Skip to main content
. 2019 Mar 7;20(7):886–890. doi: 10.1002/cbic.201800711

Table 1.

Photophysical properties of 4,5‐dihydropyridazine products.

graphic file with name CBIC-20-886-g006.jpg
λ abs/λ em [a] Stokes Φ fl [b] Intensity
R1 R2 [nm] shift [%] increase
[nm]
graphic file with name CBIC-20-886-g007.jpg graphic file with name CBIC-20-886-g008.jpg 545/628 83 0.55 13‐fold
graphic file with name CBIC-20-886-g009.jpg graphic file with name CBIC-20-886-g010.jpg 295/–
graphic file with name CBIC-20-886-g011.jpg graphic file with name CBIC-20-886-g012.jpg 546/626 80 0.52 18‐fold
graphic file with name CBIC-20-886-g013.jpg graphic file with name CBIC-20-886-g014.jpg 546/626 80 0.45 10‐fold
graphic file with name CBIC-20-886-g015.jpg graphic file with name CBIC-20-886-g016.jpg 566/643 77 0.21 threefold
graphic file with name CBIC-20-886-g017.jpg graphic file with name CBIC-20-886-g018.jpg 549/626 77 0.47 12‐fold

[a] Absorption and emission maxima were measured in CH3CN/H2O 1:1. [b] Relative fluorescence quantum yields were determined by using Nile Red in methanol as standard.