Palladium-catalyzed reactions for carbon-carbon bond formation have had a significant impact on the field of organic chemistry in recent decades. Illustrative is the 2010 Nobel Prize, awarded for “palladium-catalyzed cross couplings in organic synthesis”, and the numerous applications of these transformations in industrial settings. This thesis describes recent developments in C(sp2)-C(sp3) bond formation, focusing on alkane arylation reactions and arylative dearomatization transformations. In the first part, our contributions to the development of intramolecular C(sp3)-H arylation reactions from aryl chlorides are described (Chapter 2). The use of catalytic quantities of pivalic acid was found to be crucial to observe the desired reactivity. The reactions are highly chemoselective for arylation at primary aliphatic C-H bonds. Theoretical calculations revealed that C-H bond cleavage is facilitated by the formation of an agostic interaction between the palladium centre and a geminal C-H bond. In the following section, the development of an alkane arylation reaction adjacent to amides and sulfonamides is presented (Chapter 3). The mechanism of C(sp3)-H bond cleavage in alkane arylation reactions is also addressed through an in-depth experimental and theoretical mechanistic study. The isolation and characterization of an intermediate in the catalytic cycle, the evaluation of the roles of both carbonate and pivalate bases in reaction mechanism as well as kinetic studies are reported. Our serendipitous discovery of an arylation reaction at cyclopropane methylene C-H bonds is discussed in Chapter 4. Reaction conditions for the conversion of cyclopropylanilines to quinolines/tetrahydroquinolines via one-pot palladium(0)-catalyzed C(sp3)-H arylation with subsequent oxidation/reduction are described. Initial studies are also presented, which suggest that this transformation is mechanistically unique from other Pd catalyzed cyclopropane ring-opening reactions. Preliminary investigations towards the development of an asymmetric alkane arylation reaction are highlighted in Chapter 5. Both chiral carboxylic acid additives and phosphine ligands have been examined in this context. While high yields and enantiomeric excesses were never observed, encouraging results have been obtained and are supported by recent reports from other research groups. Finally, in part two, the use of Pd(0)-catalysis for the intramolecular arylative dearomatization of phenols is presented (Chapter 7). These reactions generate spirocyclohexadienones bearing all-carbon quaternary centres in good to excellent yields. The nature of the base, although not well understood, appears to be crucial for this transformation. Preliminary results in the development of an enantioselective variant of this transformation demonstrate the influence of catalyst activation on levels of enantiomeric excess.

Piers-Rubinsztajn (P-R) conditions, involving catalysis by tris(pentafluorophenyl)borane, were applied to siliconize triarylamines. A phenylated linear methylhydrosiloxane copolymer was utilized to create a hydrolytically-stable composite with promising optical, electrochemical and thermal properties. However, the reaction was highly exothermic, had rapid uncontrollable kinetics and produced methane as a byproduct; problematic characteristics for larger scale syntheses. Thereafter, triarylamines with bulkier substituents were studied to determine whether the kinetics could be slowed and a less volatile byproduct created. The rate of conversion was retarded significantly as expected, but not all derivatives reacted quantitatively in ambient conditions. Finally, P-R conditions were applied to methylhydrosiloxane-dimethylsiloxane copolymers. Gelation in air upon extended reaction time was effectively avoided by “finishing” excess Si-H sites using anisole. The result was the preparation of composites with up to 61 wt % arylamine content, which are expected to have significant applications as cost-effective flexible hole transport layers in organic electronic devices.

Piers-Rubinsztajn (P-R) conditions, involving catalysis by tris(pentafluorophenyl)borane, were applied to siliconize triarylamines. A phenylated linear methylhydrosiloxane copolymer was utilized to create a hydrolytically-stable composite with promising optical, electrochemical and thermal properties. However, the reaction was highly exothermic, had rapid uncontrollable kinetics and produced methane as a byproduct; problematic characteristics for larger scale syntheses. Thereafter, triarylamines with bulkier substituents were studied to determine whether the kinetics could be slowed and a less volatile byproduct created. The rate of conversion was retarded significantly as expected, but not all derivatives reacted quantitatively in ambient conditions. Finally, P-R conditions were applied to methylhydrosiloxane-dimethylsiloxane copolymers. Gelation in air upon extended reaction time was effectively avoided by “finishing” excess Si-H sites using anisole. The result was the preparation of composites with up to 61 wt % arylamine content, which are expected to have significant applications as cost-effective flexible hole transport layers in organic electronic devices.

