Abstract:We report the synthesis of the title compounds CH 2 CHDSO and CH 2 CD 2 SO and their characterization by infrared spectroscopy. The monodeuterated species occurs in two isotopically diastereomeric forms with the D atom either cis or trans oriented to the O atom. The SO infrared chromophore in these diastereomers has a strong absorption centered near 1114 and 1116 cm À1 , respectively, with an integrated band strength G 2.8 pm 2 , which renders it very suitable for infrared multiphoton excitation with a CO 2 laser, leading to the laser chemical dissociation of the reactants into deuterated ethylene and SO( 3 S À ). We have established the first successful laser chemical separation of such a diastereomer pair, with a small but significant separation factor based on the small frequency difference of the n 4 (SO stretching) fundamental mentioned above; the analysis used highresolution FTIR spectroscopy in the region of the Q branches of n 4 . Our results are discussed in relation to various aspects of stereochemical reaction dynamics in chiral and achiral sulfoxides.