Les groupements protecteurs photolabiles sont utilisés pour de nombreuses applications, notamment en neuroscience pour la libération de neurotransmetteurs avec un contrôle spatio-temporel très fin. La démocratisation des lasers pulsés infrarouges a permis la mise au point de nouveaux composés sensibles à l’excitation à deux photons, de plus en plus efficace. Cependant, l’ingénierie moléculaire des cages n’est pas la seule méthode qui peut être utilisée pour améliorer l’efficacité des de ces composés. Mon travail de thèse a ainsi abordé cette problématique sous l’angle de la nanostructuration de groupements protecteurs photolabiles sensibles à l’excitation à deux photons. Nous avons débuté cette étude avec des composés de petite taille (dimère et tétramère) basés sur des groupements photosensible type ortho-nitrophénéthyle. Nous avons ensuite fonctionnalisé des dendrimères de type polyamidoamine, cependant les propriétés photophysiques et photochimiques de ces nouveaux composés suggèrent que des interactions intramoléculaires perturbent l’efficacité de la réaction de photolibération. Des dendrimères partiellement fonctionnalisés ont ensuite été envisagés. / Photosensitive protecting groups have been used for many applications, including neuroscience for the release of neurotransmitters with an amazing spatio-temporal control. New compounds sensitive to two-photon excitation were developed with the spread out of pulsed infrared lasers. However, cages molecular engineering is not the only way to improve such compounds. This manuscript focuses on nanostructuration to improve the overall efficiency of two-photon sensitive protecting groups. We started our study with small compound as dimer and tetramer based on the ortho-nitrophenethyl architecture. Next, polyamidoamine dendrimers were tested, but photophysics and photochemistry properties of these new compounds suggest that intramolecular interactions disturb photochemical reaction. Synthesis of partially functionalized dendrimer was considering in a next step.

Des molécules ou assemblages moléculaires organiques (dérivés d’hémicyanine ou du BODIPY) ont été étudiés en solution par des méthodes optiques complémentaires : absorption stationnaire et fluorescence, absorption transitoire et fluorescence résolue en temps (échelle femtoseconde et picoseconde). Ces méthodes ont permis de caractériser différents processus tels que le transfert de charge intramoléculaire, le transfert d'énergie et le transfert d'électron photoinduit. Elles ont ainsi permis de démontrer l’intérêt de certains chromophores de type AzaBODIPY émettant dans le proche IR, dans des applications d’imagerie et de thérapie photodynamique. La photostabilité et l’absorption à deux photons ont également été étudiées dans le cas d’autres dérivés du BODIPY pouvant être appliqués à la détection d’espèces ioniques. Dans le cas des hémicyanines, des dérivés amphiphiles dotés d’une couronne reconnaissant spécifiquement certains cations ont également été étudiés sous forme de films de Langmuir-Blodgett et en présence de différents cations, le but étant de former des membranes artificielles iono- et photosensibles. / Ultrafast femtosecond transient absorption measurements (30 fs FWHM pulses) and complementary picosecond spectroscopies (20 ps FWHM pulses, streak camera detection), as well as steady state absorption and fluorescence measurements, were used to study a range of molecules and molecular assemblies. Processes such as intramolecular charge transfer, electronic energy transfer and photoinduced electron transfer were characterized. Amphiphilic azacrown-containing hemicyanine dyes and resulting iono- and photosensitive artificial membranes were studied using Langmuir-Blodgett techniques in the presence of various cations. Among a range of other molecules studied, NIR emitting aza-BODIPY dyes were studied by time-resolved methods in order to investigate their suitability for Photodynamic Therapy applications and imaging. Differently functionalized BODIPY dyes were investigated with respect to photostability, two photon absorption and ion sensing.

