Dinuclear ruthenium and iron complexes containing palladium and platinum with tri-tert-butylphosphine ligands: synthesis, structures, and bonding
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Updated: Aug 23, 2026

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
Published on: April 10, 2015
Richard D Adams1, Burjor Captain, Wei Fu
1Department of Chemistry and Biochemistry and the USC NanoCenter, University of South Carolina, Columbia, SC 29208, USA. Adams@mail.chem.sc.edu
Abstract:
The reaction of Pd(PBu(t)(3))(2) with Ru(CO)(5) yielded the dipalladium-diruthenium cluster complex Ru(2)(CO)(9)[Pd(PBu(t)(3))](2), 10. The reaction of Pt(PBu(t)(3))(2) with Ru(CO)(5) at room temperature afforded the diplatinum-diruthenium cluster complex Ru(2)(CO)(9)[Pt(PBu(t)(3))](2), 12, and the monoplatinum-diruthenium cluster PtRu(2)(CO)(9)(PBu(t)(3)), 11. All three complexes contain a diruthenium group with bridging Pd(PBu(t)(3)) or Pt(PBu(t)(3)) groups. Compound 11 can be converted to 12 by reaction with an additional quantity of Pt(PBu(t)(3))(2). The reaction of 12 with hydrogen at 68 degrees C yielded the dihydrido complex Pt(2)Ru(2)(CO)(8)(PBu(t)(3))(2)(micro-H)(2), 13. This complex contains a Ru(2)Pt(2) cluster with hydride ligands bridging two of the Ru-Pt bonds. The reaction of Fe(2)(CO)(9) with Pt(PBu(t)(3))(2) yielded the platinum-diiron cluster complex PtFe(2)(CO)(9)(PBu(t)(3)), 14, which is analogous to 11. All new complexes were characterized crystallographically. Molecular orbital calculations of 10 reveal an unusual delocalized metal-metal bonding system involving the Pd(PBu(t)(3)) groups and the Ru(2)(CO)(9) group.
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