ABSTRACT Introduction The aim of this study was to determine the current RPR positive prevalence rate at the Johannesburg Hospital and to determine whether there has been a significant decrease in the prevalence rate of RPR positive tests. Patients and Methods A retrospective analysis of all RPR results within labour ward registers was performed. A sample from 01/08/02 to 31/01/03 was used to determine the current RPR positive prevalence rate. The results from the current period were then compared to the results from a similar study in 1996. Results of two months, six months apart, of each year between these periods were also analyzed in order to determine the trend of RPR positive prevalence rates. Results The RPR prevalence rate was 4.4% compared to 19.5% in 1995/96 (p < 0.0001). Results obtained from the intervening years showed a statistically significant decrease. Conclusion RPR positive prevalence rates at Johannesburg Hospital have decreased significantly in recent years.

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This thesis concerns method development of new synthetic routes by applying electrophilic hypervalent iodine reagents, such as trifluoromethyl-benziodoxole (Togni reagent) and fluoro-benziodoxole. The first project involved the addition of an oxygen moiety and trifluoromethyl group across double and triple bonds (both groups derived from the hypervalent iodine reagent). We observed that electron donating substituents on the aromatic ring of the substrate accelerated the oxytrifluoromethylation reaction. This transformation was further expanded to halo-trifluoromethylation reaction of a vinyl silane substrate. We also developed a copper mediated cyanotrifluoromethylation reaction, which was accelerated by PCy3 additive. This transformation allowed for the creation of two new C-C bonds in a single addition reaction. The direct C-H trifluoromethylation reaction of quinones was achived using the Togni-reagent in the presence of B2pin2 additive. The intriguing additive effects of both B2pin2 and PCy3 inspired us to examine the mechanism of these transformations. Fluoro-benziodoxole is the fluoroiodane analogue of the trifluoromethylating Togni reagent. We developed a AgBF4 mediated geminal difluorination of styrenes using this fluoroiodine reagent. In this process one fluorine atom came from the fluoroiodane, while the other fluorine was derived from the tetrafluoroborate ion. A similar approach was applied for the 1,3-oxyfluorination and difluorination of cyclopropanes. Similarly, this fluorinative ring opening of unactivated cyclopropanes involved the introduction of an electrophilic fluorine atom from the fluoroiodane reagent and a nucleophilic one from the tetrafluoroborate ion. This reaction was extended to synthesis of 1,3-oxyfluorinated products. When alkenes reacted with the fluoro-benziodoxole reagent in the presence of palladium catalyst the iodofluorination reaction occurred.  Both the iodine and fluorine atoms were derived from the fluoroiodane reagent. The iodofluorination reaction with disubstituted and cyclic alkenes proceeded with high regio- and stereoselectivity.

Of several potential reagents for the indirect polarographic determination of beryllium, benzoylacetone was found to be the most attractive. A study of the relevant properties of this reagent and of the characteristics of its reaction with beryllium led to the development of a new method for the determination of beryllium with good precision at concentrations as low as 10 p.p.m. and with reasonable precision even at 2 p.p.m. Less than 0.5 mg. of beryllium is required. The method, when preceded by an appropriate mercury-cathode separation, is applicable to the determination of beryllium in copper-base alloys. The application of the method was extended to aluminium-base alloys by the development of an ion-exchange procedure for the separation, with at least 95% efficiency, of beryllium from relatively high concentrations of aluminium. A similar method is applicable to the determination of aluminium, in concentrations down to about 20 p.p.m. / Thesis / Master of Science (MS)

This report details the discovery of a method for rhodium catalyzed asymmetric conjugate additions of heteroaryl nucleophiles to α,β-unsaturated carbonyl compounds. This work has successfully employed heteraryl titanates in enantioselective conjugate addition to α,β-unsaturated carbonyl compounds for the first time. Moreover, the utility of benzofuranyl, benzothiophenyl, and pyrrolo zinc reagents has been exemplified in enantioselective conjugate additions. We have found that the precatalyst [Rh(COD)acac]/OMeBIPHEP is broadly effective for enantioselective conjugate additions. Each heterocycle tested exhibited unique reactivity with respect to both conversion and enantioselectivity; reactivities of heteroaryl zinc reagents and heteroaryl titanates in enantioselective conjugate additions to α,β-unsaturated carbonyl compounds are sometimes complementary. Efforts directed towards the development of a method for rhodium-free enantioselective conjugate addition of furan to α,β-unsaturated carbonyl compounds are also described. / text

