Preparation of Doubly Acetylide-Bridged Binuclear Platinum-Platinum and Platinum-Palladium Complexes. Structures of [{(dppe)Pt(C=CPh)2}Pt(C6F5)2] and (PMePh3)2[(C6F5)2Pt(mu-C=CPh)2Pt(C6F5)2]
- Forniés, J. 2
- Gómez-Saso, M.A. 2
- Lalinde, E. 1
- Martínez, F. 2
- Moreno, M.T. 1
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1
Universidad de La Rioja
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2
Instituto de Nanociencia y Materiales de Aragón
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ISSN: 0276-7333
Año de publicación: 1992
Volumen: 11
Número: 8
Páginas: 2873-2883
Tipo: Artículo
beta Ver similares en nube de resultadosOtras publicaciones en: Organometallics
Resumen
The reaction between [cis-Pt(C≡CR)2L2] (R = Ph, tBu; L2 = 2 PPh3, dppe, COD) and [cis-M(C6F5)2-(THF)2] (M = Pd, Pt; THF = tetrahydrofuran) in a 1:1 molar ratio affords neutral binuclear derivatives of the type [{L2Pt(C≡CR)2}M(C6F5) 2] in which the RC≡C-Pt-C≡CR group is acting as a bidentate ligand to "M(C6F5)2". In contrast, [cis-M(C6F5)2(THF)2] reacts with Q2[cis-Pt(C6F5)2(C≡CR) 2] and Q2-[Pt(C6F5)(C≡CR)3] (R = Ph, Q = PMePh3; R = tBu, Q = NBu4) to give anionic diplatinum and platinum-palladium complexes of types Q2[(C6F5)2Pt(μ-C≡CR) 2M(C6F5)2] and Q2[(C6F5)(C≡CR)Pt(μ-C≡ CR)2Pt(C6F5)2], respectively. The crystal structures of the complexes [{(dppe)Pt(C≡CPh)2}Pt(C6F5)2] (3) and (PMePh3)2[(C6F5) 2Pt(μ-C≡CPh)2Pt(C6F5) 2] (9) have been established by X-ray diffraction methods. 3 is a binuclear complex in which the unit "(dppe)Pt(σ-C≡CPh)2" acts as a chelate metallo ligand to "Pt(C6F5)2". In contrast, the crystal structure for 9 shows that two identical [(C6F5)2Pt-C≡CPh] units are joined together through η2 bonding of C≡CPh groups. This indicates that the complex is formed from the bis(σ-alkynyl)bis(pentafluorophenyl)platinate and the synthon Pt(C6F5)2 via migration of one σ-alkynyl group between the two platinum metal centers. © 1992 American Chemical Society.