Rhodium and iridium complexes containing the anion of 1-phenyl-3-methyl-4-benzoyl- pyrazolone-5, a sophisticated analogue of β-diketones

  1. Bonati, F. 2
  2. Oro, L.A. 1
  3. Pinillos, M.T. 1
  1. 1 Universidad de Zaragoza
    info

    Universidad de Zaragoza

    Zaragoza, España

    ROR https://ror.org/012a91z28

  2. 2 Università di Camerino
    info

    Università di Camerino

    Camerino, Italia

    ROR https://ror.org/0005w8d69

Revue:
Polyhedron

ISSN: 0277-5387

Année de publication: 1985

Volumen: 4

Número: 2

Pages: 357-364

Type: Article

DOI: HTTP://DX.DOI.ORG/10.1016/S0277-5387(00)84512-X SCOPUS: 2-s2.0-0002977888 GOOGLE SCHOLAR

D'autres publications dans: Polyhedron

Résumé

Several (diolefin)M(A) complexes (M = Rh, Ir) were prepared, where AH is 1-phenyl-3-methyl- 4-benzoylpyrazolone-5, a very stable asymmetric analogue of acetylacetone. In these complexes the diolefin could be replaced by one mole of (Ph2PCH2CH2)2, two of CO or of PPh3, or three of CNBut, while 1,10-phenanthroline displaced the chelating ligand to yield [(cyclooctadiene)Rh(phen)]+ (A)-. Some compounds X-Y (X-Y = iodine or MeI) added oxidatively yielding the corresponding trivalent species. Using 31P NMR spectra the presence of the expected steric isomers was detected in (Ph3P)(CO)Rh(A) and in (Ph3P) (CO)Rh(A)(X)(Y). © 1985.