Esta tese explora a potencialidade da radiação roveniente de um laser de gás carbônico para iniciar a combustão-modelo de substâncias simples oxigenadas com o bjetivo de estabelecer algumas das reações elementares relevantes ao processo de combustão. Esta tese é baseada no fato de que espécies intermediárias são geradas frequentemente em estados eletrônicos excitados no pulso do laser. O decaimento destas espécies em função do tempo foi observado pelas medidas de emissão por meio de uma fotomultiplicadora acoplada a filtros de interferência de banda estreita e, registrado em um osciloscópio de 100 MHz cuja base de tempo é gatilhada pelo laser de CO2. A evolução temporal do sinal de emissão foi analisada por um modelo cinético que compreende: 1) um processo de de pseudo-primeira ordem resultante por excitação multifotônica vibracional de colisões moduladas, e 2) decaimento através de emissão espontânea, reações químicas ou supressão radiativa. A cinética resultante das curvas experimentais foi obtida por um método de ajuste de curvas por simulação em um microcomputador. Os sistemas químicos estudados nesta tese compreendem o metanol, etanol, n-propanol, n-butanol e o éter dietílico. A eficiência na formação de C2, CH e OH foi estabelecida pela medida da intensidade e o tempo de subida da quimiluminescência determinado de acordo com o procedimento mencionado acima. A análise das curvas de subida e descida foram estudadas com o precursor puro e na presença de Ar, O2, NO, H2, Cl2, CH4 e C2H6, utilizando nestes casos pressões relativamente altas para garantir um número elevado de colisões. Nos sistemas em mistura com ar ou O2 as espécies emissivas CH e OH apresentam um prolongamento do tempo de decaimento, em geral não-exponencial. Ao mesmo tempo a intensidade relativa dos sinais de quimiluminescência atinge um máximo, sendo particularmente significativa para a espécie OH a uma determinada pressão de oxigênio. Misturas de etanol com O2/Ar resultam para a espécie OH num aumento no valor da vida média radiativa, enquanto que em misturas com CO, C2H6 e propileno (C3H6) é observado uma diminuição significativa. No caso de CO este comportamento é assumido como sendo de processos de relaxação, tendo-se para os dois últimos um processo de abstração de hidrogênio por parte da espécie OH. A presença de um inibidor de reações de radicais livres, NO, tem pouco efeito nos valores das constantes das espécies estudadas. Entretanto, a emissão da espécie OH foi totalmente suprimida em misturas do precursor com Cl2. Neste caso a observação de CH3CL por cromatografia em fase gasosa sugere que reações químicas de alguns dos fragmentos primários inibem o adicional bombeamento pelo laser. Um modo particular de se interpretar o possivel mecanismo de formação das espécies transientes, foi desenvolvido através do cálculo teórico RRKM dos principais processos primários aventados para a decomposição por excitação multifotônica vibracional da molécula de etanol. O cálculo RRKM foi modelado para a eliminação de H2O, processo majoritário a pressões baixas, e diferentes processos de cisões que passam a ter importância a intensidades elevadas de laser. O cálculo teórico mostra claramente que a eliminação de H2O é o canal preferido a baixas energias de excitação, sendo rapidamente reposto pelos outros canais a valores maiores de energia. Um efeito similar é observado para a decomposição unimolecular completa em função da pressão, onde a pressões elevadas, os processos de cisão com produção de radicais livres são dominantes como conseqüência da desativação das moléculas com energia mínima antes que sofram reação química. / This thesis explores the use of a CO2 laser to initiate combustion type reactions in a number of simple oxygen containing organic compounds. This method offers a potential tool to isolate and establish some of the elementary reactions responsible for the initial steps of combustion reactions. The core of the thesis is based on the fact that transient chemical species are generated in electronically excited