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Catalysis with Pnictogen, Chalcogen, and Halogen Bonds

Halogen‐ and chalcogen‐based σ‐hole interactions have recently received increased interest in non‐covalent organocatalysis. However, the closely related pnictogen bonds have been neglected. In this study, we introduce conceptually simple, neutral, and monodentate pnictogen‐bonding catalysts. Solutio...

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Autores principales: Benz, Sebastian, Poblador‐Bahamonde, Amalia I., Low‐Ders, Nicolas, Matile, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947745/
https://www.ncbi.nlm.nih.gov/pubmed/29558562
http://dx.doi.org/10.1002/anie.201801452
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author Benz, Sebastian
Poblador‐Bahamonde, Amalia I.
Low‐Ders, Nicolas
Matile, Stefan
author_facet Benz, Sebastian
Poblador‐Bahamonde, Amalia I.
Low‐Ders, Nicolas
Matile, Stefan
author_sort Benz, Sebastian
collection PubMed
description Halogen‐ and chalcogen‐based σ‐hole interactions have recently received increased interest in non‐covalent organocatalysis. However, the closely related pnictogen bonds have been neglected. In this study, we introduce conceptually simple, neutral, and monodentate pnictogen‐bonding catalysts. Solution and in silico binding studies, together with high catalytic activity in chloride abstraction reactions, yield compelling evidence for operational pnictogen bonds. The depth of the σ holes is easily varied with different substituents. Comparison with homologous halogen‐ and chalcogen‐bonding catalysts shows an increase in activity from main group VII to V and from row 3 to 5 in the periodic table. Pnictogen bonds from antimony thus emerged as by far the best among the elements covered, a finding that provides most intriguing perspectives for future applications in catalysis and beyond.
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spelling pubmed-59477452018-05-17 Catalysis with Pnictogen, Chalcogen, and Halogen Bonds Benz, Sebastian Poblador‐Bahamonde, Amalia I. Low‐Ders, Nicolas Matile, Stefan Angew Chem Int Ed Engl Communications Halogen‐ and chalcogen‐based σ‐hole interactions have recently received increased interest in non‐covalent organocatalysis. However, the closely related pnictogen bonds have been neglected. In this study, we introduce conceptually simple, neutral, and monodentate pnictogen‐bonding catalysts. Solution and in silico binding studies, together with high catalytic activity in chloride abstraction reactions, yield compelling evidence for operational pnictogen bonds. The depth of the σ holes is easily varied with different substituents. Comparison with homologous halogen‐ and chalcogen‐bonding catalysts shows an increase in activity from main group VII to V and from row 3 to 5 in the periodic table. Pnictogen bonds from antimony thus emerged as by far the best among the elements covered, a finding that provides most intriguing perspectives for future applications in catalysis and beyond. John Wiley and Sons Inc. 2018-03-20 2018-05-04 /pmc/articles/PMC5947745/ /pubmed/29558562 http://dx.doi.org/10.1002/anie.201801452 Text en © 2018 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-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Communications
Benz, Sebastian
Poblador‐Bahamonde, Amalia I.
Low‐Ders, Nicolas
Matile, Stefan
Catalysis with Pnictogen, Chalcogen, and Halogen Bonds
title Catalysis with Pnictogen, Chalcogen, and Halogen Bonds
title_full Catalysis with Pnictogen, Chalcogen, and Halogen Bonds
title_fullStr Catalysis with Pnictogen, Chalcogen, and Halogen Bonds
title_full_unstemmed Catalysis with Pnictogen, Chalcogen, and Halogen Bonds
title_short Catalysis with Pnictogen, Chalcogen, and Halogen Bonds
title_sort catalysis with pnictogen, chalcogen, and halogen bonds
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5947745/
https://www.ncbi.nlm.nih.gov/pubmed/29558562
http://dx.doi.org/10.1002/anie.201801452
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