High‐performance holographic polymer‐dispersed liquid crystals by incorporating hyperbranched polymers

A minute amount (0.01–0.3 wt %) of ally isocyanate functionalized hyperbranched 2,2‐bis (hydroxymethyl) propionic acid (bis‐MPA) polyester‐16‐hydroxyl (HBP) was incorporated covalently into polyurethane acrylate‐based holographic polymer dispersed liquid crystals (HPDLCs), and its effects on the compound viscosity, grating kinetics, morphology, diffraction efficiency (DE), and electro‐optical properties of the HPDLC films were examined. HBP at low concentrations (0.01–0.05%) reduced the compound viscosity and domain size of liquid crystal (LC) significantly and augmented the cure rate and saturation DE by up to threefold compared to the HBP‐free compound. At high concentrations (0.10 and 0.30%), HBP increased the compound viscosity and decreased the rate of grating formation, giving rise to distorted LC‐polymer interfaces, which caused a significant decrease in the threshold and operating voltages. The rise and decay time showed a minimum and maximum, respectively, when the compound viscosity was a minimum at 0.03% HBP. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013     

Asymmetric borane reduction of achiral ketones mediated by a chiral oxazaborolidine derived from (−)-ephedrine

Asymmetric borane reduction of achiral ketones in the presence of a chiral oxazaborolidine derived from (−)-ephedrine yielded the corresponding alcohols in optical yields of 41 – 83 % ee.     

Stability of T. Chan＇s Preconditioner from Numerical Range

A matrix is said to be stable if the real parts of all the eigenvalues are negative. In this paper, for any matrix An, we discuss the stability properties of T. Chan＇s preconditioner cU（An） from the viewpoint of the numerical range. An application in numerical ODEs is also given.     

Fluorene‐based alternating polymers containing electron‐withdrawing bithiazole units: Preparation and device applications

We report here the synthesis via Suzuki polymerization of two novel alternating polymers containing 9,9‐dioctylfluorene and electron‐withdrawing 4,4′‐dihexyl‐2,2′‐bithiazole moieties, poly[(4,4′‐dihexyl‐2,2′‐bithiazole‐5,5′‐diyl)‐alt‐(9,9‐dioctylfluorene‐2,7‐diyl)] (PHBTzF) and poly[(5,5′‐bis(2″‐thienyl)‐4,4′‐dihexyl‐2,2′‐bithiazole‐5″,5″‐diyl)‐alt‐(9,9‐dioctylfluorene‐2,7‐diyl)] (PTHBTzTF), and their application to electronic devices. The ultraviolet–visible absorption maxima of films of PHBTzF and PTHBTzTF were 413 and 471 nm, respectively, and the photoluminescence maxima were 513 and 590 nm, respectively. Cyclic voltammetry experiment showed an improvement in the n‐doping stability of the polymers and a reduction of their lowest unoccupied molecular orbital energy levels as a result of bithiazole in the polymers' main chain. The highest occupied molecular orbital energy levels of the polymers were ?5.85 eV for PHBTzF and ?5.53 eV for PTHBTzTF. Conventional polymeric light‐emitting‐diode devices were fabricated in the ITO/PEDOT:PSS/polymer/Ca/Al configuration [where ITO is indium tin oxide and PEDOT:PSS is poly(3,4‐ethylenedioxythiophene) doped with poly(styrenesulfonic acid)] with the two polymers as emitting layers. The PHBTzF device exhibited a maximum luminance of 210 cd/m² and a turn‐on voltage of 9.4 V, whereas the PTHBTzTF device exhibited a maximum luminance of 1840 cd/m² and a turn‐on voltage of 5.4 V. In addition, a preliminary organic solar‐cell device with the ITO/PEDOT:PSS/(PTHBTzTF + C₆₀)/Ca/Al configuration (where C₆₀ is fullerene) was also fabricated. Under 100 mW/cm² of air mass 1.5 white‐light illumination, the device produced an open‐circuit voltage of 0.76 V and a short‐circuit current of 1.70 mA/cm². The fill factor of the device was 0.40, and the power conversion efficiency was 0.52%. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1845–1857, 2005