The Structure of Polyfulvenes

Cationic polymerisation of 6,6-disubstituted pentafulvenes yields highly unsaturated, reactive macromolecules of high mo- . lecular weight. The mechanistic pathways leading to the polymers are discussed, and the structure XIV of the polymers has been elucidated by a combination of spectroscopic methods as well as by comparison with model compounds. In contrast to reports in the literature, the main process in thermal oligomerisation of simple pentafulvenes at 20 °c is a Diels-Alder reaction giving products of type XXI. Anionic polymerisation of pentafulvenes is initiated by traces of sodium cyclopentadienide or phenylsodium respectively. The reaction products consist of a mixture of oligomers of the series (fulvene)n. This surprising result can be explained by structure elucidation of the fulvene dimers, which gives formula XX. The mechanistic aspects of the reaction are discussed

Dispersive estimates for Schr\"odinger operators with point interactions in R3\mathbb{R}^3

The study of dispersive properties of Schr\"odinger operators with point interactions is a fundamental tool for understanding the behavior of many body quantum systems interacting with very short range potential, whose dynamics can be approximated by non linear Schr\"odinger equations with singular interactions. In this work we proved that, in the case of one point interaction in $\mathbb{R}^3$, the perturbed Laplacian satisfies the same $L^p-L^q$ estimates of the free Laplacian in the smaller regime $q\in[2,3)$. These estimates are implied by a recent result concerning the $L^p$ boundedness of the wave operators for the perturbed Laplacian. Our approach, however, is more direct and relatively simple, and could potentially be useful to prove optimal weighted estimates also in the regime $q\geq 3$.Comment: To appear on: "Advances in Quantum Mechanics: Contemporary Trends and Open Problems", G. Dell'Antonio and A. Michelangeli eds., Springer-INdAM series 201

Enhanced suppresion of localization in a continuous Random-Dimer Model

We consider a one-dimensional continuous (Kronig-Penney) extension of the (tight-binding) Random Dimer model of Dunlap et al. [Phys. Rev. Lett. 65, 88 (1990)]. We predict that the continuous model has infinitely many resonances (zeroes of the reflection coefficient) giving rise to extended states instead of the one resonance arising in the discrete version. We present exact, transfer-matrix numerical calculations supporting, both realizationwise and on the average, the conclusion that the model has a very large number of extended states.Comment: 10 pages, 3 Figures available on request, REVTeX 3.0, MA/UC3M/1/9

Proper incorporation of self-adjoint extension method to Green's function formalism : one-dimensional δ′\delta^{'}-function potential case

One-dimensional $\delta^{'}$-function potential is discussed in the framework of Green's function formalism without invoking perturbation expansion. It is shown that the energy-dependent Green's function for this case is crucially dependent on the boundary conditions which are provided by self-adjoint extension method. The most general Green's function which contains four real self-adjoint extension parameters is constructed. Also the relation between the bare coupling constant and self-adjoint extension parameter is derived.Comment: LATEX, 13 page

Dimensional crossover of a boson gas in multilayers

We obtain the thermodynamic properties for a non-interacting Bose gas constrained on multilayers modeled by a periodic Kronig-Penney delta potential in one direction and allowed to be free in the other two directions. We report Bose-Einstein condensation (BEC) critical temperatures, chemical potential, internal energy, specific heat, and entropy for different values of a dimensionless impenetrability $P\geqslant 0$ between layers. The BEC critical temperature $T_{c}$ coincides with the ideal gas BEC critical temperature $T_{0}$ when $P=0$ and rapidly goes to zero as $P$ increases to infinity for any finite interlayer separation. The specific heat $C_{V}$ \textit{vs} $T$ for finite $P$ and plane separation $a$ exhibits one minimum and one or two maxima in addition to the BEC, for temperatures larger than $T_{c}$ which highlights the effects due to particle confinement. Then we discuss a distinctive dimensional crossover of the system through the specific heat behavior driven by the magnitude of $P$. For $T<T_{c}$ the crossover is revealed by the change in the slope of $\log C_{V}(T)$ and when $T>T_{c}$, it is evidenced by a broad minimum in $C_{V}(T)$.Comment: Ten pages, nine figure

Can Light Signals Travel Faster than c in Nontrivial Vacuua in Flat space-time? Relativistic Causality II

In this paper we show that the Scharnhorst effect (Vacuum with boundaries or a Casimir type vacuum) cannot be used to generate signals showing measurable faster-than-c speeds. Furthermore, we aim to show that the Scharnhorst effect would violate special relativity, by allowing for a variable speed of light in vacuum, unless one can specify a small invariant length scale. This invariant length scale would be agreed upon by all inertial observers. We hypothesize the approximate scale of the invariant length.Comment: 12 pages no figure

Exact particle and kinetic energy densities for one-dimensional confined gases of non-interacting fermions

We propose a new method for the evaluation of the particle density and kinetic pressure profiles in inhomogeneous one-dimensional systems of non-interacting fermions, and apply it to harmonically confined systems of up to N=1000 fermions. The method invokes a Green's function operator in coordinate space, which is handled by techniques originally developed for the calculation of the density of single-particle states from Green's functions in the energy domain. In contrast to the Thomas-Fermi (local density) approximation, the exact profiles under harmonic confinement show negative local pressure in the tails and a prominent shell structure which may become accessible to observation in magnetically trapped gases of fermionic alkali atoms.Comment: 8 pages, 3 figures, accepted for publication in Phys. Rev. Let

On the Green function of linear evolution equations for a region with a boundary

We derive a closed-form expression for the Green function of linear evolution equations with the Dirichlet boundary condition for an arbitrary region, based on the singular perturbation approach to boundary problems.Comment: 9 page

Resonance-Induced Effects in Photonic Crystals

For the case of a simple face-centered-cubic photonic crystal of homogeneous dielectric spheres, we examine to what extent single-sphere Mie resonance frequencies are related to band gaps and whether the width of a gap can be enlarged due to nearby resonances. Contrary to some suggestions, no spectacular effects may be expected. When the dielectric constant of the spheres $\epsilon_s$ is greater than the dielectric constant $\epsilon_b$ of the background medium, then for any filling fraction $f$ there exists a critical $\epsilon_c$ above which the lowest lying Mie resonance frequency falls inside the lowest stop gap in the (111) crystal direction, close to its midgap frequency. If $\epsilon_s <\epsilon_b$, the correspondence between Mie resonances and both the (111) stop gap and a full gap does not follow such a regular pattern. If the Mie resonance frequency is close to a gap edge, one can observe a resonance-induced widening of a relative gap width by $\approx 5$.Comment: 14 pages, 3 figs., RevTex. For more info look at http://www.amolf.nl/external/wwwlab/atoms/theory/index.htm

The Structure of Polyfulvenes

Cationic polymerisation of 6,6-disubstituted pentafulvenes yields highly unsaturated, reactive macromolecules of high mo- . lecular weight. The mechanistic pathways leading to the polymers are discussed, and the structure XIV of the polymers has been elucidated by a combination of spectroscopic methods as well as by comparison with model compounds. In contrast to reports in the literature, the main process in thermal oligomerisation of simple pentafulvenes at 20 °c is a Diels-Alder reaction giving products of type XXI. Anionic polymerisation of pentafulvenes is initiated by traces of sodium cyclopentadienide or phenylsodium respectively. The reaction products consist of a mixture of oligomers of the series (fulvene)n. This surprising result can be explained by structure elucidation of the fulvene dimers, which gives formula XX. The mechanistic aspects of the reaction are discussed