Abstract
The title compound, C19H17PS2, results from the direct deprotonation of diphenylmethylphosphine sulfide and subsequent reaction with diphenyl disulfide. The C—P and C—S bond lengths of 1.8242 (18) and 1.8009 (18) Å, respectively, of the central P—C—S linkage are comparable to those found in the sulfonyl analogue, but are considerably longer than those reported for the dimetallated sulfonyl compound. The dihedral angle between the benzene rings of the diphenylmethyl moiety is 69.46 (7)°. No distinct intermolecular interactions are present in the crystal structure.
Highlights
The title compound, C19H17PS2, results from the direct deprotonation of diphenylmethylphosphine sulfide and subsequent reaction with diphenyl disulfide
Bond lengths of 1.8242 (18) and 1.8009 (18) Å, respectively, of the central P—C—S linkage are comparable to those found in the sulfonyl analogue, but are considerably longer than those reported for the dimetallated sulfonyl compound
As part of our studies on the synthesis of novel methandiides for the preparation of carbene complexes, we have developed a ligand and its dianionic analogue with a thiophosphoryl and sulfonyl sidearm (Schröter & Gessner, 2012)
Summary
R factor = 0.034; wR factor = 0.091; data-to-parameter ratio = 15.2. The title compound, C19H17PS2, results from the direct deprotonation of diphenylmethylphosphine sulfide and subsequent reaction with diphenyl disulfide. The C—P and C—S bond lengths of 1.8242 (18) and 1.8009 (18) Å, respectively, of the central P—C—S linkage are comparable to those found in the sulfonyl analogue, but are considerably longer than those reported for the dimetallated sulfonyl compound. The dihedral angle between the benzene rings of the diphenylmethyl moiety is 69.46 (7). No distinct intermolecular interactions are present in the crystal structure. For the sulfonyl and dimetallated sulfonyl analogues, see: Schröter & Gessner (2012).
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