TRISPHAT explained

TRISPHAT (full name tris(tetrachlorocatecholato)phosphate(1−)) is an inorganic anion with the formula often prepared as the tributylammonium or tetrabutylammonium (salt. The anion features phosphorus(V) bonded to three tetrachlorocatecholate ligands. This anion can be resolved into the axially chiral enantiomers, which are optically stable (the picture shows the Δ enantiomer).

The TRISPHAT anion has been used as a chiral shift reagent for cations.[1] It improves the resolution of 1H NMR spectra by forming diastereomeric ion pairs.

Preparation

The anion is prepared by treatment of phosphorus pentachloride with tetrachlorocatechol followed by a tertiary amine gives the anion:

PCl5 + 3 C6Cl4(OH)2 → H[P(O<sub>2</sub>C<sub>6</sub>Cl<sub>4</sub>)<sub>3</sub>] + 5 HCl

H[P(O<sub>2</sub>C<sub>6</sub>Cl<sub>4</sub>)<sub>3</sub>] + Bu3N → Bu3NH+ [P(O<sub>2</sub>C<sub>6</sub>Cl<sub>4</sub>)<sub>3</sub>]Using a chiral amine, the anion can be readily resolved.[2]

Notes and References

  1. Hassen . Ratni . Jonathan J. . Jodry . Jérôme . Lacour . E. Peter . Kündig . [''n''-Bu<sub>4</sub>N][Δ-TRISPHAT] Salt, an Efficient NMR Chiral Shift Reagent for Neutral Planar Chiral Tricarbonylchromium Complexes . . 2000 . 19 . 19 . 3997–3999 . 10.1021/om000437f.
  2. France . Favarger . Catherine . Goujon-Ginglinger . David . Monchaud . Jérôme . Lacour . Large-Scale Synthesis and Resolution of TRISPHAT [Tris(tetrachlorobenzenediolato) Phosphate(V)] Anion . . 2004 . 69 . 24 . 8521–8524 . 10.1021/jo048641q. 15549835 . .