Synthesis of photochromic 1,2-dihetarylethene using regioselective acylation of thienopyrroles

[formula: see text] The influence of catalysts, acid chlorides, and solvents in the acylation of methyl 2-methyl-4H-thieno[3,2-b]pyrrole-5-carboxylate was studied. Conditions for the regioselective acylation processes were found. Thienopyrrole-based photochrome was synthesized for the first time.     

Smectic membranes in motion: approaching the fast limits of x-ray photon correlation spectroscopy

The dynamics of the layer-displacement fluctuations in smectic membranes have been studied by x-ray photon correlation spectroscopy (XPCS). We report transitions from an oscillatory damping regime to simple exponential decay of the fluctuations, both as a function of membrane thickness and upon changing from specular to off-specular scattering. This behavior is in agreement with recent theories. Employing avalanche photodiode detectors and the uniform filling mode of the synchrotron storage ring, the fast limits of XPCS have been explored down to 50 ns.     

Kinetic theory of symmetry-dependent strength in carbon nanotubes

Carbon nanotubes yield to mechanical force by a primary dislocation dipole whose formation energy describes the thermodynamic stability of the tubule. However, the real-time strength is determined by the rate of defect formation, defined in turn by the activation barrier for the bond flip. First extensive computations of the kinetic barriers for a variety of strain-lattice orientations lead to predictions of the yield strength. Its value depends on nanotube chiral symmetry, in a way very different from the thermodynamic assessment.     

Dispersion management for solitons in a Korteweg-de Vries system

The existence of "dispersion-managed solitons," i.e., stable pulsating solitary-wave solutions to the nonlinear Schrodinger equation with periodically modulated and sign-variable dispersion is now well known in nonlinear optics. Our purpose here is to investigate whether similar structures exist for other well-known nonlinear wave models. Hence, here we consider as a basic model the variable-coefficient Korteweg-de Vries equation; this has the form of a Korteweg-de Vries equation with a periodically varying third-order dispersion coefficient, that can take both positive and negative values. More generally, this model may be extended to include fifth-order dispersion. Such models may describe, for instance, periodically modulated waveguides for long gravity-capillary waves. We develop an analytical approximation for solitary waves in the weakly nonlinear case, from which it is possible to obtain a reduction to a relatively simple integral equation, which is readily solved numerically. Then, we describe some systematic direct simulations of the full equation, which use the soliton shape produced by the integral equation as an initial condition. These simulations reveal regions of stable and unstable pulsating solitary waves in the corresponding parametric space. Finally, we consider the effects of fifth-order dispersion. (c) 2002 American Institute of Physics.     

Solution calorimetry of organic nonelectrolytes as a tool for investigation of intermolecular interactions

The paper is mainly the review and generalization of the previous publications of the authors. It demonstrates that solution calorimetry method gives the opportunities of more detailed understanding of various aspects of intermolecular interactions in solution. We are assured that prerequisite to such an understanding is the successive analysis of various solute–solvent systems from the simplest ones which include alkanes as a solute or as a solvent to the most complex systems with solvent self‐association via hydrogen bonding. Particular findings discussed in this paper are (i) an inconspicuous contribution of electrostatic solute–solvent interaction to the solvation enthalpy and, accordingly, the dominating contribution of dispersion interactions for nonspecifically solvated solutes; (ii) new, very general method for the extraction of specific interaction enthalpy from the enthalpy of solvation; (iii) new method of determination of self‐association enthalpies for the solvents associated via hydrogen bonding; (iv) new method for determination of cooperative hydrogen bonding enthalpies of proton acceptors with associated species of alcohols; (v) the unique method of experimental determination of the hydrophobic effect enthalpy. Copyright © 2007 John Wiley & Sons, Ltd.     

Fine-tuning two-particle interferometry I: Effects from temperature gradients in the source

A comprehensive model study of Bose-Einstein correlation radii in heavy ion collisions is presented. The starting point is a longitudinally and transversally expanding fireball, represented at freeze-out by an azimuthally symmetric emission function. The freeze-out temperature is allowed to feature transverse and temporal gradients. Their effects on the correlation radii are studied. In particular, we evaluate numerically their dependence on the transverse mass of the particle pairs and check a recent suggestion, based on analytical approximations, that for certain reasonable source parameters all three correlation radii satisfy simultaneously a scaling. Received: 2 July 1997 / Revised version: 25 September 1997 / Published online: 23 February 1998     

The density of rational functions in Markov systems: A counterexample to a conjecture of D. J. Newman

We construct a family of infinite Markov systems on [?1, 1] with the property that the rational functions from these systems are not dense inC[?1, 1]. This gives counterexamples to a long-standing conjecture of D. J. Newman.     

Interactions in Cp2TiX-AlH3−nXn-Et2O(NEt3) systems

Summary Cp₂TiX-AlH_3–nX_n-Et₂O(NEt₃) systems where X is Cl or Br, and n=0 or 1 have been studied by dielectrometric and calorimetric titration and by e.s.r. techniques. Bimetallic 11 compounds containing hydrogen bridges are formed in all systems. All reaction products, with the exception of Cp₂TiH₂AlHCl · Et₂O formed at 20 to 25°, are monomeric in solution. The monochloro derivative is a dimer containing both ordinary and double hydrogen bridges.