Abstract

The two-step mechanochemical preparation of carbene-pyridine complexes of palladium and platinum is reported. The organometallic products, which represent a class of commercially available catalysts, are rapidly formed in excellent yield proving solvent-free synthesis to be a viable synthetic alternative even in the case of NHC-containing compounds.

Highlights

  • The two-step mechanochemical preparation of carbene–pyridine complexes of palladium and platinum is reported

  • The organometallic products, which represent a class of commercially available catalysts, are rapidly formed in excellent yield proving solvent-free synthesis to be a viable synthetic alternative even in the case of NHCcontaining compounds

  • Solid state synthesis of organometallic adducts dates back almost 50 years,[3] little progress has been made in this field since

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Summary

Introduction

The two-step mechanochemical preparation of carbene–pyridine complexes of palladium and platinum is reported. Our group has previously reported solid-state syntheses of transition-metal coordination complexes in which target species can be formed rapidly and quantitatively by grinding together appropriate starting materials.

Results
Conclusion

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