Un tiers des urgences dentaires et un pourcentage élevé de maux de dents sont endodontie liés. Instruments rotatifs utilisés dans le traitement endodontique peuvent se briser à l'intérieur du canal radiculaire en raison de la fatigue des matériaux. Une fois cassé, l'extraction de la partie fracturée du canal est un travail difficile et ennuyeux de le patient et le dentiste. Par conséquent, l'alerte d'une fracture imminente lors de l'utilisation clinique ou développer de bonnes stratégies pour augmenter ses propriétés mécaniques sera d'une grande aide pour éviter les complications médicales / juridique. La recherche est étudié à partir de deux parties. La première partie a établi une plate-forme de test standard, simulant plusieurs paramètres de canal, propose une série de stratégies visant à améliorer la vie de la fatigue et des propriétés mécaniques de matériaux. Aussi, un système de surveillance utilisant de réseaux de Bragg (FBG) capteurs a été tentée. la raison de l'utilisation de la glycémie à jeun est sa petite taille qui est très prometteur dans l'intégration avec la pièce à main de l'équipement endodontique. dans le travail actuel, en ramassant et en analysant l'onde de contrainte par transformée de Fourier rapide (FFT), nous peut révéler la variation d'énergie et la fréquence phénomène déplaçant dans certaines fréquences caractéristiques. on espère que, avec ces informations, nous pouvons éviter / atténuer la survenue de fracture inattendue. Comme pour l'essai de fatigue, les données ont montré que la résistance à la fatigue peut être améliorée certain traitement thermique ou à mouvement alternatif méthode de rotation appliqué. tel phénomène peut être étroitement liée à la composition de la phase en ni-Ti en alliage et la contrainte de traction maximale est réduite lorsque le mouvement alternatif appliqué. études ont montré que plus la teneur de la phase martensite dans l'aiguille, l'plus de vie à la fatigue peut être atteint. Cependant, il peut être nécessaire de prendre des compromis avec l'efficacité de coupe de l'aiguille. pour cette question, nous pouvons combiner le traitement cryogénique et traitement thermique pour obtenir une meilleure résistance à la fatigue sans compromettre son efficacité de coupe. La deuxième partie est de fabriquer haute résolution, grande taille de la nouvelle Type aiguilles d'endodontie en utilisant la polymérisation à deux photons (TTP) technique. Le travail se fait à l'université de Joseph-Fourier LiPhy laboratoire, France. Contrairement à la fabrication traditionnelle du PPT, qui avait une limitation de sa taille de produits en raison du faible pouvoir lase, taux de redoublement et piézo entraîné stade, nous utilisons résine Ormocer, 130 kHz, 1W puissant laser de 532 nm à l'étape motorisé étage XY pour fabriquer une grande 800 échafaud um cellulaire bio-compatible et 1.2 cm aiguille de hauteur. aussi, pour améliorer la qualité du produit de TPP, l'approche de correction de la puissance du laser avait été tentée. Pendant TPP fabrication, la forme de focalisation laser changé lorsque la surface de la fabrication a été déplacé dans la direction z. Cela se traduit par le fait que nous avons besoin de plus afin d'assurer la taille de voxel est identique à z différent. pour corriger ce défaut, un procédé pour la correction de la puissance du laser et de la formule pour la puissance de correction sont proposées. la formule est dérivé du concept de maintien de conditions d'exposition identiques. / One third of dental emergencies and a high percentage of toothaches are endodontics related. Rotary instruments employed in endodontic treatment may break inside the root canal due to material fatigue. Once broken, extracting the fractured part from the canal is a difficult job and is annoying to both the patient and the dentist. Therefore, warning of an imminent fracture during clinical use or developing good strategies to increase its mechanical properties will be a great help to avoid medical/ legal complications. The research is studied from two parts. The first part established a standard testing platform, simulating several root canal parameters, proposing a series of strategies to improve the fatigue life and material's mechanical properties. Also, a monitoring system employing Fiber Bragg Grating (FBG) sensors has been attempted. The reason of using FBG is its small size which is very promising in integrating with the handpiece of the endodontic equipment. In the current work, by picking up and analyzing the stress wave through Fast Fourier Transform (FFT), we can reveal the energy variation and the frequency shifting phenomenon under some characteristic frequencies. It is hoped that with these information, we can avoid/alleviate the occurrence of unexpected fracture. As for the fatigue test, data showed that the fatigue life can be improved when certain heat treatment or reciprocating rotation method applied. Such phenomenon may be closely related to