Part 1: Transition-metal-catalyzed direct transformations of aromatic C-H bonds are emerging as valuable tools in organic synthesis. These reactions are attractive because of they allow for inherently efficient construction of organic building blocks by minimizing the pre-activation of substrates. Of these processes, direct arylation has recently received much attention due to the importance of the biaryl core in medicinal and materials chemistry. Also, alkyne hydroarylation has garnered interest because it allows for the atom-economical synthesis of functionalized alkenes directly from simple arenes and alkynes. Described in this thesis are number of advancements in these areas. First, palladium catalyzed direct arylation of azine N-oxides using synthetically important aryl triflates is described. Interesting reactivity of aryl triflates compared to aryl bromides was uncovered and exploited in the synthesis of a compound that exhibits antimalarial and antimicrobial activity. Also reported is the efficient, direct arylation enabled (formal) synthesis of six thiophene based organic electronic materials in high yields using simple starting materials. Additionally, the site-selective direct arylation of both sp2 and sp3 sites on azine N-oxide substrates is described. The arylation reactions are carried out in either a divergent manner or a sequential manner and is applied to the synthesis of the natural products, Papaverine and Crykonisine. Mechanistic investigations point towards the intimate involvement of the base in the mechanism of these reactions. Next, the rhodium(III)-catalyzed hydroarylation of internal alkynes is described. Good yields are obtained for a variety of alkynes and arenes with excellent regioselectivity for unsymmetrically substituted alkynes. Mechanistic investigations suggest that this reaction proceeds through arene metalation with the cationic rhodium catalyst, which enables challenging intermolecular reactivity. Part 2: Access to single enantiomer compounds is a fundamental goal in organic chemistry and despite remarkable advances in enantioselective synthesis, their preparation remains a challenge. Kinetic resolution of racemic products is an important method to access enantioenriched compounds, especially when alternative methods are scarce. Described in this thesis is the resolution of tertiary and secondary alcohols, which arise from ketone and aldehyde aldol additions. The method is technically simple, easily scalable, and provides tertiary and secondary alcohols in high enantiomeric ratios. A rationale for the unique reactivity/selectivity associated with (1S,2R)-N-methylephedrine in the resolution is proposed. Organocatalysis is a rapidly developing, powerful field for the construction of enantioenriched organic molecules. Described here is a complimentary class of organocatalysis using simple aldehydes as temporary tethers to perform challenging formally intermolecular reactions at room temperature. This strategy allows for the enantioselective, intermolecular cope-type hydroamination of allylic amines with hydroxyl amines. Also, interesting catalytic reactivity for dichloromethane is revealed.

