In digital signal processing and multimedia applications, floating-point(FP) multiplication and addition are the most commonly used operations. In addition, FP multiplication operations are frequently followed by the FP addition operations. Therefore, in order to achieve high performance and low cost, multiplication and addition are usually combined into a single unit, known as the FP Multiply-Add Fused (MAF). On the other hand, the mobile devices nowadays are rapidly developing. For this kind of devices, performance and power sustainability have to become the major trend in the research area. As a result, the mechanisms to reduce energy consumption become more important. Therefore, we propose a multi-mode FP MAF based on the concept of iterative multiplication and truncated addition, to achieve different operating modes with different errors. This MAF, with a total of seven modes, includes three modes for the FP multiply-accumulate operations, two modes for single FP multiplication operation and single FP addition operation, respectively. FP multiply-accumulate operations provide three modes to user, and this three modes have 0%, 0.328% and 1.107% of error. The 0% error is the same with the standard IEEE754 single-precision FP Multiply-Add Fused operations. For FP multiplication and FP addition operations, the proposed MAF allows users to choose two kinds of error modes, which are 0%, 0.328% error for FP multiplication and 0%, 0.781% error for FP addition. The 0% error is the same with the standard IEEE754 single-precision floating-point operations. When compared with the standard IEEE754 single-precision FP MAF, the proposed multi-mode FP MAF architecture has 4.5% less area and increase about 22% delay to achieve the effect of multi-mode. To demonstrate the power efficiency of proposed FP MAF, it is used to perform the operations of FP MAF, FP multiplication, and FP addition in the application of RGB to YUV format conversion. Experimental results show that, the proposed multi-mode FP MAF can significantly reduce power consumption when the modes with error are adopted.

Unsymmetrical discotic liquid crystals based on hexaazatriphenylene(HAT) have not been published until today.We have used tetrahydoxyquinone as the starting material to synthesis unsymmetrical discotic liquid crystals based on HAT and investigate their properties of liquid crystal.

Reaction of 3-sulfonyl acetamides with various substituted methyl acrylate derivatives furnished pyroglutamate and glutarimidess via [3+2] and [3+3] cycloaddition respectively. The results were applied to the synthesis of pyrrolizidine skeleton, tylophorine, cryptopleurine and fused bicyclic glutarimides.

This report presents improved architecture designs and implementations for a fused floating-point add-subtract unit. The fused floating-point add-subtract unit is useful for DSP applications such as FFT and DCT butterfly operations. To improve the performance of the fused floating-point add-subtract unit, the dual path algorithm and pipelining technique are applied. The proposed designs are implemented for both single and double precision and synthesized with a 45nm standard-cell library. The fused floating-point add-subtract unit saves 40% of the area and power consumption and the dual path fused floating-point add-subtract unit reduces the latency by 30% compared to the traditional discrete floating-point add-subtract unit. By combining fused operation and the dual path design, the proposed floating-point add-subtract unit achieves low area, low power consumption and high speed. Based on the data flow analysis, the proposed fused floating-point add-subtract unit is split into two pipeline stages. Since the latencies of two pipeline stages are fairly well balanced the throughput of the entire logic is increased by 80% compared to the non-pipelined implementation. / text

