This thesis presents a study of the photophysical properties of a number of fluorene molecules used for organic semiconductor lasers. These results are then combined with lasing results to assess what the important properties in an organic semiconductor laser material are. Photophysical measurements were performed on a family of oligofluorenes; results show a redshift in the peak absorption and emission wavelengths with increasing length. There is also an increase in the molar extinction coefficient and photoluminescence quantum yields of the molecules. Transition dipole moments also increase with length, but fluorescence scales slower than absorption due to self-trapping occurring at longer molecular lengths. This study was then expanded to two families of star-shaped molecules with fluorene arms and differing cores. These molecules have three arms connected to either a central benzene unit or a larger truxene core. These molecules show an increase in PLQY and roughly three times higher molar extinction coefficients than comparable linear oligofluorenes. The star-shaped molecules PLQY and transition dipole moments are both greater than their linear oligofluorene counterparts. Energy transfer was then studied in the truxene-cored molecules, which showed that the symmetry of the molecule was broken due to interactions with the solvent. Energy transfer was observed on two timescales; a fast 500 fs process which is attributed to a localisation onto a single arm to emit, and a 3-10 ps second decay component, and was assigned to resonant energy transfer between the arms. Both decays were found to be wavelength dependent. Lasing results were then obtained for the benzene cored molecules. It was found that star-shaped molecules present improved lasing characteristics with lower ASE and lasing thresholds. These results were compared with those obtained for truxene-cored molecules whose rigid core provides them with better lasing and ASE characteristics.

CoordenaÃÃo de AperfeiÃoamento de NÃvel Superior / Seja I : ∑n → Mn+1 uma imersÃo de uma variedade conexa n-dimensional ∑ em uma variedade Riemanniana completa conexa (n + 1)-dimensional M sem pontos conjugados. Suponha que a uniÃo das geodÃsicas tangentes a I nÃo cobrem M. Sobre essa hipÃtese temos dois resultados: 1. Se a cobertura universal de ∑ Ã compacta, entÃo M Ã simplesmente conexa. 2. Se I Ã um mergulho prÃprio e M Ã simplesmente conexa, entÃo I(∑) Ã um grÃfico normal sobre um subconjunto aberto de uma esfera geodÃsica. AlÃm disso, existe um conjunto estrelado aberto A M tal que A Ã uma variedade com fronteira I(∑). / Let I : ∑n → Mn+1 be an immersion of an n-dimensional connected manifold ∑ in an (n + 1)-dimensional connected completed Riemannian manifold M without conjugate points. Assume that the union of geodesics tangent to I does not cover M. Under these hypotheses we have two results: 1. M is simply connected provided that the universal covering of ∑ is compact. 2. If I is a proper embedding and M is simply connected, then I(∑) is a normal graph over an open subset os a geodesic sphere. Furthermore, there exists an open star-shaped set A M such that A is a manifold with the boundary I(∑).

