Home About us Contact
|
Home About us Contact | ||
|
|
||
Organic
Kinds of Organic Terms modified by Organic Selected AbstractsA generic approach to the impurity profiling of drugs using standardised and independent capillary zone electrophoresis methods coupled to electrospray ionisation mass spectrometryELECTROPHORESIS, Issue 9 2005Aurélie Vassort Abstract Three standardised, capillary zone electrophoresis-electrospray ionisation mass spectrometry (CZE-ESI-MS) methods were developed for the analysis of six drug candidates and their respective process-related impurities comprising a total of 22 analytes with a range of functional groups and lipophilicities. The selected backround electrolyte conditions were found to be: 60/40 v/v 10 mM ammonium formate pH 3.5/organic, 60/40 v/v 10 mM ammonium acetate pH 7.0/organic and 10 mM piperidine, pH 10.5, where the organic solvent is 50/50 v/v methanol/acetonitrile. The coaxial sheath flow consisted of either 0.1% v/v formic acid in 50/50 v/v methanol/water, or 10 mM ammonium acetate in 50/50 v/v methanol/water, depending on the mixture being analysed. Factor analysis and informational theory were used to quantify the orthogonality of the methods and predict their complementarities. The three selected CZE-ESI-MS methods allowed the identification of 21 out of 22 of all the drug candidates and their process-related impurities and provided orthogonality with four established high-performance liquid chromatography-mass spectrometry (HPLC-MS) methods. These methodologies therefore form the basis of a generic approach to impurity profiling of pharmaceutical drug candidates and can be applied with little or no analytical method development, thereby offering significant resource and time savings. [source] Multiphase Systems for the Recycling of Alkoxycarbonylation CatalystsADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 12-13 2006Jeroen J., M. de Pater Abstract This review evaluates the various multiphasic systems that have been developed for catalyst recycling in the context of alkoxycarbonylation of alkenes and alkynes. Immobilization of the catalyst on an insoluble support, such as silica, alumina, clay or a polymer, as well as immobilization in the inorganic phase of several liquid/liquid biphasic systems (aqueous/organic, ionic liquid/organic, fluorous/organic or supercritical CO2/organic) has been described. In several cases detailed information on the efficiency of catalyst separation and recycling is available. Most of the work was focused on the alkoxycarbonylation reactions of alkenes, for which several efficient methods for catalyst recycling were demonstrated. The recycling of catalyst through specific precipitation from supercritical CO2 or selective dissolution in a fluorous phase, has received only scant attention but offers many opportunities for further improvement. [source] Organic litter: dominance over stones as a source of interrill flow roughness on low-gradient desert slopes at Fowlers Gap, arid western NSW, AustraliaEARTH SURFACE PROCESSES AND LANDFORMS, Issue 1 2003David Dunkerley Abstract Thirty-six runoff plot experiments provide data on flow depths, speeds, and Darcy,Weisbach friction coefficients (f) on bare soil surfaces, and surfaces to which were added sufficient extra plant litter or surface stones to provide projected cover of 5, 10 and 20 per cent. Precision flow depth data were derived with a computer-controlled gantry and needle gauge for two different discharges for each plot treatment. Taking a fixed flow intensity (Reynolds number, Re = 150) for purposes of comparison shows means of f = 17·7 for bare soil surfaces, f = 11·4 for added stone treatments, and f = 23·8 for added litter treatments. Many individual values of f for stone treatments are lower than for the bare soil surface, but all litter treatments show increases in fcompared to bare soil. The lowering of f in stone treatments relates to the submerged volume that the stones occupied, and the associated concentration of flow onto a smaller part of the plot surface. This leads to locally higher flow intensities and lower frictional drag along threads of flow that the obstacles create. Litter causes higher frictional drag because the particles are smaller, and, for the same cover fraction, are 100 times more numerous and provide 20 times the edge or perimeter length. Along these edges, which in total exceed 2·5 m g,1 (equivalent to 500 m m,2 for a loading of 2 t ha,1), surface tension draws up water from between the litter particles. This reduces flow depth there, and as a consequence of the lower flow intensity, frictional drag rises. Furthermore, no clear passage remains for the establishment of flow