Research Article

Synthesis of Pyrazolone Derivatives and Their Nanometer Ag(I) Complexes and Physicochemical, DNA Binding, Antitumor, and Theoretical Implementations

Table 1

Analytical and physical data for Ag(I)-pyrazolone (HL1–4) complexes.

Compounds (empirical formula, calcd./found)Λm−1·cm2·mol−1)ColorElemental analysis (%) calcd. (found)
CHNM

(1) HL1(C9H9N5O) (203.20)Red53.20 (53.18)4.46 (4.46)34.47 (34.44)
(2) [Ag(HL1)2](NO3) (576.27)57.31Brown37.52 (37.51)3.15 (3.16)26.74 (26.72)18.72 (18.72)
(3) HL2(C9H8N5OCl) 237.64/239Red45.49 (45.50)3.39 (3.41)29.47 (29.45)
(4) [Ag(HL2)2](NO3) 645.15/647.6655.21Reddish brown33.51 (33.52)2.50 (2.50)23.88 (23.89)6.72 (16.71)
(5) HL3(C10H11N5O) 217.23/218Faint brown55.29 (55.31)5.10 (5.11)32.24 (32.25)
(6) [Ag(HL3)2](NO3) 2H2O 640.36/60551.06Brown37.51 (37.50)4.09 (4.11)24.06 (24.10)6.84 (16.86)
(7) HL4(C9H8N6O3) (248.20)Faint brown43.55 (43.55)32.49 (32.47)33.86 (33.85)
(8) [Ag(HL4)2](NO3) 666.27/665.2256.12Deep brown32.45 (32.43)2.42 (2.41)27.33 (27.35)6.19 (16.20)