O σκοπός της εργασίας αυτής ήταν η σύνθεση νέων αστεροειδών τριπολυμερών, τύπου An(B-C)n διαφόρων μοριακών δομών, με την τεχνική του «ζωντανού» ανιονικού πολυμερισμού. Αναπτύχθηκε μια μεθοδολογία τεσσάρων διαδοχικών σταδίων σε αντίδραση διαλείποντος έργου η οποία δίνει προϊόντα καθορισμένης μοριακής αρχιτεκτονικής. Η μέθοδος αυτή είναι επέκταση της μεθόδου in-out που χρησιμοποιήθηκε για την σύνθεση ετεροκλαδικών συμπολυμερών αστεροειδών τύπου ΑnBn. Τα νέα αστεροειδή τριπολυμερή Αn(B-C)n αποτελούνται από ένα πυρήνα διασταυρομένων μονομερών από τον οποίο εξέρχονται δύο ειδών κλάδοι θεωρητικά ίσου αριθμού, ήτοι κλάδοι ομοπολυμερούς Α και κλάδοι δι-συσταδικού συμπολυμερούς (B-C). Για το σκοπό αυτό χρησιμοποιήθηκε μια ποικιλία μονομερών και παραγόντων συνένωσης προκειμένου να επιτύχουμε το επιθυμητό αποτέλεσμα. Χρησιμοποιήθηκαν διφορετικοί πυρήνες των αστεροειδών τόσο στη φύση (διβίνυλοβενζόλιο, διμεθακρυλικός αιθυλενο-γλυκολεστέρας) όσο και στις διαστάσεις (μίγμα διβίνυλοβενζολίου/στυρενίου) προκειμένου να μελετηθεί η επίδραση που φέρουν. Η μεθοδολογία που χρησιμοποιήθηκε δίνει τη δυνατότητα του σταδιακού χαρακτηρισμού των προϊόντων ο οποίος ήταν ουσιώδης για τον τελικό χαρακτηρισμό των τριπολυμερών. Για το μοριακό χαρακτηρισμό πρόδρομων και τελικών πολυμερών χρησιμοποιήθηκαν οι τεχνικές της χρωματογραφίας αποκλεισμού μεγεθών, της στατικής σκέδασης φωτός και η φασματοσκοπία του πυρηνικού μαγνητικού συντονισμού (1H-NMR). Επιπλέον για λόγους σύγκρισης ιδιοτήτων μεταξύ γραμμικών και αστεροειδών, συντέθηκαν γραμμικά ABC τριπολυμερή χρησιμοποιώντας την μέθοδο της διαδοχικής προσθήκης. Τα τελικά πολυμερή καθαρίστηκαν από τυχόν προσμίξεις με την τεχνική της soxhlet και χρησιμοποιώντας ως διαλύτη κυκλοεξάνιο. Μελετήθηκαν οι μηχανικές ιδιότητες των ετεροκλαδικών αστεροειδών συμπολυμερών σε σύγκριση με τα αντίστοιχα γραμμικά τριπολυμερή, με σκοπό να διερευνηθεί η επίδραση της αρχιτεκτονικής στις ιδιότητες αυτές. Επιπλέον εξετάσθηκε και ο μικροφασικός διαχωρισμός τόσο των γραμμικών όσο και των αστεροειδών τριπολυμερών και ο ρόλος που παίζουν η αρχιτεκτονική και τα μοριακά χαρακτηριστικά των πολυμερών. Η πραγματοποίηση πειραμάτων δυναμικής μηχανικής ανάλυσης καθώς και διαφορικής θερμιδομετρίας σάρωσης σε αστεροειδή πολυμερή πολύστυρενίου, πολύ(μεθακρυλικού εξυλεστέρα) και πολύ(μεθακρυλικού μεθυλεστέρα) και στα αντίστοιχα γραμμικά τους πολυμερή οδήγησαν σε ενδιαφέρον συμπεράσματα. Έγινε σαφές πως η δομή και το μοριακό βάρος επηρεάζουν τις ιδιότητες των πολυμερών. / The subject of this research was the synthesis of star-shaped terpolymers An(B-C)n, using the anionic living polymerization. A 4-step methodology in patch reaction was developed which gives polymers of specific molecular structure. This method is expansion of the in-out method which is used to synthesize heteroarm-star copolymers AnBn. The new star terpolymers consist of a core from cross-linked monomers from which derive two kind of branches theoretically equal in number. One is branches of homopolymer A and the other is branches of diblock copolymer (B-C). For this aim a variety of monomers and cross-linking agents was used. Different cores were made on the nature (DVB,EGDMA) and the size (DVB/St) in order to investigate their effect. Through the synthetic methodology we were able to molecular characterize each step which was vital for the final polymer. The polymers were well characterized through specific techniques. In order to measure the molar mass (Mw and Mn) and the polydispersity, I (Mw/Mn), we used Size Exclusion Chromatography (SEC) technique. The number of the branches was calculated by the Static Light Scattering (SLS) technique. Nuclear Magnetic Resonance spectroscopy (1 H-NMR) was used to calculate the percentage of each homopolymer to the terpolymer. Moreover in order to compare the properties of star and linear terpolymers, ABC linear terpolymers were synthesized by sequential addition. The final polymers were purified through the soxhlet technique with cycloexane. The properties of heteroarm star-like terpolymers were studied comparing with that of the corresponding linear terpolymers (the block and arm lengths were equal) in order to understand the effect of the macromolecular architecture on these properties. Moreover the microphase separation was examined in order to study the effect of the architecture and the molecular characteristics on the terpolymers. The Dynamic Mechanical Analysis (DMA) and Differential Scanning Calorimetry (DSC) experiments on linear and star terpolymers with polystyrene (PS), poly(hexylmethacrylate) (PHMA) and poly(methylmethacrylate) (PMMA) result in interesting conclusions. These conclusions gave us a clear proof that the molecular characteristics and the architecture of the polymers infect their properties.

