The contamination of groundwater by arsenic is currently a major concern in Bangladesh. Arsenic in groundwater was first detected in 1993 following reports of many people suffering from arsenical diseases. Further investigations showed the extent of the problem with large areas of the country's water supply being affected and millions of people at serious risk of arsenic poisoning. Technology for arsenic removal from water already exists. However, the socioeconomic conditions which prevail in Bangladesh, do not permit implementation of this type of technology on grounds of cost. The main objective of this study was to develop a low cost technique for the removal of arsenic from contaminated groundwater using the naturally occurring iron, which is another water quality constraint in Bangladesh. The approach was to form arsenic-iron complexes by coprecipitation and adsorption of arsenic on iron. It has been demonstrated that provided the iron levels are sufficiently high (say >_ 1.2 mg/1), simple shaking of a container and allowing the arsenic-iron complex to settle out for 3 days could reduce the concentration of arsenic from 0.10 mg/l to Bangladesh standard (0.05 mg/1). In experimental program, As(III) form of arsenic was used as this form is more likely to be present in groundwater. From laboratory studies, it was shown that the removal rate was largely controlled by the Fe/As ratio, pH and the As concentration. Arsenic removal increases with increasing Fe/As ratio and is favoured by increasing pH in the range of 5 to 8. Separation of the precipitates was achieved by settlement. Following prolonged settlement, it was found that arsenic removal could exceed the removal achieved by filtration through a 0.45 μm filter paper. The experiments demonstrated that about 77% arsenic removal could be achieved from water containing 0.2 mg/l As(III), 4.0 mg/1 Fe at pH 7.5 by manual flocculation (1 min manual mixing) and 3 days settlement. The use of ordinary charcoal, which is cheap and easily available, was investigated for removal of arsenic and was found to be ineffective. From maps of the known distributions of As, Fe and pH, it was evident that 63% of the area in Bangladesh complied with the Bangladesh standard for arsenic. By interpreting the maps and applying the potential removal by coprecipitation-adsorption and settlement technique, it was estimated that a further 8% of area would comply with the Bangladesh standard freeing an additional 7 million people from arsenic contamination.

Thesis (Ph. D.)--University of Wisconsin--Madison, 1976. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.

No description available.

<p> A number of complexes FeX2Ln (X = Cl, Br; L = formamide, N-methylformamide, N,N-dimethylformamide, acetamide, benzamide, isobutyramide, urea, N-methylurea, N,N'-dimethylurea, thioacetamide, thiourea, N-methylthiourea, N,N'-dimethylthiourea, benzothiazole, aniline) have been prepared and investigated by means of Mossbauer and infrared spectroscopy and magnetic measurements. It has been possible to distinguish firstly between 4-coordinate and 6-coordinate complexes and secondly between a number of different types of 6-coordinate complexes.</p> / Thesis / Master of Science (MSc)

No description available.