threads. These findings apply to shallow interrill flows in which litter is largely immobile. The key new result from these experiments is that under these conditions, a 20 per cent cover of organic litter can generate interrill frictional retardation that exceeds by nearly 41 per cent that of a bare soil surface, and twice that contributed by the same cover fraction of surface stones. Even greater dominance by litter can be anticipated at the many dryland sites where litter covers exceed those tested here. Copyright © 2002 John Wiley & Sons, Ltd. [source] Different Morphological Organic,Inorganic Hybrid Nanomaterials as Fluorescent Chemosensors and Adsorbents for CuII IonsEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 10 2008Soo Jin Lee Abstract Functionalized silica nanotubes (FSNT), functionalized mesoporous silica (FMS), and functionalized silica nanoparticles (FSNP-15) with an immobilized phenanthroline moiety as a fluorescent receptor were fabricated by a sol,gel reaction, and their binding abilities with metal ions were evaluated by fluorophotometry in water/acetonitrile (8:2, v/v) at pH 7. They selectively recognized Cu2+ ions among other metal cations such as Co2+, Cd2+, Hg2+, Ni2+, Fe3+, Ag+, Pb2+, and Zn2+, because the Cu2+ ion selectively binds to the nitrogen atoms of the phenanthroline moiety. Among the three silica nanomaterials with the immobilized receptor 1, the sensitivity of FSNT for Cu2+ ions is better than those of FMS and FSNP-15, indicating that the adsorption capacity for metal ions is dependent on the shape and surface area of the supporting nanomaterials. FSNT (10 mg) adsorb 75,% of the Cu2+ ions (2.0,×,10,4 mM) while FSNP-15 (10 mg) adsorb only 36,%. The detection limit of FSNT for Cu2+ ions was ca. 3.0,×,10,8M. FSNT and FMS can be easily renewed by treatment with a solution of HCl and tetrabutylammonium hydroxide. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source] A Novel Copper(I) Halide Framework Templated by Organic,Inorganic Hybrid Polyoxometalate Chains Formed In Situ: A New Route for the Design and Synthesis of Porous FrameworksEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 22 2006Hua Jin Abstract A 1D organic,inorganic hybrid polyoxometalate chain has been used as a non-coordinating anionic template for the construction of a novel 3D copper halide 4,4,-bipy framework, namely [Cu3ICl(4,4,-bipy)4][CuII(1,10-phen)2Mo8O26]. X-ray diffraction experiments revealed that the title compound consists of chloride-bridged trinuclear CuI units linked by neutral organic 4,4,-bipy groups into a 3D framework with hexagon-like channels in which 1D organic,inorganic hybrid polyoxometalate chains reside. This is the first example of a 1D organic,inorganic hybrid polyoxometalate chain functioning as a novel anionic template for the construction of a 3D framework. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006) [source] Nucleophilicities and Nucleofugalities of Organic Carbonates,EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 22 2010Nicolas Streidl Abstract The kinetics of the reactions of the methyl carbonate ion with benzhydrylium ions in acetonitrile have been studied by UV/Vis spectrophotometry. Substitution of the resulting second-order rate constants and the electrophilicity parameters E of the benzhydrylium ions into the linear free energy relationship log,k = s(N + E) yielded the nucleophilicity parameters N25 = 16.03 and s25 = 0.64 for methyl carbonate in acetonitrile. The kinetics of the reverse reactions, i.e., of the solvolyses of ring-substituted benzhydryl alkyl carbonates in different aqueous solvents were followed by conductimetry. The obtained first-order rate constants and the known electrofugality parameters Ef of benzhydrylium ions were used to determine the nucleofugality parameters Nf and sf of the ROCO2, groups by using the linear free energy relationship log,k = sf(Nf + Ef). The leaving group abilities of carbonates decrease by a factor of about 300 from PhOCO2, over MeOCO2, and iBuOCO2, to tBuOCO2, in various alcoholic and aqueous solvents. tert -Butyl carbonates (tBocO-R) are, thus, considerably more stable with respect to heterolytic cleavage of the O,R bond than other organic carbonates. [source] Synthesis and Physicochemical Characterization of meso -Functionalized Corroles: Precursors of Organic,Inorganic Hybrid MaterialsEUROPEAN JOURNAL OF ORGANIC CHEMISTRY, Issue 21 2005Jean-Michel Barbe Abstract Cobalt(III) corroles exhibit an infinite selectivity for the coordination of carbon monoxide towards dioxygen and dinitrogen. This peculiar property thus allows their use as sensing devices for CO detection. Here are described the syntheses and physico-chemical