Acquisition of X-ray crystallographic data is always accompanied by structural degradation owing to the absorption of energy. The application of high-fluency X-ray sources to large biomolecules has increased the importance of finding ways to curtail the onset of X-ray-induced damage. A significant effort has been under way with the aim of identifying strategies for protecting protein structure. A comprehensive model is presented that has the potential to explain, both qualitatively and quantitatively, the structural changes induced in crystalline protein at 100 K. The first step is to consider the qualitative question: what are the radiation-induced intermediates and expected end products? The aim of this paper is to assist in optimizing these strategies through a fundamental understanding of radiation physics and chemistry, with additional insight provided by theoretical calculations performed on the many schemes presented.

Cette thèse présente une contribution originale à la compréhension et la maîtrise des mécanismes physico-chimiques qui contrôlent l’élaboration d’un nouveau matériau polymère biphasique de type Super-TPV (thermoplastique vulcanisé) contenant une phase réticulée par le procédé d’extrusion réactive. La phase caoutchoutique est constituée d’un Vinyl-PDMS de haute masse molaire qui est réticulé dynamiquement avec une matrice thermoplastique PA12 lors du procédé de mise en œuvre à l’état fondu (T≈200°C). Le premier des quatre chapitres de ce mémoire est consacré à une étude bibliographique des différents aspects fondamentaux de la réticulation radicalaire des silicones. Dans le chapitre 2, nous avons étudié le processus de réticulation radicalaire du PDMS en fonction de la température (T>160°C). Le peroxyde de dicumyle (DCP) a été utilisé comme amorceur de la réaction. Pour tenter de contrôler la réaction de réticulation à ces températures élevées, le tétraméthylpipéridyloxyde (TEMPO) a été utilisé. Nous avons ainsi montré que le temps à la transition sol-gel viscoélastique augmente en fonction de la concentration de l’inhibiteur. Des études en RMN, DSC et TGA-MS ont montré que le mécanisme à l’origine de ce temps d’inhibition est le greffage des radicaux nitroxyles sur la chaine polymère silicone. Dans le chapitre 3, un modèle original a été développé avec succès pour décrire la rhéocinétique de la réticulation radicalaire contrôlée du PDMS. Cette modélisation est basée sur le couplage de la cinétique des macro-radicaux PDMS recombinés [Rcc(t)] et la variation des modules complexes de cisaillement (G'(t) et de G"(t)). Finalement, dans le chapitre 4 ces études fondamentales ont été développées à l’élaboration d’un TPV basé sur la réticulation radicalaire de la gomme silicone dans une matrice PA12. Nous avons alors montré que l'addition du TEMPO permet d’élaborer par un procédé dynamique un nouveau Super-TPV ayant une structure et une morphologie contrôlée. / The control of macromolecular structure has recently become an important topic of polymer science from both an academic and an industrial point of view. Indeed, free-radical crosslinking of Polydimethyl-vinylmethyl-siloxane (vinyl-PDMS) rubber by organic peroxide suffers from premature crosslinking at high temperatures, which is called scorching. Consequently, the basic aim of the investigations described in this thesis is to widen and explore the network topology–crosslinking kinetics relationships and find a novel way to control free-radical crosslinking chemistry and topological parameters of final PDMS networks. The work is primarily focused on the extensive study of the crosslinking control of PDMS rubber at high temperatures. A novel composition using 2,2,6,6-tetramethylpiperidinyloxyl (TEMPO) and dicumyl peroxide (DCP) for scorch delay and control of the final network topology of the PDMS has been proposed. The work specified in this thesis is therefore directed to find a proper [TEMPO]/[DCP] ratio provided the development of a new biphasic material such as PA12/PDMS blend type TPV (Thermoplastic Vulcanizated). For this purpose a new method based on the relationship between the kinetics of the macro-radicals coupling [Rcc(t)] was derived from a fundamental kinetic model and the viscoelastic changes of the complex shear modulus (G’(t) and G”(t)). As a main result, the rheological modelling shows that this new method accurately predicts the time variation of complex shear modulus at any temperature and [TEMPO]/[DCP] ratio. Interestingly, addition of TEMPO to the TPV novel composition provided the PA12/PDMS blend compatibilization in the dynamic process and gives a new material having a controlled structure and morphology. A better insight in understanding the blend composition and the morphology development relationships is aimed at.

