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The Bimetallic Activation of White Phosphorus by trans-[RhCl(CO)(dppm)]2 Results in a Tetrahedro-Rh2P2 Moiety

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Abstract

The reaction of trans-[RhCl(CO)(dppm)]2 with P4 carried out at room temperature showed that bimetallic cooperation resulted in the cleavage of P4, giving a μ,η2-P2 (μ-κ22-P2) ligand coordinated to the two metal centres. The new complex cis-[Rh2(CO)2(μ-dppm)2(μ,η2-P2)] has been fully characterised in solution by NMR spectroscopy and in the solid state by single-crystal X-ray diffraction. The Rh–Rh distance of 2.723(18) Å is consistent with the presence of a metal–metal single bond, which was supported by theoretical analysis showing that the HOMO of the complex has metal–metal bond character. A literature survey revealed that, in most cases, the P2 unit acts as a P24– ligand, and also in the case at hand the diphosphenyl ligand behaves as an eight-electron donor with all the π* combinations occupied and donates into four empty metal combinations.

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