Complexes of Gold(III) with Hydrazones Derived from Pyridoxal: Stability, Structure, and Nature of UV-Vis Spectra

被引:1
|
作者
Kuranova, Natalia N. [1 ]
Pimenov, Oleg A. [1 ]
Zavalishin, Maksim N. [1 ]
Gamov, George A. [1 ]
机构
[1] Ivanovo State Univ Chem & Technol, Dept Gen Chem Technol, Sheremetevskii Pr 7, Ivanovo 153000, Russia
基金
俄罗斯科学基金会;
关键词
gold(III); hydrazone; pyridoxal; stability constant; speciation; DFT; molecular orbitals; UV-Vis spectra; SALICYLALDEHYDE ISONICOTINOYL HYDRAZONE; IRON CHELATORS; BLACK-GOLD; BASIS-SETS; PIH; ANALOGS; WATER; RETICULOCYTES; CONSTANTS; 3-HYDROXYPYRIDINE;
D O I
10.3390/ijms25095046
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Pyridoxal and pyridoxal 5 '-phosphate are aldehyde forms of B6 vitamin that can easily be transformed into each other in the living organism. The presence of a phosphate group, however, provides the related compounds (e.g., hydrazones) with better solubility in water. In addition, the phosphate group may sometimes act as a binding center for metal ions. In particular, a phosphate group can be a strong ligand for a gold(III) ion, which is of interest for researchers for the anti-tumor and antimicrobial potential of gold(III). This paper aims to answer whether the phosphate group is involved in the complex formation between gold(III) and hydrazones derived from pyridoxal 5 '-phosphate. The answer is negative, since the comparison of the stability constants determined for the gold(III) complexes with pyridoxal- and pyridoxal 5 '-phosphate-derived hydrazones showed a negligible difference. In addition, quantum chemical calculations confirmed that the preferential coordination of two series of phosphorylated and non-phosphorylated hydrazones to gold(III) ion is similar. The preferential protonation modes for the gold(III) complexes were also determined using experimental and calculated data.
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页数:16
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