states by the laser pulse. The time dependent behavior of this species has been observed by measuring the emission on a fast photomultiplier provided with narrow band filtres, and recording it on a 100 MHz oscilloscope triggered by the laser pulse. The time evolution of the emission signal has been analyzed by a kinetic model which includes: 1) an ill-defined pseudo-first arder process as a consequence of collisionally modulated multiphoton vibrational excitation, and 2) decay through spontaneous emission, chemical reaction ar radiative quenching. The resulting kinetics were fitted to the experimental curves by computer simulation. The chemical systems covered in this thesis include methanol, ethanol, n-propanol, n-butanol and diethyl ether. Under pulsed CO2 laser radiation, the efficiency of formation of C2, CH and OH have been established by intensity measurements and the rise time for chemiluminescence determined according to the procedure mentioned above. Emission rise times and decays were studied for the neat systems and in the presence of Ar, O2, NO, H2, CH4, and C2H6 at pressures for which collisional processes are important. Emission from the CH and OH species are sustained for longer times in the presence of air or O2 and the decay becomes distincly non-exponential. There is also a significant intensity effect which is particularly noticeable for OH which reaches a maximum at a given oxygen pressure. Mixtures af ethanol with O2/Ar result in longer lifetimes for OH whereas in mixtures with CO, C2H6 and C3H6 a significant decrease is observed. In the case af CO, this behavior is assumed ta be due to relaxation processes, while in the latter cases hydrogen abstraction by OH is presumably responsible for the decrease. The presence of the well known scavenger NO had little effect on the rate constants used to describe the emission process. On the other hand, OH emission was completely quenchend in mixtures of the precursor with Cl2. In this case, the observation of CH3Cl by gas chromatography suggests that chemical reaction of some of the primary dissociation fragments inhibits further laser pumping. An attempt to understand the possible mechanism for the formatiun of the transient species was developed through the use of an RRKM calculation of the primary dissociation processes of ethanol under multiphoton excitation. The RRKM calculations were modelled for the H2O elimination, the main process at low pressures, and different bond scission processes which may become important at higher laser intensities. The theoretical calculation clearly shows that H2O elimination is the preferred pathway at lower excitation energies but is rapidly replaced by the other channels at higher energy contents. A similar effect is observed for the complete unimolecular decomposition as a function of pressure, where at the higher pressures, the bond scission processes yielding free radicals are dominant as a consequence of the deactivation of the molecules with threshold energies before they can undergo chemical reaction.

Neste trabalho, foram investigados os processos de migração e dissociação do éxciton em filmes ultrafinos de poli(9,9 dioctilfluoreno) (PFO) com espessura menores que o raio típico de migração excitônica (10 nm) próximos de interface semicondutora orgânica e inorgânica. Os filmes de PFO foram produzidos utilizando a técnica de <span style=\'color:black;font-style:italic;language:PT-BR\'>spin-coating<span style=\'color:black;language:PT-BR\'> a partir de soluções de PFO em clorofórmio e em tolueno. Sabe-se que ao se utilizar o clorofórmio como solvente, os filmes de PFO apresentam uma estrutura amorfa. Com isso foi possível obter filmes com espessuras menores que o raio de migração do éxciton com qualidades ideais para o estudo de processos fotofísicos. Esses filmes foram depositados sobre uma camada de nanopartículas de dióxido de titânio (TiO<span style=\'color:black;language:PT-BR\'>2<span style=\'color:black;language:PT-BR\'>) formando assim uma interface orgânica/inorgânica. Técnicas