Abstract
This article presents the synthesis and characterization of a series of robust high-valent organometallic nickel (Ni) complexes stabilized by a functionalized PC(sp3)P pincer ligand. Notably, the nickel center, covalently confined within the 3D ligand framework, demonstrates predictable coordination and redox behavior, coupled with remarkable stability across oxidation states +2, +3, and +4. These states were found to interconvert via one-electron transfer reactions. Among these complexes, the Ni(III)-PC(sp3)P species was identified as an efficient catalyst for the mild and selective hydrosilylation of alkenes, operating through a nonoxidative reaction mechanism.
| Original language | English |
|---|---|
| Article number | e202500618 |
| Journal | Chemistry - A European Journal |
| Volume | 31 |
| Issue number | 28 |
| DOIs | |
| State | Published - 19 May 2025 |
Bibliographical note
Publisher Copyright:© 2025 Wiley-VCH GmbH.
Keywords
- csp3-carbometalated
- high-valent
- hydrosilylation
- nickel
- pincer complexes