TABLE 2.
Compound | λabs (nm) | λema (nm) | Φfb |
---|---|---|---|
1a | 631 | 647 | 0.70 |
1b | 630 | 647 | 0.72 |
1c | 629 | 648 | 0.70 |
1d | 632 | 651 | 0.65 |
2a | 640 | 658 | 0.70 |
2b | 638 | 657 | 0.74 |
2c | 636 | 659 | 0.67 |
2d | 641 | 662 | 0.65 |
2e | 650 | 674 | 0.26 |
Symmtrical dyes 1a–d and rotaxanes 2a–e were excited at 580 nm and emission was monitored in the 600–750 nm region for estimating Φf.
Fluorescence quantum yields (error limit ± 5 %) were determined for using 4,4-[bis(N,N-dimethylamino)phenyl] squaraine dye as the standard (Φf = 0.70 in CHCl3) Molar absorptivities were typical of squaraine dyes 1a–d having log ε = 5.4, squaraine rotaxanes 2a–e having log ε = 5.6.