>Magister Scientiae - MSc / This study describes the synthesis and characterisation of Cu(II) and V(IV) complexes of tri- and quadridentate ligands L1 and L2 formed by condensation of ethylenediamine with acetylacetonate in 1:1 and 1:2 molar ratio, respectively. Encapsulation of these metal complexes in the nanocage of zoilite-Y generates new heterogeneous catalysts. These catalysts were synthesized employing the flexible ligand method encapsulation technique.The structures of these encapsulated complexes were established on the basis of various physico-chemical and spectroscopic studies. The results indicated that the complexes did not hinder or modify the framework or structure of the zeolite, confirming successful immobilization of Schiff-bases through the voids of zeolite Y.These encapsulated complexes were screened as heterogeneous catalysts for various oxidation reactions such as such as phenol, benzene, styrene and cyclohexene using a green oxidant (H2O2).For comparison, the corresponding neat complexes were screened as potential homogeneous catalysts for these oxidation reactions. The results proved that the corresponding homogeneous systems described here represent an efficient and inexpensive method for oxidation of phenol, benzene, styrene and cyclohexene, having advantages over heterogeneous catalysis are its high activity and selectivity and short reaction times. Its major problem is its industrial application regarding principally the separation of the catalyst from the products.The size of the substrate has a significant effect on the conversion by encapsulated complexes such as in styrene oxidation. Therefore, it was established that steric effects of the substrates play a critical role in the poor reactive nature of the encapsulated complexes.In general, the percentage conversion decreased upon encapsulation of complexes in zeolite Y. All catalysts studied proved to be potential catalysts for the various oxidation reactions.It has been shown in this study that encapsulation can effectively improve product selectivity but requires a longer reaction time in most cases for maximum activity.Furthermore,oxovanadium complexes were more reactive than copper-based catalysts in all oxidation reactions tested in this study.A reaction mechanism study revealed that the activity of the encapsulated and neat complexes occurs through either formation of peroxovanadium (V) or hydroperoxidecopper(II) intermediate species.The studies in this thesis, therefore, conclude that the Cu(II) and V(IV) complexes encapsulated in Y-zeolite are active heterogeneous catalysts for the selective oxidation of various substrates. Encapsulation of the metal complexes in the super cages (-cages) of the zeolite matrix has the advantages of solid heterogeneous catalysts of easy separation and handling, ruggedness, thermostability, reusability (regeneration of the deactivated catalysts) as well as share many advantageous features of homogeneous catalysts.

Thesis advisor: Amir H. Hoveyda / Chapter 1. We have developed a single-vessel catalytic protocol for double protoboryl additions to terminal alkynes with B2(pin)2 promoted by Cu complex derived from chiral N-heterocyclic carbene (NHC), to achieve enantiomerically enriched versatile vicinal diborons. Since an alkenyl(pinacolato)boron, which was in situ generated by the first protoboration of a terminal alkyne, can serve as an effective substrate for the second protoboration (alkenylboron can allow delocalization of π electrons of olefin to a partially vacant p orbital on boron), single-vessel catalytic process with 2 equiv. of B2(pin)2 in the presence of sulfonate-bearing chiral NHC–Cu complex, affords enantiomerically enriched 1,2-diborons in up to 93% yield and 97.5:2.5 enantiomeric ratio (e.r.). Site-selective Pd-catalyzed cross-coupling with alkenyl bromide shows the versatility of the resulting diboron compounds, which delivers the coupling product efficiently. Interestingly, only the less hindered, primary C–B bond on vicinal diboron compound participates in the cross coupling. Chapter 2. Cu-catalyzed protocol for selective formation of α-alkenylborons has been demonstrated. With achiral NHC–Cu complex, readily prepared from commercially