Abstract
We report the first spectroscopic observation of the tin hydride radical in the infrared spectral region. Vibration rotation transitions of the ten stable isotopic forms of SnH in the 2п3/2 component of its ground state were recorded with a CO-LMR-spectrometer. The isotopic structure, the ∧-doubling in the 2п3/2 substate and the hyperfine splitting due to the tin isotopes 115Sn, 117Sn and 119Sn have been resolved for the first time. A set of effective molecular parameters of the X 2п3/2 state is given.