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The packaging does not serve as a mere containment but also can be designed to play a key role in preserving the product from quality-deteriorating factors, including oxygen, light irradiation, and foodborne pathogenic microorganisms (e.g., Escherichia coli). There has been a growing interest in employing ultra-porous metal-organic frameworks (MOF) with visible light-responsive antibacterial mechanisms to generate reactive oxygen species (ROS) that can eliminate bacteria via an oxidative burst. MOF is made of inorganic metal ions/nodes/clusters/secondary building units linked by organic bridge ligands, where titanium dioxide (TiO2) and tetrakis(4-carboxyphenyl)porphyrin) (TCPP) were selected for these components, respectively. TiO2 is an exceptional UV-A/B/C-blocker; meanwhile, TCPP dye performs a remarkable photocatalytic ability even under visible light, on top of its macro-heterocyclic structure that is ideal as a MOF linker. Both have good compatibility but suffer from the notorious tendency to self-quench/aggregate. The incorporation of MOF-based conjugates into a polymeric matrix, like cellulose, is among the proven-successful solutions. Cellulose is the Earth's most abundant and naturally biodegradable, and cellulose nanofibril (CNF) was particularly chosen for its high specific surface area and surface activity. However, a straightforward, cheap, and environmentally friendly approach of multicycle homogenization (0-25 passes) was conducted to solve neat cellulose's challenge of natural hydrophilicity, where low pressure (<10 MPa) was applied to prevent the common over-shearing effect. The antibacterial efficacy of CNF films functionalized with TiO2-TCPP conjugate on inhibiting E. coli growth was analyzed with and without light of different intensities (3000 and 6000 lux). The positive impacts of CNFs' promoted fibrillation and subsequent inter/intra-molecular hydrogen bonding post-homogenization were evidenced in an array of functional properties, i.e., crystallinity, TiO2-TCPP conjugate dispersion, surface smoothness, mechanical properties, thermal stability, hydrophobicity, oxygen barrier (comparable to ethylene-vinyl alcohol (EVOH), a commercial high-barrier polymer), and 100%-antibacterial rate (under 6000 lux after 72 hours). Varying optimum cycles of homogenization demonstrated the prospect of the proposed homogenization approach in preparing CNF with diverse processability and applicability. These findings also exhibited a promising potential for a myriad of high-barrier, UV-blocking, and/or visible light-responsive antibacterial film applications, including food packaging and biomedical. / Doctor of Philosophy / Packaging is useful not only as a container but can also be designed to help prevent products from being spoiled due to various reasons such as oxidation, light, and bacterial contamination. Researchers have discovered the promising antibacterial feature of the metal-organic framework (MOF). Packaging made with MOF technology can harness light and oxygen in the environment to produce a special form of oxygen called reactive oxygen species (ROS) that can kill unwanted bacteria. MOF is an extremely porous sponge-like material made of two ingredients: an inorganic metal cluster and an organic linker; in this study, titanium dioxide (TiO2) and a porphyrin called TCPP were selected, respectively. TiO2 is an excellent ultraviolet blocker, while TCPP has a unique, ring-like geometry that is ideal for use as a linker and an antimicrobial feature that works well under the visible light spectrum. The pair are compatible but still suffer from MOF's notorious challenge, where it tends to clump together because of its tiny size. To resolve this problem, TiO2-TCPP MOF can be deposited evenly in a cast made of polymer. Cellulose has been proven to work effectively as a polymeric cast; moreover, it is natural, biodegradable, and in abundant supply. A type of nanosized cellulose—cellulose nanofibril (CNF)—was specifically chosen because its high surface area and activity are useful when blended with other materials. However, cellulose is naturally a poor water-repellant that is not ideal for packaging applications. As a solution, cellulose can be treated with a homogenization technique by passing the material through a very narrow hole under high pressure. Homogenization can be problematic as it possibly damages the cellulose's structure, and its high pressure can also be expensive and energy consuming. Therefore, low pressure with multiple cycles was applied in this work. CNF-TiO2-TCPP films were tested for their ability to slow down E. coli bacteria growth with and without light of varying brightness to compare its light-sensitive antimicrobial feature. Homogenization was found helpful in producing higher-quality CNF, which improved several of the film's final characteristics, including an even material dispersion, structural order, smoothness, strength, heat resistance, and water repellency. Most importantly, it produced films with oxygen barrier ability comparable to commercial high-barrier plastics and completely eliminated bacteria after 72 hours. The optimum number of homogenization cycles was found to be dependent on the desired characteristics and application. Overall, these findings carry a promising potential for a variety of applications, including food packaging and the biomedical field.

