Home About us Contact
|
Home About us Contact | ||
|
|
||
Efficient
Kinds of Efficient Terms modified by Efficient Selected AbstractsEfficient and fair scheduling for two-level information broadcasting systemsCONCURRENCY AND COMPUTATION: PRACTICE & EXPERIENCE, Issue 18 2008Byoung-Hoon Lee Abstract In a ubiquitous environment, there are many applications where a server disseminates information of common interest to pervasive clients and devices. For an example, an advertisement server sends information from a broadcast server to display devices. We propose an efficient information scheduling scheme for information broadcast systems to reduce average waiting time for information access while maintaining fairness between information items. Our scheme allocates information items adaptively according to relative popularity for each local server. Simulation results show that our scheme can reduce the waiting time up to 30% compared with the round robin scheme while maintaining cost-effective fairness. Copyright © 2008 John Wiley & Sons, Ltd. [source] Efficient and sensitive method of DNA silver staining in polyacrylamide gelsELECTROPHORESIS, Issue 1 2005Lujiang Qu Abstract DNA silver staining is widely used to detect DNA fragment in polyacrylamide gel with high sensitivity. Conventional procedures of the silver staining involve several steps, which take about 40 min to 2 h in total. To improve the efficiency of DNA silver staining, a more efficient protocol is developed in this study. The procedure comprises only four steps including impregnating, rinsing, developing, and stopping, and could be completed within 20 min. Nitric acid and ethanol in the silver-impregnation step of the new procedure eliminates the need for prior treatment of gels with a fixing solution and following rinse prior to impregnation with silver. The procedure has high sensitivity and long storage lifetime. The minimum detectable mass of DNA is 0.44 and 3.5 ng in denaturing and nondenaturing polyacrylamide gel, respectively. [source] Synthesis of New Phenanthroline-Based Heteroditopic Ligands , Highly Efficient and Selective Fluorescence Sensors for Copper(II) IonsEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 21 2006Peter Comba Abstract The heteroditopic phenanthroline derivatives 5,6-bis(2-pyridylcarboxamido)-1,10-phenanthroline (H2L1) and 5,6-bis[(4-methoxy-2-pyridyl)carboxamido]-1,10-phenanthroline (H2L2) have been prepared and characterized, together with their luminescent ruthenium(II) complexes [Ru(bpy)2(H2L1,2)](PF6)2 and [Ru(H2L1)3](PF6)2 and the corresponding iron(II) complex [Fe(H2L1)3](PF6)2. In these complexes, the metal ion is coordinated by the bidentate phen site of H2L. The luminescence of the ruthenium complexes (,ex = 450 nm, ,em ca. 620 nm) is completely quenched by Cu2+ ions in the micromolar concentration range and, to a lesser extent, by other metal ions. At pH 5, the response of the luminescent sensors is highly Cu2+ -selective. Heterodinuclear complexes [Ru(bpy)2(LM)](PF6)2, [Ru(LM)3](PF6)2, and [Fe(LM)3](PF6)2 have been isolated for M = Cu2+, Ni2+, Co2+, and Pd2+. It is suggested that M is coordinated to the tetradentate N4 site of L by two deprotonated amide N atoms and two pyridyl groups. This coordination type is confirmed by the EPR spectrum of the compound [RuII(bpy)2(L1CuII)](PF6)2.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source] Highly Efficient and Practical Pyrrolidine,Camphor-Derived Organocatalysts for the Direct ,-Amination of AldehydesEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 29 2010Pang-Min Liu Abstract A series of pyrrolidine,camphor-derived organocatalysts (1,4) were designed and synthesised. These organocatalysts were used for direct ,-amination of aldehydes with dialkyl azodicarboxylates to give the desired ,-aminated products in high chemical yields (up to 92,%) and with high to excellent levels of stereoselectivity (up to >99,% ee). The reactions proceeded rapidly (within 5 min) with low catalyst loading (5 mol-%) at ambient temperature. Enantioselective aminations of asymmetric ,,,-disubstituted aldehydes in the catalytic system were studied, with reasonable to high stereoselectivities (up to 75,% ee) being obtained. The utility of this methodology was demonstrated with the synthesis of derivatives of ,-amino-,-butyrolactone and a tetrasubstitutedcyclohexane-derived amino alcohol with high stereoselectivities. Transition models were proposed for the asymmetric ,-amination reactions; they involve hydrogen-bond interactions between the nucleophilic