the phase composition in Ni-Ti Alloy and the maximum tension stress is decreased when reciprocating movement applied. Studies showed that the more content of martensite phase in the needle, the more fatigue life can be achieved. However, it may need to take compromise with needle's cutting efficiency. For this issue, we can combine cryogenic treatment and heat treatment to get better fatigue life without compromising with its cutting efficiency. The second part is to fabricate high resolution, large size of new type endodontic needles by employing two-photon polymerization (TTP) technique. The work is done in the university of Joseph-Fourier LiPhy lab, France. Unlike traditional TPP manufacturing, which had a limitation of its products size due to small lase power, repetition rate and piezo driven stage, we use Ormocer resin, 130 kHz, 1W powerful 532 nm laser with step motor driven X-Y stage to fabricate high bio-compatible 800 µm cell scaffold and 1.2 cm height needle. Also, to improve the product quality of TPP, the laser power correction approach had been attempted. During TPP fabrication, the laser focusing shape changed when the fabrication surface was moved up in z direction. This results in that we need more power to ensure the voxel size is the same at different z. To correct such defect, a method of the laser power correction and formula for the correcting power are proposed. The formula is derived from the concept of keeping exposure condition the same.

The purpose of this thesis is to investigate the nonlinear phenomena known as doubly-stimulated, non-degenerate two-photon emission (ND-2PE) in Gallium Arsenide (GaAs). 2PE refers to the simultaneous emission of two-photons as electrons move from the conduction band in a direct gap semiconductor to the valence band. Following the same path for describing one-photon emission (1PE) we describe 2PE as a product of the irradiance, and the negative of the loss which in this case is two-photon absorption, , the negative coming from the population inversion. We attempt to observe 2PE by using a frequency non-degenerate pump-probe experiment in which a third beam optically excites a 4 µm thick GaAs sample. We use nondegenerate beams in hopes of utilizing the 3-orders of magnitude enhancement seen in twophoton absorption (2PA) by going to extreme nondegeneracy (END) to enhance 2PE. GaAs is chosen due to the availability of the appropriate wavelengths, the maturity of the GaAs technology, its use in optoelectronic devices and its ability to be electrically pumped. During the experimental development we learn how to effectively etch and manipulate thin GaAs samples and model the transmission spectrum of these samples using thin film transmission matrices. We are able to match the measured transmission spectrum with the theoretical transmission spectrum. Here we etch the bulk GaAs left on the sample leaving only the 4 µm thickness of molecular beam epitaxial grown GaAs plus additional layers of aluminum gallium arsenide (AlGaAs). These samples were grown for us by Professor Gregory Salamo of the University of Arkansas. iv Using the pump-probe experiment on the 4 µm GaAs sample, we measure the change of the 2PA due to the presence of optically excited carriers. The goal is to reduce the 2PA signal to zero and then invert the 2PA signal indicating an increase in transmission indicative of 2PE when the population is inverted. Our results show that we achieve a 45% reduction in the 2PA signal in a 4 μm thick GaAs sample due to the excited carriers. Unfortunately, we currently cannot experimentally determine whether the reduction is strictly due to free-carrier absorption (FCA) of our pump or possibly due to a change in the two-photon absorption coefficient. We measure the transmission of various wavelengths around the bang gap of GaAs as a function of excitation wavelength and achieve a transmittance of ~80% which we attribute to possibly be one photon gain (1PG) at 880 nm. We also go to cryogenic temperatures to concentrate the carriers near the bottom of the conduction band and improve the theoretical gain coefficient for 2PE. Unfortunately, we do not observe a measurable change in 2PA with the addition of optically excited carriers. Along with FCA of our infrared pump we suspect that the difficulties in this first set of experiments are also a result or radiative recombination due to amplified spontaneous emission reducing our free carrier density along with the fact that 4 m is too thick for uniform excitation. We now have 1 m samples from Professor Gregory Salamo which we hope will give better and more definitive results

