Photon gluon fusion cross sections at HERA energy

We present cross sections for heavy flavour production through photon gluon fusion in electron proton collisions at HERA energy. The electron photon vertex is taken into account explicitly, and theQ ² of the exchanged photon ranges from nearly zero (almost real photon) to the kinematically allowed maximum. In our approach the scale is set by the mass of the produced quarks. Our formalism is also applicable to the production of light quarks as long as the invariant mass of the pair is sufficiently high, so we also give cross sections for \(u\bar u,d\bar d\) and \(s\bar s\) production.     

Magydardiendiol,diterpenoid with a new skeleton from magydaris panacifolia (umbelliferae).

Three new diterpenoids with a substituted α-cyclogeraniol skeleton have been isolated from the umbelliferae $\text{Magydaris panacifolia}$ (Vahl) Lange, for which the names of magydar-2,13-dien-11,17-diol, $\text{1}$, magydar-2,10 (20), 13-trien-17-ol, $\text{2}$, and magydar-2,10(20), 13-trien-17-yl acetate, $\text{3}$, are proposed. The structures of these substances have been deduced from spectroscopic and chemical data.     

Chimie des complexes de metaux de transition avec des hydrocarbures cyanes : III. Quelques observations sur la conformation et la reactivite de complexes dicyclopentadienyles du molybdene et du tungstene

A new class of cyclic telluronium salts has been prepared. All the salts are stable in solution in CHCl₃ or dimethylsulphoxide (DMSO). Conductivity measurements in DMSO and dimethylformamide (DMF) have shown that considerable ion pairing occurs in solution. Infrared, ¹H, ¹³C, ¹²⁵Te NMR, and mass spectra are reported and discussed.     

CHEMILUMINESCENCE FROM THE OXIDATION OF AUXIN DERIVATIVES

Abstract— The thiophenyl ester of indole-3-acetic acid and indole-3-acetonitrile produce chemiluminescence in aerated dimethylsulfoxide in the presence of potassium t -butoxide. The emitter is the aromatic aldehyde. In the case of acetonitrile, the other product expected from the cleavage of an intermediate dioxetane, cyanate/isocyanate, has also been identified. Other auxins also chemiluminesce under similar conditions, but the emitters have not been properly identified.
These systems are models for the peroxidase catalyzed oxidation of indole-3-acetic acid to indole-3-carboxaldehyde and as such support the earlier inference (Vidigal et al , 1975) that the excited aldehyde is generated in the enzymic process.
An additional result is the observation of an exciplex between excited indole-3-carboxaldehyde and the thiophenylester of indole-3-acetic acid. This appears to be the first case of chemical generation of an exciplex by a route other than radical ion reaction, presumably by the dioxetane route.