Methanesulfonyl-polarized halogen bonding enables strong halide recognition in an arylethynyl anion receptor. Issue 13 (25th January 2019)

• Record Type: Journal Article
• Authors: Lohrman, Jessica A.; Deng, Chun-Lin; Shear, Trevor A.; Zakharov, Lev N.; Haley, Michael M.; Johnson, Darren W.
• Is Part Of: Chemical communications. Volume 55:Issue 13(2019)
• Page Start: 1919
• Page End: 1922
• Publication Date: 2019-01-25
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1039/c8cc09251f
• Languages: English
• ISSNs: 1359-7345

Abstract

Abstract : Easy-to-synthesize methanesulfonyl substituents are introduced as a way to polarize C–I halogen bond donors for reversible halide binding in competitive media. Abstract : A 3, 5-bis((2-iodophenyl)ethynyl)pyridinium scaffold was synthesized which introduces the use of methanesulfonyl withdrawing groups to polarize iodine halogen bonding units for anion binding. We investigate the capability of this receptor to bind halides in polar media, while further probing the structure–property relationship of this well-polarized yet under-explored halogen bonding system.