Organometallic chemistry and biochemistry have been merged in the last two decades into a new field: bioorganometallic chemistry. This new research area was devoted to the synthesis of new organometallic compounds and their biological and medical effects against some types of diseases, such as cancer and malaria. For several years, the use of ferrocene in bioorganometallic chemistry has been growing rapidly, and several promising applications have been developed since ferrocene is a stable, nontoxic compound and has good redox properties. This review will focus on ferrocenyl compounds which have been biologically evaluated against certain diseases. This area has attracted many researchers due to the promising results of some ferrocene compounds in the medicinal applications.

A hydrazone ligand (HL) containing the thiophene moiety has been prepared via condensation of thiophene-2-carbohydrazide with 1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carbaldehyde. The complexes of copper(II), nickel(II), cobalt(II), manganese(II), zinc(II), palladium(II), iron(III), ruthenium(III), uranyl(VI), and titanium(IV) with the ligand were prepared in good yield from the reaction of the ligand with the corresponding metal salts. The ligand and complexes were characterized using infrared, mass spectra, nuclear magnetic resonance, electronic absorption spectra, electron spin resonance, and magnetic moment measurements as well as elemental and thermal analyses. The results showed that the complexes are enolic by nature, whilst the ratio between the metal ion and the ligand depends on the acidity of the metallic ions and their oxidation numbers.

The coordination chemistry of N 0 -((1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)methylene)-2-hydroxybenzohydrazide with copper(II), nickel(II), cobalt(II), manganese(II), zinc(II), palladium(II), iron(III), ruthenium(III), uranyl(VI), and titanium(IV) has been studied. The ligand and its complexes was characterized by elemental and thermal analyses, magnetic moments and conductivity measurements as well as spectroscopic techniques such as infrared, mass spectra, nuclear magnetic resonance, electron spin resonance and electronic absorption spectra. The spectral data showed that the ligand is monobasic tridentate coordinated via the enolic carbonyl oxygen of the hydrazide moiety, azomethine nitrogen and pyrazolone oxygen atoms.

Abstract:The reaction products resulting from the interaction between kaolin ore and ammonium sulphate depend on molar ratios between reactants, reaction temperature and time of interaction. The reaction products were characterized by means of XRD. They were composed of silica, unreacted kaolin ore, traces of iron, magnesium, calcium, titanium and NH,Al(SO,), and (NH,),Al(SO,),. The last compound was produced alone at 553 K, whereas mixtures of them were produced between 553 and 823 K after a short time of interaction (0.5 h). On other hand the former compound was produced alone after longer heating (c. 2 h). At 823 K, a mixture composed of Al,(SO,) and NH,AI(SO,), was identified after 0.5 h, whereas anhydrous aluminium sulphate was detected alone after heating the reaction mixture for 2 h. The transformation of (NH,),AI(SO,), into NH,Al(SO,), and alumina leads to a decrease in the percentages of extracted alumina from kaolin ore at relatively higher temperatures and/or longer heating of reaction mixtures. The investigation was also devoted to establishing the possible reactions which lead to the formation of Fe,O,, MgO, CaO and TiO, as soluble salts together with aluminium compounds. The percentages of their extraction are low compared with the original quantities found in kaolin ore. From the obtained results, both Al,(SO,), and NH,Al(SO,), can be prepared from local kaolin with a reasonable degree of purity which makes it possible to produce them for use for different industrial and pharmaceutical purposes.

The work in this paper was devoted to investigating some nanosized iron oxide pigments prepared by microemulsion technique. The role of concentration of iron salt and surfactant (cetyltrimethylammonium bromide) on the produced iron oxide was studied. The techniques employed to characterize the samples were thermogravimetric analysis, X-ray diffractometry, transmission electron microscope, infrared spectroscopy, and diffuse reflectance spectroscopy. The results revealed that the particle size of the prepared sample using 0.2 M iron sulfate and 3.2 wt% of surfactant was in the range 7–9 nm. Increasing the concentration of either iron salt or the surfactant increased the particle size of the obtained ferric oxide. The diffuse reflectance measurements showed that the charge transfer/electron pair transition absorption peak, which is closely related to the reddish color of the oxide, was shifted to a longer wavelength (blue shift) by decreasing the dimension of the particles. The samples were tested as pigments. They showed different tints of red color and were found to be promising for applications as pigments in the field of paint manufacturing.