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. Author manuscript; available in PMC: 2014 Feb 20.
Published in final edited form as: Bioconjug Chem. 2013 Jan 16;24(2):215–223. doi: 10.1021/bc3005073

Table 4.

Photophysical properties of functionalized merocyanines.

dye name % yield
(from enol
ether)
solvent QYa εb QY × ε λmax (nm)
absorption
λmax (nm)
emission
mero60 21 DMSO 0.37 126000 46620 593 620
MeOH 0.02 133000 2660 591 614
BuOH 0.16 132000 21120 593 616
H2O <0.01 106000 11 595 608
mero61 26 DMSO 0.37 100000 37035 570 595
MeOH 0.07 167000 11690 565 588
BuOH 0.17 146000 24820 570 592
H2O 0.03 131000 3930 565 586
mero62 21 DMSO 0.20 135000 27000 597 615
MeOH 0.09 140000 12600 590 608
BuOH 0.18 139000 25020 594 614
H2O 0.10 36000 3600 585 608
mero87 33 DMSO 0.34 140000 47600 592 620
MeOH 0.06 107000 6420 588 620
BuOH 0.21 111000 23310 591 622
H2O 0.02 81000 1620 592 616
mero60-BME - DMSO 0.66 124000 81870 595 618
mero61-BME - DMSO 0.55 116000 63800 570 594
mero62-BME - DMSO 0.41 142000 58220 596 614
mero87-BME - DMSO 0.27 105000 28350 590 620
I-SOc - BuOH 0.54 134000 72000 587 618
OcOH 0.98 125000 123000 587 617
- MeOH 0.08 143000 11440 586 615
a

Quantum yield of fluorescence, error ± 10%.

b

Molar extinction coefficient, error ± 10%.

c

Values for I-SO as reported in ref.9 are included for comparison (see Discussion and Conclusions).