Repozytorium
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Kolekcje
Inne
Platinum(II) complexes with tris(2-carboxyethyl)phosphine, X-ray structure and reactions with polar solvents and glutathione.
Autorzy
Rok wydania
2015
Czasopismo
Journal of Organometallic Chemistry
Numer woluminu
791
Strony
124-129
DOI
10.1016/j.jorganchem.2015.05.050
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
It has recently been found that P(C2H4COOH)3 (TCEP), used in the reduction of S–S bonds, promoted reaction of cisplatin with Sp1 zinc finger protein and Cu(I) transporters. However Pt complexes with TCEP were not investigated. New platinum(II) complexes with (TCEP): trans-[PtCl2(TCEP)2] (1) and cis-[PtCl2(TCEP)2]·1.25H2O (2) were fully characterized by IR, 1H, 13C, 31P, 195Pt NMR and ESI-MS spectroscopic techniques. Structures of trans-[PtCl2{P(C2H4COOD)3}2] (1a) and cis-[PtCl2(TCEP)2]·1.25H2O (2) have been determined by X-ray crystallography. Complexes are stable in non-aqueous DMSO and DMF. In aqueous solutions Cl ligands are substituted by COO groups of phosphines. In the mixtures DMSO + H2O and DMF + H2O coordination of COO groups proceeds to a lesser extent and 1 partly isomerizes forming cis-[PtCl2(TCEP)2] and cis-[PtCl{P(C2H4COOH)3-κP}{P(C2H4COOH)2(C2H4COO)-κO,κP}]. The latter complex is also formed in solution of 2 in DMSO + H2O and DMF + H2O. The degrees of isomerization and substitution of Cl ligands in aqueous solutions are higher. NMR data indicate that complexes interact with reduced glutathione (GSH). Compound 2 in D2O forms complex with GS ligand coordinated to platinum via S atom and NH cysteinyl group.
Słowa kluczowe
platinum, Phosphine, Trans-cis isomerization, gluthatione
Adres publiczny
http://dx.doi.org/10.1016/j.jorganchem.2015.05.050
Strona internetowa wydawcy
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