espectroscópicas, tais como, microscopia confocal de fluorescência (LSCM), microscopia de imagem do tempo de vida (FLIM), fotoluminescência de onda contínua e resolvida no tempo bem como espectroscopia de absorção foram utilizadas no presente trabalho. Inicialmente o espectro de fotoluminescência dos filmes de PFO foram caracterizados através da dependência da intensidade da transição puramente eletrônica <span style=\'color:black;font-style:italic;language:PT-BR\'>I<span style=\'color:black;language:PT-BR\'>, largura da linha a meia altura <span style=\'font-family:Symbol;color:black;language:PT-BR\'>G<span style=\'color:black;language:PT-BR\'>o<span style=\'color:black; language:PT-BR\'>, energia da transição puramente eletrônica <span style=\'color:black;font-style:italic;language:PT-BR\'>E<span style=\'color:black;language:PT-BR\'> e parâmetro de Huang-Rhys <span style=\'color:black;font-style:italic;language:PT-BR\'>S<span style=\'color:black;language:PT-BR\'> variando a temperatura. Verificou-se que a intensidade pode ser descrita em termos da ativação térmica da migração do éxciton. Além disso, a temperatura introduz uma desordem térmica que afeta diretamente o tamanho dos segmentos conjugados que é observado em termos dos parâmetros, <span style=\'font-family:Symbol;color:black;language:PT-BR\'>G<span style=\'color:black;language:PT-BR\'>o<span style=\'color:black; language:PT-BR\'>, <span style=\'color:black;font-style:italic; language:PT-BR\'>E<span style=\'color:black;language:PT-BR\'> e <span style=\'color:black;font-style:italic;language:PT-BR\'>S<span style=\'color:black;language:PT-BR\'>. Com os filmes de PFO produzidos com o solvente tolueno foi observado que frações de fase <span style=\'font-family:\"Times New Roman\";color:black;font-style:italic; language:EL\'>&#946;<span style=\'font-family:\"Times New Roman\"; color:black;language:EL\'> <span style=\'color:black;language:PT-BR\'>já são induzidas nesses filmes e que esta fase não está dispersa na matriz amorfa e sim em forma de domínios formados por moléculas na fase <span style=\'font-family:\"Times New Roman\";color:black;font-style:italic; language:EL\'>&#946; <span style=\'color:black;language:PT-BR\'>que correspondente ao ordenamento nos anéis aromáticos do PFO. Também foi observado que nos filmes com espessura menor que 10 nm preparados em clorofórmio, a fase <span style=\'font-family:\"Times New Roman\";color:black;font-style:italic; language:EL\'>&#946;<span style=\'font-family:\"Times New Roman\"; color:black;language:EL\'> <span style=\'color:black;language:PT-BR\'>é induzida e sugerimos que isso ocorre devido a forte interação filme/substrato. Além disso, outros métodos bem conhecidos na literatura, tais como, tratamento a vapor de tolueno e ciclos térmicos de resfriamento/aquecimento foram utilizados para induzir a fase <span style=\'font-family:\"Times New Roman\";color:black;font-style:italic; language:EL\'>&#946;<span style=\'font-family:\"Times New Roman\"; color:black;language:EL\'> <span style=\'color:black;language:PT-BR\'>em filmes de PFO amorfo. Com relação aos filmes contendo a interface TiO<span style=\'color:black;language:PT-BR\'>2<span style=\'color:black;language:PT-BR\'>/PFO, a dissociação do éxciton na interface foi observada através da redução da intensidade da fotoluminescência. Em filmes ultrafinos, a eficiência do processo de dissociação do éxciton na interface é superior a 90%. A partir desses resultados, obteve-se que o raio de migração do éxciton no PFO é de (13 <span style=\'font-family:Symbol;color:black;language:PT-BR\'>±<span style=\'color:black;language:PT-BR\'> 3) nm. Além disso, devido à alta fluência (~ 10<span style=\'color:black;language:PT-BR\'>25<span style=\'color:black;language:PT-BR\'> fótons/cm<span style=\'color:black;language:PT-BR\'>2<span style=\'color:black;language:PT-BR\'>s), efeitos de autoaniquilamento de éxcitons em filmes ultrafinos foram observados nas medidas de tempo de decaimento radiativo. Por fim, em filmes de PFO (contendo a fase <span