Strategies are provided for enhancing adherence and motivation, as well as facilitating medical communication.”
“The hydrosilylation of cyclohexanone and acetone with triethysilane and diphenysilane catalyzed by polymer-supported Rh(I) complex has been investigated. Two terpolymers of styrene, divinylbenzene, and 1-vinylimidazole (S/DVB/VI) or N-vinylpyrrolidinone (S/DVB/NVP) were used as the catalysts supports. Physical characterization

of these materials has involved the measurements of the structural parameters in the dry and swollen states by DSC, the nitrogen BET adsorption method and inverse steric exclusion chromatography ISEC. From these results it can be concluded that the original polymer structure has been changed during the complex attachment giving rise to materials of higher porosity. X-ray photoelectron selleck inhibitor BAY 73-4506 spectroscopy XPS, IR, and AAS spectroscopy were used to characterization of heterogeneous complexes before and after use. The effect of the morphology of the support on the catalytic properties of the polymer-supported Rh(I) species was tested in the hydrosilylation of ketones and correlated with the reaction mechanism. It was demonstrated that the high selectivity of homogeneous rhodium complex toward the silyl ethers can be partially reversed to the dehydrogenative silylation

products by a proper choice of polymer support with favorable microporous structure. Recycling tests demonstrated high stability of the supported catalysts during prolonged use. The constant selectivity of the supported catalysts demonstrated during recycling experiments showed that they could be useful for practical application. (C) 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2012″
“Efficient electrophosphorescence is demonstrated using single-layer organic light-emitting devices (OLEDs) containing fac-tris(2-phenylpyridine) iridium (III) [Ir(ppy)(3)], bis(1-phenylisoquinoline)-(acetylacetonate) iridium (III) [PQIr], and iridium(III) bis[(4,6-difluorophenyl)-pyridinato-N,C-2']picolinate Small molecule library in vivo [FIrpic] for emission in the green, red, and

blue, respectively. Peak forward-emitted external quantum (eta(EQE)) and power efficiencies (eta(P)) of eta(EQE) = (16.9 +/- 0.4)% and eta(P) = (65.0 +/- 1.1)lm/W, eta(EQE) = (12.0 +/- 0.4)% and eta(P) (8.3 +/- 1.1 ) lm/W, and eta(EQE) (10.9 +/- 0.3)% and eta(P) (28.1 +/- 1.1)lm/W, are obtained for optimized green, red, and blue OLEDs, respectively. Devices are doped uniformly with the phosphorescent guest, and contain a continuously-varying host composition from predominately hole-transporting material (HTM) at the anode to predominately electron transporting material (ETM) at the cathode. The highly tunable composition gradient allows for the optimization of electron-hole charge balance and low-voltage operation while maintaining charge and exciton confinement.