η6-Coordination of a ruthenium(II) organometallic fragment to the arene ring of N,C,N-pincer metal complexes

Publication date

2008

Authors

Bonnet, S.A.
Lutz, M.ORCID 0000-0003-1524-9629ISNI 0000000352600916
Spek, A.L.ISNI 0000000389231413
van Koten, G.ISNI 0000000389131797
Klein Gebbink, R.J.M.ISNI 0000000388707889

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Abstract

Stable heterobimetallic complexes of the type [MX(NCN)Ru(C5R5)]+ (R = H or Me), where the phenylene ring of an NCN-pincer ligand coordinates first to a platinum or palladium center via a σ-bond, and second to a ruthenium organometallic fragment via a π-bond, are synthesized in a single step involving electrophilic attack of a cationic Ru species on the aryl metal complex. X-ray crystal structures and solution NMR agree on the simultaneous presence of orthogonal η6- and η1-coordination axes. 195Pt NMR and electrochemistry show that the η6-coordinated ruthenium fragment has a strong electron-withdrawing effect on the pincer metal, which leads to a diminished nucleophilicity of the platinum center toward electrophiles such as SO2.

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Bonnet, S A, Lutz, M, Spek, A L, van Koten, G & Klein Gebbink, R J M 2008, 'η6-Coordination of a ruthenium(II) organometallic fragment to the arene ring of N,C,N-pincer metal complexes', Organometallics, vol. 27, no. 2, pp. 159-162.