characterization of meso mono-, bis- and tris(triethoxysilyl)-functionalized corroles, precursors of organic,inorganic materials. The corrole ring formation was achieved in every case using the "2+1" method involving the reaction of two equivalents of an encumbered dipyrromethane with one equivalent of an aromatic aldehyde in the presence of a catalytic amount of trifluoroacetic acid. The functionalization of the corrole by triethoxysilyl chains was carried out by a condensation reaction of an isocyanate, bearing a triethoxysilyl termination, either on an amino or hydroxy group. Each final compound and intermediate were characterized by various physico-chemical techniques such as 1H NMR, UV/Vis, MALDI/TOF or EI mass spectrometry and elemental analysis. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005) [source] Retraction: Human telomeric G-quadruplex: targeting with small moleculesFEBS JOURNAL, Issue 5 2010Amit Arora Retraction: The following review from FEBS Journal, 'Human telomeric G-quadruplex: targeting with small molecules' by Amit Arora, Niti Kumar, Tani Agarwal and Souvik Maiti, published online on 27th November 2009 in Wiley InterScience (www.interscience.wiley.com), has been retracted by agreement between the authors, the journal Editor-in-Chief Professor Richard Perham and Blackwell Publishing Ltd. The retraction has been agreed due to overlap between this review and the following reviews: Published in Organic & Biomolecular Chemistry, 'A hitchhiker's guide to G-quadruplex ligands' by David Monchaud and Marie-Paule Teulade-Fichou. Volume 6 Issue 4, 2008, pages 627-636. Published in BioChimie, 'Targeting telomeres and telomerase' by Anne De Cian, Laurent Lacroix, Celine Douarre, Nassima Temime-Smaali, Chantal Trentesaux, Jean-Francois Riou and Jean-Louis Mergny. Volume 90 Issue 1, 2008, pages 131-155. [source] Ultrathin, Organic, Semiconductor/Polymer Blends by Scanning Corona-Discharge Coating for High-Performance Organic Thin-Film TransistorsADVANCED FUNCTIONAL MATERIALS, Issue 17 2010Hee Joon Jung Abstract A new thin-film coating process, scanning corona-discharge coating (SCDC), to fabricate ultrathin tri-isopropylsilylethynyl pentacene (TIPS-PEN)/amorphous-polymer blend layers suitable for high-performance, bottom-gate, organic thin-film transistors (OTFTs) is described. The method is based on utilizing the electrodynamic flow of gas molecules that are corona-discharged at a sharp metallic tip under a high voltage and subsequently directed towards a bottom electrode. With the static movement of the bottom electrode, on which a blend solution of TIPS-PEN and an amorphous polymer is deposited, SCDC provides an efficient route to produce uniform blend films with thicknesses of less than one hundred nanometers, in which the TIPS-PEN and the amorphous polymer are vertically phase-separated into a bilayered structure with a single-crystalline nature of the TIPS-PEN. A bottom-gate field-effect transistor with a blend layer of TIPS-PEN/polystyrene (PS) (90/10 wt%) operated at ambient conditions, for example, indeed exhibits a highly reliable device performance with a field-effect mobility of approximately 0.23 cm2 V,1 s,1: two orders of magnitude greater than that of a spin-coated blend film. SCDC also turns out to be applicable to other amorphous polymers, such as poly(, -methyl styrene) and poly(methyl methacrylate) and, readily combined with the conventional transfer-printing technique, gives rise to micropatterned arrays of TIPS-PEN/polymer films. [source] Electronic Structure and Geminate Pair Energetics at Organic,Organic Interfaces: The Case of Pentacene/C60 HeterojunctionsADVANCED FUNCTIONAL MATERIALS, Issue 23 2009Stijn Verlaak Abstract Organic semiconductors are characterized by localized states whose energies are predominantly determined by electrostatic interactions with their immediate molecular environment. As a result, the details of the energy landscape at heterojunctions between different organic semiconductors cannot simply be deduced from those of the individual semiconductors, and they have so far remained largely unexplored. Here, microelectrostatic computations are performed to clarify the nature of the electronic structure and geminate pair energetics at the pentacene/C60 interface, as archetype for an interface between a donor molecule and a fullerene electron acceptor. The size and orientation of the molecular quadrupole moments, determined by material choice, crystal orientation, and thermodynamic growth parameters of the semiconductors, dominate the interface energetics. Not only do quadrupoles produce direct electrostatic interactions with charge carriers, but, in addition, the discontinuity of the quadrupole