enamine formed in situ and the nitrogen source. [source] Efficient and Chirally Specific Synthesis of Phenanthro-Indolizidine Alkaloids by Parham-Type CycloacylationEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 2 2010Ziwen Wang Abstract A concise, efficient and modular route involving Parham-type cycloacylation as the key step has been used to synthesize six enantiopure phenanthro-indolizidine alkaloids 1a,c. The preparation of enantiomerically pure tylophora alkaloids and their seco analogues on a large-scale is now feasible. The alcohol intermediates 8a,c, which are difficult to prepare by other synthetic methodologies, have been synthesized by a metallation,cyclization,reduction sequence in excellent yields. [source] A Novel, Highly Efficient, One-Pot Synthesis of 1,4-Dihydroquinoline Derivatives in the Presence of a Pd(OAc)2/DABCO Catalytic SystemEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 29 2009Xiao-Jin Wu Abstract The Pd(OAc)2/DABCO catalytic system was first found to be highly efficient for C,N cross-coupling reactions. With the aid of this transformation, a variety of new 1,4-dihydroquinoline derivatives were synthesized from o -halobenzaldehydes and various ,-enaminones in good to excellent yields. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source] Efficient and Selective Method for the Synthesis of Dihydrodipyridopyrazines Based on the Pd-Catalysed Amination of HalopyridinesEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 22 2009Oana-Irina Patriciu Abstract A novel methodology for the efficient and selective synthesis of isomers A and B of N -substituted dihydrodipyridopyrazines was developed. The key step is the intermolecular coupling of aminopyridines and halonitropyridines/dihalopyridines in the presence of a catalyst system composed of Pd(OAc)2/Xantphos. This system displays good functional group compatibility and the desired C,N bond-forming process proceeds in good yields. Cyclization of suitable nitro-substituted N,N, -dipyridinylamines produces monosubstituted dihydrodipyridopyrazines, which can easily be alkylated to give a large variety of unsymmetrical 5,10-dialkyl-5,10-dihydrodipyrido[2,3- b:2,,3,- e]pyrazines (isomers A) and 5,10-dialkyl-5,10-dihydrodipyrido[2,3- b:3,,2,- e]pyrazines (isomers B). (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009) [source] Silica-Immobilized NHC,CuI Complex: An Efficient and Reusable Catalyst for A3 -Coupling (Aldehyde,Alkyne,Amine) under Solventless Reaction ConditionsEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 13 2008Min Wang Abstract A novel silica-immobilized NHC,CuI complex was developed and used as a highly efficient catalyst in the three-component coupling reactions of aldehydes, alkynes and amines (A3 -coupling). The reactions were applicable to aromatic and aliphatic aldehydes, alkynes and amines, and generated the corresponding propargylamines in good yields only in the presence of SiO2,NHC,CuI (2 mol-%) at room temp. under solvent-free reaction conditions. Moreover, the catalyst was quantitatively recovered from the reaction mixture by a simple filtration and reused for ten cycles with almost consistent activity.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source] Efficient, Rhodium-Catalyzed Hydrogenation of ,-Dehydroamino Acid Esters with Chiral Monodentate Aminophosphanes Bearing Two Binaphthyl GroupsEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 32 2007Luc Eberhardt Abstract All four stereoisomers of 4-{4,5-dihydro-3H -dinaphtho[2,1- c:1,,2,- e]azepin-4-yl}dinaphtho[2,1- d:1,,2,- f][1,3,2]dioxaphosphepine have been prepared from (R or S)-1,1,-binaphthyl-2,2,-diyl chlorophosphite and the appropriate dinaphtho-azepine. When reacted with [Rh(1,5-cyclooctadiene)2]BF4, highly active catalysts for the hydrogenation of ,-dehydroamino acid esters were obtained. The highest enantioselectivities (up to 99,% ee) were achieved with the phosphoramidites having two chiral binaphthyl groups with opposite configurations. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007) [source] An Efficient and Diastereoselective Intramolecular 1,3-Dipolar Cycloaddition of Cyclic Azomethine Ylides and NitronesEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 14 2006Rafael Pedrosa Abstract Nitrones and azomethine ylides formed by condensation of chiral 2-formyl-perhydro benzoxazines and N -substituted hydroxylamines or cyclic ,-amino acids cyclize intramolecularly yielding polycyclic isoxazolidine or pyrrolidine derivatives, respectively, with total diastereoselectivity. On the contrary, stabilized azomethine ylides derived from methyl prolinate undergo the cyclization products in very low yields.