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Conformational analysis of Se-esters of diselenophosphinic acids has been performed and their polarities have been determined using the methods of dipole moments and quantum chemistry (DFT [B3PW91/6-311++G(df,p)]+CPCM). In solution, the studied compounds exist as an equilibrium of several conformers with staggered gauche and trans- or eclipsed cis-orientation of the substituents relative to the P=Se bond. The presence of eclipsed cis-conformations is explained by the formation of intramolecular H⋯Se bonds involving the hydrogen atom of the Se-alkyl(benzyl) or phenyl substituents at the phosphorus atom and the selenium atom of the P=Se group.

Conformational analysis of tris(3-methylphenyl)phosphine and its chalcogenides has been performed by methods of dipole moments, IR spectroscopy, and quantum chemistry [DFT B3PW91/6-31G(df,p)]. In solution, these compounds exist as an equilibrium of conformers with gauche- and cis-arrangement of the substituents at the phosphorus atom relative to the P=X bond (X = lone electron pair, O, S, Se).