Table 7.
Photophysical properties of 1H-pyridines 8.
| Compound | R1 | R2 | λmax,abs [nm]a (ε [L·mol−1·cm−1]) | λmax,em [nm]b (Φf)c | Stokes shift Δ ν̃ [cm−1] |
| 8a | Ph | Ph | 274 (20300), 324 (20100), 417 (7700) | 557 (<0.01) | 6000 |
| 8b | p-MeOC6H4 | Ph | 261 (16200), 307 (31300), 419 (11000) | 565 (<0.01) | 6200 |
aRecorded in dichloromethane, T = 293 K, c(8) = 10−6 M; brecorded in dichloromethane, T = 293 K, c(8) = 10−7 M (λexc = 420 nm); cfluorescence quantum yields were determined relative to coumarin153 (Φf = 0.54) as a standard in ethanol [58].