Affiliation:
1. Division of Applied Chemistry Graduate School of Engineering Hokkaido University Sapporo Hokkaido 060-8628 Japan
2. Institute for Chemical Reaction Design and Discovery (WPI-ICReDD) Hokkaido University Sapporo Hokkaido 060-0021 Japan
Abstract
AbstractThe combination of a nickel(II) catalyst and a mechanoredox catalyst under ball‐milling conditions promotes mechanical‐force‐driven C−N cross‐coupling reactions. In this nickel(II)/mechanoredox cocatalyst system, the modulation of the oxidation state of the nickel center, induced by piezoelectricity, is used to facilitate a highly efficient aryl‐amination reaction, which is characterized by a broad substrate scope, an inexpensive combination of catalysts (NiBr2 and BaTiO3), short reaction times, and an almost negligible quantity of solvents. Moreover, this reaction can be readily up‐scaled to the multi‐gram scale, and all synthetic operations can be carried out under atmospheric conditions without the need for complicated reaction setups. Furthermore, this force‐induced system is suitable for excitation‐energy‐accepting molecules and poorly soluble polyaromatic substrates that are incompatible with solution‐based nickel(II)/photoredox cocatalysts.
Funder
Japan Society for the Promotion of Science London
Japan Science and Technology Corporation
Cited by
1 articles.
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