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. 2019 Aug 6;10(39):9028–9037. doi: 10.1039/c9sc02287b

Table 1. Photophysical properties of ASiPa and NIR-ASiPa analogues.

Inline graphic
R 1 (alkyl) R 2 (EWG) λ abs a /nm λ em b /nm Φ F c
ASiPa1 Me H 452 612 0.33 d
ASiPa2 Bn H 469 623 0.34 e
ASiPa3 Propargyl H 473 628 0.25 e
NIR-ASiPa1 Me CO2Bn 669 685 0.42 f
NIR-ASiPa2 Propargyl COCH3 676 694 0.31 e
NIR-ASiPa3 Propargyl COCF3 684 707 0.27 e
NIR-ASiPa4 Propargyl SO2CF3 694 713 0.25 e
NIR-ASiPa5 Bn COCF3 684 704 0.29 e
NIR-ASiPa6 Cyclic urea 674 690 0.22 e

aMaximum absorption wavelength.

bMaximum emission wavelength in PBS (pH 7.4).

cFluorescence quantum yield.

dDetermined in methanol using fluorescein as the reference (ΦF = 0.95 in 0.1 M NaOH).18

eDetermined in ethanol using rhodamine 101 (ΦF = 0.915 in EtOH) as the reference dye.

fDetermined in CH3CN using Nile blue (ΦF = 0.27 in ethanol) as the reference dye.