available imidazolinium salt, various terminal alkynes are converted to internal alkenylborons in up to 93% yield with high to exclusive α selectivity. Propargyl ethers, amides and aryl alkynes are proved to be suitable substrates. Utility of α-alkenylborons is demonstrated by conversion to methyl ketone and synthesis of cyclic alkenylboron compound. In addition, when Cu complex bearing a stronger electron-donating NHC is used, the site selectivity of protoboration reaction becomes reversed, which delivers the alternative isomer, β-alkenylboron efficiently. By altering the steric and electronic nature of NHC, site selectivity is dramatically changed. Mechanistic basis for site selectivity is presented. Chapter 3. Efficient and selective protocol for synthesis of enantiomerically enriched silylborons is described. In the presence of achiral NHC–Cu complex, site- and stereoselective protosilyl additions to terminal alkynes afford a wide range of alkyl- and aryl-substituted (E)-β-alkenylsilanes. Chiral monodentate NHC−Cu complex promotes enantioselective protoboration of alkyl- or alkenyl-bearing alkenylsilanes, delivering vicinal borosilanes with up to 96.5:3.5 e.r. When an alkene bearing both silyl and aryl groups is utilized, on the other hand, geminal silylboron is obtained with high enantio- (93:7–98.5:1.5 e.r.) and site selectivity (up to >98% geminal). In this case, we have reasoned that the electronic attribute of aryl unit is more dominant than the silyl group to control site selectivity. To demonstrate the utility of the Cu-catalyzed transformation, we have illustrated the formal synthesis of bruguierol A, natural product active against Gram-positive and also Gram-negative bacteria. The key intermediate geminal borosilane is provided by sequential NHC–Cu-catalyzed protosilylation and protoboration of terminal alkyne in 77% overall yield with 97.5:2.5 e.r. and 97% site selectivity. Additionally, stereochemical models to account for levels and trends in site- and enantioselectivity are proposed. Chapter 4. New methods for enantioselective protonation of 2-B(pin)-bearing allylcopper, which is in situ generated by site-selective Cu–B addition to 1,1-disubstituted allene, are presented. Transformations are promoted by a chiral NHC–Cu complex, affording an alkenylboron containing α-carbon stereogenic center. Enantiomerically enriched aryl-, heteroaryl- and silyl-bearing alkenylborons are generated in high yield (up to 98%) and selectivities (up to >98% site selectivity and 96.5:3.5 e.r.). To explore the utility of enantiomerically enriched alkenylborons, we have developed Cu-catalyzed enantioselective allylic alkenyl addition to allylic phosphate. A chiral NHC–Cu complex promotes the allylic substitution of enantiomerically enriched alkenylboronic acid with ally phosphate to deliver 1,4-diene in 62% yield with 96:4 d.r. (>98% stereoselectivity). Chapter 5. We have developed a single-vessel, multicomponent process to synthesize N-bearing quaternary carbon stereogenic centers with exceptional diastereo- (>98:2 d.r. for all cases) and high enantioselectivity (88:12 to >99:1 e.r. except one case). Especially, protecting group-free ketoimine (“N–H” ketoimine), which can be prepared by alkylation of a readily available nitrile, has been utilized for the study. The transformation of “N–H” ketoimine is very useful because the obtained amine has no protecting group, which allows us to avoid the deprotection step as well as to be able to choose appropriate protecting group for subsequent chemical reactions. By oxidation of α-tertiary carbamine with NaBO3, β-amino ketones (Mannich reaction product) are obtained in up to 83% yield. A stereochemical model to account for the level of diastereo- and enantioselectivity are presented using DFT calculations. To show the utility of the present method, we have synthesized a medicinally active compound, which was studied for Alzheimer’s disease. The Cu-catalyzed protocol delivers the core structure of the target molecule with exclusive diastereo- and enantioselectivity (>98:2 d.r. and 99.5:0.5 e.r.). / Thesis (PhD) — Boston College, 2016. / Submitted to: Boston College. Graduate School of Arts and Sciences. / Discipline: Chemistry.

