Synthesis and catalytic activity of trihalotin-iridium complexes

  1. Uson, R. 1
  2. Oro, L.A. 1
  3. Fernandez, M.J. 1
  4. Pinillos, M.T. 1
  1. 1 Universidad de Zaragoza
    info

    Universidad de Zaragoza

    Zaragoza, España

    ROR https://ror.org/012a91z28

Revista:
Inorganica Chimica Acta

ISSN: 0020-1693

Año de publicación: 1980

Volumen: 39

Número: C

Páginas: 57-60

Tipo: Artículo

SCOPUS: 2-s2.0-0007982130 GOOGLE SCHOLAR

Otras publicaciones en: Inorganica Chimica Acta

Resumen

The addition of phosphine derivatives and SnX2 (X = Cl or Br) to solutions of [IrCl(COD)]2 (COD) = 1,5-cyclooctadiene) leads to the preparation of the pentacoordinated complexes [Ir(SnX3)(COD)L2], which carbonylated or hydrogenated at ordinary pressure and at room temperature yield [Ir(SnCl3(CO)2L2] or, respectively, [Ir(SnCl3)H2L2]. The latter catalyze both the hydrogenation and the isomerization of n-heptene; the rates of these reactions decrease with decreasing basicity of the phosphine. © 1980.