Free-electron attachment to thymine and partially deuterated thymine, where D replaces H at all carbon atoms, is studied in the electron energy range from about 0 to 15 eV. The formation of fragment anions that are formed by the loss of one or two H (D) atoms is analyzed as a function of the incident electron energy using a crossed electron/neutral beam apparatus in combination with a quadrupole mass spectrometer. By using partially deuterated thymine and quantum-chemical calculation a bond selectivity for the loss of one and two hydrogen atoms is observed that is determined only by the kinetic energy of the incident electron.

Spin-1 2 compounds A3Cu3AlO2(SO4)4 (A=K, Rb, and Cs) have one-dimensional (1D) inequilat-eral diamond-chains. We analyze the temperature dependence of the magnetic susceptibility and determine the magnetic exchange interactions. In contrast to azurite, a dimer is formed on one of the sides of the diamond. From numerical analyses of the proposed model, we find that the dimer together with a nearly isolated 1D Heisenberg chain characterize magnetic properties including magnetization curve and magnetic excitations. This implies that a dimer-monomer composite chain without frustration is a good starting point for describing these compounds.

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