Neutral and anionic pentafluorophenyl isonitrile complexes of palladium and platinum(II) and their reactivity towards amines

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

    Universidad de Zaragoza

    Zaragoza, España

    ROR https://ror.org/012a91z28

Revista:
Transition Metal Chemistry Weinheim

ISSN: 0340-4285

Año de publicación: 1984

Volumen: 9

Número: 7

Páginas: 277-279

Tipo: Artículo

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DOI: 10.1007/BF00624474 SCOPUS: 2-s2.0-0021463499 GOOGLE SCHOLAR

Otras publicaciones en: Transition Metal Chemistry Weinheim

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Resumen

The (n-Bu4N)[M(C6F5)3(CNR)] complexes (M=Pd or Pt; R=p-Tolyl, Me, Cy or t-Bu, prepared from (n-Bu4N)[M(C6F5)3(tht)] (tht = tetrahydrothiophene) and the appropriate isocyanide, RNC, prove to be unreactive towards benzylamine or MeOH. The trans-[Pd(C6F5)2(CNR)2] complexes react slowly with benzylamine to give the corresponding carbene complexes trans-[Pd(C6F5)2{C(NHR)(NHBz)}2], the rate of the reaction decreasing in the order:p-Tolyl > Me > Cy ≫t-Bu (for R=t-Bu the carbene complex cannot be prepared). In the corresponding Pt complexes a marked decrease in reactivity is observed and only the most reactive isonitrile complex (R=p-Tolyl) gives the carbene complex trans-[Pt(C6F5)2{C(NHTolyl-p)(NHBz)}2}. The cis-[M(C6F5)2(CNTolyl)2] complexes do not show any change in reactivity compared to the corresponding trans-complexes, and give cis[M(C6F5)2{C(NHTolyl-p)(NHBz)}2]. © 1984 Verlag Chemie GmbH.