Ligand Centered Reactivity of a Transition Metal Bound Geometrically Constrained Phosphine

We report on the electronic properties, coordination chemistry and reactivity of metal complexes of a planar acridane-derived geometrically constrained phosphine, P(NNN). Despite no longer exhibiting a constrained geometry when coordinated to metal centres, the P(NNN) phosphine retains its ability to activate polar E−H bonds (including those of amines and ammonia).

Abstract

The electronic properties, coordination chemistry and reactivity of metal complexes of a planar (C _2v symmetric) acridane-derived geometrically constrained phosphine, P(NNN), are described. On complexation to metal centers, the phosphine was found to adopt a distorted trigonal pyramidal structure with a high barrier to pyramidal inversion (22.3 kcal/mol at 298 K for Au[P(NNN)]Cl). Spectroscopic data and theoretical calculations carried out at the density functional level of theory indicate that P(NNN) is a moderate σ-donor, with significant π-acceptor properties. Despite the distortion undergone by the phosphorus atom on coordination to metal centers, the P(NNN) ligand retains its ability to react with small molecule substrates with polar E−H bonds (MeOH, NH₂Ph, NH₃). It does so in a concerted fashion across one of the P−N bonds, and reversibly in the case of amine substrates. This cooperative bond activation chemistry may ultimately prove beneficial in catalysis.

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