O Cu e suas ligas têm diferentes aplicações na sociedade moderna devido as excelentes propriedades elétricas, condutividade térmica, resistência à corrosão dentre outras propriedades. Estas aplicações podem ser em válvulas, tubulações, panelas para absorção de energia solar, radiadores para automóveis, condutores de corrente e eletrônico, elementos de termostatos e partes estruturais de reatores nucleares, como, por exemplo, bobinas para campo toroidal para um reator de fusão nuclear. Dentre as ligas utilizadas em reatores nucleares, podemos destacar Cu-Be, Cu-Sn e Cu-Pt. O Ni e o Co, freqüentemente são adicionados às ligas de Cu para que a solubilidade seja deslocada para temperaturas mais elevadas com relação aos sistemas binários de Cu-Sn e Cu-Pt. A adição de Ni-Pt ou Ni-Sn ao Cu em porcentagens iguais ou inferiores a 1,5 % aliado a tratamentos termos-mecânico alteram as propriedades do Cu. Estudamos neste trabalho sete diferentes ligas: três ligas de Cu-Ni-Pt 1 (97,99 % Cu - 1,55 % Ni - 0,46 % Pt), 2 (99,33 % Cu - 0,23 % Ni -0,43 % Pt) 3 (98,01 % Cu - 0,48 % Ni - 1,51 % Pt); três ligas de Cu-Ni-Sn 4 (98,31% Cu - 1,12 % Ni - 0,58 % Sn), 5 (98,79 % Cu – 0,57 % Ni - 0,65 % Sn), 6 (98,39% Cu – 0,46 % Ni – 1,16 % Sn) e Cu eletrolítico 0 (0,0058 % Pb - 0,0007 % Fe - 0,0036 % Ni - 0,0024 % Ag). As referentes ligas foram desenvolvidas a partir de um forno a arco voltaico e passaram por tratamentos termo-mecânicos pré-determinados. As microestruturas foram analisadas diretamente por microscopia óptica e microscopia eletrônica de varredura / EDS e indiretamente por medidas de dureza Vickers e condutividade elétrica. O objetivo deste trabalho, portanto, foi observar e constatar os efeitos da mudança da microestrutura em relação às propriedades dureza e condutividade elétrica. / The Cu and its alloys have different applications in the owed modern society the excellent electric properties, thermal conductivity, resistance to the corrosion and other properties. These applications can be in valves, pipes, pots for absorption of solar energy, radiators for automobiles, current driver, electronic driver, thermostats elements and structural parts of nuclear reactors, as, for example, reels for field toroidal for a reactor of nuclear coalition. The alloys used in nuclear reactors, we can highlight Cu-Be, Cu-Sn and Cu-Pt. Ni and Co frequently are added to the Cu alloys so that the solubility is moved for temperatures more elevated with relationship to the binary systems of Cu-Sn and Cu-Pt. The addition of Ni-Pt or Ni-Sn to the Cu in the same or inferior percentages to 1,5% plus thermomechanical treatments changes the properties of the copper. We studied the electric conductivity and hardness Vickers of the Cu-Ni-Pt and Cu-Ni-Sn and compared with the electrolytic Cu. In the proposed flowcharts, breaking of the obtaining of the ingot, we proceeded with thermo mechanical treatments.

Thesis advisor: Amir H. Hoveyda / Chapter One: An overview of Cu-catalyzed enantioselective allylic substitutions with organometallic reagents. Chapter Two: Development of Cu-catalyzed enantioselective allylic alkylations of allylic chlorides with Grignard reagents for the formation of all-carbon quaternary stereogenic centers is disclosed. Chapter Three: Development of Cu-catalyzed enantioselective allylic substitutions of allylic phosphates with alkyl, aryl, and heterocyclic aluminum reagents for the formation of quaternary stereogenic centers is discussed. / Thesis (MS) — Boston College, 2010. / Submitted to: Boston College. Graduate School of Arts and Sciences. / Discipline: Chemistry.

