Improved Parameterization for Combined Isotopomer Analysis of Diatomic Spectra and Its Application to HF and DF

A new way of representing vibration-rotation term values for multiple isotopomers of a given electronic state of a diatomic molecule is presented which resolves problems associated with the way the conventional combined isotopomer expansion represents the atomic mass-dependent JWKB and Born-Oppenheimer breakdown correction terms. Its application to infrared and microwave data for HF and DF yields new Dunham expansion coefficients and Born-Oppenheimer breakdown correction terms for this species. This procedure is implemented in a generally available computer program for fitting to various types of data involving one or several electronic states of multiple isotopomers of a diatomic molecule. Copyright 1999 Academic Press.     

Proton polarization in the14N(3He,p)16O reaction near 10 MeV and reaction mechanisms

The angular distribution of the proton polarization has been measured between 30° and 110° in the CM system near 10 MeV laboratory energy. It provides a sensitive test of theoretical fits to the cross section angular distribution. The reaction mechanism is largely direct below 70° and evidence has been found for a deuteron-cluster transfer. Nuclear Reactions¹⁴N³(He,p),E=9.8 MeV; measuredP(E,θ), σ(E,θ); DWBA and deuteron transfer analysis; deduced dominant mechanism of forward angle amplitudes.     

Deutron transfer in the 3He(3He,p)5Li reaction

Evidence supporting the transfer of deuteron cluster in the reaction ³He(³He, $\text{p}$)⁵Li is presented. This entails a selection of total angular momentum in a two-nucleon transfer reaction.