Synthesis and structural characterization of a new dinuclear platinum(III) complex, [Pt2Cl4(NH3)2{μ‐HN=C(O)But}2]

Cisplatin plays an important role in treating many tumors. However, its pharmacological potential is limited by several side effects (nephrotoxicity, neurotoxicity, hair loss) and the resistance of many cancer types. In the effort of overcome resistance to cisplatin, more than 3000 platinum complexe...

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Veröffentlicht in:Acta crystallographica Section B, Structural science, crystal engineering and materials Structural science, crystal engineering and materials, 2022-12, Vol.78 (6), p.835-841
Hauptverfasser: Vinci, Doriana, Chateigner, Daniel
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Sprache:eng
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Zusammenfassung:Cisplatin plays an important role in treating many tumors. However, its pharmacological potential is limited by several side effects (nephrotoxicity, neurotoxicity, hair loss) and the resistance of many cancer types. In the effort of overcome resistance to cisplatin, more than 3000 platinum complexes have been synthesized in the past 45 years, but only about 30 have demonstrated adequate pharmacological platinum(III) complexes have been synthesized and their structure determined, because some of these exhibit antitumor and catalytic activity for the oxidation of olefins. Herein the synthesis of a new dinuclear platinum(III) complex with two butyl(amidato) bridging ligands, namely [Pt2Cl4(NH3)2{μ‐HN=C(O)But}2], is reported. The complex was characterized by means of nuclear magnetic resonance (1H and 195Pt NMR) and infrared spectroscopy, and the crystal structure determined using X‐ray single‐crystal diffraction. This complex, to the best of our knowledge, is the first dinuclear complex of PtIII with two butyl(amidato) bridging ligands with a head‐to‐tail configuration. The synthesis and the structural characterization of a new dinuclear platinum(III) complex are presented. Lantern‐shaped platinum(III) complexes have been shown to have antitumor activity, so this new complex should be screened through antitumor screening tests.
ISSN:2052-5206
2052-5192
2052-5206
DOI:10.1107/S2052520622009660