This research project originated from interest in assessing the potential of enzyme technology (particularly laccase-based systems) for the biomodification of sisal specialty fibres by using environmentally friendly processes. This doctoral work focused on two different research lines, namely: biobleaching and enzymatic functionalization of sisal pulp fibres. The study was started by assessing the use of natural, potentially cost-effective phenolic compounds as substitutes for expensive, potentially toxic laccase mediators. The tendency of natural phenols to either promote delignification or couple onto pulp was examined with a view to assessing their potential for either bleaching or functionalizing sisal fibres. In the biobleaching study, totally chlorine free (TCF) sequences were implemented in order to compare the efficiency of a selected natural mediator and a well-known synthetic mediator, both in the presence and absence of a xylanase pre-treatment. The effluents resulting from each stage in the sequence were analysed with a view to assessing the environmental impact of the laccase treatments ¿a scarcely explored aspect of biobleaching sequences. The xylanase stage proved highly efficient in reducing the HexA content of sisal fibres and in boosting the bleaching effect of the laccase treatments. The proposed TCF sequences provided high-cellulose sisal pulp with brightness above 80% ISO and a reduced HexA content; also, they exhibited improved performance and a reduced impact on effluent properties relative to the use of the synthetic mediator. Two different approaches to fibre functionalization were explored, namely: lignin modification (biografting) and cellulose modification (laccase¿TEMPO oxidation). Biografting of phenolic compounds was for the first time studied in sisal pulp. Covalent binding of the originally assayed phenolic compounds to sisal fibres during the laccase treatment was exposed by a novel analytical approach based on pyrolysis-GC/MS. The phenolic compound showing the highest tendency to couple to fibres was selected to investigate biografting under different reaction conditions and to evaluate the extent of phenol coupling via various pulp properties. Biografting efficiency was enhanced by refining the fibres prior to the enzyme treatment, which provided improved strength-related properties in the resulting paper. The use of the laccase-TEMPO system to oxidatively modify cellulose and improve strength-related properties in sisal pulp was for the first time evaluated as an environmentally friendly alternative to existing halide-based systems. The first part of this study revealed that the laccase¿TEMPO system considerably improved wet strength in sisal pulp by effect of the formation of a substantial amount of aldehyde groups in cellulose chains that facilitated inter-fibre bonding through hemiacetal linkages. The influence of process variables on various properties of the oxidized fibres and resulting paper was assessed by using a three-variable statistical plan. The conditions maximizing functionalization and the improvement in paper strength properties were used to design treatments of increased efficiency that exposed the potential of laccase¿TEMPO oxidation for biorefining pulp fibres. Analytical methods including pyrolysis-GC/MS, polyelectrolyte titration, conductimetric titration, carbohydrate determination by HPLC, fibre morphology analysis by SEM and thermogravimetry were used to both characterize the raw material and gain a better understanding of the reaction mechanisms behind the different laccase-based treatments. Some of the analyses were performed by collaborating research groups at IRNAS (Seville, Spain) and the Department of Chemical Engineering of the University of Huelva (Spain). Also, part of this doctoral work was conducted at the Institute of Paper Science and Technology of the Georgia Institute of Technology (Atlanta, USA).

ZnO is one of the most important materials for electronics, optoelectronics, piezoelectricity and optics. With a wide band gap of 3.37eV and an exiton binding energy of 60meV, ZnO 1D nanostructures exhibit promising properties in a lot of optical device applications. It is also an important piezoelectric material and has applications in a new category of nanodevices, nano-piezotronics. Demonstrated prototype of devices includes nanogenerators, piezoelectric-FET, and a series of evolutive devices based on the concept of nanogenerator. This is based on working principle of a semiconductor and piezoelectric coupled property. This thesis is about the growth, characterization and device fabrication of ZnO nanowires and nanobelts for sensors and UV detectors. First, the fundamental synthesis of ZnO nanostructurs is investigated, particularly polar surface dominated nanostructues, to illustrate the unique growth configurations of ZnO. Detail study in this part includes nanobelts, nanorings, nanocombs, nanonetworks, and nanodiskettes synthesis. Important factors in driving the nanostructure synthesis mechanism are analyzed, such as the chemical activities of different surface of ZnO and the polar surface dominated effects. Then, the devices fabricated methods using individual nanowires/nanobelts and their electrical transport properties were carefully characterized. In this part, dominant factors which are critical for nanobelt device performance are investigated, such as the contact properties, interface effects, and durability testing. Also, a metal doping method is studied to explore the controlling and modification of nanowire electric and optical properties. Further more, I will present the surface functionalization of nanobelt for largely improving its electrical, optoelectronic and chemical performance. Surface functionalization of nanobelts is proven to be an effective method in enhancing the semiconductor and metal contact. Piezoelectric field-effect transistors will be demonstrated as a powerful approach as chemical sensors. Finally, a technique is illustrated for functionalizing the surfaces of ZnO nanobelts for enhancing its UV sensitivity by over five orders of magnitude. This demonstrates an effective approach for fabricatiing ultrasensitive UV detectors. The research results presented in this thesis have made great contribution to the growth, device fabrication and novel applications of ZnO nanostructures for photonics, optoelectronics and sensors.