This research project is concentrated on tuning the properties of small organic molecules, namely polyacenes, tropones and thiepins, by incorporating redox-active transition metal centers π-bonded to terminal cyclopentadienyl ligands. Organometallic-fused acenequinones, tropones, thiepins and cyclopentadiene-capped polyacenes were synthesized and characterized. This work was divided into three parts: first, the synthesis of ferrocene-fused acenequinones, cyclopentadiene-capped acenequinones and their subsequent aromatization to polyacenes; second, the synthesis of ferrocene-fused tropones, thiotropones and tropone oxime; and third, the synthesis of ferrocene-fused thiepins. Ferrocene-fused quinones are the precursors to our target complexes. Our synthetic route to ferrocenequinones involved two-fold aldol condensation between 1,2-diformylferrocene and naphthalene-1,4-diol or anthracene-1,4-diol, and four-fold condensation between 1,2-diformylferrocene and 1,4-cyclohexanedione. Reduction of ferrocene-fused quinones with borane in THF resulted in ferrocene-fused dihydroacenes. Attempts to reduce ferrocene-fused acenequinones with sodium dithionite led to metal-free cyclopentadiene- (Cp-) capped acenequinones. Cp-capped acenequinones were aromatized to bis(triisopropylsilyl)ethynyl polyacenes by using lithium (triisopropylsilyl)acetylide (TIPSC≡CLi) with subsequent dehydroxylation by stannous chloride. The compounds were characterized by using spectroscopic methods and X-ray crystallography. Further, the electronic properties of these compounds were studied by using cyclic voltammetry and UV-visible spectroscopy. Cyclic voltammetry showed oxidation potentials of Cp-capped TIPS-tetracene and bis-Cp-capped TIPS-anthracene as 0.49 V and 0.61 V, respectively (vs. ferrocene/ferrocenium). The electrochemical band gaps were 2.15 eV and 2.58 eV, respectively. Organic thin-film transistor device performance of Cp-capped polyacenes was studied using solution deposition bottom-contact, bottom-gate (BCBG) device architecture and the resulting performance parameters are described herein. Similarly, we are also interested in potential applications of metallocene-fused tropones and derivatives as organic electronic materials. Condensation of 1,2-diformylferrocene with acetone or 1,3-diphenylacetone in the presence of KOH resulted in the ferrocene-fused tropone (η5-2,4-cyclopentadien-1-yl)[(1,2,3,3a,8a-η)-1,6-dihydro-6-oxo-1-azulenyl]iron (1, R = H, E = O) and its 5,7-diphenyl derivative (1, R = Ph, E = O) as previously reported by Tirouflet. The use of piperidine as base resulted in Michael addition of piperidine to one of the carbon-carbon double bonds of the tropones. Lawesson’s reagent converted the ferrocene-fused tropones to either a thiotropone (1, R = H, E = S) or a detached 5,7-diphenylazulenethiol (2). Reaction of the ferrocene-fused thiotropone with hydroxylamine gave the corresponding oxime (1, R = H, E = NOH). Products were characterized by using spectroscopic methods and X-ray crystallography. Their electronic properties were studied by using cyclic voltammetry and UV-visible spectroscopy. The third project involved the two-fold aldol condensation of 1,2-diformylferrocene with dimethylthioglycolate S-oxide in the presence of freshly distilled triethylamine, which gave mono- and di-dehydrated products. Deoxygenation of the ferrocene-fused thiepin S-oxide with 2-chloro-1,3,2-benzodioxaphosphole in the presence of pyridine resulted in the corresponding thiepin. The ester groups of the thiepin and thiepin S-oxide were hydrolyzed under basic conditions to give carboxylic acids, which were converted into acid chlorides using oxalyl chloride. Attempts to decarboxylate the thiepin and thiepin S-oxide diacids resulted in decomposition.

Fused floating-point arithmetic units such as a floating-point fused Dot-Product (fused DP) and a floating-point fused Add-Subtract (fused AS) are employed for the implementation of the butterfly unit of the FFT due to their characteristics of low power and less area. In addition, the fused DP has less delay and lower error. Among the elements of the fused DP, two internal mantissa multipliers occupy the largest area and consume the largest power. A Multiple-Constant Multiplier (MCM) architecture has high speed, low power consumption, and small area compared to a conventional multiplier. The MCM is used for the internal mantissa multiplier, providing a solution for low power and high performance. Despite the benefits of the MCM, it lacks precision compared to a conventional multiplier. Due to this, the butterfly unit using the MCM has higher error. In this report, a new architecture of the butterfly unit has been designed by merging conventional MCMs. The new architecture provides two options. It either reduces the error or it lowers the power compared to a conventional MCM butterfly unit. / text

No description available.

Konstanz, Univ., Diplomarbeit, 2007.

