Band‐gap engineering of polythiophenes via dithienophosphole doping

A series of polythiophenes doped with dithieno[3,2‐b:2′,3′‐d]phosphole units at varying levels (0–17%) were synthesized and characterized. Polymer work up provided two series of polymers from chloroform (C) and hexanes (H) for each doping level, respectively. Systematic structure–property studies revealed that the C‐series polymers generally had higher molecular weights than the H‐series, but also slightly higher relative dithienophosphole concentrations, both having a significant impact on the photophysical and electrochemical properties of the polymers. Furthermore, the presence of the dithienophosphole units also stabilizes the LUMO levels, whereas the HOMO levels remain dominated by the thiophene units, resulting in desirable electronics for an interaction with acceptor materials, such as 1‐(3‐methoxycarbonyl)propyl‐1‐phenyl[6,6]C₆₁. Importantly, increasing amount of dithienophosphole doping results in increased conductivities for the polymers in their oxidized state, while concurrently significantly stabilizing the neutral polythiophenes toward oxidation under environmental conditions. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

Characterization of Standard Reference Material 2942, Ce-ion-doped glass, spectral correction standard for UV fluorescence

Standard Reference Material (SRM) 2942 is a cuvette-shaped, Ce-ion-doped glass, recommended for use for relative spectral correction of emission from 320 to 430 nm and day-to-day performance verification of steady-state fluorescence spectrometers. Properties of this standard that influence its effective use or contribute to the uncertainty in its certified emission spectrum were explored here. These properties include its photostability, absorbance, dissolution rate in water, anisotropy and temperature coefficient of fluorescence intensity. The expanded uncertainties in the certified spectrum are about 9% around the peak maximum at 330 nm, using an excitation wavelength of 310 nm. The SRM also exhibits a strong resistance to photodegradation, with no measurable decrease in fluorescence intensity even after 25 h of irradiation with UV light>280 nm from a Xe lamp.     

Synthesis and Crystal Structure of an Organic-Polyoxometalate (POM) Hybrid Compound Containing a Keggin Type Mo–Si Polyanion

Abstract  

Complex (1), which is comprised of a typical Keggin type anion, four protonated 3-amino-1,2,4-triazole (AmTAZ) ligands, one nitrate anion and an area of disordered unidentifiable species was synthesized via hydrothermal methods followed by slow evaporation. The structure is held together through a web of hydrogen bonding and crystallizes in the monoclinic space group P2₁/c with unit cell dimensions of a = 13.789(3) b = 15.551(3) c = 24.401(7) ?, β = 93.898(8)°, V = 5220(2) ?³ Z = 4, D = 2.896 Mg/m³.     

MICROEMULSIONS: A CONTEMPORARY OVERVIEW

The literature on microemulsions from 1975-1979 has been reviewed.     

On surface tension modelling using the level set method

The paper describes and compares the performance of two options for numerically representing the surface tension force in combination with the level set interface‐tracking method. In both models, the surface tension is represented as a body force, concentrated near the interface, but the technical implementation is different: the first model is based on a traditional level set approach in which the force is distributed in a band around the interface using a regularized delta function, whereas in the second, the force is partly distributed in a band around the interface and partly localized to the actual computational cells containing the interface. A comparative study, involving analysis of several two‐phase flows with moving interfaces, shows that in general the two surface tension models produce results of similar accuracy. However, in the particular case of merging and pinching‐off of interfaces, the traditional level set model of surface tension produces an error that results in non‐converging solutions for film‐like interfaces (i.e. ones involving large contact areas). In contrast, the second model, based on the localized representation of the surface tension force, displays consistent first‐order convergence. Copyright © 2008 John Wiley & Sons, Ltd.     

Zum Nachweis und zur Bestimmung des Stickstoffs in organischen K?rpern

Ohne Zusammenfassung     

Gouy phase compensation in quasi-phase matching

In any focussed nonlinear interaction the focus induced phase shift, known as the Gouy phase shift, provides an imperfection in phase matching for any linearly invariant material. However, using an appropriately designed quasi-phase matched structure it is theoretically possible to compensate for the deleterious effects of the Gouy phase shift, allowing a symmetric frequency response and tighter optimal focussing than in a uniform material.