Phosphorus-Selenium chemistry has seen a surge in development over the last five to ten years thanks to the optimisation of the synthesis of 2,4-diphenyl-1,3,2,4-diselenadiphosphetane-2,4-diselenide, Woollins' Reagent. This selenium analogue of the well known Lawesson's Reagent has proved itself to be a valuable asset to modern inorganic chemistry, providing a route to novel heterocycles, as well as acting as a selenation reagent with a wide range of functional groups. A series of new ammonium phenylphosphonamidodiselenoate ligands were synthesised via the reaction of Woollins' Reagent with a range of amines. The products were obtained in high yields and could be used as ligands for the synthesis of novel metal complexes. The reaction of diisopropylamine N-isopropyl-P-phenylphosphonamidodiselenoate with nickel(II) acetate produces a dimeric structure, whilst the reaction with copper(II) acetate yields a beautiful cluster of the form Cu₆Se₃L₆. The phenylphosphonamidodiselenoate ligands were further reacted with a range of cis-Pt(PR₃)₂Cl₂ complexes to form a library of 20 novel compounds, which were studied by ³¹P{¹H}, ⁷⁷Se{¹H} and ¹⁹⁵Pt{¹H} NMR spectroscopy. The X-ray crystal structure of one of these compounds was obtained, which confirmed the atom connectivity and spatial arrangement of the complexes and the geometry around the platinum centre. During investigations into the above-mentioned platinum complexes, it was postulated that an increase in steric bulk of the phosphine ligands would aid crystallisation of the products. As such, trimesityl-, dimesitylphenyl- and mesityldiphenyl phosphine were synthesised and reacted with elemental sulfur and selenium and hydrogen peroxide, as well as Pt(cod)Cl₂ and K₂[PtCl₄], yielding nine new structures, all of which were characterised by X-ray crystallography, ³¹P{¹H}, ¹³C{¹H} and ¹H NMR spectroscopy. Finally Woollins' Reagent was reacted directly with a selection of metal complexes, yielding some new insights into its reactivity with inorganic moieties, which has been relatively sparsely reported until now.

The objective of this study was to synthesize new energetic, strained, saturated polycyclic compounds. For this purpose, new methodology has been developed, as follows: (i) Ketenes have been generated in situ via treatment of aldo-, keto- or alkenoic acid with either toluenesulfonyl chloride or 2-chloro-1-methylpyridfniurn iodide (Mulkaiyama's reagent). The reactive intermediates thereby generated have been found to undergo intramolecular [2+2] cycloaddition reactions in these systems.