Time Dependent Density Functional Theory offers a good accuracy/computational cost ratio among different methods used to predict the electronic structure for molecules of practical interest. The Coupled Electronic Oscillator (CEO) formalism was recently shown to accurately predict Nonlinear Optical (NLO) properties of organic chromophores when combined with Time Dependent Density Functional Theory. Unfortunately, CEO does not lend itself easily to interpretation of the structure activity relationships of chromophores. On the other hand, the Sum Over States formalism in combination with semiempirical wavefunction methods has been used in the past for the design of simplified essential states models. These models can be applied to optimization of NLO properties of interest for applications. Unfortunately, TD-DFT can not be combined directly with SOS because state-to-state transition dipoles are not defined in the linear response TD approach. In this work, a second order CEO approach to TD-DFT is simplified so that properties of double excited states and state-to-state transition dipoles may be expressed through the combination of linear response properties. This approach is termed the a posteriori Tamm-Dancoff approximation (ATDA), and validated against high-level wavefunction theory methods. Sum over States (SOS) and related Two-Photon Transition Matrix formalism are then used to predict Two-Photon Absorption (2PA) profiles and anisotropy, as well as Second Harmonic Generation (SHG) properties. Numerical results for several conjugated molecules are in excellent agreement with CEO and finite field calculations, and reproduce experimental measurements well.

<p>Highly correlated quantum chemical methods have been appliedto study the photophysical properties of substituted benzenes.With the inclusion of spin-orbit coupling, the phosphorescencesof these molecules have been calculated usingMulti-CongurationalSelf- Consistent Field (MCSCF) quadraticresponse theory. The Herzberg-Teller approximation has beenadopted to evaluate the vibronic contributions tophosphorescence.</p><p>The performance of hybrid density functional theory (DFT) atthe B3LYP level is examined in comparison to the MP2, CCSD andCCSD(T) methods for the geometry and permanent dipole moment ofp-aminobenzoic acid. The time-dependent DFT/B3LYP method isapplied to calculate the two-photon absorption of a series ofZinc-porphyrin derivatives in combination with a two-statemodel. The transitions between excited singlet and tripletstates of Zinc and Platinum based organometallic compounds havebeen computed using DFT quadratic response theory. The resultsare used to simulate the non-linear propagation of laser pulsesthrough these materials utilizing a dynamical wave propagationmethod.</p>

<p>Two-photon excited fluorescence microscopy (TPM) has become a standard biological imaging tool due to its simplicity and versatility. The fundamental contrast mechanism is derived from fluorescence of intrinsic or extrinsic markers via simultaneous two-photon absorption which provides inherent optical sectioning capabilities. The NIR-II wavelength window (1000–1350 nm), a new biological imaging window, is promising for TPM because tissue components scatter and absorb less at longer wavelengths, resulting in deeper imaging depths and better contrasts, compared to the conventional NIR-I imaging window (700–1000 nm). However, the further enhancement of TPM has been hindered by a lack of good two-photon fluorescent imaging markers in the NIR-II. </p><p>In this dissertation, we design and characterize novel two-photon imaging markers, optimized for NIR-II excitation. More specifically, the work in this dissertation includes the investigation of two-photon excited fluorescence of various highly conjugated porphyrin arrays in the NIR-II excitation window and the utilization of nanoscale polymersomes that disperse these highly conjugated porphyrin arrays in their hydrophobic layer in aqueous environment. The NIR-emissive polymersomes, highly conjugated porphyrins-dispersed polymersomes, possess superb two-photon excited brightness. The synthetic nature of polymersomes enables us to formulate fully biodegradable, non-toxic and surface-functionalized polymersomes of varying diameters, making them a promising and fully customizable multimodal diagnostic nano-structured soft-material for deep tissue imaging at high resolutions. We demonstrated key proof-of-principle experiments using NIR-emissive polymersomes for in vivo two-photon excited fluorescence imaging in mice, allowing visualization of blood vessel structure and identification of localized tumor tissue. In addition to spectroscopic characterization of the two-photon imaging agents and their imaging capabilities/applications, the effect of the laser setup (e.g., repetition rate of the laser, peak intensity, system geometry) on two-photon excited fluorescence measurements is explored to accurately measure two-photon absorption (TPA) cross-sections. A simple pulse train shaping technique is demonstrated to separate pure nonlinear processes from linear background signals, which hinders accurate quantification of TPA cross-sections.</p> / Dissertation

