Neutral PtRh2 and PtRh4 tetraalkynyl complexes. X-ray crystal structures of {Pt(C=CBut)4[Rh2(μ-X)(COD)2] 2} (X = Cl, OH)

  1. Ara, I. 2
  2. Berenguer, J.R. 1
  3. Forniés, J. 2
  4. Lalinde, 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

Revista:
Organometallics

ISSN: 0276-7333

Año de publicación: 1997

Volumen: 16

Número: 18

Páginas: 3921-3926

Tipo: Artículo

DOI: 10.1021/OM9702587 SCOPUS: 2-s2.0-0000335586 WoS: WOS:A1997XU43800011 GOOGLE SCHOLAR

Otras publicaciones en: Organometallics

Repositorio institucional: lock_openAcceso abierto Editor

Resumen

The reaction of 2 equiv of [Rh(COD)(acetone)2]+ with the dianionic homoleptic species [Pt(C≡CR)4]2- (R = But (1a), SiMe3 (1b)) in acetone (molar ratio 2:1) gives the expected neutral trinuclear adducts {Pt(μ-C-C≡CR)4[Rh(COD)]2} (R = But (2a), SiMe3 (2b)) in moderately good yield. Further reaction of 2a with the binuclear [Rh(μ-X)(COD)]2 (X = Cl, OH) derivatives (molar ratio 1:1) produces the formation of unusual pentanuclear {Pt(μ-C=CBut)4-[Rh2(μ-X)(COD) 2]2} complexes (X = Cl (3a), OH (4a)), which are formed by a dianionic "Pt-(C≡CBut)4" fragment and two dinuclear cationic "Rh2(COD)2(μ-X)" units connected through bridging alkynyl ligands. The molecular structures of complexes 3a and 4a have been established by X-ray crystallography.