Fiche publication
Date publication
octobre 2016
Journal
Chemical science
Auteurs
Membres identifiés du Cancéropôle Est :
Dr DELSUC Marc-André
Tous les auteurs :
Maugeri L, Asencio-Hernández J, Lébl T, Cordes DB, Slawin AMZ, Delsuc MA, Philp D
Lien Pubmed
Résumé
The halogen bond (XB) donor properties of neutral 1,4-diaryl-5-iodo-1,2,3-triazoles are explored using a combination of computational and experimental results and are shown to be competitive in halogen bonding efficiency with the classic pentafluoroiodobenzene XB donor. The SNAr reactivity of these donors permits the facile assembly of an iodotriazole functionalised with a 3-oxypyridine XB acceptor, thus generating a molecular scaffold capable of undergoing dimerisation through the formation of two halogen bonds. The formation of this halogen-bonded dimer is demonstrated by (1)H and DOSY NMR experiments and a plausible structure generated using DFT calculations.
Référence
Chem Sci. 2016 Oct;7(10):6422-6428
