Crown-shapped tetrametalic imidoyl complexes of palladium. X- ray structure of [Pd2 {m-C(C6 F5 )=NMe}2 (mu-Cl)(mu-CH3 CO2 )]2
- Uson, R. 1
- Fornies, J. 1
- Espinet, P. 1
- Lalinde, E. 1
- García, Agustín. 1
- Jones, P.G. 2
- Meyer-Base, K. 2
- Sheldrick, G.M. 2
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1
Universidad de Zaragoza
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2
University of Göttingen
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ISSN: 0300-9246
Año de publicación: 1986
Volumen: 2
Páginas: 259-264
Tipo: Artículo
beta Ver similares en nube de resultadosOtras publicaciones en: Journal of the Chemical Society-Dalton Transactions
Resumen
The complexes [{[Pd2{μ-C(C6F5)=NR1} 2](μ-X1)(μ-X2)}n] (R1 = Me or p-tolyl; X1 = X2 = Cl) and their derivatives (X1 = Cl, X2 = MeCO2 or CF3CO2; X1 = X2 = MeCO2 or CF3CO2), obtained by metathetical reactions with the corresponding silver salts, are shown to be tetrametallic (n = 2) by molecularweight determinations. Their structures are discussed on the basis of 1H and 19F n.m.r. data. The crystal structure of the title complex has been solved by X-ray diffraction methods [space group P21/n, a = 14.380(4), b = 19.980(4), c = 15.976(4) Å, β = 103.51(3)°, Z = 4, R′ = 0.046 for 5 428 unique observed reflections]. The tetrametallic molecule is crown-shaped. The bond lengths at palladium reflect the strong trans influence of the imidoyl-C atom; the Pd-Cl bonds trans to C are amongst the longest known.