Chelating P,N versus P,P Ligands: Differing Reactivity of Donor-Stabilized Pt(η<sup>2</sup>-PhC⋮CPh) Complexes Toward Diphenylacetylene
作者:Christian Müller、Rene J. Lachicotte、William D. Jones
DOI:10.1021/om010924a
日期:2002.3.1
The thermal activation of the eta(2)-diphenylacetylene complex (PN)Pt(eta(2)-PhC=CPh) (1) (PN = (diisopropylphosphinodimethylamino)ethane leads to the formation of the platinacyclopenta-2,4-diene compound (PN)Pt(CPh)(4) (3), which can be quantitatively obtained by reaction of 1 with 1 equiv of diphenylacetylene. Two transient intermediates are observed by P-31 NMR spectroscopy during the course of the latter reaction. These species were independently synthesized and characterized. Hexaphenylbenzene is catalytically generated by reaction of 1 in the presence of excess diphenylacetylene. In contrast, no reaction of diphenylacetylene with (dippe)Pt(eta(2)-PhC=CPh) (2) (dippe = bis(diisopropylphosphino)ethane) was observed.