Amide-based tripodal receptors for selective anion recognition
✍ Scribed by Gülşen Öztürk; Mehmet Çolak; Mahmut Toğrul
- Publisher
- Springer Netherlands
- Year
- 2010
- Tongue
- English
- Weight
- 342 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0923-0750
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Anion recognition properties of D-ribose-based receptors aand b-1 were measured by 1 H NMR in CDCl 3 and MeCN-d 3 . Receptor b-1 showed effective binding with anions by cooperative hydrogen bonds of cisdiol. The anomeric isomer a-1 is a less effective anion receptor which has similar cis-diol as a r
## Abstract magnified image Neutral classes of amide‐based macrocycle have been synthesized and the anion binding abilities are assessed by UV‐vis titration and ^1^H nmr experiments. Results indicate that higher anion binding abilities are observed for H~2~PO~4~^−^, F^−^ and AcO^−^, but almost no
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