Home About us Contact
|
Home About us Contact | ||
|
|
||
Polymeric
Terms modified by Polymeric Selected AbstractsPolymeric, Molecular, and Cation/Anion Arrangements in Chloro-, Bromo-, and Iododiruthenium(II,III) Carboxylate CompoundsEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 12 2003M. Carmen Barral Abstract The synthesis and characterization of the anhydrous compounds [Ru2X(,-O2CR)4] [R = CH2CH2OPh, X = Cl (1a), Br (2a), I (3a); R = CMePh2, X = Br (5a), I (6a)] and of the solvated complexes [Ru2X(,-O2CR)4(H2O)] [R = CH2CH2OPh, X = Cl (1b), I (3b); R = CMePh2, X = Cl (4b), Br (5b), I (6b)] are described. Thermogravimetric analyses have been used to confirm the anhydrous or solvated natures of the complexes. The crystal structures of 1b·2MeOH, 3b·0.5H2O, and 4b have been investigated by X-ray diffraction and none of them shows the usual polymeric arrangement reported for tetracarboxylatodiruthenium(II,III) compounds. The structure of 3b·0.5H2O consists of cationic and anionic units, [Ru2(,-O2CCH2CH2OPh)4(H2O)2][Ru2I2(,-O2CCH2CH2OPh)4], and represents the first reported crystal structure of a tetracarboxylato(iodo)diruthenium(II,III) derivative. The structures 1b·2MeOH and 4b each show the presence of discrete dinuclear molecules. The crystal structure of [Ru2Cl(,-O2CCMePh2)4(H2O)] demonstrates that diruthenium compounds with the same halide and carboxylate ligands may adopt polymeric or discrete molecular dispositions. Magnetic susceptibility measurements of the complexes in the 2,300 K range have been carried out. Complex 2a shows a strong antiferromagnetic coupling, consistent with the existence of linear chains in the solid state. The complexes [Ru2X(,-O2CR)4(H2O)] show weak through-space antiferromagnetic coupling, in accordance with non-polymeric structures. The magnetic behaviour of 1a, 3a, 5a, and 6a suggests a mixture of arrangements. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003) [source] Red-Emitting Polyfluorenes Grafted with Quinoline-Based Iridium Complex: "Simple Polymeric Chain, Unexpected High Efficiency"ADVANCED FUNCTIONAL MATERIALS, Issue 1 2010Zhihua Ma Abstract A series of red-light emitting electrophosphorescent polyfluorenes (PFs) with varying content of a quinoline-based iridium complex, (PPQ)2Ir(acac) (bis(2,4-diphenylquinolyl-N,C2,) iridium(acetylacetonate)), in the side chain are synthesized by Suzuki polycondensation. Because of the efficient Förster energy transfer from the PF main chain to (PPQ)2Ir(acac) and direct charge trapping on the complex, the electroluminescent emission from PF is nearly completely quenched, even though the amount of iridium complex incorporated into the polymers is as low as 1,mol %. Based on a single-layer device configuration, a luminous efficiency of up to 5.0,cd A,1 with a luminance of 2000,cd m,2 and Commission Internationale de L'Eclairage coordinates of (0.63, 0.35) (x, y) is realized, which is far superior to that of previously reported red-light emitting PFs containing benzothiazole- and isoquinoline-based iridium complexes. This result is beyond expectations, especially when considering that the simple polymeric chain involved has no additional charge-transporting moieties. Noticeably, the device efficiency remains as high as 4.2,cd A,1 with a luminance of 4000,cd m,2 even at current densities of 100,mA cm,2. Further optimization of the device configuration by incorporating an additional electron-injection layer leads to improved efficiencies of 8.3 and 7.5,cd A,1 at luminances of 100 and 1000,cd m,2, respectively. This state-of-the-art performance indicates that covalently attaching quinoline-based iridium complexes to a PF backbone is a simple and effective strategy to develop high-efficiency red-light emitting electrophosphorescent polymers. [source] Loss of tocopherols and formation of degradation compounds at frying temperatures in oils differing in degree of unsaturation and natural antioxidant contentJOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE, Issue 14 2002Daniel Barrera-Arellano Abstract Samples of oils of different degrees of unsaturation, namely palm olein, olive oil, high-linoleic sunflower oil, high-oleic sunflower oil, rapeseed oil and soybean oil, were heated at 180,°C for 2, 4, 6, 8 and 10,h in the presence or absence of their natural antioxidants. Also, tocopherol-stripped oils were supplemented with ,-tocopherol (500,mg,kg,1), ,-tocopherol (500,mg,kg,1) or a mixture of ,-, ,-, ,- and ,-tocopherols (250,mg,kg,1 each) and heated under the same conditions. Losses of tocopherols and formation of polymeric triacylglycerols were followed. Total polar compounds were also evaluated after 10,h of heating. Results demonstrated that tocopherols were lost very rapidly, in the expected order, with ,-tocopherol being the least stable. Polymeric and polar compound formation during heating was inhibited to a variable extent, being more dependent on the natural content and type of tocopherols than on the degree of unsaturation of the oil. For example, polymeric and polar compound contents in soybean oil were significantly lower than those found in high-linoleic sunflower oil. However, the expected influence of