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source] Polystyrene-Supported 1,5,7-Triazabicyclo[4.4.0]dec-5-ene as an Efficient and Reusable Catalyst for the Thiolysis of 1,2-Epoxides under Solvent-Free ConditionsEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 5 2006Francesco Fringuelli Abstract Polystyrene-supported 1,5,7-triazabicyclo[4.4.0]dec-5-ene (PS-TBD) is an effective basic catalyst for the thiolysis of the 1,2-epoxides 1a,e by the aryl- and alkyl-substituted thiols 2A,E under solvent-free conditions while its activity is remarkably reduced in MeCN. The reactions are totally anti -diastereoselective and generally highly C-, regioselective. The corresponding hydroxy sulfides have been isolated in excellent yields and the catalyst has been easily recovered and reused with no loss in terms of efficiency and selectivity of the process. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source] Asymmetric Reduction of Ketones Under Mild Conditions Using NaBH4 and TarB-NO2: An Efficient and Unusual Chiral Acyloxyborohydride Reducing System,EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 24 2005David B. Cordes Abstract High enantioselectivities are obtained for the reduction of a series of ketones using the inexpensive and mild reducing agent NaBH4 with TarB-NO2 (1). This easily prepared tartaric acid-based reagent combines a Lewis acid with carboxylic acids in a single bifunctional reagent. When combined with NaBH4, the resulting chiral acyloxyborohydride mediates the reduction of aromatic ketones to provide the product alcohols in enantiomeric excesses of 93,98,%. Several aliphatic ketones were also reduced with moderate to excellent enantioselectivity. A unique mechanism is provided with supporting calculations for the proposed active species and transition state. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005) [source] Efficient Photosensitized Splitting of Thymine Dimer by a Covalently Linked Tryptophan in Solvents of High PolarityEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 6 2005Qin-Hua Song Abstract Tryptophan-thymine dimer model compounds used to mimic the repair reaction of DNA photolyase have been synthesized. The photosensitized cleavage of the dimer by the covalently linked tryptophan is strongly solvent-dependent with the reaction rates increasing in increasingly polar solvents, for example, the quantum yield , = 0.004 in THF/hexane (5:95) and 0.093 in water. The fluorescence of the tryptophan residue is quenched by the dimer moiety by electron transfer from the excited tryptophan to the dimer. Fluorescence-quenching studies indicated that the electron transfer was efficient in polar solvents. The splitting efficiency of the dimer radical anion within the tryptophan·+,dimer·, species is also remarkably solvent-dependent and increases with the polarity of the solvents. The back-electron-transfer reaction in the charge-separated species, which competes with cleavage, was suppressed in polar solvents. These results are in contrast to those of earlier solvent-dependent studies of indole-dimer systems, but they can be rationalized in terms of the differences in the distances between the chromophore unit and the attached dimer. The pH-dependent measurements of the splitting reaction and the deuterium isotope effect showed that the tryptophan radical cation within the charge-separated species does not deprotonate prior to the cleavage of the dimer radical anion. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005) [source] Efficient and selective tumor cell lysis and induction of apoptosis in melanoma cells by a conditional replication-competent CD95L adenovirusEXPERIMENTAL DERMATOLOGY, Issue 8 2010Lothar F. Fecker Please cite this paper as: Efficient and selective tumor cell lysis and induction of apoptosis in melanoma cells by a conditional replication-competent CD95L adenovirus. Experimental Dermatology 2010; 19: e56,e66. Abstract:, The high mortality of melanoma demands the development of new strategies, and gene therapy may be considered provided improvements in efficacy and selectivity. Overexpression of the death ligand CD95L/FasL has been shown in previous studies as highly effective for apoptosis induction in melanoma cells. For efficient and selective targeting of melanoma, a conditional replication-competent adenoviral vector was constructed (Ad5-FFE-02), which drives CD95L expression by a