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Com o objetivo de verificar o consumo alimentar e o estado nutricional em relação ao zinco de crianças submetidas a um programa de suplementação com ferro, foram estudadas 150 crianças com idade entre 2 e 7 anos, que pertenciam a por 2 creches do município de São Paulo. O período de estudo foi de 7 meses, dividido em três fases (F0, F1 e F2); onde avaliou-se em cada fase a dieta oferecida e a concentração de zinco no eritrócito das crianças. Na fase inicial do estudo (F0) avaliou-se a dieta normal oferecidas nas creches e o estado nutricional inicial das crianças; na F1, a creche ST recebeu o alimento fortificado com ferro e a creche SM recebeu o mesmo alimento porém sem a fortificação. Já na F2, a creche ST recebeu o alimento sem fortificação e a SM o alimento fortificado. Pelos resultados obtidos pode-se concluir que: as dietas se apresentaram deficientes em caloria e zinco para a creche ST e também em ferro para a creche SM, não estando adequada especialmente para as crianças acima de 4 anos; a fortificação do queijo \"petit suisse\" com ferro aminoquelato não causou mudança na concentração de zinco nos eritrócitos das crianças analisadas ao longo do estudo, embora o estado nutricional das mesmas em relação a este mineral encontrava-se deficiente podendo ser atribuido à qualidade da dieta. / Aiming to value the food consumption and the nutritional status of zinc on infants submitted to an iron supplementation program, were studied 150 pre-schollars aged 2 to 7 years old of two nurseries (ST e SM) in the city of São Paulo. Studies were seven month, based on three stages (F0, F1 e F2), where was assessed the diets offered and the erythrocite zinc on infants, in the each stage. In the initial stage (F0), were assessed the regular diets offered by the nurseries and the initial nutritional status on infants; in the F1), the diets from nursery ST had meals supplemented with iron and the diets from nursery SM had the same meals although without the supplementation. In F2), the diets from nursery ST had meals without the supplementation and the diets from nursery SM the meals supplemented with iron. According with the results we can conclude: the diets were calories and zinc deficient to nursery ST and iron defícient to nursery SM, also; the iron supplementation in the \"petit suisse\" cheese with aminoquell iron did not cause any change in the erythrocite zinc concentration of the children being studied although the nutritional status were zinc deficient due to a quality of the diets.

A range of inorganic materials, with structures based on transition metal centred polyhedra linked through simple or polyatomic anions, has been synthesised and fully characterised. These materials were prepared using a variety of synthetic methods, including the direct high temperature, solid state reactions, and hydrothermal techniques in fluoride rich media. The materials produced were structurally characterised by powder (PXD) and single crystal (SXD) X-ray diffraction techniques with further analysis via infrared and UV/visible/near-infrared spectroscopies, thermogravimetric analysis and scanning electron microscopy. Copper (II) phosphates and related materials have potential applications derived from their near-infrared (NIR) radiation absorbing properties. A range of complex copper phosphate phases in the Cu-P-O or A-Cu-P-O systems, where A is a Group 1 or 2 element, has been synthesised and characterised. The intensity and positions of absorptions in the NIR region found for these materials and derived from d-d transitions on copper, are dependent upon the copper ion coordination geometry and the ligand field produced by the surrounding anions. K2CuP2O7 and the phases A3Cu3(PO4)3 (A = Sr, Ca) were all found to absorb strongly in the NIR region. The NIR absorbance spectrum could be modified further by introducing fluoride into the Cu(II) ligand environment and Cu2PO4F was shown to have a very strong, broad NIR absorption spectrum.

