On covering bridged plane triangulations with balls

We show that every plane graph of diameter 2r in which all inner faces are triangles and all inner vertices have degree larger than 5 can be covered with two balls of radius r. © 2003 Wiley Periodicals, Inc. J Graph Theory 44: 65–80, 2003     

Total synthesis of anachelin H

[structure: see text] The first total synthesis of anachelin H is reported. Starting from L-Ser, a stereodivergent synthesis of the polyketide fragment resulting in all possible diastereoisomers is described. The alkaloid peptide fragment is prepared via a tellurium-mediated oxidative aza annulation as the key step. Coupling of the fragments gave synthetic anachelin H, which was found to be identical to a sample of the natural product, thus confirming the configuration by total synthesis.     

The RHIM of the Immune Adaptor Protein TRIF Forms Hybrid Amyloids with Other Necroptosis-Associated Proteins

TIR-domain-containing adapter-inducing interferon-β (TRIF) is an innate immune protein that serves as an adaptor for multiple cellular signalling outcomes in the context of infection. TRIF is activated via ligation of Toll-like receptors 3 and 4. One outcome of TRIF-directed signalling is the activation of the programmed cell death pathway necroptosis, which is governed by interactions between proteins that contain a RIP Homotypic Interaction Motif (RHIM). TRIF contains a RHIM sequence and can interact with receptor interacting protein kinases 1 (RIPK1) and 3 (RIPK3) to initiate necroptosis. Here, we demonstrate that the RHIM of TRIF is amyloidogenic and supports the formation of homomeric TRIF-containing fibrils. We show that the core tetrad sequence within the RHIM governs the supramolecular organisation of TRIF amyloid assemblies, although the stable amyloid core of TRIF amyloid fibrils comprises a much larger region than the conserved RHIM only. We provide evidence that RHIMs of TRIF, RIPK1 and RIPK3 interact directly to form heteromeric structures and that these TRIF-containing hetero-assemblies display altered and emergent properties that likely underlie necroptosis signalling in response to Toll-like receptor activation.     

Insights into the oxidation of propylene oxide through the analysis of experiments and kinetic modeling

Cyclic ethers are important intermediates in the oxidation of hydrocarbons and biofuels. Studying the oxidation and pyrolysis of cyclic ethers will help in improving our understanding of this functional group and provide consistency to the base mechanism where they play an important role. In this aspect, propylene oxide has been investigated in this study by obtaining ignition delay time measurements in the rapid compression machine and shock tube. The experiments were performed in a range of pressures varying from 10 to 40 bar at different equivalence ratios (0.5–2.0) and dilution percentages. Additionally, speciation measurements in the shock tube at pyrolysis conditions have been performed at a pressure of 40 bar to explore the isomerization pathways. A detailed kinetic mechanism was developed to describe both the oxidation and pyrolysis chemistry of propylene oxide. The mechanism is not only able to predict the data obtained from this study but also reproduces the data from the literature in a consistent trend. For a better understanding of the oxidation and pyrolysis chemistry of propylene oxide, the kinetic analyses were performed using the developed mechanism to comprehend the important reaction pathways and sensitive reactions. At the investigated regime, the consumption of propylene oxide through its isomerization channels is the critical pathway that controls the reactivity of the fuel.     

An experimental and kinetic modeling study on the oxidation of 1,3-dioxolane

The modern catalytic or enzymatic advances allow the production of novel biofuel. Among them, 1,3-dioxolane can be produced from formaldehyde and ethylene glycol, both can be obtained from biomass. In this study, the oxidation of 1,3-dioxolane is studied at stoichiometric conditions. The ignition delay times of 1,3-dioxolane/O₂/inert mixtures were measured in a shock tube and in a rapid compression machine at pressures of 20 to 40 bar and temperatures ranging from 630 to 1300 K. The pressure profiles recorded in the rapid compression machine show a first stage of ignition enlightening the influence of the low temperature chemistry of combustion. Furthermore, mole fraction profiles of the stable intermediates produced during the oxidation of 1,3-dioxolane were measured in a jet-stirred reactor at 10 bar. Following these observations, a detailed kinetic model was developed with reaction rate coefficients and thermochemical data calculated by theoretical calculations or estimated by analogies to suitable molecules. In order to get an insight into the most important reaction pathways brute force sensitivity analysis and reaction pathway analysis were performed with the proposed model and discussed. It became clear that in the fuel-in-air case for the alkylhydroperoxide of 1,3-dioxolane the ring opening beta-scission pathway is favored against the further alkane-like second addition to molecular oxygen, which leads to a limited negative temperature coefficient.     

ATLAS discovery potential for a heavy charged Higgs boson

The sensitivity of the ATLAS detector to the discovery of a heavy charged Higgs boson is presented. Assuming a heavy SUSY spectrum, the most promising channels above the top quark mass are H^± → tb and H^± → τ^±ν_τ which provide coverage in the low and high tanβ regions up to ∼ 600 GeV. The achievable precisions on the charged Higgs mass and tanβ determination are also discussed. The H^± → W^± h⁰ channel, though restricted to a small MSSM parameter space, shows a viable signal in NMSSM where the parameter space is less constrained. The observation of the channel H⁻ → τ⁻_L ν_τ + c.c. may constitute a distinctive evidence for models with singlet neutrinos in large extra dimensions.     

Spin texture and magnetoroton excitations at nu=1/3

Neutral spin texture (ST) excitations at nu=1/3 are directly observed for the first time by resonant inelastic light scattering. They are determined to involve two simultaneous spin flips. At low magnetic fields, the ST energy is below that of the magnetoroton minimum. With increasing in-plane magnetic field these mode energies cross at a critical ratio of the Zeeman and Coulomb energies of eta(c)=0.020+/-0.001. Surprisingly, the intensity of the ST mode grows with temperature in the range in which the magnetoroton modes collapse. The temperature dependence is interpreted in terms of a competition between coexisting phases supporting different excitations. We consider the role of the ST excitations in activated transport at nu=1/3.     

Nuclear quantum effects on the thermal expansion coefficient of hexagonal boron nitride monolayer

This work examines the importance of vibrational delocalization on a basicthermomechanical property of a hexagonal boron nitride monolayer, namely its thermalexpansion coefficient (TEC). Using a recently parametrized bond-order potential of theTersoff type, the TEC was theoretically obtained from the thermal variations of thelattice parameter a(T) calculated using threedifferent methods: (i) the quasiharmonic approximation; (ii) its anharmonic improvementbased on self-consistent phonons; (iii) fully anharmonic Monte Carlo simulations possiblyenhanced within the path-integral framework to account for nuclear quantum effects. Theresults obtained with the three methods are generally consistent with one another and withother recently published data, and indicate that the TEC is negative at least up to ca.700 K, quantum mechanical effects leading to a significant expansion by about 50% relativeto the classical result. Comparison with experimental data on bulk hexagonal BN suggestssignificant differences, which originate from possible inaccuracies in the model that tendto underestimate the lattice parameter itself, and most likely from the 2D nature of themonolayer and the key contribution of out-of-plane modes. The effects of isotopic purityin the natural abundances of boron are found to be insignificant.     

High‐Yield Formation of Substituted Tetracyanobutadienes from Reaction of Ynamides with Tetracyanoethylene

A high‐yielding sequence of [2+2] cycloaddition–retroelectrocyclization of ynamides with tetracyanoethylene (TCNE) is described. The reaction provided tetracyanobutadiene (TCBD) species, which were characterized by various techniques. DFT and TD‐DFT calculations were also performed to complement experimental findings.