Design, synthesis, and carbon-heteroatom coupling reactions of organometallic nickel(IV) complexes

Author:

Camasso Nicole M.1,Sanford Melanie S.1

Affiliation:

1. Department of Chemistry, University of Michigan, 930 North University Avenue, Ann Arbor, MI 48109, USA.

Abstract

Taking advantage of four for a nickel Metal atoms change their oxidation state—i.e., lose or gain electrons—relatively easily. This is a major reason why metal compounds accelerate so many chemical reactions. Camasso and Sanford now report a straightforward way to prepare complexes of nickel in the +4 oxidation state, based on careful tuning of the coordination environment around the metal center (see the Perspective by Riordan). These complexes could prove useful in coupling carbon to oxygen, nitrogen, or sulfur, and complement more traditional nickel catalysts that operate in lower oxidation states. Science , this issue p. 1218 ; see also p. 1203

Funder

NSF

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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