Distortion of cyclopentadienyl rings in cyclopentadienyl-palladium complexes: crystal structures of [Pd(C5H5)Cl(PMe2Ph)] and [Pd(C5H5)(Ph2PCH2CH2PPh2)][PF6]

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Cross, R.J. and Hoyle, R.W. and Kennedy, A.R. and Manojlovic-Muir, L.J. and Muir, K.W. (2001) Distortion of cyclopentadienyl rings in cyclopentadienyl-palladium complexes: crystal structures of [Pd(C5H5)Cl(PMe2Ph)] and [Pd(C5H5)(Ph2PCH2CH2PPh2)][PF6]. Journal of Organometallic Chemistry, 468 (1-2). pp. 265-271. ISSN 0022-328X (http://dx.doi.org/10.1016/0022-328X(94)80059-6)

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Abstract

The structures of [Pd(C5H5)Cl(PMe2Ph)] and [Pd(C5H5(dppe)]PF6(dppe = Ph2PCH2CH2PPh2) have been determined by X-ray analysis. Both are μ5-cyclopentadienyl compounds, with the Cp ring nearly perpendicular to the PdPCl or PdP2 plane. Comparison of their molecular geometries with those of other cyclopentadienyl-palladium complexes of the types PdCpLL′ and PdCpL2 reveals the existence of a complete range of ring-PdLL′ or ring-PdL2 orientations and suggests that the usual assignment of structures of these types as either staggered or eclipsed is not realistic. Likewise, the patterns of long and short C---C bonds of the Cp rings do not in general follow the sequences expected for the idealized geometries, although large librational distortions of the C5H5 rings in most of the compounds limit the accuracy of these determinations. The lengths of the Pd---C(Cp) bonds appear to be much more dependent on the relative trans influences of L and L′ than on the ring orientations.

ORCID iDs

Cross, R.J., Hoyle, R.W., Kennedy, A.R. ORCID logoORCID: https://orcid.org/0000-0003-3652-6015, Manojlovic-Muir, L.J. and Muir, K.W.;
  • Item type:Article
    ID code:1323
    Dates:
    Date
    Event
    12 April 2001
    Published
    Subjects:Science > Chemistry
    Department:Faculty of Science > Pure and Applied Chemistry
    Depositing user:Users 45 not found.
    Date deposited:28 Jun 2006
    Last modified:11 Nov 2024 08:19
    URI:https://strathprints.strath.ac.uk/id/eprint/1323
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