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. 2023 Aug 2;19:1155–1160. doi: 10.3762/bjoc.19.83

Table 2.

Data of absorption and fluorescence spectra of compounds 4ai, 9a, and 10a.a

Compound UV–vis Photoluminescence
maxλabs, nm ε, 103,
M–1·cm–1
(λ, nm)
λex, nm maxλem, nm Stokes shift,
nm; eV
Quantum yield Φflb

4a 260; 302 30.3 ± 0.7
(260)
300; 320 419 117; 1.15 0.22 ± 0.01
4b 260; 302 38.3 ± 0.7
(260)
300; 320 428 126; 1.21 0.23 ± 0.01
4c 262; 302 22.2 ± 0.8
(262)
300; 320 409 107; 1.07 0.16 ± 0.01
4d 260; 301 35.1 ± 0.9
(260)
300; 320 414 113; 1.12 0.15 ± 0.01
4e 262; 301 22.7 ± 0.9
(262)
300; 320 416 115; 1.14 0.18 ± 0.01
4f 260; 302 27.6 ± 0.8
(260)
300; 320 415 113; 1.12 0.20 ± 0.01
4g 261; 300 41.5 ± 0.9
(261)
300; 320 411 111; 1.12 0.20 ± 0.01
4h 265; 305 32.4 ± 1.0
(265)
300; 310 421 116; 1.12 0.23 ± 0.01
4i 263; 301 26.2 ± 0.8
(263)
300; 310 431 130; 1.24 0.09 ± 0.00
9a 259; 303 40.0 ± 0.9
(261)
305 433 130; 1.23 0.19 ± 0.01
10a 261; 288 34.9 ± 0.5
(259)
290 440 152; 1.49 0.11 ± 0.01

aIn EtOH solution, c = 1.0·10−5 mol·L−1. bQuantum yield determined relative to quinine sulfate standard in 0.5 M H2SO4f = 0.546).