tetracycline-inducible promoter. For restricting its replication to melanoma cells, the adenoviral E1A gene is controlled by a tyrosinase-derived promoter. Furthermore, adenoviral E1B was deleted and a mutated E1A was used to preferentially support replication in tumor cells. Proving its high selectivity and efficiency, strong expression of E1A and doxycycline-dependent induction of CD95L were characteristic for tyrosinase-positive melanoma cells after Ad5-FFE-02 transduction, whereas absent in non-melanoma cell lines. Importantly, Ad5-FFE-02-mediated cell lysis was restricted to melanoma cells, and induction of apoptosis was found only in tyrosinase and CD95 expressing cells. Finally, the combination of adenoviral replication and CD95L-mediated apoptosis resulted in an enhanced repression of melanoma cell growth. This new adenoviral vector may provide a basis for an efficient targeting of melanoma. [source] Computational cardiac atlases: from patient to population and backEXPERIMENTAL PHYSIOLOGY, Issue 5 2009Alistair A. Young Integrative models of cardiac physiology are important for understanding disease and planning intervention. Multimodal cardiovascular imaging plays an important role in defining the computational domain, the boundary/initial conditions, and tissue function and properties. Computational models can then be personalized through information derived from in vivo and, when possible, non-invasive images. Efforts are now established to provide Web-accessible structural and functional atlases of the normal and pathological heart for clinical, research and educational purposes. Efficient and robust statistical representations of cardiac morphology and morphodynamics can thereby be obtained, enabling quantitative analysis of images based on such representations. Statistical models of shape and appearance can be built automatically from large populations of image datasets by minimizing manual intervention and data collection. These methods facilitate statistical analysis of regional heart shape and wall motion characteristics across population groups, via the application of parametric mathematical modelling tools. These parametric modelling tools and associated ontological schema also facilitate data fusion between different imaging protocols and modalities as well as other data sources. Statistical priors can also be used to support cardiac image analysis with applications to advanced quantification and subject-specific simulations of computational physiology. [source] Combined Confocal Microscopy and Stereology: a Highly Efficient and Unbiased Approach to Quantitative Structural Measurement in TissuesEXPERIMENTAL PHYSIOLOGY, Issue 6 2002Katherine Howell Understanding the relationship of the structure of organs to their function is a key component of integrative physiological research. The structure of the organs of the body is not constant but changes, both during growth and development and under conditions of sustained stress (e.g. high altitude exposure and disease). Recently, powerful new techniques have become available in molecular biology, which promise to provide novel insights into the mechanisms and consequences of these altered structure-function relationships. Conventionally structure-function relationships are studied by microscopic examination of tissue sections. However, drawing conclusions about the three-dimensional structure of an organ based on this two-dimensional information frequently leads to serious errors. The techniques of stereology allow precise and accurate quantification of structural features within three-dimensional organs that relate in a meaningful way to integrated function. For example, knowledge of changes in the total surface area of the capillary endothelium in an organ can be related directly to changes in fluid filtration and permeability, or knowledge of total vessel length and mean radius allows deductions about vascular resistance. Confocal microscopy adds enormously to the power of stereological approaches. It reduces the difficulties and labour involved in obtaining suitable images. Moreover, when used in conjunction with new analytical software, it allows convenient application of stereology to small samples and those in which it is essential to maintain a specific orientation for interpretation. The information obtained will allow us to examine in a quantitative manner the altered structure-function relationships produced by manipulation of single genes and regulatory pathways in whole organisms. [source] Efficient and Long-Living Light-Emitting