Cette thèse présente la conception, la synthèse et l'étude photophysique de divers dérivés d'azophénine comme modèles structurels mono-bloc pour l'éméraledine qui est une forme de polyaniline à valence mixte. L'azophénine est une molécule conjuguée en forme d'étoile contenant à la fois des résidus de quinone diimine et de phénylamine tous deux contenus dans l'émeraldine. Cependant l'azophénine et l'émeraldine sont tout deux reconnus pour ne pas être émissifs. Le défi était alors de donner des propriétés d’émissions à l'azophénine à température ambiante avant toute investigation photophysique. L'objectif à long terme étant de rendre la polyaniline, connu pour être peu dispendieuse, attractive en tant que matériau donneur efficace dans une cellule solaire de type « bulk-heterojunction ». En raison des problèmes de faible solubilité des polymères, l'utilisation de modèles beaucoup plus soluble est une nécessité. Les modifications structurelles considérées comprennent l'ancrage des fonctions pontées d'éthynyle en position para- des quatre groupes phényls d'azophénine. Ces fonctions sont des groupes aromatiques encombrés de type truxène, des composés organométalliques trans-bis(trialkylphosphine) platine(II), des colorants de porphyrines de zinc(II) et de Bodipy. Elles présentent toutes une fluorescence ou une phosphorescence, signal pouvant être utilisé pour mesurer les interactions électroniques entre ces groupements et le noyau central. Leurs propriétés photophysiques sont étudiées en détail en utilisant la spectroscopie d'absorption et d'émission UV-Visible stationnaire et ultra-rapide résolue dans le temps. La DFT et la TDDFT sont également utilisés pour les optimisations des géométries (DFT) et pour déterminer la nature et les positions de l'absorption de la bande de transfert de charge (TDDFT). Le chapitre 2 présente la synthèse et la caractérisation d'un dérivé en étoile d'azophénine autour d’un noyeau truxène appelé TertTruQ. Le couplage de résidus encombrés de truxène avec de l'azophénine a amélioré l'activité photophysique du premier niveau singulet de ce dérivé à 77 K. Les hypothèses étant que le taux de désactivation non radiatif a diminué les rotations autour des axes des liaisons C-N en raison de la taille du truxène. De plus, cette nouvelle azophénine substituée s'est révélée être fluorescente à l'état solide à température ambiante. En raison de ces nouvelles observations, les propriétés d'émission des dérivés de l’éméraldine sont réexaminées. Une fluorescence faible à ~ 780 nm à 77 K, confirmée par le spectre d'excitation, a démontré la présence d'une faible émission de type fluorescence CT dans le proche-IR pour TertTruQ. Nous pouvons en conclure que l'azophénine fournit un modèle utile pour identifier quelle modification structurelle simple peut être effectuée pour rendre l’éméraldine émissive, si possible à température ambiante. De plus, lorsqu'une espèce non luminescente devient émissive, ce changement s'accompagne d'une augmentation de sa durée de vie à l’état excitée, propriétés recherchées pour des applications dans le domaine des cellules solaires. Ce travail a été publié dans Physical Chemistry Chemical Physics, 2017, 19, 21532-21539. Le chapitre 3 décrit la synthèse et la caractérisation des azophénines contenant du trans-bis(trialkylphosphine)diéthynyl-platine(II) formant les dérivés di- et tétra-substitués DiTruPtQ et TertTruPtQ. Les deux complexes présentent une fluorescence et une phosphorescence des "bras" organométalliques à 298 K en solution. En outre, l'effet d'atome lourd du platine permet d'explorer les propriétés de l’état triplet de l'azophénine. Cependant, la phosphorescence recherchée de l'état triplet CT n'a pas été considérée probablement en raison des processus rapides non radiatifs. Ce travail a été publié dans Organometallics, 2017, 36(3), 572-581. Le chapitre 4 présente l'effet du