Thesis advisor: Amir H. Hoveyda / Chapter 1. In this chapter, the ability of chiral bidentate N-heterocyclic carbenes (NHCs) to activate alkylmetal reagents directly in order to promote C&#8210;C bond forming reactions in the absence of a Cu salt is presented. Highly regio- and enantioselective Cu-free allylic alkylation reactions of di- and trisubstituted allylic substrates with organomagnesium, organozinc, and organoaluminum reagents are demonstrated. Chiral bidentate sulfonate-bearing NHC-Zn and NHC-Al complexes are isolated and fully characterized. Based on crystal structures of these catalytic complexes, mechanistic details regarding Cu-free allylic alkylations with alkylmetal reagents are proposed. Chapter 2. New methods for efficient and highly enantioselective Cu-catalyzed allylic alkylation reactions of a variety of trisubstituted allylic substrates with alkylmagnesium and alkyl-, aryl-, 2-furyl-, and 2-thiophenylaluminum reagents are presented. Transformations are promoted by a chiral NHC complex in the presence of commercially available, inexpensive and air stable CuCl2*H2O. Enantiomerically enriched compounds containing difficult-to-access all-carbon quaternary stereogenic centers are obtained. Chapter 3. New methods for highly site- and enantioselective Cu-catalyzed allylic alkylation reactions of allylic phosphates with vinylaluminum reagents are presented. The requisite vinylaluminums are prepared by reaction of readily accessible terminal alkynes with DIBAL-H and used directly without further purification. Vinyl additions are promoted in the presence of a chiral bidentate sulfonate-based NHC complex and a Cu salt. The desired SN2' products are obtained in >98% E selectivities, >98% SN2' selectivities, >98% group selectivities (<2% i-Bu addition) and high enantioselectivities. The enantioselective total synthesis of the natural product bakuchiol highlights the versatility of the one-pot hydroalumination/Cu-catalyzed enantioselective allylic vinylation process. Chapter 4. Efficient and highly site-selective Cu-catalyzed hydroboration reactions of 1,2-disubstituted aryl olefins with bis(pinacolato)diboron (B2(pin)2) are presented. Transformations are promoted by an NHC-Cu complex in the presence of MeOH, affording only secondary &#946;-boronate isomers. A Cu-catalyzed method for the synthesis of enantiomerically enriched secondary alkylboronates promoted by chiral NHC complexes is disclosed. Chapter 5. A new method for efficient and site-selective tandem Cu-catalyzed copper-boron additions to terminal alkynes with B2(pin)2 in the presence of an NHC-Cu complex is demonstrated. In a one-pot process, Cu-catalyzed hydroboration of alkynes provides vinylboronates in situ, which undergo a second site-selective hydroboration to afford vicinal diboronates. Highly Enantiomerically enriched diboronates obtained through Cu-catalyzed enantioselective dihydroboration in the presence of chiral bidentate sulfonate-based NHC-Cu complex are obtained. The control of site selectivity in the first-stage hydroboration of alkynes is critical for efficient and highly enantioselective reactions in the tandem dihydroboration. Functionalizations of the vicinal diboronates described herein underline the significance of the current method. / Thesis (PhD) — Boston College, 2010. / Submitted to: Boston College. Graduate School of Arts and Sciences. / Discipline: Chemistry.