the degree of unsaturation was evident when oils were unprotected or possessed identical initial antioxidant contents. Finally, levels of degradation compounds after 10,h of heating were not dependent on the remaining content of antioxidants. © 2002 Society of Chemical Industry [source] Polymeric (,2 -nitrato-,2O:O,)(,2 -nitrato-,2O:O)(,4 -pyridinium-4-thiolato-,4S:S:S:S)disilver(I)ACTA CRYSTALLOGRAPHICA SECTION C, Issue 6 2004Yu-Biao Chen The title compound, [Ag2(NO3)2(C5H5NS)]n, was obtained from the reaction of silver nitrate with bis(4-pyridyl) disufide (4-PDS) in a mixture of ethanol and water, which suggests that the disulfide bond of 4-PDS can be cleaved under mild conditions. The structure of the title compound is a two-dimensional infinite array in which the asymmetric unit contains two Ag atoms, a pyridinium-4-thiolate molecule and two nitrate groups. Each pyridinium-4-thiolate molecule acts as a ,4 bridge, linking four Ag atoms, with Ag,S bond distances of 2.4870,(19), 2.5791,(19), 2.5992,(19) and 2.848,(2),Å. The Ag,Ag distances lie in the range 2.889,(2),3.049,(1),Å. [source] Construction of New Heteroselenometallic Clusters: Formation of Crownlike [Et4N]4 [(,5 -WSe4)(CuI)5(,-I)2] and Octahedral Polymeric [(,6 -WSe4)Cu6I4 (py)4]n from Planar [Et4N]4 [(,4 -WSe4)Cu4I6] with Additional Faces.CHEMINFORM, Issue 38 2006Qian-Feng Zhang Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source] Recyclable Polymeric ,-Acid Catalyst Effective on Mannich-Type Reaction in Water.CHEMINFORM, Issue 31 2006Yukio Masaki Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source] Crystal Structure and Excited Optical Nonlinearity of a 1D Polymeric [W2O2S6Cu4(NCMe)4] n Cluster.CHEMINFORM, Issue 38 2004Hegen Zheng Abstract For Abstract see ChemInform Abstract in Full Text. [source] ChemInform Abstract: Bromoplumbates with One-Dimensional Polymeric and Isolated Anions: (Bn4P)2[Pb3Br8], (Bn4P)2 [Pb3Br8(dmf)2], (Bn4P)[PbBr3], (Bn4P)2[PbBr4], and (Bn4P)4[Pb2Br4].CHEMINFORM, Issue 12 2002Henriette Groeger Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source] Rationally Designed, Polymeric, Extended Metal,Ciprofloxacin ComplexesCHEMISTRY - A EUROPEAN JOURNAL, Issue 22 2005Dong-Rong Xiao Dr. Abstract Reactions of the antimicrobial fluoroquinolone ciprofloxacin (cfH) with metal salts in the presence of aromatic polycarboxylate ligands or under basic conditions produce fourteen new metal,cfH complexes, namely, [Ba2(cf)2(1,4-bdc)(H2O)2],H2O (1), [Sr6(cf)6(1,4-bdc)3(H2O)6],2,H2O (2), [M2(cfH)2(bptc)(H2O)2],8,H2O (M = Mn(3) and Cd(4)), [M(cfH)(1,3-bdc)] (M = Mn(5), Co(6), and Zn(7)), [Zn2(cfH)4(1,4-bdc)](1,4-bdc),13,H2O (8), [Ca(cfH)2(1,2-Hbdc)2],2,H2O (9) and [M(cf)2],2.5,H2O (M = Mn(10), Co(11), Zn(12), Cd(13), and Mg(14)) (1,4-bdc = 1,4-benzenedicarboxylate, bptc = 3,3,,4,4,-benzophenonetetracarboxylate, 1,3-bdc = 1,3-benzenedicarboxylate, 1,2-bdc = 1,2-benzenedicarboxylate). Their structures were determined by single-crystal X-ray diffraction analyses and further characterized by elemental analyses, IR spectra, and thermogravimetric analyses. The structures of 1 and 2 consist of unique two-dimensional arm-shaped layers. Compounds 3 and 4 are isostructural and feature one-dimensional structures formed from the interconnection of [M2(cfH)2(H2O)2] dimers with bptc ligands. Compounds 5,7 are isostructural and contain double-chain-like ribbons constructed from [M2(cfH)2(CO2)2] dimers and 1,3-bdc. Compound 8 consists of a pair of [Zn(cfH)2]2+ fragments bridged by a 1,4-bdc into a dinuclear dumbbell structure. Compound 9 is a neutral monomeric complex. To the best of our knowledge, compounds 1,9 are the first examples of metal-quinolone complexes that contain aromatic polycarboxylate ligands. Compounds 10,14 are isostructural and exhibit interesting two-dimensional rhombic grids featuring large cavities with dimensions of 13.6×13.6 Å. Up to now, polymeric extended metal,cfH complexes have never been reported. [source] Influence of Metal Nanoparticles on the Electrocatalytic Oxidation of Glucose by Poly(NiIIteta) Modified ElectrodesELECTROANALYSIS, Issue 5 2010Pratap Azad Abstract Conductive polymeric [NiII(teta)]2+ (teta=C-meso-5,5,7,12,12,14-hexamethyl-1,4,8,11-tetra-azacyclotetradecane) films (poly(Ni)) have been deposited on the surface of glassy carbon (GC), Nafion (Nf) modified GC (GC/Nf) and Nf stabilized Ag and Au nanoparticles (NPs) modified GC (GC/Ag-Nf and GC/Au-Nf) electrodes. The cyclic voltammogram of the resulting electrodes, show a well defined redox peak due to oxidation and reduction of poly(Ni) system in 0.1,M NaOH. They show electrocatalytic activity towards the oxidation of glucose. AFM studies reveal the formation of poly(Ni) film on the modified electrodes. Presence of metal NPs increases electron transfer rate and electrocatalytic oxidation current by improving the communication within the Nf and poly(Ni) films. In the presence of metal NPs, 4 fold increase in current for glucose oxidation was observed. [source] Nucleophilic Addition of Water and Alcohols to Dicyanonitrosomethanide: Ligands with Diverse Bonding Modes in Magnetically Coupled d-Block ComplexesEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 