Fig. 7: Photocatalyzed reduction of dinitro substrates using different reductants. | Nature Communications

Fig. 7: Photocatalyzed reduction of dinitro substrates using different reductants.

From: Modifying electron injection kinetics for selective photoreduction of nitroarenes into cyclic and asymmetric azo compounds

Fig. 7

Isolated yields are reported. Standard conditions for cyclic azo product conversion were as follows: 1.0 mol% HF (0.50 μmol), substrate (0.05 mmol) and tripropylamine (1.20 mmol) under light irradiation for 10 h. Standard conditions for diamino product conversion were as follows: 1.0 mol % of HF (0.50 μmol), substrate (0.05 mmol) and Na2S (1.20 mmol) under light irradiation for 2 h.

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