Crystal structure of {μ2-1,2-bis[(4-methylphenylsulfanyl]-3-oxoprop-1-ene-1,3-diyl-1:2κ2C3:C1}dicarbonyl-1κ2C-[μ2-methylenebis(diphenylphosphane)-1:2κ2P:P′](triphenylphosphane-2κP)ironplatinum(Fe—Pt), [(OC)2Fe(μ-dppm){μ-C(=O)C(4-MeC6H4SCH2)=CCH2SC6H4Me-4}Pt(PPh3)]

Acta Crystallographica Section E: Crystallographic Communications

卷:76

Ahmed Said Mohamed¹  Michael Knorr²  Isabelle Jourdain²  Lukas Brieger³  Carsten Strohmann³ 

[1] Centre D'Etude et de Recherche de Djibouti, Djibouti;

[2] Institut UTINAM UMR 6213 CNRS, Université Bourgogne Franche-Comté, 16 Route de Gray, 25030 Besançon, France;

[3] Institute for Inorganic Chemistry, Faculty of Chemistry and Chemical Biology, TU Dortmund University, Otto-Hahn Str. 6, 44227 Dortmund, Germany;

关键词: crystal structure;    internal alkyne;    iron;    platinum;    heterobimetallic;    metal–metal bond;    dimetallcyclopentenone;    bis(diphenylphosphino)methane;    thioether;    hydrogen bonding;   

DOI  :  10.1107/S2056989020007859

来源: DOAJ

【 摘 要 】

The title compound, [FePt(C19H18OS2)(C18H15P)(C25H22P2)(CO)2], 1, [(OC)2Fe(μ-dppm)(μ-C(=O)C(CH2SC6H4Me-4)=CCH2SC6H4Me-4)Pt(PPh3)], represents the first example of a diphosphane-bridged heterobimetallic Fe—Pt dimetallacyclopentenone complex resulting from a bimetallic activation of metal-coordinated carbonyl ligand with an internal alkyne, namely 1,4-bis(p-tolylthio)but-2-yne. The bridging μ2-C(=O)C(CH2SC6H4Me-4)=CCH2SC6H4Me-4 unit (stemming from a carbon–carbon coupling reaction between CO and the triple bond of the alkyne dithioether) forms a five-membered dimetallacyclopentenone ring, in which the C=C bond is π-coordinated to the Fe center. The latter is connected to the Pt center through a short metal–metal bond of 2.5697 (6) Å.

【 授权许可】

Unknown