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. 2020 Oct 12;11(44):12212–12220. doi: 10.1039/d0sc04751a

Fig. 2. (a) Nanosecond time-resolved transient difference absorption spectra of Ir-Rho-G2 in deaerated CH3CN; λex = 355 nm. The inset shows the decay trace of the signal at 575 nm. (b) Singlet oxygen emission spectra of Ir-Rho-G2 and rose bengal in CH3CN with an excitation wavelength of 514.5 nm.

Fig. 2