Sum-of-Squares Results for Polynomials Related to the Bessis–Moussa–Villani Conjecture

We show that the polynomial S _m,k (A,B), that is the sum of all words in noncommuting variables A and B having length m and exactly k letters equal to B, is not equal to a sum of commutators and Hermitian squares in the algebra R〈X,Y〉, where X ²=A and Y ²=B, for all even values of m and k with 6≤k≤m−10, and also for (m,k)=(12,6). This leaves only the case (m,k)=(16,8) open. This topic is of interest in connection with the Lieb–Seiringer formulation of the Bessis–Moussa–Villani conjecture, which asks whether Tr (S _m,k (A,B))≥0 holds for all positive semidefinite matrices A and B. These results eliminate the possibility of using “descent + sum-of-squares” to prove the BMV conjecture.     

Manifestation of magnetically induced spatial dispersion in the cubic semiconductors ZnTe, CdTe, and GaAs

Nonreciprocal birefringence due to magnetically induced spatial dispersion was observed in the T _d-class cubic semiconductors ZnTe, CdTe, and GaAs near the fundamental absorption edge. The dispersion of the parameters A and g, describing the contributions from terms of the type B _ik_j to the diagonal and off-diagonal components of the permittivity tensor ε _ij(ω,B,k), is determined for ZnTe and CdTe. Analysis of the dispersion and anisotropy of the nonreciprocal birefringence shows that in ZnTe, CdTe, and GaAs, in contrast to magnetic semiconductors of the type Cd_1−x Mn_xTe, it is due excitonic mechanisms. Pis’ma Zh. éksp. Teor. Fiz. 69, No. 7, 514–519 (10 April 1999)     

Conformational analysis of <Emphasis Type="Italic">o</Emphasis>-allylphenol by density functional and IR spectroscopy methods

The two-dimensional cyclic potential energy surfaces for internal rotation of the allyl substituent and its vinyl fragment in o-allylphenol (o-APh) depending on the OH group orientation relative to the allyl substituent were constructed by a B3LYP/6-31G method. It is shown that o-APh exists in the gas phase as a mixture of eight non-planar rotamers (A, B, C, D, E, F, G, and H) and their eight optical isomers (A ₁, B ₁, C ₁, D ₁, E ₁, F ₁, G ₁, and H ₁). An intramolecular H-bond (IHB) O–H...π occurs only in four rotamers (A, B, A ₁, and B ₁). The content of such rotamers in the gas phase is 47.2% (as calculated by the B3LYP/cc-pVTZ method). Taking into account the solvation effect in the polarizable continuum model (PCM) for a solution of o-APh in cyclohexane decreases the total content of rotamers with an IHB (A and B) to 37.7%. The ratio of rotamers with OH groups bonded by an IHB and with free OH groups that is predicted theoretically agrees with the value measured experimentally from IR spectra of o-APH in CCl₄ solution.     

Properties and structure of GaAs films grown by molecular beam epitaxy on GaAs substrates with the (100), (111)A, and (111)B orientations

The structural perfection of GaAs epitaxial films grown by molecular beam epitaxy on substrates with the (100), (111)A, and (111)B orientations is investigated by double-crystal and triple-crystal x-ray diffractometry. It is found that the ratio γ of the molecular fluxes of arsenic and gallium has a strong influence on the structural quality of the epitaxial films. The optimum values of the parameter γ are found for each of the substrate orientations (100), (111)A, and (111)B. Zh. Tekh. Fiz. 69, 68–72 (July 1999)     

Reduction of Quantum Systems with Arbitrary First Class Constraints and Hecke Algebras

We propose a method for reduction of quantum systems with arbitrary first-class constraints. An appropriate mathematical setting for the problem is the homology of associative algebras. For every such algebra A and subalgebra B with augmentation ɛ there exists a cohomological complex which is a generalization of the BRST one. Its cohomology is an associative graded algebra Hk ^*(A,B) which we call the Hecke algebra of the triple (A,B,ɛ). It acts in the cohomology space H ^*(B,V) for every left A module V. In particular the zeroth graded component $Hk^{0}(A,B)$ acts in the space of B invariants of $V$ and provides the reduction of the quantum system. Received: 15 June 1998 / Accepted: 25 January 1999     

