[η(5)-cyclopentadienyl-η(3)-allyl(acetonitrile)rhodium] tetrafluoroborate | 171977-52-9

• 英文名称: [η(5)-cyclopentadienyl-η(3)-allyl(acetonitrile)rhodium] tetrafluoroborate
• CAS: 171977-52-9
• 化学式: BF₄*C₁₀H₁₃NRh
• 分子量: 336.93
• InChiKey: DPKJPAAJXUTFPW-UHFFFAOYSA-N

反应信息

• 作为产物：
  描述：

  silver tetrafluoroborate 、 (η(5)-cyclopentadienyl-η(3)-allyl)chloridorhodium 、 乙腈 以89.9%的产率得到[η(5)-cyclopentadienyl-η(3)-allyl(acetonitrile)rhodium] tetrafluoroborate
  参考文献：
  名称：

  Synthesis and investigation of mono- and binuclear cyano-bridged complexes of rhodium, ruthenium, and palladium

  摘要：

  Binuclear Rh-III and Ru-II complexes of the [M(1)-CN-M(2)](BF4-)-B-+ (M(1) and/or M(2) are (eta(5)-Cp)(eta(3)-C3H5)Rh and (eta(6)-C6H6)(eta(3)-C3H5)Ru) type, heteronuclear organometallic compound (eta(5)-CP)(eta(3)-C3H5)RhCNPd(eta(3)-C3H5)Cl, and mononuclear Rh-III and Ru-II complexes [(eta(3)-C3H5)LM(MeCN)](BF4-)-B-+ (M = Rh, L = eta(5)-Cp; M = Ru, L = eta(6)-C6H6) were synthesized. An electrochemical study of these compounds in solutions demonstrates that the bond between the bridged CN ligand and the metal atoms is rather strong, and there is no dissociation into mononuclear fragments in solutions. The kinetics of the reaction of [(eta(5)-Cp)(eta(3)-C3H5)Rh(MeCN)](BF4-)-B-+ with halide ions was studied by electrochemical methods. The ligand exchange proceeds by a bimolecular dissociative-exchange mechanism.

  DOI：

  10.1007/bf00696933