The interactions between anionic, crosslinked gels and cationic surfactants have been investigated. When exposed to oppositely charged surfactant, the gel collapses into a dense complex of polyion and micelles. During deswelling, the gel phase separates into a micelle-rich, collapsed surface phase, and a swollen, micelle-free core, both still part of the same network. As more surfactant is absorbed, the surface phase grows at the expense of the core, until the entire gel has collapsed. Polyacrylate (PA) gels with dodecyl- (C12TAB), and cetyltrimethylammonium bromide (C16TAB), as well as hyaluronate gels with cetylpyridinium chloride, have been studied. Kinetic experiments have been performed on macro- as well as microgels, using micromanipulator assisted light microscopy for the latter. A surfactant diffusion controlled deswelling model has been employed to describe the deswelling. The deswelling kinetics of PA microgels have been shown to be controlled by surfactant diffusion through the stagnant layer surrounding the gel, as the surface phase is relatively thin for the major part of the deswelling. For macroscopic PA gels the surface phase is thicker, and the kinetics with C12TAB were therefore also influenced by diffusion through the surface phase, while for C16TAB they were dominated by it. Relevant parameters have also been determined using equilibrium experiments. An irregular, balloon-forming deswelling pattern, mainly found for macrogels, as well as unexpectedly long lag times and slow deswelling for microgels, are reported and discussed. The microstructure of fully collapsed PA/C12TAB complexes has been studied using small-angle X-ray scattering. A cubic Pm3n structure was found at low salt concentration, which melted into a disordered micellar phase as the salt concentration was increased. Further increasing the salt concentration dissolved the micelles, resulting in no ordering.