remplacement des ions H+ labiles sur le fragment HN^N par des fragments BF2+ pour former des cycles, fournissant ainsi un cadre plus rigide pour l'azophénine. En effet, la fluorescence CT proche-IR a été observée à 298 et 77 K. Cependant, malgré la présence de Pt dans les groupes pendants, aucune phosphorescence n'a été détectée. Les calculs de DFT ont suggéré que l'état triplet de plus faible énergie était très faible (0,975 eV (BQ) et 0,84 eV (TertPtBQ)) induisant une plus grande probabilité de processus non radiatifs, depeuplant ainsi efficacement l'état triplet. Ce travail a été accepté à Inorganic Chemistry, 2017. Le chapitre 5 présente les colorants fluorescents de porphyrine de zinc(II) et BODIPY bien connus, qui ont été liés à l'azophénine pour former DiBodipyQ, TertBodipyQ et PorBodipyQ. Le spectre d'absorption des BODIPY se situe dans une gamme où la porphyrine n'absorbe pas beaucoup. Ainsi, la combinaison de ces deux chromophores avec la formation d'une bande de CT faible permet d'améliorer la collecte du rayonnement solaire. Par conséquent, il était important de vérifier que l'énergie collectée pourrait facilement être transférée d'un chromophore à l'autre. En effet, on a observé 1BODIPY * → 1porphyrine zinc(II) et 1BODIPY * → 1CT (azophénine) avec une désactivation efficace de 1porphyrine zinc(II) ~~> 1CT (azophénine). Ce travail a été soumis à Chemistry: A European Journal. / Abstract: This thesis presents the design, synthesis and photophysical investigation of various azophenine derivatives as “one unit” structural models for emeraldine, a mixed-valence form of polyaniline. Azophenine is a star-shaped cross-conjugated molecule containing both quinone diimine and phenyl amine residues included in emeraldine but both, azophenine and emeraldine, are reported notoriously non-emissive. The challenge was to render azophenine emissive at room temperature prior any photophysical investigation. The long-term objective is to render polyaniline, in one form or the other, useful in bulk heterojunction solar cell in the active layer as it is not expensive. Because of solubility issues, the use of models becomes very appealing. The considered structural modifications include the anchoring of ethynyl-bridged functions at the para-position of the four phenyl groups of azophenine. These functions are the bulky truxene aromatic, the organometallic trans-bis(trialkylphosphine)platinum(II) pendent groups, and zinc(II)porphyrin and BODIPY dyes. All these functions exhibit fluorescence or phosphorescence, signal that can be used to monitor any electronic interaction between these pendent groups and the central core. Their photophysical properties were investigated in detail using steady-state and ultrafast time-resolved UV-vis absorption and emission spectroscopy. DFT and TDDFT were also employed for geometry optimizations (DFT) and nature and positions of the CT absorption (TDDFT). Chapter 2 introduces the synthesis and characterization of a truxene-based star-shaped azophenine derivative called TertTruQ. The coupling of bulky truxene residues with azophenine improved the photophysical activity of the lowest energy singlet excited state (i.e. CT state) of this derivative at 77 K. Speculations are that the rate for non-radiative deactivation, namely internal conversion, decreased upon slowing down the rotations around the N-C bonds due to the size of truxene. Moreover, this new substituted azophenine turned out to be fluorescent in the solid state at room temperature. Because of these interesting new observations, the emission properties of emeraldine base form were re-examined. A weak fluorescence at ~780 nm at 77 K, confirmed by the excitation spectrum, demonstrated the presence a CT near-IR fluorescence for TertTruQ. Thus, azophenine provides a useful model to identify what simple structural modification that can be performed to