Abstract
Observations are reported on the rotationally resolved 3d2Δ2p2Π electronic transition in the LiHe van der Waals molecule. These observations, which represent the first optical double-resonance measurements of the rovibrational structure of any alkalirare-gas molecule, have been analyzed, using standard techniques, to yield values for the 3d2Δ state well depth De=430(70) cm1 and equilibrium separation re=3.6(1)a0. The experimental scheme, which should allow spectroscopy of excited states in a number of excimer molecules, is also described.