This thesis presents results of novel methodologies applied to oriented systems. Both pure liquid crystalline materials as well as molecules oriented in liquid crystalline matrices have been studied. In particular this thesis presents investigations related to various aspects of NMR in liquid crystalline media, such as, assignment of resonances and the study of director dynamics of spinning liquid crystals in different phases and with different symmetry. Simplified methods for structure determination of solutes dissolved in liquid crystal solvents have been proposed. Diffusion ordered spectroscopy has been used to study a mixture of liquid crystals of opposite diamagnetic susceptibility at its coexistent phase. The methods presented represent novel techniques to characterize the liquid crystalline phase. NMR spectroscopy which has become a method of choice for understanding ordering mechanisms of mesogens requires a robust method for obtaining assignments of the NMR spectra of various nuclei that are found in the mesogens [1, 2]. It turns out that the spectra in the isotropic phase and in the nematic phase of a liquid crystal molecule are very different due to the presence of chemical shift anisotropy in the mesophase spectrum. There are a host of methodologies available for assigning spectra in the isotropic phase [3]. These methods however fail, when applied to the spectrum of the molecules in the mesophase due to the dominating role of strong anisotropic interactions, such as homonuclear couplings among protons. Problems arising while assigning spectral lines of liquid crystals in their nematic phase have been dealt with in chapter 2. To circumvent these problems, a property of the liquid crystal molecules under off-magic angle sample spinning can be utilized. It has been shown by Courtieu et al. [4] that the director/symmetry axis of a Δχ + ve liquid crystal aligns along the spinning axis for θ between 0 ° and θm, where θ is the angle between the spinning axis and the magnetic field and θm = 54.7° is the magic angle. It may be noted that the spectrum of θ = 0° spinning angle corresponds to the normal static spectrum, while the spectrum of θ = θm corresponds to the isotropic spectrum. In an earlier study, Teearr et al. [5] had recorded the 13C liquid crystal spectra as a function of very closely spaced θ values from 90° all the way up to 0°. From these plots of chemical shift versus the angle of spinning, it is possible to follow the trajectory of each 13C line from its position from θ = θm to θ = 0° and then match the spectrum in the isotropic phase (equivalently the magic angle sample spinning spectrum of the nematic phase) to the spectrum of the static sample in the nematic phase. However this method requires recording spectra at closely spaced angle intervals, so that one can unambiguously follow the trajectory of each of the lines without missing out any crossover of trajectories. However, this operation is time consuming. In this thesis we propose an alternate method, where we utilize the fact that the above trajectory has a very distinct relationship to the isotropic and anisotropic chemical shift and the problem of assignment does not require a continuous variation of angles, but just a few selected experiments should enable the assignment of the spectrum in the anisotropic phase. Thus the method of assignment has been made simpler and faster. It is shown that in addition to the assigned isotropic spectrum, only one other Off-magic angle spinning spectrum whose spinning angle θ is accurately known is necessary to obtain the complete assignment of the static spectrum. This procedure is non-trivial due to possibilities of errors in assignments arising out of inaccuracies in the knowledge of chemical shifts and the spinning angle. A computational procedure is proposed to take into account deviations arising out of non-ideal experimental conditions. A discussion regarding the details of the procedure and also situations where there can be ambiguities and how they can be resolved has been elaborated. The developed method has been demonstrated on a well known thermotropic liquid crystalline system, N-(4-ethoxybenzylidene)-4-n-butlyaniline [EBBA]. Since assignment of resonances in the nematic phase is a primary requirement for any further analysis regarding the ordering and deeper understanding of the role of various substituents in the mesogens we believe our novel prescription will be of immense use and utility. The third chapter presents the study of director dynamics in a lyotropic liquid crystal composed of Potassium laurate, 1-Decanol and D2O [6] under variable angle sample spinning using 2H NMR spectrum of D2O. A very interesting interplay of the magnetic orienting torque due to interaction of the liquid crystal director with the magnetic field and viscous torque arising from the viscosity of the sample on the director comes to fore. The relative magnitude of these torques has a direct bearing on the spectral pattern and line shapes observed, providing valuable insights into magnetohydrodynamics of the spinning liquid crystals. This study leads to even more interesting behavior for liquid crystals which deviate from uniaxial symmetry. This competition between magnetic and viscous torques has been quantitatively visualized by simulation of the 2H spectrum. It has been possible to visualize the observed spread in the director distribution arising out of viscous torque in terms of the energetics of the system under fast spinning. If the magnetic torque dominates over the viscous torque, then the equilibrium corresponds to the director orientation of δ = 0° where the energy is at its minimum. However the viscous and magnetic torques can become comparable as it may happen if the spinning angle is close to the magic angle or when the Δχ of the system is small. In those circumstances additional energy from the viscous torque causes the distribution of the director orientation to spread further away from δ = 0° for a positive Δχ liquid crystal. The trigonometric factor [P2(cosθ)∗P2(cosδ)] being proportional to the total energy of the system has been plotted against the spinning angle. The spectrum of the biaxial phase [7] as a function of the spinning angle shows more interesting director distribution. Here the patterns of the director distribution are observed on either side of the magic angle due to the presence of more than one director. The patterns observed also have information about the symmetry of the phase. This work provides insights into magnetohydrodynamics of spinning liquid crystals and can also be of relevance to samples of biological interest such as bicelles with protein oriented in them [8]. The fourth chapter deals with a novel characterization method relevant for the biaxial phase [9]. As an off shoot of the previous chapter, it effectively overcomes the disadvantages of the previous experimental methods which require simulation and line shape fitting to extract useful parameters. The chapter also presents the measurement of geometrical parameters of oriented solutes in phases exhibiting biaxial symmetry. The measured parameters show the effect of the onset of biaxiality as significant deviation in the value of the measured parameter. The utility of liquid crystalline media as solvents in high resolution NMR spectroscopy has been very rewarding since the pioneering work of Saupe and Englert [6]. The intramolecular interactions within solutes are only partially averaged. As a result one obtains a liquid like spectrum while at the same time very useful anisotropic interactions such as dipolar couplings, chemical shift anisotropies, quadrupolar couplings and anisotropic part spin-spin J couplings are extracted [10]. NMR spectra of molecules dissolved in thermotropic liquid crystals have long been used to obtain structural and orientational information. As the same time the complexity of the spectrum increases with the increase in the number of spins and the reduction in symmetry of the molecule, which can make the spectral analysis forbidding. Generally proton spectra have been used to obtain the geometry of the proton skeleton of the molecule and the information that includes dilute X nuclei such as 13C and 15N are available only from satellites which are buried in the intense proton spectrum. Different inequivalent dilute spins coupled to protons form different coupled spin systems in their natural abundance and appear as satellites in the proton spectra. Identification of transitions belonging to each of the spin system is essential to determine heteronuclear dipolar couplings, which is a formidable task. The fifth chapter deals with development of the techniques to obtain the complete structure of the dissolved molecules including nuclei other than protons in their natural abundance. The use of inverse experiments has been elaborated to overcome the problems of sensitivity and complexity for solute molecules having larger number of spins. In the present study using HSQC and HMQC experiments, we have selectively detected spectra of each inequivalent rare spin coupled to protons in pyrazine, pyrimidine and pyridazine dissolved in thermotropic Phase 4 and Phase 5 liquid crystal solvents. This way we could obtain enhancement in the intensity of satellites signals without the interference from the signals connected to the major isotopomers. Besides, we could resolve a complex spectrum into its sub-spectra corresponding to individual 13C and 15N isotopomers. This separation of the spectra corresponding to individual sub-spin systems makes analysis easy and helps analyze larger systems with higher number of spins and lower symmetry. Besides 1H-1H dipolar couplings, 13C-1H and 15N-1H dipolar couplings have been determined in natural abundance, thereby giving the complete dipolar coupling network between all the spins in the molecule. In this treatment pyrazine, pyrimidine and pyridazine have been used as examples of methodology developed. It is expected that the method will be of wider use for several other similar systems. Chapter six describes the diffusion ordered spectroscopic investigation [11] of a phase arising out of mixing together two liquid crystals having opposite signs of diamagnetic susceptibility anisotropy [12]. Towards this end we have used CH3CN as a probe molecule. The spectrum of CH3CN has with it the information about the parallel or perpendicular orientation of the phase. Such a mixture of liquid crystals have shown interesting behavior at the critical temperature where the two phases seem to coexist. It has been an interesting question to understand what exactly happens for the molecular orientation when the macroscopic anisotropy Δχ vanishes. Earlier Jokisaari et al. [13] have varied the temperature very finely taking due precautions to maintain homogeneity and stability of temperature to the tune of ±0.05K across the sample volume. Their observation of a powder pattern exactly in the critical temperature was interpreted as arising out of a distribution of directors equally oriented in all directions. In our experiments we have measured the diffusion coefficient of the probe molecule i.e. acetonitrile as we change the temperature of the system through the critical temperature. At the critical temperature we have a situation of being able to measure the parallel and perpendicular orientational diffusion coefficients simultaneously. The measurements show that the parallel component of the diffusion coefficient has reduced and the perpendicular component has increased in comparison to the trend in the immediate neighboring temperatures, thereby indicating that at the exact critical condition the liquid crystal mixture consists of an isotropic distribution of molecules. As a check to rule out any exchange of molecules in different domains of parallel and perpendicular orientations an EXSY experiment was conducted with a mixing time which was same as that of the diffusion delay in the DOSY experiment. The EXSY spectrum showed no exchange cross peaks between the two orientations, this confirms that the anisotropy of the diffusion vanishes at the critical temperature. Nematic liquid crystals exhibit a rich variety of phases and properties. NMR is a very powerful tool to study the various phases at the microscopic and molecular level. It has also turned out that some of these properties can be usefully utilized for investigation of both small and large molecules by NMR. Thus this thesis has attempted to expand several of the techniques already available for various applications and extend the utility of NMR for the study of partially ordered systems.

