phosphane, P(C7H7)3, as a Tripodal Tetradentate Ligand in Cationic, Five-coordinate Complexes of Platinum(II) and Palladium(II)

نویسندگان

  • Max Herberhold
  • Thomas Schmalz
  • Wolfgang Milius
  • Bernd Wrackmeyer
چکیده

Chloride abstraction, using AgPF6, from tri(1cyclohepta-2,4,6-trienyl)phosphane platinum and palladium dichloride, [P]MCl2 [M = Pt (1), Pd (2)], affords the complexes {[P]MCl}PF6 [M = Pt (3), Pd (4)] in good yields. The central metal is coordinated by the chloro ligand, the phosphorus atom and by three η2-C=C units, one of each C7H7 ring. This assignment of a highly symmetrical C3v structure is based on a consistent set of NMR data (1H, 13C, 31P, 195Pt NMR), in agreement with NMR data of the corresponding known neutral iridium and rhodium complexes [P]MCl [M = Ir (5), Rh (6)]. The chemical shift δ103Rh of 6 was determined, and a nearly linear relationship δ195Pt / δ103Rh was established.

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Platinum(II) and Palladium(II) Dichalcogenolene Complexes Containing the Ligand Tri(1-cyclohepta-2,4,6-trienyl)phosphane. Molecular Structure, Intramolecular Dynamics in Solution, and the Absolute Signs of Coupling Constants

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تاریخ انتشار 2002