A new free radical chain process for the allylation of hydrocarbons and some other substrates utilizing substituted allyl bromides (R-H + C=C-C-Br -> R-C-C=C + HBr) has been developed. Good to excellent yields were observed in all cases. Kinetic chain measurements and competition experiments were performed in order to elucidate the mechanism of the reaction. Overall, the results are consistent with a free radical chain process with bromine atom as the chain carrier. Substitution effects on the reactivity of the allyl bromides (CH2=C(Z)CH2Br) and their influence on the overall reaction rate were studied by conducting several competition experiments. The relative rate constants for addition of benzyl radical to CH2=C(Z)CH2Br are: Z=CN(180), COOEt(110), Ph(65), H(1.0). The trend of electronegativity/reactivity of these reactions was very similar to that reported for addition of benzyl radical to substituted alkenes. Other than alkyl aromatics (PhCH3, PhCH(CH3)2), other substrates (i.e., 2- propanol, phenyl cyclopropane) were also tested for this allylation reaction. The magnitude and scope of these reactions, and their synthetic utility is discussed. / Ph. D.

The stable free radical polymerization methodology for production of controlled macromolecules was investigated using a novel monomer, 2-vinylnaphthalene. Initial polymerizations resulted in molecular weight distributions typical of conventional free radical polymerization techniques (>2.0). Manipulation of the initiator concentration and the molar ratio of initiator to nitroxide demonstrated no significant control over the resulting polymer products. Analysis of the polymerization kinetics for a 2-vinylnaphthalene polymerization performed in the presence and absence of the free radical initiator revealed identical monomer consumption profiles as well as pseudo first order kinetics indicating a significant degree of the thermal polymerization was occurring at the polymerization temperature (130°C). Comparison of the thermal polymerization propensity of 2-vinylnaphthalene and styrene revealed an increased tendency for 2-vinylnapthahlene to undergo thermal polymerization. Styrene is considered highly active in its propensity to thermally polymerize. However, an Arhenius analysis using in situ FTIR was employed to determine the activation energy for the thermal polymerization of styrene and 2-vinylnaphthalene. The 2-vinylnaphthalene activation energy for thermal polymerization was determined for the first time to be almost 30 kJ/mol less than styrene. A novel modified Mayo mechanism was proposed for the 2-vinylnaphthalene thermal initiation mechanism. Moreover, this thermal initiation was employed to initiate nitroxide mediated polymerizations of styrene. This first use of a 2-vinylnaphthalene initiating system resulted in polystyrene with a large macrocyclic initiating fragment. The presence of the initiating moiety was studied using both UV-Vis spectroscopy and 1H NMR spectroscopy. The extension of stable free radical polymerization to the acrylate monomer family was examined using a novel nitroxide mediator, N-tert-butyl-N-[1-diethylphosphono-(2,2-dimethylpropyl)] nitroxide (DEPN). The synthesis of DEPN was monitored using in situ FTIR spectroscopy to determine optimum reaction conditions. The purified nitroxide was subsequently employed in the synthesis of various block and random acrylate copolymers. The production of a unique amphiphilic block copolymer consisting of acrylic sequences was achieved. Poly(t-butyl acrylate-b-2ethylhexyl acrylate-b-t-butyl acrylate) was synthesized using the SFRP process. The t-butyl functionalities were subsequently removed in a post-polymerization acid catalyzed hydrolysis. The effect of steric bulk and electronic factors on the resulting SFRP process was also investigated and revealed similar polymerization kinetics for various alkyl acrylates. However, addition of a hydroxyl containing monomer, 2-hydroxyethyl acrylate, resulted in an increase in the polymerization rate up to 2 times. The rate enhancement was attributed to hydrogen bonding effects and this was confirmed using the unprecedented addition of dodecanol, which also demonstrated a significant rate enhancement. Block copolymers were also achieved using a novel difunctional nitroxide synthesized from 4-hydroxy TEMPO and 1,6-hexamethylene diisocyanate. The identity of the nitroxide was confirmed using mass spectrometry and 1H NMR. The dinitroxide was used in the polymerization of styrene and subsequently used to produce symmetric ABA triblock copolymers with t-butyl styrene using a unique two-step polymerization route. In addition, the dinitroxide demonstrated an increased tendency for decomposition due to the complex mediation equilibrium. The decomposition was studied using GPC to evaluate the decomposition effects on the polymerization. Results of the research efforts presented herein are written as individual research reports with contributing authors and pertinent literature reviews presented at the beginning of each chapter. / Ph. D.