Survival and extinction in cyclic and neutral three-species systems

We study the ABC model ( A + B↦2B, B + C↦2C, C + A↦2A), and its counterpart: the three-component neutral drift model ( A + B↦2A or 2B, B + C↦2B or 2C, C + A↦2C or 2A.) In the former case, the mean-field approximation exhibits cyclic behaviour with an amplitude determined by the initial condition. When stochastic phenomena are taken into account the amplitude of oscillations will drift and eventually one and then two of the three species will become extinct. The second model remains stationary for all initial conditions in the mean-field approximation, and drifts when stochastic phenomena are considered. We analyzed the distribution of first extinction times of both models by simulations of the master equation, and from the point of view of the Fokker-Planck equation. Survival probability vs. time plots suggest an exponential decay. For the neutral model the extinction rate is inversely proportional to the system size, while the cyclic model exhibits anomalous behaviour for small system sizes. In the large system size limit the extinction times for both models will be the same. This result is compatible with the smallest eigenvalue obtained from the numerical solution of the Fokker-Planck equation. We also studied the behaviour of the probability distribution. The exponential decay is found to be robust against certain changes, such as the three reactions having different rates. Received 14 August 2002 and Received in final form 14 February 2003 / Published online: 1 April 2003 RID="a" ID="a"e-mail: ita@physics.ubc.ca     

Formality Theorem for Hochschild Cochains via Transfer

We construct a 2-colored operad Ger _∞ which, on the one hand, extends the operad Ger _∞ governing homotopy Gerstenhaber algebras and, on the other hand, extends the 2-colored operad governing open-closed homotopy algebras. We show that Tamarkin’s Ger _∞-structure on the Hochschild cochain complex C ^•(A, A) of an A _∞-algebra A extends naturally to a Ger⁺_￥{{\bf Ger}^+_{\infty}}-structure on the pair (C ^•(A, A), A). We show that a formality quasi-isomorphism for the Hochschild cochains of the polynomial algebra can be obtained via transfer of this Ger⁺_￥{{\bf Ger}^+_{\infty}}-structure to the cohomology of the pair (C ^•(A, A), A). We show that Ger⁺_￥{{\bf Ger}^+_{\infty}} is a sub DG operad of the first sheet E ¹(SC) of the homology spectral sequence for the Fulton–MacPherson version SC of Voronov’s Swiss Cheese operad. Finally, we prove that the DG operads Ger⁺_￥{{\bf Ger}^+_{\infty}} and E ¹(SC) are non-formal.     

Theoretical description of fluctuations in free-standing smectic-A films including spatial non-uniformity of their elastic characteristics

A theoretical study is reported of fluctuations in smectic layer displacements and of the correlations between them in free-standing smectic-A films formed of liquid-crystal compounds with smectic-A-isotropic liquid (Sm-A-I) and Sm-A-nematic (Sm-A-N) bulk phase transitions. The study took into account the dependence of the elastic constants for bending, K, and tension (compression), B, of smectic layers on distance to the free film surfaces. The calculations are compared with the results obtained within Hołyst’s model for spatially uniform, free-standing smectic-A films. It has been established that, below the temperature at which smectic order in the bulk of a liquid crystal disappears, taking into account the profiles of the elastic moduli K and B does not produce noticeable differences from this model. However, at temperatures considerably above the Sm-A-I and Sm-A-N phase transitions, their inclusion results in considerable discrepancies from the predictions of Hołyst’s model. Fiz. Tverd. Tela (St. Petersburg) 41, 1882–1889 (October 1999)     

Cantor–Bernstein Theorem for Pseudo-BCK-Algebras

We prove that if A and B are orthogonally σ-complete commutative pseudo-BCK-algebras such that A is isomorphic to a direct factor in B, and also B is isomorphic to a direct factor in A, then A and B are isomorphic. As a consequence we obtain previously known results for MV-algebras (by De Simone, Mundici and Navara), pseudo-MV-algebras (by Jakubík) and lattice-ordered groups (again by Jakubík). Supported by the Research and Development Council of the Czech Government, the research project MSM 6198959214.     

