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Table 5 Alkene epoxidation with different H2O2 content

From: Glutaraldehyde-crosslinked Rhizopus oryzae whole cells show improved catalytic performance in alkene epoxidation

Entrya

Substrate

Content of H2O2 (mmol)

Initial reaction rateb (mmol/L/h)

Conversion (%)c

yield (%)c

1

1

93.99 ± 6.41

57.21 ± 0.82

49.17 ± 1.22

2

2.5

121.87 ± 9.26

91.99 ± 0.04

74.5 ± 1.99

3

5

176.15 ± 1.78

99.89 ± 0.08

91.37 ± 1.94

4

7.5

232.88 ± 1.76

99.65 ± 0.07

92.04 ± 3.08

5

10

239.81 ± 5.23

99.73 ± 0.11

86.75 ± 0.24

6

15

–

74.53 ± 5.6

67.96 ± 8.45

7

30

–

20.56 ± 7.12

12.8 ± 1.99

8

45

–

6.37 ± 5.28

6.25 ± 0.89

9

1

4.22 ± 0.09

22.17 ± 0.35

8.13 ± 0.54

10

2.5

4.35 ± 0.91

49.15 ± 0.36

36.68 ± 1.97

11

5

5.29 ± 0.05

62.11 ± 0.33

45.77 ± 2.3

12

7.5

5.79 ± 0.19

66.44 ± 0.91

56.24 ± 3.95

13

10

6.34 ± 2.35

63.95 ± 1.41

56.3 ± 0.59

14

1

6.31 ± 0.3

15.91 ± 0.88

14.25 ± 2.1

15

2.5

6.62 ± 1.18

68.82 ± 0.42

50.02 ± 3.94

16

5

9.23 ± 2.65

83.53 ± 0.42

65.35 ± 4.49

17

7.5

9.59 ± 0.19

89.02 ± 0.64

76.56 ± 1.22

18

10

9.72 ± 1.39

84.79 ± 1.15

70.38 ± 1.69

  1. aA mixture of alkene (1 mmol), octanoic acid (1 mmol), 30% (v/v) H2O2 (1−10 mmol), and Na3C6H5O7 (3.5 mmol) in toluene (1.5 mL) was shaken at 180 rpm and 30 °C
  2. bThe value obtained at 30 min for pinene and 60 min for octene and styrene, respectively
  3. cThe value obtained at 6 h for pinene, 50 h for octene and 58 h for styrene, respectively