1 2010Anthony S. R. Chesman Abstract Ligands resulting from the transition-metal-promoted nucleophilic addition of water or an alcohol to dicyanonitrosomethanide ions (dcnm) have been utilised in the formation of a large series of polynuclear complexes. Addition of water to dcnm results in formation of carbamoylcyanonitrosomethanide (ccnm); deprotonation of this ligand gives amidocarbonyl(cyano)nitrosomethanide (acnm), which has been incorporated into the trinuclear complex [Cu3(acnm)2(dmae)2(H2O)2] [dmae = 2-(dimethylamino)ethoxide] (1) which shows strong antiferromagnetic coupling with an exchange coupling constant, J = ,500 cm,1. [Cu(acnm)(NH3)2], (2) marks the first instance of acnm facilitating the formation of a coordination polymer, namely a 1D chain with intramolecular hydrogen bonding. Attempts to synthesise 2 through different reaction conditions instead resulted in the mononuclear [Cu(acnm)(NH3)2(py)] (py = pyridine) (3). The addition of ethanol to dcnm results in cyano[imino(ethoxy)methyl]nitrosomethanide (cenm) which features in the mononuclear [Cu(cenm)2(H2O)2] (4) and polymeric {[Cu(cenm)2]2·H2O}, (5). The latter is the first example of the cenm ligand in a coordination polymer and has a highly unusual coordination mode through the nitrile groups and extremely weak antiferromagnetic coupling. {[Mn3(ccnm)2(EtOH)2(OAc)4]·2EtOH}, (6) and (Et4N)2[Cu(ccnm)4] (7) contain previously unobserved coordination modes of the ccnm ligand while the complex [Mn(cmnm)3Mn(bipy)(MeOH)](ClO4) (8) {cmnm = cyano[imino(methoxy)methyl]nitrosomethanide, bipy = 2,2,-bipyridine} displays weak antiferromagnetic coupling between manganese atoms with J = ,1.44 cm,1. A change in the solvent systems used in the synthesis of 7 results in the formation of the mononuclear complexes [Mn(bipy)2(dcnm)2] (9) or [Mn(bipy)2(H2O)(dcnm)](dcnm)·H2O (10) and [Mn(bipy)2(dcnm)(H2O)](dcnm) (11). The addition of ethlyene glycol monomethyl ether to dcnm gives cyano[imino(2-methoxyethoxy)methyl]nitrosomethanide (cgnm) and the formation of [Cu(cgnm)2(H2O)2] (12). [source] Polymeric, Molecular, and Cation/Anion Arrangements in Chloro-, Bromo-, and Iododiruthenium(II,III) Carboxylate CompoundsEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 12 2003M. Carmen Barral Abstract The synthesis and characterization of the anhydrous compounds [Ru2X(,-O2CR)4] [R = CH2CH2OPh, X = Cl (1a), Br (2a), I (3a); R = CMePh2, X = Br (5a), I (6a)] and of the solvated complexes [Ru2X(,-O2CR)4(H2O)] [R = CH2CH2OPh, X = Cl (1b), I (3b); R = CMePh2, X = Cl (4b), Br (5b), I (6b)] are described. Thermogravimetric analyses have been used to confirm the anhydrous or solvated natures of the complexes. The crystal structures of 1b·2MeOH, 3b·0.5H2O, and 4b have been investigated by X-ray diffraction and none of them shows the usual polymeric arrangement reported for tetracarboxylatodiruthenium(II,III) compounds. The structure of 3b·0.5H2O consists of cationic and anionic units, [Ru2(,-O2CCH2CH2OPh)4(H2O)2][Ru2I2(,-O2CCH2CH2OPh)4], and represents the first reported crystal structure of a tetracarboxylato(iodo)diruthenium(II,III) derivative. The structures 1b·2MeOH and 4b each show the presence of discrete dinuclear molecules. The crystal structure of [Ru2Cl(,-O2CCMePh2)4(H2O)] demonstrates that diruthenium compounds with the same halide and carboxylate ligands may adopt polymeric or discrete molecular dispositions. Magnetic susceptibility measurements of the complexes in the 2,300 K range have been carried out. Complex 2a shows a strong antiferromagnetic coupling, consistent with the existence of linear chains in the solid state. The complexes [Ru2X(,-O2CR)4(H2O)] show weak through-space antiferromagnetic coupling, in accordance with non-polymeric structures. The magnetic behaviour of 1a, 3a, 5a, and 6a suggests a mixture of arrangements. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003) [source] The effect of polymers and surfactants on the pour point of palm oil methyl estersEUROPEAN JOURNAL OF LIPID SCIENCE AND TECHNOLOGY, Issue 4 2007Cheah Han Sern Abstract The objective of this research was to find some additives suitable to reduce the pour point (PP) of palm oil methyl esters. The PP properties of palm oil methyl esters (biodiesel) were evaluated with commercially available polymeric and surfactant compounds with various polarities, molecular sizes and structures. The compounds under study were poly(ethylene glycol), poly(methyl methacrylate), poly(ethylene-co-vinyl acetate), poly(styrene-co-maleic anhydride), poly(ethylene glycol) distearate, poly-(octadecyl methacrylate), poly(1-decene), poly(maleic anhydride- alt -1-octadecene), caprylic acid sodium salt, N -lauroylsarcosine sodium salt, polyoxyethylene(2) cetyl ether and polyoxyethylene(10) cetyl ether. Seven out of the twelve polymeric compounds tested were miscible in palm oil methyl esters due to similar polarities of the solute and biodiesel. The blends of the resultant seven polymeric compounds in palm oil methyl esters were evaluated respectively for their effect on the PP property. Poly-(maleic anhydride- alt -1-octadecene) was able to improve the PP of palm oil methyl esters from 12 to 