Modulating Chalcogen Bonding and Halogen Bonding Sigma‐Hole Donor Atom Potency and Selectivity for Halide Anion Recognition

A series of acyclic anion receptors containing chalcogen bond (ChB) and halogen bond (XB) donors integrated into a neutral 3,5‐bis‐triazole pyridine scaffold are described, in which systematic variation of the electronic‐withdrawing nature of the aryl substituents reveal a dramatic modulation in sig...

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Detalles Bibliográficos
Autores principales: Docker, Andrew, Guthrie, Charles H., Kuhn, Heike, Beer, Paul D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518858/
https://www.ncbi.nlm.nih.gov/pubmed/34297867
http://dx.doi.org/10.1002/anie.202108591

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8518858/
https://www.ncbi.nlm.nih.gov/pubmed/34297867
http://dx.doi.org/10.1002/anie.202108591

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