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Chemistry. 2008;14(29):8980-5. doi: 10.1002/chem.200801089.

P--P bond cleavage of tetraphenyltetraphosphane-1,4-diide facilitated by nickel(0).

Chemistry (Weinheim an der Bergstrasse, Germany)

Santiago Gómez-Ruiz, Stefan Zahn, Barbara Kirchner, Winfried Böhlmann, Evamarie Hey-Hawkins

Affiliations

  1. Institut für Anorganische Chemie der Universität Leipzig, Johannisallee 29, 04103 Leipzig, Germany.

PMID: 18712742 DOI: 10.1002/chem.200801089

Abstract

One equivalent of [Na2(thf)5-(P4Ph4)] (1) reacts with one equivalent of [Ni(cod)2] (cod=1,5-cyclooctadiene) to give the unexpected ionic compound [Na(Et2O)3][Na3(Et2O)2Ni3(micro-P2Ph2)2-(P2Ph2)3] (2), whereas the reaction of [Ni(cod)2] with the less reactive [K2(pmdeta)2(P4Ph4)] (3) leads to the formation of [K(pmdeta)]2[Ni(P4Ph4)-(P2Ph2)] (4) (PMDETA=NMe(CH2CH2NMe2)2), in which K--Ni interactions are observed. The calculations for 4 confirm the structural parameters obtained by X-ray diffraction studies. A shared electron number (SEN) analysis was applied to investigate the K...Ni interactions. These studies indicate a SEN value of a typical three-center, two-electron bond for K1-Ni-K2 indicating a covalent contribution in the interaction between nickel and potassium.

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