Higher-order QED corrections to single-W production in electron-positron collisions

Four-fermion processes with a particle lost in the beam pipe are studied at LEP to perform precision tests of the electroweak theory. Leading higher-order QED corrections to such processes are analyzed within the framework of the Structure Functions (SF) approach. The energy scale entering the QED SF is determined by inspection of the soft and collinear limit of the O(alpha) radiative corrections to the four-fermion final states, paying particular attention to the process of single-W production. Numerical predictions are shown in realistic situations for LEP experiments and compared with existing results. A Monte Carlo event generator, including exact tree-level matrix elements, vacuum polarization, higher-order leading QED corrections and anomalous trilinear gauge couplings, is presented.Comment: LaTeX (using elsart), 21 pages, 8 .ps figure

Light Pair Correction to Bhabha Scattering at Small Angle

This work deals with the computation of electron pair correction to small angle Bhabha scattering, in order to contribute to the improvement of luminometry precision at LEP/SLC below 0.1% theoretical accuracy. The exact QED four-fermion matrix element for $e^+e^-\to e^+e^-e^+e^-$, including all diagrams and mass terms, is computed and different Feynman graph topologies are studied to quantify the error of approximate calculations present in the literature. Several numerical results, obtained by a Monte Carlo program with full matrix element, initial-state radiation via collinear structure functions, and realistic event selections, are shown and critically compared with the existing ones. The present calculation, together with recent progress in the sector of $O(\alpha^2)$ purely photonic corrections, contributes to achieve a total theoretical error in luminometry at the 0.05% level, close to the current experimental precision and important in view of the final analysis of the electroweak precision data.Comment: LaTeX2e, 28 pages, 8 figures include

Light-Pair Corrections to Small-Angle Bhabha Scattering in a Realistic Set-up at LEP

Light-pair corrections to small-angle Bhabha scattering have been computed in a realistic set-up for luminosity measurements at LEP. The effect of acollinearity and acoplanarity rejection criteria has been carefully analysed for typical calorimetric event selections. The magnitude of the correction, depending on the details of the considered set-up, is comparable with the present experimental error.Comment: 6 pages, LaTeX (elsart.sty), 4 tables, 1 figur

On the abundance of Lithium in T Coronae Borealis

We have obtained high resolution echelle spectroscopy of the recurrent nova T CrB. We find that the surface lithium abundance in T CrB is signifcantly enhanced compared to field M giants, where it is not detectable. We offer possible explanations for this in terms of either a delay in the onset of convection in the giant star, enhanced coronal activity due to star-spots or the enhancement of Li resulting from the nova explosion(s).Comment: 3 pages, 1 figure (a and b), accepted by MNRA

One-step preparation of enantiopure L- or D-amino acid benzyl esters avoiding the use of banned solvents

The enantiomers of amino acid benzyl esters are very important synthetic intermediates. Many of them are currently prepared by treatment with benzyl alcohol and p-toluenesulfonic acid in refluxing benzene or carbon tetrachloride, to azeotropically remove water, and then precipitated as tosylate salt by adding diethyl ether. Here, we report a very efficient preparation of eight l- or d-amino acid benzyl esters (Ala, Phe, Tyr, Phg, Val, Leu, Lys, Ser), in which these highly hazardous solvents are dismissed using cyclohexane as a water azeotroping solvent and ethyl acetate to precipitate the tosylate salt. With some work-up modifications and lower yield, the procedure can be applied also to methionine. Chiral HPLC analysis shows that all the benzyl esters, including the highly racemizable ones such as those of phenylglycine, tyrosine and methionine, are formed enantiomerically pure under these new reaction conditions thus validating the solvents replacement. Contrariwise, toluene cannot be used in place of benzene or carbon tetrachloride because leading to partially or totally racemized amino acid benzyl esters depending on the polar effect of the amino acid \u3b1-side chain as expressed by Taft\u2019s substituent constant (\u3c3*)