SUGRA hybrid inflation with shift symmetry

We propose a solution to the η  -problem in supergravity (SUGRA) hybrid inflation using a Nambu–Goldstone-like shift symmetry within a new class of models. The flatness of the tree-level inflaton potential is ensured by shift symmetry invariance of the Kähler potential, while a small symmetry breaking term in the superpotential gives rise to a slope of the potential at loop-level. In the proposed class of inflation models, potentially dangerous couplings between the inflaton and the moduli sector are avoided. We also discuss under which conditions the predicted spectral index can be in agreement with the best-fit-value of the latest WMAP observation ns∼0.96$n_{\mathrm{s}}\sim 0.96$, corresponding to a hilltop-type inflaton potential at loop-level.     

Chaotic inflation in supergravity with Heisenberg symmetry

We propose the introduction of a Heisenberg symmetry of the Kähler potential to solve the problems with chaotic inflation in supergravity, as a viable alternative to the use of shift symmetry. The slope of the inflaton potential emerges from a small Heisenberg symmetry breaking term in the superpotential. The modulus field of the Heisenberg symmetry is stabilized and made heavy with the help of the large vacuum energy density during inflation. The observable predictions are indistinguishable from those of typical chaotic inflation models, however the form of the inflationary superpotential considered here may be interpreted in terms of sneutrino inflation arising from certain classes of string theory.     

Highly regioselective synthesis of trifluoromethyl derivatives of pyrazolo[1,5-a]pyrimidines bearing fused cycloalkane rings using (2-ethoxycycloalkenyl)-2,2,2-trifluoroethanones

8-Trifluoromethyl-6,7-dihydro-5H-1,4,8a-triaza-s-indacene and 9-trifluoromethyl-5,6,7,8-tetrahydropyrazolo[5,1-b]quinazolines were efficiently generated by condensation of 5(3)-aminopyrazoles with (2-ethoxycycloalkenyl)-2,2,2-trifluoroethanones and isolated in excellent yields. The regiochemistry of the prepared compounds was established by ¹H, ¹³C and ¹⁹F NMR spectroscopy and X-ray diffraction analysis.     

Si-Fluoro substituted quasisilatranes (N → Si) FYSi(OCH2CH2)2NR

The reaction of fluorosilanes XYSiF₂ (X = Y = F; X = F, Y = Ph; X = Ph, Y = Me) with diethanolamines and their O-trimethylsilyl derivatives affords novel Si-fluoro substituted quasisilatranes 3, 5 and 9. These compounds were characterized by the multinuclear NMR spectroscopy and X-ray diffraction analysis. Experimental and theoretically calculated electron density distribution functions in crystal structure of 9 have shown that the N → Si coordination bond corresponds to polar bond with pronounced ionic contribution. Calculated N → Si bond order in the compound 9 does not exceed 1/3 of the normal Si-N bond. A strong N → Si coordination bond exists in compounds 3, 5 and 9 the length of which varies in the range 1.98-2.175 Å.     

Dual fluorescence from an isonido ReIII rhenacarborane phosphine complex, [7,10-mu-H-7-CO-7,7-(PPh3)2-isonido-7,8,9-ReC2B7H9

The complex [7,10-mu-H-7-CO-7,7-(PPh3)2-isonido-7,8,9-ReC2B7H9] has been synthesized by treatment of the complex salt [NHMe3][3,3-Cl2-3,3-(CO)2-closo-3,1,2-ReC2B9H11] with PPh3 in refluxing THF (tetrahydrofuran) and isolated as intensely colored orange-red microcrystals. Spectroscopic NMR and IR data have suggested that the product has a highly asymmetric structure with two inequivalent PPh3 ligands and a single CO ligand. Measurement of 11B NMR spectra in particular have indicated seven distinct boron vertexes, although the resulting cage degradation by removal of two BH vertexes was confirmed only following X-ray crystallographic analysis, which revealed the pentadecahedral isonido-7,8,9-ReC2B7 architecture. The 11B NMR resonances span an enormous chemical shift range (Deltadelta = 113), and this appears to be a direct consequence of the deshielding of the boron vertex directly opposite the quadrilateral |ReCCB| aperture. The new complex has been shown by electrochemical measurements to undergo a reversible one-electron oxidation. Digitally simulated cyclic voltammograms support a proposed square scheme (E(1/2) = 0.58, 0.69 V vs ferrocene) involving a reversible isonido-closo transition of the metallacarborane cage. Most unusually for a metallacarborane complex, ambient temperature solutions in CH2Cl2 and DMF have been shown to be intensely turquoise-blue fluorescent (lambda(em) = 442 nm, Phi = 0.012). Fluorescence spectroscopy measurements in MeTHF (2-methyltetrahydrofuran) glass at 77 K have indicated that the likely cause of such a broad emission is dual fluorescence (lambda(em) = 404, 505 nm), with both emissions displaying vibronic structure. Following excited-state lifetime decay analysis, the emissive behavior has been accredited to metal-perturbed 1IL states, with the lower energy emission arising from a slight geometric distortion of the initially excited complex.     