style=\'font-family:\"Times New Roman\";color:black;font-style:italic; language:EL\'>&#946;<span style=\'font-family:\"Times New Roman\"; color:black;language:EL\'>) <span style=\'color:black;language:PT-BR\'>depositados sobre o TiO<span style=\'color:black;language:PT-BR\'>2<span style=\'color:black;language:PT-BR\'>, somente os éxcitons das regiões amorfas migram até a interface do TiO<span style=\'color:black;language:PT-BR\'>2<span style=\'color:black;language:PT-BR\'> e são dissociados por ela. A energia térmica a temperatura ambiente promove uma maior eficiência da dissociação do éxciton do que em baixas temperaturas (~5 K). No entanto, mesmo em temperatura ambiente, as moléculas de fase <span style=\'font-family:\"Times New Roman\";color:black;font-style:italic; language:EL\'>&#946;<span style=\'font-family:\"Times New Roman\"; color:black;language:EL\'> <span style=\'color:black;language:PT-BR\'>atuam como centros de captura dos éxcitons competindo com o processo de dissociação. A partir desses resultados, obteve-se que o raio de transferência de energia no PFO é igual a (3,5 <span style=\'color:black;text-decoration:underline;language:PT-BR\'>+<span style=\'color:black;language:PT-BR\'> 0,5) nm.<span style=\'color:black; language:PT-BR\'> <![if !vml]> <![endif]> / In this work, we investigated the process of exciton dissociation and migration in ultra-thin films of poly (9,9 dioctilfluoreno) (PFO) with a thickness smaller than the typical radius of excitonic migration (10 nm) and near to organic and inorganic semiconductor interface. The PFO films were produced using the spin-coating technique from a PFO solution in chloroform and toluene. It is known that when using chloroform as solvent, the PFO films have an amorphous structure. Thus, it was possible to obtain films that have thicknesses smaller than the radius of the exciton migration qualities, which is ideal to study photophysical processes. These films were deposited on the titanium dioxide (TiO<span style=\'language:EN\'>2<span style=\'language:EN\'>) nanoparticles layer forming an organic/inorganic interface. Spectroscopic techniques such as fluorescence confocal microscopy (LSCM), fluorescence lifetime imaging microscopy (FLIM), continuous wave photoluminescence and time resolved and absorption spectroscopy were used in this study. First, the photoluminescence spectrum of PFO films were characterized by the dependence of the purely electronic transition intensity <span style=\'font-style:italic;language:EN\'>I<span style=\'language:EN\'>, full width at half maximum <span style=\'font-family:Symbol;language:EN\'>G<span style=\'language: EN\'>o<span style=\'language:EN\'>, purely electronic transition energy <span style=\'font-style:italic;language:EN\'>E<span style=\'language:EN\'> and Huang-Rhys parameter <span style=\'font-style:italic;language:EN\'>S <span style=\'language:EN\'>with the temperature. It was showed that the intensity can be described according to thermal activation of the exciton migration. Furthermore, the temperature introduces a thermal disorder affecting directly the conjugated segment length which is observed according to the parameters, <span style=\'font-family:Symbol;language:EN\'>G<span style=\'language: EN\'>o<span style=\'language:EN\'>, <span style=\'font-style: italic;language:EN\'>E<span style=\'language:EN\'> e <span style=\'font-style:italic;language:EN\'>S<span style=\'language:EN\'>. The PFO films produced with the solvent toluene analysis showed that the fractions of <span style=\'font-family:\"Times New Roman\";font-style:italic;language:EN\'>&#946;<span style=\'language:EN\'> phase are already induced and that this phase is not dispersed in the amorphous matrix. On the order hand, they are shaped domains formed by <span style=\'font-family:\"Times New Roman\";font-style:italic;language:EN\'>&#946;<span style=\'language:EN\'> phase molecules that are related to the PFO aromatic rings organization. It was also observed that the films with thickness smaller than 10 nm prepared using