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Frontiers in Halogen and Chalcogen‐Bond Donor Organocatalysis

Non‐covalent molecular interactions on the basis of halogen and chalcogen bonding represent a promising, powerful catalytic activation mode. However, these “unusual” non‐covalent interactions are typically employed in the solid state and scarcely exploited in catalysis. In recent years, an increased...

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Detalles Bibliográficos
Autores principales: Bamberger, Julia, Ostler, Florian, Mancheño, Olga García
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6919929/
https://www.ncbi.nlm.nih.gov/pubmed/31894187
http://dx.doi.org/10.1002/cctc.201901215
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author Bamberger, Julia
Ostler, Florian
Mancheño, Olga García
author_facet Bamberger, Julia
Ostler, Florian
Mancheño, Olga García
author_sort Bamberger, Julia
collection PubMed
description Non‐covalent molecular interactions on the basis of halogen and chalcogen bonding represent a promising, powerful catalytic activation mode. However, these “unusual” non‐covalent interactions are typically employed in the solid state and scarcely exploited in catalysis. In recent years, an increased interest in halogen and chalcogen bonding has been awaken, as they provide profound characteristics that make them an appealing alternative to the well‐explored hydrogen bonding. Being particularly relevant in the binding of “soft” substrates, the similar strength to hydrogen bonding interactions and its higher directionality allows for solution‐phase applications with halogen and chalcogen bonding as the key interaction. In this mini‐review, the special features, state‐of‐the‐art and key examples of these so‐called σ‐hole interactions in the field of organocatalysis are presented.
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spelling pubmed-69199292019-12-30 Frontiers in Halogen and Chalcogen‐Bond Donor Organocatalysis Bamberger, Julia Ostler, Florian Mancheño, Olga García ChemCatChem Minireviews Non‐covalent molecular interactions on the basis of halogen and chalcogen bonding represent a promising, powerful catalytic activation mode. However, these “unusual” non‐covalent interactions are typically employed in the solid state and scarcely exploited in catalysis. In recent years, an increased interest in halogen and chalcogen bonding has been awaken, as they provide profound characteristics that make them an appealing alternative to the well‐explored hydrogen bonding. Being particularly relevant in the binding of “soft” substrates, the similar strength to hydrogen bonding interactions and its higher directionality allows for solution‐phase applications with halogen and chalcogen bonding as the key interaction. In this mini‐review, the special features, state‐of‐the‐art and key examples of these so‐called σ‐hole interactions in the field of organocatalysis are presented. John Wiley and Sons Inc. 2019-08-30 2019-11-07 /pmc/articles/PMC6919929/ /pubmed/31894187 http://dx.doi.org/10.1002/cctc.201901215 Text en © 2019 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 Minireviews
Bamberger, Julia
Ostler, Florian
Mancheño, Olga García
Frontiers in Halogen and Chalcogen‐Bond Donor Organocatalysis
title Frontiers in Halogen and Chalcogen‐Bond Donor Organocatalysis
title_full Frontiers in Halogen and Chalcogen‐Bond Donor Organocatalysis
title_fullStr Frontiers in Halogen and Chalcogen‐Bond Donor Organocatalysis
title_full_unstemmed Frontiers in Halogen and Chalcogen‐Bond Donor Organocatalysis
title_short Frontiers in Halogen and Chalcogen‐Bond Donor Organocatalysis
title_sort frontiers in halogen and chalcogen‐bond donor organocatalysis
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6919929/
https://www.ncbi.nlm.nih.gov/pubmed/31894187
http://dx.doi.org/10.1002/cctc.201901215
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