render emeraline emissive, if possible at room temperature. Again, when a non-luminescent species becomes emissive, this change is accompanied by an increase of its excited state lifetime. Longer excited state lifetimes are more prone to solar cell applications. This work has been published in Physical Chemistry Chemical Physics, 2017. Chapter 3 describes the synthesis and characterization of trans-bis(trialkylphosphine)diethynyl-platinum(II)-containing azophenines forming the di- and tetra-substituted derivatives DiTruPtQ and TertTruPtQ. Both complexes exhibit fluorescence and phosphorescence of the organometallic “arms” at 298 K in fluid solution. Moreover, the heavy atom effect of platinum gave the possibility of exploring the triplet state properties of azophenine. However, the sought phosphorescence from the triplet CT state was not seen most presumably due to the fast non-radiative processes. This work has been published in Organometallics, 2017, 36(3), 572-581. Chapter 4 presents the effect of the replacement of the labile H+ ions on the HN^N moiety by BF2+ fragments to form cycles thus providing a more rigid framework for azophenine. Indeed, the CT near-IR fluorescence was observed both at 298 and 77 K. However, despite the presence of Pt in the pendent groups, no phosphorescence was detected. DFT computations suggested that the low-lying triplet state was very low (0.975 (BQ) and 0.84 eV) inducing a higher probability of non-radiative processes thus efficiently depleting the triplet state. This work has been submitted to Inorganice Chemistry. Chapter 5 introduces the well-known BODIPY and zinc(II)porphyrin fluorescent dyes, which were linked to azophenine to form DiBodipyQ, TertBodipyQ and PorBodipyQ. The absorption spectrum of Bodipy lies in a range where porphyrin does not absorb very much. So, the combination of these two chromophores along with the formation of a low-lying CT band improves the light collection of the solar radiation. Consequently, it was important to verify that the collected energy could easily transferred from one chromophore to another. Indeed, the 1Bodipy* → 1zinc(II)porphyrin and 1Bodipy* → 1CT(azophenine) were observed along with an efficient deactivation from 1zinc(II)porphyrin ~~> 1CT(azophenine).

The work in this thesis was undertaken to explore both the effect of heteroatoms on the semiconducting properties of star-shaped thienoacenes, and to expand the scope of these materials to fields outside of organic semiconductors. Overall, new star-shaped molecules were prepared with a view towards applications such as thin film transistors, as the organic linker component in metal-organic frameworks, and as ligands that could coordinate to transition metals through the sulfur atom. The first chapter describes the properties of star-shaped molecules, the theory underlying their semiconducting behaviour, and the previous work that motivated the research contained herein. The second chapter of this thesis outlines the synthetic methodology that was utilized to achieve the molecular targets, as well as the characterization techniques that are used to reveal the properties of organic semiconductors. The third chapter of this thesis describes the synthesis and optoelectronic properties of novel nitrogen-containing semiconductor molecules called thienoacridines, and their comparison to carbon-and-sulfur based analogues, thienoanthracenes. The fourth and fifth chapters concern the synthesis of functionalized star shaped thienylbenzene molecules. In Chapter 4, these molecules are decorated with carboxylic acid groups so that they may act as tetrapodal MOF linkers. In Chapter 5, they are equipped with N-aryl(azomethine)thiophene moieties to explore sulfur coordination and act as ligands. The sixth chapter provides conclusion to this work, and possible future directions of the research conducted herein.