Electrochemical CellsADVANCED FUNCTIONAL MATERIALS, Issue 9 2010Rubén D. Costa Abstract Three new heteroleptic iridium complexes that combine two approaches, one leading to a high stability and the other yielding a high luminescence efficiency, are presented. All complexes contain a phenyl group at the 6-position of the neutral bpy ligand, which holds an additional, increasingly bulky substituent on the 4-position. The phenyl group allows for intramolecular ,,, stacking, which renders the complex more stable and yields long-living light-emitting electrochemical cells (LECs). The additional substituent increases the intersite distance between the cations in the film, reducing the quenching of the excitons, and should improve the efficiency of the LECs. Density functional theory calculations indicate that the three complexes have the desired ,,, intramolecular interactions between the pendant phenyl ring of the bpy ligand and the phenyl ring of one of the ppy ligands in the ground and the excited states. The photoluminescence quantum efficiency of concentrated films of the complexes improves with the increasing size of the bulky groups indicating that the adopted strategy for improving the efficiency is successful. Indeed, LEC devices employing these complexes as the primary active component show shorter turn-on times, higher efficiencies and luminances, and, surprisingly, also demonstrate longer device stabilities. [source] Multifunctional Fluorene-Based Oligomers with Novel Spiro-Annulated Triarylamine: Efficient, Stable Deep-Blue Electroluminescence, Good Hole Injection, and Transporting Materials with Very High TgADVANCED FUNCTIONAL MATERIALS, Issue 24 2009Zuoquan Jiang Abstract A series of fluorene-based oligomers with novel spiro-annulated triarylamine structures, namely DFSTPA, TFSTPA, and TFSDTC, are synthesized by a Suzuki cross-coupling reaction. The spiro-configuration molecular structures lead to very high glass transition temperatures (197,253,°C) and weak intermolecular interactions, and consequently the structures retain good morphological stability and high fluorescence quantum efficiencies(0.69,0.98). This molecular design simultaneously solves the spectral stability problems and hole-injection and transport issues for fluorene-based blue-light-emitting materials. Simple double-layer electroluminescence (EL) devices with a configuration of ITO/TFSTPA (device A) or TFSDTC (device B)/ TPBI/LiF/Al, where TFSTPA and TFSDTC serve as hole-transporting blue-light-emitting materials, show a deep-blue emission with a peak around 432,nm, and CIE coordinates of (0.17, 0.12) for TFSTPA and (0.16, 0.07) for TFSDTC, respectively, which are very close to the National Television System Committee (NTSC) standard for blue (0.15, 0.07). The maximum current efficiency/external quantum efficiencies are 1.63,cd A,1/1.6% for device A and 1.91,cd A,1/2.7% for device B, respectively. In addition, a device with the structure ITO/DFSTPA/Alq3/LiF/Al, where DFSTPA acts as both the hole-injection and -transporting material, is shown to achieve a good performance, with a maximum luminance of 14,047,cd m,2, and a maximum current efficiency of 5.56,cd A,1. These values are significantly higher than those of devices based on commonly usedN,N,-di(1-naphthyl)- N,N,-diphenyl-[1,1,-biphenyl]-4,4,-diamine (NPB) as the hole-transporting layer (11,738,cd m,2 and 3.97,cd A,1) under identical device conditions. [source] Realising Reliable, Durable, Energy Efficient and Cost Effective SOFC Systems (Real-SOFC)FUEL CELLS, Issue 6 2009P. Holtappels Dr. No abstract is available for this article. [source] Dye-Doped Polyhedral Oligomeric Silsesquioxane (POSS)-Modified Polymeric Matrices for Highly Efficient and Photostable Solid-State LasersADVANCED FUNCTIONAL MATERIALS, Issue 20 2009Roberto Sastre Abstract Here, the design, synthesis, and characterization of laser nanomaterials based on dye-doped methyl methacrylate (MMA) crosslinked with octa(propyl-methacrylate) polyhedral oligomeric silsesquioxane (8MMAPOSS) is reported in relation to their composition and structure. The influence of the silicon content on the laser action of the dye pyrromethene 567 (PM567) is analyzed in a systematic way by increasing the weight proportion of POSS from 1 to 50%. The influence of the inorganic network structure is studied by replacing the 8MMAPOSS comonomer by both the monofunctionalized heptaisobutyl-methacryl-POSS (1MMAPOSS), which defines the nanostructured linear network with the POSS cages appearing as pendant groups of the