Repozytorium

Interaction of ruthenium(II) and ruthenium(III) ions with 5-methyl-1,2,4-triazolo[1,5-α]pyrimidin-7(4H)-one.

Autorzy

Marzena Fandzloch

Andrzej Wojtczak

Jerzy Sitkowski

Iwona Łakomska

Rok wydania

2014

Czasopismo

Polyhedron

Numer woluminu

67

Strony

410-415

DOI

10.1016/j.poly.2013.09.022

Kolekcja

Naukowa

Język

Angielski

Typ publikacji

Artykuł

Streszczenie

Ru(II) and Ru(III) complexes with 5-methyl-1,2,4-triazolo[1,5-a]pyrimidin-7(4H)-one (HmtpO) of the formula cis-[RuCl2(dmso)3(HmtpO)] (1) and trans-[RuCl4(dmso)(H2mtpO)]·4H2O (2) have been synthesized and characterized using different spectroscopic techniques (IR, 1H–15N HMBC, 1H–13C HSQC, 1H–13C HMBC and EPR). Spectroscopic studies reveal a monodentate coordination of the heterocycle ligand (HmtpO) via N3 to the ruthenium(II) and ruthenium(III) ions. In addition, the X-ray crystal structure was determined for complex (2). The compound crystallized in the triclinic group P1¯. The asymmetric unit of the structure consists of two complex molecules (2a and 2b) and 8 water molecules. The equatorial positions are occupied by four chloride ions, while the N3 bonded, protonated H2mtpO+ and S-bonded dmso ligands are located in axial positions. Complex (1) has been screened for in vitro cytotoxicity against two human cells: non-small cell lung carcinoma (A549) and breast cancer (T47D). The ruthenium(II) complex was found to be less active than cisplatinum.

Słowa kluczowe

Ruthenium(II) complex, Ruthenium(III) complex, 15N NMR, EPR, X-ray, Triazolopyrimidine, In vitro cytotoxicity

Adres publiczny

http://dx.doi.org/10.1016/j.poly.2013.09.022

Strona internetowa wydawcy

http://www.elsevier.com

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Use of 1,2,4-triazolo[1,5-α]pyrimidines to design new "piano-stool" ruthenium(II) compounds.

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