The 1980's heralded the discovery and identification of extra-pituitary sources of the neurohypophysial hormone oxytocin in non-neural tissues of several animal species. The presence, location and biosynthesis of significant amounts of oxytocin in the ovarian corpus luteum was followed by the immunocytochemical demonstration of an oxytocin-like peptide in the testicular interstitial cells. Leydig cells, which comprise up to 80% of the testicular intertubular cell population, are known to synthesize testosterone in situ. Indirect evidence indicated that an oxytocin-like peptide was also present in Leydig cells. The question arose whether this peptide was synthesized de novo by Leydig cells or was taken up and stored by the cells following biosynthesis at some other intra- and/or extra-gonadal source(s). Since luteinizing hormone (LH) and ascorbate are known to augment the production of oxytocin in ovarian granulosa cells, varying concentrations of these two stimulants were used to monitor the biosynthesis of oxytocin from isolated Leydig cells in culture. / Ph. D.

Ganglion cell death in glaucoma is caused by a variety of insults that include ischemia, insufficient neurotrophic support and oxidative stress. Experimental studies were therefore conducted on cell cultures to determine how serum deprivation (to mimic insufficient neurotrophic support) or oxidative glutamate toxicity (GB), cause oxidative stress and induce retinal cell death. Moreover, studies were carried out to deduce whether selected sulphur containing compounds can blunt any negative influences to cells in culture and/or a defined ischaemic insult to the rat retina in situ, as this might suggest their use for the treatment of glaucoma. Serum deprivation and GB caused generation of reactive oxygen species (ROS) and apoptosis-like death to transformed retinal ganglion cells (RGC-5 cells). RGC-5 cells were more susceptible to the detrimental effects of GB than serum deprivation. RGC-5 cells subjected to serum deprivation appear to die by mechanisms that resemble classical apoptosis more closely than that caused by GB and the phase between the maximal generation of ROS and cell death were different. Cell death caused by serum deprivation was caspase-dependent but this was not the case for GB. Moreover, of the two sulphur compounds sulbutiamine and N-acetyl cysteine (NAC), sulbutiamine blunts the effect of serum deprivation more effectively. In addition, the pan caspase inhibitor z-VAD-fmk attenuated the negative effect of serum deprivation to RGC-5 cells while the necroptosis inhibitor (necrostsatin-1) counteracted solely the insult of GB. The sulphur containing compounds, ACS1 and ACS 67 which release hydrogen sulphide (H2S) slowly and NAC (a pro-cysteine GSH precursor) attenuated GB-induced cell death of RGC-5 cells. In contrast, sulbutiamine (a lipophilic thiolic thiamine derivative) was particularly effective in protecting RGC-5 cells from an insult of serum deprivation. Moreover, all of the sulphur compounds directly sequestered different types of ROS but with varying efficiency. Common features by which all tested sulphur containing agents seem to elicit a mode of action include the stimulation of GSH and the antioxidant enzyme glutathione-S-transferase (GST) as well as to scavenge excess free radicals. Moreover, the slow release of H₂S from the ACS compounds appears to protect cells from oxidative stress through increasing the level of GSH, modulation of the cystine uptake transporter xCT, stimulation of the oxidative stress related transcription factor Nrf2 and the stimulation of pro-survival signalling pathways. The slow releasing H₂S sulphur compound ACS67 also counteracts a number of detrimental influences to the rat retina in situ because of ischemia/reperfusion that includes damage to their ganglion cells. This suggests that such sulphur compounds might find a use in the treatment of glaucoma where ischemia probably plays a part in the disease process.

