- Abstract:
- Neutral tetradentate halogen bond donor foldamers were synthesised and exhibit enhanced anion affinities over their hydrogen bonding analogues, displaying iodide selectivity over lighter halide, carboxylate and dihydrogen phosphate anions. A foldamer with a chiral (S)-binaphthol motif was demonstrated to distinguish between enantiomers of chiral anions.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
- Version:
- Publisher's version
- Files:
-
-
(pdf, 1.8MB)
-
- Publisher copy:
- 10.1039/c7cc00727b
-
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- Grant:
- Doctoral Training in Synthesis for Biology and Medicine (EP/L015838/1)
- Grant:
- FP7/2007–2014, ERC Advanced Grant Agreement No. 267426
- Publisher:
- Royal Society of Chemistry Publisher's website
- Journal:
- Chemical Communications Journal website
- Volume:
- 53
- Issue:
- 16
- Pages:
- 2483-2486
- Publication date:
- 2017-02-21
- DOI:
- EISSN:
-
1364-548X
- ISSN:
-
1359-7345
- Pubs id:
-
pubs:679451
- URN:
-
uri:004facf7-ceb9-46c7-a6ce-b51bd75e5003
- UUID:
-
uuid:004facf7-ceb9-46c7-a6ce-b51bd75e5003
- Local pid:
- pubs:679451
- Paper number:
- 16
- Language:
- English
- Copyright holder:
- Borissov et al.
- Copyright date:
- 2017
- Notes:
- This article is licensed under a Creative Commons Attribution 3.0 Unported Licence.
Journal article
Neutral iodotriazole foldamers as tetradentate halogen bonding anion receptors
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+ Engineering and Physical Sciences Research Council
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Agency for Science,
Technology and Research, Singapore
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+ European Research Council
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