In Chapter 1, I discuss the synthesis and characterization of lithium tris(pyrazolyl)hydroborato complexes, [TpR1,R2]Li. Group 1 [TpR1,R2]M complexes serve as key starting points to access many other main group and transition metal complexes; however, the synthesis and crystal structures of [Tp R1,R2]Li has not been reported. Molecular structures of [TpBut]Li and [TpBut,Me]Li show these complexes are trigonal pyramidal, an unusual geometry for lithium. These complexes are also able to bind small molecules to form four-coordinate pseudo-tetrahedral complexes, [Tp]Li-L (L = MeCN, pzButH, and H2O). The binding constants for the association of acetonitrile to [TpBut]Li and [TpBut,Me]Li are 0.84M-1 and 0.96M-1, respectively, indicating that the dissociation of MeCN is facile in solution. In addition, [TpBut,Me]Li serves as transmetallating agent to yield the cadmium halide complexes, [TpBut,Me]CdX (X = Cl, Br, I). In Chapter 2, I discuss the synthesis and characterization of organometallic cadmium complexes supported by the nitrogen-rich multidentate ligands, tris(pyridylthio)methane, [Tptm]H; tris(1-methyl-imidazolylthio)methane, [TitmMe]H; and tris(1-methyl-benzimidazolylthio)methane, [TitmiPrBenz]H. These ligands are in the nascent stages of development and there are only a few metal [Tptm] and [TitmMe] complexes in the literature. An investigation of the reactivity of [L]CdN(SiMe3)2, [L]CdOSiMe3, and [L]CdOSiPh3 ([L] = [Tptm], [TitmMe], [TitmiPrBenz]) shows these complexes provide access to a variety of organometallic cadmium complexes, [L]CdX, (X = OAc, Cl, Br, O2CH, NCO). The characterization of cadmium acetate and formate complexes is significant due to their structural similarity with the metal bicarbonate intermediate formed by zinc and cadmium-substituted carbonic anhydrase. In addition, the synthesis and characterization of cadmium methyl complexes, [L]CdMe, is discussed. The application of heat to a mixture of [TitmiPrBenz]H and CdMe2 results in isomerization of the ligand to [S3-TitmiPrBenz]CdMe. This sulfur-rich [S3-TitmiPrBenz] ligand is not reported in the literature and is ripe for further investigation. The solid state structures of these compounds provide a comparison with biologically relevant [Tp] or [Tm] cadmium methyl complexes in the literature. In Chapter 3, I describe the synthesis and structural characterization of [BmButBenz]M (M = Na, K) and [BmRBenz]Ca(THF)2 (R = Me, But) are discussed. The sulfur-rich tripodal ligand tris(imidazolylthio)hydroborato, [Tm], was previously designed to serve as a softer version of the [Tp] ligand. Metal [Tm] complexes are prevalent in the literature and have often been used as molecular mimics of sulfur-rich enzyme active sites. Recently, the benzannulated [TmRBenz]M complexes were reported and were found to promote k3 coordination toward the metal center. To allow for an in-depth investigation of the newly synthesized [BmRBenz] class of ligand, the [BmButBenz]M (M = Na, K, Ca) complexes were synthesized and compared to previously reported metal [BmMeBenz]M complexes. Additionally, the [BmMeBenz]2Ca(THF)2 was synthesized and characterized via X-ray diffraction. The molecular structure of [BmMeBenz]2Ca(THF)2 shows the complex is monometallic with an uncommon eight-coordinate dodecahedral calcium center. [BmMeBenz]2Ca(THF)2 is the first molecular structure of calcium coordinated to the [Tm] or [Bm] ligand class. In Chapter 4, I discuss the synthesis and characterization of mercury alkyl complexes supported by the [TmMe], [BmR], [TmRBenz] and [BmRBenz] ligands (R = Me or But). As previously mentioned, [Tm]M complexes are considered biologically relevant molecular models of enzyme active sites. With this in mind, [TmBut]HgR (R = Me,Et) complexes have served as mimics for the mercury detoxification enzyme MerB. A previous study by our group showed that the adoption of multiple coordination modes of the ligand in [TmBut]HgR plays a significant role in the activation of the Hg-C bond toward protonolysis. The molecular structures of the [TmR], [BmR], [TmRBenz], and [BmRBenz] mercury alkyl complexes show that they adopt various coordination modes, ranging from k1 to k3. Preliminary competition experiments in which benzenethiol was added to [TmR]HgEt and [TmRBenz]HgEt indicate that the Hg-C bond in [TmMeBenz]HgEt was cleaved faster than that in [TmMe]HgEt. Conversely, the Hg-C bond in [TmBut]HgEt was cleaved faster than that in [TmButBenz]HgEt, indicating that benzannulation and the size of the R-group on the [Tm] ligand play important roles in Hg-C bond cleavage.

