2024-03-28T09:05:53Zhttp://digital.csic.es/dspace-oai/requestoai:digital.csic.es:10261/1338602016-10-20T09:18:06Zcom_10261_31com_10261_3col_10261_284
Reversible opening of the triangular structure of a sulfido-bridged ZrRh2 early-late heterobimetallic complex induced by Bis-(diphenylphosphino)methane
Hernandez-Gruel, Marc A. F.
Lahoz, Fernando J.
Dobrinovich, Isabel T.
Modrego, Francisco J.
Oro, Luis A.
Pérez-Torrente, Jesús J.
Ministerio de Educación y Ciencia (España)
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.
2016-06-21T12:49:52Z
2016-06-21T12:49:52Z
2007
2016-06-21T12:49:52Z
artículo
Organometallics 26(10): 2616-2622 (2007)
http://hdl.handle.net/10261/133860
10.1021/om061092p
eng
Postprint
http://dx.doi.org/10.1021/om061092p
Sí
openAccess
American Chemical Society