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Bidentate Lewis Acids Derived from o‐Diethynylbenzene with Group 13 and 14 Functions
Starting from 1,2‐diethynylbenzene, a series of bidentate Lewis acids was prepared by means of hydrometalations, in particular hydrosilylation, hydroboration, hydroalumination and terminal metalation based on group 13 and 14 elements. In the case of terminal alkyne metalation, the Lewis‐acidic galli...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507440/ https://www.ncbi.nlm.nih.gov/pubmed/34637192 http://dx.doi.org/10.1002/open.202100198 |
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author | Rudlof, Jens Aders, Niklas Lamm, Jan‐Hendrik Neumann, Beate Stammler, Hans‐Georg Mitzel, Norbert W. |
author_facet | Rudlof, Jens Aders, Niklas Lamm, Jan‐Hendrik Neumann, Beate Stammler, Hans‐Georg Mitzel, Norbert W. |
author_sort | Rudlof, Jens |
collection | PubMed |
description | Starting from 1,2‐diethynylbenzene, a series of bidentate Lewis acids was prepared by means of hydrometalations, in particular hydrosilylation, hydroboration, hydroalumination and terminal metalation based on group 13 and 14 elements. In the case of terminal alkyne metalation, the Lewis‐acidic gallium function was introduced using triethylgallium under alkane elimination. A total of six different Lewis acids based on a semiflexible organic scaffold were prepared, bearing −SiClMe(2), −SiCl(2)Me, −SiCl(3), −B(C(6)F(5))(2), −AlBis(2) (Bis=bis(trimethylsilyl)methyl) and −GaEt(2) as the corresponding functional units. In all cases, the Lewis acid functionalisation was carried out twice and the products were obtained in good to excellent yields. In the case of the twofold gallium Lewis acid, a different structural motif in the form of a polymer‐like chain was observed in the solid state. All new bidentate Lewis acids were characterised by multinuclear NMR spectroscopy, CHN analysis and X‐ray diffraction experiments. |
format | Online Article Text |
id | pubmed-8507440 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85074402021-10-18 Bidentate Lewis Acids Derived from o‐Diethynylbenzene with Group 13 and 14 Functions Rudlof, Jens Aders, Niklas Lamm, Jan‐Hendrik Neumann, Beate Stammler, Hans‐Georg Mitzel, Norbert W. ChemistryOpen Full Papers Starting from 1,2‐diethynylbenzene, a series of bidentate Lewis acids was prepared by means of hydrometalations, in particular hydrosilylation, hydroboration, hydroalumination and terminal metalation based on group 13 and 14 elements. In the case of terminal alkyne metalation, the Lewis‐acidic gallium function was introduced using triethylgallium under alkane elimination. A total of six different Lewis acids based on a semiflexible organic scaffold were prepared, bearing −SiClMe(2), −SiCl(2)Me, −SiCl(3), −B(C(6)F(5))(2), −AlBis(2) (Bis=bis(trimethylsilyl)methyl) and −GaEt(2) as the corresponding functional units. In all cases, the Lewis acid functionalisation was carried out twice and the products were obtained in good to excellent yields. In the case of the twofold gallium Lewis acid, a different structural motif in the form of a polymer‐like chain was observed in the solid state. All new bidentate Lewis acids were characterised by multinuclear NMR spectroscopy, CHN analysis and X‐ray diffraction experiments. John Wiley and Sons Inc. 2021-10-12 /pmc/articles/PMC8507440/ /pubmed/34637192 http://dx.doi.org/10.1002/open.202100198 Text en © 2021 The Authors. Published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Full Papers Rudlof, Jens Aders, Niklas Lamm, Jan‐Hendrik Neumann, Beate Stammler, Hans‐Georg Mitzel, Norbert W. Bidentate Lewis Acids Derived from o‐Diethynylbenzene with Group 13 and 14 Functions |
title | Bidentate Lewis Acids Derived from o‐Diethynylbenzene with Group 13 and 14 Functions |
title_full | Bidentate Lewis Acids Derived from o‐Diethynylbenzene with Group 13 and 14 Functions |
title_fullStr | Bidentate Lewis Acids Derived from o‐Diethynylbenzene with Group 13 and 14 Functions |
title_full_unstemmed | Bidentate Lewis Acids Derived from o‐Diethynylbenzene with Group 13 and 14 Functions |
title_short | Bidentate Lewis Acids Derived from o‐Diethynylbenzene with Group 13 and 14 Functions |
title_sort | bidentate lewis acids derived from o‐diethynylbenzene with group 13 and 14 functions |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8507440/ https://www.ncbi.nlm.nih.gov/pubmed/34637192 http://dx.doi.org/10.1002/open.202100198 |
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