Crystal structure of dicarbon-yl[μ2-methyl-enebis(di-phenyl-phosphane)-κ2 P: P'][μ2-2-(2,4,5-tri-methyl-phen-yl)-3-oxoprop-1-ene-1,3-di-yl](tri-phenyl-phosphane-κ P)ironplatinum(Fe- Pt)-di-chloro-methane-toluene (1/1/2), [(OC)2Fe(μ-dppm)(μ-C(=O)C(2,4,5-C6H2Me3)=CH)Pt(PPh3)]

Acta Crystallogr E Crystallogr Commun. 2019 Nov 22;75(Pt 12):1902-1906. doi: 10.1107/S2056989019015573. eCollection 2019 Dec 1.

Abstract

The title compound, [FePt(C12H12O)(C18H15P)(C25H22P2)(CO)2]·2C7H8·CH2Cl2 or [(OC)2Fe(μ-dppm)(μ-C(=O)C(2,4,5-C6H2Me3)=CH)Pt(PPh3)], represents an example of a diphosphane-bridged heterobimetallic dimetalla-cyclo-pentenone complex resulting from a bimetallic activation of 1-ethynyl-2,4,5-tri-methyl-benzene and a metal-coordinated carbonyl ligand. The bridging μ2-C(=O)C(2,4,5-C6H2Me3)=CH unit (stemming from a carbon-carbon coupling reaction between CO and the terminal alkyne) forms a five-membered dimetalla-cyclo-pentenone ring, in which the C=C bond is π-coordinated to the Fe centre. The latter is connected to the Pt centre through a short metal-metal bond of 2.5770 (5) Å. In the crystal, the complex is solvated by one di-chloro-methane and two toluene mol-ecules.

Keywords: C—H⋯π inter­actions; bis­(di­phenyl­phosphino)methane; crystal structure; heterobimetallic; hydrogen bonding; iron; metal–metal bond dimetalla­cyclo­pentenone; platinum; terminal alkyne.

Grants and funding

This work was funded by Deutsche Forschungsgemeinschaft grant . Verband der Chemischen Industrie grant .