L’avènement des lasers impulsionnels nanosecondes à femtosecondes a permis un développement rapide de techniques permettant de sonder et/ou de transformer les matériaux à l’échelle locale par des processus d’absorption non linéaire. Ce saut technologique a vu l’émergence de nombreuses applications associées au phénomène de confinement spatial. La stéréolithographie 3D par photopolymérisation biphotonique constitue un exemple typique d’application à forte valeur ajoutée qui offre de prometteuses perspectives en terme d’écriture à l’échelle nanométrique. Un enjeu fondamental constitue alors l’élaboration de nouveaux photoamorceurs très réactifs et activables à deux photons. Dans ce contexte, ce manuscrit présente une étude photophysique et photochimique de deux séries de photoamorceurs biphotoniques ‘Donneur/Accepteur’ intégrants des stilbènes comme relais électroniques avec pré-organisation dans des structures bichromophores. Les processus primaires photoinduits, les mécanismes de photoamorçage, la photoréactivité à l’echelle locale sont décrits et étudiés méthodiquement. Enfin, le potentiel appliqué de cette nouvelle génération de photoamorceurs est mis en évidence en microfabrication multiphotonique à travers l’élaboration de structure 3D à l’échelle µm. / The advent of pulsed laser technologies has promoted the rapid growth of new emerging research domains which aim at probing and/or transforming materials at local scale using non linear absorption processes. A large range of applications takes benefit of the inherent spatial containment observed in non linear absorption processes so as to control photoreactions at nm-scale. The field of multiphoton fabrication (or stereolithography) addresses this fundamental issue and has developed rapidly so that it is no longer a rapid prototyping technology but a real manufacturing technique that is commercially available. The development of multiphoton stereolitography also requires highly reactive two-photon activable (2PA) initiators whose design and elaboration are the subject of considerable molecular engineering research. In this context, the present manuscript describes the photophysical and photochemical properties of two series of 2PA initiators. Such novel D--A structures have be designed by associating distinctive Donor and Acceptor groups into stilbene arms used as ‘electron relay’ and organized into a (multi)branched architecture. The photoinduced primary processes, the global photoinitiating mechanisms as well as the photoreactivity are described methodically. We finally demonstrate the applied potential of this new type of two-photon initiators in multiphoton stereolitography.

A distribuição de pesos moleculares (DPM) de um polímero afeta as propriedades mecânicas, térmicas e reológicas do material. Além disso, a análise em tempo real de uma reação de polimerização é uma tarefa complicada e, consequentemente, os procedimentos de controle devem ser baseados em valores gerados pelos modelos. Por isso, é extremamente importante ter dados confiáveis sobre distribuições de pesos moleculares, melhorar a eficiência dos métodos existentes e desenvolver novos métodos capazes de prever as heterogeneidades das reações de polimerização. Experimentalmente, a DPM pode ser obtida usando técnicas como a cromatografia de permeação em gel. Para predizer a DPM, vários métodos foram desenvolvidos nas ultimas décadas. Um dos principais é o dos momentos estatísticos, baseado em conceitos puramente estatísticos, que não conseguem descrever completamente a DPM. Além disso, as aproximações com método de Galerkin usam polinômios ortogonais - no caso especifico polinômios de Laguerre - cujos coeficientes são calculados empregando os momentos estatísticos e a distribuição é gerada resolvendo um número de equações definido pelo usuário, relacionado à precisão desejada. Enfim, o método das funções geradoras de probabilidades foi utilizado para prever as DPMs, porém necessitando uma inversão da transformada de Laplace, que introduz problemas numéricos nem sempre possíveis de serem resolvidos. No presente trabalho, o sistema rigoroso de equações diferenciais ordinárias foi resolvido, com objetivo de reduzir as imprecisões e as limitações introduzidas pelas aproximações. Obter diretamente a DPM completa requer a resolução de um sistema contendo cerca de 2Nmax até 3Nmax equações diferenciais ordinárias rígidas, tarefa que há alguns anos era inviável devido a limitações relacionadas à capacidade de cálculo. Foi modelada a DPM para uma reação de polimerização radicalar livre de estireno e de metacrilato de metila. Um interesse especial foi dado à taxa de terminação que é, no momento, um dos temas mais investigados em polimerização por radicais livres. Os resultados das simulações foram comparados com dados experimentais tirados de reatores convencionais e, subsequentemente, com dados experimentais provenientes de um millireactor não convencional. / It is well known that the molecular weight distribution (MWD) of a synthetic polymer affects its mechanical, thermal and rheological properties. Furthermore, the on-line analysis for polymerization reaction is a difficult task and, consequently, the control procedures must rely on values given by models. As such, it is extremely important to have reliable data on the MWD, improve the efficiency of existing methods and develop new ones to predict the heterogeneities of polymerization reactions. Experimentally, the MWD can be obtained using techniques such as Gel Permeation Chromatography (GPC). To predict the MWD, many methods have been developed over the last decades. One of the main methods is the statistical moment treatment, which is based on a pure statistical concept and do not describe the whole MWD. Moreover, Galerkin approximation uses orthogonal polynomials -in general Laguerre polynomials- whose coefficients are calculated exploiting the statistical moment definition and the distribution is generated by solving a user-defined number of equations based on the desired precision. Finally, probability-generating functions that have been used to predict MWDs require Laplace transforms inversions, introducing numerical issues that must be bypassed and are not always solvable. It has been decided to base the approach without adopting any of these methods but directly solving the rigorous ordinary differential equation (ODE) system in order to reduce the inaccuracies and the limitations introduced by approximations. The direct obtention of the MWD requires the resolution of a system containing approximately 2Nmax up to 3Nmax stiff ODE equations that, a few years ago, was unfeasible due computational time limitations. The MWDs for a free radical styrene polymerization system and a methyl methacrylate system have been modeled. A special focus was given to the termination rate constant, which is, at the present, one of the most investigated topics in free radical polymerization. The results of the simulations were compared to experimental data taken from conventional reactors and, subsequently, to experimental data coming from an unconventional millireactor.

