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Disila- and digermabenzenes
Reactions of isolable disilynes and digermynes with alkynes can result in the formation of the corresponding disila- (DSBs) and digermabenzenes (DGBs), wherein two carbon atoms of the benzene ring are replaced by silicon or germanium atoms. Detailed structural and spectroscopic analyses of these DSB...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Royal Society of Chemistry
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132941/ https://www.ncbi.nlm.nih.gov/pubmed/34040726 http://dx.doi.org/10.1039/d1sc00130b |
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author | Sasamori, Takahiro |
author_facet | Sasamori, Takahiro |
author_sort | Sasamori, Takahiro |
collection | PubMed |
description | Reactions of isolable disilynes and digermynes with alkynes can result in the formation of the corresponding disila- (DSBs) and digermabenzenes (DGBs), wherein two carbon atoms of the benzene ring are replaced by silicon or germanium atoms. Detailed structural and spectroscopic analyses of these DSBs and DGBs have revealed that they exhibit considerable aromaticity, comparable to that of benzene. However, in contrast to the all-carbon system benzene, these DSBs and DGBs are highly reactive toward small molecules such as oxygen, hydrogen, 1,3-dienes, and water. During the investigation of their reactivity, we discovered that a 1,2-DGB works as a catalyst for the cyclotrimerization of arylalkynes, which provides access to the corresponding 1,2,4-triarylbenzenes. In this perspective article, our recent progress in the area of DSB and DGB chemistry is summarized. |
format | Online Article Text |
id | pubmed-8132941 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-81329412021-05-25 Disila- and digermabenzenes Sasamori, Takahiro Chem Sci Chemistry Reactions of isolable disilynes and digermynes with alkynes can result in the formation of the corresponding disila- (DSBs) and digermabenzenes (DGBs), wherein two carbon atoms of the benzene ring are replaced by silicon or germanium atoms. Detailed structural and spectroscopic analyses of these DSBs and DGBs have revealed that they exhibit considerable aromaticity, comparable to that of benzene. However, in contrast to the all-carbon system benzene, these DSBs and DGBs are highly reactive toward small molecules such as oxygen, hydrogen, 1,3-dienes, and water. During the investigation of their reactivity, we discovered that a 1,2-DGB works as a catalyst for the cyclotrimerization of arylalkynes, which provides access to the corresponding 1,2,4-triarylbenzenes. In this perspective article, our recent progress in the area of DSB and DGB chemistry is summarized. The Royal Society of Chemistry 2021-03-26 /pmc/articles/PMC8132941/ /pubmed/34040726 http://dx.doi.org/10.1039/d1sc00130b Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Sasamori, Takahiro Disila- and digermabenzenes |
title | Disila- and digermabenzenes |
title_full | Disila- and digermabenzenes |
title_fullStr | Disila- and digermabenzenes |
title_full_unstemmed | Disila- and digermabenzenes |
title_short | Disila- and digermabenzenes |
title_sort | disila- and digermabenzenes |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8132941/ https://www.ncbi.nlm.nih.gov/pubmed/34040726 http://dx.doi.org/10.1039/d1sc00130b |
work_keys_str_mv | AT sasamoritakahiro disilaanddigermabenzenes |