Interaction force between incompatible star-polymers in dilute solution

We consider a low-density assembly of spherical colloids, such that each is clothed by L end-grafted chemically incompatible polymer chains either of types A or B. These are assumed to be dissolved in a good common solvent. We assume that colloids are of small size to be considered as star-polymers. Two adjacent star-polymers A and B interact through a force F originating from both excluded-volume effects and chemical mismatch between unlike monomers. Using a method developed by Witten and Pincus (Macromolecules 19, 2509 (1986)) in the context of star-polymers of the same chemical nature, we determine exactly the force F as a function of the center-to-center distance h. We find that this force is the sum of two contributions F _e and F _s. The former, that results from the excluded volume, decays as F _e∼A _L h ^-1, with the L -dependent universal amplitude A _L∼L ^3/2. While the second, which comes from the chemical mismatch, decays more slowly as F _s∼χB _L h ^{-1 - τ}, where τ is a critical exponent whose value is found to be τ 0.40, and χ is the standard Flory interaction parameter. We find that the corresponding L-dependent universal amplitude is B _L∼L ^{3 + τ /2}. Theses forces are comparable near the cores of two adjacent star-polymers, i.e. for h∼h _c∼a (a is the monomer size). Finally, for two star-polymers of the same chemical nature (A or B), the force F that simply results from excluded-volume effects coincides exactly with F _e, and then the known result is recovered. Received 2 October 2000 and Received in final form 24 January 2001     

<Emphasis Type="Italic">SO</Emphasis>(3,1)-Invariant Approach to Dipole Radiation

The aim of the present work is to revisit the theory of the dipole radiation, within an SO(3,1)-gauge invariant formulation, by solving the Maxwell equations. Thus, we obtain the two interconnected components, A _B , B=1,2, of the vector potential A, in terms of Hankel and Legendre polynomials. Finally, for the pure dipole-like radiation, the observables, regarded as phasors, the Umov–Poynting vector components and the well-known Larmor formula for the effective radiated power are explicitly derived.     

Bound states and critical behavior of the Yukawa potential

We investigate the bound states of the Yukawa potential V (r)=−λexp(−αr)/r, using different algorithms: solving the Schr?dinger equation numerically and our Monte Carlo Hamiltonian approach. There is a critical α = α_C, above which no bound state exists. We study the relation between α_C and λ for various angular momentum quantum number l, and find in atomic units, α_C(l) = λ[A ₁ exp(−l/B ₁) + A ₂ exp(−l/B ₂)], with A ₁ = 1.020(18), B ₁ = 0.443(14), A ₂ = 0.170(17), and B ₂ = 2.490(180).     

e + e − pair production in ultrarelativistic heavy-ion collisions at intermediate impact parameters

Using the semiclassical Green’s function in the Coulomb field, we analyze the probabilities of single and multiple e ⁺ e ⁻ pair production at a fixed impact parameter b between colliding ultrarelativistic heavy nuclei. We perform calculations in the Born approximation with respect to the parameter Z _Bα and exactly in Z _Aα, where Z _A and Z _B are the charge numbers of the corresponding nuclei. We also obtain the approximate formulas for the probabilities valid for Z _Aα, Z _Bα ≲ 1. The text was submitted by the authors in English.     