Fouling properties of materials such as polyethylene glycol (PEG) have been extensively studied over the past decades. Traditionally, the factors believed to result in protein adsorption resistance have included i) steric exclusion arising from the compression of longer chains and ii) grafting density contribution which may provide shielding from the underlying material. Recent studies have suggested that PEG interaction with water may also play a role in its ability to resist protein adsorption suggesting that steric exclusion may not be the only mechanism occurring during PEG/protein interactions. Star-shaped PEG polymers have been utilized in protein adsorption studies due to their high PEG segment concentration, which allows to increase the PEG chain grafting density compared to that achieved with linear PEG chains. Most studies that have investigated the interactions of tethered linear and star-shaped PEG layers with proteins have considered linear PEG molecules with molecular weights several orders of magnitude smaller than those considered for star-shaped PEG molecules (i.e. 10 000 g/mol vs. 200 000 g/mol, respectively). Additionally, the star-shaped PEG molecules which have been considered in the literature had up to ~70 arms and were therefore modeled by hard-sphere like structures and low chain densities near the surface due to steric hindrance. This resulted in some difficulties to achieve grafted PEG chain overlap for star molecules. Here, triethoxysilane end-functionalized linear PEG molecules have been synthesized and utilized to form star-shaped PEG derivatives based on ethoxy hydrolysis and condensation reactions. This resulted in PEG stars with up to ~4 arms, which were found to result in grafted star-shaped PEG chains with significant chain overlap. Linear PEG derivatives were synthesized so that their molecular weight would match the overall molecular weight of the star-shaped PEG molecules. These 2 PEG molecular architectures were covalently self-assembled to hydroxylated silicon wafers and the thickness, grafting density, and conformation of these films were studied. The adsorption of human albumin (serum protein) on linear and star-shaped PEG films was compared to that obtained on control samples, i.e. uncoated silicon wafers. Both film architectures were found to significantly lower albumin adsorption. / Ph. D.

O poli(ε-caprolactona) (PCL) é um polímero biocompatível e biodegradável, aprovado pelo Food and Drug Administration (FDA) para ser usado como biomaterial. Diversos estudos utilizando sua forma linear ou ramificada têm demonstrado resultados promissores para seu uso no desenvolvimento de dispositivos médicos e em aplicações na área farmacêutica. O objetivo deste trabalho foi utilizar o PCL com estrutura estrelada (PCLE) para obter microesferas biorreabsorvíveis. Primeiramente realizou-se a avaliação das propriedades físico-químicas do PCLE por meio da cromatografia de permeação em gel (GPC), ressonância magnética de prótons (1H-RMN) e carbono (13C-RMN), calorimetria exploratória diferencial (DSC) e espectrometria por infravermelho com transformada de Fourier (FT-IR). A avaliação toxicológica do PCLE foi obtida por meio do ensaio de citotoxicidade utilizando células CHO-K1 e o corante vital 5-(3-carboximethoxifenil)-2-(4,5-dimetiltiazolil)-3-(4-sulfofenil) tetrazolium e do acoplador de elétrons fenazine metilssulfato (MTS/PMS). O ensaio de biodegradação foi conduzido em pH 7,4 na presença de lipase a 37 ºC. Após essas análises o PCLE foi utilizado para preparação de esferas por meio de emulsão complexa A/O/A. O PCLE foi caracterizado como um polímero de baixa massa molar, com dispersão de tamanho unimodal e cerca de 68,8 % de suas moléculas apresentaram estrutura estrelada com três braços. Em relação às propriedades térmicas o PCLE apresentou temperatura de fusão de 57,3 ºC e temperatura de transição vítrea de -54,3 ºC. A avaliação da citotoxicidade mostrou que o extrato de PCLE é compatível com o metabolismo celular. As microesferas obtidas a partir do PCLE, por emulsão A/O/A apresentaram polidispersão de tamanho. / The poly(ε-caprolactone) (PCL) is a biocompatible and biodegradable polymer which has been approved by Food and Drug Administration (FDA). Many studies that are using its linear or branched form have showed promising results