Formation of a regular fullerene nanochain lattice

A vicinal Au(11 12 12) surface, naturally patterned into a rectangular superlattice, has been used as a template to prepare C60 nanostructures with long-range order and uniform size. At a coverage of 0.1 monolayer and at room temperature, a two-dimensional long-range ordered superlattice of molecular nanochains is achieved, which perfectly replicates the periodicity of the template surface. The fullerene nanochains are found to be located exclusively on the face-centered cubic stacking domains at the lower step edges. Our experiments demonstrate that highly periodic molecular nanochains can be fabricated through a site-selective anchoring method.     

Halogen bonding in supramolecular chemistry

Halogen bonding is the noncovalent interaction where halogen atoms function as electrophilic species. The energetic and geometrical features of the interaction are described along with the atomic characteristics that confer molecules with the specific ability to interact through this interaction. Halogen bonding has an impact on all research fields where the control of intermolecular recognition and self-assembly processes plays a key role. Some principles are presented for crystal engineering based on halogen-bonding interactions. The potential of the interaction is also shown by applications in liquid crystals, magnetic and conducting materials, and biological systems.     

Mutual induced coordination in halogen-bonded anionic assemblies with (6,3) cation-templated topologies

We describe the use of halogen bonding for the deliberate construction of cation-templated anionic (6,3) networks thanks to a strategy based on the mutual induced fitting of the valences of the building blocks.     

Superfluorinated Ionic Liquid Crystals Based on Supramolecular,Halogen‐Bonded Anions

Unconventional ionic liquid crystals in which the liquid crystallinity is enabled by halogen‐bonded supramolecular anions [C_nF_{2 n+1}‐I⋅⋅⋅I⋅⋅⋅I‐C_nF_{2 n+1}]⁻ are reported. The material system is unique in many ways, demonstrating for the first time 1) ionic, halogen‐bonded liquid crystals, and 2) imidazolium‐based ionic liquid crystals in which the occurrence of liquid crystallinity is not driven by the alkyl chains of the cation.     

The Quantum Hydrodynamics System in Two Space Dimensions

In this paper we study global existence of weak solutions for the quantum hydrodynamics system in two-dimensional energy space. We do not require any additional regularity and/or smallness assumptions on the initial data. Our approach replaces the WKB formalism with a polar decomposition theory which is not limited by the presence of vacuum regions. In this way we set up a self consistent theory, based only on particle density and current density, which does not need to define velocity fields in the nodal regions. The mathematical techniques we use in this paper are based on uniform (with respect to the approximating parameter) Strichartz estimates and the local smoothing property.     

Fluorinated PLGA Nanoparticles for Enhanced Drug Encapsulation and 19F NMR Detection

In the continuous search for multimodal systems with combined diagnostic and therapeutic functions, several efforts have been made to develop multifunctional drug delivery systems. In this work, through a covalent approach, a new class of fluorinated poly(lactic-co-glycolic acid) co-polymers (F-PLGA) were designed that contain an increasing number of magnetically equivalent fluorine atoms. In particular, two novel compounds, F₃-PLGA and F₉-PLGA, were synthesized and their chemical structure and thermal stability were analyzed by solution NMR, DSC, and TGA. The obtained F-PLGA compounds were proven to form in aqueous solution colloidal stable nanoparticles (NPs) displaying a strong ¹⁹F NMR signal. The fluorinated NPs also showed an enhanced ability to load hydrophobic drugs containing fluorine atoms compared to analogous pristine PLGA NPs. Preliminary in vitro studies showed high cell viability and the NP ability to intracellularly deliver and release a functioning drug.     

Equivalent detector models for the simulation of efficiency response of an HPGe detector with PENELOPE code

ABSTRACT

In this work, some ‘equivalent’ models for the simulation of efficiency response of a High-Purity Germanium (HPGe) detector, installed inside a ‘low background’ bunker in the Engineering Department of the University of Palermo, were developed. The main feature was to attribute the uncertainties of the model to only one of the parameters, the dead layer of the detector, keeping unchanged the other data provided by the manufacturer. With this technique, using the Monte Carlo PENELOPE code in the 2011 version, the efficiency response was evaluated and compared with the previous one performed with MCNP5 code.

The validation of equivalent models is performed by comparing the simulation results with that of experimental spectrometric measurements of calibrated point sources and characterized volumetric sources such as a Marinelli beaker and an air filter reduced to a ‘packet-sample’.

The use of equivalent models makes the evaluation of efficiency curves with a Monte Carlo code easier and faster, and requires only a few experimental values for validation.