field at the interface induces permanent interface dipoles. That discontinuity is particularly striking for an interface with C60 molecules, which by virtue of their symmetry possess no quadrupole. Consequently, at a pentacene/C60 interface, both the vacuum-level shift and geminate pair dissociation critically depend on the orientation of the pentacene ,-system relative to the adjacent C60. [source] Functional Chromium Wheel-Based Hybrid Organic,Inorganic Materials for Dielectric ApplicationsADVANCED FUNCTIONAL MATERIALS, Issue 20 2009Vito Di Noto Abstract The first example of organic,inorganic hybrid materials based on the embedding of a chromium,nickel wheel cluster {[(n-C3H7)2NH2]- [Cr7NiF8(O2C4H5)16]} (Cr7Ni) into poly(methyl methacrylate) (PMMA) and the characterization of the dielectric properties of the obtained material is described. By an optimized copolymerization of the methacrylate-functionalized chromium,nickel wheel with methyl methacrylate in a cluster/monomer 1:200 molar mixture, a homogeneous hybrid material CrNi_MMA200 is obtained. The electrical responses of the non-doped PMMA and of the hybrid material were studied by broadband dielectric spectroscopy (BDS) from 0.01,Hz to 10,MHz and over the temperature range of 5,115,°C. The permittivity profiles reveal two relaxation peaks in the materials, which correspond to the , and , relaxation modes of the PMMA matrix. The position of these modes shifts toward higher frequencies as temperature increases. BDS is a powerful tool revealing the intimate miscibility of the various components of the hybrid material, thus indicating that, on a molecular scale, the material proposed is a homogeneous system. Finally, a value of the dielectric constant of 2.9 at 25,°C and 1,kHz is determined. This value is noticeably lower than the value of 3.2 obtained for pristine PMMA prepared following the same synthesis protocol. Thus, these results classify the hybrid CrNi_MMA200 as an appealing starting material for the development of dielectric polymeric layers for the development of innovative capacitors, transistors, and other microelectronic devices. The vibrational properties of the hybrid materials are investigated by Fourier-transform infrared (FT-IR) and Raman spectroscopy, whereas the thermal behavior is analyzed by thermogravimetric analysis (TGA). Swelling experiments are used to qualitatively evaluate the crosslinking density of the hybrid materials. The integrity of the wheels once embedded in the macromolecular backbone is confirmed by extended X-ray absorption fine structure (EXAFS) and electron spin resonance (EPR) spectroscopic measurements. [source] Hybrid Nanofiber Growth: One-Pot Synthesis of Functional Helicoidal Hybrid Organic,Inorganic Nanofibers with Periodically Organized Mesoporosity (Adv. Funct.ADVANCED FUNCTIONAL MATERIALS, Issue 18 2009Mater. Luminescent nanofibers are grown with controlled alignment of twisted nanochannels, as described by K. Valle and co-workers on page 2896. Tuning of the main synthesis parameters (sol-gel conditions, temperatures, choice of surfactants and inorganic precursors) allows the fine control of morphology, porosity-architecture, and organic chemical functionalization in order to prepare useful functional nanofibers. [source] One-Pot Synthesis of Functional Helicoidal Hybrid Organic,Inorganic Nanofibers with Periodically Organized MesoporosityADVANCED FUNCTIONAL MATERIALS, Issue 18 2009Frédéric Rambaud Abstract The one-pot synthesis and properties of multifunctional hybrid mesoporous organosilica fibers with helical shapes are described. These hybrid mesoporous fibers are prepared without chiral elements and functionalized with a large variety of organic R functions (R,=,alkylthiols, phenylsulfonates, alkylphosphonates, dansyl, aminopropyl, fluoroalkyl, etc.). The resulting nanomaterials are thoroughly characterized by a variety of techniques. The use of a synergetic combination of achiral molecules as co-directing structuring agents, a surfactant, and an organofunctional silica precursor R-Si(OR)3 allows, via carefully tuning of the main synthesis parameters and processing conditions, to control the shape, which is the anisotropic factor, of the hybrid nanofibers. The functionalization of the hybrid materials with fluorescent molecules (dansyl) and gold nanoparticles opens possibilities for sensor and catalytic applications, respectively. Moreover, these hybrid nanofibers can be easily transferred in organic solvents or in a "green" solvent such as water to make stable colloidal dispersions. This tunable functionality of nanofibers also allows their transferability into a variety of polymeric hosts (PVDF, PVBu, and PVP) allowing the formation of