Ionic platinum(II) complexes [PtCl(PPh3)(L∧L)][BF4] {L∧L = 2,2′-bipyridyl (1) 1,10-phenanthroline (2)} and [PtCl(PPh3)(L)2][BF4] {L = pyridine (3), dimethyl sulfoxide (4)} were synthesized by dehalogenation of cis-[PtCl2(PPh3)(NCMe)], followed by reaction with the suitable ligand. Chelating nitrogen ligands L∧L afforded single products, which were structurally characterized. In the other cases mixtures of geometric (L = pyridine) and/or coordination (L = dimethyl sulfoxide) isomers were observed in solution. In these cases the structures of the less soluble isomers were obtained via single crystal X-ray diffraction. All the complexes were tested in vitro for their antiproliferative activity on three human tumor cell lines: MSTO-211H, HeLa and HepG2.
Synthesis and antiproliferative activity of ionic platinum(II) triphenylphosphino complexes
BELLI, DANIELA;LABELLA, LUCA;MARCHETTI, FABIO;SAMARITANI, SIMONA;
2016-01-01
Abstract
Ionic platinum(II) complexes [PtCl(PPh3)(L∧L)][BF4] {L∧L = 2,2′-bipyridyl (1) 1,10-phenanthroline (2)} and [PtCl(PPh3)(L)2][BF4] {L = pyridine (3), dimethyl sulfoxide (4)} were synthesized by dehalogenation of cis-[PtCl2(PPh3)(NCMe)], followed by reaction with the suitable ligand. Chelating nitrogen ligands L∧L afforded single products, which were structurally characterized. In the other cases mixtures of geometric (L = pyridine) and/or coordination (L = dimethyl sulfoxide) isomers were observed in solution. In these cases the structures of the less soluble isomers were obtained via single crystal X-ray diffraction. All the complexes were tested in vitro for their antiproliferative activity on three human tumor cell lines: MSTO-211H, HeLa and HepG2.File | Dimensione | Formato | |
---|---|---|---|
Polyhedron PtBio2016.pdf
solo utenti autorizzati
Tipologia:
Versione finale editoriale
Licenza:
NON PUBBLICO - Accesso privato/ristretto
Dimensione
863.24 kB
Formato
Adobe PDF
|
863.24 kB | Adobe PDF | Visualizza/Apri Richiedi una copia |
Samaritani_807164.pdf
Open Access dal 01/12/2018
Tipologia:
Documento in Post-print
Licenza:
Creative commons
Dimensione
512.94 kB
Formato
Adobe PDF
|
512.94 kB | Adobe PDF | Visualizza/Apri |
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.