chloroform, the <span style=\'font-family:\"Times New Roman\";font-style:italic;language:EN\'>&#946;<span style=\'language:EN\'> phase is induced, which may be occurring due to the strong interaction observed between film and substrate. Other methods reported in the literature, such as toluene steam treatment and thermal cycles of cooling/heating were used to induce <span style=\'font-family:\"Times New Roman\";font-style:italic;language:EN\'>&#946;<span style=\'language:EN\'> phase in amorphous PFO films as well. The exciton dissociation at the interface in films containing TiO<span style=\'language:EN\'>2<span style=\'language:EN\'>/PFO interface were observed by reduction of photoluminescence intensity; and this same efficiency in ultra-thin films is higher than 90%. From these results, it was reported that the exciton migration radius in PFO is (13 <span style=\'font-family:Symbol;language:EN\'>±<span style=\'language:EN\'> 3) nm. Furthermore, effects of excitons annihilation in ultra-thin films were observed in the decay time radiative measurements due to high fluency (~ 10<span style=\'language:EN\'>25<span style=\'language:EN\'> photons/cm<span style=\'language:EN\'>2<span style=\'language:EN\'>s). Finally, in PFO films (with the <span style=\'font-family:\"Times New Roman\";font-style:italic;language:EN\'>&#946;<span style=\'language:EN\'> phase) deposited on the TiO<span style=\'language:EN\'>2 <span style=\'language:EN\'>just the exciton of amorphous regions migrates to the TiO<span style=\'language:EN\'>2<span style=\'language:EN\'> interface, which dissociates them. The thermal energy at room temperature promotes higher efficiency than the exciton dissociation at low temperatures (~ 5 K). However, even at room temperature, the <span style=\'font-family:\"Times New Roman\";font-style:italic;language:EN\'>&#946;<span style=\'language:EN\'> phase molecules act as the most important molecules to capture exciton, competing to the exciton dissociation process. These results conducted to conclude that the energy transfer radius in PFO is equal to (3.5 <span style=\'text-decoration:underline;language:EN\'>+<span style=\'language: EN\'> 0.5) nm. <![if !vml]> <![endif]>

Genom att samla kunskap om psykoser och analysera spel och film utvecklar vi ett grafiskt koncept för ett skräckspel. Genom intervjuer tar vi reda på hur konceptet uppfattas av spelare och spelutvecklare. Konceptet saknade grafiskt narrativ, vilket gjorde att spelets tema tolkades olika av alla respondenter. Vi diskuterar vikten av ett grafiskt narrativ, och hur spelets grafiska stil kan fortsätta utvecklas.

La mobilité du monde est permanente et cependant fugace, pour partie visible et invisible. La peinture contient à la fois un espace immobile mais mouvant, plan mais profond. Une couleur rehausse sa complémentaire et le sec réagit à l’humide. Cette succession de dualités sensibles, observable dans mes tableaux, instaure une tension. Cette dernière me permet de restituer avec justesse les liens qui se tressent entre les éléments participant du visible. La peinture dans sa profondeur propre creuse une distance qui servira de base à l’agrandissement de la sensation spatiale par l’écart. Elle prend naissance dans le rapport au lointain provenant de l’observation du paysage naturel et des éléments mouvants qui le constituent. De l’imprégnation qui en résulte ressort une structure constante du visible par-delà les particularismes, ce que l’acte pictural vise à saisir avec justesse par-delà l’apparence. La discontinuité entre les éléments impliqués dans le réel et l’incidence du vide fondateur de l’espace est un point de correspondance entre le visible du monde et celui de la peinture. L’usage de la réserve et l’emploi de formes ouvertes, de lignes discontinues obtenues par dissociation du geste, entre autres subterfuges déjouant la volonté consciente d’évoquer, sont parmi les moyens plastiques dont je me dote pour atteindre une correspondance structurelle au visible. La mobilité du monde naturel instaure celle de la