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Table 3 The 1H NMR data for the H2L Schiff base and its complexes

From: Spectroscopic, docking, antiproliferative, and anticancer activity of novel metal derivatives of phenylacetohydrazide Schiff base on different human cancer cell lines

Compound

1H NMR data, ppm

H2L

12.51 (s, 1H, OHketo), 11.85, 11.35 (s, 2H, OHenol), 10.00 (s, 1H, NH), 9.22 (s, 1H, CH=Nketo), 8.91 (s, 1H, CH=Nenol), 7.18–8. 25 (m, 10H, aromatic), 4.00 (s, 2H, CH2keto), 3.62 (s, 2H, CH2enol)

[Zn2(HL)2](CH3COO)2

9.43 (s, 2H, CH=N), 8.03–6.65 (m, 22Haromatic), 3.62 (d, 2H, CH2), 3.56 (d, 2H, CH2), 1.87 (s, 6H, 2CH3)

[Cd2(HL)2](CH3COO)2

9.27 (s, 2H, CH=N), 7.89–6.50(m, 22Haromatic), 3.66 (s, 4H, 2CH2), 1.85 (s, 6H, 2CH3)

[Pt(H2L)Cl2]. 2.5H2O

12.89 (s, 1H, OH), 10.00 (s, 1H, OH), 9.51 (s, 1 H, CH=N), 8.65–7.25 (m, 11Haromatic), 3.95 (s, 2H, CH2)