Abstract
Modular diboronic acid receptors R-1 and S-1 were synthesized and found to be selective fluorescent chemosensors for saccharides. The fluorescence intensity of R-1 and S-1 increased on addition of saccharides due to the formation of intramolecular 1:1 cyclic complexes. In general, R-1 has higher binding constants and produces a higher fluorescent response with saccharides than S-1. The fluorescence intensity of receptors R-1 and S-1 increased on addition of saccharides due to the formation of intramolecular 1:1 cyclic complexes. In general, R-1 has higher binding constants and produces a higher fluorescent response with saccharides than S-1.
Original language | English |
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Pages (from-to) | 1223-1229 |
Number of pages | 7 |
Journal | European Journal of Organic Chemistry |
Volume | 2012 |
Issue number | 6 |
DOIs | |
Publication status | Published - Feb 2012 |
Keywords
- sensors
- fluorescence
- boronic acid
- chirality
- receptors
- saccharides