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. Author manuscript; available in PMC: 2021 Apr 19.
Published in final edited form as: Nat Chem. 2020 Oct 19;12(12):1123–1130. doi: 10.1038/s41557-020-00554-5

Fig. 2.

Fig. 2.

Panel of flavylium heptamethine dyes and their photophysical properties. a) Heterocycle structures and absorption wavelength maxima visualized graphically on the electromagnetic spectrum. b) Absorption and c) Emission profiles (ex. 885 nm) of selected polymethine dyes. d) Hammett plot relating σm substituent constants (ref. 50) to absorption and emission wavelengths of dyes 1–6 and 9–11. e) Brightness (defined as ελ×ΦF) of the heptamethine derivatives at relevant excitation wavelengths (λ = 785 nm (dark grey), λ = 980 nm (light grey), and λ = 1064 nm (white). Error bars represent the propagated error from standard deviations in ε and ΦF measurements.