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
Summary
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.
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