Abstract
We report a rotaxane based on a simple urea motif that binds Cl− selectively as a separated ion pair with H+ and reports the anion binding event through a fluorescence switch-on response. The host selectively binds Cl− over more basic anions, which deprotonate the framework, and less basic anions, which bind more weakly. The mechanical bond also imparts size selectivity to the ditopic host.
Original language | English |
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Pages (from-to) | 5315-5319 |
Number of pages | 5 |
Journal | Angewandte Chemie - International Edition |
Volume | 57 |
Issue number | 19 |
DOIs | |
Publication status | Published - 4 May 2018 |
Bibliographical note
Funding Information:M.D. thanks the University of Southampton and EPSRC (EP/ L505067/1) for financial support. S.M.G. acknowledges funding from the European Research Council (Consolidator Grant Agreement no. 724987). S.M.G. thanks the Royal Society for a Research Fellowship. L.Q. acknowledges financial support from a John A. Lamberton scholarship. The authors gratefully acknowledge support from the Royal Society (International Exchange grant). The authors thank P. Horton and G. Tizzard of the UK National Crystallography Service for assistance with the analysis of 1, 1·HBF4, and 1·HCl.
Publisher Copyright:
© 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.
Keywords
- anions
- fluorescence
- mechanical bonds
- rotaxanes
- sensors
ASJC Scopus subject areas
- Catalysis
- General Chemistry