6,°C when 2,wt-% was added. The cloud point was reduced from 12.9 to 8.1,°C, and the cold filter plugging point was reduced from 12 to 7,°C, whilst the flash point value remained unchanged at 156,°C when 2,wt-% of poly(maleic anhydride- alt -1-octadecene) was added to the palm oil methyl esters. [source] Stem Cell Aligned Growth Induced by CeO2 Nanoparticles in PLGA Scaffolds with Improved Bioactivity for Regenerative MedicineADVANCED FUNCTIONAL MATERIALS, Issue 10 2010Corrado Mandoli Abstract Hybrid 2D polymeric,ceramic biosupports are fabricated by mixing a nanostructured CeO2 powder with 85:15 poly(D,L -lactic- co -glycolic acid) (PLGA)/dichloromethane solutions at specific concentrations, followed by solvent casting onto pre-patterned molds. The mold patterning allows the orientation of ceramic nanoparticles into parallel lines within the composite scaffold. The ability of the produced films to host and address cell growth is evaluated after 1, 3, and 6 days of culturing with murine derived cardiac and mesenchymal stem cells (CSCs and MSCs), and compared with PLGA films without ceramics and loaded with nanostructured TiO2. Aligned cell growth is observed only for scaffolds that incorporate oriented ceramic nanoparticles, attributed to the nanoceramic ability to modulate the roughness pitch, thus improving cell sensitivity towards the host surface features. Better CSC and MSC proliferative activity is observed for CeO2 composites with respect to either TiO2 -added or unfilled PLGA films. This evidence may be related to the nanostructured CeO2 antioxidative properties. [source] Cone calorimeter testing of S2 glass reinforced polymer compositesFIRE AND MATERIALS, Issue 7 2009Alexander B. Morgan Abstract With the ever increasing demand for fuel savings on vehicles, there is a strong push to replace metal with polymeric + fiber (carbon/glass) composites. However, the replacement of metal with polymeric composites can lead to additional fire risk. Our study focused on glass fiber reinforced polymer composites meant for vehicular structural applications, and flammability performance of these composites was studied by cone calorimetery. The effects of fiberglass loading, nanocomposite use (clay, carbon nanofiber) and polymer type (epoxy, phenolic) were studied under a heat flux of 50kW/m2 to better understand the potential effects that these variables would have on material flammability. It was found that as fiberglass loading increased, flammability decreased, but at a cost to structural integrity of the residual polymer + fiber char. The use of nanocomposites has little effect on reducing flammability in this set of samples, but the use of phenolic resins in comparison with epoxy resins was found to yield the greatest improvements in flammability performance. Further, the phenolic system yielded a higher level of structural integrity to the final polymer + fiberglass char when compared with the other polymer systems of low heat release. Copyright © 2009 John Wiley & Sons, Ltd. [source] Integrated Multifunctional Nanosystems for Medical Diagnosis and TreatmentADVANCED FUNCTIONAL MATERIALS, Issue 21 2009*Article first published online: 9 OCT 200, Donglu Shi Abstract This article provides an overview on the development of integrated multifunctional nanosystems for medical diagnosis and treatment. In particular, a novel system is developed specifically for achieving simultaneous diagnosis and treatment of cancer. Critical issues are addressed on the architecture and assembly of nanocomponents based on medical requirements: targeted in vivo imaging, controlled drug release, localized hyperthermia, and toxicity. Nanotube-based carriers are summarized with surface functionalized properties. Other types of nanocarriers are also included such as super paramagnetic composite nanospheres and biodegradable hydroxylapatite nanoparticles. In addition, polymeric-based nanosystems are introduced with several novel features: they can be bio-dissolved due to environmental pH and temperature fluctuations. The nanocarriers are surface tailored with key functionalities: surface antibodies for cell targeting, anti-cancer drug loading, and magnetic nanoparticles for both hyperthermia and MRI. Future requirements, aims, and trends in the development of multifunctional nanosystems, particularly with intelligent functionalities for fundamental studies, are also provided. [source] A Delivery System for Self-Healing Inorganic Films,ADVANCED FUNCTIONAL MATERIALS, Issue 22 2008Harvey A. Liu Abstract Multilayer composites that utilize polymeric and brittle inorganic films are essential components for extending the lifetimes and exploiting the flexibility of many electronic devices. However, crack formation within the brittle inorganic layers that arise from defects as well as the flexing of these multilayer composite materials allows the influx of atmospheric water, a major source of device degradation. Thus, a composite material that can initiate self-healing upon the influx of environmental water through defects or stress-induced cracks would find potential applications in multilayer composite materials for permeation barriers. In the present