Fig. 3: Catalytic activity and substrate scope. | Nature Communications

Fig. 3: Catalytic activity and substrate scope.

From: Bio-inspired asymmetric Zn-N2O2 single-atom catalysts via natural skeleton for efficient N-alkylation of nitroarenes with alcohols

Fig. 3: Catalytic activity and substrate scope.

a Kinetic curves and b comparison of TOFs for various commercial and reported catalysts in the model reaction of nitrobenzene and benzyl alcohol. c1c5 Substrate applicability: a Reaction conditions: nitro compounds (0.2 mmol), alcohols (0.6 mmol), KOH (0.54 mmol), petroleum ether (6 mL), Zn/CS (0.09 mol% [Zn], Zn: PhNO2), reacted at 120 °C for 21 h. b Reaction time was 36 h. c Toluene (4 mL), Zn/CS (0.17 mol% [Zn]), reacted at 130 °C for 24 h. d Zn/CS (0.17 mol% [Zn]), reacted at 130 °C for 36 h. e Reacted at 120 °C for 48 h. f Zn/CS (0.17 mol% [Zn]), reacted at 130 °C for 48 h. g Toluene (4 mL), Zn/CS (0.17 mol% [Zn]), reacted at 130 °C for 36 h. h Toluene (4 mL), Zn/CS (0.17 mol% [Zn]), reacted at 130 °C for 48 h. i Zn/CS (0.3 mol% [Zn]), reacted at 130 °C for 21 h. Yields of the product were isolated yield, and the corresponding NMR spectra were shown in the supporting information.

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