The forward-backward multiplicity correlations,the single hemisphere multiplicity distributions and the mean cluster size in high energye + e − and hadron-hadron collisions

Data on multiplicity distributions inp collisions at 0.3, 0.546, 1.0 and 1.8 GeV CM energy from recent experiments at FNAL and its relation to previous experiments are analyzed. Fits to the data and a critical discussion of the results are presented.Partially supported by CONICET     

Infrared photodissociation spectroscopy of electrosprayed ions in a Fourier transform mass spectrometer

Previous gas-phase methods for infrared photodissociation spectroscopy (IRPD) require sample volatility. Our method instead uses electrospray ionization to introduce even large nonvolatile molecules into a Fourier transform mass spectrometer, where extended (>15 s) ion storage makes possible high sensitivity spectral measurements with an OPO laser over a range of 3050-3800 cm(-1). The spectra of 22 gaseous proton-bound amino acid complexes are generally correlated with the H-stretching frequencies established for O-H and N-H functional groups in solution. For theoretical structure predictions of the Gly2H+ and N-acylated Asp2H+ dimers, IRPD spectra clearly differentiate between the predicted lowest energy conformers. In contrast to solution, in the gas phase the glycine zwitterion is approximately 20 kcal/mol less stable than the neutral; however, glycine is clearly zwitterionic in the gaseous GlyLysH+ dimer. The level of theory is inadequate for the larger Lys2H+ dimer, as all low energy predicted structures have free carboxyl O-H groups, in contrast to the IR spectrum. IRPD appears to be a promising new technique for providing unique information on a broad range of biomolecular and other gaseous ions, especially on noncovalent bonding involving O-H and N-H groups.     

Highly stereospecific epimerization of alpha-amino acids: conducted tour mechanism

The highly stereospecific and regiospecific recognition of alpha-amino acids exhibited by a novel Co(III) metal complex embodied in the experimental work (Nature 1999, 401, 254) is rationalized from the energetics and structural characteristics with the use of density functional calculations. The steric repulsion between the chiral center of the receptor [Co(III) complex] and alanine has been a cause for the discrimination of complex stabilities. The energies evaluated for all possible alanine binding modes clearly reveal regiospecificity. Our main emphasis is laid on the base-catalyzed epimerization reaction that drives the stereospecific recognition to near completion. The conducted tour mechanism is found to be the most likely candidate. A similar role by the equivalent Zn(II) complex is found.     

Kinetics and mechanism of the aminolysis of aryl N-ethyl thiocarbamates in acetonitrile

The aminolysis of aryl N-ethyl thiocarbamates (EtNHC(=O)SC(6)H(4)Z) with benzylamines (XC(6)H(4)CN(2)NH(2)) in acetonitrile at 30.0 degrees C is investigated. The rates are faster than the corresponding values for aryl N-phenyl thiocarbamates (PhNHC(=O)SC(6)H(4)Z), reflecting a stronger push to expel the leaving group by EtNH than the PhNH nonleaving group in a concerted process. The negative rho(XZ) (-0.86) and failure of the reactivity-selectivity principle found are consistent with the concerted mechanism. The kinetic isotope effects involving deuterated nucleophiles (k(H)/k(D) = 1.5-1.7) and low Delta H(++) with large negative Delta S(++) values suggest a hydrogen bond cyclic transition state.     

Fabric‐hydrogel composite membranes for culturing microalgae in semipermeable membrane‐based photobioreactors

In this article, we demonstrate that hydrogel‐based composite membranes are used as semipermeable materials for the construction of photobioreactors (PBRs). PBRs are developed to culture microalgae using nutrients dissolved in seawater, and thus they need to be fabricated with membranes possessing sufficient material‐transport properties. While hydrogels are characterized by their highly swelling nature in water and therefore have desirable transport of dissolved matter, they lack the mechanical strength to be cast into thin structures of large surface area. This issue motivated us to design a new concept, i.e., fabric‐hydrogel composite membranes ( FHCM s). A cotton fabric inside the hydrogel matrix endows the composite with tensile strength, which enables casting of FHCM s into thin membranes. Several FHCM s were prepared with 2‐hydroxyethyl methacrylate ( HEMA ), cross‐linking poly(ethylene glycol) dimethacrylate ( PEGDMA ) and a sheet of gauze by controlling the composition of the monomers and water. In the permeability measurement of nitrate ions, a key ingredient for the growth of microalgae, the permeability coefficient reached as high as 1.2 x 10^?8 m² min^?1, which is roughly three times higher than that of a commercially available semipermeable membrane (3.3 x 10^?9 m² min^?1). In the following evaluation of microalgal culture, a PBR constructed with a FHCM was able to maintain sufficient ion concentration and pH of the culture broth, supporting microalgal growth. These results suggest that the composite membranes with hydrogel and fabric have potential in the application of microalgal culture for bio‐diesel production in a marine environment. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2016 , 54, 108–114     

Band alignment and defect states in amorphous GaInZnO thin films grown on SiO2/Si substrates

The band alignment and defect states of GaInZnO thin films grown on SiO₂/Si via radio frequency (RF) magnetron sputtering were investigated by using X‐ray photoelectron spectroscopy, reflection electron energy loss spectroscopy, thermally stimulated exo‐electron emission and photo‐induced current transient spectroscopy.The band gap via reflection electron energy loss spectroscopy was 3.2 eV. The defect states via photo‐induced current transient spectroscopy and thermally stimulated exo‐electron emission were at 0.24, 0.53, 1.69 and 2.01 eV below the conduction band minimum of GIZO thin films, respectively. The defect states at 0.24 and 0.53 eV are related to the field‐effect mobility, and the defect stated at 1.69 and 2.01 eV is related to the oxygen vacancy defect. Copyright © 2016 John Wiley & Sons, Ltd.     

Thermal and electro-optical properties of cerium-oxide-doped liquid-crystal devices

Doping with cerium (IV) oxide (CeO₂) nanoparticles can significantly enhance the thermal stability and electro-optical (EO) properties of nematic liquid crystal (NLC) systems. Thermal stability was improved without aggregation and reduction of transmittance by adding CeO₂ nanoparticles in a liquid crystal medium. In particular, the EO properties greatly improved in CeO₂-dispersed NLC cells. The threshold voltage reduced from 3.027 to 2.279 V and the response time decreased from 13.097 to 9.970 ms with increased CeO₂ nanoparticles in the NLC cells. The improved properties of liquid crystals doped with CeO₂ nanoparticles depend on the anchoring energy and the electric field of the CeO₂-dispersed liquid crystal displays.