This dissertation is a summary of my research developing the synthesis and assembly of functional materials from nanoscale building blocks and studying their emergent properties. Chapter 1 introduces superatoms as exciting atomically precise supramolecular building blocks for materials design. Bottom-up assembly of these superatoms into materials with increased dimensionality (0D, 1D, 2D, and 3D) offers exciting opportunities to create novel solid-state compounds with tailored functions for widespread technological applications. I review recent advances to assemble superatomic materials and focus on assemblies from metal chalcogenide clusters and fullerenes. In subsequent chapters, I employ several of these nanoscale superatoms as the precursors to functional materials. Chapter 2 describes the synthesis and structural characterization of a hybrid solid-state compound assembled from two building blocks: a nickel telluride superatom and an endohedral fullerene. Although a varied library of binary superatomic solids has been assembled from fullerenes, this is the first demonstration of a superatomic assembly using an endohedral fullerene as a building block. Lu3N@C80 fullerenes are dimerized in this new solid-state compound with an unpreceded orientation of the encapsulated metal nitride cluster. I explore the structural characterization of this material supported with computational evidence to explain the dimerization and orientation of the endohedral fullerenes. In Chapter 3 I begin to detail my exploration into assembling superatoms at micro and meso-scales –which will be the focus of Chapters 3-5. Polymers offer attractive mechanical and self-assembly properties that when combined with the attractive redox, optical, and magnetic properties of molecular clusters, these materials chart new paths to developing advanced materials and technologies. Chapter 3 describes charge transfer interactions between perylene diimide and cobalt telluride superatoms that drive the assembly of a solid-state compound from these two building blocks and inspired the design of a diblock copolymer template. Chapters 4 and 5 detail the synthesis and characterization of a polymer with functionalized cobalt selenide side units. I describe a cationic homopolymer in Chapter 4 and diblock copolymer in Chapter 5 synthesized from ring opening polymerization of norbornene-derived monomers. Chapter 4 describes potential applications of the homopolymer system such as thin film fabrication. Chapter 5 discusses the self-assembly of the redox-active diblock copolymer into cross-linkable vesicle structures that can encapsulate molecular cargo. Finally, in Chapter 6 I introduce a new molecular building block to form gold metal surface bonds. Bisaminocyclopropenylidenes (BACs) are a class of carbenes that, much like N-heterocyclic carbenes, have been widely employed for catalysis but have yet to be explored for materials design. This chapter describes the structure and binding orientation of a BAC on an Au(111) surface. Each of these chapters illustrates how the synthetic flexibility of molecular building blocks enables the design of functional materials with tunable properties.

Abstract not available

Thesis (M. Phil.)--University of Hong Kong, 2006. / Title proper from title frame. Also available in printed format.

Thesis (Ph. D.) in Physics--University of Maine, 2001. / Includes vita. Includes bibliographical references (leaves 96-102).

published_or_final_version / abstract / Electrical and Electronic Engineering / Master / Master of Philosophy

The goal of this research is to obtain the adsorption mechanisms of toxic mercury-containing species (Hg, HgCl and HgCl2) and carbon dioxide (CO2) on inorganic solid surfaces using theoretically predicted results because experiments have been unable to unravel the involved issues. The understanding of the adsorption mechanisms of the mercury species and carbon dioxide from flue gases is important when considering mercury capture from coal-fired power plants, artisanal gold mining, and cement manufacturing industries. The current research attempts to explain each adsorption mechanism for mercury species, and those for carbon dioxide adsorption, on the surfaces through optimized geometries, energies and thermodynamic data.To investigate this research, density functional theory, which is one of useful tools for analyzing reactions on solid surfaces, was used to determine first principles-based theoretical adsorption models. Mainly, results from computational work indicate that mercury-containing species and carbon dioxide adsorption on calcium oxide surfaces and elemental mercury adsorption on a gehlenite surface are exothermic reactions. Calcium oxide is a promising adsorbent for oxidized mercury (HgCl and HgCl2), but not for elemental Hg. Interestingly, the elemental mercury, which is the major form (> 90%) in the flue gases of the coal-combustion power plants, is chemisorbed on a gehlenite surface, which is partially composed of calcium oxide and comes from a mineral transition at high temperature. Strong adsorption on this inorganic sorbent is enhanced at high temperatures even though this adsorption process is exothermic. In addition, CaO surfaces are effective at capturing CO2, generating calcium carbonate compounds at flue gas temperatures, and water vapor enhances its adsorbability due to a larger CO2 adsorption energy. The current research shows that inorganic sorbents are not only effective in removing the elemental and oxidized forms of mercury but also in mineralizing CO2 at high temperatures into a solid form. The mercury species and carbon dioxide adsorption mechanisms investigated in this research may be utilized in the application of more efficient mercury and carbon dioxide control technologies. Future work will examine the reaction transition state and predict the kinetic data of the carbonation reactions, and, additionally, may prove the hypothesis that H2O molecules play a role as catalysts, increasing reaction rates.