As estruturas do tri(hidroximetil) amino metano complexado com cobre Cu(II), Cu[NH2C(COH3)3]2+H2O e do tri(hidroximetil)amino metano dopado com prata Ag(I), Ag[NH2C(COH3)3] foram determinados por difração de raios-x. O complexo contendo íons de cobre refinou até um R de 0.034 e foram encontradas as seguintes características principais: sistema cristalino monoclínico; grupo espacial C2/c, a=12.955(2)&#197; b=10.793(1)&#197; c=10.091(2)&#197; &#946=116.62&#176; V=1261.3(6)&#1973; Z=4; xDc=1.694(2)g/cm-3; &#955(K&#945Mo)=0.71073&#197; das reflexões medidas 1441 tinham I&#62 3&#948 (I). O íon de cobre está coordenado por pares de átomos de oxigênio e nitrogênio os quais formam uma pirâmide de base quadrada, o oxigênio da molécula de água ocupa o outro vértice da pirâmide. A determinação dessa estrutura é utilizada na interpretação da formação de complexos de cobre com tri(hidroximetil) amino metano em função do pH. A estrutura do tri(hidroximetil) amino metano dopado com prata apresentou as seguintes características: sistema cristalino ortorrômbico; grupo espacial Pna21; a=7.800(2)&#197; b=8.810(3)&#197; c=8.850(2)&#197; V=608.85(4)&#1973; Dc=1.329g/cm-3; Dm=1.337g/cm-3; 435 reflexões com I&#62 3&#948 (I); R=0.13; o carbono central é coordenado tetraedricamente por três átomos de carbono do tri(hidroximetil) e um nitrogênio do grupo amino. As estruturas do tris dopado com níquel, e do tris dopado com zinco apresentam-se isomorfa com a estrutura do tris dopado com prata. / The crystal structures of the tri(hydroxymethyl) amine methane complexed with cooper Cu[NH2C(COH3)3]2+H2O and the silver Ag[NH2C(COH3)3] doped into the tri(hydroxymethyl) amine methane have been determined by x-ray diffraction. The complex involving Cu++ refined to final R-factor of 0.034, and the following main features were found: the crystal system is monoclinic and its space group is C2/c, a=12.955(2)&#197; b=10.793(1)&#197; c=10.091(2)&#197; &#946=116.62&#176; V=1261.3(6)&#1973; Z=4; Dc=1.694(2)g/cm-3; &#955(K&#945Mo)=0.71073&#197; from measures done, 1441 had I&#62 3&#948 (I). The Cu++ is coordinated by couples of atoms of oxygen and nytrogen, which form a base of a quadrangular pyramid, the pyramid vertex is formed by the oxygen of the water molecule. The determination of this structure is used to interpret the rise of tri(hydroxymethyl) amine methane and complexed with Cooper varying the pH. The silver doped into the structures of tris(hydroxymethyl) amine methane presented the following features: crystal system is orthorrombic; space group is Pna21; a=7.800(2)&#197; b=8.810(3)&#197; c=8.850(2)&#197; V=608.85(4)&#1973; Dc=1.329 g/cm-3; Dm=1.337 g/cm-3; R=0.13; 435 reflections with I&#62 3&#948 (I) the central carbon is coordinated tetrahedrally by three atoms of carbon from tri(hydroxymethyl) and a nitrogen from the amine group.

This work describes a novel technique to prepare ultra-thin composite Pd-porous metal membranes for H2 separation. This novel technique consists of the gradual smoothing of the Porous Metal (PM) support's surface with several layers of pre-activated alumina particles of different sizes. The deposition of coarse, fine and ultra-fine alumina particles resulted in the narrowing of the PM' surface pore size distribution. The excellent surface smoothness achieved after the grading of the PM 's surface support allowed for the preparation of gas tight Pd layers as thin as 5.6?m. The Pd layers were extremely uniform due to the presence of the grade layer and strongly attached to the support. Composite Pd membranes prepared on graded supports showed H2 permeance as high as 50 m3/(m2 h bar0.5) at 500ºC and ideal selectivities (H2/He) as high as 27000. Moreover, the H2 permeance and ideal selectivity were stable over 1100 hours at 500ºC in H2 atmosphere. Composite Pd-Cu membranes showed H2 permeance as high as 30 m3/(m2 h bar0.5) at 450ºC and ideal selectivities (H2/He) as high as 900. The H2 permeance and ideal selectivity of Pd-Cu membranes were stable over 500 hours at 450ºC in H2 atmosphere. The outstanding long-term H2 permeance and ideal selectivity stability of all composite Pd and Pd-Cu membranes represented a breakthrough in composite Pd membrane synthesis. The thermal stresses arising from the mismatch in the coefficient of thermal expansion between the Pd film and the support were determined by means of x-ray diffraction. The results indicated that the release of stresses began to occur at temperatures close to 400ºC. Also, the release of stresses took place with a visible sintering of Pd clusters within the thin Pd film. The stresses due to the absorption of H2 were also studied and modeled. It was estimated that the maximum compressive stress under which these composite Pd membranes were characterized was equal to 260 MPa.

