Diferent coordination modes of the 1,1,1-tris(diphenylphosphinomethyl)ethane ligand in gold(I) and gold(III) complexes

  1. Fernández, E.J. 1
  2. Gimeno, M.C. 2
  3. Laguna, A. 2
  4. Laguna, M. 2
  5. López-de-Luzuriaga, J.M. 1
  6. Olmos, E. 1
  1. 1 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    ROR https://ror.org/0553yr311

  2. 2 Instituto de Nanociencia y Materiales de Aragón
    info

    Instituto de Nanociencia y Materiales de Aragón

    Zaragoza, España

    ROR https://ror.org/031n2c920

Aldizkaria:
Journal of Organometallic Chemistry

ISSN: 0022-328X

Argitalpen urtea: 1996

Alea: 514

Zenbakia: 1-2

Orrialdeak: 169-175

Mota: Artikulua

SCOPUS: 2-s2.0-0030591557 WoS: WOS:A1996UQ50400024 GOOGLE SCHOLAR

Beste argitalpen batzuk: Journal of Organometallic Chemistry

Laburpena

The synthesis of pentafluorophenyl mono-or poly-nuclear gold(I) and/or gold(III) complexes with the tridentate ligand (PPh2CH2)3CCH3 (tdppme) are described in different coordination modes not represented thus far. The reaction of the free phosphine with gold(I) or gold(III) derivatives in different molar ratios gives [{Au(C6F5)}3( μ3-η3-tdppme)], [{Au(C6F5)}2( μ-η2-tdppmeO)], [Au(C6F5)3(η1-tdppme)] or [Au(C6F5)2(η2-tdppme)]Cl. The mononuclear derivatives further react with gold(I) or gold(III) species giving rise to di-or tri-nuclear complexes which contain the triphosphine acting as a μ3-η3, μ-η2, μ-η3 or η2 ligand.