polymeric chains, and also by a new 8-hydrogenated POSS incorporated as additive to the polymeric matrices. The new materials exhibit enhanced thermal, optical, and mechanical properties with respect to the pure organic polymers. The organization of the molecular units in these nanomaterials is studied through a structural analysis by solid-state NMR. The domain size of the dispersed phase assures a homogeneous distribution of POSS into the polymer, thus, a continuous phase corresponding to the organic matrix incorporates these nanometer-sized POSS crosslinkers at a molecular level, in agreement with the transparency of the samples. The silicon,oxygen core framework has to be covalently bonded into the polymer backbone instead of being a simple additive and both the silica content and crosslinked degree exhibit a critical influence on the laser action. [source] Photocrosslinkable Polythiophenes for Efficient, Thermally Stable, Organic PhotovoltaicsADVANCED FUNCTIONAL MATERIALS, Issue 14 2009Bumjoon J. Kim Abstract Photocrosslinkable bromine-functionalized poly(3-hexylthiophene) (P3HT-Br) copolymers designed for application in solution-processed organic photovoltaics are prepared by copolymerization of 2-bromo-3-(6-bromohexyl) thiophene and 2-bromo-3-hexylthiophene. The monomer ratio is carefully controlled to achieve a UV photocrosslinkable layer while retaining the ,,, stacking feature of the conjugated polymers. The new materials are used as electron donors in both bulk heterojunction (BHJ) and bilayer type photovoltaic devices. Unlike devices prepared from either P3HT:PCBM blend or P3HT-Br:PCBM blend without UV treatment, photocrosslinked P3HT-Br:PCBM devices are stable even when annealed for two days at the elevated temperature of 150,°C as the nanophase separated morphology of the bulk heterojunction is stabilized as confirmed by optical microscopy and grazing incidence wide angle X-ray scattering (GIWAXS). When applied to solution-processed bilayer devices, the photocrosslinkable materials show high power conversion efficiencies (,2%) and excellent thermal stability (3 days at 150,°C). Such performance, one of the highest obtained for a bilayer device fabricated by solution processing, is achieved as crosslinking does not disturb the ,,, stacking of the polymer as confirmed by GIWAXS measurements. These novel photocrosslinkable materials provide ready access to efficient bilayer devices thus enabling the fundamental study of photophysical characteristics, charge generation, and transport across a well-defined interface. [source] Parsimonious finite-volume frequency-domain method for 2-D P,SV -wave modellingGEOPHYSICAL JOURNAL INTERNATIONAL, Issue 2 2008R. Brossier SUMMARY A new numerical technique for solving 2-D elastodynamic equations based on a finite-volume frequency-domain approach is proposed. This method has been developed as a tool to perform 2-D elastic frequency-domain full-waveform inversion. In this context, the system of linear equations that results from the discretization of the elastodynamic equations is solved with a direct solver, allowing efficient multiple-source simulations at the partial expense of the memory requirement. The discretization of the finite-volume approach is through triangles. Only fluxes with the required quantities are shared between the cells, relaxing the meshing conditions, as compared to finite-element methods. The free surface is described along the edges of the triangles, which can have different slopes. By applying a parsimonious strategy, the stress components are eliminated from the discrete equations and only the velocities are left as unknowns in the triangles. Together with the local support of the P0 finite-volume stencil, the parsimonious approach allows the minimizing of core memory requirements for the simulation. Efficient perfectly matched layer absorbing conditions have been designed for damping the waves around the grid. The numerical dispersion of this FV formulation is similar to that of O(,x2) staggered-grid finite-difference (FD) formulations when considering structured triangular meshes. The validation has been performed with analytical solutions of several canonical problems and with numerical solutions computed with a well-established FD time-domain method in heterogeneous media. In the presence of a free surface, the finite-volume method requires 10 triangles per wavelength for a flat topography, and fifteen triangles per wavelength for more complex shapes, well below the criteria required by the staircase approximation of