Abstract
The first excited electronic state of TII was investigated by laser excitation and laser fluorescence spectroscopy. Almost completely resolved rotational fine structure was observed with the help of a collimated molecular beam and a single-mode cw dye laser. From the derived Dunham parameters Y lk a RKR potential for the excited state is calculated. The unusual shape of the potential energy curve can be understood as originating from an avoided crossing of the ionic ground-state potential and a non-bonding covalent state of the atomic asymptote (6p) 2P 1 2 (TI)+(5p) 5 2P 3 2 (I).
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