La thérapie photodynamique est fondée sur l’activation sélective par la lumière de médicaments appelés photosensibilisateurs. Non toxique en l’absence d’excitation lumineuse, le photosensibilisateur est capable, une fois excité, de transférer son énergie pour former de l’oxygène singulet qui induit la mort de la cellule. L’utilisation d’une excitation biphotonique offre de nouvelles perspectives pour la thérapie photodynamique du cancer. En effet, la dépendance quadratique de l’absorption à deux photons (ADP) avec l’intensité du laser permet une très grande sélectivité spatiale, ce qui rend possible un traitement plus sélectif des tumeurs, et la lumière infra-rouge utilisée permet le traitement de tumeurs plus profondes. Dans ce travail, nous avons développé une famille de nano-objets tout organiques pour la thérapie photodynamique biphotonique. Ils présentent des sections efficaces d’ADP très élevées dans la gamme spectrale d’intérêt biologique et leur efficacité a été démontrée in vitro. / Photodynamic therapy is based on the selective activation by light of drugs called photosensitizers. Non-toxic in the absence of excitation light, the photosensitizer is able, upon excitation, to transfer energy to produce singlet oxygen, which induces cell death. Two-photon excitation offers new perspectives for photodynamic therapy of cancer. Indeed, the quadratic dependence of two-photon absorption (TPA) with the laser intensity allows high spatial selectivity, which enables a more selective treatment of tumors, and the use of infrared light allows treatment of deeper tumors. In this work, we have developed a family of fully organic nano-objects for two-photon photodynamic therapy. They exhibit very high TPA cross-sections in the biological spectral range of interest and their efficiency has been demonstrated in vitro.

Les techniques de fluorescence sont des outils de choix pour l’étude et la compréhension fine des processus biologiques. Ceci requiert toutefois l’utilisation de sondes fluorescentes parfaitement adaptées au but visé et répondant aux différentes exigences requises pour l’application visée. Dans ce cadre, nous nous sommes plus particulièrement intéressés à l’élaboration de sondes biphotoniques de pH adaptées à une mesure très sensible de faibles variations de pH autour du pH neutre. Les variations et gradients de pH sont en effet impliqués dans un certain nombre de processus biologiques importants et peuvent être associées à des dysfonctionnements liés à certaines maladies. Dans ce cadre, nous avons développé de nouvelles sondes fluorescentes de pH fluorescentes présentant à la fois un comportement ratiométrique, une forte sensibilité autour du pH neutre et facilement excitables dans le proche IR par absorption à deux photons. Ces sondes de structure quadrupolaire et bolamamphiphile permettent ainsi la détection ratiométrique du pH dans des environnements biologiques au moyen d'une excitation biphotonique dans le proche IR. En parallèle, nous nous sommes intéressés à l’élaboration de nanoparticules hyperbrillantes dédiées à l’imagerie biologique par microscopie de fluorescence induite par excitation à deux photons. Nous nous sommes plus particulièrement attachées au design de nanoparticules organiques fluorescentes constituées de molécules organiques de bas poids moléculaire (FONs). Cette approche offre en effet une grande flexibilité et la possibilité d’accéder à des nanosondes ayant des brillances comparables aux très populaires quantum dots mais moins toxiques et plus facilement dégradables. L’ingénierie moléculaire des fluorophores utilisés pour la préparation des FON est cruciale puisqu’elle influence fortement à la fois les propriétés photophysiques (brillance, couleur…) et leur propriétés physico-chimiques (stabilité chimique et structurale, stabilité colloïdale). Dans ce contexte, une librairie de nouveaux chromophores dipolaires a été synthétisée et utilisées pour la préparation de FON par la méthode de nano-précipitation. Leurs propriétés ont été étudiées afin de déterminer la relation entre la structure du chromophore et les propriétés globales des nanoparticules constituées de ces colorants. Ce travail a permis d’identifier les paramètres structuraux permettant d’accéder à des nanoparticules présentant à la fois une brillance exceptionnelle, une émission modulable du vert au rouge et proche IR et une remarquable stabilité colloïdale. Ces nanoparticules présentent des potentialités majeures pour l’imagerie in vivo par excitation et détection dans le proche IR. / Fluorescence-based techniques are popular tools for the study and understanding of biological processes. This has prompted continuous research aimed at the development of a wide range of fluorescent probes specifically designed for specific applications. Among them, fluorescent pH probes are of much interest as pH variations or gradients are involved in many biological events and anomalous alterations are often related to the onset of dysfunctions and diseases. In this framework we have