Core‐and‐Surface‐Functionalized Polyphenylene Dendrimers for Solution‐Processed,Pure‐Blue Light‐Emitting Diodes Through Surface‐to‐Core Energy Transfer

Several pyrene‐based polyphenylene dendrimers (PYPPDs) with different peripheral chromophores (PCs) are synthesized and characterized. Deep blue emissions solely from the core are observed for all of them in photoluminescence spectra due to good steric shielding of the core and highly efficient surface‐to‐core Förster resonant energy transfers (FRETs). Device performances are found in good correlation with the energy gaps between the work function of the electrodes and the frontier molecular orbital (FMO) levels of the PCs. Pure blue emission, luminance as high as 3700 cd m⁻² with Commission Internationale de l'Éclairage 1931 (CIE_xy) = (0.16, 0.21), and a peak current efficiency of 0.52 cd A⁻¹ at CIE_xy = (0.17, 0.20) are achieved. These dendrimers are among the best dendritic systems so far for fluorescent blue light‐emitting materials.

     

Two-dimensional microrheology of freely suspended liquid crystal films

Smectic liquid crystals form freely-suspended, fluid films of highly uniform structure and thickness, making them ideal systems for studies of hydrodynamics in two dimensions. We have measured particle mobility and shear viscosity by direct observation of the gravitational drift of silica spheres and smectic islands included in these fluid membranes. In thick films, we observe a hydrodynamic regime dominated by lateral confinement effects, with the mobility of the inclusion determined predominantly by coupling of the fluid flow to the fixed boundaries of the film. In thin films, the mobility of inclusions is governed primarily by coupling of the fluid to the surrounding air, as predicted by Saffman-Delbrück theory.     

Synthesis, structure, and reactivity of carbene-stabilized phosphorus(III)-centered trications [L3P]3+

Carbene-stabilized [L(3)P](+3) cations have been synthesized for the first time by a reaction between 1-chloro-2,3-bis(dialkylamino)cyclopropenium salts and P(SiMe(3))(3). In addition, the first structural characterization of such an entity is reported. Consistent with the X-ray data, density functional calculations indicate that these P-centered cations, despite their high positive charge, still feature a nonbonding electron pair on the P-atom (HOMO) and a very low-lying LUMO depicting them as poor σ-donors and excellent π-acceptors.     

An improved decision support model for scheduling production in an engineer-to-order manufacturer

4OR - This paper outlines a mathematical model to solve a scheduling problem for a company engineering and producing propellers to order. Nonås and Olsen (Comput Oper Res...     

Tris(benzophenoneimino)phosphane and Related Compounds

A new group of bases with benzophenoneiminyl (bpi) moiety has been synthesized and characterized in this work. The title compound tris(benzophenoneimino)phosphane (P(bpi)₃) 1 was prepared with a convenient one-pot approach: benzophenone imine was deprotonated using MeMgCl and reacted with PBr₃ in diglyme. The method could be considered as a method of choice for preparing other (amino)phosphanes in case lithio-intermediates and/or protonated phosphane is out of consideration. Phosphane 1 is further used to prepare a range of related phosphonium cations and phosphazenes. Phosphonium cations were deprotonated to assess the stability of the resulting phosphonium ylides. In some cases, the bulky substances were capable of forming P−N heterocycles. Experimental (MeCN) and computational (MeCN, THF, gas-phase) basicities of benzophenone imine, phosphane 1 , phosphonium ylides, and phosphazenes, as well as some representative XRD structures, are presented and discussed.     

ChemInform Abstract: The Chemistry of Phosphorus Suboxides.

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