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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...

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Autores principales: Rudlof, Jens, Aders, Niklas, Lamm, Jan‐Hendrik, Neumann, Beate, Stammler, Hans‐Georg, Mitzel, Norbert W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
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.
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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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