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Título: | Reversible opening of the triangular structure of a sulfido-bridged ZrRh2 early-late heterobimetallic complex induced by Bis-(diphenylphosphino)methane |
Autor: | Hernandez-Gruel, Marc A. F.; Lahoz, Fernando J. CSIC ORCID; Dobrinovich, Isabel T. CSIC; Modrego, Francisco J. CSIC ORCID; Oro, Luis A. CSIC ORCID; Pérez-Torrente, Jesús J. CSIC ORCID | Fecha de publicación: | 2007 | Editor: | American Chemical Society | Citación: | Organometallics 26(10): 2616-2622 (2007) | Resumen: | Reaction of the early - late heterobimetallic complexes [Cp tt 2Zr(μ3-S)2{M(CO)} 2(μ-dppm)] (M = Rh, Ir) with dppm (bis-(diphenylphosphino)methane) yields the compounds [Cptt 2Zr(μ-S)2M(μ- CO)2(μ-dppm)M(η2-dppm)] (M = Rh (3), Ir (4)). The molecular structure of 3 shows a bent trimetallic ZrRhRh chain with tetrahedral, trigonal-bipyramidal, and square-pyramidal geometries, respectively. This trinuclear compound exhibits a mixed-valence Rh(II) - Rh(0) metal - metal bonded unit that results from the unusual chelating coordination of the metalloligand [Cptt 2Zr(S)2]2- and is further stabilized by the presence of two unsymmetrical bridging carbonyl ligands, which interact with the unsaturated Rh(II) metal. The formation of 3 is reversible, and the equilibrium 1 + dppm ⇄ 3 has been observed in solution (K ≈ 16 at 22 °C in C6D6). The opening of the triangular core in the heterotrimetallic compound [Cptt 2Zr(μ 3-S)2-{Rh(CO)}{Ir(CO)}(μ-dppm)] (5) is not selective and gives the compounds [Cptt 2Zr(μ-S) 2Rh(μ-CO)2(μ-dppm)Ir(η2-dppm)] (6) and [Cptt 2Zr(μ-S)2Ir(μ-CO) 2(μ-dppm)Rh(η2-dppm)] (7) in a 3:1 molar ratio. | Versión del editor: | http://dx.doi.org/10.1021/om061092p | URI: | http://hdl.handle.net/10261/133860 | DOI: | 10.1021/om061092p | Identificadores: | doi: 10.1021/om061092p issn: 0276-7333 e-issn: 1520-6041 |
Aparece en las colecciones: | (ICMA) Artículos |
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Reversible Opening.pdf | 1,69 MB | Adobe PDF | Visualizar/Abrir |
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