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Benzaldehyde thiosemicarbazone complexes of platinum: Syntheses, structures and cytotoxic properties

Reaction of 4-R-benzaldehyde thiosemicarbazones (H2L-R) with [Pt(PPh3)2Cl2] and K2[PtCl4] afforded the [Pt(PPh3)(L-R)] and [Pt(HL-R)2] complexes, respectively, which have shown remarkable cytotoxicity towards HL-60 and U-937 cell lines. [Display omitted] ► Mixed-ligand complexes of Pt of benzaldehyd...

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Bibliographic Details
Published in:Polyhedron 2012-09, Vol.45 (1), p.177-184
Main Authors: Halder, Sarmistha, Paul, Piyali, Peng, Shie-Ming, Lee, Gene-Hsiang, Mukherjee, Asama, Dutta, Sushanta, Sanyal, Utpal, Bhattacharya, Samaresh
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Language:English
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Summary:Reaction of 4-R-benzaldehyde thiosemicarbazones (H2L-R) with [Pt(PPh3)2Cl2] and K2[PtCl4] afforded the [Pt(PPh3)(L-R)] and [Pt(HL-R)2] complexes, respectively, which have shown remarkable cytotoxicity towards HL-60 and U-937 cell lines. [Display omitted] ► Mixed-ligand complexes of Pt of benzaldehyde thiosemicarbazones have been prepared. ► The thiosemicarbazones are C,N,S-coordinated to Pt in these complexes. ► Bis-thiosemicarbazone complexes of Pt have also been synthesized. ► Complexes of both types show remarkable cytotoxicity. The reaction of 4-R-benzaldehyde thiosemicarbazones (denoted in general as H2L-R, where H2 stands for the two dissociable protons and R (R=OCH3, CH3, H, Cl and NO2) for the substituent on the phenyl ring) with [Pt(PPh3)2Cl2] in the presence of NEt3 afforded a family of organometallic complexes of platinum(II) of the type [Pt(PPh3)(L-R)]. Reaction of the same group of ligands with K2[PtCl4] in the presence of NEt3 afforded complexes of the type [Pt(HL-R)2]. The crystal structure of [Pt(PPh3)(L-CH3)] and [Pt(HL-CH3)2] have been determined. In the [Pt(PPh3)(L-R)] complexes, the benzaldehyde thiosemicarbazones are coordinated to platinum as dianionic tridentate C,N,S-donors. In the [Pt(HL-R)2] complexes, the benzaldehyde thiosemicarbazones are coordinated to the metal center as bidentate N,S-donors, forming five-membered chelate rings, and with reference to the structure of the uncoordinated thiosemicarbazone ligand, this coordination mode is associated with a change in stereochemistry around the CN bond. All the [Pt(PPh3)(L-R)] and [Pt(HL-R)2] complexes display intense absorptions in the visible and ultraviolet regions. The cytotoxic effects of these complexes, examined on the human leukemia cell line HL-60 and human lymphoma cell line U-937, have shown that all the [Pt(PPh3)(L-R)] and [Pt(HL-R)2] complexes are cytotoxic in nature and their IC50 values indicate their potential use as antitumor agents.
ISSN:0277-5387
DOI:10.1016/j.poly.2012.07.037