developed a series of promising two-photon pH fluorescent molecular probes. These quadrupolar bolaamphiphilic probes are of great interest, as they combine a steep pH dependence of their optical properties close to neutral pH, ratiometric behavior and large response to two-photon (2P) excitation in the NIR region. As such they offer much promise for ratiometric detection of the pH in biological environments and in situ monitoring of acidification. In parallel, we have been interest in the design of ultrabright nanoparticles for bioimaging purpose (in particular highly sensitive optical imaging). We chose to focus on Fluorescent Organic Nanoparticles made of organic molecules with low molecular weight (FONs) as they offer a flexible route and promising alternatives to toxic quantum dots. In this case the design of the dye used as building blocks of the FONs is of crucial importance and strongly influence the chemical and physical properties of the nanoparticles generated, such as their one and two-photon brightness and both their structural and colloidal stability. In that context a library of novel dipolar chromophores have been synthesized and used to prepare FONs using the nanoprecipitation method. Their properties were thoroughly investigated in order to determine the relationship between the molecular design of the isolated dye and the overall properties of the nanoparticles made of these dyes. As a result, Hyperbright FONs emitting in the green to NIR region and combining giant brightness and remarkable stability have been achieved. They offer major promise for bioimaging based on both excitation and detection in the NIR region.

L’utilisation de nano-objets luminescents en milieu biologique est devenue très répandue, notamment en vue d’applications biomédical est elles que l’imagerie, la thérapie et le diagnostic. Jusqu’à récemment, les principaux travaux réalisés dans ce domaine concernaient les nanoparticules de silice dopées ou fonctionnalisées avec des molécules organiques, les nanoparticules d’or et les nanoparticules semi-conductrices (quantum dots, i.e., QDs). Toutefois, un certain nombre de limitations demeurent pour les applications dans le domaine du vivant, en lien notamment avec des problèmes de stabilité, de biocompatibilité et de toxicité ou encore de biodégradabilité. En parallèle,un certain nombre de molécules organiques fluorescentes non-toxiques ont été utilisées comme sondes fluorescentes en milieu biologique, mais leur brillance demeure limitée. L’idée directrice de la thèse est de concevoir et synthétiser de nouveaux chromophores organiques présentant une émission modulable (du visible au proche infrarouge) et adaptés à la préparation de nanoparticules organiques fluorescentes (FONs) combinant à la fois une brillance extrêmement élevée, une excellente stabilité colloïdale et une photostabilité adaptée à leur utilisation en imagerie in vitro et in vivo. De tels nanoobjets ultra-brillants pourraient alors représenter une alternative très intéressante aux nanoparticules actuellement les plus utilisées en imagerie de fluorescence du vivant (QDs). Le manuscrit décrit la synthèse et les propriétés de plusieurs classes de molécules fluorescentes spécifiquement conçues pour former des telles FONS par auto-assemblage dans l’eau. La préparation de ces FONs est présentée et leurs propriétés étudiées et discutées. Enfin des applications concrètes en bio-imagerie sont présentées. / Nowadays the use of bright luminescent nano-objects in biological environment is a topic that is gaining more and more importance, especially for biomedical applications such as imaging, the rapyand diagnostic. So far, numerous studies have been conducted with gold nanoparticles, silica nanoparticles (doped or functionalized with organic molecules), as well as semiconductor nanoparticles (quantum dots, i.e., QDs). However, most of these nanoparticles suffer from drawbacks (in terms of stability, biocompatibility, eco-toxicity or degradability). On the other hand, several nontoxic fluorescent molecular probes have been widely used, but most of the time their brightness remain modest in biological environments compared to QDs. Our idea is to engineer new organicchromophores with tunable emission wavelength (from visible to near infrared) for further preparation of organic fluorescent nanoparticles (so called FONs) that display giant one-photon and two-photonbrightness, as well as good colloidal and chemical stability, and suitable photostability for in vitro andin vivo imaging. As such, these FONs would represent interesting alternatives to QDs for use in bioimaging. This manuscript describes the synthesis and characterization of new classes of fluorescent molecules specifically engineered as building blocks for the fast preparation of such nanoparticles byself-aggregation in water. The FONs were fully characterized from both morphological and photophysical points of view and further used in bioimaging.

