Planarity relations for the sextic centrifugal distortion constants of triangular triatomic molecules

Four linearly independent linear combinations of the ten sextic centrifugal distortion coefficients of triangular triatomic molecules are presented. These combinations are formed in such a way that the resulting expressions depend only on the equilibrium geometry and the harmonic force field parameters of the molecule, quantities which are ordinarily known to considerably better precision than the sextic constants. The relations obtained thus constitute a set of planarity constraints on the ten sextic coefficients which arise in connection with the Nielsen-Amat expansion of the Darling-Dennison Hamiltonian. The planarity expressions can be utilized to effect a reduction of the sextic portion of the Hamiltonian.     

Photoluminescence of Al x Ga1−x As/GaAs quantum well heterostructures grown by molecular beam epitaxy

Nominally undoped Al_xGa_1–xAs grown by molecular beam epitaxy from As₄ species at elevated substrate temperatures of 670°C exhibits well-resolved excitonic fine structure in the low-temperature photoluminescence spectra, if the effective As-to-(Al+Ga) flux ratio on the growth surface is kept within a rather narrow range of clearly As-stabilized conditions. In contrast to previous results on Al_xGa_1–xAs of composition 0.15not to shift in energy by changing the excitation intensity. This implies a simple freeelectron carbon-acceptor recombination mechanism for the line without any participation of a donor. In Al_xGa_1–xAs of composition close to the direct-to-indirect cross-over point, two distinct LO-phonons separated by 34 and 48 meV from the (D ⁰,C ⁰) peak position at x=0.43 were observed which were before only detectable by Raman scattering experiments. The intensity of the carbon-impurity related luminescence lines in bulk-type Al_xGa_1–xAs and GaAs layers was found to be strongly reduced, as compared to the excitonic recombination lines, if the respective active layer was covered by a very thin confinement layer of either GaAs on top of Al_xGa_1–xAs or vice versa grown in the same growth cycle.     

Energy Decay for the Strongly Damped Nonlinear Beam Equation and Its Applications in Moving Boundary

We study the existence and energy decay of solutions for the strongly damped nonlinear beam equation. We apply a method based on Nakao method to show that the solution decays exponentially, and to obtain precise estimates of the constants in the estimates. Finally, we discuss its applications in moving boundary.     

The role of resolved virtual photons in the production of forward jets at HERA

The measurement of forward jet cross sections has been suggested as a promising probe of new small x parton dynamics and the question is whether the new HERA data provide an indication of this. In this paper the influence of resolved photon processes has been investigated and it has been studied to what extent the inclusion of such processes in addition to normal deep inelastic scattering leads to agreement with data. It is shown that two DGLAP evolution chains from the hard scattering process towards the proton and the photon respectively, are sufficient to describe effects observed in the HERA data, which have been attributed to BFKL dynamics. Received: 11 March 1999 / Published online: 18 June 1999     

Resonant-cavity light-emitting diodes: quantum noise and spatial emission characteristics

We demonstrate the interplay between the intensity noise and the spatial emission characteristics of resonant-cavity light-emitting diodes. First, we find that the total aperture intensity noise exhibits a sub-shot noise behavior in a quite large pumping regime. Second, we investigate the angular, spectral, and spatial emission characteristics of the devices by controlling the shape and width of the angular intensity distribution via temperature detuning of the quantum well wavelength and the cavity resonance wavelength. Finally, the angular and aperture resolved intensity noise exhibit a super-shot noise behavior in contrast to that of the total emission. We explain this difference with anticorrelations between various radial components which increase with the temperature-tuned extension of the spatial emission. PACS 85.60.Jb; 42.50.L; 23.20.En     

Two-dimensional poroelastic acoustical foam shape design for absorption coefficient maximization by topology optimization method

Optimal shape design of a two-dimensional poroelastic acoustical foam is formulated as a topology optimization problem. For a poroelastic acoustical system consisting of an air region and a poroelastic foam region, two different physical regions are continuously changed in an iterative design process. To automatically account for the moving interfaces between two regions, we propose a new unified model to analyze the whole poroelastic acoustical foam system with one set of governing equations; Biot's equations are modified with a material property interpolation from a topology optimization method. With the unified analysis model, we carry out two-dimensional optimal shape design of a poroelastic acoustical foam by a gradient-based topology optimization setting. The specific objective is the maximization of the absorption coefficient in low and middle ranges of frequencies with different amounts of a poroelastic material. The performances of the obtained shapes are compared with those of well-known wedge shapes, and the improvement of absorption is physically interpreted.     