This thesis involves the design and development of reagents for the recovery of base metals (specifically zinc, nickel and cobalt) in hydrometallurgical solvent extraction processes. The work aims to demonstrate how ligand design can affectively tune the strength and selectivity of extractants to achieve efficient recovery of the desired base metals. Chapter 1 reviews current solvent extraction processes used in extractive metallurgy, encompassing both the well established technologies developed for sulfate streams as well as those more recently explored for treating chloride streams. Also reviewed, is the nature of the chemical binding involved in the three key modes of extraction; namely cation transport, anion transport and metal salt transport. Chapter 2 summarises the methodologies that have been established during this research for the appropriate testing of these reagents. Chapter 3 deals exclusively with the processing of zinc sulfide ores with an aim to design reagents to achieve concentration and separation of zinc in chloride hydrometallurgical circuits. The amido functionalised reagents that are reported have a common structural feature with ligands that have been previously studied by the Tasker group (Ross J. Ellis Thesis, University of Edinburgh, 2009). A six membered chelate ring is formed by a protonated amino nitrogen atom and an amido oxygen atom in a sequence of the type R2HN+-CH2-NR-CO-R. This differs from those previously studied which have a sequence of the type R2HN+-CH2-CHR-CO-NR2. The pro-ligands (L) operate via an anion exchange mechanism (Equation 1) whereby two protonated ligands (LH+) coordinate to the outersphere of anionic zinc(II) or iron(III) chloridometalates from acid chloride solutions using both N-H and C-H hydrogen-bond donors. pH dependent solvent extraction experiments have concluded that this reagent series achieves zinc(II) loading with pH0.5 values that are competitive with the previous ligand series (Ross J. Ellis Thesis, University of Edinburgh, 2009). Chloride concentration dependent solvent extraction experiments have demonstrated that the reagents show an unusually good selectivity for ZnCl4 2- over chloride or FeCl4 - in equilibrium of the type; yLorg + yH+ +MClx y- ⇌ [(LH)yMClx](org) (1) The development of bidentate and tridentate pyrazolone-based pro-ligands for the extraction of nickel and cobalt from mixed metal sulfate streams is considered in Chapters 4 and 5. These reagents (LH) operate via metal cation transport, where an inner-sphere complex of nickel(II) or cobalt(II) is formed with the ligand (L-) see Equation 2. A combination of N, O and S donors has been incorporated into 1-phenyl-3-methyl-4- acylpyrazol-5-ones and their respective 4-acylpyrazolone oximes in order to tune the bidentate ligands (L-) for optimal coordination with nickel(II) or cobalt(II). Substituent effects have also been investigated, by synthesising a series of 1-(2-X-phenyl)-3-methyl-4- acylpyrazol-5-one oximes [X = Cl, H]. Substitution in the 3-position of the phenol group in phenolic oximes has been reported to increase extractant strength for copper by two orders of magnitude (Ross S. Forgan Thesis, University of Edinburgh, 2008). Similar improvements were not observed in this study. The nature of this effect has been attributed to buttressing of hydrogen-bonds, where the substituent forms a stabilising, bifurcated hydrogen-bond between the oximic hydrogen and the pyrazolonic oxygen. yLHorg + My+ ⇌ [(L)yM]org + yH+ (2) Tridentate analogues of the oxime reagents above have been prepared as imines derived from anilines contained o-O, S or N donor atoms. It was hoped that these would give high spin octahedral nickel(II) complexes in extraction processes. They proved to be weak extractants. Chapter 6 focuses of the development of bidentate pyrazolethiones for the selective extraction of cobalt from manganese in acidic sulfate streams. These reagents have been designed to favour coordination to metals in a tetrahedral geometry as shown by L. Emeleus and A. Smith for copper and zinc (Lucy Emeleus Thesis, University of Edinburgh 1999 and Andrew Smith Thesis, University of Edinburgh 2000).

Organometallic compounds derived from tin, boron, and zinc, have been used extensively in transition metal-catalysed cross-coupling, and continue to hold status as the go-to reagents to form new carbon-carbon bonds. Recently, organosilicon compounds have emerged as an attractive alternative to these established reagents, benefitting from low toxicity, low cost, and general ease of handling. While the fundamental reactivity of arylsilane reagents (Ar-SiR3) is well known, their role in transition metal-catalysed reactions is generally less well studied. This thesis comprises an investigation into the effect of ortho-substitution of these arylsilane reagents, and specifically, their application in gold-catalysed direct arylation. In Chapter 2, the transmetalation of these reagents to gold(III) is assessed using a combination of in situ reaction monitoring coupled with kinetic simulations. This allowed a scale of reactivity to be constructed for a range of structurally diverse arylsilanes, and uncovered that more sterically hindered arylsilanes actually exhibit accelerated rates of transmetalation. In Chapter 3, the reactivity of ortho-substituted arylsilanes in gold-catalysed arylation is addressed. The majority of arylsilanes tested in the previous chapter were found to be unable to undergo coupling, despite the viability of transmetalation having been demonstrated. Slight modification of the ortho-substituent, to incorporate a tethered ligand, was found to have a dramatic effect on reactivity, and allowed the coupling of a variety of substrates. The nature of the ligand, as well as the substitution of the tether was found to have a significant impact on the rate of coupling. Chapter 4 describes the way in which the reactivity of ortho-substituted arylsilanes might be exploited in a 'Catch and Release' protocol for catalyst recovery. This aims to combine the established benefits of homogeneous and heterogeneous catalysis to offer an alternative to current methods of catalyst recycling in industrial chemistry. A number of different 'Catch and Release' mechanisms were considered, and the validity of the concept was demonstrated in a monophasic system.

Estágio realizado na Universidade de Granada e orientado pelo Prof. Maldonado-Hódar / Tese de mestrado integrado. Engenharia Química. Faculdade de Engenharia. Universidade do Porto. 2008