Neste trabalho, demonstramos a fabricação de microambientes tridimensionais para investigar o crescimento celular. Inicialmente, desenvolvemos um sistema de microfabricação que utiliza fotopolimerização via absorção de dois fótons, com o qual se pode fabricar um conjunto de microestruturas com formas e espaçamentos pré-determinados. Este sistema de fabricação utiliza pulsos de femtossegundos, provenientes de um laser de Ti:safira operando em 790 nm. A intensidade destes pulsos é alta o bastante para induzir a absorção de dois fótons no fotoiniciador, o qual é responsável por promover a polimerização em uma resina acrílica. A natureza não linear da absorção de dois fótons confina a excitação ao volume focal, permitindo a fabricação de estruturas tridimensionais com alta resolução espacial. Para a obtenção dos microambientes, foi necessário o desenvolvimento de um sistema opto-mecânico de movimentação, tanto do feixe quando do substrato da amostra. Com esta técnica, fabricamos microambientes compostos de estruturas com diferentes formas (paralelepípedos, cilindros e cones) e espaçamentos, os quais foram caracterizados através de microscopia óptica e eletrônica. Para demonstrar a viabilidade destes microambientes para a investigação do crescimento celular, estes foram utilizados para monitorar o desenvolvimento da célula Michigan Cancer Foundation-7 (MCF-7), uma linhagem celular de adenocarcinoma de mama que apresenta fenótipo tumoral amplamente utilizada como modelo de estudo para câncer de mama. Observamos, via microscopia óptica de transmissão e fluorescência, o desenvolvimento das células MCF-7 nos distintos microambientes. Nossos resultados indicam uma melhor aderência e, portanto, desenvolvimento celular nas microestruturas cilíndricas. Observamos ainda uma maior densidade de células nos microambientes com estruturas separadas de 12 &micro;m, a qual diminui com o aumento do espaçamento, de tal forma que para o microambiente com 30 &micro;m, por exemplo, poucas células são observadas. Portanto, nossos resultados demonstram que os microambientes desenvolvidos são viáveis para estudos mais aprofundados em biologia celular, com potenciais aplicações em engenharia de tecido. / In this work we have demonstrated the fabrication of tridimensional microenvironments for the investigation of cell growth. Initially we have developed a two-photon absorption photopolymerization microfabrication system, which allows producing a set of microstructures with predetermined forms and spacing. This fabrication system uses femtosecond pulses from a Ti: sapphire laser operating at 790 nm. These pulses are intense enough to induce two-photon absorption by the photoinitiator, that is responsible for promoting the polymerization in an acrylic resin. The nonlinear nature of the two-photon absorption confines the excitation to the focal volume, allowing the fabrication of tridimensional structures with high spatial resolution. In order to obtain the microenvironments, it was necessary to develop a movement system for both the laser beam and the sample substrate. With this technique we have fabricated microenvironments composed by structures with different geometries (parallelepipeds, cylinders and cones) and spacing, which were characterized by optical and scanning electron microscopes. To demonstrate the feasibility of the microenvironments for the investigation of cell growth, the samples were used to monitor de development of the Michigan Cancer Foundation-7 cell (MCF-7), a lineage of breast adenocarcinoma that has a tumoral phenotype and is highly used as a model in breast cancer studies. We have observed, through conventional optical and fluorescence microscopy, the growth of the MCF-7 cells in the various microenvironments. Our results indicate a better adhesion and, therefore, better development of cells on the cylindrical microstructures. We also observe a higher cell density in the microenvironments with microstructures having a spacing of 12 &micro;m, which reduces as the distance between microstructures increases, in such a way that for the microenvironment with 30 &micro;m spacing, for example, just a few cells are observed. Thus, our results demonstrate that the produced microenvironments are applicable in deeper studies in microbiology, with potential application in tissue engineering.