This thesis describes the synthesis of a host of polynuclear iron complexes synthesised with phenolic oxime ligands, fundamentally developing the coordination chemistry of iron with these ligands. The metallic cores that occur within iron phenolic oxime clusters were found to contain almost exclusively oxo-centred triangles and oxo-centred tetrahedra. We found that we could alter the reaction conditions or derivatise the ligands and develop these basic building blocks into more elaborate arrays, exerting a degree of control over creating larger or smaller clusters. Chapter one describes the syntheses, structures and magnetic properties of new iron complexes alongside previously synthesised related complexes (4, 5, 8, 9 and 15) containing salicylaldoxime (saoH2) or derivatised salicylaldoximes (RsaoH2). These are [Fe3O(OMe)(Ph-sao)2Cl2(py)3]·2MeOH (1·2MeOH), [Fe3O(OMe)(Ph-sao)2Br2(py)3]·Et2O (2·Et2O), [Fe4(Ph-sao)4F4(py)4]·1.5MeOH (3·1.5MeOH), [Fe6O2(OH)2(Et-sao)2(Et-saoH)2(O2CPh)6] (4), [HNEt3]2[Fe6O2(OH)2(Et-sao)4(O2CPh(Me)2)6]·2MeCN (5·2MeCN), [Fe6O2(O2CPh)10(3-tBut-5-NO2-sao)2(H2O)2]·2MeCN (6·2MeCN), [Fe6O2(O2CCH2Ph)10(3-tBut-sao)2(H2O)2]·5MeCN (7·5MeCN), {[Fe6Na3O(OH)4(Me-sao)6(OMe)3(H2O)3(MeOH)6]·MeOH}n (8·MeOH) and [HNEt3]2[Fe12Na4O2(OH)8(sao)12(OMe)6(MeOH)10] (9). The predominant building block appears to be the triangular [Fe3O(R-sao)3]+ species which can self-assemble into more elaborate arrays depending on reaction conditions. The four hexanuclear and two octanuclear complexes of formulae [Fe8O2(OMe)4(Mesao) 6Br4(py)4]·2Et2O·MeOH (10·2Et2O·MeOH), [Fe8O2(OMe)3.85(N3)4.15(Mesao) 6(py)2] (11), [Fe6O2(O2CPh-4-NO2)4(Me-sao)2(OMe)4Cl2(py)2] (12), [Fe6O2(O2CPh-4-NO2)4(Et-sao)2(OMe)4Cl2(py)2]·2Et2O·MeOH (13·2Et2O·MeOH), [HNEt3]2[Fe6O2(Me-sao)4(SO4)2(OMe)4(MeOH)2] (14) and [HNEt3]2[Fe6O2(Etsao) 4(SO4)2(OMe)4(MeOH)2] (15) all are built from series of edge-sharing [Fe4( μ4- O)]10+ tetrahedra. Complexes 10 and 11 display a new μ4-coordination mode of the oxime ligand and join a small group of Fe-phenolic oxime complexes with nuclearity greater than six. Chapter three then introduces co-ligands to the reaction scheme to compete with the salicylaldoxime ligands for metal coordination sites. Five tetranuclear and two nononuclear complexes are stabilised with salicylaldoxime (saoH2) or derivatised salicylaldoximes (R-saoH2) in conjunction with either 1,4,7- triazocyclononane (tacn), 2-hydroxymethyl pyridine (hmpH) or 2,6-pyridine dimethanol (pdmH2), [Fe4O2(sao)4(tacn)2]·2MeOH (16·MeOH), [Fe4O2(Mesao) 4(tacn)2]·2MeCN (17·2MeCN), [Fe4O2(Et-sao)4(tacn)2]·MeOH (18·MeOH), [Fe9NaO4(Et-sao)6(hmp)8]·3MeCN·Et2O (19·3MeCN·Et2O), [Fe4 (Etsao) 4(hmp)4]·Et-saoH2 (20·Et-saoH2), [Fe4(Ph-sao)4(hmp)4]·2MeCN (21·2MeCN) [Fe9O3(sao)(pdm)6(N3)7(H2O)] (22). Chapter four straps two salicylaldoxime units together in the 3-position, using ligands with aliphatic a,W-aminomethyl links, allowing the assembly of the polynuclear complexes [Fe7O2(OH)6(H2L1)3(py)6](BF4)5·6H2O·14MeOH (23·6H2O·14MeOH), [Fe6O(OH)7(H2L2)3][(BF4)3]·4H2O·9MeOH (24·4H2O·9MeOH) and [Mn6O2(OH)2(H2L1)3(py)4(MeCN)2](BF4)5(NO3)·3MeCN·H2O·5py (25·3MeCN·H2O·5py). In each case the metallic skeleton of the cluster is based on a trigonal prism in which two [MIII 3O] triangles are tethered together via three helically twisted double-headed oximes. The latter are present as H2L2- in which the oximic and phenolic O-atoms are deprotonated and the amino N-atoms protonated, with the oxime moieties bridging across the edges of the metal triangles. Both the identity of the metal ion and the length of the straps connecting the salicylaldoxime units have a major impact on the nuclearity and topology of the resultant cage, with, perhaps counter-intuitively, the longer straps producing the “smallest” clusters.

No description available.

The synthesis of diiron thiolate complexes was carried out using two ligands that were expected to furnish improved catalytic activity, solubility in water, and stability to the metal complexes. The water-soluble phosphine 1,3,5-triaza-7- phosphaadamantane, PTA, coordinates to the Fe centers forming the disubstituted complex (m-pdt)[Fe(CO)2PTA]2, which presents one PTA in each iron in a transoid arrangement. Substitution of one CO ligand in the (m-pdt)[Fe(CO)3]2 parent complex forms the asymmetric (m-pdt)[Fe(CO)3][Fe(CO)2PTA]. Enhanced water solubility was achieved through reactions with electrophiles, H+ and CH3 +, which reacted with the N on the PTA ligand forming the protonated and methylated derivatives, respectively. The 1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene), IMes, was reacted with (m-pdt)[Fe(CO)3]2 yielding the asymmetric (m-pdt)[Fe(CO)3][Fe(CO)2IMes], an electron rich, air stable complex that does not show reactivity with H+. Electrocatalytic production of hydrogen was studied for the all-CO, bis-PMe3, mono- and di-PTA FeIFeI complexes, as well as the PTA-protonated and -methylated derivatives. The all-CO species produce H2, in the presence of the weak HOAc, at their second reduction event, FeIFe0 ?? Fe0Fe0, that occurs at ca. ??1.9 V, through an EECC mechanism. The mono- and di-substituted phosphine complexes present electrocatalytic production of H2 from the Fe0FeI redox state; this reduction takes place at ??1.54 V for (m-pdt)[Fe(CO)3][Fe(CO)2PTA], and at ca. ??1.8 for the disubstituted PMe3 and PTA derivatives. A positive charge on the starting complex does not have an effect on the production of H2. It was found that the protonated and methylated derivatives are not the catalytic species for H2 production. At their first reduction event the neutral precursor forms, and catalysis occurs from the FeIFeI complex in all cases. The possibility of enhanced catalytic activity in the presence of H2 O was explored by conducting electrochemical experiments in the mixed CH3CN:H2O solvent system for the PTA-substituted complexes. The reduction potential of the catalytic peak is shifted to more positive values by the presence of H2 O. The cyclic voltammogram of {(m-pdt)[Fe(CO)2(PTA?? H)]2}2+ in CH3CN:H2O 3:1 shows the reduction of a more easily reduced species in the return scan. This curve-crossing event provides evidence for the (h2-H2)FeII intermediate proposed in the ECCE mechanism.