study, the reactive metal oxide precursor TiCl4 is encapsulated within the pores of a degradable polymer, poly(lactic acid) (PLA). Electrospun PLA fibers are found to be reactive to atmospheric water leading to the hydrolysis of the degradable polymer shell and subsequent release of the reactive metal oxide precursor. Release of the reactive TiCl4 from the pores results in hydrolysis of the metal oxide precursor, forming solid titanium oxides at the surface of the fibers. The efficacy of this self-healing delivery system is also demonstrated by the integration of these reactive fibers in the polymer planarization layer, poly(methyl methacrylate), of a multilayer film, upon which an alumina barrier layer is deposited. The introduction of nanocracks in the alumina barrier layer lead to the release of the metal oxide precursor from the pores of the fibers and the formation of titanium dioxide nanoparticles within the crack and upon the thin film surface. In this study the first delivery system that may find utility for the self-healing of multilayer barrier films through the site-specific delivery of metal oxide nanoparticles through smart reactive composite fibers is established. [source] Structural Changes in the BODIPY Dye PM567 Enhancing the Laser Action in Liquid and Solid Media,ADVANCED FUNCTIONAL MATERIALS, Issue 16 2007I. García-Moreno Abstract In the search for more efficient and photostable solid-state dye lasers, newly synthesized analogs of the borondipyrromethene (BODIPY) dye PM567, bearing the polymerizable methacryloyloxypropyl group at position 2 (PMoMA) or at positions 2 and 6 (PDiMA), have been studied in the form of solid copolymers with methyl methacrylate (MMA). The parent dye PM567, as well as the model analogs bearing the acetoxypropyl group in the same positions, PMoAc and PDiAc, respectively, have been also studied both in liquid solvents and in solid poly(MMA) (PMMA) solution. Although in liquid solution PMoAc and PDiAc have the same photophysical properties as PM567, PDiAc exhibited a photostability up to 10 times higher than that of PM567 in ethanol under 310,nm-irradiation. The possible stabilization factors of PDiAc have been analyzed and discussed on the basis of the redox potentials, the ability for singlet molecular oxygen [O2(1,g)] generation, the reactivity with O2(1,g), and quantum mechanical calculations. Both PMoAc and PDiAc, pumped transversally at 532,nm, lased in liquid solution with a high (up to 58,%), near solvent-independent efficiency. This enhanced photostabilization has been also observed in solid polymeric and copolymeric media. While the solid solution of the model dye PDiAc in PMMA showed a lasing efficiency of 33,%, with a decrease in the laser output of ca.,50,% after 60,000 pump pulses (10,Hz repetition rate) in the same position of the sample, the solid copolymer with the double bonded chromophore, COP(PDiMA-MMA), showed lasing efficiencies of up to 37,%, and no sign of degradation in the laser output after 100,000 similar pump pulses. Even under the more demanding repetition rate of 30,Hz, the laser emission from this material remained at 67,% of its initial laser output after 400,000 pump pulses, which is the highest laser photostability achieved to date for solid-state lasers based on organic polymeric materials doped with laser dyes. This result indicates that the double covalent linkage of the BODIPY chromophore to a PMMA polymeric matrix is even more efficient than the simple linkage, for its photostabilization under laser operation. [source] Cover Picture: Anisotropy and Dynamic Ranges in Effective Properties of Sheared Nematic Polymer Nanocomposites (Adv. Funct.ADVANCED FUNCTIONAL MATERIALS, Issue 12 2005Mater. Abstract Forest and co-workers report on p.,2029 that nematic polymer nanocomposite (NPNC) films can be processed in steady shear flows, which generate complex orientational distributions of the nanorod inclusions. Distribution functions for a benchmark NPNC (11,vol.-% of 1,nm,×,200,nm rods) are computed for a range of shear rates, yielding a bifurcation diagram with steady states at very low (logrolling) and high (flow-aligning) shear rates, and limit cycles (tumbling, wagging, kayaking) at intermediate shear rates. The orientational distributions dictate the effective conductivity tensor of the NPNC film, which is computed for all distribution functions, and extract the maximum principal conductivity enhancement (Emax, averaged in time for periodic distributions) relative to the matrix. The result is a "property bifurcation diagram" for NPNC films, which predicts an optimal shear rate that maximizes Emax. Nematic, or liquid-crystalline, polymer nanocomposites (NPNCs) are composed of large aspect ratio, rod-like or platelet, rigid macromolecules in a matrix or solvent, which itself may be aqueous or polymeric. NPNCs are engineered for high-performance material applications, ranging across mechanical, electrical, piezoelectric, thermal, and barrier properties. The rods or platelets possess enormous property contrasts relative to the solvent, yet the composite properties are strongly affected by the orientational distribution of the