This thesis describes the synthesis of a low modulus, thermally conductive thermal interface materials (TIM) using metal decorated nanotubes as fillers. TIMs are very important in electronics because they act as a thermally-conductive medium for thermal transfer between the interface of a heat sink and an electronic package. The performance of an electronic package decreases with increasing operating temperature, hence, there exists a need to create a TIM which has high thermal conduction to reduce the operating temperature. The TIM in this study is made from metal decorated multi-walled carbon nanotubes (MWCNT) and Vinnapas®BP 600 polymer. The sample was functionalized using mild oxidative treatment with nitric acid (HNO3) or, with N-Methly-2-Pyrrolidone (NMP). The metals used for this experiment were copper (Cu), tin (Sn), and nickel (Ni). The metal nanoparticles were seeded using functionalized MWCNTs as templates. Once seeded, the nanotubes and polymer composites were made with or without sodium dodecylbenzene sulfonate (SDBS), as a surfactant. Thermal conductivity (k) measurement was carried out using ASTM D-5470 method at room temperature. This setup best models the working conditions of a TIM. The TIM samples made for this study showed promise in their ability to have significant increase in thermal conduction while retaining the polymer’s mechanical properties. The highest k value that was obtained was 0.72 W/m-K for a well dispersed aligned 5 wt percent Ni@MWCNT sample. The Cu samples underperformed both Ni and Sn samples for the same synthesis conditions. This is because Cu nanoparticles were significantly larger than those of Ni and Sn. They were large enough to cause alloy scattering and too large to attach to the nanotubes. Addition of thermally-conductive fillers, such as exfoliated graphite, did not yield better k results as it sunk to the bottom during drying. The use of SDBS greatly increased the k values of the sample by reducing agglomeration. Increasing the amount of metal@MWCNT wt percent in the sample had negative or no effect to the k values. Shear testing on the sample shows it adheres well to the surface when pressure is applied, yet it can be removed with ease.

There are several studies in order to control drug delivery, decrease the toxicity of drugs and also for novel biomedical applications. It is necessary to be able to control the release of the drug within the body by using drug delivery systems. Mesoporous silica compounds have only been discovered twenty years ago and they have already attracted many researchers to study these materials for several applications. SBA-15 particles have a highly ordered regular structure and are a good matrix for guest-host applications. The aim of this study is to be able to address whether the surface functionalization of SBA-15 samples would improve the loading of a drug into these particles. The synthesized SBA-15 particles were surface functionalized by post - grafting synthesis method in order to be used as carrier materials for drug delivery. Amoxicillin was used as a model drug. These mesoporous materials have been characterized using X-ray diffraction (XRD), small-angle X-ray spectroscopy (SAXS), fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), N2 adsorption/ desorption, solid-state silicon nuclear magnetic resonance (Si-NMR), high-performance liquid chromatography (HPLC), ultra-violet (UV) spectroscopy, elemental and thermo gravimetric analysis (TGA). The effect of concentration difference and the type of alkoxysilanes used for the functionalization have been discussed in terms of loading amoxicillin and controlling the delivery. Drug delivery systems have many further applications that still need to be investigated in areas such as neurosciences, cancer and biomedical engineering.

