Table 1 The effects of various reaction conditions on the oxidative cleavage of coumarin-3-carboxylic acid with A-CQDs/W.

From: Pseudohomogeneous metallic catalyst based on tungstate-decorated amphiphilic carbon quantum dots for selective oxidative scission of alkenes to aldehyde

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Entry

Catalyst

PTC (mmol)

Solvent

H2O2/Substrate (mmol/mmol)

T (°C)

Conversion (%)a

Yield (%)b

1

H2O

3/1

90

Trace

Trace

2

Na2WO4 (0.02 mmol)

H2O

3/1

90

Trace

Trace

3

A-CQDs/W (1 mol%)

H2O

0

90

Trace

Trace

4

A-CQDs (1 mg)

H2O

3/1

90

73

61

5

A-CQDs (10 mg)

 

H2O

3/1

90

75

63

6

A-CQDs/W (0.25 mol%)

H2O

3/1

90

79

69

7

A-CQDs/W (0.5 mol%)

H2O

3/1

90

88

75

8

A-CQDs/W (1 mol%)

H2O

3/1

90

95

86

9

A-CQDs/W (1.5 mol%)

H2O

3/1

90

86

73

10

A-CQDs/W (1 mol%)

0.1

H2O

3/1

90

87

73

11

A-CQDs/W (1 mol%)

H2O

2/1

90

79

68

12

A-CQDs/W (1 mol%)

H2O

4/1

90

71

62

13

A-CQDs/W (1 mol%)

H2O/EtOH

3/1

90

90

83

14

A-CQDs/W (1 mol%)

H2O/Toluene

3/1

90

88

57

15

A-CQDs/W (1 mol%)

H2O/CH3CN

3/1

90

71

20

16

A-CQDs/W (1 mol%)

Pure EtOH

3/1

90

80

61

17

A-CQDs/W (1 mol%)

H2O

3/1

RT

trace

trace

18

A-CQDs/W (1 mol%)

H2O

3/1

50

21

17

19

A-CQDs/W (1 mol%)

H2O

3/1

70

84

67

  1. Reaction conditions: Coumarin-3-carboxylic acid (1 mmol), H2O (1.5 mL), 90 °C, 3 h.
  2. aConversions were calculated based on initial mmol of coumarin-3-carboxylic acid.
  3. bIsolated Yields.