Synthesis and reactivity of palladium complexes with N,N'-di-p-tolyl-formamidine,- triazene or formamidinato ligands. Insertion of CNC6H4Me-p, CS2 or CO2 into Pd-N bond

  1. Usón, R. 2
  2. Fornies, J. 2
  3. Espinet, P. 2
  4. Lalinde, E. 1
  1. 1 Universidad de Zaragoza
    info

    Universidad de Zaragoza

    Zaragoza, España

    ROR https://ror.org/012a91z28

  2. 2 Instituto de Nanociencia y Materiales de Aragón
    info

    Instituto de Nanociencia y Materiales de Aragón

    Zaragoza, España

    ROR https://ror.org/031n2c920

Revue:
Journal of Organometallic Chemistry

ISSN: 0022-328X

Année de publication: 1987

Volumen: 334

Número: 3

Pages: 399-408

Type: Article

SCOPUS: 2-s2.0-22844432891 WoS: WOS:A1987K682300015 GOOGLE SCHOLAR

D'autres publications dans: Journal of Organometallic Chemistry

Résumé

The syntheses of complexes containing the HL ligands N,N′-di-p-tolylformamidine (TolNCHNHTol) (Tol = p-MeC6H4) and N,N⇔-di-p-tolyltriazene (TolNN- NHTol) are described. The complexes are of the types cis-[Pd(C6F5)2(HL)2], trans-[Pd(C6F5)Cl(HL)2] and cis-[Pd(C6F5)2(PPh3)(HL)], with the HL ligands acting as monodentate ligands via the imino N atom. A N,N′-di-p-tolylformamidinato complex, cis-(NBun 4) | Pd(C6F5)2{N(tol)CHN(Tol)} | is also described. It undergoes irreversible insertion of CNTol of CS2, or reversible insertion of CO2, into one NPd bond. While the CS2 insertion product is an S,S-bonded dithiocarbamate-type complex, the product arising from the CO2 insertion contains a six-membered palladiacycle with the ligand O,N-bonded to the Pd atom. © 1987.