functional homogeneous nanocomposite hybrid membranes. [source] Rewritable Holographic Structures Formed in Organic,Inorganic Hybrid Materials by Photothermal ProcessingADVANCED FUNCTIONAL MATERIALS, Issue 16 2009Hiroshi Kakiuchida Abstract Holographic and direct-written structures are fabricated in tin-doped silicophosphite thin plates containing rhodamine 6G dye by a photothermal process based on the principle of glass softening/frozen-in behavior. To be highly processable by photothermal treatment and stable at room temperature after processing, the intrinsic viscoelastic property is improved by increasing the crosslinking density of the network structure, and the photothermal conditions for efficient transfer of the irradiated photons to thermal phonons are explored. Then, the excellent rewritability and reliability of the fine processed structure are found by examining the writing/erasing repetition. Furthermore, the origins of the changes in refractive index due to photothermal treatment are classified into density change and photobleaching, and the dynamics of the formation process of holographic gratings are studied by measuring refractive index changes as functions of irradiation time and wavelength. As a result, it is found that the holographic structure consists of spatial modulation of the refractive index and the refractive index change results primarily from the change in the frozen structure, although there is a slight influence by photobleaching. [source] Optically-Pumped Lasing in Hybrid Organic,Inorganic Light-Emitting DiodesADVANCED FUNCTIONAL MATERIALS, Issue 13 2009Myoung Hoon Song Abstract Here, the use of metal oxide layers both for charge transport and injection into an emissive semiconducting polymer and also for the control of the in-plane waveguided optical modes in light-emitting diodes (LEDs) is reported. The high refractive index of zinc oxide is used to confine these modes away from the absorbing electrodes, and include a nano-imprinted grating in the polymer layer to introduce distributed feedback and enhance optical out-coupling. These structures show a large increase in the luminescence efficiency over conventional devices, with photoluminescence efficiency increased by up to 45%. Furthermore, optically-pumped lasing in hybrid oxide polymer LEDs is demonstrated. A tuneable lasing emission is also obtained in a single device structure by employing a graduated thickness of a zinc oxide inter-layer. This demonstrates the scope for using such architectures to improve the external efficiency of organic semiconductor LEDs, and opens new possibilities for the realization of polymer injection lasers. [source] Temperature Responsive Solution Partition of Organic,Inorganic Hybrid Poly(N -isopropylacrylamide)-Coated Mesoporous Silica Nanospheres,ADVANCED FUNCTIONAL MATERIALS, Issue 9 2008Po-Wen Chung Abstract A series of poly(N -isopropylacrylamide)-coated mesoporous silica nanoparticle materials (PNiPAm-MSNs) has been synthesized by a surface-initiated living radical polymerization with a reversible addition,fragmentation chain transfer (RAFT) reaction. The structure and the degree of polymerization of the PNiPAm-MSNs has been characterized by a variety of techniques, including nitrogen sorption analysis, 29Si and 13C solid-state NMR spectroscopy, transmission electron microscopy (TEM), and powder X-ray diffraction (XRD). The thermally induced changes of the surface properties of these polymer-coated core,shell nanoparticles have been determined by examining their partition activities in a biphasic solution (water/toluene) at different temperatures. [source] Self-Assembled Organic,Inorganic Hybrid Elastic Crystal via Biomimetic MineralizationADVANCED MATERIALS, Issue 33 2010Halei Zhai Organic,inorganic hybrid rhombs with regular shape and a lamellar superstructure are biomimetically fabricated by the cooperative self-assembly of bovine serum albumin (BSA), sodium bis-2-ethylhexyl sulfosuccinate (AOT), and calcium phosphate (see figure). Although crystalline calcium phosphate is the main component, the hybrid crystals are elastic and they can be flexible under external stresses. [source] Accounting for Interference, Scattering, and Electrode Absorption to Make Accurate Internal Quantum Efficiency Measurements in Organic and Other Thin Solar CellsADVANCED MATERIALS, Issue 30 2010George F. Burkhard Accurately measuring internal quantum efficiency requires knowledge of absorption in the active layer of a solar cell. The experimentally accessible total absorption includes significant contributions from the electrodes and other non-active layers. We suggest a straightforward method for calculating the active layer contribution