Reaction of the Organometallic Planar Tetracoordinate Carbon Compound [(Cp<sub>2</sub>Zr)<sub>2</sub>(μ-C⋮CCH<sub>3</sub>)(μ-(η<sup>1</sup>-C:η<sup>2</sup>-C,C)-CH<sub>3</sub>CCCH<sub>3</sub>)]<sup>+</sup>[BPh<sub>4</sub>]<sup>-</sup> with Alkyl Isocyanides

Dirk Röttger, Jörg Pflug, Gerhard Erker, Sirpa Kotila, Roland Fröhlich

Organometallics · 1996 · 13 citations · 7 references

Concepts

Abstract

The [(Cp 2 Zr) 2 (μ-CH 3 CCCH 3 )(μ-C⋮CCH 3 )] + BPh 4 - complex ( 4 ) reacts readily with alkyl isocyanides RN⋮C by displacement of the bridging 2-butyne ligand to give the cationic [(μ-acetylide)(μ-isonitrile)(Cp 2 Zr) 2 ] complexes 6a − c in high yield (∼80%). The X-ray crystal structure analysis of an example ( 6c ) revealed the μ-(η 1 -C:η 2 -C,N) coordination of the isonitrile ligand.

References

7