Ce doctorat portait sur le développement de nanoparticules (NPs) photosensibles constituées d’un cœur photolysablepoly(acrylate d'o-nitrobenzyle) (polymère hydrophobe biocompatible - PANB) et d’une couronne basée sur un dérivé du dextrane (polysaccharide bactérien, hydrophile et biodégradable). Dans un premier temps, le PANB-N3 a été synthétisé par i) polymérisation radicalaire contrôlée (SET-LRP) de l’acrylate d’o-nitrobenzyle puis ii) modification chimique de l’extrémité de chaîne par une fonction azoture. En parallèle, le dextrane a été hydrophobisé par quelques chaînes grasses dotées d’un groupe alcyne (obtention du DexAlcyne-15). Ces polymères précurseurs peuvent alors réagir par chimie click CuAAC (Cycloaddition azide-alcyne catalysée par Cu(I)) pour engendrer divers glycopolymères greffés Dex-g-PANB. Dans un deuxième temps, les NPs ont été formulées par deux procédés puis caractérisées en termes de taille, recouvrement en dextrane (quantité par gramme de PANB, épaisseur de la couche surfacique) et stabilité colloïdale en milieu salin, en présence de tensioactif compétitif ou dans un milieu de culture (DMEM). Le procédé de nanoprécipitation a été appliqué aux Dex-g-PANB présentant de fortes fractions massiques en PANB (>40%) alors que le procédé d’émulsion-évaporation de solvant organique a été mis en œuvre en utilisant le DexAlcyne-15 comme tensioactif hydrosoluble et le PANB-N3 comme matériau hydrophobe. Grâce à leurs fonctionnalités complémentaires, une réaction CuAAC peut (ou non) avoir lieu à l’interface liquide/liquide pendant l’élaboration des NPs et conduire à l’obtention de NPs « non clickées » ou « clickées ». Enfin, le caractère photosensible des NPs a été validé par irradiation UV en observant une disparition progressive des NPs résultant de la photolyse des PANB. Afin d’utiliser ces NPs comme systèmes stimulables de délivrance de médicaments, un anticancéreux (Doxorubicine - Dox) a été encapsulé au sein des NPs, pendant leur élaboration. Cette encapsulation a été optimisée et les NPs chargées de DOX ont été caractérisées en termes de taille et d’efficacité d’encapsulation. La libération de la DOX hors des NPs a ensuite été suivie par simple diffusion, ou provoquéepar irradiation UV. Enfin, le potentiel biologique de ces NPs a été évalué vis-à-vis d’une lignée cellulaire tumorale humaine d'origine intestinale isolée d'un adénocarcinome colique (Caco-2). Après vérification de leur biocompatibilité et de la résistance des Caco-2 aux irradiations UV, nous avons pu montrer que les NPs chargées pouvaient libérer suffisamment de DOX en seulement 30 secondes d’irradiation (puissane: 54mW/cm2) pour éradiquer plus de 50% de ces cellules cancéreuses. / This work was focused on the development of light-sensitive nanoparticles (NPs) based on a photodegradable poly(o-nitrobenzyl acrylate) core(PNBA, hydrophobic and biocompatible polymer) and a dextran derivative shell (dextran is a biodegradable and hydrophilic bacterial polysaccharide). Firstly, PNBA-N3 was synthesized by i) Single-Electron Transfer Living Radical Polymerization (SET-LRP) of o-nitrobenzyl acrylate then ii) introduction of one azide end-function. In the same time, DexAlkyne-15 carrying several alkyne groups was produced by hydrophobization of dextran. Such DexAlkyne-15 and PNBA-N3 can react by CuAAC (Cu(I)-catalyzed azide-alkyne cycloaddition) click chemistry leading to Dex-g-PNBA glycopolymers with various macromolecular parameters. Secondly, NPs were produced by comparing two processes then characterized in terms of size, dextran amount, shell thickness and colloidal stability in NaCl or cell culture media, or in presence of one strong surfactant. On one hand, NPs were made by nanoprecipitation of Dex-g-PNBA exhibiting high PNBA weight fractions (>40 %). On the other hand, NPs were produced by emulsion-evaporation of the organic solvent using DexAlkyne-15 as water-soluble surfactant and PNBA-N3 as hydrophobic materials. In this case, in situ CuAAC occurred (or not) at the liquid/liquid interface during the NPs formulation, leading to “clicked” and “not-clicked” NPs. Finally, NPs disruption was studied by UV irradiation according the PNBA chains photolysis. To use such NPs as smart drug delivery systems, Doxorubicin (DOX - an anticancer agent), was loaded inside the NPs during their elaboration. The experimental conditions were optimized to enhance the DOX encapsulation. The kinetics release of encapsulated DOX were studied by diffusion or under UV irradiation. Finally, the biological potential of these NPs was estimated towards Caco-2 (continuous line of heterogeneous human epithelial colorectal adenocarcinoma cells). After checking the NPs biocompatibility and theCaco-2 strength under UV irradiation, we proved that such loaded NPs can release enough DOX under 30 second irradiation (power: 54mW/cm2) to decrease the Caco-2 viability about more than 50%.

