yadagiri Gopalakrishna Tullimilli 
Chunyan Chi 
Issue Date: 10-May-2023
Citation: Yi Han, Jun Zhu, Shaoqiang Dong, Yijie Eng, Tao tao, Yadagiri Gopalakrishna Tullimilli, Chunyan Chi (2023-05-10). Bisazapentalene Dication: Global Aromaticity and Open-Shell Singlet Ground State. Organic Letters 25 (19) : 3380 - 3385. ScholarBank@NUS Repository. https://doi.org/https://pubs.acs.org/doi/abs/10.1021/acs.orglett.3c00870
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
Abstract: Antiaromatic moieties fused in polycyclic π-conjugated molecules usually exhibit strong localized antiaromaticiy. Herein, we reported the synthesis and properties of a bisazapentalene dication (BAP2+) obtained from in situ two-electron oxidation of neutral species 8. Noteworthily, it possesses global aromaticity and an open-shell singlet ground state. This study underlines the importance of heteroatoms in determining the delocalization of π-electrons and the aromaticity of molecules in their oxidized states.
Source Title: Organic Letters
URI: https://scholarbank.nus.edu.sg/handle/10635/249388
ISSN: 1523-7060
1523-7052
DOI: https://pubs.acs.org/doi/abs/10.1021/acs.orglett.3c00870
Rights: Attribution-NonCommercial-NoDerivatives 4.0 International
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