Research Article: [μ-1,6-Bis(diphenyphosphan­yl)hexane-1:2κ2P:P′]deca­carbonyl-1κ3C,2κ3C,3κ4C-triangulo-triruthenium(0)

Date Published: May 01, 2012

Publisher: International Union of Crystallography

Author(s): Omar bin Shawkataly, Siti Syaida Sirat, Ching Kheng Quah, Hoong-Kun Fun.

http://doi.org/10.1107/S1600536812014614

Abstract

The title triangulo-triruthenium(0) compound, [Ru3(C30H32P2)(CO)10], contains a triangle of singly bonded Ru atoms. The phosphane-bridged Ru—Ru distance [2.9531 (2) Å] is significantly longer than the non-bridged Ru—Ru distances [2.8842 (2) and 2.8876 (2) Å] . The bis­(diphenyl­phosphan­yl)hexane ligand bridges the Ru—Ru bond. Each phosphane-substituted Ru atom bears one equatorial and two axial terminal carbonyl ligands, whereas the unsubstituted Ru atom bears two equatorial and two axial terminal carbonyl ligands. The dihedral angles between the benzene rings attached to each P atom are 72.75 (7) and 82.02 (7)°. The mol­ecular structure is stabilized by an intra­molecular C—H⋯O hydrogen bond involving a methyl­ene group of the phosphane ligand and an axial carbonyl O atom, which generates an S(6) ring motif. In the crystal, mol­ecules are linked via C—H⋯O hydrogen bonds into layers parallel to (100).

Partial Text

For general background to triangulo-triruthenium clusters with structures of the general type Ru3(CO)10L (where L is a group 15 bidentate ligand), see: Bruce et al. (1982 ▶); Coleman et al. (1984 ▶); Teoh et al. (1990 ▶); Diz et al. (2001 ▶); Shawkataly et al. (2006 ▶, 2011 ▶); Churchill et al. (1977 ▶). For the preparation of the title compound, see: Bruce et al. (1983 ▶). For hydrogen-bond motifs, see: Bernstein et al. (1995 ▶). For the stability of the temperature controller used in the data collection, see: Cosier & Glazer (1986 ▶).

 

Source:

http://doi.org/10.1107/S1600536812014614