Abstract

The reaction of [Ru 3(CO) 10(μ-dppm)] ( 1) with dppmSe at 66 °C affords [Ru 3(CO) 8(μ-dppm) 2] ( 2), [Ru 3(CO) 7(μ 3-CO)(μ 3-Se)(μ-dppm)] ( 3), [Ru 3(CO) 5(μ 3-CO)(μ 3-Se)(μ-dppm) 2] ( 4) and [Ru 3(CO) 6(μ 3-CO)(μ 3-Se)(μ-dppm)(η 1-Ph 2PCH 2P( O)Ph 2)] ( 5) in 7%, 5%, 9% and 33% yields, respectively. A similar reaction between 1 with dppmS gives [Ru 3(CO) 7(μ 3-S) 2(μ-dppm)] ( 6), [Ru 3(CO) 7(μ 3-CO)(μ 3-S)(μ-dppm)] ( 7) [Ru 3(CO) 5(μ 3-CO)(μ 3-S)(μ-dppm) 2] ( 8) and [Ru 3(CO) 6(μ 3-CO)(μ 3-S)(μ-dppm)(η 1-Ph 2PCH 2P( O)Ph 2)] ( 9) in 8%, 7%, 14% and 35% yields, respectively. Treatment of 1 with PhSeSePh at 66 °C affords the dinuclear compound [Ru 2(CO) 4(μ-SePh) 2(μ-dppm)] ( 10) in 14% yield. Thermolysis of 5 and 9in refluxing toluene at 110 °C gives 4 and 8, respectively. The molecular structures of 4, 9 and 10 have been determined by single-crystal X-ray diffraction studies. The cores of the new clusters 4, 5, 8 and 9 consist of metal triangles capped by μ 3-sulfur or selenium atoms with the bidentate ligand bridging in equatorial positions. In compounds 4 and 8, two bidentate dppm ligands bridge the Ru 3 triangle in such a way that each ligand bridges two ruthenium atoms and one Ru–Ru edge remains unbridged. Compounds 5 and 9 contain one bridging dppm ligand and one dangling dppm mono-oxide ligand Ph 2PCH 2P( O)Ph 2 coordinated to the rear metal atom at an equatorial position. The molecular structure of 10 shows classical “sawhorse” structure with two bridging SePh ligands as well as the dppm ligand.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.