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A Study of Unsaturated Pyrazolate-Bridged Diruthenium Carbonyl Complexes

  • Yi-Hwa Song
  • , Yun Chi
  • , Yao-Lun Chen
  • , Chao-Shiuan Liu
  • , Wei-Li Ching
  • , Arthur J. Carty
  • , Shie-Ming Peng
  • , Gene-Hsiang Lee

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

Abstract

The reaction of Ru3(CO)12 with approximately 3 equiv of 3,5-di-tert-butylpyrazole, (dbpz)H, in hexane at 170 °C in a stainless steel autoclave afforded the unsaturated, pyrazolate-bridged diruthenium complex [Ru2(CO)5(dbpz)3] (2). The spectroscopic and structural analysis indicated that this compound contains a vacant coordination site at one axial position trans to the Ru-Ru linkage. This compound reacted with CO at room temperature to give the saturated complex [Ru2(CO)6(dbpz)2] (1b); its structure is analogous to that of the previously determined complexes [Ru2(CO6(pz)2], pz = pyrazolate and 3,5-dimethyl pyrazolate, except that the equatorial CO ligands show a skew arrangement, an indication of steric constraints within the coordination sphere. Treatment of 2 with benzyl isocyanide or with pyridine in toluene leads to the formation of substitution products [Ru2(CO)4(L)(dbpz)2], L = CNCH2Ph and pyridine, in which the incoming donor ligand occupies an equatorial position at the saturated Ru center. The structural significance of this pyrazolate-bridged diruthenium complex 2 is discussed.
Original languageEnglish
Pages (from-to)4735-4742
JournalOrganometallics
Volume21
Issue number22
Online published1 Oct 2002
DOIs
Publication statusPublished - 28 Oct 2002
Externally publishedYes

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