When E- or Z-l-methyl-l-phenyl-2-neopentylsilene was generated by the retro-Diels-Alder vacuum-sealed tube thermolysis of its corresponding anthracene adduct, in the presence of various alkoxysilanes, only one diastereomeric adduct was formed in each case, showing that the reactions are stereospecific. An x-ray crystal structure of the methoxytriphenylsilane adduct of the E-silene confirmed its relative configuration as (R,S) or (S,R). This demonstrated that the addition of alkoxysilanes to silenes is stereospecific and syn. The relative configurations of similar alkoxysilane and alkoxystannane adducts to E- and Z-l-methyl-l-phenyl-2-neopentylsilene were assigned based on a combination of xray structures and *3C NMR data. A strong, nonbonded oxygen-metal interaction is apparent in all of those compounds studied. Treatment of the alkoxystannane adducts with alkyl lithium reagents results in tin-lithium exchange in some cases. The results indicate that the resulting <x-lithio alkoxysilanes are not configurationally stable in either THF or hydrocarbon solvents. The reaction of tert butyl lithium with a-trimethylsilylvinylmethylphenylchlorosilane in hydrocarbon solvents yields E- and Z-l-methyl-l-phenyl-2-neopentyl-2-trimethylsilylsilene. In the absence of any traps these silenes undergo a novel tert butyl lithium catalyzed rearrangement to 2-phenyl-3-trimethylsilyl-5,5-dimethyl-2-silahex-3-ene. These silenes were also trapped as their [4+2] cycloadducts with anthracene. The Z-isomer of the anthracene adduct was separated and its stereochemistry confirmed by an x-ray crystal structure. The anthracene adducts of both E- and Z-l-methyl-1-phenyl-2-neopentyl-2-trimethylsilylsilene undergo a facile, stereospecific decomposition at temperatures as low as 190°C to regenerate their respective silenes, the mildest stereospecific route to a silene yet reported. The E- and Z-silenes react stereospecifically with methanol under vacuum-sealed tube conditions. The stereochemistry of the addition is syn and a common mechanism is proposed for the addition of alcohols and the addition of alkoxysilanes to silenes.

Au cours de ce travail de thèse, la Cellulose Nanofibrillée (CNF) a été isolée à partir de fibres de paille d’avoine puis modifiée chimiquement par des alcoxysilanes en milieu aqueux. La CNF silylée a ensuite été utilisée pour élaborer de nouveaux matériaux composites et mousses biosourcés.Le chapitre I présente quelques aspects généraux concernant les nanocelluloses, en particulier la NFC et ses applications dans le domaine des matériaux composites et des mousses.Le chapitre II est consacré à la fonctionnalisation de la CNF par le méthyltriméthoxysilane - choisi comme alcoxysilane modèle - ainsi qu’à la caractérisation du matériau silylé. Plusieurs paramètres réactionnels (pH, temps de réaction, concentration initiale en silane) ont été étudiés et optimisés, à partir de deux protocoles expérimentaux distincts. Les modifications ont été caractérisées à l’échelle moléculaire par différentes techniques physico-chimiques. Les propriétés des nanofibrilles silylées, comme la morphologie, cristallinité, mouillabilité, hygro-copicité et stabilité thermique, ont ensuite été évaluées.Dans le chapitre III, l’impact de la silylation sur les propriétés mécaniques et hygroscopiques de composites à matrice acide poly(lactique) ou matrice polydiméthylsiloxane chargés en NFC a été évalué.Pour finir, l’impact de la silylation sur les propriétés de mousses élaborées à partir de NFC lyophilisées a été étudié dans le chapitre IV (porosité, propriétés en compression, conductivité thermique, mouillabilité, hygroscopicité et oléophilicité). / In this thesis, nanofibrillated cellulse (NFC) has been isolated from oat straw and chemically modified by alkoxysilanes in water medium. Silylated NFC has been subsequently used to elaborate novel biobased composite materials and foamsChapter I presents some general aspects about nanocelluloses – in particular Nanofibrillated Cellulose (NFC) - and their use in composite materials and foams.Chapter II is dedicated to the functionalization of NFC by methyltrimethoxysilane - chosen as a model silane - and to the comprehensive examination of the silylated material. Reaction conditions such as pH, reaction time and initial silane concentration have been particularly in-vestigated and optimized using two distinct experimental protocols. The modifications have been characterized at the molecular level by various physicochemical techniques. The proper-ties of the silylated nanofibrils i.e. the morphology, crystallinity, wettability, hygroscopicity and thermal stability, have been subsequently examined. Chapter III investigates the impact of silylation on the mechanical and hygroscopic properties of NFC-reinforced composites prepared with two distinct polymeric matrices: poly(lactic acid) (PLA) and polydimethylsiloxane (PDMS).Chapter IV examines the impact of silylation on the properties of NFC-foams prepared by freeze drying, in particular on the porosity, compressive properties, thermal conductivity, wet-tability, hygroscopicity and oleophilicity.

