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

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.

Complexation of Gold(III) with Pyridoxal 5'-Phosphate-Derived Hydrazones in Aqueous Solution.

Today, complexes of gold(I) and gold(III) are recognized as promising drugs for the treatment of bacterial infectious diseases and oncological diseases, respectively. It is of interest to broaden the area of potential use of gold(III) compounds to the pathogenic microorganism as well. The first step towards the development of new antibacterial drugs based on Au3+ complexes is the study of their stability in an aqueous solution. The present contribution reports on the investigation of gold(III) complexation with five hydrazones derived from a well-known biologically active compound, pyridoxal 5'-phosphate (one of the aldehyde forms of the B6 vitamin). The complex formation in aqueous solutions was confirmed by mass spectrometry and fluorescent spectroscopy. The stoichiometric composition of the complexes formed and their stability constants were determined using a UV-Vis titration method. The complexes are quite stable at physiological values of pH, as the speciation diagrams show. The results of the paper are helpful for further studies of gold(III) complexes interaction with biomacromolecules.

Structural and Phase Transformations and Physical and Mechanical Properties of Cu-Al-Ni Shape Memory Alloys Subjected to Severe Plastic Deformation and Annealing.

Using the methods of electron microscopy and X-ray analysis in combination with measurements of the electrical resistance and magnetic susceptibility, the authors have obtained data on the peculiar features of pre-martensitic states and martensitic transformations, as well as subsequent decomposition, in the alloys with shape memory effect of Cu-14wt%Al-3wt%Ni and Cu-13.5wt%Al-3.5wt%Ni. For the first time, we established the microstructure, phase composition, mechanical properties, and microhardness of the alloys obtained in the nanocrystalline state as a result of severe plastic deformation under high pressure torsion and subsequent annealing. A crystallographic model of the martensite nucleation and the rearrangements ß1→ß1' and ß1→γ1' are proposed based on the analysis of the observed tweed contrast and diffuse scattering in the austenite and the internal defects in the substructure of the martensite.