Gold Coordination by a Tertiary Phosphine with Three Thioether Functions

  1. Fuchs, S. 1
  2. López-De-Luzuriaga, J.M. 12
  3. Olmos, M.E. 1
  4. Sladek, A. 1
  5. Schmidbaur, H. 1
  1. 1 Technical University Munich
    info

    Technical University Munich

    Múnich, Alemania

    ROR https://ror.org/02kkvpp62

  2. 2 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    ROR https://ror.org/0553yr311

Revista:
Zeitschrift für Naturforschung. B, A Journal of Chemical Sciences

ISSN: 0932-0776

Año de publicación: 1997

Volumen: 52

Número: 2

Páginas: 217-220

Tipo: Artículo

SCOPUS: 2-s2.0-0040563400 GOOGLE SCHOLAR

Otras publicaciones en: Zeitschrift für Naturforschung. B, A Journal of Chemical Sciences

Resumen

The reaction of tris(phenylthiomethyl)phosphine with equimolecular amounts of [AuPPh3]+[BF4]- affords the complex (tris(phenylthiomethyl)phosphine)(triphenylphosphine)-gold(I) tetrafluoroborate 1 in good yield. The X-ray diffraction analysis of this product shows an unusual conformation with the three CH2SPh arms of the phosphine folded back towards the metal atom shielding the P-Au-P' unit. The reaction of the same substrate with Bis(tetrahydrothiophene)gold(I) perchlorate in a 1:1 molar ratio leads to the displacement of both weakly coordinated tht ligands, and a dimeric product [AuP(CH2Sph)3]2(ClO4)2 2 is obtained.