Zwitterionic inorganic benzene valence isomer with σ-bonding between two π-orbitals
Despite the large number of plausible isomers of benzene (C6H6), only four valence isomers [(CH)6] have been experimentally detected, all of which are nonionic and possess skeletal frameworks built from localized C-C bonds. Herein, we present the isolation of a diazatetraborabenzene analogue of a hy...
Main Authors: | , , , , |
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Format: | Journal Article |
Language: | English |
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2020
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Online Access: | https://hdl.handle.net/10356/139272 |
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author | Su, Bochao Ota, Kei Xu, Kai Hirao, Hajime Kinjo, Rei |
author2 | School of Physical and Mathematical Sciences |
author_facet | School of Physical and Mathematical Sciences Su, Bochao Ota, Kei Xu, Kai Hirao, Hajime Kinjo, Rei |
author_sort | Su, Bochao |
collection | NTU |
description | Despite the large number of plausible isomers of benzene (C6H6), only four valence isomers [(CH)6] have been experimentally detected, all of which are nonionic and possess skeletal frameworks built from localized C-C bonds. Herein, we present the isolation of a diazatetraborabenzene analogue of a hypothetical zwitterionic valence isomer of benzene. Therein, two electrons are delocalized over the four boron atoms in the six-membered B4N2 ring, which is a result of the σ-bonding interaction between two odd-electron B-B π-orbitals. Simple treatment with a crown ether leads to the formation of a paramagnetic potassium-doped radical ion pair that exhibits a thermally populated triplet character. |
first_indexed | 2024-10-01T06:22:05Z |
format | Journal Article |
id | ntu-10356/139272 |
institution | Nanyang Technological University |
language | English |
last_indexed | 2024-10-01T06:22:05Z |
publishDate | 2020 |
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spelling | ntu-10356/1392722020-05-18T07:50:24Z Zwitterionic inorganic benzene valence isomer with σ-bonding between two π-orbitals Su, Bochao Ota, Kei Xu, Kai Hirao, Hajime Kinjo, Rei School of Physical and Mathematical Sciences Science::Chemistry Potassium Hydrocarbons Despite the large number of plausible isomers of benzene (C6H6), only four valence isomers [(CH)6] have been experimentally detected, all of which are nonionic and possess skeletal frameworks built from localized C-C bonds. Herein, we present the isolation of a diazatetraborabenzene analogue of a hypothetical zwitterionic valence isomer of benzene. Therein, two electrons are delocalized over the four boron atoms in the six-membered B4N2 ring, which is a result of the σ-bonding interaction between two odd-electron B-B π-orbitals. Simple treatment with a crown ether leads to the formation of a paramagnetic potassium-doped radical ion pair that exhibits a thermally populated triplet character. MOE (Min. of Education, S’pore) 2020-05-18T07:50:23Z 2020-05-18T07:50:23Z 2018 Journal Article Su, B., Ota, K., Xu, K., Hirao, H., & Kinjo, R. (2018). Zwitterionic inorganic benzene valence isomer with σ-bonding between two π-orbitals. Journal of the American Chemical Society, 140(38), 11921-11925. doi:10.1021/jacs.8b08025 0002-7863 https://hdl.handle.net/10356/139272 10.1021/jacs.8b08025 30205673 2-s2.0-85053662031 38 140 11921 11925 en Journal of the American Chemical Society © 2018 American Chemical Society. All rights reserved. |
spellingShingle | Science::Chemistry Potassium Hydrocarbons Su, Bochao Ota, Kei Xu, Kai Hirao, Hajime Kinjo, Rei Zwitterionic inorganic benzene valence isomer with σ-bonding between two π-orbitals |
title | Zwitterionic inorganic benzene valence isomer with σ-bonding between two π-orbitals |
title_full | Zwitterionic inorganic benzene valence isomer with σ-bonding between two π-orbitals |
title_fullStr | Zwitterionic inorganic benzene valence isomer with σ-bonding between two π-orbitals |
title_full_unstemmed | Zwitterionic inorganic benzene valence isomer with σ-bonding between two π-orbitals |
title_short | Zwitterionic inorganic benzene valence isomer with σ-bonding between two π-orbitals |
title_sort | zwitterionic inorganic benzene valence isomer with σ bonding between two π orbitals |
topic | Science::Chemistry Potassium Hydrocarbons |
url | https://hdl.handle.net/10356/139272 |
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