Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 27th March 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 77, 2018
Previous Article Next Article

Triazole-bearing calixpyrroles: strong halide binding affinities through multiple N–H and C–H hydrogen bonds

Author affiliations

Abstract

Triazole-bearing calixpyrroles (TCPs) were synthesized as artificial anion binding receptors. The additional C–H⋯X hydrogen bonding interaction induced strong binding affinity towards halide ions. Using this strong binding affinity, Cl was successfully extracted from the aqueous to organic phase.

Graphical abstract: Triazole-bearing calixpyrroles: strong halide binding affinities through multiple N–H and C–H hydrogen bonds

Back to tab navigation

Supplementary files

Publication details

The article was received on 06 Aug 2018, accepted on 03 Sep 2018 and first published on 04 Sep 2018


Article type: Communication
DOI: 10.1039/C8CC06385K
Citation: Chem. Commun., 2018,54, 10863-10865

  •   Request permissions

    Triazole-bearing calixpyrroles: strong halide binding affinities through multiple N–H and C–H hydrogen bonds

    H. Kim, K. Hong, J. H. Lee, P. Kang, M. Choi and W. Jang, Chem. Commun., 2018, 54, 10863
    DOI: 10.1039/C8CC06385K

Search articles by author

Spotlight

Advertisements