Table 2.
|
4T‐PBI |
5T‐PBI [16] |
6T‐PBI |
7T‐PBI |
---|---|---|---|---|
λ abs,max [a] [nm] |
533 |
531 |
531 |
529 |
ϵ max [a] [103 M−1 cm−1] |
67.5 |
64.8 |
67.2 |
69.2 |
λ abs,max [b] [nm] |
522 |
519 |
519 |
564 |
λ em,max [b,c] [nm] |
530 |
523 |
533 |
527 |
λ em,max [b,d] [nm] |
530 |
523 |
527 |
527 |
[b] [cm−1] |
218 |
329 |
220 |
221 |
Φ fl [b], [e] [%] |
<1.0 |
<1.0 |
<1.0 |
<1.0 |
[a] CH2Cl2, c 0=10−5 M. [b] Cyclohexane, c 0=10−7 M. [c] λ ex=350 nm. [d] λ ex=480 nm. [e] The fluorescence quantum yields of the PBI subunit were measured relative to N,N′‐bis(2,6‐diisopropylphenyl)‐1,6,7,12‐tetraphenoxy‐perylene‐3,4 : 9,10‐bis(dicarboximide) as a reference [27] at four different excitation wavelengths in the spectral region of the PBI subunit.