nanophase. Nematic polymer film processing flows are shear-dominated, for which orientational distributions are well known to be highly sensitive to shear rate and volume fraction of the nematogens, with unsteady response being the most expected outcome at typical low shear rates and volume fractions. The focus of this article is a determination of the ranges of anisotropy and dynamic fluctuations in effective properties arising from orientational probability distribution functions generated by steady shear of NPNC monodomains. We combine numerical databases for sheared monodomain distributions[1,2] of thin rod or platelet dispersions together with homogenization theory for low-volume-fraction spheroidal inclusions[3] to calculate effective conductivity tensors of steady and oscillatory sheared mesophases. We then extract maximum scalar conductivity enhancement and anisotropy for each type of sheared monodomain (flow-aligned, tumbling, kayaking, and chaotic). [source] Well-Defined Fullerene Nanowire Arrays,ADVANCED FUNCTIONAL MATERIALS, Issue 8 2003Y.-G. Guo Abstract Fullerene nanowire arrays with well-defined size and length have been prepared by a controllable technique. Fullerene molecules such as C60 are introduced into the pores of anodic aluminum oxide (AAO) templates under a direct current (DC) electric field and polymerized in the pores. Structure analysis shows that the C60 nanowires are mainly polycrystalline, and a rhombohedral polymeric phase is observed in their vibration spectra. The electrical conductivity of so-prepared nanowire arrays show a semiconducting behavior. The ability to fabricate the fullerene nanowire arrays with controlled structures represents an important step toward the development of chemical sensors and nanoscale electronic devices based on fullerenes. [source] Combinatorial Polymer Scaffold Libraries for Screening Cell-Biomaterial Interactions in 3D,,ADVANCED MATERIALS, Issue 11 2008Yanyin Yang A combinatorial method for screening cell,biomaterial interactions in 3D is presented; polymeric, salt-leached scaffolds with varied composition and properties are present in a 96-well plate. Previous high-throughput approaches for screening cell,material interactions have focused on planar 2D surfaces or films. However, biomaterials are commonly used in a 3D scaffold format and cells behave more physiologically when cultured in 3D. [source] A Combinatorial Approach to Heterogeneous Asymmetric Aquacatalysis with Amphiphilic Polymer-Supported Chiral Phosphine-Palladium ComplexesADVANCED SYNTHESIS & CATALYSIS (PREVIOUSLY: JOURNAL FUER PRAKTISCHE CHEMIE), Issue 12-13 2006Yukinari Kobayashi Abstract A library of amphiphlic polystyrene-poly(ethylene glycol) (PS-PEG) resin-supported chiral phosphine ligands was prepared by the split method using porous miniature reactors. A polymeric (R)-2-(diphenylphosphino)binaphthyl (MOP) ligand anchored onto the PS-PEG resin by an (S)-alanine tether unit was identified through the library-based screening to be an effective chiral ligand for the asymmetric palladium-catalyzed ,-allylic substitution under heterogeneous aqueous conditions. [source] Evaluation of trimedlure dispensers by a method based on thermal desorption coupled with gas chromatography,mass spectrometryJOURNAL OF APPLIED ENTOMOLOGY, Issue 9-10 2008C. Alfaro Abstract Knowledge about the behaviour of trimedlure (TML) dispensers is essential to ensure the efficacy of monitoring and control methods based on TML as attractant. There are several commercially available TML dispensers, and each of them has a different useful life and TML release profile. Their emission is also affected differently by environmental factors. Even the same type of dispenser sometimes shows an important variability in the TML release rate. Because of the importance of methods based on TML lures in the control of the Mediterranean fruit fly and the influence of the TML dispenser on the efficacy of these control methods, we developed a non-destructive flow-through system to measure the TML release rate. This volatile collection method (VCM) adsorbs TML vapour on a Tenax TA desorption tube, and TML is quantified by Thermal desorption coupled with gas chromatography/mass spectrometry. Two types of TML dispensers, a polymeric (Aralure) and a mesoporous (Epalure), were field aged during 3 months. The TML release rates of these dispensers were determined by both, VCM and solvent extraction method. In this study, the correlation between both measurement methods is shown. A field trial has also been carried out to correlate trap catches and TML emission of each type of tested dispenser. The VCM allows a quick and accurate evaluation of the current behaviour of commercial dispensers along their useful life. It also allows comparing the TML release rate between different dispensers. We believe that the VCM can be useful for dispenser manufacturers to determine seasonal dispenser performance before a new product is introduced in the market, and to rapidly verify TML dispenser release when field-aged dispenser efficacy is in question. Thus, it can be employed as a quality control of commercial dispensers. [source] Increased sialylation