. 2022 Jul 12;88(10):6364–6373. doi: 10.1021/acs.joc.2c01137

Table 3. Average ¹H NMR Yields Obtained in the ATRA Reaction and Relevant Redox Potentials of the Photocatalysts^a.

photocatalyst	E_ox (V)	E_ox^* (V)	¹H NMR yield (%)
[Ru(bpy)₃](PF₆)₂	1.42	–0.86	64 ± 3(80)^b
4CzIPN	1.51	–1.09	10 ± 1
pDTCz-DPmS	1.57	–1.44	16 ± 2

Redox potentials reported vs SCE and in DCM unless otherwise noted. Values in parentheses indicate the ¹H NMR yield obtained in the literature. Reaction conditions followed are those shown in Figure 3 (refer to SI for further details).

Value taken from ref (30) using 455 nm irradiation and MeCN as the solvent.

Table 3. Average 1H NMR Yields Obtained in the ATRA Reaction and Relevant Redox Potentials of the Photocatalystsa.

Table 3. Average ¹H NMR Yields Obtained in the ATRA Reaction and Relevant Redox Potentials of the Photocatalysts^a.