Designing an application specific integrated circuit (ASIC) must be starting with careful preparations, otherwise the chip will not be as good as possible. The theoretical studies must cover everything from the chip circuits to the application structure. In mobile applications there is extremely important that the current consumption becomes minimized because the battery power is limited. The power reductions studies must include the most power costing circuits on the chip. When the whole circuit or segments of the circuit is not in use, they must switch fast and simple into another mode that consume nearly none power. This mode is called sleep-mode. If the sleep-mode has very low leakage currents, the lifetime of the application will dramatically increase. This report studies the most power costing circuits in smartcard application ASIC. The chip should be used to control a LCD display on the smartcard. The circuits that have been investigated are level shifters, charge pumps and LCD drivers, also sleep-mode configuration possibilities have been investigated. Other small preparing work is also included in the thesis.

A system packaging level approach on liquid crystal polymer (LCP) was proposed for low cost, lightweight, and compact wireless communication systems. Via technology was explored for V-band W-band transitions and an active cooling system that are essential for compact multilayer integration. RF MEMS switches were fabricated and integrated at the component level to enable multi-functional devices with optimal performance. A pattern reconfigurable antenna for MIMO applications and 3D phase shifters for phased array antennas that use RF MEMS switches were presented. In addition, a lightweight expandable array was designed and measured with up to 256 elements on multilayer LCP integrated at the system level. Furthermore, a 60 GHz multilayer transceiver front end device with simultaneous transmit and receive was designed and measured for low cost 60 GHz applications. The wide variety of multilayer LCP applications integrated at the system level shows a promising future for the next generation low cost lightweight wireless communication systems.

