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. 2019 Nov 8;25(70):16088–16098. doi: 10.1002/chem.201903657

Figure 5.

Figure 5

Spectrofluorimetric titration of 8 b with ct DNA (A, c L=10 μm, c DNA=1.49 mm; c DNA in base pairs) in BPE buffer (c Na+=16 mm, pH 7.0; with 5 % v/v DMSO), 22AG (B, c L=5 μm, c 22AG=285 μm; c 22AG in oligonucleotide) in K‐phosphate buffer (c K+=73 mm, pH 7.0; with 5 % v/v DMSO) and PSS (C, c L=10 μm, c PSS=195 μm) in BPE buffer (c Na+=16 mm, pH 7.0; with 2.5 % v/v DMSO); λ ex=515 nm. Red: Spectra of the pure ligand solutions; blue: spectra at the end of the titrations. The arrows indicate the changes in emission intensity upon addition of the host molecule. Insets: Plot of the relative fluorescence intensity I/I 0 (corrected with regard to the change of the absorption at the excitation wavelength) versus c DNA/c L or c PSS/c L. Inset pictures in A: Fluorescence colors of 8 b in the absence and in the presence of ct DNA; λ ex=366 nm. The contrast and brightness were enhanced by 30 % without changing the true colors (cf. Figure S5).