Resonance formation in electron collisions with pyrimidine-like targets

In this thesis we apply the R-matrix method to study low-energy « 15 eV) elastic and inelastic electron collisions with the diazine molecules (pyrazine, pyrimidine and pyridazine), (2 and 4) oxopyrimidines and the RNA nucleobase uracil. We use these molecules as models for the pyrimidinic DNA nucleobases. The main goal of this work is to study resonance formation in these targets. We test various standard scattering models (Static Exchange, Static Exchange plus Polarization, CloseCoupling) to identify those that produce the most accurate results; we also study simplified versions of these models that allow us to provide detailed insights into the resonance formation. We compare our elastic (for pyrazine and pyrimidine) and inelastic (for pyrimidine) cross sections with available experimental data and find a good agreement. A methodology based on the time-delay analysis is applied that allowed us to find and characterize in det ail many new resonances not previously identified. We find an unexpectedly large number of resonances. Most of the new resonances have core-excited shape character and many of them do not enhance (significantly) the elastic or inelastic cross sections for collisions with the molecule in the ground state. These resonances, however, significantly enhance the elastic cross sections for collisions with mole<:ules in electronic excited states. The discovery of a large number of these resonances and their unusual properties are novel and unexpected results. We find that oxygen substitution of the pyrimidine ring does not lead to significant changes in the resonance formation : the resonances in pyrimidinic molecules are associated with the ring structure. We conclude that the picture of resonance formation in pyrimidines is much more complex than expected. Most of the work presented in this thesis has been published in peer-reviewed journals.EThOS - Electronic Theses Online ServiceGBUnited Kingdo