Synthesis and reactivity of bimetallic acetylide-bridged Pt-Pt complexes. Crystal and molecular structure of [(PPh3)(C6F5)Pt(mu-C=CPh)2Pt(C6F5)(PPh3)]

  1. Berenguer, J.R. 1
  2. Forniés, J. 1
  3. Martínez, F. 1
  4. Cubero, J.C. 1
  5. Lalinde, E. 3
  6. Moreno, M.T. 3
  7. Welch, A.J. 2
  1. 1 Instituto de Nanociencia y Materiales de Aragón
    info

    Instituto de Nanociencia y Materiales de Aragón

    Zaragoza, España

    ROR https://ror.org/031n2c920

  2. 2 University of Edinburgh
    info

    University of Edinburgh

    Edimburgo, Reino Unido

    ROR https://ror.org/01nrxwf90

  3. 3 Universidad de La Rioja
    info

    Universidad de La Rioja

    Logroño, España

    ROR https://ror.org/0553yr311

Montrer des affiliations +
Revue:
Polyhedron

ISSN: 0277-5387

Année de publication: 1993

Volumen: 12

Número: 14

Pages: 1797-1804

Type: Article

beta Ver similares en nube de resultados
SCOPUS: 2-s2.0-0001603316 WoS: WOS:A1993LQ07600013 GOOGLE SCHOLAR

D'autres publications dans: Polyhedron

Résumé

The binuclear double-bridged acetylide complexes [Pt(μ-CCR)(C6F5)PPh3)]2 [R = Ph (1), But (2), SiMe3 (3)] have been synthesized from [trans-Pt(CCR)2(PPh3)2] and [cis-Pt(C6F5)2(THF)2] (THF = tetrahydrofuran). The crystal structure of [Pt(μ-CCPh) (C6F5)(PPh3)]2 (1) has been established by X-ray diffraction methods. The structure shows that two identical [(PPh3)(C6F5)PtCCPh] units are joined together through η2-bonding of MCCPh units. This indicates that the complex is formed via a rearrangement of groups between the two metal centres. Treatment of [Pt(μ-CCR)(C6F5)(PPh3)]2 with L (L = PPh3, py = pyridine) produces simple bridge-cleavage reactions giving the mono-nuclear complexes [trans-Pt(C6F5)(CCR)(PPh3)L] (4-9). © 1993.