of polymeric ,-IgA1 in patients with IgA nephropathyJOURNAL OF CLINICAL LABORATORY ANALYSIS, Issue 1 2002Joseph C.K. Leung Abstract The mechanism of mesangial IgA deposition is poorly understood in IgA nephropathy (IgAN). Abnormal glycosylation of carbohydrate moieties in the hinge region of the IgA molecule has recently attracted much attention. In this report, we studied galactosylation and sialylation profiles in ,- and ,-IgA1 from patients with IgAN. Total serum IgA1 was isolated from patients with IgAN or healthy controls by jacalin-affinity chromatography. Six fractions of molecular weight (MW) 50,1,000 kDa were separated by fast protein liquid chromatography (FPLC). Four lectin-binding assays were used to study the sialylation and the presence of terminal galactose or N-acetylgalactosamine (GalNAc) in the O-linked carbohydrate moieties of ,- or ,-IgA1. Maackia amurensis agglutinin (MAA) and Sambucus nigra agglutinin (SNA) lectin recognize ,(2,3)- and ,(2,6)-linked sialic acid, respectively. Peanut agglutinin (PNA) and Helix aspersa (HA) lectin recognize terminal galactose and GalNAc, respectively. Reduced HA was demonstrated in macromolecular , or ,-IgA1 (300,825 kDa) isolated from patients with IgAN (P < 0.05 compared with healthy controls). Lambda- but not ,-IgA1 from patients with IgAN bound less to PNA (P < 0.05). The ,(2,3)-linked sialic acid content in ,- but not ,-IgA1 of MW 150,610 kDa from patients was higher than that of controls (P < 0.005). The ,(2,6)-linked sialic acid content in ,-IgA1 (300,825 kDa) and ,-IgA1 (150,610 kDa) from patients was also higher than that of controls. This unusual glycosylation and sialylation pattern of the ,-IgA1 may have important implications for the pathogenesis of IgAN, as both the masking effect of sialic acid on galactose and the reduced galactosylation will hinder the clearance of macromolecular ,-IgA1 by asialoglycoprotein receptor of hepatocytes. The negative charge from sialic acid may also favor mesangial deposition of macromolecular ,-IgA1 in IgAN. J. Clin. Lab. Anal. 16:11,19, 2002. © 2002 Wiley-Liss, Inc. [source] Update on Bioabsorbable Stents: From Bench to ClinicalJOURNAL OF INTERVENTIONAL CARDIOLOGY, Issue 5 2006F.A.C.C., RON WAKSMAN M.D. Permanent metallic stents are associated with limitations such as continued mechanical stress, transfer to the tissue, and continued biological interaction with the surrounding tissue. They are also associated with late stent thrombosis and artifacts when non-invasive technologies such as MRI and MSCT are used. The potential advantages of bioabsorbable polymeric or metallic stents are to leave no stent behind, they are fully compatible with MRI and MSCT imaging, and are not associated with late stent thrombosis. This review covers the different stent programs as they move from bench to bed and clinical trials. Bioabsorbable stents are considered the next frontier of stenting and we will discuss their potential to fulfill this promise in interventional cardiology. [source] Intravascular bioresorbable polymeric stents: A potential alternative to current drug eluting metal stentsJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 11 2007Tahmer Sharkawi Abstract Stent implantation following angioplasty is the standard treatment of coronary artery disease necessitating interventional procedures. The use of stents as a platform for local drug delivery is a popular strategy to achieve local pharmacological treatment to the diseased artery. Drug eluting stents (DES) are now largely preferred to bare metal stents when stent implantation is necessary. Lately, there have been several reports questioning the long-term safety of DES. An alternative to these drug eluting metal stents are bioresorbable polymeric stents (BPS) because of the many advantages of bioresorbable material. However, the fundamental differences in polymeric and metallic materials make the development of such an alternative a significant challenge. This review discusses the different advantages of BPS and the many constrains and requirements of such devices. An up to date commented review of published data concerning BPS is presented. Considerations are given on using BPS as local drug delivery systems as well as on evaluating BPS performances. © 2007 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 96: 2829,2837, 2007 [source] Biophysical characterization of polymeric and liposomal gene delivery systems using empirical phase diagramsJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 10 2006Marika Ruponen Abstract A major problem with the pharmaceutical use of nonviral gene delivery systems arises from their limited characterization due to their size and heterogeneity. In this study, we provide a more intuitive view of their structure and behavior employing an empirically based phase diagram approach. Complexes formed between plasmid DNA and four cationic carriers (a monovalent lipid, the same monovalent lipid combined with a helper lipid, polylysine, and a branched form of polyethyleneimine), at both positive and negative nitrogen/phosphorous ratios, are characterized employing dynamic light scattering, circular dichroism, and extrinsic