A challenging application space exists for high-aspect-ratio, high-fidelity dielectrics in micro-electro-mechanical system (MEMS), microelectronic, and photonic applications. Photosensitive polymers are widely used in these fields because they are relatively easy to process and pattern, and have good mechanical properties. Photosensitive polynorbornene (PNB)-based dielectrics have been shown to have high sensitivity, excellent photodefinition properties, and high mechanical strength making them suitable for MEMS, microelectronic packaging, and photonic applications. PNB-based dielectrics can be functionalized with epoxide, carboxylic acid, or fluorinated alcohol groups. Epoxy or carboxylic acid groups can be used to provide cross-linkable sites, resulting in improved chemical and thermal properties while fluorinated alcohol groups can provide solubility in aqueous base. The focus of this study has been on the epoxy-based cross-linking of ultraviolet and electron beam (e-beam) sensitive negative-tone PNB-based dielectrics. The impact of multifunctional epoxy-based additives on the cross-linking, photolithographic properties, and adhesion properties of the photosensitive PNB dielectric was investigated. High aspect ratio features of 13:1 (height:width) were produced in 40 µm thick films (a single coat) with straight side-wall profiles and high fidelity. Contrast values as high as 33.4 were obtained at doses below 15 mJ/cm2. To evaluate the polymer's suitability to MEMS and microelectronics applications, epoxy cross-linking reactions were studied as a function of processing condition through Fourier transform infrared spectroscopy (FTIR), nanoindentation, swelling and dielectric measurements. The fully cross-linked films had an elastic modulus of 2.9 GPa and hardness of 0.18 GPa which can improve the mechanical compliance of the packaging device. To explore the feasibility of the PNB dielectric as a highly sensitive e-beam resist for nano scale fabrication, the e-beam initiated reaction between PNB cross-linking sites and the multifunctional epoxy cross-linkers was investigated. In this study, the interaction of an e-beam with the PNB mixture and its compounds was investigated. The contrast, photodefinability, and e-beam activation of the components in the PNB formulations were studied. The PNB polymer had very high e-beam sensitivity and contrast. It was shown that the addition of a photoacid generator (PAG) to the polymer-epoxy mixture enhanced the contrast and sensitivity. Formulations with the additional cross-linker showed improved contrast, sensitivity, and substrate adhesion. 100 nm structures with 13.5 nm line edge roughness (LER) were fabricated. The influence of the developing time, the developer concentration, PEB, and film thickness on the contrast and sensitivity were studied. Structures with contrast values as high as approximately 8 were fabricated at doses as low as 0.38 µC/cm2. The acid-catalyzed epoxy ring opening reaction of the PNB dielectric was studied using FTIR spectroscopy. The photo and thermal acid generation initiated epoxy ring opening reactions and subsequent cross-linking of polymer. Additionally, polymer properties were characterized as a function of processing conditions for this polymer system. It was shown that thermal cure conditions have a substantial impact on the mechanical and electrical properties of the polymer. The rate and ultimate conversion of the epoxy ring opening reaction increased with increasing cure temperature, resulting in a higher degree of cross-linking at cure temperatures above 140°C. Degradation reactions occurred at temperatures above 160°C, indicating loss of epoxide cross-linking groups and linkages. These hypotheses were supported by electrical and mechanical property studies. It was shown that curing the PNB polymer at 160°C for 1 h after develop resulted in full epoxy ring opening and highest cross-link density. This sample showed lower dielectric constant (3.9), residual stress (20 MPa), and solvent swelling (3.1%). Variable frequency microwave (VFM) processing of the PNB dielectric was studied to investigate the rapid curing of the polymer at lower temperatures. The FTIR results showed that the microwave reaction rates were higher at each isothermal cure temperature compared to convective heating, indicating that the rapid VFM curing of PNB at low temperatures is feasible. The PNB film was fully cross-linked after 15 min VFM cure at the low temperature of 150˚C. The shortest time to fully cure the polymer was found to be 5 min at 160°C. Also, the feasibility of rapid VFM