Multinuclear magnetic resonance and X-ray characterization of platinum(II) complexes with substituted-1,2,4-triazolo[1,5-a]pyrimidines

•Platinum(II) coordination compound as potent anticancer agent.•15N NMR can be used to determinate a coordination mode of triazolopyrimidine.•X-ray determination.

Mononuclear, square-planar platinum(II) complexes having general formula cis-[PtI2(L)2], where L = 7-isobutyl-5methyl-1,2,4-triazolo[1,5-a]pyrimidine (ibmtp) (1), 5,7-diethyl-1,2,4-triazolo[1,5-a]pyrimidine (detp) (2), 5,6,7-trimethyl-1,2,4-triazolo[1,5-a]pyrimidine (tmtp) (3) and 5-methyl-1,2,4-triazolo[1,5-a]pyrimidin-7(4H)-one (HmtpO) (4) have been synthesized and characterized by infrared and multinuclear magnetic resonance (1H, 13C, 15N, 195Pt) spectroscopy. The solid-state structure of cis-[PtI2(dptp)2]·2dmf (5) has been determined by X-ray diffraction method. X-ray structure and spectroscopical parameters revealed that the heterocyclic ligands are coordinated to platinum(II) ion via N(3).