(Amidomethyl)dimethylsilanol hydrohalides: Synthesis, NMR and IR studies. Characteristic features of the electronic structure from high-resolution X-ray study and quantum chemical calculation

(C,O)-chelate silanol hydrohalides RC(O)NHCH₂SiMe₂OH · HHal (2a,b and 5b), and their precursors, (C,O)-chelate chlorosilanes RC(O)NHCH₂SiMe₂Cl (6a,b) and disiloxanes [RC(O)NHCH₂SiMe₂]₂O (8a,b) (R = Me (a), Ph (b); Hal = Cl (2), Br (5)), were obtained by several routes. The original scheme of hydrolysis of the above chlorides was discussed in detail. X-ray analysis has shown that the silanol hydrohalogenides PhC(O)NHCH₂SiMe₂OH · HX (2b and 5b) in the crystal exist in the form of cation-anion pairs [PhC(O)NHCH₂SiMe₂(OH₂)]⁺ · X⁻ (14b · Cl⁻ and 14b · Br⁻) assembled by H-bonds in a 3D framework. The Si atom in the cation has a trigonal bipyramidal configuration with the oxygen atom of the carbonyl group and protonated hydroxyl exo-substituent in axial positions. The endocyclic Si-O bonds are equal with an average of 1.905 Å while the exocyclic Si-O bonds are 1.979 and 2.009 Å, for Hal = Cl and Br, respectively.Quantum chemical calculations have shown that the cation [PhC(O)NHCH₂SiMe₂(OH₂)]⁺ (14b) is stable only in the crystal. Based on a high-resolution X-ray study and a quantum chemical calculation, it was found that the chemical bonding pattern in the OSiO axial fragment of the cation 14b corresponds to a three-centred four electron interaction. The cation 14b should be considered as a silylium cation stabilized by coordinated H₂O molecules rather than a silyloxonium ion.     

Simplified spectral phase interferometry for direct electric-field reconstruction by using a thick nonlinear crystal

We propose and demonstrate a novel implementation of spectral-shearing interferometry (SSI) for reconstructing the electric field of ultrashort pulses by utilizing asymmetric group velocity matching in a long nonlinear crystal. The proposed configuration eliminates the requirement for a linearly chirped auxiliary pulse that is in common in all existing SSI methods, relying on nonlinear conversion to produce a spectral shear.     

Experimental observations of tyre deformation characteristics on heavy mining vehicles under static and quasi-static loading

Due to large sidewall and bead thicknesses, multi-piece rims are necessary for use with large off-the-road (OTR) tyres. This paper presents the testing protocol and observed load/deflection and vertical/sidewall deflection characteristics of three Goodyear OTR tyre assemblies, namely, (1) a radial 29.5R29 (2) a bias-ply 29.5-29, and (3) a bias-ply 26.5-26. Localized tyre deformations and rim displacements were measured using optical displacement transducers and post-processing high-speed camera images using digital image analysis software. A validation analysis illustrated a maximum difference of 4.05% of vertical wheel displacements between the aforementioned methods. Quasi-static tests show the maximum values of vertical rim displacement and lateral tyre deflection are in the range of 72.2–78.9 mm and 23.3–27.1 mm, respectively, for a severe excitation condition. Differences ranging from 0.2% to 21.5% for maximum vertical and lateral tyre deflections were found between static load tests and engineering data provided by the tyre manufacturer. Linear relationships were observed for both vertical wheel displacement and lateral tyre deflection versus load for all tests. This study demonstrates a thorough methodology to study deflection characteristics of heavy duty OTR tyres and the collected data could be very useful in the development of numerical models of wheel and tyre assemblies for mining vehicles.     

Tests of discrete symmetries with the neutral kaon system at the KLOE and KLOE-2 experiments

The KLOE-2 experiment continues and extends the program of its predecessor KLOE in the field of discrete symmetry tests with the K meson system, among other studies which comprise light meson spectroscopy, dark matter searches and γγ physics. Together, KLOE and KLOE-2 have recorded the largest sample (almost 8 fb^??1) of e⁺e^? collisions at the energy equal to ? meson mass, amounting to 2.4 × 10¹⁰ of produced ? mesons. We report on the latest results and ongoing analyses of KLOE and KLOE-2 concerning discrete symmetry tests and measurements of symmetry-violating observables. A measurement of the CPT violation sensitive asymmetry in semileptonic decays of K˙S with 1.7 fb^??1 of KLOE data will be presented, which improves the sensitivity w.r.t. previous measurements about twice. Moreover, status of direct tests of T and CPT in transitions of neutral kaons performed with the ? →K˙SK˙L → πeν, 3π⁰(2π) processes will be reported, followed by the search of the CP-violating decay K˙S → 3π⁰ using the data recently acquired by KLOE-2.     

Electro-optical characterization of Ge–Se–Te glasses

Chalcogenide bulk glasses Ge₂₀Se_80−xTe_x for x(0,15) have been prepared by systematic replacement of Se by Te. Selected glasses have been doped with Ho, Er and Pr, and samples have been characterized by transmission spectroscopy, measurements of dc electrical conductivity and low-temperature photoluminescence. Absorption coefficients have been derived from measured transmittance and estimated reflectance. Arrhenius plots of dc electrical conductivity, in the measured temperature range 300–460 K, are characterized by single activation energies roughly equal to the half of the optical gap. Activation energies deduced from Arrhenius plots reveal a systematic decrease with increasing Te content. Similarly, both absorption and low-temperature photoluminescence spectra reveal shifts of absorption edge and/or dominant luminescence band to longer wavelength due to Te → Se substitution. Samples doped with Ho and Er exhibit a strong luminescence at 1200 and 1540 nm due to ⁵I₆ → ⁵I₈ and ⁴I_13/2 → ⁴I_15/2 transitions of Ho³⁺ and Er³⁺ ions, respectively. Pr doped samples exhibit only a relatively weak luminescence peak at 1590 nm, which we tentatively assign to ³F₃ → ³H₄ transition of Pr³⁺ ions. Absorption of the base glass luminescence at 1460 and 1520 nm has been observed at low temperature on samples doped with Pr and Er, respectively.