Submitted by Cleide Dantas (cleidedantas@ufpa.br) on 2014-04-08T17:15:22Z No. of bitstreams: 2 license_rdf: 23898 bytes, checksum: e363e809996cf46ada20da1accfcd9c7 (MD5) Dissertacao_EfeitoAdicoesNi.pdf: 5757867 bytes, checksum: 8a77abd3b782bdae2352df421372bf23 (MD5) / Approved for entry into archive by Ana Rosa Silva (arosa@ufpa.br) on 2014-09-01T15:39:57Z (GMT) No. of bitstreams: 2 license_rdf: 23898 bytes, checksum: e363e809996cf46ada20da1accfcd9c7 (MD5) Dissertacao_EfeitoAdicoesNi.pdf: 5757867 bytes, checksum: 8a77abd3b782bdae2352df421372bf23 (MD5) / Made available in DSpace on 2014-09-01T15:39:57Z (GMT). No. of bitstreams: 2 license_rdf: 23898 bytes, checksum: e363e809996cf46ada20da1accfcd9c7 (MD5) Dissertacao_EfeitoAdicoesNi.pdf: 5757867 bytes, checksum: 8a77abd3b782bdae2352df421372bf23 (MD5) Previous issue date: 2013 / CAPES - Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / Este trabalho estudou a influência dos teores dos solutos Mg e Ni na modificação das propriedades térmicas, elétricas e mecânicas de uma liga Al-Cu-Fe para aplicação como condutor de energia elétrica. Para a realização do presente estudo, as ligas foram obtidas por fundição unidirecional horizontal, a partir da base do alumínio de pureza comercial com adição dos teores 0,05%p Cu e [0,24 a 0,28]%p Fe. Tal base foi modificada em uma primeira etapa com teores de 0,45, 0,60 e 0,80%p Mg. As ligas obtidas com estes teores tiveram suas propriedades estudadas para que se selecionasse um teor de Mg para posterior adição de Ni à liga. O estudo destas propriedades na primeira etapa passou pela análise das propriedades térmicas: velocidade de solidificação (VL) e taxa de resfriamento (Ṫ). A caracterização elétrica estudou a propriedade condutividade elétrica (φ) e o levantamento das propriedades mecânicas: limite de resistência à tração (σ) e microdureza Vickers (HV). A liga com adição de Ni passou por tratamentos térmicos de envelhecimento, por 1, 4 e 8h. Estas amostras foram analisadas em um microscópio eletrônico de varredura - MEV pelos sinais de elétrons retroespalhados – ERE e espectroscopia de energia dispersiva – EDS. Como resultados do estudo, encontrou-se que adições de Mg influenciaram significativamente a viscosidade das ligas, elevando as velocidades de solidificação nos instantes finais. Os ensaios de microdureza das amostras envelhecidas mostraram que houve um acréscimo significativo de dureza na quarta hora de envelhecimento, da mesma forma que as análises de EDS mostraram que a concentração de Ni também elevou-se nesta condição de tratamento. / This work studied the influence of Mg and Ni solute content on the modification of the thermal, electrical and mechanical properties of an Al-Cu-Fe alloy for application as an electrical conductor. To realize the present study, the alloys were obtained by unidirectional horizontal casting, starting from the commercial pure aluminum with the addition of 0.05wt% Cu and [0.24 to 0.28]wt% Fe content. This basis was modified on a first stage with 0.45, 0.60 and 0.80wt% of Mg content. The alloys obtained with these contents had its properties studied for the selection of a Mg content for further Ni addition at the alloy. The study of these properties on the first stage passed through the analysis of the thermal properties: growth rate (VL) and cooling rate (Ṫ). The electrical characterization studied the electrical conductivity property (φ) and the following mechanical properties were determined: ultimate tensile strength (σ) and Vickers microhardness (HV). The alloy which has Ni additions passed through ageing heat treatments of 1, 4 and 8 hours. These samples were analyzed in a scanning electron microscope – SEM by the electrons backscattered – EBS and energy dispersive spectroscopy – EDS signals. As a result of the research, it was found that Mg additions had significantly influenced the alloys viscosity, increasing its growth rates at the final moments of the solidification. The microhardness tests for the aged samples showed that they suffered a significant gain of hardness at the fourth hour of ageing, also, the EDS analysis showed that Ni content increased at the same treating conditions.