Biological processes at the cellular level take place in heterogeneous environments, and usually involve only a small number of molecules. They tend to exhibit strong time dependent fluctuations, as a result, and are, therefore, intrinsically stochastic. The present thesis describes some of the efforts I have made during the course of my research work to develop simple, analytically tractable models of a selection of biologically-inspired problems in which this kind of stochasticity is a central ingredient. These problems are: (i) single molecule enzyme activity (ii) intermittency in single enzymes, (iii) liquids crystal dynamics (iv) modulation of electron transfer kinetics during photosynthesis, and (v) anomalous polymer translocation dynamics. All of these problems can be defined in terms of quantity that changes randomly in time because of environmental fluctuations with broad distributions of relaxation times. In this thesis I show that a generalization of a model that describes simple Brownian Motion can be used to understand many of the dynamical aspects of these problems.

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In this thesis the main objectives were to improve the liquid crystal shutters and to develop a stereoscopic vision application called 3D Dual View. The vision quality of a 3D system based on active glasses is direct related to the performance of the liquid crystal shutters. There are a lot of parameters that plays an important role in the quality of 3D glasses. Thus, efforts were concentrated in the organization of the liquid crystal molecules between the substrates and in the liquid crystal itself. We studied different configurations of shutters using nematic liquid crystal and ferroelectric liquid crystal (smectic), with and without polymer. Furthermore, the ferroelectric samples were analyzed using a full optical snapshot matrix Mueller polarimenter made by UBO (Université de Bretagne Occidentale) in partnership with Télécom-Bretagne. The second part was the development of 3D Dual View System. It is a stereoscopic vision system based on a mixture of active and passive 3D solution which displays a 3D image that can be viewed simultaneously by two spectators, but from different perspectives. To allow two different points-of-view of a scene or object in three dimensions, the system has to multiplex four images, one pair to form the 3D image for one viewer in one perspective and the other pair for the second viewer in other perspective. We describe different techniques to multiplex and demultiplex the video streams taking into account the physiological aspects, market, image quality and the crosstalk. The crosstalk between the images leads to an effect called ghosting, which the viewer sees a low intensity image that belongs to the other viewer. Then, we also characterized the ghosting effect (crosstalk) and proposed an algorithm of ghostbusting to compensate it.

Primarily, newly developed, high sensitive and accurate methods for thermal characterization of liquids using photothermal radiometry are presented. Two experimental configurations are suggested, tested and validated with usual liquid materials. These methods are used to study polymer dispersed liquid crystal samples. Dynamic thermal properties of samples are analysed verses amplitude varying applied electric field with constant frequency as well as versus frequency varying electric field with constant amplitude. Our results clearly show the thermal properties of the samples are prone to depolarizing field effects at the lower frequencies of the applied electric field. The experimental results are modeled against existing theories to predict electric properties of the sample composites. Second part of the manuscript describes the development of a novel photothermal technique based on thermoelectric effect. This technique is particularly useful for thermally characterizing thermoelectric materials without using a separate sensor for measuring induced temperature changes. A theoretical and experimental study is presented. The experiments are done on polyaniline - carbon nanotube composite pellets by measuring Seebeck voltage generated by the samples upon heating by a modulated laser beam. Additional infrared radiometry experiments are done on the same samples and the results are in good agreement with those previously found. Later on, the possibility of photothermoelectric materials to be used as sensors for finding thermal transport properties of materials with a thermal wave resonant cavity is suggested.

Because of the tremendous amount of media streaming, video calling and high definition TV and gaming, the biggest challenge for the wireless industry is the increasing demand of high data rates. Utilization of mm-wave frequencies is an attractive option to meet this high demand. Recent advances in low cost semiconductor technologies allow realization of low-cost on-chip RF front-ends in the high millimeter wave (mm-wave) frequencies, making it possible to realize compact systems for these application areas. Although integrated circuits (ICs) are one of the main building blocks of a mm-wave system, in order to realize a fully functional wireless system, cost-effective antenna design and packaging are two important pre-conditions. Researchers have investigated and reported low-cost electronics packaging up to 100 GHz to a great extent on ceramic substrates, but mm-wave packaging above 100 GHz is relatively less explored, particularly on organic substrates. This Ph.D. dissertation demonstrates the design and development of microwave and mm-wave on-chip and on-package antennas and organically packaged components and modules ranging from 20 GHz to 170 GHz. The focus of this research was to design and develop mm-wave components and modules on LCP, to investigate the viability of this organic substrate and development of fabrication techniques in the K- (18-26.5 GHz), V- (50 to 70 GHz), W- (75 to 110 GHz), and D- (110 to 170 GHz) bands. Additionally, a demonstration of a micro-machined on-chip antenna has also been presented. This dissertation is divided in three parts: (1) characterization of liquid crystal polymer from 110 to 170 GHz. (2) development of highly radiation efficient on-chip and AiP antennas, and (3) development of mm-wave modules with the integration of antennas.