The reaction of the tertiary phosphine sulfides R3PS (R = Ph, Me2N or C6H11) with X2 (X2 = I2, Br2, IBr or ICl); structural characterisation of the CT complexes (Me2N)3PSI2 and Ph3PS(I0.89Br0.11)Br and the ionic compound [{(Me2N)3PS}2S]2+ 2[Br3]

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Wendy I. Cross, Stephen M. Godfrey, Sheena L. Jackson, Charles A. McAuliffe and Robin G. Pritchard


Abstract

The reactions of the tertiary phosphine sulfides R3PS (R = Ph, Me2N or C6H11) with X2 (X = I or Br) and IX (X = Br or Cl) have been studied. Reaction of R3PS with I2 or IX results in quantitative isolation of the CT complexes R3PSIX (X = I, Br or Cl), except for Ph3PS with I2 which produces the unusual compound (Ph3PSI2)2I2, which has been crystallographically characterised by earlier workers. The crystal structure of (Me2N)3PSI2 has been determined and compared to Ph3PSI2, previously described. The greater d(I–I) for (Me2N)3PSI2, 2.856(1) Å, compared to that of 2.823(1) Å for Ph3PSI2 clearly illustrates that d(I–I) in R3PSI2 compounds is sensitive to R, although this effect is less pronounced when compared to that of analogous R3PSeI2 compounds. The crystal structure of the product from the reaction of Ph3PS with IBr has also been determined and represents the first example of a tertiary phosphine sulfide interhalogen CT complex. It has the formula Ph3PS(I0.89Br0.11)Br and is isomorphous with Ph3PSI2. The reaction of R3PS with Br2 is complex. In the case of Ph3PS, phosphorus–sulfur bond cleavage occurs quantitatively to produce Ph3PBr2 and elemental sulfur. Reaction of (Me2N)3PS with Br2 gives, as one product, [{(Me2N)3PS}2S][Br3]2 in moderate (ca. 30%) yield. This unusual dication is compared to the previously reported [(But3PTe)2Te][SbF6]2. Tricyclohexylphosphine sulfide reacts with Br2 in solvents of low relative permittivity (Et2O) to produce the 1∶1 addition complex (C6H11)3PSBr2; however, dissolution of this material in solvents of higher relative permittivity results in phosphorus–sulfur bond cleavage to produce (C6H11)3PBr2 and elemental sulfur.


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