Superfícies de silício (100) foram inicialmente pré-ativadas em uma solução diluída de ácido fluorídrico contendo PdCl2. Após essa etapa, filmes finos de Cu-Ni-P foram quimicamente depositados utilizando-se um banho químico contendo 15g/l NiSO4.6H2O; 0.2 g/l CuSO4.5H2O; 15 g/l Na2HPO2.H2O e 60 g/l Na3C6H5O7.2H2O na temperatura de 80ºC onde foi adicionado NH4OH até que o pH da solução atingisse 8,0. Foi observado que as porcentagens estequiométricas de Ni e Cu variaram substancialmente no intervalo de 1 a 3min, e se tornaram praticamente estáveis em 50% e 35%, respectivamente, quando o tempo de deposição foi superior a 3min. Além disso, a porcentagem de P permaneceu quase constante em torno de 17-18% para todos os tempos de deposição. A distribuição de alturas nas imagens FE-SEM resultou bimodal para tempos na faixa de 1 e 3min onde a predominância do modo de maior altura aumentou substancialmente para o tempo de 3min. Tal fato serviu para corroborar a evolução da morfologia superficial de grãos menores com diâmetros na faixa de 0,02 a 0,1µm, predominantemente compostos de Ni, para grãos maiores, na faixa de 0,1 a 0,3µm e predominantemente compostos de Cu. Após um recozimento a 100oC durante 10min em ambiente 20%O2+80%N2, observou-se uma mudança na morfologia superficial em que os aglomerados de fósforo (Po) desapareceram enquanto que os grãos que compunham a imagem não mudaram substancialmente de tamanho após o recozimento. Apesar do desaparecimento dos aglomerados, a concentração de fósforo ainda apresentou valor semelhante ao valor de antes do recozimento (~17-18%). As análises de difração de raios X (XRD) indicaram o aparecimento de um pico de difração alargado ao redor de 22,6º característico de óxido de fósforo (P2O5) com estrutura vítrea amorfa significando que o fósforo em estado puro foi transformado na sua forma oxidada. Por outro lado, picos substancialmente menos intensos de NiO, Ni3P e Si5P6O25 foram observados. Verificou-se também para os filmes recozidos em N2+O2 que a resistividade aumentou para todos os tempos de deposição e o poder termoelétrico medido resultou quase independente do tempo de deposição e, portanto, foi quase independente da espessura do filme para as diferentes temperaturas medidas na faixa de 40 a 120ºC. / Silicon surfaces (100) were initially pre-activated in a diluted hydrofluoric acid solution containing PdCl2. After this step, Cu-Ni-P thin films were chemically deposited using a chemical bath containing 15g/l NiSO4.6H2O; 0.2 g/l CuSO4.5H2O; 15 g/l Na2HPO2.H2O e 60 g/l Na3C6H5O7.2H2O at the temperature of 80°C where NH4OH was added until the pH of the solution reached 8.0. It was observed that the stoichiometric percentages of Ni and Cu varied substantially for deposition time in the range of 1 to 3min, and became practically invariant at 50% and 35%, respectively, when the deposition time was greater than 3min. In addition, the percentage of P remained almost constant at around 17-18% for all the deposition times. The distribution of heights in the FE-SEM images resulted bimodal for times in the range of 1 and 3min where the predominance of the higher average height mode increased substantially for the time of 3min. This fact allowed one to corroborate the superficial morphology passing from smaller grains with diameters in the range of 0.02 to 0.1µm, predominantly composed of Ni to larger grains in the range of 0.1 to 0.3µm with Cu predominant composition. After an annealing at 100°C for 10min in a 20%O2+80%N2 environment, the phosphorus (Po) agglomerates disappeared while the size of the grains did not change substantially after the annealing. Despite the disappearance of the agglomerates, the phosphorus concentration still