Interfacial electronic structure of vanadyl naphthalocyanine on highly ordered pyrolytic graphite

We present a core and valence region spectroscopic analysis of the interfacial electronic structure of thin films of vanadyl naphthalocyanine (VONc) deposited onto highly oriented pyrolytic graphite (HOPG). X-ray photoelectron spectroscopy indicates the predominantly ionic character of the vanadyl metal center coordinated by the heterocycle and affords the bandgap in the thin VONc films. Valence band photoelectron spectroscopy points to the existence of three different adsorption geometries of VONc on the HOPG surface. The distribution of the different geometries can be systematically influenced in a simple post-deposition processing step, with an immediate effect on the interfacial electronic environment. We find spectroscopic evidence in the valence levels that VONc grows on HOPG most likely in a 2D-gas fashion rather than by nucleation and growth of islands. These data allow us to predict accurately the interface dipole in the case of a broad class of dipolar organic semiconductors, based simply on molecular dipole moment, polarizability and molecular diameter. This ability provides an important step towards rational optimization of energy level alignment in organic electronics.     

Hosing instability in the blow-out regime for plasma-wakefield acceleration

The electron hosing instability in the blow-out regime of plasma-wakefield acceleration is investigated using a linear perturbation theory about the electron blow-out trajectory in Lu et al. [in Phys. Rev. Lett. 96, 165002 (2006)10.1103/PhysRevLett.96.165002]. The growth of the instability is found to be affected by the beam parameters unlike in the standard theory Whittum et al. [Phys. Rev. Lett. 67, 991 (1991)10.1103/PhysRevLett.67.991] which is strictly valid for preformed channels. Particle-in-cell simulations agree with this new theory, which predicts less hosing growth than found by the hosing theory of Whittum et al.     

Gas-phase reactivity of silver and copper coordinated monosaccharide cations studied by electrospray ionization and tandem mass spectrometry

The analytical distinction of the most common isomeric underivatized hexoses was investigated by means of mass spectrometry experiments. Electrospray ionization and tandem mass spectrometry were used in the analysis of silver and copper-coordinated monosaccharides (D-glucose, D-galactose, D-fructose, O-methyl-alpha-D-glucose and O-methyl-beta-D-glucose). The results show that cationization by Ag(+) allows the differentiation of the three first monosaccharides while the complexes formed by association of Cu(+) with these three monosacharides display a similar reactivity that prevents stereoisomer distinction. Unlike copper, silver adduct-ions of both alpha and beta anomeric O-methyl-D-glucoses exhibit specific decomposition patterns (i.e. a loss of methanol for the alpha-anomer and a loss of silver hydride for the beta-anomer), which allow an easy characterization. A theoretical survey of selected complexes, based on the use of DFT calculations were carried out on both anomers in order to rationalize the experimental findings.     

Determination of the angular and energy dependence of hard constituent scattering from π0 pair events at the CERN intersecting storage rings

We present data on proton-proton collisions, obtained at the CERN Intersecting Storage Rings, in which two roughly back-to-back π⁰'s of high transverse momentum (p_T) were produced. The angular distribution of the dipion axis relative to the collision axis is found to be independent of both the effective mass m of the dipion system and the centre-of-mass energy √s of the proton-proton collision. The cross-sections $\text{d}\text{σ}\text{d}\text{m}$ at the values of √s satisfy a scaling law of the form $\text{d}\text{σ}\text{d}\text{m}\text{=}\text{G(x)}\text{m}{}^{\mathrm{n}}\text{,}\text{where}\text{x = m(π}{}^0\text{, π}{}^0\text{)//trs}\text{and}\text{n = 6.5 ± 0.5}$. We show from our data that the leading π⁰ carries most of the momentum of the scattered parton. Given this fact, the axis of the dipion system follows closely the direction of the scattered constituents, and we exploit this to determine the angular dependence of the hard-scattering subprocess. We also compare our data with the lowest order QCD predictions using structure functions as determined in deep-inelastic scattering and fragmentation functions from electron-positron annihilation.     

A measurement of single electrons,electron pairs,and associated phenomena,in proton-proton collisions at the CERN ISR

Measurements of single-electron production in proton-proton collisions at the CERN ISR are presented for five centre-of-mass energies √s = 23.5, 30.6, 44.8, 52.7, and 62.4 GeV. The invariant cross sections for single electrons with transverse momenta of 0.60 to 4.7 GeV/c are given. Measurements of electron-positron pairs and measurements of charged hadrons produced in association with the single electrons, are also reported.     

Inclusive production cross sections of resonances in 32 GeV/c K+p interactions

The inclusive production of resonances is systematically studied in K⁺p interactions at 32 GeV/c. Total production cross sections are given for three baryon resonances, five vector and three 2⁺ tensor mesons. We also compare the central and fragmentation components of the total production cross sections with quark model predictions.     

Synthesis of Enantiomerically Pure Substituted Cyclopentenes from (−)-Quinic Acid

The synthesis of a large variety of enantiomerically pure substituted reactive cyclopentenes 16, 23, 24 and 28 have been synthesized from the readily available (?)-quinic acid 1 . The straightforward strategy involves a high-yielding intramolecular aldolization-dehydration of acyclic 1,6-dialdehydes 13, 18, 19 and 27 obtained by oxidative cleavage of cyclohexanediols 5, 7, 11 and 12 , using either lead tetraacetate or triphenylbismuth carbonate. Neither sulfoxide formation nor racemization of the intermediate dialdehydes at the oxygenated chiral centre was observed. Transformation of the thioacetal 25 to the corresponding ketone 26 using phenylselenic anhydride is also described.     

Two body correlations between negative pions in pp interactions at 69 GeV/c

Correlations between two π^? in pp interactions at 69 GeV/c are presented in terms of longitudinal and transversal variables. The dominant feature is the existence of a strong shortrange positive correlation between the two π^? in the central region.