No description available.

The current thesis addresses the various facets of the chemistry of photocytotoxic iron complexes including their syntheses, characterization, evaluation of the anti-proliferative activities in various cancer cell lines upon photo-exposure, mechanism of cell death, the cellular uptake, localization inside cells, the interaction with double stranded DNA and their ability to induce DNA photocleavage. Chapter I presents a general introduction to cancer and the anticancer agents. It covers various procedures available for cancer treatment and different aspects of chemotherapy are discussed in details. The mechanism of action of several chemotherapeutic agents, the DNA cleavage pathways and the anticancer activity of bleomycins are delineated. Photo-chemotherapy or photodynamic therapy which has emerged as an alternative treatment modality is described. It also contains a brief description of ideal photosensitizers and the ones that are currently approved. The potential of transition metal complexes as photo-chemotherapeutic agents is discussed based on the recent literature reports on the prospective photocytotoxic metal complexes, the photo-release of cytotoxic molecules from metal complexes, the DNA cleavage activities and their cytotoxicities. The biochemistry of iron and its medical utility which prompted the development of iron based cytotoxins has been presented. The objective of the present investigation is also defined in this chapter. Chapter II describes the syntheses, characterization, evaluation of visible light induced cytotoxicity and interaction with DNA of a series of iron(II) bis-terpyridine complexes. Some interesting redox behaviour observed for two of the complexes has been described in details and rationalized from theoretical calculations. The DNA binding affinities of the complexes and their ability to induce DNA photocleavage in green light are discussed. The importance of this work lies in the remarkable photocytotoxic behaviour of the iron(II) complexes with visible light which was not reported earlier. Chapter III addresses the syntheses of a series of iron(III) catecholate complexes which upon irradiation with red light can initiate photoreactions to generate cytotoxic species and induce death in HeLa, HaCaT, MCF-7 and A549 cells. The mechanisms of cell death, effect of the complexes on the cell cycle under various conditions, the uptake inside cells and the cellular localization of the complexes are studied. The DNA binding affinities of the five complexes and their ability to induce DNA photocleavage in red light are also presented here. These are the first iron based complexes to show red light induced photocytotoxicity. Chapter IV addresses the drawbacks associated with the aforementioned iron(III) catecholates and their modification with a mitochondria targeting triphenylphosphonium unit. The synthesis, characterization, photocytotoxicities in HeLa, HaCaT, MCF-7 and A549, cell death mechanisms and cellular uptake and localization of four iron(III) complexes are discussed. Chapter V describes the syntheses, characterization and the biological activities of carbohydrate appended iron(III) complexes and their non-glucose analogues. The selective and faster internalization of the glyco-conjugated complexes in HeLa cells has been studied using various spectroscopic and microscopic techniques. The red light induced cytotoxicities of the complexes, their effect on the progression of the cell cycle with and without irradiation and the mechanisms of cell death are explored. DNA binding abilities and photocleavage of DNA are also discussed. Chapter VI presents the syntheses, characterization of a series of iron(III) complexes of a pyridoxal derivative and their salicyldehyde analogues for exploring their differential photocytotoxicity and cellular uptake in cancer cells compared to normal cells. The visible light induced cytotoxicities of the complexes in HeLa, HaCaT, MCF-7 A549 cells and HPL1D cells, their effect on the progression of the cell cycle in dark and light, the mechanisms of cell death and the localization of the complexes inside the cells are explored. The references have been compiled at the end of each chapter and given as superscripts in the text. The complexes presented in this thesis are indicated by bold-faced numbers. Crystallography data of the complexes that are structurally characterized by single crystal X-ray crystallography are given in CIF format in the enclosed CD (Appendix-I). Due acknowledgements have been made wherever the work described is based on the findings of other investigators. Any unintentional omission that might have happened due to oversight is regretted. INDEX WORDS: Iron complexes • Crystal structure • Red light induced cytotoxicity • Cellular imaging • DNA binding • DNA photocleavage.