Cross sections for multi-particle final states at a linear collider

In this paper total cross sections for signals and backgrounds of top- and Higgs-production channels in e ⁺ e^- collisions at a future linear collider are presented. All channels considered are characterized by the emergence of six-particle final states. The calculation takes into account the full set of tree-level amplitudes in each process. Two multi-purpose parton level generators, HELAC/PHEGAS and AMEGIC + + , are used, and their results are found to be in perfect agreement.Received: 26 November 2003, Revised: 15 January 2004, Published online: 3 March 2004     

Dynamics of the surface layer in cyanobiphenyl-aerosil nanocomposites with a high silica density

Composites were prepared from an aerosil and 4-n-alkyl-4'cyanobiphenyls with five to eight carbon atoms in the alkyl chain. Their high silica density of ∼7 g aerosil in 1 cm³ of liquid crystal (LC) allows the observation of the behaviour of a thin cyanobiphenyl layer (having nearly a monolayer structure) on the silica particles. The systems are investigated by dielectric spectroscopy (10^-2-10⁹ Hz) in a large temperature range (220-370 K). All the composites show a (main) relaxation process at frequencies much lower than the processes observed for the bulk LC that was assigned to the dynamics of the molecules in the surface layer. The temperature dependence of its characteristic frequencies obeys the Vogel-Fulcher-Tammann law, which is found to be typical for glass-forming liquids. The quasi two-dimensional character of the glass transition in the surface layer is discussed for the first time. At the nematic-to-isotropic transition temperature of the bulk, the composites show a continuous decrease of the characteristic frequencies as a function of the alkyl chain length, while the bulk LCs show the well known odd-even behaviour. The magnitude and temperature dependence of the slow relaxation process in the composites (molecules on an outer surface) agree with those of the same molecules confined to the nanopores of molecular sieves (internal surface).     

Bounded imaginary powers of differential operators on manifolds with conical singularities

 We study the minimal and maximal closed extension of a differential operator A on a manifold B with conical singularities, when A acts as an unbounded operator on weighted L _p -spaces over B, 1<p<∞. Under suitable ellipticity assumptions we can define a family of complex powers A ^z , zℂ. We also obtain sufficient information on the resolvent of A to show the boundedness of the purely imaginary powers. Examples concern unique solvability and maximal regularity for the solution of the Cauchy problem for the Laplacian on conical manifolds as well as certain quasilinear diffusion equations. Received: 12 June 2001; in final form: 3 June 2002 / Published online: 1 April 2003 Mathematics Subject Classification (2000): 35J70, 47A10, 35K57     

Gain competition effect in dual-wavelength dye lasers

In this paper, we present a theoretical model for the gain competition in dual-wavelength dye lasers. For this purpose the rate equations under the steady-state conditions have been used. The degree of the gain competition is shown to depend on the polarization of the two laser beams. The dependence of the gain competition on various working parameters such as pumping power, dye concentration and the reorientation rate of the molecules or solvent viscosity is studied for two different cases of parallel and orthogonal polarizations. The results of our model show dramatically different behaviors in the two proposed cases.     

Formation of nanosystems under near-equilibrium copper condensation in an ultrapure inert medium

Mechanisms of the self-organization of nanosystems at the condensation of the extremely weak steady flows of copper vapors obtained in magnetron sputtering in an ultrapure argon are studied. It is shown that the free-energy minimization near equilibrium condensation creates prerequisites for the self-organization of statistically homogeneous layers of nanoclusters and determines the transition to the formation of nanosystems in the form of fractal networks. Original Russian Text ? V.I. Perekrestov, A.S. Kornyushchenko, Yu.A. Kosminskaya, 2007, published in Pis’ma v Zhurnal éksperimental’noĭ i Teoreticheskoĭ Fiziki, 2007, Vol. 86, No. 12, pp. 879–883.     

Stark structure of the Yb3+ ion levels in (YbxY1?x)2Ti2O7 and the crystal field in rare-earth titanates with a pyrochlore structure

The absorption spectra of Yb₂Ti₂O₇ single crystals and the luminescence and luminescence excitation spectra of Y₂Ti₂O₇: Yb (1%) polycrystals were studied in the temperature range 4.2–300 K. The spectra were analyzed in terms of the crystal-field theory and the exchange-charge model. Based on the set of crystal-field parameters found for Yb₂Ti₂O₇, analogous sets of parameters were determined for other rare-earth titanates and proved to be in reasonable agreement with all available experimental data. __________ Translated from Fizika Tverdogo Tela, Vol. 47, No. 8, 2005, pp. 1376–1380. Original Russian Text Copyright ? 2005 by Klimin, Popova, Chukalina, Malkin, Zakirov, Antic-Fidancev, Goldner, Aschehoug, Dhalenne.     

Reaction of aroyl- and hetaroyltrifluoroacetones with acylhydrazines: Regioselectivity and tautomerism of the condensation products

Acylhydrazines react with 1,3-diketones of the general formula CF₃COCH₂COR (where R is an aryl or hetaryl group) at both carbonyl groups. The reaction at the trifluoroacetyl group is favored by donor substituents in the aromatic ring of the 1,3-diketone or by the 2-furyl and, especially, 2-thienyl group as a hetaryl substituent, as well as by elevated temperature. The condensation products at the carbonyl group contiguous to the aryl or hetaryl ring have the structure of 5-hydroxy-4,5-dihydropyrazoles and do not undergo tautomeric transformations in solution. The condensation products at the trifluoroacetyl group have either 5-hydroxy-4,5-dihydropyrazole or hydrazone structure and give rise to ring-chain tautomeric equilibrium in solution. Electron-withdrawing substituents in the aromatic ring of the 1,3-dicarbonyl fragment and CDCl₃ as solvent favor formation of the cyclic tautomer. The state of the tautomeric equilibrium is weakly sensitive to structural variations in the hydrazine component.