that minimizes error by subtracting optically-modeled electrode absorption from experimentally measured total absorption. [source] MnII(TCNE)3/2(I3)1/2,A 3D Network-Structured Organic-Based Magnet and Comparison to a 2D AnalogADVANCED MATERIALS, Issue 23 2010Kevin H. Stone MnII(TCNE)3/2(I3)1/2 and MnII(TCNE)[C4(CN)8]1/2 [tetracyanoethylene (TCNE)] are organic-based magnets with 3D and 2D extended network structures with vastly different magnetic behavior. They have similar ferrimagnetic coupled layers of MnII(TCNE),, with different interlayer couplings, which lead, respectively, to net ferrimagnetic (Tc,=,171,K) and antiferromagnetic (Tc,=,68,K) order. [source] Phosphorescent Hybrid Organic,Inorganic Light-Emitting DiodesADVANCED MATERIALS, Issue 19 2010Henk J. Bolink Competitive efficacy and power conversion efficiency (15,cd,A,1 and above 9,lm,W,1, respectively) are obtained for a hybrid organic,inorganic light-emitting diode (HyLED) with air-stable metal oxides as electrodes. Thanks to the use of a phosphorescent iridium complex and a Cs-doped ZnO cathode, performances approaching those of standard solution-processed organic LEDs can be obtained. [source] Nanostructured Organic,Inorganic Composite Materials by Twin Polymerization of Hybrid MonomersADVANCED MATERIALS, Issue 20 2009Stefan Spange Abstract Forming two structurally different but associated polymer structures in a single step is a possible route for the production of nanostructured materials. By means of twin polymerization of specially constructed monomers consisting of two different covalently bonded building blocks (hybrid monomers), this route is realized. What is important is that two different macromolecular structures are formed from one monomer in a single process. The two polymers formed can be linear, branched, or cross-linked structures. The molecular composition of the hybrid monomer defines the degree of cross-linking of the corresponding macromolecular structures that is theoretically possible. [source] Organic,Inorganic Sol,Gel Composites Incorporating Semiconductor Nanocrystals for Optical Gain ApplicationsADVANCED MATERIALS, Issue 17 2009Miri Kazes Organic-inorganic sol-gel composite incorporating highly emitting CdSe/ZnS quantum dots and CdSe/CdS/ZnS quantum rods is reported. Optical gain measurements conducted on a quantum rod/sol-gel composite film show stable room temperature amplified spontaneous emission under ambient conditions. [source] Metal-Containing Carbon Nitride Compounds: A New Functional Organic,Metal Hybrid MaterialADVANCED MATERIALS, Issue 16 2009Xinchen Wang The electronic and optical functions of polymeric C3N4 can be easily modified by the inclusion of metal species such as Fe in its structure. The metal species lowers the bandgap and expands the light absorption of the material further into the visible region of the electromagnetic spectrum, while keeping a sufficient overpotential for carrying out oxidation reactions. [source] Self-Assembly: Molecular Self-Assembled Monolayers and Multilayers for Organic and Unconventional Inorganic Thin-Film Transistor Applications (Adv. Mater.ADVANCED MATERIALS, Issue 14-15 200915/2009) A self-assembled monolayer (SAM) of azo stillbazolium sandwiched between two conductive electrodes is shown. The upper and lower electrodes are doped silicon and a Hg drop, respectively, a configuration often used for measuring the conductivity of SAMs and multilayers of hybrid organic and inorganic materials. The evaluation and implementation of these unconventional materials in complex device architectures is highlighted in the review on page 1407 by Sara DiBenedetto et al. [source] Molecular Self-Assembled Monolayers and Multilayers for Organic and Unconventional Inorganic Thin-Film Transistor ApplicationsADVANCED MATERIALS, Issue 14-15 2009Sara A. DiBenedetto Abstract Principal goals in organic thin-film transistor (OTFT) gate dielectric research include achieving: (i) low gate leakage currents and good chemical/thermal stability, (ii) minimized interface trap state densities to maximize charge transport efficiency, (iii) compatibility with both p- and n- channel organic semiconductors, (iv) enhanced capacitance to lower OTFT operating voltages, and (v) efficient fabrication via solution-phase processing methods. In this Review, we focus on a prominent class of alternative gate dielectric materials: self-assembled monolayers (SAMs) and multilayers (SAMTs) of organic molecules having good insulating properties and large capacitance values, requisite properties for addressing these challenges. We first describe the formation and properties of SAMs on various surfaces (metals and oxides), followed by a discussion of fundamental