From Dimethylamine to Pyrrolidine: The Development of an Improved Nickel Pincer Complex for Cross-Coupling of Nonactivated Secondary Alkyl Halides
Replacement of a dimethyl amino group of the amidobis(amine) nickel(II) pincer complex (1), [((N2N)-N-Me)-Ni-Cl], by a pyrrolidino group resulted in a new nickel(II) pincer complex (2), [((PNNN)-N-yr-N-Me)Ni-Cl]. Complex 2 is an efficient catalyst for Kumada and Suzuki-Miyaura cross-coupling of nonactivated secondary alkyl halides, while complex 1 is largely inactive. The significant activity difference is tentatively attributed to a minimal structural difference, which leads to a more hemilabile ligand.
Pyrrolidine_ACS-rev-Hu1.pdf
openaccess
158.32 KB
Adobe PDF
31d8586d3dfb6e5124938ae23b087f4b
Pyrrolidine_ACS_SI-rev-hu1.pdf
openaccess
2.5 MB
Adobe PDF
3b66d9ff2097edb05e91e30fae2d3e81