O(,x2) FD methods. Comparisons between the frequency-domain finite-volume and the O(,x2) rotated FD methods also show that the former is faster and less memory demanding for a given accuracy level, an attractive feature for frequency-domain seismic inversion. We have thus developed an efficient method for 2-D P,SV -wave modelling on structured triangular meshes as a tool for frequency-domain full-waveform inversion. Further work is required to improve the accuracy of the method on unstructured meshes. [source] High Molar Extinction Coefficient Ion-Coordinating Ruthenium Sensitizer for Efficient and Stable Mesoscopic Dye-Sensitized Solar Cells,ADVANCED FUNCTIONAL MATERIALS, Issue 1 2007D. Kuang Abstract Ru(4,4-dicarboxylic acid-2,2,-bipyridine) (4,4,-bis(2-(4-(1,4,7,10-tetraoxyundecyl)phenyl)ethenyl)-2,2,-bipyridine) (NCS)2, a new high molar extinction coefficient ion-coordinating ruthenium sensitizer was synthesized and characterized using 1H,NMR, Fourier transform IR (FTIR), and UV/vis spectroscopies and cyclic voltammetry. Using this sensitizer in combination with a nonvolatile organic-solvent-based electrolyte, we obtain a photovoltaic efficiency of 8.4,% under standard global AM,1.5 sunlight. These devices exhibit excellent stability when subjected to continuous thermal stress at 80,°C or light soaking at 60,°C for 1000,h. An electrochemical impedance spectroscopy study revealed that device stability is maintained by stabilizing the TiO2/dye/electrolyte and Pt/electrolyte interface during the aging process. The influence of Li+ present in the electrolyte on the device photovoltaic parameters was studied, and the FTIR spectral and photovoltage transient study showed that Li+ coordinates to the triethyleneoxide methylether side chains on the K60 sensitizer molecules. [source] Bright and Efficient, Non-Doped, Phosphorescent Organic Red-Light-Emitting Diodes,ADVANCED FUNCTIONAL MATERIALS, Issue 12 2004Y.-H. Song Abstract Ir(III) metal complexes with formula [(nazo)2Ir(Fppz)] (1), [(nazo)2Ir(Bppz)] (2), and [(nazo)2Ir(Fptz)] (3) [(nazo)H,= 4-phenyl quinazoline, (Fppz)H,=,3-trifluoromethyl-5-(2-pyridyl) pyrazole, (Bppz)H,=,3- t -butyl-5-(2-pyridyl) pyrazole, and (Fptz)H,=,3-trifluoromethyl-5-(2-pyridyl) triazole] were synthesized, among which the exact configuration of 1 was confirmed using single-crystal X-ray diffraction analysis. These complexes exhibited bright red phosphorescence with relatively short lifetimes of 0.4,1.05,,s in both solution and the solid-state at room temperature. Non-doped organic light-emitting diodes (OLEDs) were fabricated using complexes 1 and 2 in the absence of a host matrix. Saturated red electroluminescence was observed at ,max,=,626,nm (host-emitter complex,1) and 652,nm (host-emitter complex,2), which corresponds to coordinates (0.66,0.34) and (0.69,0.31), respectively, on the 1931 Commission Internationale de l'Eclairage (CIE) chromaticity diagram. The non-doped devices employing complex,1 showed electroluminance as high as 5780,cd,m,2, an external quantum efficiency of 5.5,% at 8,V, and a current density of 20,mA,cm,2. The short phosphorescence lifetime of 1 in the solid state, coupled with its modest ,,, stacking interactions, appear to be the determining factors for its unusual success as a non-doped host-emitter. [source] Efficient and Photostable ZnS-Passivated CdS:Mn Luminescent Nanocrystals,ADVANCED FUNCTIONAL MATERIALS, Issue 2 2004H. Yang Abstract Efficient and photostable ZnS-passivated CdS:Mn (CdS:Mn/ZnS core/shell) nanocrystals were synthesized using reverse micelle chemistry. CdS:Mn/ZnS core/shell nanocrystals exhibited much improved luminescent properties (quantum yield and photostability) over organically (n -dodecanethiol-) capped CdS:Mn nanocrystals. This is the result of effective, robust passivation of CdS surface states by the ZnS shell and consequent suppression of non-radiative recombination transitions. The dependence of photoluminescence (PL) intensity has been observed as a function of UV irradiation time for both organically and inorganically capped CdS:Mn nanocrystals. Whereas organically capped CdS:Mn nanocrystals exhibit a significant reduction of PL intensity, CdS:Mn/ZnS core/shell nanocrystals exhibit an increased PL intensity with UV irradiation. XPS (X-ray photoelectron spectroscopy) studies reveal that UV irradiation of CdS:Mn/ZnS nanocrystals in air atmosphere induces the photo-oxidation of the ZnS shell surface, leading to the formation of ZnSO4. This photo-oxidation product is presumably responsible for the enhanced PL