remained unchanged (~ 17-18%). X-ray diffraction (XRD) analysis showed a broad diffraction peak around 22.6º, which is characteristic of an amorphous vitreous structure (P2O5). In addition, substantially less intense peaks showing small amounts of NiO, Ni3P and Si5P6O25 were observed. It was also verified for the N2+O2 annealed films that the resistivity increased for practically all the deposition times and the measured thermoelectric power was almost independent of the deposition time and, therefore, was also independent of the film thickness for the various temperatures in the range from 40 to 120ºC.

An electron momentum spectrometer at the Australian National University has been used to study various aspects of different solid state systems. EMS is a transmission mode technique and involves the collision of the incident electron with a bound electron, after which both electrons are ejected and measured in coincidence. Through well defined reaction kinematics the complete valence spectral momentum density A(ɛ,q) can be measured. The spectrometer has been used to measure the spectral momentum densities (spectral functions) of single crystal targets, as well as targets in disordered states. A new spin polarised electron source was constructed and implemented in the ANU spectrometer, which was used to measure spin dependent features of ferromagnetic samples.¶ This thesis is divided into seven chapters, the first chapter is an introduction into the field of electron momentum spectroscopy, highlighting what has been measured before and how the technique has progressed to its present state. Some comparisons to other experimental techniques will be made.¶ The second chapter describes the ANU EMS spectrometer in detail. The technique requires some technical and advanced equipment that is often used in novel ways. The production of thin (20 nm) free standing targets will be detailed, along with the experimental chamber and electronics used to run the apparatus and collect data. The determination of the energy and momentum resolution of the experiment is also described.¶ The third chapter will detail the design and construction of the new spin polarised electron source. The results of commissioning and characterizing the new source will be presented.¶ Chapters four through six will present the measured results. The fourth chapter will detail the single crystalline measurements for the group eleven noble metals (Cu, Ag and Au). Each sample was measured along three high symmetry directions and compared to a DFT calculation using the LDA and a FP-LMTO basis. The fifth chapter will include the results from samples that were in disordered states, a measurement which is unique to the EMS technique. The polycrystalline and amorphous states of the Si and Ge semiconductors are presented and conclusions are made to the degree of difference in the results and to which theoretical approach to the unique amorphous state of the semiconductors best matches the EMS results. The sixth chapter includes results of ferromagnetic iron, measured using the spin polarised electron source. The spectrometer was used to measure spin-polarised electron-energy-loss-spectroscopy (SPEELS) and magnetic electron-Compton profiles. A theoretical investigation is also presented in chapter six which details the advancements required in the spin polarised electron gun to measure an accurate spin-polarised EMS spectra of a ferromagnetic Fe sample.¶ Chapter 7 includes the summary of all the results presented and conclusions reached from the comparison of the measured EMS spectra and various theoretical calculations. A discussion is presented about the future directions and possibilities of the EMS technique.