The purpose of this study was to explore the feasibility of re-treating artifacts previously conserved by PEG impregnation with alkoxysilanes. The study tried to evaluate pros and cons of re-conserving artifacts with this type of silanes. A series of experiments were conducted focusing on small, wood samples from the Vasa Museum Collection, to test different re-conservation methods. Three different procedures involving alkoxysilanes were implemented in order to re-conserve the samples. The study revealed the techniques are an efficient re-conservation method in which highly satisfactory results can be achieved. The re-treated samples present minimal volumetric distortion without significant collapse or shrinkage of the wood structures. This minimal distortion is primarily produced by the transition from swollen waterlogged wood to a dry conserved wood, and not as a result of collapse or shrinkage during treatment. Due to the negligible thickness of the polymer coating (a few microns), the samples acquire physical properties extremely close to the original dry wood. Moreover, other physiochemical properties are obtained from the consolidation with alkoxysilanes; the re-conserved wood becomes hydrophobic, chemically inert, resistant to chemical attacks (e.g., acids or bases), and resistant to ultraviolet light. These newly acquired characteristics drastically reduce the preventive conservation measures needed in museum display cabinets or during transport. Despite the excellent results, the procedure is not reversible, thus does not comply with one of the main premises traditionally accepted in conservation. Therefore, a careful study assessing benefits and disadvantages in a case-by-case basis should be assessed by conservators, restorers, and curators before applying this method to waterlogged material culture.

Ce travail de thèse concerne l'auto-structuration de particules magnétiques dans une matrice cristal liquide nématique (CLN). Par l'élaboration de matériaux nouveaux combinant propriétés magnétiques et structurations des particules, cette étude s'inscrit dans le domaine, en plein essor, de la recherche de matériaux adaptatifs. P. Poulin, le premier, a mis en évidence de nouvelles interactions colloïdales induites par l'élasticité d'un fluide nématique suspendant. L'obtention d'une structuration contrôlée des particules microniques via la matrice nématique passe par un contrôle précis de l'ancrage des molécules de CLN sur la surface des particules de fer. Ainsi, après une caractérisation approfondie de l'état de surface du fer, de nombreux traitements capable d'engendrer un ancrage homéotrope des nématogènes en contact avec la surface ont été réalisés sur des plaques servant de système modèle. Deux approches ont été explorées, l'une consiste en une modification de l'état de surface du fer, l'autre, beaucoup plus prometteuse, consiste en une modification de la surface par dépôt de molécules amphiphiles. Ces traitements transposées aux particules de fer avec succès, ont permis d'obtenir l'ancrage homéotrope fort indispensable à l'obtention des défauts topologiques induisant l'auto-alignement des particules. La réponse magnétique des particules de fer soumises à un champ, observée en microscopie optique, a permis de calculer précisément, grâce à un logiciel de calcul de force magnétique par éléments finis, les contributions attractives et répulsives de la force induite par les distorsions du CLN entre les particules et ainsi, de construire le profil complet de cette force.

