Triphenylphosphine-stabilized diphenyl-arsenium, -stibenium, and -bismuthenium salts

Nathan L. Kilah, Simon Petrie, Robert Stranger*, J. Wolfram Wielandt, Anthony C. Willis, S. Bruce Wild

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    47 Citations (Scopus)

    Abstract

    Two series of triphenylphosphine-stabilized diphenyl-arsenium, -stibenium, and -bismuthenium salts of the types [(Ph3P)EPh2]PF 6 (where E = As, Sb, Bi) and [(Ph3P)2EPh 2]PF6 (where E = Sb, Bi) have been synthesized and their structures and bonding investigated by X-ray crystallography and density functional theory at the PBE/TZP level. The coordination geometries around the central group 15 elements are distorted trigonal pyramidal in the mono(triphenylphosphine) complexes and distorted trigonal bipyramidal in the bis(triphenylphosphine) complexes, where in each case the stereochemically active lone pair of the six-electron, angular diphenyl-arsenium, -stibenium, or -bismuthenium ion occupies an equatorial position in the trigonal plane containing the C-E-C bonds. For the complexes [(Ph3P)EPh 2]-PF6 (E = As, Sb, Bi), the theoretical results for the cations are consistent with the dative covalent formulation [Ph 3P→EPh2]+, especially for E = As and Sb, but for [(Ph3P)2EPh2]PF6 (E = Sb, Bi) the bonding between the phosphines and the stibenium or bisthmuthenium ion is best described as an induced dipole-ion interaction.

    Original languageEnglish
    Pages (from-to)6106-6113
    Number of pages8
    JournalOrganometallics
    Volume26
    Issue number25
    DOIs
    Publication statusPublished - 3 Dec 2007

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