In the present study the effects of addition of organically functionalized boehmite nano-particles on the mechanical properties of epoxy polymers were analyzed. Nanosize platelets of boehmite powders were produced via a hydrothermal process from the raw material aluminum trihydroxide Al(OH)3 provided by a a chemical supplier, but which in future studies can be replaced by local resources of aluminum trihydroxide available in Seydisehir, Turkey. The ground aluminum trihydroxide particles were submitted to a two-step preliminary ageing procedure in different pH media. Particles were then converted to boehmite nanoparticles via hydrothermal ageing at high pressure and temperature. The product&lsquo / s chemical identity, size, structure and morphology were characterized with XRD, FT-IR, SEM and PSA analyses. By controlling the pH and the ageing time as parameters, hexagonal shaped nanoplatelets were obtained with dimensions ranging from 100 to 500 nm. Aiming at using these nanoparticles into surface coating polymers, the most favorable shape is the plate-like morphology, leading to adopting the last hydrothermal condition in the rest of the study. v The boehmite crystal surfaces are furnished with hydroxyls which can potentially be reacted with epoxy monomers of bisphenol A diglycidyl ether with the help of tin (II) chloride as catalyst through ring-opening reactions. The FT-IR and quantitative analyses indicated that this surface functionalization is possible under a temperature 80 oC and a weight ratio of 5:1 epoxy monomer to boehmite powder These novel inorganic/organic hybrid materials were then mixed with epoxy/hardener resin mixture to obtain nanocomposites. The properties of the composites were characterized accordingly with tensile, impact, micro hardness, micro-scratch tests, DMA analysis and observed with SEM analysis. A deterioration of the tensile strength from the neat polymer was observed, with a distinct trend between the functionalized and non-functionalized boehmite-epoxy polymers. The functionalized polymers showed a less deteriorative character. The tensile modulus instead showed a little improvement of (4%) in 5wt% loaded polymers. DMA analysis results revealed an improved glass transition temperature in the nanocomposites as well as in storage and loss modulus. As aimed in this work, the functionalized boehmite-epoxy polymers displayed a clear improvement in comparison to both non-functionalized and neat polymers in surface coating properties in hardness and scratch resistance.

From medicine to aerospace, innovation in multiple fields will not occur without addressing current questions that still exist in polymer behavior and manipulation. This dissertation represents the research carried out over the course of three separate experiments using rheometry as the key technique to explore the behavior of polymer composites. In all three studies, polymer composites were investigated for changes to their known physical properties caused through the addition of a filler or functionalization. Chapter Two examines the possibility of enhancing poly(4-methyl-1-pentene) through the use of soluble carbon nanotubes. In this series of experiments, carbon nanotubes were covalently functionalized using reductive alkylation with a dodecyl group to render them easily soluble in the same organic solvents as low molecular weight poly(4-methyl-1-pentene). The polymer and the functionalized nanotubes were dissolved together in carbon tetrachloride then the solvent is removed leaving the functionalized nanotubes uniformly dispersed in the polymer matrix. The composites were then compression molded and the changes to the physical properties were explored. The functionalized nanotube filler generally acted to plasticize the samples producing transparent but colored polymers. The samples had a lower modulus and glass transition which was the opposite found by Clayton et al. using sonicated pristine carbon nanotubes. Polyurethanes have a growing significance in the biomedical field, and we explore the possibility fine tuning the properties of a polyurethane for such uses in Chapter Three. Here, self healing Polycarbonate polyurethanes (PCU) were synthesized with two different soft segments, Nippollan 964 and T-5652, and characterized with dielectric analysis (DEA), differential scanning calorimetry (DSC) and rheometry. The extra methyl group acted to produce a crystalline-like ordered hard segment that caused the 964 PCU to become Arrhenius in the glass transition region where the 5652 PCU had followed WLF behavior. Results showed the pendent methyl group acted to impart a crystalline-like character to the 964 PCU making it a candidate for applications that would be suited to a stiffer polymer. In Chapter Four we explore the possibility of increasing the wearability and comfort of contact lenses through increased hydration. The hydrogels 2-hydroxyethylmethacrylate (HEMA) and glycidyl methacrylate (GMA) solutions were created in three concentrations; neat, 50/50 and 60/40. Into these samples [Cu2({μ2-CO2}R)4(axial)2] (Cu(II) 4-hydroxybenzoic acid (MHBC) were dissolved 0.05% by weight. The samples were then polymerized via UV polymerization and compression molded. The experiments performed included penetration resistance , water absorption, micro hardness and glass transition. Addition of the MHBC acted to increase the water uptake of the samples but also reduced their ability to withstand mechanical penetration. With further study into crosslinking of the polymers, the MHBC could show promise in increasing hydration for commercial use.