O estudo do eletrorrevestimento de tântalo sobre aço e sobre cobre foi realizado na mistura eutética FLINAK (29,2% LiF - 11,7% NaF - 59,1% KF - % em massa) contendo 15% em massa de K2TaF7. Foram estudadas as influências da densidade de corrente catódica, do tempo de eletrólise, da temperatura e da natureza do substrato sobre as eficiências de correntes catódicas e a morfologia dos revestúnentos. Depósitos de tântalo lisos, brilhantes, aderentes e uniformes foram obtidos com alta eficiência de corrente catódica usando os seguintes parâmetros: densidade de corrente catódica de 23 mA/cm2 a 50 mA/cm2, temperatura de 750°C e tempo de eletrólise de 30 minutos a 120 minutos. Os revestimentos obtidos nestas condições possuem espessuras de 18 µm a 41 µm. Os depósitos de tântalo sobre aço e sobre cobre são constituídos de tântalo puro, sem formação de camada de difusão. Ensaios de eletrodeposição de camadas delgadas de tântalo em catodos de formas e geometrias complexas mostraram o bom poder de cobertura do tântalo. Curvas potencial de circuito aberto x tempo, feitas à temperatura ambiente em soluções de ácido nítrico a 40%, a 50% e a 60% em massa, ácido clorídrico a 3,6% em massa e ácido sulfúrico a 80% em massa, mostraram ótima concordância entre o potencial de circuito aberto estacionário do tântalo maciço comercial e dos revestimentos de tântalo sobre cobre nestes meios. Curvas potencial de circuito aberto x tempo feitas à temperatura ambiente em meio de ácido clorídrico a 3,6% em massa, para revestimentos sobre aço mostraram que a semelhança com o tântalo maciço só é observada em depósitos recentes, o que foi atribuído à difusão do ferro do substrato para a superficie do revestimento. Ensaios gravimétricos mostraram que a velocidade de corrosão dos revestimentos é comparável com a do tântalo comercial, em meios de ácido nítrico a 40% e a 50% em massa, à temperatura de ebulição. / The study of tantalum electroplating on copper and carbon steel has been carried out in FLINAK eutectic (29.2% LiF -11.7% NaF -59.1% KF - wt%) containing 15wt% K2TaF7. The effects of current cathodic density, time of electrolysis, temperature and substrate kind have been studied in relation to the cathodic current efficiencies and the coating morphology. Tantalum deposits, with good smoothness, brightness, adherence and uniformity were obtained with high cathodic efficiency, using the following conditions: 23 mA/cm2 to 50 mA/cm2 cathodic current densities, 30 minutes to 120 minutes electrolysis time interval and 750°C temperature. Under these conditions the coatings are about 18 µm to 41 µm thick. The deposits obtained on carbon steel and copper are both constituted of pure tantalum without formation of interdiffusion layer. The results of tantalum thin coatings electrodeposition on cathodes of complex geometrics and shapes showed the good throwing power of tantalum. Open circuit potential x time curves have been recorded for massive tantalum and for tantalum coatings on copper in 40 wt%, 50 wt% and 60 wt% nitric acid, 3.6 wt% hydrochloric acid and 80 wt% sulfurie acid at room temperature. They showed similar stationary open-circuit poteutial values for both the massive tantalum and the tantalum coatings. Open circuit potential x time curves for tantalum coatings on carbon steel performed in 3.6%wt hydrochloric acid at room temperature showed that the similarity with massive tantalum exists only with recent deposits, because of iron diffusion from substrate to coating surface. Gravimetric tests showed comparable corrosion rate values for massive tantalum and tantalum coatings in boiling 40wt% and 50wt% nitric acid.

This study focuses on novel approaches to the modeling and construction of devices used in ion beam and vacuum systems. Turbulent computational fluid dynamics simulations were performed to model the air flow into an ion funnel system. The results of these simulations were coupled one-way with electrodynamics simulations of the fields generated by the ion funnel. Using the turbulence kinetic energy (k), a spatially varying estimation of the fluctuating component of the velocity field was calculated. These resulting simulations more accurately predicted the ion transmission through the system. Using fused deposition modeling (FDM) novel construction methods for the ion funnel and the vacuum chamber components the ion funnel system utilizes were developed. An FDM fabricated frame, in the shape of the ion funnel, was quickly and inexpensively produced. This frame supported a flexible printed circuit board that served as both the lenses of the ion funnel and power distribution circuit. The transmission of ions was as good as the traditionally constructed ion funnel. The device cost and weighed less and had lower intrinsic impedance, requiring less power to be driven. FDM was also used to produce vacuum components by post-processing using electroplating. Initial tests to determine whether electroplating would adequately produce a hermetic seal for vacuum components were performed. It was observed that thinner plated components could not withstand the stresses required from the gaskets and flanges to adequately seal, subsequently cracking. Thicker samples adequately sealed against atmosphere and maintained this seal over the entire test period. A proof of concept KF-25 full nipple was produced and processed using electroplating. The device was able to reach and ultimate pressure of 1 x 10-6 Torr, however, it was not able to reach the ultimate pressure of the chamber, which was 5 x 10-7 Torr due to the inability to be adequately cleaned of contaminant water.