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An Unusual and Facile Synthetic Route to Alumoles
Reaction of the aluminum dialkynyl LAl(CCR)(2) (L=N,N‐chelate ligand and R=organic group) with B(C(6)F(5))(3) proceeds through an intermediate with Al⋅⋅⋅η(2)‐C≡C side‐on coordination to form the alumoles (2, 4, 6). A distinctive reaction pattern indicates a new facile synthetic route to aluminum‐con...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318123/ https://www.ncbi.nlm.nih.gov/pubmed/32160361 http://dx.doi.org/10.1002/anie.202000899 |
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author | Li, Jiancheng Wu, Peng Jiang, Wenjun Li, Bin Wang, Binju Zhu, Hongping Roesky, Herbert W. |
author_facet | Li, Jiancheng Wu, Peng Jiang, Wenjun Li, Bin Wang, Binju Zhu, Hongping Roesky, Herbert W. |
author_sort | Li, Jiancheng |
collection | PubMed |
description | Reaction of the aluminum dialkynyl LAl(CCR)(2) (L=N,N‐chelate ligand and R=organic group) with B(C(6)F(5))(3) proceeds through an intermediate with Al⋅⋅⋅η(2)‐C≡C side‐on coordination to form the alumoles (2, 4, 6). A distinctive reaction pattern indicates a new facile synthetic route to aluminum‐containing heterocycles. The synthetic process is described, and the characterization of compounds and computational calculations were carried out. Furthermore, alumoles 2 and 4 exhibit an aggregation‐induced emission (AIE) of the bright yellow fluorescence. |
format | Online Article Text |
id | pubmed-7318123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73181232020-06-29 An Unusual and Facile Synthetic Route to Alumoles Li, Jiancheng Wu, Peng Jiang, Wenjun Li, Bin Wang, Binju Zhu, Hongping Roesky, Herbert W. Angew Chem Int Ed Engl Communications Reaction of the aluminum dialkynyl LAl(CCR)(2) (L=N,N‐chelate ligand and R=organic group) with B(C(6)F(5))(3) proceeds through an intermediate with Al⋅⋅⋅η(2)‐C≡C side‐on coordination to form the alumoles (2, 4, 6). A distinctive reaction pattern indicates a new facile synthetic route to aluminum‐containing heterocycles. The synthetic process is described, and the characterization of compounds and computational calculations were carried out. Furthermore, alumoles 2 and 4 exhibit an aggregation‐induced emission (AIE) of the bright yellow fluorescence. John Wiley and Sons Inc. 2020-04-23 2020-06-15 /pmc/articles/PMC7318123/ /pubmed/32160361 http://dx.doi.org/10.1002/anie.202000899 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Li, Jiancheng Wu, Peng Jiang, Wenjun Li, Bin Wang, Binju Zhu, Hongping Roesky, Herbert W. An Unusual and Facile Synthetic Route to Alumoles |
title | An Unusual and Facile Synthetic Route to Alumoles |
title_full | An Unusual and Facile Synthetic Route to Alumoles |
title_fullStr | An Unusual and Facile Synthetic Route to Alumoles |
title_full_unstemmed | An Unusual and Facile Synthetic Route to Alumoles |
title_short | An Unusual and Facile Synthetic Route to Alumoles |
title_sort | unusual and facile synthetic route to alumoles |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318123/ https://www.ncbi.nlm.nih.gov/pubmed/32160361 http://dx.doi.org/10.1002/anie.202000899 |
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