Abstract
Over the last fifty years, the use of nickel catalysts for facilitating organic transformations has
skyrocketed. Ni(0) sources act as useful precatalysts because they can enter a catalytic cycle through
ligand exchange, without needing to undergo additional elementary steps. However, most Ni(0)
precatalysts are synthesized with stoichiometric aluminum–hydride reductants, pyrophoric reagents that
are not atom-economical and must be used at cryogenic temperatures. Here, we demonstrate that Ni(II)
salts can be reduced on preparative scale using electrolysis to yield a variety of Ni(0) and Ni(II) complexes
that are widely used as precatalysts in organic synthesis, including bis(1,5-cyclooctadiene)nickel(0)
[Ni(COD)2]. This method overcomes the reproducibility issues of previously reported methods by
standardizing the procedure, such that it can be performed anywhere in a robust manner. It can be easily
transitioned to large scale through an electrochemical recirculating flow process. We anticipate that this
work will accelerate adoption of preparative electrochemistry for the synthesis of low-valent
organometallic complexes in academia and industry.
Supplementary materials
Title
Supporting Info
Description
Experimental details and procedures, optimization data, and copies of NMR spectra
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