Enhancing the enantioselective recognition and sensing of chiral anions by halogen bonding
authors Lim, JYC; Marques, I; Ferreira, L; Felix, V; Beer, PD
nationality International
journal CHEMICAL COMMUNICATIONS
keywords AMINO-ACIDS; RECEPTORS; CATALYSIS; WATER; ION; EXPLORATION; SENSORS; FIELD
abstract Chiral halogen bonding (S)-BINOL-based receptors are demonstrated to enhance the enantioselective recognition and sensing of chiral anions compared to their hydrogen bonding analogues. Computational studies attribute this behaviour to the strict linearity of halogen bonding (XB) and steric environment conferred by the XB donor groups bridged by the (S)-BINOL motif.
publisher ROYAL SOC CHEMISTRY
issn 1359-7345
year published 2016
volume 52
issue 32
beginning page 5527
ending page 5530
digital object identifier (doi) 10.1039/c6cc01701k
web of science category Chemistry, Multidisciplinary
subject category Chemistry
unique article identifier WOS:000374035800005
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journal analysis (jcr 2017):
journal impact factor 6.290
5 year journal impact factor 6.064
category normalized journal impact factor percentile 83.918
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