Issue 8, 2013

A rotaxane host system containing integrated triazole C–H hydrogen bond donors for anion recognition

Abstract

Two rotaxanes incorporating a 3,5-bis(triazole)-pyridinium axle component have been prepared using either an anion templated amide condensation or ring closing metathesis (RCM) clipping strategy. The respective yields of interlocked receptor were found to be significantly higher when the RCM clipping synthetic route was used. Proton NMR titration experiments in competitive 1 : 1 CDCl3–CD3OD solvent media reveal that the rotaxane prepared by the clipping procedure is selective for halide anions over larger, more basic oxoanions. Interestingly, the interlocked host displays an unusual preference for bromide over other halide anions.

Graphical abstract: A rotaxane host system containing integrated triazole C–H hydrogen bond donors for anion recognition

Supplementary files

Article information

Article type
Paper
Submitted
16 נוב 2012
Accepted
18 דצמ 2012
First published
11 ינו 2013

Org. Biomol. Chem., 2013,11, 1326-1333

A rotaxane host system containing integrated triazole C–H hydrogen bond donors for anion recognition

N. G. White and P. D. Beer, Org. Biomol. Chem., 2013, 11, 1326 DOI: 10.1039/C2OB27229F

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