Materiais nanocompósitos híbridos polímero-argila nos quais lamelas nanométricas de argila montmorilonita são encapsuladas e dispersas em matriz polimérica são em geral mais rígidas, tenazes e resistentes do que os materiais poliméricos convencionais e tem o potencial de aplicações em revestimentos e filmes com propriedades de barreira. Dentre as várias técnicas de preparação de nanocompósitos poliméricos, as técnicas de polimerização \"in-situ\" em emulsão e mini-emulsão vem sendo empregada na síntese de látices híbridos com lamelas de argilas encapsuladas pelo polímero. Neste trabalho foram preparados látices híbridos de poliestireno e argila montmorilonita esfoliada através de dois métodos: no primeiro, a polimerização em emulsão e miniemulsão convencional na presença de argila modificada com sal quaternário de amônio é realizada com surfatante catiônico; no segundo método, um surfatante aniônico reativo foi usado para modificar uma argila natural sódica e empregada na polimerização em emulsão. Os resultados obtidos tanto para a polimerização em emulsão como em miniemulsão empregando idênticos reagentes (argila organofílica modificada e surfatante catiônico) mostraram boa conversão, aumento na velocidade de polimerização com aumento da concentração de surfatante e de argila, aumento na temperatura de pico na máxima velocidade de decomposição (TG), aumento no módulo de armazenamento no patamar vítreo e no patamar borrachoso (DMTA) com aumento da concentração de argila, encontrando um valor mínimo em ambos a 5% de argila. Apesar dessas características positivas, não foi obtida a encapsulação das lamelas da argila que era o objetivo principal do trabalho. Por outro lado, o método de polimerização em emulsão não convencional com surfatante reativo mostrou baixa eficiência na conversão mas que se mostrou eficaz na encapsulação das lamelas da argila para os látices com baixa conversão e elevado diâmetro de partícula. / Polymer-clay nanocomposite materials, in which nanometer-thick layers of clay dispersed in polymers, are generally stiffer, stronger, and tougher than normal polymeric materials and can be potentially useful in a variety of applications. These polymer-clay nanocomposites can be prepared in several ways, namely by emulsion \"in-situ\" polymerisation where polymer chains are coagulated on silicate layers producing capped silicate layers are more or less uniformly dispersed in aqueous medium. The objective of this work is to prepare polymer-clay hybrid latexes with exfoliated clay platelets encapsulated inside latex particles in order to improve the exfoliation of the clay platelets in the final polymeric film. To achieve this objective two separate approaches have been investigated, first by conventional emulsion polymerization and miniemulsion polymerization in the presence of montmorillonite clay modified by cationic surfactant and in the other approach a reactive anionic surfactant was used to modify the natural montmorillonite clay layers by emulsion polymerization. The results for both the emulsion polymerization as in miniemulsion using identical reagents (organoclay modified and cationic surfactant) showed good conversion, polymerization rate increased with increasing concentration of surfactant and clay, increased peak temperature at maximum speed decomposition (TG), an increase in storage modulus in the glassy plateau and the rubbery plateau (DMTA) with increasing concentration of clay, finding a minimum value in both the 5% clay. Despite these positive characteristics, encapsulation was not obtained from lamellar clay that was the main objective. Moreover, the method of emulsion polymerization with non-conventional reactive surfactant showed low conversion efficiency but has proved effective in the encapsulation of the lamellae of the clay for the lattices with low conversion and high particle diameter.

