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Table 3 Physical and analytical data for the newly synthesized pyridinium hydrazones 2–33

From: Novel amphiphilic pyridinium ionic liquids-supported Schiff bases: ultrasound assisted synthesis, molecular docking and anticancer evaluation

Comp no

R

Y

mp °C

λmax (nm)

Fluorescence

2

C8H17

I

104–105

222, 330, 430

+

3

C9H19

I

91–93

220, 332, 432

+

4

C10H21

I

110–112

220, 332, 430

+

5

C11H23

I

82–83

220, 332, 430

+

6

C12H25

I

72–73

220, 330, 430

+

7

C14H29

I

86–88

220, 332, 430

+

8

C16H33

I

78–80

220, 332, 430

+

9

C18H37

I

98–99

220, 332, 430

+

10

C8H17

PF6

Yellow crystals

64–65

220, 330, 430

+

11

C8H17

BF4

Yellow crystals

80–82

220, 332, 430

+

12

C8H17

COOCF3

Yellow crystals

74–76

220, 332, 430

+

13

C9H19

PF6

Yellow crystals

69–70

220, 330, 428

+

14

C9H19

BF4

Yellow crystals

88–90

222, 328, 426

+

15

C9H19

COOCF3

Yellow crystals

96–98

222, 332, 424

+

16

C10H21

PF6

Yellow syrup

220, 330, 428

+

17

C10H21

BF4

Colorless syrup

220, 330, 428

+

18

C10H21

COOCF3

Yellow syrup

222, 334, 432

+

19

C11H23

PF6

Yellow syrup

220, 330, 428

+

20

C11H23

BF4

Yellow syrup

220, 330, 426

+

21

C11H23

COOCF3

Colorless syrup

222, 332, 430

+

22

C12H25

PF6

Yellow syrup

222, 330, 430

+

23

C12H25

BF4

Yellow syrup

218, 332, 430

+

24

C12H25

COOCF3

Colorless syrup

220, 336, 428

+

25

C14H29

PF6

Yellow syrup

220, 332, 428

+

26

C14H29

BF4

Yellow syrup

220, 336, 430

+

27

C14H29

COOCF3

Colorless syrup

220, 330, 428

+

28

C16H33

PF6

Yellow syrup

220, 338, 432

+

29

C16H33

BF4

Yellow syrup

218, 332, 428

+

30

C16H33

COOCF3

Colorless syrup

220, 334, 430

+

31

C18H37

PF6

Yellow syrup

220, 330, 428

+

32

C18H37

BF4

Yellow syrup

220, 330, 432

+

33

C18H37

COOCF3

Colorless syrup

220, 332, 430

+

figure 1