peinture ainsi que celle du regard qui y déambule dans une relation de transfert et de continuité qui est l’objet de cette recherche. / The mobility of the world is constant and however fleeting, partly visible and invisible. Painting contains at the same time motionless and moving, flat and deep space. A colour enhances its complementary one and the dry reacts to the wet. This succession of sensitive dualities, which canbe seen in my paintings, sets up some tension. The latter allows me to accurately restore the links that are twining the involved elements of the visible. Painting in its own depth delves a distance which will serve as an enlargement of the spatial sensation. It originates in the reference to the distant coming from the observation of natural landscape and the moving elements that are part ofit. The impregnation that ensues brings out an abiding structure of the visible across the particularities, what the pictorial act aims at pointing with accuracy beyond the surface. The discontinuity between the elements which are involved in the real and the impact of the emptiness of the space are an interchange of the visible of the world and the painting one. The use of blank areas and open forms, of discontinuous lines which were made from dissociation of gesture, among other subterfuge eluding the aware will of conjuring up, are among the plastic means I useto get a structural correspondence with the visible. The mobility of the natural world sets up the mobility of painting such as the one of the act of looking which strolls around it in a relationship of transfer and continuity which is the object of this research.

Conselho Nacional de Desenvolvimento Científico e Tecnológico / A retrospective study including the analysis of the cerebrospinal fluid (CSF) of dogs neurologically affected was conducted by the Neurology Service (NS) of the Veterinary Teaching Hospital (VTH) at the Federal University of Santa Maria (FUSM), between 2004 and 2015. The aim of this study was to analyze the results of the CSF of dogs with neurological signs, and compare the changes found in the CSF in two sampling sites in the same patient and see if this test helped the clinician to strengthen clinical suspicion of the major diseases of the central nervous system. Of the 507 patients that underwent CSF analysis, only the analysis of 144 (26.5%) dogs were suited to inclusion criteria. The main diagnosed neurological diseases were distemper (21.6% [n=31]), intervertebral disc disease (IVDD) (52.7% [n=76]), intracranial (IC) tumors (13.2% [n=19]) and tumors which affected the spinal cord (SC) (8.3% [n=12]). Lymphocytic pleocytosis was present in 78.3% (29/37) of samples from dogs with canine distemper and in 23.2% (10/43) of samples from dogs with IVDD. The albuminocytologic dissociation was found in 73% (19/26) of samples from dogs with IC tumors and in 64.3% (9/14) of the samples from dogs with tumors involving the SC. For dogs affected by IVDD, there was statistical significance (p <0.05) between the degree of neurological dysfunction and the total nucleated cells (TNC) and total protein (TP). In 29 dogs, CSF was collected from both the cistern magna (CM) and the lumbar cistern (CL) and in 12 (41.4%) the results were different between the samples of the same dog, where two cases (6, 9%) showed alterations in the sample collected cranial to the injury. It can be concluded that the lymphocytic pleocytosis was the main alteration found in the CSF of dogs with distemper and IVDD and albuminocytologic dissociation in tumors, intracranial and affecting the spinal cord. Dogs affected by IVDD had more severe neurological signs as TNC and TP increased and the CSF was altered even collected cranial to the lesion site and helped the clinician to strengthen the clinical suspicion., but not confirm, the major neurological diseases in dogs. / Foi realizado um estudo retrospectivo dos resultados do líquido cerebroespinhal (LCE) de cães, atendidos pelo Serviço de Neurologia (SN) do Hospital Veterinário Universitário (HVU) da Universidade Federal de Santa Maria (UFSM), de 2004 a 2015, com o objetivo de analisar os resultados obtidos do LCE de cães com sinais neurológicos, e comparar as alterações encontradas no LCE em dois locais de colheita no mesmo paciente e verificar se esse exame auxiliou o clínico em reforçar a suspeita clínica das principais doenças do sistema nervoso central. Dos 507 pacientes que foram submetidos à análise do LCE, apenas as análises de 144 (26,5%) cães se adequaram aos critérios de inclusão. Dentre estes, cães com cinomose representaram 21,6% (n=31), doença do disco intervertebral (DDIV) 52,7% (n=76), tumores intracranianos (IC) 13,2% (n=19) e tumores envolvendo a medula espinhal (ME) 8,3% (n=12). A pleocitose linfocítica esteve presente em 78,3% (29/37) das amostras de cães com cinomose e em 23,2% (10/43) das amostras de cães com DDIV. Já a dissociação albuminocitológica foi encontrada em 73% (19/26) das amostras de cães com tumores IC e em 64,3% (9/14) das amostras de cães com tumores envolvendo a ME. Para os cães acometidos pela DDIV, houve significância estatística (p < 0,05) entre o grau de disfunção neurológica e o total de células nucleadas e total de proteínas encontrados no LCE destes cães. Em 29 cães, houve a colheita do LCE tanto na cisterna magna (CM) quanto na cisterna lombar (CL) e em 12 (41,4%) os resultados foram diferentes entre as duas amostras colhidas do mesmo cão, onde dois (6,9%) apresentaram alteração na amostra colhida cranial à lesão. Pode-se concluir que a pleocitose linfocítica foi a principal alteração encontrada no LCE de cães com cinomose e DDIV e dissociação albuminocitológica nas neoplasias, intracranianas e medulares, cães acometidos pela DDIV apresentaram sinais neurológicos mais severos conforme o TCN e o TP aumentaram e o LCE sofreu alteração, mesmo colhido cranial ao local da lesão e auxiliou o clínico em reforçar a suspeita clínica, mas não confirmou, as principais doenças neurológicas em cães.

Le but principal de ma thèse de doctorat est d’étudier la dissociation de noyaux exotiques. Ces noyaux sont peu liés et présentent une structure en halo dominante. Ceci conduit à des propriétés très particulières, telles que des rayons beaucoup plus grands que ceux des noyaux voisins. Les noyaux 6He et 11Li sont des exemples typiques, et sont décrits par des structures alpha+n+n et 9Li+n+n, respectivement. La principale technique expérimentale pour étudier ces noyaux consiste à développer des faisceaux d’ions radioactifs, et à mesurer la section efficace de dissociation sur des cibles lourdes. Les données expérimentales nécessitent donc le développement de modèles théoriques précis pour leur interprétation.<p><p>Mon travail a consisté en le développement de la méthode eikonale pour décrire les processus de diffusion élastique et de dissociation. Cette méthode nécessite les fonctions d’onde du projectile qui, dans le cas présent, est décrit par une structure à trois corps. Cette situation rend les calculs particulièrement difficiles, en particulier pour la réaction de dissociation où les fonctions d’onde du continu à trois corps sont nécessaires. Les fonctions d’onde à trois corps sont décrites dans le cadre des coordonnées hypersphériques, à la fois pour les états liés et pour les états de diffusion.<p><p>J'ai d'abord calculé les sections efficaces de dissociation de 6He en utilisant des fonctions d'onde & / Doctorat en Sciences / info:eu-repo/semantics/nonPublished

The Diploma Thesis deals with preparation of one phoshonate and two phospinate derivatives of dipicolylamine. Dissociation constants of prepared ligands were determined by potentiometric and NMR titration. Coordination properties of the compounds were studied by combination of potentiometry and UV-VIS spectrophotometry. Stability constants of complexes with selected transition metal ions (Cu2+ , Ni2+ a Zn2+ ) and alkali-earth metals ions (Ca2+ , Mg2+ ) were calculated. Acid-base and coordination properties in the solid state were studied by X-ray diffraction on single-crystals.

