SYNTHESIS, INFRARED AND NMR STUDIES OF SOME SULFATO DIORGANOSTANNIC DERIVATIVES

  • DAOUDA NDOYE
    Université Cheikh Anta Diop, Faculté des Sciences et Techniques, Département de Chimie, Laboratoire de Chimie Minérale et Analytique (LACHIMIA), Dakar, Sénégal
  • LIBASSE DIOP
    Université Cheikh Anta Diop, Faculté des Sciences et Techniques, Département de Chimie, Laboratoire de Chimie Minérale et Analytique (LACHIMIA), Dakar, Sénégal
    dlibasse@gmail.com

Abstract

EthylendiammoniumSO4•SnBu2Cl2•1/4ethylendiammoniumCl2 (A), 2ethylendiammoniumSO4•SnBu2Cl2 (B) and Cy2NH2SO4H•Cy2NH2SnBu2Cl3 (C) complexes have been obtained on allowing ethylendiammoniumSO4 and Cy2NH2HSO4 to react respectively with SnBu2Cl2 in specific ratios. The molecular structures of these compounds have been determined on the basis of infrared and NMR data. The suggested structures are dimeric and tetrameric, the tin atom being hexacoordinated, the sulphate anions behaving as a monochelating ligand or non-coordinating and only involved in hydrogen bonds. The hydrogenosulfate is a non-sigma coordinating anion but only involved in hydrogen bonds of acetic acid type or NH…O bonds. The presence of dimeric [(SnBu2Cl3)2]2- in one of the structures is noteworthy. The key role of the cations involved in hydrogen bonds is outlined.

Cuvinte cheie

cation chloro bridges dinuclear dimer hydrogen bonds monochelating and non-sigma involved sulphate anion non-sigma involved HSO4- Td symmetry