factors governing charge transport through SAMs. The last section focuses on the roles that SAMs and SAMTs play in OTFTs, such as surface treatments, gate dielectrics, and finally as the semiconductor layer in ultra-thin OTFTs. [source] Lanthanide-Containing Light-Emitting Organic,Inorganic Hybrids: A Bet on the FutureADVANCED MATERIALS, Issue 5 2009Luís D. Carlos Abstract Interest in lanthanide-containing organic,inorganic hybrids has grown considerably during the last decade, with the concomitant fabrication of materials with tunable attributes offering modulated properties. The potential of these materials relies on exploiting the synergy between the intrinsic characteristics of sol,gel derived hosts (highly controlled purity, versatile shaping and patterning, excellent optical quality, easy control of the refractive index, photosensitivity, encapsulation of large amounts of isolated emitting centers protected by the host) and the luminescence features of trivalent lanthanide ions (high luminescence quantum yield, narrow bandwidth, long-lived emission, large Stokes shifts, ligand-dependent luminescence sensitization). Promising applications may be envisaged, such as light-emitting devices, active waveguides in the visible and near-IR spectral regions, active coatings, and bio-medical actuators and sensors, opening up exciting directions in materials science and related technologies with significant implications in the integration, miniaturization, and multifunctionalization of devices. This review provides an overview of the latest advances in Ln3+ -containing siloxane-based hybrids, with emphasis on the different possible synthetic strategies, photoluminescence features, empirical determination [source] Nanomechanical Properties of Bioinspired Organic,Inorganic Composite Films,ADVANCED MATERIALS, Issue 7 2007Z. Burghard Nacre-like thin films are fabricated via a bioinspired route combining chemical bath deposition of the inorganic component (TiO2) and layer-by-layer alternate adsorption of oppositely charged polyelectrolytes for the organic component (see figure). Nanoindentation testing revealed an increase in hardness and Young's modulus imparted by the alternate-layer architecture of the composite films. [source] Organic Heteroepitaxy: p -Sexiphenyl on Uniaxially Oriented ,-Sexithiophene,ADVANCED MATERIALS, Issue 18 2006M. Oehzelt Organic,organic heteroepitaxy using two rodlike aromatic molecules shows that p -sexiphenyl aligns predominantly parallel to an underlying uniaxially oriented ,-sexithiophene film (see figure) although there is no lattice match of the two layers. The structure of both layers is determined and the results suggest that a simple transfer of the well-established models of inorganic epitaxy cannot explain the heterostructures formed here. [source] Super-Stable, High-Quality Fe3O4 Dendron,Nanocrystals Dispersible in Both Organic and Aqueous SolutionsADVANCED MATERIALS, Issue 11 2005M. Kim High-quality Fe3O4 nanocrystals coated with stearate groups are successfully converted to dendron-coated nanocrystals (dendron,nanocrystals). Poly(ethylene glycol) oligomers are used as major terminal groups for the dendron ligands, which afford excellent dispersibility of the dendron,nanocrystals in a broad spectrum of solvents, ranging from dichloromethane to water (see Figure). [source] Why Isn't More US Farmland Organic?JOURNAL OF AGRICULTURAL ECONOMICS, Issue 2 2010Nicolai V. Kuminoff D81; Q18 Abstract We develop a theoretical model to assess the dollar compensation required to induce conventional growers to convert to organic. The model incorporates the uncertainty in producers' expectations about future returns and about the impact of policy changes on these expectations in particular. We demonstrate that a new policy which favours organic can have opposing effects on the rate of conversion. An increase in relative returns to organic today will increase conversion rates. However, if the future of the policy programme is uncertain, its introduction can increase the value of waiting to switch, which will decrease conversion rates. We then develop an empirical switching regression model that enables direct estimation of the value associated with being able to postpone the conversion decision until some of the uncertainty is resolved. The model is applied to data on organic and conventional soybeans before and after major changes in US farm policy toward organic growers. The results suggest that sunk costs associated with conversion to organic coupled with uncertainty about future returns can help to explain why there is so little organic farmland in the USA. [source] | |||||||||||||||||||||||||||||||||||||||||||||||||||||||