Mamalian protein ubiquitination and SUMOylation are reversible post translational modifications, which are involved in a multitude of important complex regulatory processes within the cell. Current mass spectrometry approaches that involve bottom-up proteomics to comprehensively analyse these modifications, have proved to be problematic. In this work, analytical approaches are carried out to improve and enhance the comprehensive analysis of these modifications. Tryptic proteolysis of ubiquitinated proteins results in the generation of isopeptides bearing adi-glycine (GG) remnant. Current mass spectrometry approaches used to identify these isopeptides are predominantly reliant on detecting the signature mass shift of the GG remnant (114.043 Da). The lack of sequence information from the GG remnant post MS/MS acquisition results in database search algorithms falsely identifiying these isopeptides. Reductive methylation chemistry was employed to derivatize these isopeptides. Upon collision induced dissociation of the isopeptides two robust ions were released from the iso-N-terminus of the GG remnant ; i) an a1’ ion at m/z 62.09, corresponding to the G of the remnant and ii) a b2’ ion at m/z 147.11, corresponding to the full GG remnant. Post-acquisition data extraction of these unique diagnostic ions demonstrated enhanced selectivity towards identifying these isopeptides. Tryptic proteolysis of SUMOylated proteins results in the generation of isopeptides bearing a substantial iso-C-terminal SUMO remnant. The CRA(K) (Consecutive Residue Addition tolysines (K)) approach combined independant use of proteolytic enzymes and unbiased consecutive residue addition of amino acids pertaining to these iso-C-terminal SUMOremnants, on all lysine residues. This approach enabled the identification of analytically useful novel wildtype isopeptides derived from the proteolysis of SUMO(1/2/3)ylated proteins, bearing GG, TGG and QTGG remnants. The analytically useful isopeptides derived from proteolysis of SUMO(2/3)ylated proteins lacked robust diagnostic information from their iso-C-terminal bearing TGG and QTGG remnants. Reductive methylation chemistry was utilised to derivatize these isopeptides and enabled diagnostic a’ and b’ ions to be released from their iso-N-termini; i) a1’ (m/z 133.13),b2’ (m/z 262.17) and b4’ (m/z 376.22) ions, corresponding to the QTGG remnant and ii) (m/z106.10), b2’ (m/z 191.14) and b3’ (m/z 248.14) ions, corresponding to the TGG remnant. Post-acquisition data extraction of these unique diagnostic ions, enabled comprehensive structural elucidation of these isopeptides and enhanced selectivity towards identification.

There is an extensive debate in the adult literature on whether recognition memory can better be explained by a single- or a dual-process account. Single-process accounts assume that a single memory strength signal underlies recognition. Dual-process accounts propose two independent processes, namely recollection (slow and associated with contextual details) and familiarity (fast and automatic). The aim of this dissertation was to advance this debate using a cognitive developmental approach. By investigating age-related changes of recognition memory across childhood as a function of theoretically motivated experimental manipulations, predictions drawn from single- and dual-process models of recognition memory were tested. We adapted the Process Dissociation Paradigm (PDP; Jacoby, 1991) to disentangle processes underlying recognition memory in 5-, 7-, and 11-year-olds and adults using a Dual-Process Signal Detection cognitive modelling approach (DPSD; Yonelinas, 1996). Experiments 1 – 6 demonstrated that 5-year-olds are able to recollect items based on perceptual details. Consistent with dual-process theory, across all age groups a response time limit decreased recollection while leaving familiarity unaffected (Chapter 2). Converging evidence consistent with dissociations during childhood was found after repeated item presentation (Chapter 3). Finally, after a thorough empirical validation of our approach, the new paradigm was used to investigate the developmental perceptual to semantic shift (Chapter 4). These findings, using a double dissociation logic, have advanced the theoretical debate on the nature of recognition memory by showing that one process is insufficient to account for the developmental and experimental findings reported here. Recollection and familiarity follow different developmental trajectories and are affected by encoding and retrieval manipulations (i.e., repetition and time limits). This provides a challenge for existing theories of recognition memory.

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