for medical devices and controlled drug delivery applications. The aim of this research was the use of star-shaped PCL (PCLE) to prepare bioreabsorbable microspheres. At first, the physical-chemical properties were characterized by Gel Permeation Chromatography (GPC), Protons Resonance Magnetic Nuclear (1H-RMN), Carbon Resonance Magnetic Nuclear (13C-RMN), Differential Scanning Calorimetry (DSC) and Fourier Transformed Infrared Spectroscopy (FT-IR). The toxicological property was investigated by colorimetric assay using CHO-K1 cells and the vital dye (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) (MTS) and the electron acceptor phenazine methosulfate (PMS). The biodegradation behavior was evaluated in the presence of lipase at 37 ºC and pH 7.4. The microspheres were prepared by complex emulsion W/O/W. The PCLE was characterized as low molecular weight polymer with monomodal distribution and about 68,8 % of the molecules were three-arm branched. The melting and glass transition temperatures were 57.3 ºC and -54.3 ºC, respectively. The cytotoxicity evaluation showed that PCLE extract was cell compatible. The obtained microspheres showed diameter polydispersity.

O poli(ε-caprolactona) (PCL) é um polímero biocompatível e biodegradável, aprovado pelo Food and Drug Administration (FDA) para ser usado como biomaterial. Diversos estudos utilizando sua forma linear ou ramificada têm demonstrado resultados promissores para seu uso no desenvolvimento de dispositivos médicos e em aplicações na área farmacêutica. O objetivo deste trabalho foi utilizar o PCL com estrutura estrelada (PCLE) para obter microesferas biorreabsorvíveis. Primeiramente realizou-se a avaliação das propriedades físico-químicas do PCLE por meio da cromatografia de permeação em gel (GPC), ressonância magnética de prótons (1H-RMN) e carbono (13C-RMN), calorimetria exploratória diferencial (DSC) e espectrometria por infravermelho com transformada de Fourier (FT-IR). A avaliação toxicológica do PCLE foi obtida por meio do ensaio de citotoxicidade utilizando células CHO-K1 e o corante vital 5-(3-carboximethoxifenil)-2-(4,5-dimetiltiazolil)-3-(4-sulfofenil) tetrazolium e do acoplador de elétrons fenazine metilssulfato (MTS/PMS). O ensaio de biodegradação foi conduzido em pH 7,4 na presença de lipase a 37 ºC. Após essas análises o PCLE foi utilizado para preparação de esferas por meio de emulsão complexa A/O/A. O PCLE foi caracterizado como um polímero de baixa massa molar, com dispersão de tamanho unimodal e cerca de 68,8 % de suas moléculas apresentaram estrutura estrelada com três braços. Em relação às propriedades térmicas o PCLE apresentou temperatura de fusão de 57,3 ºC e temperatura de transição vítrea de -54,3 ºC. A avaliação da citotoxicidade mostrou que o extrato de PCLE é compatível com o metabolismo celular. As microesferas obtidas a partir do PCLE, por emulsão A/O/A apresentaram polidispersão de tamanho. / The poly(ε-caprolactone) (PCL) is a biocompatible and biodegradable polymer which has been approved by Food and Drug Administration (FDA). Many studies that are using its linear or branched form have showed promising results for medical devices and controlled drug delivery applications. The aim of this research was the use of star-shaped PCL (PCLE) to prepare bioreabsorbable microspheres. At first, the physical-chemical properties were characterized by Gel Permeation Chromatography (GPC), Protons Resonance Magnetic Nuclear (1H-RMN), Carbon Resonance Magnetic Nuclear (13C-RMN), Differential Scanning Calorimetry (DSC) and Fourier Transformed Infrared Spectroscopy (FT-IR). The toxicological property was investigated by colorimetric assay using CHO-K1 cells and the vital dye (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) (MTS) and the electron acceptor phenazine methosulfate (PMS). The biodegradation behavior was evaluated in the presence of lipase at 37 ºC and pH 7.4. The microspheres were prepared by complex emulsion W/O/W. The PCLE was characterized as low molecular weight polymer with monomodal distribution and about 68,8 % of the molecules were three-arm branched. The melting and glass transition temperatures were 57.3 ºC and -54.3 ºC, respectively. The cytotoxicity evaluation showed that PCLE extract was cell compatible. The obtained microspheres showed diameter polydispersity.

