Please use this identifier to cite or link to this item:
https://scidar.kg.ac.rs/handle/123456789/10070
Title: | Kinetics of the substitution reactions of some Pt(II) complexes with 5'-GMP and L -histidine |
Authors: | Jovanovic, Snezana Petrović, Biljana Čanović, Dragan Bugarčić, Živadin |
Issue Date: | 2011 |
Abstract: | The reactions of platinum(II) complexes, [PtCl2(dach)] (dach = (1R,2R)-1,2-diaminocyclohexane) and [PtCl2(en)] (en = ethylenediamine) with biologically relevant ligands such as 5'-GMP (guanosine-5'-monophosphate) and l-His (l-histidine) were studied by UV-vis spectrophotometry, 1H NMR spectroscopy, and high-performance liquid chromatography (HPLC). Spectrophotometrically, these reactions were investigated under pseudo-first-order conditions at 310 K in 25 mM Hepes buffer (pH 7.2) and 10 mM NaCl to prevent the hydrolysis of the complexes. The [PtCl 2(en)] complex reacts faster than [PtCl2(dach)] in the reaction with studied nucleophiles. This confirms the fact that the reactivity of studied Pt(II) complexes depends on the structure of the inert bidentate ligand. Also, the substitution reactions with l-His are always faster than the reactions with nucleotide 5'-GMP. The reactions of [PtCl2(dach)] and [PtCl2(en)] complexes with l-histidine are studied by 1H NMR spectroscopy. The obtained rate constants are in agreement with those obtained by UV-vis. The same reactions were studied by HPLC comparing the obtained chromatograms during the reaction. The changes in intensity of signals of the free and coordinated ligand show that after a few days there is only one dominant product in the system. © 2010 Wiley Periodicals, Inc. |
URI: | https://scidar.kg.ac.rs/handle/123456789/10070 |
Type: | article |
DOI: | 10.1002/kin.20537 |
ISSN: | 0538-8066 |
SCOPUS: | 2-s2.0-78650619758 |
Appears in Collections: | Faculty of Science, Kragujevac |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
PaperMissing.pdf Restricted Access | 29.86 kB | Adobe PDF | View/Open |
Items in SCIDAR are protected by copyright, with all rights reserved, unless otherwise indicated.