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Table 1 Physical data for organotin(IV) derivatives of 3,4-methylenedioxy-6-nitrophenylpropenoic acid (L1), 3,4-methylenedioxyphenylpropenoic acid (L2) and 2,3-methylenedioxybenzoic acid (L3)

From: ATR-FTIR spectroscopy detects alterations induced by organotin(IV) carboxylates in MCF-7 cells at sub-cytotoxic/-genotoxic concentrations

Compound no.

General Formula

Molecular Formula

MolecularWeight

M.P. (°C)

Yield (%)

Elemental Analysis % Calculated (Found)

      

C

H

N

Ligand 1

(L1)

C10H7O6N

237

278

80

50.63 (50.45)

2.95 (2.80)

5.91 (5.87)

1

Bu3Sn(L1)

C22H33O6NSn

527

143–146

89

50.09 (50.23)

6.26 (6.30)

2.65 (2.70)

2

BuSnCl(L1)2

C24H21O12N2SnCl

684.5

142–145

70

42.07 (42.24)

3.07 (3.15)

4.09 (4.04)

3

Ph3Sn(L1)

C28H21O6NSn

587

207–210

80

57.24 (54.43)

3.58 (3.60)

2.38 (2.45)

4

Bu2Sn(L1)2

C28H30O12N2Sn

706

196–199

73

47.60 (47.74)

4.25 (4.16)

3.97 (4.01)

Ligand 2

(L2)

C10H8O4

192

238

90

62.50 (62.30)

4.17 (4.23)

-

5

Et2Sn(L2)2

C24H24O8Sn

560

177–179

81

51.43 (51.39)

4.28 (4.24)

-

6

Me2Sn(L2)2

C22H20O8Sn

532

247–248

73

49.62 (49.98)

3.76 (3.70)

-

7

Ph3Sn(L2)

C28H22O4Sn

542

180–181

84

61.99 (62.25)

4.06 (3.98)

-

8

Bu2Sn(L2)2

C28H32O8Sn

616

134–136

68

54.54 (54.68)

5.19 (5.08)

-

Ligand 3

(L3)

C8H6O4

166

165

65

57.83 (57.72)

3.61 (3.70)

-

9

Bu2Sn(L3)2

C24H28O8Sn

564

180–184

78

51.06 (51.20)

4.96 (5.01)

-

10

BuSn(L3)3

C28H24O12Sn

672

220–222

74

50.0 (50.10)

3.57 (3.58)

-

11

Me3Sn(L3)

C11H14O4Sn

330

150–151

68

40.0 (41.8)

4.24 (4.01)

-

12

Et2Sn(L3)2

C20H20O8Sn

508

210–215

80

47.24 (47.23)

3.94 (3.81)

-