emission, serving as a passivating layer. [source] Synthesis of Some Novel Thioxanthenone-Fused Azacrown Ethers, and Their Use as New Catalysts in the Efficient, Mild, and Regioselective Conversion of Epoxides to , -Hydroxy Thiocyanates with Ammonium ThiocyanateHELVETICA CHIMICA ACTA, Issue 7 2007Hashem Sharghi Abstract The regioselective ring-opening reactions of some epoxides with ammonium thiocyanate in the presence of a series of new 9H -thioxanthen-9-one-fused azacrown ethers, i.e., 7,11 (Scheme,1), and also of dibenzo[18]crown-6 (12), Kryptofix®22 (13), and benzo[15]crown-5 (14) were studied (Tables 1 and 2). The epoxides were subjected to cleavage by NH4SCN in the presence of these catalysts under mild conditions in various aprotic solvents. Reagents and conditions were identified for the synthesis of individual , -hydroxy thiocyanates in high yield and with more than 90% regioselectivity. The results can be discussed in terms of a four-step mechanism (Scheme,2): 1) formation of a complex between catalyst and NH4SCN, 2) release of SCN, from the complex, 3) reaction of the released SCN, at the sterically less hindered site of the epoxide, and 4) regeneration of the catalyst. The major advantages of this method are the high regioselectivity, the simple regeneration of the catalyst, the reuse of it through several cycles without a decrease of activity, and the ease of workup of the reaction mixtures. [source] Llama-derived single-domain intrabodies inhibit secretion of hepatitis B virions in mice,HEPATOLOGY, Issue 1 2009Benedikte Serruys Hepatitis B virus (HBV) infections cause 500,000 to 700,000 deaths per year as a consequence of chronic hepatitis, cirrhosis, and hepatocellular carcinoma. Efficient and safe antivirals to treat chronically infected patients and consequently to prevent development of hepatocellular carcinoma are still awaited. We isolated five single-domain antibodies (VHHs) that recognize the most abundant envelope protein (S) of HBV. VHHs, when expressed and retained in the endoplasmic reticulum as intrabodies, reduced levels of secreted hepatitis B surface antigen (HBsAg) particles in a cellular HBV model. In a hydrodynamics-based HBV mouse model, these intrabodies caused a marked reduction in HBsAg concentrations and a 10- to >100-fold reduction in the concentration of HBV virions in plasma. Conclusion: VHHs potently inhibited secretion of HBV virions in vivo, showing that this approach might be useful in the treatment of HBV. To our knowledge, this is the first report of intrabody-mediated inhibition of viral secretion in mammals. (HEPATOLOGY 2009;49:39-49.) [source] Efficient Visible-Light Emission from Dye-Doped Mesostructured OrganosilicaADVANCED MATERIALS, Issue 47 2009Norihiro Mizoshita Efficient and color-tunable visible-light emission is achieved in fluorescent dye-doped oligo(phenylenevinylene),silica mesostructured films through fluorescence resonance energy transfer from a blue-light-emitting organosilica to a yellow-light-emitting dye (see figure). Tuning of the composition realizes pseudo white-light emission with a quantum yield of 67%. Utilization of both walls and pores of the mesostructured organosilicas is effective to construct highly functional systems. [source] Highly Efficient and Color-Stable Deep-Blue Organic Light-Emitting Diodes Based on a Solution-Processible DendrimerADVANCED MATERIALS, Issue 47 2009Lei Wang A color-stable blue organic light-emitting diode is obtained utilizing a solution-processible fluorescent , -conjugated dendrimerG0 (see image), with a maximum luminance efficiency of 5.3,cd A,1. Efficient green, red, and white OLEDs are also demonstrated by doping G0 with phosphorescent dyes. Combining high device efficiency with solution processibility, G0 becomes one of the best blue-emitting materials for fabricating flat-panel displays and white-light lighting panels via solution processing. [source] Efficient, Stable Bulk Charge Transport in Crystalline/Crystalline Semiconductor,Insulator BlendsADVANCED MATERIALS, Issue 44 2009Avinesh Kumar Efficient and stable ambipolar charge transport in the bulk of crystalline/crystalline P3HT/HDPE systems, as evidenced by time-of-flight (TOF) photoconductivity measurements, is found. Interestingly, certain blend compositions displayed significantly enhanced bulk charge-transport properties compared to neat P3HT, with ,TOF measured for 80:20,wt% P3HT:PE blends being up to one order of magnitude higher than those found in neat P3HT. [source] | ||||||||||||||||||||||||||||||||||||||||||||||||||||