The ring opening polymerization of D,L-lactide (DLLA) using multifunctional hydroxyl-terminated initiators and catalyst/coinitiator systems based on Sn(Oct)2 afforded the preparation of star-shaped, poly(D,L-lactide)s (PDLLA)s of controlled molar mass, narrow molar mass distributions, and well-defined chain end functionality. Various modifications of star-shaped PDLLA resulted in macromolecules with tailored functionalities for biomedical applications. Star-shaped PDLLAs were modified to contain photoreactive methacrylate end groups and subsequent photo-crosslinking was performed. Photo-crosslinked networks based on methacrylated star-shaped PDLLAs exhibited thermal properties and mechanical performance that were superior to current approved clinical adhesives. In addition, the thermal and mechanical properties of the networks were strongly dependent on the composition and molar mass of the star-shaped PDLLA precursors. Tensile strengths in the range of 8-21 MPa were obtained while the Young's modulus increased from 12 to 354 MPa and were higher for networks based on urethane containing polymers. Star-shaped PDLLAs bearing complementary adenine and thymine terminal units were also prepared. The hydrogen bonding associations between complementary PDLLA macromolecules depended strongly on molar mass and hence, the concentration of multiple hydrogen bonding units. 1H NMR spectroscopy confirmed the formation of hydrogen-bonded complexes with a 1:1 optimal stoichiometry and an association constant of 84 M-1. The hydrogen-bonded complexes also exhibited significantly higher solution viscosities than non-blended polymer solutions of similar molar mass and concentration. Thermoreversible associations of PDLLA-based complementary polymers were observed in the melt phase and the melt viscosity of a blended complex was consistently an order of magnitude higher than non-functionalized star-shaped PDLLA of similar molar mass. Furthermore, melt electrospinning of the hydrogen-bonded complexes successfully resulted in fibers of significantly larger diameter (9.8 ± 2.0 µm) compared to the individual precursors (PDLLA-A = 4.0 ± 0.6 µm and PDLLA-T = 4.4 ± 1.0 µm). These results suggested that thermoreversibility, as well as the strength of the hydrogen bonding interactions between the end groups of the tailored star-shaped PDLLA-based supramolecular polymers controlled the fiber diameter in the melt electrospinning process. Highly ordered microporous honeycomb structures were developed on photo-functional star-shaped PDLLA surfaces. The pore dimensions were dependent on polymer solution concentration, polymer molar mass and relative humidity. The combination of self-organizing and cross-linking techniques resulted in free-standing, PDLLA membranes with high chemical stability as well as higher mechanical strength for further material patterning. Amikacin, an antibiotic commonly used for treating infections was successfully encapsulated in star-shaped PDLLA fibers that were electrospun from solution. Preliminary results suggested that molecular architecture influenced the encapsulation of the antibiotic and subsequent drug release profile. / Ph. D.

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