https://commons.ru.ac.za/vital/access/manager/Index ${session.getAttribute("locale")} 5 The development of amine-based extractants for separation of base metals in a sulfate medium https://commons.ru.ac.za/vital/access/manager/Repository/vital:4559 Wed 12 May 2021 19:26:07 SAST ]]> Synthesis, characterisation and biological activity of 2-(methylthiomethyl)anilines, 2-(methylthio)anilines, their Schiff-base derivatives and metal(II) (Co, Ni, Cu) complexes https://commons.ru.ac.za/vital/access/manager/Repository/vital:4562 Co(II) > Ni(II). The Schiff-base derivatives were prepared from the ligands and para-methoxysalicylaldehyde and their Cu(II) complexes were synthesized in order to determine their biological activity. The Schiff-base ligands were found to be less active than their parent ligands. The Cu(II) complexes are not soluble in water, DMSO or DMF, as a result and could not be evaluated for their biological activity. Based on the good results from the antimicrobial evaluation, the antiplasmodial activity of some of the Co(II), Ni(II) and Cu(II) complexes of the thiomethylated ligands against Plasmodium falciparum (FCR-3) was determined. At 50 μM concentration level, the Cu(II) complexes show activity equal or better than the prophylactic chloroquine. The Cu(II) complexes with the methoxy-substituted demonstrated exceptional activity but their Co(II) and Ni(II) analogues did not show any activity. The cytotoxicity of the active Cu(II) complexes at 50 μM concentration was determined against the breast cancer cell line (MDA-MB-231). The compounds destroyed the cancer cell in the range of 28–40%, thus showing their preferred activity against the parasitic cell instead of the cancer cell. The selectivity demonstrated by these compounds have shown them to be potential antimalarial agents and this could be further investigated.]]> Wed 12 May 2021 17:24:20 SAST ]]> The coordination chemistry of Rhenium(V) with multidentate no-donor ligands https://commons.ru.ac.za/vital/access/manager/Repository/vital:10370 Wed 12 May 2021 17:22:09 SAST ]]> Rhenium (I) and (V) complexes with potentially mulidentate ligands containing the Amino group https://commons.ru.ac.za/vital/access/manager/Repository/vital:10386 Wed 12 May 2021 16:31:06 SAST ]]> Synthesis, characterization and antimicrobial activity of copper (II) complexes of some hydroxybenzaldimines and their derivatives https://commons.ru.ac.za/vital/access/manager/Repository/vital:4534 Wed 12 May 2021 16:27:58 SAST ]]> Synthesis, crystal structures and molecular modelling of rare earth complexes with bis(2-pyridylmethyl)amine and its derivatives : a quantum chemical investigation of ligand conformational space, complex intramolecular rearrangement and stability https://commons.ru.ac.za/vital/access/manager/Repository/vital:39517 Wed 12 May 2021 16:00:53 SAST ]]> Effects of Axial Ligands on the Photosensitising Properties of Silicon Octaphenoxyphthalocyanines https://commons.ru.ac.za/vital/access/manager/Repository/vital:4553 600 nm) in dimethylsulphoxide solution. All the ligands were transformed into the dihydroxy silicon octaphenoxyphthalocyanine with varying degrees of phototransformation quantum yields ranging in order from 10⁻³ to 10⁻⁵ depending on the axial ligand involved. During and after axial ligand transformations a photodegredation of the dihydroxy silicon octaphenoxy phthalocyanine was observed upon continued irradiation. The oligomers were found to undergo the same axial ligand transformation process with a phototransformation quantum yield of 10⁻⁵ The singlet oxygen quantum yields of the unaggregated monomeric silicon octaphenoxy phthalocyanines were all found to be approximately 0.2 with the exception of a compound with two (trihexyl)siloxy axial substituents that had a singlet oxygen quantum yield of approximately 0.4 in dimethylsulphoxide solutions. The oligomers showed a surprising trend of an increase in singlet oxygen quantum yield with an increase in phthalocyanine ring number up to the pentamer and then a dramatic decrease to the nonamer. The triplet quantum yield and triplet lifetime were determined by laser flash photolysis for selected compounds and no correlation was observed with any of these properties and the singlet oxygen quantum yields. These selected compounds all fluoresce and a very good correlation was found between the fluorescence lifetimes determined experimentally by laser photolysis and the Strickler-Berg equation for the non-aggregated compounds. Electrochemical measurements also indicate the importance of the axial ligands upon the behaviour of the phthalocyanines as cyclic voltammetric behaviour was determined by the nature of the axial ligand.]]> Thu 13 May 2021 14:52:35 SAST ]]>