This thesis presents the study of organofunctional alkoxysilane coatings to prevent high temperature oxidation of Sm-Co powders. Sm-Co are important permanent magnetic alloys, owing to their high Curie temperature and large values of magnetocrystalline anisotropy. They possess stable magnetic properties in the temperature range -40 to 120 °C which makes them very attractive candidates for automobile’s electric motors. However, the environmental conditions for such applications are a sum of high temperatures, humidity, fuels and salts which provide perfect breeding ground for corrosion. In this study we report the high temperature oxidation resistance of Sm2Co17 powders coated with four common commercially available organofunctional silanes; (3-aminopropyl)trimethoxysilane (APTMS), (3-aminopropyl)triethoxysilane (APTES), methyltrimethoxysilane (MTMS) and (3-glycidyloxypropyl)trimethoxysilane (GPTMS). The as received powder was a multimodal mixture of many sizes and shapes which represented a typical ball milling product. The thermal analyses of the powders suggested that the powders without surface coatings had profound affinity towards oxidation. The thermal properties of sieved uncoated powders revealed that the small powders were more susceptible to oxidation than the large powders due to their large specific surface area. The isothermal properties of coated powders revealed that the powders coated with silanes had at least 10 times higher resistance to oxidation as compared to uncoated powders heated at 400 °C for 10 h. The non-isothermal tests conducted from room temperature to 500 °C also revealed that the uncoated powders gained 6 times more mass as compared to the powders coated with an ideal (MTMS) silane. The microstructural analysis of the uncoated powders heated from 400 °C to 550 °C revealed diffusion of oxygen, instable intermetallic phases which resulted in a redistribution of alloying elements, precipitation of alloying elements and formation of a featureless shell (approximately 20 µm in thickness) that surrounded the unreacted core. The coated powders on the other hand showed homogenous distribution of alloying elements, stable intermetallic phases and limited the shell thickness (1 µm). The thermo-magnetic properties of Sm-Co powders showed that the thermal instability also affected the magnetic properties adversely. It was found that the magnetic properties were deteriorated with a decrease in powder size. The energy dispersive spectroscopic (EDS) analyses showed that the small powders contained higher oxygen content than the large powders. Moreover XRD analysis also revealed that the small powders contain higher residual strains and smaller crystallite size which can play their role in deteriorating magnetic properties. It was found that surface modification by silanization improve the thermo-magnetic properties by effectively shielding the powder surfaces from surface oxidation. The rheological properties Sm-Co/PA12 composites revealed that the viscosity of the composites was increased with decreasing powder size due to the presence of rough surfaces and sharp corners in small powders. The rheological properties of the melts containing coated powders revealed that the silane layer acted as a lubricant and decreased the melt viscosity. It was found that coating the powders with silanes not only improve the rheological properties but also improve the other physical properties such as glass transition temperature the loss modulus by modifying the interfacial layer between the polymer matrix (PA12) and the powder. It results in a decrease in viscosity, a broadening of the glass transition temperature and a change in the damping properties of the composites. The dynamic mechanical properties of Sm-Co/PA12 composites showed that the storage modulus was increased with decreasing powder size. The results were expected as the rough surfaces act as local welding points between the powder and the polymer matrix. It was found that the surface modification improve the storage modulus. It is assumed that the silanes modify the interfacial properties which not only resulted in increasing the storage modulus but also broadened the glass transition temperature, Tg and damping, tanδ peaks. From the thermogravimetric, microstructural, rheological and magnetic analyses it can be concluded that the silanes are the effective coatings in preventing high temperature oxidation, stabilizing microstructure, enhancing mechanical properties, and improving rheological and magnetic properties. / <p>QC 20121205</p>

