Search results for " density"

Durability of a strach-based biodegradable polymer

2007

Abstract The photo-oxidation and the photo-stabilization of a commercial biodegradable polymer have been investigated in order to establish the possibility of using this polymer as raw material for films for agriculture. The degradation has been followed by measuring the mechanical properties as a function of photo-oxidation time and in particular by following the elongation at break. The virgin polymer, made from maize starch and a synthetic biodegradable polyester, shows poor resistance to the UV irradiation as observed by the fast decay of the elongation at break, but the presence of small amounts of conventional UV stabilizers strongly improves the durability of this polymer. The UV sta…

Effect of conductivity of hole injection layer on the performance of a blue light emitting solution processable OLED

2005

The performance of blue emitting OLED devices, using a polyspiro as blue light emitting polymer, were studied as a function of the conductivity of a novel hybrid hole injection material. The hole injection material is based on a polyarylamine using a molecular magnet as oxidant. The charge density and the luminance of the devices changed considerably with increasing conductivity of the hole injection layer. The change in device performance can be attributed to a change from a hole limited device to a balanced charge carrier device and eventually to an electron limited device. The performance of the optimized device configuration is significantly improved with respect to a device making use …

Efficient photovoltaic and electroluminescent perovskite devices.

2015

Planar diode structures employing hybrid organic–inorganic methylammonium lead iodide perovskites lead to multifunctional devices exhibiting both a high photovoltaic efficiency and good electroluminescence. The electroluminescence strongly improves at higher current density applied using a pulsed driving method.

Perimeter leakage current in polymer light emitting diodes

2009

Observation of leakage current paths through the device perimeter in standard poly(phenylene vinylene)-based light-emitting devices is reported. Perimeter leakage currents govern the diode performance in reverse and low positive bias and exhibit an ohmic character. Current density correlates with the perimeter-to-area ratio thus indicating that leakage currents are mainly confined on polymer regions in the vicinity of metallic contact limits (device perimeter). © 2008 Elsevier B.V. All rights reserved.

Viscometry of polyelectrolyte solutions: Star-like versus linear poly[[2-(methacryloyloxy)ethyl] trimethylammonium iodide] and specific salt effects

2017

Abstract The intrinsic viscosities, [η], of the 3-arm star polyelectrolyte in pure water are for a given molar mass considerably lower than for the linear product because of the higher monomer concentration and charge density in isolated coils. These effects are much more pronounced than in the case of uncharged macromolecules. Extra salt (NaCl, NaI, CaCl2) reduces the solution viscosities of the 3-arm star polymer less than of the linear product. The transition of [η] from the value in pure water to the minimum saturation value at high salt concentrations follows a Boltzmann sigmoid. In saline solvents the changes of the viscosities with rising polymer concentration depend strongly on the …

Understanding the origin of the asynchronicity in bond-formation in polar cycloaddition reactions. A DFT study of the 1,3-dipolar cycloaddition react…

2012

The origin of the asynchronicity in bond-formation in polar cycloadditions has been studied by an ELF analysis of the electron reorganisation along the 1,3-dipolar cycloaddition of Padwa's carbonyl ylide 4 with the 1,2-benzoquinone 8. This reaction presents an unexpected asynchronous bond-formation, which is initialised through the nucleophilic attack of Padwa's carbonyl ylide on the carbonyl oxygen atom of the strongly electrophilically activated 1,2-benzoquinone. The present study allows for the establishment that along an asynchronous bond-formation, the more favourable two-center interaction begins at the most electrophilic center, which is the center with the highest spin density achie…

1996

The major new developments in electron crystallography and high resolution imaging of organic molecules are discussed. The aim is to show that the recent rapid advances in computer technology have made it possible to analyze molecules at a level or resolution which was impossible less than a decade ago, thus bringing the concept of molecular design to produce specific physical properties much nearer to realization

Counterion-mediated attraction and kinks on loops of semiflexible polyelectrolyte bundles.

2006

The formation of kinks in a loop of bundled polyelectrolyte filaments is analyzed in terms of the thermal fluctuations of charge density due to polyvalent counterions adsorbed on the polyelectrolyte filaments. It is found that the counterion-mediated attraction energy of filaments depends on their bending. By consideration of curvature elasticity energy and counterion-mediated attraction between polyelectrolyte filaments, the characteristic width of the kink and the number of kinks per loop is found to be in reasonable agreement with existing experimental data for rings of bundled actin filaments.

Monte Carlo simulations of the polymer glass transition: From the test of theories to material modeling

1997

We present results on the glass transition in polymer melts using Monte Carlo simulations of the bond fluctuation lattice model. There are two questions we address in this work. What is the temperature dependence of the entropy density in such a model polymer melt and how well is it described by theories like the Gibbs-DiMarzio theory of the glass transition? And to what degree is one able to map the Hamiltonian of such an abstract lattice model onto a specific polymer material and use it to model the large scale and long time properties of a realistic polymer melt?

d-Glucose as a multivalent chiral scaffold for combinatorial chemistry

2002

Due to their high density of functional groups and their availability in a variety of diastereomeric forms, monosaccharides are considered attractive scaffolds for combinatorial chemistry that allow the attachment and defined spatial alignment of up to five different pharmacophoric groups. For their application in combinatorial syntheses on solid phase, a set of selectively removable hydroxy protecting groups in combination with a cleavable anchor is required. Herein, we report on the construction and use of a versatile multivalent glucose building block for parallel synthesis on the solid phase.