Bis‐benzimidazolium‐palladium system catalyzed Suzuki‐Miyaura coupling reaction of aryl bromides under mild conditions

Bis‐benzimidazolium salts were prepared successfully from commercially available and inexpensive o‐phenylenediamine through a series of simple reactions. The bis‐NHC‐Pd complexes prepared in situ can catalyze Suzuki‐Miyaura cross‐coupling reaction under very mild conditions in aqueous media with excellent yields. The efficiency of this reaction is demonstrated by its compatibility with a range of functional groups. Di‐ortho‐substituted biaryls could be accomplished in 89–99% yields. Moreover, the rigorous exclusion of air or moisture is not required in these transformations.     

Molecular Encapsulation of Trimeric Chromium Carboxylate Clusters in Metal–Organic Frameworks and Propylene Sorption

Oxo-bridged trimeric chromium acetate clusters [Cr₃O(OOCCH₃)₆(H₂O)₃]NO₃ have been encapsulated for the first time in the mesoporous cages of the chromium terephthalate MIL-101(Cr). The isolated clusters in MIL-101(Cr) have increased affinity towards propylene compared to propane, due to generation of a new kind of pocket-based propylene-binding site, as supported by DFT calculations.     

Mechanical and electrical response variation of the polyurethane–tin oxide–carbon nanotube composite microfiber depending on the chemical solution

Toward the goal of smart sensor systems for wearable electronics, polymer microfiber‐based free‐standing sensors benefit from excellent flexibility, decent ductility, and easy wearability in comparison with thin‐film‐based sensing devices. Herein, we report a hydrophobic and conducting single‐strand microfiber‐based liquid‐phase chemical sensor consisting of polyurethane (PU), tin oxide (SnO₂), and carbon nanotube (CNT) composites with applying a (1H,1H,2H,2H‐heptadecafluorodec‐1‐yl) phosphonic acid (HDF‐PA)‐based self‐assembled monolayer. The free‐standing HDF‐PA‐treated PU–SnO₂–CNT composite microfiber showing selective filtering properties with the repellency of water and the penetration of an organic solvent is electrically and mechanically characterized. Finally, the single‐strand HDF‐PA‐treated PU–SnO₂–CNT composite microfiber‐based chemical sensor, which shows excellent mechanical properties and aqueous stability, is demonstrated to detect the presence of a chemical in pure water or counterfeit gasoline in pure gasoline by observing mechanical changes, especially variations in the length and diameter of the fiber, and monitoring the electrical resistance change. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 495–502     

Self‐emulsion polymerization of amphiphilic monomers—a green route to synthesis of polymeric nanoscaffolds

Self‐emulsion polymerization (SEP), a green route developed by us for the polymerization of amphiphilic monomers, does not require any emulsifier or an organic solvent except that the water‐soluble initiators such as 2,2′‐azobis[2‐(2‐imidazolin‐2‐yl)propane]dihydrochloride (VA‐044) and potassium persulfate (KPS) are only used. We report here the polymer nanoscaffolds from a number of amphiphilic monomers, which can be used for in situ encapsulation of a variety of nanoparticles. As a demonstration of the efficacy of these nanoscaffolds, the synthesis of a biocompatible hybrid nanoparticle (nanohybrid), prepared by encapsulating Fe₃O₄ magnetic nanoparticle (Fe₃O₄ MNPs) in poly(2‐hydroxyethyl methacrylate) in water, for MRI application is presented. The nanohybrid prepared following the SEP in the form of an emulsion does not involve the use of any stabilizing agent, crosslinker, polymeric emulsifier, or surfactant. This water‐soluble, spherical, and stable nanohybrid containing Fe₃O₄ MNPs of average size 10 ± 2 nm has a zeta potential value of ?41.89 mV under physiological conditions. Magnetic measurement confirmed that the nanohybrid shows typical magnetic behavior having a saturation magnetization (Ms) value of 32.3 emu/g and a transverse relaxivity (r2) value of 29.97 mM^?1 s^?1, which signifies that it can be used as a T2 contrast agent in MRI. © 2019 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019