Neste trabalho estudamos o processo de absorção de dois fótons em compostos azoaromáticos, abordando tanto aspectos fundamentais quanto aplicados. Moléculas azo-aromáticos têm recebido especial atenção nos últimos anos devido as suas potencias aplicações em dispositivos para armazenamento óptico de informação, modulação da luz e geração de relevos em superfície, processes estes associados ao mecanismo de foto isomerização. Os trabalhos apresentados nessa tese tiveram como principal foco explorar o fenômeno de absorção de dois fótons, utilizando a propriedade de foto-isomerização das moléculas azo-aromáticas. Nosso objetivo foi estudar as vantagens que podem ser obtidas pela utilização de pulsos intensos de luz, que interagem de maneira não linear com a matéria, para desenvolver aplicações utilizando compostos azo-aromáticos. Inicialmente, estudamos o processo de absorção de dois fótons em uma nova família de compostos azo-aromáticos, denominados Salen Dyes. Investigamos a influencia da presença de íons metálicos no processo de absorção de dois fótons dessas moléculas. Nossos resultados mostraram que, devido a ausência de conjugação entre as estruturas azo-aromáticas conectadas pelo metal, este tem pouca influência no processo não linear estudado. Pelo uso de um modelo de soma de estado para a seção de choque de absorção de dois fótons, fomos capazes de determinar os momentos de dipolo de transição destas moléculas. Em seguida, implementamos uma técnica para estudar o processo de armazenamento óptico, induzido através da orientação molecular dos compostos azo-aromáticos, via absorção de dois fótons. Observamos que de fato é possível se observar birrefringência induzida por dois fótons nestas moléculas, a qual esta confinada ao volume focal, conforme demonstrado pela obtenção de armazenamento tri-dimensional. Finalmente, exploramos o processo de controle coerente via formatação de pulsos ultra-curtos para manipular o processo de birrefringência induzida por dois fótons em compostos azo-aromáticos. Foi demonstrado que apenas a através da manipulação da fase do pulso ultra-curto, é possível modular a birrefringência induzida em filmes de compostos azo-aromáticos. / Here we investigated fundamental and applied aspects of the two-photon absorption process in azoaromatic compounds. Azoaromatic molecules have been studied in the last few years due to their applications in optical storage devices, light modulators and surface relief gratings, processes related to the photo-isomerization mechanism. The main focus of the results presented in this thesis was to explore the two-photon absorption process, taking advantage of the intrinsic photo-isomerization of the azo-aromatic chromophores. Our main goal was to study the advantages of utilizing intense pulses, which promote nonlinear excitation, to develop application with azo-aromatic compounds. Initially, we studied the two-photon absorption process in a new class of azo-aromatic compounds, named Salen Dyes. We investigated the influence of metal ions, presented in the Salen Dyes structure, on the two-photon absorption spectrum. Our results revealed that the metals have practically no influence in the nonlinear optical properties due to the lack of conjugation between the azo-moieties in the Salen Dyes. Through a theoretical model based on a sum-over-states calculation, we were able to determine the transition dipole moment of these molecules. Subsquently, we implememnted a technique to study the two-photon induced birefringence, resulting from the molecular re-orientation, in azo-aromatic compounds. We observed that the two-photon induced birefringence is confined to the focal volume, s demonstrated in a three dimensional optical storage experiment. Finally, we used coherent control processes to manipulate the two-photon induced birefringence in azo-compounds. It was demonstrated that it is possible to modulate the optically induced birefringence by manipulating the phase of the ultra-short pulses, via pulse shaping techniques.