dye fluorescence as methods sensitive to various aspects of the structure of the complexes. These measurements were performed as a function of pH and ionic strength to perturb the electrostatic contacts that are key to complex formation. Using a multidimensional eigenvalue approach, the data are presented in the form of a colored, five dimensional diagram. The resultant eight empirical phase diagrams display three to five variably resolved phases. In contrast, the phase diagram of the plasmid alone showed only two to three such phases. Each state is assigned to a particular form of the complex in terms of their size, extent of collapse and conformation of the associated DNA component. The utility of this approach is then briefly discussed. © 2006 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 95:2101,2114, 2006 [source] Small-molecule release from poly(D,L -lactide)/poly(D,L -lactide-co-glycolide) composite microparticlesJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 9 2005Emily J. Pollauf Abstract Addition of biodegradable polymer shells surrounding polymeric, drug-loaded microparticles offers the opportunity to control drug release rates. A novel fabrication method was used to produce microparticles with precise control of particle diameter and the thickness of the polymer shell. The effect of shell thickness on release of a model drug, piroxicam, has been clearly shown for 2- to 15-µm thick shells of poly(D,L -lactide) (PDLL) surrounding a poly(D,L -lactide-co-glycolide) (PLG) core and compared to pure PLG microspheres loaded with piroxicam. Furthermore, the core-shell microparticles are compared to microspheres containing blended polymers in the same mass ratios to demonstrate the importance of the core-shell morphology. Combining PDLL(PLG) microcapsules of different shell thicknesses allows nearly constant release rates to be attained for a period of 6 weeks. © 2005 Wiley-Liss, Inc. and the American Pharmacists Association J Pharm Sci 94:2013,2022, 2005 [source] Synthesis of polymeric 1-iminopyridinium ylides as photoreactive polymersJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 4 2010Daniel Klinger Abstract Two synthetic routes to polymeric 1-imino pyridinium ylides as new photoreactive polymeric architectures were investigated. In the first approach, polymerization of newly synthesized 1-imino pyridinium ylide containing monomers yielding their polymeric analogues was achieved by free radical polymerization. Alternatively, reactive precursor polymers were synthesized and converted into the respective 1-imino pyridinium ylide polymers by polymer analogous reactions on reactive precursor polymers. Quantitative conversion of the reactive groups was achieved with pentafluorophenyl ester containing polymers and newly synthesized photoreactive amines as well as by the reaction of poly(4-vinylbenzoyl azide) with a photoreactive alcohol. The polymers obtained by both routes were examined regarding their photoreaction products and kinetics in solution as well as in thin polymer films. Contact angle measurements of water on the polymer films before and after irradiation showed dramatic changes in the hydrophilicity of the polymers. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 832,844, 2010 [source] One-pot synthesis of ABC miktoarm star terpolymers by coupling ATRP, ROP, and click chemistry techniquesJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 12 2009Yanfeng Zhang Abstract We report on the one-pot synthesis of well-defined ABC miktoarm star terpolymers consisting of poly(2-(dimethylamino)ethyl methacrylate), poly(,-caprolactone), and polystyrene or poly(ethylene oxide) arms, PS(- b -PCL)- b -PDMA and PEO (- b -PCL)- b -PDMA, taking advantage of the compatibility and mutual tolerability of reaction conditions (catalysts and monomers) employed for atom transfer radical polymerization (ATRP), ring-opening polymerization (ROP), and click reactions. At first, a novel trifunctional core molecule bearing alkynyl, hydroxyl group, and bromine moieties, alkynyl(OH)Br, was synthesized via the esterification reaction of 5-ethyl-5-hydroxymethyl-2,2-dimethyl-1,3-dioxane with 4-oxo-4-(prop-2-ynyloxy)butanoic acid, followed by deprotection and monoesterification of alkynyl(OH)2 with 2-bromoisobutyryl bromide. In the presence of trifunctional core molecule, alkynyl(OH)Br, and CuBr/PMDETA/Sn(Oct)2 catalytic mixtures, target ABC miktoarm star terpolymers, PS(- b -PCL)- b -PDMA and PEO(- b -PCL)- b -PDMA, were successfully synthesized in a one-pot manner by simultaneously conducting the ATRP of 2-(dimethylamino)ethyl methacrylate (DMA), ROP of ,-caprolactone (,-CL), and the click reaction with azido-terminated PS (PS- N3) or azido-terminated PEO (PEO- N3). Considering the excellent tolerability of ATRP to a variety of monomers and the fast expansion of click chemistry in the design and synthesis of polymeric and biorelated materials, it is quite anticipated that the one-pot concept can be applied to the preparation of well-defined polymeric materials with more complex chain architectures. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 3066,3077, 2009 [source] | ||||||||||||||||||||||