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. 2022 Jun 9;10:880257. doi: 10.3389/fchem.2022.880257

TABLE 1.

Optimization table of photocatalyst for the synthesis of 4a a .

graphic file with name FCHEM_fchem-2022-880257_wc_tfx1.jpg
Entry Photocatalyst Light source Solvent (3 ml) Time (min) Isolated yields (%)
1 White light (18 W) H2O/EtOH (2:1) 15 57
2 Na2 eosin Y (0.2 mol%) White light (18 W) H2O/EtOH (2:1) 5 78
3 Na 2 eosin Y (0.5 mol%) White light (18 W) H 2 O/EtOH (2:1) 5 93
4 Na2 eosin Y (1 mol%) White light (18 W) H2O/EtOH (2:1) 5 93
5 Erythrosin B (0.5 mol%) White light (18 W) H2O/EtOH (2:1) 5 51
6 Phenanthrenequinone (0.5 mol%) White light (18 W) H2O/EtOH (2:1) 5 53
7 Rhodamine B (0.5 mol%) White light (18 W) H2O/EtOH (2:1) 5 72
8 Acenaphthenequinone (0.5 mol%) White light (18 W) H2O/EtOH (2:1) 5 57
9 Riboflavin (0.5 mol%) White light (18 W) H2O/EtOH (2:1) 5 64
10 9H-xanthen-9-one (0.5 mol%) White light (18 W) H2O/EtOH (2:1) 5 60
11 Fluorescein (0.5 mol%) White light (18 W) H2O/EtOH (2:1) 5 77
12 Rose bengal (0.5 mol%) White light (18 W) H2O/EtOH (2:1) 5 68
a

Reaction conditions: benzaldehyde (1 mmol), malononitrile (1 mmol), resorcinol (1 mmol) in H2O/EtOH (2:1) (3 ml), white LED (18 W), and various photocatalysts at rt. Bold values provides optimal conditions for reaction.