curing of PNB in air was studied. All samples VFM-cured (140˚C-180˚C) in air showed no signs of oxidation. The electrical and mechanical properties of VFM-cured films were characterized and compared with thermally cured films to determine the effectiveness of the VFM processing. VFM-cured samples showed higher degree of cross-linking than thermally-cured samples, which was congruent with the FTIR results. Improved or equivalent properties were obtained for VFM-cured samples at shorter cure cycles and lower cure temperatures compared to thermally-cured films. The PNB dielectric was also used as an overcoat material to make micro and nano fluidic channels. In this work, incorporation of advanced micro/nano fluidics with high-sensitivity photonic sensors was demonstrated. 500 nm to 50 µm channels were fabricated by thermal decomposition of epoxy-based PNB polymers. Microdisks with quality factors of over 106 were presented in complementary metal-xide-semiconductor (CMOS) compatible SiN on oxide technology. These ultra-high quality factor SiN resonators were demonstrated in the visible range for the first time. The fluidic structures were interfaced with photonics for index and florescence sensing. This study was a collaboration with Dr. Ehsan Shahhosseini from the Photonics Group at Georgia Tech.

This research explores the capacity for functional photoreception in larvae of the mountain pine beetle (Dendroctonus ponderosae), an extremely important forest pest insect that is well adapted for development beneath the bark of pine trees. Phototaxis tests, gene expression analysis and development experiments were integrated to assess mountain pine beetle larvae for light sensitivity. When presented with a phototaxis choice test, larvae preferred dark over light microhabitats, revealing that larvae sense and respond behaviourally to light. Long wavelength opsin transcription was identified in all life stages, including eggs and larvae, suggesting that D. ponderosae possesses extraretinal photosensitive capabilities across its life cycle. The long wavelength opsin could function in phototaxis or the development phenology of immature beetles, while the ultraviolet opsin, only found to be expressed in pupae and adults, is likely to function in dispersal via the compound eyes. Results from two development experiments reveal an effect of photoperiod treatment on beetle development rate when reared from the egg stage, but not when reared from mature larvae, indicating that a critical photosensitive life stage(s) must occur in D. ponderosae prior to the third larval instar. An effect of photoperiod on adult emergence rates, however, appears to be independent of larval rearing conditions. The discovery of opsin expression and negative phototaxis in eyeless mountain pine beetle larvae, in addition to an effect of photoperiod on immature development and adult emergence rates, suggest that light and photoperiodism likely function in survival and life cycle coordination in this species. / Graduate / 2018-10-17

We proposed and demonstrated the first account of large-area, semi-transparent, tandem photosensitive nanocrystal skins (PNSs) constructed on flexible substrates operating on the principle of photogenerated potential buildup, which avoid the need for applying an external bias and circumvent the currentmatching limitation between junctions. We successfully fabricated and operated the tandem PNSs composed of single monolayers of colloidal water-soluble CdTe and CdHgTe nanocrystals (NCs) in adjacent junctions on a Kapton polymer tape. Owing to the usage of a single NC layer in each junction, noise generation was significantly reduced while keeping the resulting PNS films considerably transparent. In each junction, photogenerated excitons are dissociated at the interface of the semi-transparent Al electrode and the NC layer, with holes migrating to the contact electrode and electrons trapped in the NCs. As a result, the tandem PNSs lead to an open-circuit photovoltage buildup equal to the sum of those of the two single junctions, exhibiting a total voltage buildup of 128.4 mV at an excitation intensity of 75.8 μW cm⁻² at 350 nm. Furthermore, we showed that these flexible PNSs could be bent over 3.5 mm radius of curvature and cut out in arbitrary shapes without damaging the operation of individual parts and without introducing any significant loss in the total sensitivity. These findings indicate that the NC skins are promising as building blocks to make low-cost, flexible, large-area UV/visible sensing platforms with highly efficient full-spectrum conversion.