Electron Shuttle in <i>N</i>-Heteroaromatic Ni Catalysts for Alkene Isomerization
Maxime Tricoire, Ding Wang, Thayalan Rajeshkumar, Laurent Maron, Grégory Danoun, Grégory Nocton
Abstract
High Resolution Image Download MS PowerPoint Slide Simple N -heteroaromatic Ni(II) precatalysts, (L)NiMe 2 (L = bipy, bipym), were used for alkene isomerization. With an original reduction method using a simple borane (HB(Cat)), a low-valent Ni center was formed readily and showed good conversion when a reducing divalent lanthanide fragment, Cp* 2 Yb, was coordinated to the (bipym)NiMe 2 complex, a performance not achieved by the monometallic (bipy)NiMe 2 analogue. Experimental mechanistic investigations and computational studies revealed that the redox non-innocence of the L ligand triggered an electron shuttle process, allowing the elusive formation of Ni(I) species that were central to the isomerization process. Additionally, the reaction occurred with a preference for mono-isomerization rather than chain-walking isomerization. The presence of the low-valent ytterbium fragment, which contributed to the formation of the electron shuttle, strongly stabilized the catalysts, allowing catalytic loading as low as 0.5%. A series of alkenes with various architectures have been tested. The possibility to easily tune the various components of the heterobimetallic catalyst reported here, the ligand L and the divalent lanthanide fragment, opens perspectives for further applications in catalysis induced by Ni(I) species.