Abstract
A novel benzthiazole-based fluorescent receptor was synthesized, and its anion recognition properties were compared with those of similarly designed benzimidazole-based receptors. The selectivity of this receptor for the recognition of dihydrogen phosphate is enhanced by employing hydrogen bonding, in which cooperative polarization effect to the carbonyl group of amide linkages is lacking.
Original language | English |
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Pages (from-to) | 807-810 |
Number of pages | 4 |
Journal | Tetrahedron Letters |
Volume | 50 |
Issue number | 7 |
DOIs | |
Publication status | Published - 2009 Feb 18 |
All Science Journal Classification (ASJC) codes
- Biochemistry
- Drug Discovery
- Organic Chemistry