Espécies carbonílicas tripletes formadas quimicamente no escuro, por exemplo, durante a peroxidação de lipídios, têm reatividade química análoga à de radicais alcoxilas. Aventou-se que tais espécies possam estar implicadas na fisiopatologia de doenças degenerativas (\"estresse carbonílico\"). A pesquisa dos efeitos de espécies tripletes sobre algumas biomoléculas e consequentes respostas biológicas, propostas e pesquisadas no período 1970 - 1990 (hipótese de \"fotoquímica sem luz\" dos Profs. G. Cilento, IQUSP, e Emil H. White, Johns Hopkins University), encontrou empecilhos instrumentais e relativamente poucas propostas foram confirmadas. Com o uso de técnicas de alta resolução, tais como EPR, HPLC e MS, este trabalho teve como objetivo analisar intermediários e produtos de tais processos e estudar mecanismos de reação de acetona triplete, produzida quimicamente pela decomposição térmica de 3,3,4,4-tetrametildioxetano (TMD) ou, enzimaticamente, pela oxidação aeróbica de isobutanal (IBAL), catalisada por peroxidase de raiz forte (HRP), na presença de aminoácidos e proteínas. Este trabalho demonstra a formação de um radical acetila, presumidamente formado da clivagem α de acetona triplete, e um radical terciário centrado em carbono, formado pela abstração de hidrogênio do IBAL. Resultados de espectrometria de massas demonstraram a formação de três diferentes adutos entre o radical terciário de IBAL, com L-Trp. Aventou-se que um dos produtos era resultante de alteração no nitrogênio e os outros no carbono 3, ambos no anel indólico. Observou-se também a formação de produto correspondente ao radical hidroxipropionil com L-Trp. Também se observaram dois produtos de L-Trp típicos de sua oxidação por oxigênio singlete, a formilquinurenina, e um aduto de função álcool. A formação de base de Schiff entre o L-Trp estudado e o IBAL também é apresentada. A formação de oxigênio singlete foi evidenciada indiretamente via EPR utilizando o spin trap TEMP e através de um captador de adição-9,10 (tipo Diels-Alder) em derivado de antraceno. Foram realizados, também, experimentos com precursores de melanina e demonstrou-se a formação de espécies excitadas do ácido 5,6-dihidroxi-indol-2-carboxílico (DHICA) que poderiam explicar a formação de produtos de DNA tipicamente resultantes de reação fotoquímica, mas na ausência de luz. Tais resultados corroboram a reação de espécies tripletes com biomoléculas, possibilitando a compreensão de número significativo de eventos biológicos conhecidos, mas teoricamente \"proibidos\" de ocorrer no estado fundamental, em tecidos não expostos à luz / Electronically excited triplet carbonyl species formed as products of some biochemical reactions, such as lipid peroxidation, behave similarly as alcoxyl radicals. It has long been hypothesized that such excited species could have a role in some diseases (\"carbonyl stress\"). Research of chemical lesions of triplet carbonyls over biomolecules and their biological response took place principally from 1970 to 1990 (the \"photochemistry without light\" hypothesis proposed by Profs. G. Cilento, IQUSP, and Emil H. White, Johns Hopkins University), but it suffered from the lack of required instrumentation, and just few cases of photo(bio)chemistry without light were confirmed. The aim of this work, using high resolution techniques (EPR, HPLC, and MS), is to analyze the reaction products of excited triplet acetone with aminoacid and protein targets. Triplet acetone was produced from the thermal decomposition of 3,3,4,4-tetramethyldioxetane (TMD) or from the aerobic oxidation of isobutanal (IBAL) catalyzed by horseradish peroxidase (HRP). We revealed the generation of acetyl radical, putatively originated from α-cleavage of triplet acetone, and a carbon-centered tertiary radical, proposed as an IBAL radical formed by hydrogen abstraction from IBAL. Mass spectrometry showed production of three adducts from the reaction of IBAL radical with L-Trp, one of them at the nitrogen 1 and the other two at carbon 3 from the amino acid indole ring. Two adducts with m/z correspondent to the reaction between L-Trp (at carbon 3) and a hydroxypropionyl radical, and two products typically formed from singlet oxygen (formylkynurenine and an alcohol L-Trp adduct) were also observed. A Schiff base between L-Trp and IBAL was also observed. Singlet oxygen production from triplet-triplet energy transfer from excited acetone to ground state molecular oxygen was indirectly showed by EPR spin trapping with TEMP, and by MS using the anthracene derivative EAS to trap (9,10-cycloaddition) of 18O2 (1Δg). Other data reported here include the demonstration of excited species formed when DHICA, a melanin precursor, was oxidized. These results might explain the generation of DNA photochemical products (thymine dimers) in the absence of light. Altogether, we collect strong and significant evidence in this thesis that corroborate the reactivity of triplet excited species with a couple of biomolecules, providing insights over some reportedly known molecular events that are theoretically forbidden to occur in the ground state but happen in tissues non-exposed to light