Limits for two-photon ande + e − decay widths of positron-electron scattering resonances for√s=1.78 to 1.92 MeV

Motivated by the observation of energy- and momentum-correlatede ⁺ e ^? pairs in heavy ion collisions, a search for resonances ine ⁺ e ^? scattering at the corresponding energies has been made. Thee ⁺ e ^? decay channel is analyzed in a time window from ～ 10^?13 s to ～ 10^?11 s with a set-up optimized for low-background detection of delayede ⁺ e ^? decays. The two-photon decay channel of a hypothetical resonance is investigated by measuring the two-photon annihilation-in-flight excitation function. New upper limits for the partiale ⁺ e ^? decay width Γ_ee of a few meV are derived for total centre-of-mass energies √s between 1.78 and 1.92 MeV, taking into account the dilepton as well as the two-photon decay of a neutral resonance.     

New pressure DSC cell and some applications

Physical properties and chemical reactions can be investigated by pressure DSC. There are 3 possibilities of sample preparation with respect to the contact with the furnace atmosphere which are illustrated by typical applications:

On the order conditions of Runge-Kutta methods with higher derivatives

Summary Runge-Kutta methods have been generalized to procedures with higher derivatives of the right side ofy=f(t,y) e.g. by Fehlberg 1964 and Kastlunger and Wanner 1972. In the present work some sufficient conditions for the order of consistence are derived for these methods using partially the degree of the corresponding numerical integration formulas. In particular, methods of Gauß, Radau, and Lobatto type are generalized to methods with higher derivatives and their maximum order property is proved. The applied technique was developed by Crouzeix 1975 for classical Runge-Kutta methods. Examples of simple explicit and semi-implicit methods are given up to order 7 and 6 respectively.     

Synthesis of 3,6-diaminophthalimides for ureidophthalimide-based foldamers

[reaction: see text]. Herein, we report an improved methodology for the synthesis of a variety of 3,6-diaminophthalimides in high yields. This enables decoration of the periphery of foldamers with a wide range of functionalities.     

Determination of the antiproton-to-electron mass ratio by precision laser spectroscopy of pHe+

A femtosecond optical frequency comb and continuous-wave pulse-amplified laser were used to measure 12 transition frequencies of antiprotonic helium to fractional precisions of (9-16)x10(-9). One of these is between two states having microsecond-scale lifetimes hitherto unaccessible to our precision laser spectroscopy method. Comparisons with three-body QED calculations yielded an antiproton-to-electron mass ratio of Mp/me=1836.152674(5).