Acta Crystallographica Section E: Crystallographic Communications (Jan 2015)

Crystal structure of O-isopropyl [bis(trimethylsilyl)amino](tert-butylamino)phosphinothioate

  • Oleksandr O. Kovalenko,
  • Vasyl Kinzhybalo,
  • Oleksii A. Brusylovets,
  • Tadeusz Lis

DOI
https://doi.org/10.1107/S205698901402622X
Journal volume & issue
Vol. 71, no. 1
pp. o37 – o38

Abstract

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[Bis(trimethylsilyl)amino](tert-butylimino)thiophosphorane reacts in benzene with isopropyl alcohol via 1,2-addition of an iPrO–H bond across the P=N bond, resulting in the title compound, C13H35N2OPSSi2. In the molecule, the P atom possesses a distorted tetrahedral environment involving two N atoms from (Me3Si)2N– and tBuNH– groups, one O atom from an iPrO group and one S atom, therefore the molecule has a stereocenter on the P atom but crystal symmetry leads to a racemate. In the crystal, a pair of enantiomers form a centrosymmetric dimer via a pair of N—H...S hydrogen bonds.

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