Dialkylsilanediols are a novel class of non-hydrolyzable analogues of the tetrahedral intermediate of amide hydrolysis, shown to be good inhibitors of HIV-1 protease, angiotensin converting enzyme (ACE), and thermolysin. An impediment to utilization of these silanediol structures, however, has been the methods for their assembly. This research describes the reductive lithiation of hydridosilanes and alkoxysilanes, and the use of the resulting silyl anions to develop efficient methods to synthesize silanediol precursors. In the first part of research, lithiation of hydridosilanes was studied. As part of this study, a simple 1H NMR method was developed for monitoring and analyzing the progress of lithiation. In addition, this method was converted to a titration for silyllithium reagents using BHT as an internal standard. Silanediols 107 and 177 are analogues of a potent chymase inhibitor, NK-3201 (82). In the second part, diphenylsilanes 108 and 170, precursors to silanediols 107 and 177, were synthesized using addition of silyllithium to sulfinimine 113 as a key step. In the third part, lithiation of alkoxysilanes was studied. (Si,O)-Dianions, generated from lithiation of silane alcohol 175 or 2,2-diphenyl-1-oxa-2-silacyclopentane (225), were reacted with a wide variety of electrophiles to give potentially useful silicon-containing building blocks. Addition of the (Si,O)-dianion 284 to sulfinimines gave silanediol inhibitor precursors with full control of stereochemistry. In the last part, a new method featuring 1,1-diphenyl-2-azaallyllithium chemistry were utilized to synthesize a series of protected α-amino silanes 323, 329 - 331. / Chemistry

[pt] Os métodos de recuperação terciária ou avançada de petróleo (EOR) permitem fatores de recuperação de até 70 por cento. A injeção de surfactantes aniônicos, amplamente empregados em EOR químico, pode se tornar inviável devido às perdas após precipitação, difusão para o interior de poros sem conectividade e especialmente adsorção sobre a superfície da rocha reservatório. Este trabalho almejou modificar a superfície de nanopartículas de sílica com alcoxisilanos para que possam ser utilizadas como nanocarreadores de surfactantes aniônicos em EOR químico, diminuindo desta forma as perdas por adsorção. Técnicas de caracterização foram empregadas para confirmar a modificação ocorrida na superfície da sílica, obtendo-se graus de modificação estimados entre 11 e 14 por cento. A inserção de grupos alquila (C8 e C16) na superfície da sílica aumentou significativamente a interação com o surfactante aniônico (dodecil sulfato de sódio, SDS), em comparação com as nanopartículas sem modificação, ampliando em até 11x a quantidade de surfactante retido na superfície das nanopartículas. Os nanomateriais híbridos obtidos possuem maior capacidade de manter adsorvido o tensoativo em soluções aquosas e salinas, bem como liberá-lo quando na interface salmoura/óleo. Ao fim, as nanopartículas de sílica modificadas contendo surfactante adsorvido na sua superfície atuaram sinergicamente na redução da tensão interfacial, sem afetar o desempenho do surfactante após liberação na interface água/óleo. Sendo assim, as nanopartículas modificadas com alcoxisilanos obtidas neste trabalho podem atuar como nanocarreadores de surfactantes em fluidos de injeção para EOR químico. / [en] The tertiary oil recovery methods or enhanced oi recovery (EOR) allow a recovery factor up to 70 percent. The injection of anionic surfactants, widely used in chemical EOR, could become unfeasible due to losses after precipitation, diffusion to the interior of non-connected pores and specially adsorption over reservoir rock surface. This work aimed to modify the surface of silica nanoparticles with alkoxysilanes in order to be used as surfactant nanocarriers in chemical EOR, reducing surfactant loss by adsorption. Characterization techniques were employed to confirm the modifications on silica surface, obtaining degrees of modification between 11 and 14 percent. The attachment of alkyl groups (C8 and C16) on the silica surface raised significantly the interaction with an anionic surfactant (sodium dodecyl sulfate, SDS), in comparison to bare silica nanoparticles, increasing up to 11x the amount of adsorbed surfactant over silica s surface. The hybrid nanomaterials obtained in this work have a high capacity to keep the tensoactive in aqueous solutions and brine, as well as releasing it at the brine/oil interface. Finally, the modified silica nanoparticles containing surfactant adsorbed on their surface showed a synergy in reducing interfacial tension, without affecting the surfactant performance after the release at the water/oil interface. Thus, the nanoparticles modified with alkoxysilanes obtained in this work can act as surfactant nanocarriers in injection fluids for chemical EOR.