On the well‐posedness of a mathematical model of quorum‐sensing in patchy biofilm communities

We analyze a system of reaction–diffusion equations that models quorum‐sensing in a growing biofilm. The model comprises two nonlinear diffusion effects: a porous medium‐type degeneracy and super diffusion. We prove the well‐posedness of the model. In particular, we present for the first time a uniqueness result for this type of problem. Moreover, we illustrate the behavior of model solutions in numerical simulations. Copyright © 2011 John Wiley & Sons, Ltd.     

Core, shell, and surface-optimized dendrimers for blue light-emitting diodes

We present a novel core-shell-surface multifunctional structure for dendrimers using a blue fluorescent pyrene core with triphenylene dendrons and triphenylamine surface groups. We find efficient excitation energy transfer from the triphenylene shell to the pyrene core, substantially enhancing the quantum yield in solution and the solid state (4-fold) compared to dendrimers without a core emitter, while TPA groups facilitate the hole capturing and injection ability in the device applications. With a luminance of up to 1400 cd/m(2), a saturated blue emission CIE(xy) = (0.15, 0.17) and high operational stability, these dendrimers belong to the best reported fluorescence-based blue-emitting organic molecules.     

Coordination chemistry of perhalogenated cyclopentadienes and alkynes. XXVIII new high-yield synthesis of monobromoferrocene and simplified procedure for the synthesis of pentabromoferrocene. Molecular structures of 1,2,3-tribromoferrocene and 1,2,3,4,5-pentabromoferrocene

Monobromoferrocene (1) was obtained in 95% yield from ferrocene via lithiation with tert-BuLi/KO-tert-Bu and bromination with dibromotetrachloroethane. Starting from 1 mixtures of 1,2-dibromoferrocene (2) and apparently unreacted 1 (ranging from 80:20 to 50:50, depending on the reaction conditions) can be obtained via a lithiation- zincation- bromination sequence. These mixtures can be transferred directly with a tenfold excess of Lithium-tetramethylpiperidinide, followed by bromination with 1,1,2,2-tetrabromoethane to pentabromoferrocene (3), in an overall yield of 36% starting from ferrocene. The molecular structures of 3 and of 1,2,3-tribromoferrocene (4) have been determined by X-Ray diffraction.     

Direct experimental evidence for an enamine radical cation in SOMO catalysis

SOMO catalysis has lately obtained large interest as a new and powerful version of enantioselective organocatalysis which includes radical steps initiated by a one-electron oxidation. The intermediate enamine radical cation has been postulated, but has not been observed directly so far. This communication now reports the direct detection of this key intermediate.     

Activation/Inhibition Effects during the Coelectrodeposition of PtAg Nanoparticles: Application for ORR in Alkaline Media

PtAg bimetallic nanoparticles for oxygen reduction reaction (ORR) in alkaline media were prepared by pulse electrodeposition (PED). During PED the reduction of Ag⁺ ions predominates, thus an increased Ag content in the co‐deposit is accomplished. The mechanism for this anomalous co‐deposition was elucidated by potential pulse experiments, which revealed that nuclei formation mainly occurs via the reduction of Pt²⁺ ions. The growth of the particles is diffusion controlled leading to the formation of a Ag shell covering a PtAg alloyed region. However, the shell is not growing homogeneously on the PtAg alloy. Hence, regions of the PtAg alloy are exposed, which exhibit an enhanced ORR activity compared to a pure Ag surface.     

Evaporation of single component viscous liquids in a metal falling film evaporator

Heat transfer for single component falling film evaporation has been investigated in a stainless steel single tube falling film evaporator. The tube had a heated length of 2,500 mm. Propylene glycol and cyclohexanol have been used as evaporating media. Liquid film running down the tube, is formed on the inner side of the tube. For the distribution of liquid two different devices were examined. Process equipment was operated in pump-around mode with the distillate being condensed and recycled. Results show that none of the available correlations for heat transfer in falling film evaporation is able to describe the results qualitatively as well as quantitatively. Using different film distribution devices, a significant influence of the Reynolds number for the transition from laminar to turbulent flow is seen. However, differences between experimental results and correlations in literature cannot be explained only by usage of different film distributions, in particular when the correlation is based on measurements with a different tube length. A model approach is presented for cyclohexanol as evaporating medium with a flat weir as film distributor.     

Azodioxy compounds as precursors for C-radicals and their application in thermal styrene difunctionalization

An atom-economic thermal α,β-difunctionalization of various styrenes with readily prepared azodioxy compounds is reported. Mechanistic studies reveal that the starting azodioxy compounds can thermally be cleaved to the corresponding C-nitroso compounds, which under these thermal conditions further homolyze to generate reactive C-radicals along with the persistent NO radical. In the presence of a styrene, C-radical addition with subsequent nitrosylation followed by tautomerization is occurring, resulting in an overall styrene β-alkylation-α-oximation reaction.

An atom-economic thermal α,β-difunctionalization of various styrenes with readily prepared azodioxy compounds is reported.