Laurdan and Prodan as Polarity-Sensitive Fluorescent Membrane Probes

The steady-state and dynamic fluorescence spectral properties of 2-dimethylamino-6-lauroylnaphthalene (LAURDAN) and several other naphthalene derivatives are summarized to illustrate their sensitivity to the polarity of the environment. Results obtained both in solvents of different polarity and in phospholipid vesicles in two phase states are presented. The emission red shift observed in polar solvents and in the phospholipid liquid–crystalline phase is explained on the basis of dipolar relaxation of solvent molecules surrounding the fluorescent naphthalene moiety of these probes. In phospholipid environments, experimental evidence is shown that excludes the intramolecular relative reorientation of the dimethylamino and carbonyl groups in the naphthalene and the reorientation of the entire fluorescent moiety. The solvent dipolar relaxation observed for LAURDAN and PRODAN in phospholipid bilayers has been attributed to a small number of water molecules present at the membrane interface. A comparison between LAURDAN emission in phospholipid vesicles prepared in D₂O and in H₂O is also presented. The definition and the derivation of the generalized polarization function are also discussed.     

UNA generalizzazione del problema di burnside relativo all'esponente 4

An automorphism σ of order (a divisor of)n of the groupG is calledn-splitting if for everyg∈G. In this paper we prove that a 2-group admitting a 4-splitting automorphism, is locally finite.     

A variational approach to chaotic dynamics in periodically forced nonlinear oscillators

We prove that a class of problems containing the classical periodically forced pendulum equation displays the main features of chaotic dynamics. The approach is based on the construction of multibump type heteroclinic solutions to periodic orbits by the use of global variational methods.     

Lipschitz and path isometric embeddings of metric spaces

We prove that each sub-Riemannian manifold can be embedded in some Euclidean space preserving the length of all the curves in the manifold. The result is an extension of Nash C ¹ Embedding Theorem. For more general metric spaces the same result is false, e.g., for Finsler non-Riemannian manifolds. However, we also show that any metric space of finite Hausdorff dimension can be embedded in some Euclidean space via a Lipschitz map.     

Hausdorff measures of subgroups of \mathbb{R }/\mathbb{Z } and \mathbb{R }

For a sequence $\underline{u}=(u_n)_{n\in \mathbb{N }}$ of integers, let $t_{\underline{u}}(\mathbb{T })$ be the group of all topologically $\underline{u}$ -torsion elements of the circle group $\mathbb{T }:=\mathbb{R }/\mathbb{Z }$ . We show that for any $s\in ]0,1[$ and $m\in \{0,+\infty \}$ there exists $\underline{u}$ such that $t_{\underline{u}}(\mathbb{T })$ has Hausdorff dimension $s$ and $s$ -dimensional Hausdorff measure equal to $m$ (no other values for $m$ are possible). More generally, for dimension functions $f,g$ with $f(t)\prec g(t), f(t)\prec \!\!\!\prec t$ and $g(t)\prec \!\!\!\prec t$ we find $\underline{u}$ such that $t_{\underline{u}}(\mathbb{T })$ has at the same time infinite $f$ -measure and null $g$ -measure.     

Time-division multiplexing of the orbital angular momentum of light

We present an optical setup for generating a sequence of light pulses in which the orbital angular momentum (OAM) degree of freedom is correlated with the temporal one. The setup is based on a single q plate within a ring optical resonator. By this approach, we demonstrate the generation of a train of pulses carrying increasing values of OAM, or, alternatively, of a controlled temporal sequence of pulses having prescribed OAM superposition states. Finally, we exhibit an "OAM-to-time conversion" apparatus that divides different input OAM states into different time bins. The latter application provides a simple approach to digital spiral spectroscopy of pulsed light.     

Chemical and Mechanical Characterization of Licorice Root and Palm Leaf Waste Incorporated into Poly(urethane-acrylate) (PUA)

A poly(urethane-acrylate) polymer (PUA) was synthesized, and a sufficiently high molecular weight starting from urethane-acrylate oligomer (UAO) was obtained. PUA was then loaded with two types of powdered ligno-cellulosic waste, namely from licorice root and palm leaf, in amounts of 1, 5 and 10%, and the obtained composites were chemically and mechanically characterized. FTIR analysis of final PUA synthesized used for the composite production confirmed the new bonds formed during the polymerization process. The degradation temperatures of the two types of waste used were in line with what observed in most common natural fibers with an onset at 270 °C for licorice waste, and at 290 °C for palm leaf one. The former was more abundant in cellulose (44% vs. 12% lignin), whilst the latter was richer in lignin (30% vs. 26% cellulose). In the composites, only a limited reduction of degradation temperature was observed for palm leaf waste addition and some dispersion issues are observed for licorice root, leading to fluctuating results. Tensile performance of the composites indicates some reduction with respect to the pure polymer in terms of tensile strength, though stabilizing between data with 5 and 10% filler. In contrast, Shore A hardness of both composites slightly increases with higher filler content, while in stiffness-driven applications licorice-based composites showed potential due to an increase up to 50% compared to neat PUA. In general terms, the fracture surfaces tend to become rougher with filler introduction, which indicates the need for optimizing interfacial adhesion.     

Electrochemically controlled formation/dissociation of phosphonate-cavitand/methylpyridinium complexes

The phosphorus-bridged cavitand 1 self-assembles very efficiently in CH2Cl2 with either the monopyridinium guest 2+ or the bispyridinium guest 3(2+). In the first case a 1:1 complex is obtained, whereas in the second case both 1:1 and 2:1 host-guest complexes are observed. The association between 1 and either one of the guests causes the quenching of the cavitand fluorescence; in the case of the adduct between 1 and 3(2+), the fluorescence of the latter is also quenched. Cavitand complexation is found to affect the reduction potential values of the electroactive guests. Voltammetric and spectroelectrochemical measurements show that upon one-electron reduction both guests are released from the cavity of 1. Owing to the chemical reversibility of such redox processes, the supramolecular complexes can be re-assembled upon removal of the extra electron from the guest. Systems of this kind are promising for the construction of switchable nanoscale devices and self-assembling supramolecular materials, the structure and properties of which can be reversibly controlled by electrochemical stimuli.