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. 2022 Sep 30;12:16395. doi: 10.1038/s41598-022-20699-2

Table 5.

Comparison of the activity of B-V-PIL/W for one-pot tandem alcohol oxidation/Knoevenagel condensation reaction with some reported catalysts.

Entry Catalyst Time (h) Catalyst amount Condition Yield (%) Ref.
1 B-V-PIL/W 1.5 40 mg H2O2/H2O:EtOH (2:1)/70 °C 94 This work
2 NH2-UiO-66(Zr) 40 20 mg Trifluorotoluene: CH3CN/O2/light irradiation 4.6 39
3 NH2-MIL-101(Fe) 40 20 mg Trifluorotoluene: CH3CN/O2/light irradiation 72 39
4 Ti-MOF-NH2 48 100 mg p-Xylene/UV irradiation 32 40
5 Zr-MOF-NH2 48 100 mg p-Xylene/UV irradiation 91 40
6 UoB-2a 1.5 2 mol% Alcohol oxidation in solvent-free condition/TBHP/Knoevenagel condensation in EtOH 94 38
7 Cu3TATAT-3b 12 8 mol% CH3CN/O2/75 °C 95 41
8 Fe3O4@SiO2@PEI@Ru(OH)X 22 100 mg O2/110 °C for alcohol oxidation step/Knoevenagel condensation step at r.t. 90.2 42
9 NH2-MIL-125(Ti) 40 20 mg Trifluorotoluene: CH3CN/O2/light irradiation 3.3 39
10 MNP@PIL/Wc 6d 4 mol% Alcohol oxidation in H2O2, H2O, 90 °C/Knoevenagel condensation step at r.t. 94 43

aNi‐based metal–organic framework.

bH6TATAT = 5,5,5-(1,3,5-Triazine-2,4,6 triyl)tris(azanediyl)triisophtalate.

cTungstate-loaded triazine-based magnetic Poly(Bis-imidazolium ionic liquid).

dOxidation step at 90 °C (4 h) + Knoevenagel condensation step at room temperature (2 h).