Quantitative conversion spectroscopy of the ultrasoft isomeric transition of uranium-235 and the electronic structure of uranium oxides

Combined measurements of conversion electron spectra and the decay constant (76.5 eV, (1/2)⁺→(7/2)⁻) of the E3-isomeric transition of the uranium-235 nucleus have been performed with collection of the isomer atoms on an indium surface. The conversion spectra are interpreted as corresponding to a mixture of two different oxides A and B of uranium, one of which (A) is similar to UO₂, and the other (B) consists of a uranium-oxygen cluster based on the linear uranyl group O-U-O. From a set of mixed experimental spectra conversion spectra have been found corresponding to the chemical states A and B of the isomer atoms, and the variation of the absolute intensities of the conversion lines has been quantitatively investigated for them by varying the chemical composition of the isomer atoms and the ratio between the intensities of various conversion lines of the B spectrum. Experimental ratios between the intensities of the conversion lines are compared with the expected ratios in accordance with the distribution of the 6p electron density in the uranyl group. It is concluded that the experimental data agree with the calculation and that abrupt violations of proportionality of the partial probabilities of conversion of the electron density near the nucleus are absent. In accordance with the hypothesis of proportionality of the partial probabilities of conversion, an experimental estimate is given of the degree of localization of the deep-lying uranium 6p _1/2 shell during formation of the chemical bond in the uranyl group: around 70% of the 6p _1/2 electron density remains in the quasi-atomic uranium shell and around 30% is transferred to hybrid molecular orbitals. Zh. éksp. Teor. Fiz. 112, 574–595 (August 1997)     

Comment: “On the computation of molecular auxiliary functions<Emphasis Type="Italic">A</Emphasis><Subscript>n</Subscript>and<Emphasis Type="Italic">B</Emphasis><Subscript>n</Subscript>”

Guseinov, Mamedov, Kara and Orbay (Pramana - J. Phys. 56, 691 (2001)) propose methods for evaluating the molecular auxiliary functionsA _n(p) andB _n(pt) for the range 17 ≤n ≤ 60 and 25 ≤pt ≤ 60. However, their procedure forA _n(p) is not new, and that forB _n(pt) is less efficient for their target range than another well-known method. Their approach does have merit for smaller non-zero values ofpt. Two minor errors in table 1 of their paper are also identified.     

A Statistical Mechanics Approach for a Rigidity Problem

We focus the problem of establishing when a statistical mechanics system is determined by its free energy. A lattice system, modelled by a directed and weighted graph (whose vertices are the spins and its adjacency matrix M will be given by the system transition rules), is considered. For a matrix A(q), depending on the system interactions, with entries which are in the ring Z[a ^q :a∈R ⁺] and such that A(0) equals the integral matrix M, the system free energy β _A (q) will be defined as the spectral radius of A(q). This kind of free energy will be related with that normally introduced in Statistical Mechanics as proportional to the logarithm of the partition function. Then we analyze under what conditions the following statement could be valid: if two systems have respectively matrices A,B and β _A = β _B then the matrices are equivalent in some sense. Issues of this nature receive the name of rigidity problems. Our scheme, for finite interactions, closely follows that developed, within a dynamical context, by Pollicott and Weiss but now emphasizing their statistical mechanics aspects and including a classification for Gibbs states associated to matrices A(q). Since this procedure is not applicable for infinite range interactions, we discuss a way to obtain also some rigidity results for long range potentials.     

EPR of trivalent iron ions in a LiCaAlF6 crystal

The orientational dependences of the EPR spectra of Fe³⁺-doped LiCaAlF₆ single crystals (space group P31c, Z=2), grown at the Laboratory of Magnetic Radio Spectroscopy at Kazan’ State University, have been investigated in detail. The spectrum is described by a trigonal spin Hamiltonian with the following parameters: B ₂₀=40.072×10⁻⁴ cm⁻¹, B ₄₀=−5.799×10⁻⁴ cm⁻¹, B ₄₃=−4.281×10⁻⁴ cm⁻¹, A _s=24.33±1, A _p=6.13±1, g _∥=g _⊥=2.00217±0.0003. A theoretical calculation of the hyperfine structure parameters shows that they are described quite well when allowance is made for the overlapping of the wave functions of the paramagnetic center and the ligands (F⁻). Fiz. Tverd. Tela (St. Petersburg) 39, 488–490 (March 1997)