The transport gap of organic semiconductors studied using the combination of direct and inverse photoemission

The combination of valence band photoemission and inverse photoemission spectroscopy is applied to study the densities of occupied and unoccupied states of perylene derivative and phthalocyanine organic layers on inorganic semiconductors. The ionisation energies and electron affinities are determined and it is proposed that the transport gap of the materials can be evaluated from the distance of the HOMO and LUMO edges. The resulting values for the transport gap which are somewhat smaller than other published data are in good agreement with e.g. electrical measurements. The experimental spectra are compared with simulated ones obtained by density functional theory calculations.     

Fractal dimensions of lanthanum ferrite samples by adsorption isotherm method

Fractal dimensions of three different samples of lanthanum ferrite were computed using single adsorption method. The fractal Dubinin–Radushkevitch isotherm was used to fit directly the experimental nitrogen adsorption data. Avnir–Jaroniec method for fractal dimension determination was also used. Low and intermediate fractal dimensions were obtained according to BET specific surface areas.     

Molecular motion in solid ammonia trimethylalane

Solid state ²H NMR has been used to study molecular motion in deuterated ammonia trimethylalane (CH₃)₃AlND₃. From analysis of the ²H NMR lineshape between 123 and 298 K, reorientation of the -ND₃ group about the molecular Al-N axis is shown to occur at a rate higher than 10⁸ s^-1, and simulation of partially relaxed ²H NMR lineshapes shows that the reorientation can be described as a 3-site 120° jump motion. From the temperature dependence of the ²H spin-lattice relaxation time, the activation energy for this motion is estimated to be 9.3±0.3 kJ mol^-1. There is no evidence from either ²H or ²⁷Al NMR data for any site-exchange between the sites occupied by the -ND₃ and -CH₃ groups. The anisotropy of the dynamics of (CH₃)₃AlND₃ indicates that the orientation of the Al-N bond is highly constrained, presumably by a strong interaction between the electric dipoles of neighboring molecules.     

Massless gauge bosons other than the photon

Gauge bosons associated with unbroken gauge symmetries, under which all standard model fields are singlets, may interact with ordinary matter via higher-dimensional operators. A complete set of dimension-six operators involving a massless U(1) field, gamma('), and standard model fields is presented. The mu-->egamma(') decay, primordial nucleosynthesis, star cooling, and other phenomena set lower limits on the scale of chirality-flip operators in the 1-15 TeV range if the operators have coefficients given by the corresponding Yukawa couplings. Simple renormalizable models induce gamma(') interactions with leptons or quarks at two loops, and may provide a cold dark matter candidate.     

New Evidence for Liquid-Liquid Transitions in Polymers

The morphology changes in polyethylene (PE) and polypropylene (PP) melts were studied by rheometrical and x-ray methods. The dependence of viscosity on temperature exhibits reproducible, characteristic inflections within given temperature ranges. Throughout the transition range the variation of viscosity of PE is slower than in adjacent regions. The temperature dependences of the position, height, and half-width of the x-ray amorphous peak also show inflections in the same temperature range as viscosity. However, while the position of the amorphous peak and therefore the distance between chains varies in the transition range slower than in adjacent regions, the half-width and height asSociated to short range order and molecular chain mobility, respectively, change faster in the transition range than outside it. This means that morphological transformations at the molecular chains level, occurring in the transition range, have to be assigned to an increase of the length of parallel packed chain segments, as well as to the faster decrease of the short range order. The variation of melt viscosity and melt density supports this interpretation. Similar results were obtained for PP melts.     

Hemin interaction with bare and 4,4'-thio-bis-benzene-thiolate covered n-GaAs (110) electrodes

Cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS) investigations on the redox behavior of hemin at bare and 4,4'-thio-bis-benzene-thiolate (TBBT) covered n-GaAs (110) electrodes in dimethylsulfoxide (DMSO) revealed the high irreversibility of the electroreduction process, which appeared to be closely related to the stable adsorbed species strongly interfering with the electronic properties of the semiconducting substrate. The subsequent exploration of the hemin-modified electrodes by second harmonic generation (SHG), X-ray photoelectron spectroscopy (XPS) and atomic force microscopy (AFM) measurements pointed to significant differences between the iron protoporphyrin species adsorbed on the bare- and TBBT-GaAs (110) electrodes. Only Fe(2+) species having a flat configuration with the porphyrin plane oriented parallel to the surface were detected on GaAs, unlike the TBBT-GaAs, where Fe(2+) and Fe(3+) species having both flat and vertical adsorption positions could be observed. These differences originate from the mutual interactions between the solvent, hemin and dithiolate molecules as well as their competition for the surface sites found to play a key role in the electrochemical process under discussion.     

Die quantitative F?llung von Blei als basisches Bleisalicylat

Ohne Zusammenfassung     

Total oxidation of benzene using Cu-Cr mixed oxide as catalyst

Benzene total oxidation on a Cu-Cr supported catalyst was investigated using the work function method. Above 300°C, the majority of the oxygen species on the surface was O²⁻ in the absence or in the presence of hydrocarbon.     

Paclitaxel-Loaded Magnetic Nanoparticles Based on Biotinylated N-Palmitoyl Chitosan: Synthesis,Characterization and Preliminary In Vitro Studies

A considerable interest in cancer research is represented by the development of magnetic nanoparticles based on biofunctionalized polymers for controlled-release systems of hydrophobic chemotherapeutic drugs targeted only to the tumor sites, without affecting normal cells. The objective of the paper is to present the synthesis and in vitro evaluation of the nanocomposites that include a magnetic core able to direct the systems to the target, a polymeric surface shell that provides stabilization and multi-functionality, a chemotherapeutic agent, Paclitaxel (PTX), and a biotin tumor recognition layer. To our best knowledge, there are no studies concerning development of magnetic nanoparticles obtained by partial oxidation, based on biotinylated N-palmitoyl chitosan loaded with PTX. The structure, external morphology, size distribution, colloidal and magnetic properties analyses confirmed the formation of well-defined crystalline magnetite conjugates, with broad distribution, relatively high saturation magnetization and irregular shape. Even if the ability of the nanoparticles to release the drug in 72 h was demonstrated, further complex in vitro and in vivo studies will be performed in order to validate the magnetic nanoparticles as PTX delivery system.