Binding constants (Kasoc, M−1)a calculated for 3 and the sodium salts of anionic analytes in 15% water in DMSO.
| Anion | K asoc | Quench (%) | FWHM (nm) | Shift (nm) |
|---|---|---|---|---|
| F− | NDb | 5 | 119 | 0 |
| Cl− | <10 | 6 | 113 | 6 |
| Br− | <10 | 3 | 113 | 0 |
| NO3− | NR | +2 | 120 | 0 |
| HSO4− | NR | 0 | 118 | 0 |
| CH3CO2− | <100b | +7 | 115 | 12 |
| H2PO4− | 1.65 × 106 | 18 | 113 | 14 |
| H2P2O72− | 5.82 × 105 | 24 | 113 | 14 |
| HAsO42− | 3.55 × 106 | 25 | 116 | 12 |
| AMP | 1.61 × 105 | 12 | 111 | 18 |
| ADP | <100c | 9 | 117 | 6 |
| ATP | <100c | 7 | 120 | 6 |
| GlyP | 2.70 × 105 | 12 | 119 | 9 |
| MPA | 8.20 × 104 | 8 | 115 | 10 |
| PhPA | <100 | 0 | 116 | 14 |
| EMPA | <100 | +2 | 119 | 6 |
The Kasoc values were calculated based on the change in fluorescence intensity upon an incremental addition of each anion (sodium salts in water). All fitting errors were <15%. λexc = 370 nm. The association constants were calculated using non-linear least-square fitting. NR – no appreciable response was observed.
ND – not determined due to what appears to be a partial deprotonation of the sensor and the ensuing complex equilibria.
K asoc was not determined due to the biphasic nature of the isotherm.